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Mônica Barbosa De Melo

Dados pessoais

  • HS Health Sciences
  • LS Life Sciences
  • MU Multidisciplinary
  • PS Physical Sciences
  • SH Social Sciences & Humanities
# Nome Links Grande Área Área
1 Carlos Alberto LONGUI Ciências da Saúde Medicina
2 Cristiane KOCHI Ciências da Saúde Medicina
3 Fernando CENDES Ciências da Saúde Medicina
4 Iscia Teresinha Lopes CENDES Ciências Biológicas Genética
5 José Paulo Cabral De VASCONCELLOS Ciências da Saúde Medicina
6 Keila Miriam Monteiro De CARVALHO Ciências da Saúde Medicina
7 Kleber Yotsumoto FERTRIN Ciências da Saúde Medicina
8 Marcelo Ribeiro Da Silva BRIONES Ciências Biológicas Microbiologia
9 Osmar MONTE Ciências da Saúde Medicina
10 Sofia Helena Valente De Lemos MARINI Ciências da Saúde Medicina
11 Vera Lúcia Gil Da Silva LOPES Ciências Biológicas Genética
Figura 1. Número de publicações por ano e por tipo, considerando todas as publicações.
  1. Life Sciences Cell Biology
    Ana Carolina Lima CAMARGO; Victor De Haidar E BERTOZZO; Costa Sueli MS; Júlia Nicoliello Pereira De CASTRO; Thiago Adalton Rosa RODRIGUES et al. 2023. Comparative transcriptome analysis of endothelial colony-forming cells from hbsc and hbss patients with sickle cell retinopathy. In: 26th human genome meeting ? hugo. Brasil.
  2. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Ana Carolina Lima CAMARGO; Júlia Nicoliello Pereira De CASTRO; Victor De Haidar E BERTOZZO; Costa Sueli MS; Thiago Adalton Rosa RODRIGUES et al. 2023. Identification of potential transcription factors and micrornas associated with proliferative sickle cell retinopathy in hbsc and hbss patients using in silico analyses. In: X-meeting / bsb 2023. Brasil.
  3. Life Sciences Cell Biology
    Júlia Nicoliello Pereira De CASTRO; Costa Sueli MS; Mirta Tomie ITO; Ana Carolina Lima CAMARGO; Souza B B et al. 2023. In-silico comparison of potentially secreted proteins from endothelial colony-forming cells in ischemic stroke and sickle cell anemia. In: X-meeting / bsb 2023. Brasil.
  4. Health Sciences Medicine (miscellaneous)
    Júlia Nicoliello Pereira De CASTRO; Costa Sueli MS; Ana Carolina Lima CAMARGO; Mirta Tomie ITO; Souza B B et al. 2023. Prediction of regulatory factors of differentially expressed genes in sickle cell anemia and ischemic stroke. In: 26th human genome meeting ? hugo. Brasil.
  5. Health Sciences Infectious Diseases
    Thiago Adalton Rosa RODRIGUES; Yuri De Carvalho Oiamore SILVA; Júlia Nicoliello Pereira De CASTRO; Ana Carolina Lima CAMARGO; Souza B B et al. 2023. Association variants at the afap1 (rs4619890); and tmco1 (rs2814471) as a risk factor for primary open-angle glaucoma development in a brazilian cohort. In: 26th human genome meeting ? hugo. Brasil.
  6. Life Sciences Neuroscience (miscellaneous)
    Thiago Adalton Rosa RODRIGUES; Souza B B; Victor De Haidar E BERTOZZO; Júlia Nicoliello Pereira De CASTRO; Ana Carolina Lima CAMARGO et al. 2023. Associação da variante rs7137828 (atxn2) com o desenvolvimento de gpaa e aumento da relação escavação/disco vertical em uma amostra da população brasileira. In: Simpósio de pós-graduação em oftalmologia - 11ª. jornada paulista de oftalmologia;. Brasil.
  7. Life Sciences Genetics
    Ana Vitória Volpato JENSEN; Thiago Adalton Rosa RODRIGUES; Ana Carolina Lima CAMARGO; Ana Rafaela Carvalho MONTE; Gabrielle Maria Giovanna Da Silva GONÇALVES et al. 2023. Evaluation of rs7426380 in the efemp1 gene as a risk factor for primary open-angle glaucoma development in a brazilian cohort. In: 26th human genome meeting ? hugo. Brasil.
  8. Life Sciences Genetics
    Mônica Barbosa De MELO; Thiago Adalton Rosa RODRIGUES; Souza B B; Victor De Haidar E BERTOZZO; Júlia Nicoliello Pereira De CASTRO et al. 2022. Association of variants in the foxc1 ; atxn2 and txnrd2 genes with primary open angle glaucoma in a brazilian population. In: Arvo annual meeting. Estados Unidos.
  9. Life Sciences Cell Biology
    Júlia Nicoliello Pereira De CASTRO; Costa Sueli MS; Ana Carolina Lima CAMARGO; Mirta Tomie ITO; Souza B B et al. 2022. Transcriptomic analysis of circulating endothelial colony-forming cells in patients with sickle cell anemia and ischemic stroke. In: American society of human genetics annual meeting. Estados Unidos.
  10. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Ana Carolina Lima CAMARGO; Victor De Haidar E BERTOZZO; Costa Sueli MS; Júlia Nicoliello Pereira De CASTRO; Thiago Adalton Rosa RODRIGUES et al. 2022. Identification of fzd3 and sema3a as potentially secreted proteins involved in proliferative sickle cell retinopathy. In: American society of human genetics annual meeting. Estados Unidos.
  11. Life Sciences Cell Biology
    Júlia Nicoliello Pereira De CASTRO; Costa Sueli MS; Mirta Tomie ITO; Ana Carolina Lima CAMARGO; Souza B B et al. 2022. Transcriptomic-based secretome analysis of circulating endothelial colony-forming cells in patients with ischemic stroke and sickle cell anemia. In: Iii escola paranaense de bioinformática 2022. Brasil.
  12. Life Sciences Developmental Biology
    Ana Carolina Lima CAMARGO; Victor De Haidar E BERTOZZO; Costa Sueli MS; Júlia Nicoliello Pereira De CASTRO; Thiago Adalton Rosa RODRIGUES et al. 2022. Identification of mirnas associated with pathological angiogenesis in in proliferative sickle cell retinopathy. In: Iii escola paranaense de bioinformática 2022. Brasil.
  13. Life Sciences Genetics
    Mônica Barbosa De MELO; Manoel Vinicius Rocha ARAKI; Yuri De Carvalho Oiamore SILVA; Thiago Adalton Rosa RODRIGUES; Flavia Fialho BAJANO et al. 2021. Association of abca1 rs2472493 and gas7 rs9913911 variants with poag in a brazilian population. In: Association for research in visual and ophthalmology annual meeting. Estados Unidos.
  14. Life Sciences Genetics
    Rodrigues Thiago Adalton ROSA; Souza B B; Victor De Haidar E BERTOZZO; Júlia Nicoliello Pereira De CASTRO; Costa Vital P et al. 2021. Evaluation of genetic variants associated with primary open angle glaucoma in a brazilian population. In: Brazilian congress of genetics. Brasil.
  15. Life Sciences Neuroscience (miscellaneous)
    Victor De Haidar E BERTOZZO; Sueli Matilde Da Silva COSTA; Souza B B; Cruz P R S; Marina Gonçalves Monteiro VITURINO et al. 2021. Candidate genes involved in sickle cell retinopathy. In: 66th brazilian congress of genetics. Brasil.
  16. Life Sciences Genetics
    Vasconcellos J P C; Yuri De Carvalho Oiamore SILVA; Thiago Adalton Rosa RODRIGUES; Francisco Carenzi Da SILVA; Mônica ALVES et al. 2020. Association of sall1 rs1362756 and six1/six6 rs33912345 variants with poag in a brazilian population. In: Association for reserach in vision and ophthalmology annual meeting. Estados Unidos.
  17. Health Sciences Pharmacology (medical)
    Mônica Barbosa De MELO; Marina Gonçalves Monteiro VITURINO; Neto Jamil M; Alicia B ROQUE; Gessica F S BORGES et al. 2020. Analysis of cfb (r32q - rs641153) and cfh (rs1410996) variants as risk factors for age-related macular degeneration in a brazilian population. In: Association for research in vision and ophthalmology annual meeting. Estados Unidos.
  18. Life Sciences Parasitology
    R PINTO; F GOMES; A MARTINI; Daniel BORGES; E BARBOSA et al. 2020. Quality of life in keratoconus: evaluation with keratoconus outcomes specific questionnaire (korq). In: Association for research in vision and ophthalmology annual meeting. Estados Unidos.
  19. Health Sciences Medicine (miscellaneous)
    E BARBOSA; A ELOY; A F BARBOSA; C TAVARES; R PINTO et al. 2020. Meibomian gland dysfunction and ocular surface findings in rosacea patients. In: Association for research in visual and ophthalmology annual meeting. Estados Unidos.
  20. Life Sciences Genetics
    Marcelo Luís OCCHIUTTO; Mônica Barbosa De MELO; José Paulo Cabral De VASCONCELLOS; Thiago Adalton Rosa RODRIGUES; Flavia Fialho BAJANO et al. 2020. Associação dos polimorfismos do gene apoe com glaucoma primário de ângulo aberto em uma amostra da população brasileira. In: 64º congresso brasileiro de oftalmologia. Brasil.
  21. Life Sciences Genetics
    Manoel Vinicius Rocha ARAKI; Yuri De Carvalho Oiamore SILVA; Thiago Adalton Rosa RODRIGUES; Flavia Fialho BAJANO; Rui Barroso SCHIMITI et al. 2020. Associação das variantes abca1 (rs2472493) e gas7 (rs9913911) com gpaa em uma população brasileira. In: 64º congresso brasileiro de oftalmologia. Brasil.
  22. Health Sciences Radiology, Nuclear Medicine and Imaging
    Mônica Barbosa De MELO; Marina Gonçalves Monteiro VITURINO; Jamil Miguel NETO; Alicia Buffoni ROQUE; Gessica F S BORGES et al. 2020. Analysis of cfb (r32q ? rs641153) and cfh (rs1410996) variants as risk factors for age-related macular degeneration in a brazilian population. In: 64º congresso brasileiro de oftalmologia. Brasil.
  23. Life Sciences Genetics
    Vasconcellos J P C; Yuri De Carvalho Oiamore SILVA; Thiago Adalton Rosa RODRIGUES; Francisco Carenzi Da SILVA; Rui Barroso SCHIMITI et al. 2020. Association of sall1 rs1362756 and six1/six6 rs33912345 variants with poag in a brazilian population. In: 64º congresso brasileiro de oftalmologia. Brasil.
  24. Life Sciences Cell Biology
    Svidnicki Paulo VINICIUS; Mônica Barbosa De MELO; José Paulo Cabral De VASCONCELLOS; Shi Song RONG; Anna LARSON et al. 2019. Apex 1 as a new candidate gene for glaucoma. In: Arvo annual meeting. Estados Unidos.
  25. Health Sciences Genetics (clinical)
    Gislene Pereira GIL; Galina ANANINA; Mariana MASCHIETTO; Sheila Soares LIMA; Sueli Matilde Da Silva COSTA et al. 2019. Altered dna methylation profile in placentas from pregnant women with sickle cell disease. In: 69th american society of human genetics annual meeting. Estados Unidos.
  26. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Gislene Pereira GIL; Ananina GALINA; Mariana MASCHIETTO; Baptista Letícia C; Da Silva Costa Sueli MATILDE et al. 2019. Dna methylation profile in placentas of sickle cell anemia women. In: International federation of placenta associations meeting; 2019. Estados Unidos.
  27. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Sueli Matilde Da Silva COSTA; Mirta Tomie ITO; Souza B B; Pedro Rodrigues Sousa Da CRUZ; Marina Gonçalves Monteiro VITURINO et al. 2018. Identification of candidate genes involved in proliferative sickle cell retinopathy by rnaseq. In: Association for research in vision and ophthalmology annual meeting. Estados Unidos.
  28. Health Sciences Medicine (miscellaneous)
    Mônica Barbosa De MELO; Mirta Tomie ITO; Sueli Matilde Da Silva COSTA; Baptista Letícia C; Gabriela Queila De Carvalho SIQUEIRA et al. 2018. Gene expression analysis of endothelial cells from sickle cell anemia patients and its relation with stroke. In: 68th american society of human genetics annual meeting. Estados Unidos.
  29. Health Sciences Genetics (clinical)
    Baptista Letícia C; Costa Maria LAURA; Souza B B; Costa F F; Mônica Barbosa De MELO. 2018. Transcriptome of placentas from two pregnancies of a patient with sickle cell disease. In: International congress of genetics. Brasil.
  30. Life Sciences Genetics
    Vasconcellos J P C; Souza B B; Jamil Miguel NETO; Ricardo Yuji ABE; Rui Barroso SCHIMITI et al. 2017. Snp rs11024102 in plekha7 as a risk factor for pacg development in a brazilian population. In: World glaucoma congress 2017. Holanda.
  31. Life Sciences Molecular Biology
    Gabriela Queila De Carvalho SIQUEIRA; Souza B B; Murilo Guimarães BORGES; Mirta Tomie ITO; Ananina GALINA et al. 2017. Exome sequencing of extreme phenotypes identifies potential novel genes as modifiers of leg ulcer in sickle cell anemia. In: American society of human genetics 67th annual meeting. Brasil.
  32. Life Sciences Genetics
    Milena Atique TACLA; Souza B B; Camila ZANGALLI; Daniela STANCATO; Ananina GALINA et al. 2017. Evaluation of genetic polymorphisms in the determination of optic disc parameters and circumpapillary retinal nerve fiber layer thickness in normal individuals in a sample of the brazilian population. In: American society of human genetics 67th annual meeting. Brasil.
  33. Health Sciences Genetics (clinical)
    Baptista Letícia C; Maria Laura COSTA; Surita Fernanda G; Parpinelli Mary A; Souza B B et al. 2017. Analysis of placenta transcriptome in patients with hemoglobin sc disease. In: 11th annual conference - academy for sickle cell and thalassemia - ascat. Brasil.
  34. Health Sciences Medicine (miscellaneous)
    Mirta Tomie ITO; Sueli Matilde Da Silva COSTA; Albuquerque Dulcinéia M; Baptista Letícia C; Gabriela Queila De Carvalho SIQUEIRA et al. 2017. Gene expression analysis of endothelial cells with stroke in sickle cell patients. In: Genética 2017 - brazilian-international congress of genetics. Brasil.
  35. Health Sciences Genetics (clinical)
    Jhonathan A A FERNANDEZ; Sueli Matilde Da Silva COSTA; Ana C CARNEIRO; Raquel A LAURIA; Souza B B et al. 2017. Novel compound heterozygous mutations in ush2a gene associated with usher syndrome type ii. In: Xvii workshop de genética. Brasil.
  36. Life Sciences Cell Biology
    Mônica Barbosa De MELO; Leticia De Carvalho BAPTISTA; Regiane FERREIRA; Fernanda SURITA; Dulcineia Martins ALBUQUERQUE et al. 2016. Expression profile of inflammatory genes in placenta from sickle cell disease patients. In: 13th international congress of human genetics. Brasil.
  37. Life Sciences Genetics
    Mônica Barbosa De MELO; Caique MARTINS; Mariana B OLIVEIRA; Sueli Matilde Da Silva COSTA; Vasconcellos J P C. 2016. Analysis of the col8a2 and slc4a11 genes and of the tgc intronic expansion in the tcf4 gene in families with fuchs endothelial corneal distrophy (fecd). In: American society of human genetics meeting. Brasil.
  38. Life Sciences Cell Biology
    Hugo Freire NUNES; Vasconcellos J P C; Iscia Teresinha Lopes CENDES; Benilton De Sá CARVALHO; Murilo Guimarães BORGES et al. 2015. Whole exome sequencing in a family with primary open angle glaucoma. In: American society of human genetics 65th annual meting. Estados Unidos.
  39. Health Sciences Infectious Diseases
    Mariana B OLIVEIRA; Vasconcellos J P C; Costa Vital P; Mônica Barbosa De MELO. 2015. Elevated il1-beta level in plasma is associated with primary open angle glaucoma in a brazilian population. In: Arvo 2015 annual meting. Estados Unidos.
  40. Life Sciences Cell Biology
    Pedro Rodrigues Sousa Da CRUZ; Galina ANANINA; Marcos André BEZERRA; Wagner M AVELAR; A C Amato FILHO et al. 2015. Characterizing brazilian sickle cell anemia patients. In: American society of human genetics 65th annual meting. Brasil.
  41. Life Sciences Neurology
    Souza B B; Vasconcellos J P C; Benilton De Sá CARVALHO; Murilo Guimarães BORGES; Patrícia Aline O R Aguiar ARAÚJO et al. 2015. Whole exome sequencing in a family with early onset primary angle-closure glaucoma. In: American society of human genetics 65th annual meting. Estados Unidos.
  42. Health Sciences Immunology and Allergy
    Paulo Vinícius SVIDNICKI; Vasconcellos J P C; Helber D Teles CALDEIRA; Mariana B OLIVEIRA; Hugo Freire NUNES et al. 2015. Exome sequencing analysis in a primary open angle glaucoma brazilian family. In: American society of human genetics 65th annual meting. Estados Unidos.
  43. Life Sciences Genetics
    Medina Flávio MACCORD; Augusto Lopes Alves Da MOTTA; Walter Y TAKAHASHI; Pedro Carlos CARRICONDO; Mario Martins Dos Santos MOTTA et al. 2014. Association of the y402h polymorphism of cfh gene with response of exudative amd to intravitreal vegf inhibitors in the brazilian population. In: Arvo 2014 annual meeting. Estados Unidos.
  44. Health Sciences Immunology and Allergy
    Mariana B OLIVEIRA; José Paulo Cabral De VASCONCELLOS; Vital Paulino COSTA; Mônica Barbosa De MELO. 2014. Inflammatory cytokines in aqueous humor and plasma are associated with primary open angle glaucoma in a brazilian population. In: Arvo 2014 annual meting. Estados Unidos.
  45. Health Sciences Genetics (clinical)
    Ana Luiza ARAÚJO; Eugênio Santana De FIGUEIREDO; Pedro Rodrigues Sousa Da CRUZ; Bruno Batista De SOUZA; Carlos Eduardo Leite ARIETA et al. 2014. Identification of structural alterations in the cx50 gene in patients with congenital cataracts. In: American society of human genetics 64th annual meeting. Estados Unidos.
  46. Life Sciences Genetics
    Mônica Barbosa De MELO; Galina ANANINA; Marcos André BEZERRA; Aderson S ARAÚJO; Cruz P R S et al. 2014. High degree of admixture in an urban brazilian population. In: American society of human genetics 64th annual meeting. Estados Unidos.
  47. Health Sciences Genetics (clinical)
    Vasconcellos J P C; Paulo Vinícius SVIDNICKI; Carolina Ayumi BRAGHINI; Mônica Barbosa De MELO. 2014. New mutations in the myoc gene in patients with juvenile open-angle glaucoma. In: American society of human genetics 64th annual meeting. Estados Unidos.
  48. Life Sciences Animal Science and Zoology
    Leticia De Carvalho BAPTISTA; Regiane FERREIRA; Fernanda SURITA; Mary Angela PARPINELLI; Kleber Y FERTRIN et al. 2014. Alteração na expressão de genes relacionados à inflamação na placenta de paciente com anemia falciforme. In: Congresso brasileiro de hematologia; hemoterapia e terapia celular - hemo 2014. Brasil.
  49. Life Sciences Genetics
    Leticia De Carvalho BAPTISTA; Fertrin K Y; Regiane FERREIRA; Carolina LANARO; Dulcineia Martins ALBUQUERQUE et al. 2014. Hyperexpression of inflammatory genes in placental tissue in patients with hemoglobin sc disease. In: 56th ash annual meeting. Estados Unidos.
  50. Life Sciences Neurology
    Mônica Barbosa De MELO; Daniela Prescila Dezidério SACCONI; Galina ANANINA; Fábio Endo HIRATA; Priscila Hae Hyun RIM et al. 2013. Contribution of cfh y402h polymorphism and cfhr3/cfhr1 deletion to age-related macular degeneration in brazil. In: Arvo 2013 annual meeting. Estados Unidos.
  51. Life Sciences Genetics
    Mariana B OLIVEIRA; José Paulo Cabral De VASCONCELLOS; Vital Paulino COSTA; Galina ANANINA; Mônica Barbosa De MELO. 2013. Association between il1a; il1b and tnfa polymorphisms and glaucoma in a brazilian population. In: Arvo 2013 annual meeting. Estados Unidos.
  52. Health Sciences Neurology (clinical)
    Mônica Barbosa De MELO; Pedro Rodrigues Sousa Da CRUZ; Galina ANANINA; Sérgio Pereira FILHO; Rodrigo P C LIRA et al. 2013. Analysis of pedf levels and pedf gene promoter polymorphisms (-790t>c; -358g>a) in a cohort of brazilian patients with and without sickle cell retinopathy. In: Asia arvo 2013. Estados Unidos.
  53. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; Bruno Batista De SOUZA; Mariana B OLIVEIRA; Vital Paulino COSTA; Mônica Barbosa De MELO. 2013. Asb10 gene variants in primary open angle glaucoma brazilian patients. In: Asia arvo 2013. Estados Unidos.
  54. Health Sciences Medicine (miscellaneous)
    Mônica Barbosa De MELO; Pedro Rodrigues Sousa Da CRUZ; Tânia R ZACCARIOTTO; Fábio Nero MITSUUSHI; Sérgio A Pereira FILHO et al. 2012. Angiopoietin-2 may play a role as protective factor in sickle cell retinopathy. In: 2012 association for research in vision and ophthalmology annual meeting. Estados Unidos.
  55. Health Sciences Radiology, Nuclear Medicine and Imaging
    José Paulo Cabral De VASCONCELLOS; Bibiana Amélia Cosim Dos SANTOS; Rodrigo SECOLIN; Fábio Rossi TORRES; Carolina Ayumi BRAGHINI et al. 2012. Investigation of candidate loci for primary open angle glaucoma in a brazilian family through snp array. In: 2012 association for research in vision and ophthalmology annual meeting. Estados Unidos.
  56. Life Sciences Genetics
    Galina ANANINA; Farid MENAA; Marcos André BEZERRA; Aderson S ARAÚJO; Pedro Rodrigues Sousa Da CRUZ et al. 2012. Copy number variations in a cohort of brazilian sickle cell anemia patients with and without cerebrovascular accident. In: American society of human genetics 62nd annual meeting. Estados Unidos.
  57. Life Sciences Genetics
    Mariana B OLIVEIRA; José Paulo Cabral De VASCONCELLOS; Vital Paulino COSTA; Mônica Barbosa De MELO. 2012. Association between il1a; il1b and tnfa polymorphisms and glaucoma in a brazilian population. In: American society of human genetics 62nd annual meeting. Estados Unidos.
  58. Life Sciences Genetics
    Hugo Freire NUNES; Mariana B OLIVEIRA; José Paulo Cabral De VASCONCELLOS; Vital Paulino COSTA; Mônica Barbosa De MELO. 2012. Investigation of rs4236601 and rs4977756 snps in a primary open- angle glaucoma brazilian population. In: American society of human genetics 62nd annual meeting. Estados Unidos.
  59. Health Sciences Genetics (clinical)
    Mônica Barbosa De MELO; Gislene Pereira GIL; Galina ANANINA; Mariana B OLIVEIRA; Márcio José Da SILVA et al. 2012. Polymorphism in the hmox-1 gene is associated with high levels of hbf in brazilian patients with sickle cell anemia. In: American society of human genetics 62nd annual meeting. Estados Unidos.
  60. Life Sciences Neuroscience (miscellaneous)
    Pedro Rodrigues Sousa Da CRUZ; Tânia R ZACCARIOTTO; Fábio Nero MITSUUSHI; Sérgio A Pereira FILHO; Rodrigo P C LIRA et al. 2012. Soluble icam-1 levels are associated to a protective prognosis in sickle cell retinopathy. In: American society of human genetics 62nd annual meeting. Estados Unidos.
  61. Life Sciences General Biochemistry, Genetics and Molecular Biology
    Bibiana Amélia Cosim Dos SANTOS; Mônica Barbosa De MELO; Carolina Ayumi BRAGHINI; Rodrigo SECOLIN; Fábio Rossi TORRES et al. 2011. Investigation of candidate loci for primary open angle glaucoma in a brazilian family through snp array. In: European human genetics conference 2011. Holanda.
  62. Life Sciences Genetics
    Carolina Ayumi BRAGHINI; José Paulo Cabral De VASCONCELLOS; Daniela STANCATO; Márcio José Da SILVA; Anderson TAVARES et al. 2011. Cyp1b1 as a modifier gene for two brazilian families with juvenile-onset open angle glaucoma harboring the c433r mutation in the myoc gene. In: European human genetics conference 2011. Holanda.
  63. Life Sciences Genetics
    Fábio E HIRATA; Priscila Hae Hyun RIM; Andréa Mara Simões TORIGOE; Enzo A FULCO; Anderson TAVARES et al. 2011. Loc387715/arms2 polymorphism analysis in brazilian patients with age-related macular degeneration. In: 2011 association for research in vision and ophthalmology annual meeting. Estados Unidos.
  64. Health Sciences Genetics (clinical)
    Mônica Barbosa De MELO; Gislene Pereira GIL; Galina ANANINA; Mariana B OLIVEIRA; Márcio José Da SILVA et al. 2011. Analysis of the polymorphism -930 a/g (rs9932581) in the cyba gene in pediatric patients with sickle cell anemia. In: 12th international congress of human genetics/61st annual meeting of the american society of human genetics. Estados Unidos.
  65. Life Sciences Genetics
    Galina ANANINA; José Paulo Cabral De VASCONCELLOS; Renato VICENTINI; Farid MENAA; Fernando Ferreira COSTA et al. 2011. Genomic variation in a brazilian population. In: 12th international congress of human genetics/61st annual meeting of the american society of human genetics. Estados Unidos.
  66. Health Sciences Medicine (miscellaneous)
    Farid MENAA; Marcos André BEZERRA; Aderson S ARAÚJO; Galina ANANINA; Pedro Rodrigues Sousa Da CRUZ et al. 2011. Evaluating genomic copy number variations in a brazilian population of adult sickle cell anemia patients with and without stroke complication. In: 12th international congress of human genetics/61st annual meeting of the american society of human genetics. Estados Unidos.
  67. Life Sciences Neurology
    Mônica Barbosa De MELO; Jayter Silva De PAULA; Mariana B OLIVEIRA; Renata PELEGRINO; Gislene Pereira GIL et al. 2010. Copy number variation analysis of a primary open angle glaucoma brazilian familiy. In: 2010 annual meeting of the association for research in vision and ophthalmology. Estados Unidos.
  68. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; Taís TANNO; Paulo Maurício Do Amor Divino MIRANDA; Flávia CALLEFO; Edi Lúcia SARTORATO et al. 2010. Coexistence of glaucomatous phenotype and mitochondrial mutation in a three generation brazilian family. In: 2010 annual meeting of the association for research in vision and ophthalmology. Estados Unidos.
  69. Life Sciences Genetics
    Priscila Hae Hyun RIM; Fábio E HIRATA; Andréa Mara Simões TORIGOE; Luís Alberto MAGNA; Mônica Barbosa De MELO et al. 2010. Genética e prevenção da cegueira: estudo dos fatores de risco que influenciam o desenvolvimento da degeneração macular relacionada à idade em uma população brasileira. In: Xxii congresso brasileiro de genética médica. Brasil.
  70. Life Sciences Genetics
    Carolina Ayumi BRAGHINI; Mônica Barbosa De MELO. 2010. Avaliação dos genes myoc e cyp1b1 em famílias portadoras de glaucoma primário de ângulo aberto. In: Xviii congresso interno de iniciação científica da unicamp. Brasil.
  71. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; Carolina Ayumi BRAGHINI; Anderson TAVARES; Sérgio Ricardo Elias Pião JR; Gislene Pereira GIL et al. 2009. New mutation in the myoc gene; c1187_1188inscccaga; segregates with juvenile open angle glaucoma in a brazilian family. In: Association for research in vision and ophthalmology. Estados Unidos.
  72. Life Sciences Neuroscience (miscellaneous)
    Pedro Rodrigues Sousa Da CRUZ; Maria De Fátima SONATI; Fernando Ferreira COSTA; Gislene Pereira GIL; Anderson TAVARES et al. 2009. Analysis of the role of pedf gene polymorphisms in the sickle cell retinopathy. In: 55o congresso brasileiro de genética. Brasil.
  73. Life Sciences Genetics
    Carolina Ayumi BRAGHINI; José Paulo Cabral De VASCONCELLOS; Fernanda Caroline SOARDI; Anderson TAVARES; Sérgio Ricardo Elias Pião JR et al. 2009. New mutation in the myoc gene; c.1187_1188inscccaga; segregates with juvenile open-angle glaucoma in a brazilian family. In: 55o congresso brasileiro de genética. Brasil.
  74. Life Sciences Neuroscience (miscellaneous)
    Pedro Rodrigues Sousa Da CRUZ; Anderson TAVARES; Mônica Barbosa De MELO. 2009. Análise do papel de polimorfismos nos genes vegf e pedf na retinopatia falciforme. In: Xvii congresso interno de iniciação científica da unicamp. Brasil.
  75. Life Sciences Genetics
    Carolina Ayumi BRAGHINI; José Paulo Cabral De VASCONCELLOS; Anderson TAVARES; Mônica Barbosa De MELO. 2009. Avaliação dos genes myoc e cyp1b1 em famílias portadoras de glaucoma primário de ângulo aberto. In: Xvii congresso interno de iniciação científica da unicamp. Brasil.
  76. Life Sciences Genetics
    Alessandro SANTANA; Mauro WAISWOL; Enyr Saran ARCIERI; Flávio RICHETI; José Paulo Cabral De VASCONCELLOS et al. 2008. Mutation (tyr56stop) in thegamma d-crystallin gene causing autosomal dominant congenital cataract in a brazilian family. In: Association for research in vision and ophthalmology (arvo) 2008 annual meeting. Estados Unidos.
  77. Health Sciences Infectious Diseases
    Mônica Barbosa De MELO; Maurício Della PAOLERA; Cristiano Caixeta UMBELINO; Niro KASAHARA; Mylene Neves ROCHA et al. 2008. Molecular analysis of the cyp1b1 gene in congenital glaucoma brazilian patients. In: Association for research in vision and ophthalmology (arvo) 2008 annual meeting. Estados Unidos.
  78. Life Sciences Genetics
    Niro KASAHARA; Cristiano Caixeta UMBELINO; José Paulo Cabral De VASCONCELLOS; Murilo Resende MELO; Maurício Della PAOLERA et al. 2008. Mt.1gene promotersingle nucleotide polymorphism in brazilian patients with primary open angle glaucoma. In: Association for research in vision and ophthalmology (arvo) 2008 annual meeting. Estados Unidos.
  79. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; A REIS; C STEFANI; Anderson TAVARES; Carolina Ayumi BRAGHINI et al. 2008. Genotype/phenotype correlation in two brazilian families harboring the cys433arg mutation in the myoc gene. In: 58ª annual meeting of the american society of human genetics (ashg). Estados Unidos.
  80. Life Sciences Genetics
    Enyr Saran ARCIERI; Rafael Saran ARCIERI; Emerson Soares De Souza FRANÇA; Fernanda Caroline SOARDI; Fernanda L CALAIS et al. 2008. Análise molecular do gene pax6 em pacientes com aniridia. In: Xviii congresso brasileiro de prevenção da cegueira e reabilitação visual. Brasil.
  81. Health Sciences Infectious Diseases
    Mônica Barbosa De MELO; Maurício Della PAOLERA; Cristiano Caixeta UMBELINO; Niro KASAHARA; Mylene Neves ROCHA et al. 2007. Molecular analysis of the cyp1b1 gene in congenital glaucoma brazilian patients. In: 57ª annual meeting of the american society of human genetics (ashg). Estados Unidos.
  82. Life Sciences Developmental Biology
    José Paulo Cabral De VASCONCELLOS; Anderson TAVARES; Iscia Teresinha Lopes CENDES; Cláudia Vianna Maurer MORELLI; Rodrigo SECOLIN et al. 2007. Analysis of candidate loci in primary open angle glaucoma families. In: 57ª annual meeting of the american society of human genetics (ashg). Estados Unidos.
  83. Life Sciences Genetics
    Mônica Barbosa De MELO; Alessandro SANTANA; Mauro WAISWOL; Enyr Saran ARCIERI; Flávio RICHETI et al. 2007. New mutation in the alpha-a crystallin gene causing autosomal dominant congenital cataract. In: Association for research in vision and ophthalmology (arvo) 2007 annual meeting. Estados Unidos.
  84. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; Cristiano Caixeta UMBELINO; Maurício Della PAOLERA; Niro KASAHARA; Mylene Neves ROCHA et al. 2007. Optineurin gene evaluation in primary open angle glaucoma brazilian patients. In: Association for research in vision and ophthalmology (arvo) 2007 annual meeting. Estados Unidos.
  85. Life Sciences Genetics
    Emerson Soares De Souza FRANÇA; Fernanda Caroline SOARDI; Fernanda L CALAIS; Mônica Barbosa De MELO; José Paulo Cabral De VASCONCELLOS et al. 2007. Análise molecular do gene pax6 em pacientes com aniridia. In: 53o congresso brasileiro de genética. Brasil.
  86. Life Sciences Parasitology
    Aglair Veridiana CELESTINO; Anderson TAVARES; Cíntia Moura ARCANJOLETO; Bianca KNEIPP; Flávio Mccord MEDINA et al. 2006. Avaliação de polimorfismos no gene opa1 em pacientes brasileiros com glaucoma primário de ângulo aberto. In: World ophthalmology congress. Brasil.
  87. Health Sciences Genetics (clinical)
    Flávio RICHETI; Renata Maria NORONHA; Ricardo Temudo Lessa WAETGE; Luís Eduardo Procópio CALLIARI; Osías Francisco De SOUZA et al. 2006. Avaliação dos polimorfismos c-106t e acn no gene alr2 e suscetibilidade ao desenvolvimento de retinopatia diabética em pacientes com diabetes tipo 1. In: World ophthalmology congress. Brasil.
  88. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO; Wener CELLA; Bianca KNEIPP; Mylene Neves ROCHA et al. 2006. Mutation screening of foxc1 and pitx2 genes in brazilian patients with axenfel-rieger malformations. In: World ophthalmology congress. Brasil.
  89. Life Sciences Genetics
    Mônica Barbosa De MELO; José Paulo Cabral De VASCONCELLOS; Wener CELLA; Bianca KNEIPP; Mylene Neves ROCHA et al. 2006. Axenfeld-rieger syndrome: coexistence of mutations in the foxc1 and gja1genes. In: World ophthalmology congress. Brasil.
  90. Life Sciences Genetics
    Cristiano Caixeta UMBELINO; José Paulo Cabral De VASCONCELLOS; Maurício Della PAOLERA; Niro KASAHARA; Geraldo Viecente De ALMEIDA et al. 2006. Investigação das alterações e50k e t34t no exon 4 do gene optn em pacientes com glaucoma primário de ângulo aberto. In: World ophthalmology congress. Brasil.
  91. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; Aglair Veridiana CELESTINO; Anderson TAVARES; Cíntia Moura ARCANJOLETO; Bianca KNEIPP et al. 2006. Analysis of opa1 gene polymorphisms in brazilian patients with primary open angle glaucoma. In: Annual meeting of the association for research in vision and ophthalmology. Estados Unidos.
  92. Life Sciences Neurology
    Mônica Barbosa De MELO; Flávio RICHETI; Renata Maria NORONHA; Ricardo Temudo Lessa WAETGE; Luís Eduardo Procópio CALLIARI et al. 2006. Ac(n) and c(-106)t polymorphisms of the aldose reductase gene and susceptibility to diabetic retinopathy in brazilian patients with type 1 diabetes mellitus. In: Annual meeting of the association for research in vision and ophthalmology. Estados Unidos.
  93. Health Sciences Medicine (miscellaneous)
    Vânia P A WOBETO; E T ROSIM; Mônica Barbosa De MELO; Ricardo Temudo Lessa WAETGE; Luís Eduardo Procópio CALLIARI et al. 2005. Polimorfismo da haptoglobina e retinopatia diabética. In: Congresso brasileiro de patologia clínica/ medicina laboratorial. Brasil.
  94. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO; Wener CELLA; Bianca KNEIPP; Mylene Neves ROCHA et al. 2005. Mutation screening of foxc1 and pitx2 genes in brazilian patients with axenfeld-rieger malformations. In: Association for research in vision and ophthalmology. Estados Unidos.
  95. Life Sciences Genetics
    Mônica Barbosa De MELO; José Paulo Cabral De VASCONCELLOS; Wener CELLA; Bianca KNEIPP; Mylene Neves ROCHA et al. 2005. Axenfeld-rieger syndrome: coexistence of mutations in the foxc1 and gja1 genes. In: Association for research in vision and ophthalmology. Estados Unidos.
  96. Social Sciences & Humanities Psychology (miscellaneous)
    Carlos Alberto LONGUI; Cristiane KOCHI; Mônica Barbosa De MELO; Murilo Rezende MELO; Lilian MARTELO et al. 2005. Parental origin of x chromosome: influence on height determination in patients with turner syndrome and normal control boys. In: European society for paediatric endocrinology (espe) / 7th joint meeting in collaboration with apeg; appes; jspe and slep. Estados Unidos.
  97. Life Sciences Genetics
    Wener CELLA; José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO; Bianca KNEIPP; Vital Paulino COSTA. 2005. Aspectos genéticos da síndrome de axenfeld-rieger: descrição de novas mutações nos genes foxc1 e gja1 em pacientes brasileiros. In: Xxxiii congresso brasileiro de oftalmologia. Brasil.
  98. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; Rui Barroso SCHIMITI; Vital Paulino COSTA; Norisvaldo César BRESSANIM; Fernando Ferreira COSTA et al. 2004. Pro59his: a novel mutation inthe gja1 gene in a brazilian family with oculodentodigitaldysplasia. In: Association for research in vision and ophthalmology. Estados Unidos.
  99. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; Wener CELLA; Mônica Barbosa De MELO; Bianca KNEIPP; Vital Paulino COSTA. 2004. Síndrome de axenfeld-rieger: associação à mutação no gene da conexina 43 humana (gja1)?. In: Xix reunião anual da federação de sociedades de biologia experimental - fesbe. Brasil.
  100. Life Sciences Genetics
    Mônica Barbosa De MELO; Vital Paulino COSTA; Norisvaldo César BRESSANIM; Rui Barroso SCHIMITI; José Paulo Cabral De VASCONCELLOS. 2004. Nova mutação no gene da conexina 43 (gja1) em uma família com displasia óculo-dento-digital. In: Xix reunião anual da federação de sociedades de biologia experimental - fesbe. Brasil.
  101. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; Rui Barroso SCHIMITI; Norisvaldo César BRESSANIM; Mônica Barbosa De MELO; Vital Paulino COSTA. 2003. Descrição de uma família com síndrome de displasia óculo-dento- digital e glaucoma. In: Xxxi congresso brasileiro de oftalmologia. Brasil.
  102. Life Sciences Genetics
    Wener CELLA; José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO; Dulcinéia ALBUQUERQUE; Vital Paulino COSTA. 2003. Rastreamento de mutações no genes pitx2 em pacientes com anomalia e síndrome de axenfeld-rieger. In: Xxxi congresso brasileiro de oftalmologia. Brasil.
  103. Life Sciences Genetics
    Carmen Silvia Passos LIMA; Manoela Marques ORTEGA; Hélvia NASCIMENTO; Mônica Barbosa De MELO; M T TEORI et al. 2002. Polymorphism of glutathione s-transferase mu1 (gstm1) gene in multiple myeloma. In: 7th meeting of the european hematology association. Itália.
  104. Health Sciences Medicine (miscellaneous)
    Carmen Silvia Passos LIMA; Manoela Marques ORTEGA; Mônica Barbosa De MELO; Irene Lorand METZE; Cármino Antônio De SOUZA et al. 2002. Predictive role of p53 deletion for short survival in patients with multiple myeloma. In: 7th meeting of the european hematology association. Itália.
  105. Life Sciences Cancer Research
    Carmen Silvia Passos LIMA; Manoela Marques ORTEGA; Mônica Barbosa De MELO; Irene Lorand METZE; Cármino Antônio De SOUZA et al. 2002. P53 gene deletion as a prognostic factor in multiple myeloma. In: 44th annual meeting of the american society of hematology. Estados Unidos.
  106. Health Sciences Neurology (clinical)
    Manoela Marques ORTEGA; Mônica Barbosa De MELO; Irene Lorand METZE; Cármino Antônio De SOUZA; Fernando Ferreira COSTA et al. 2002. Predictive role of p53 deletion for short survival in patients with multiple myeloma. In: 48o congresso nacional de genética. Brasil.
  107. Health Sciences Immunology and Allergy
    Carmen Silvia Passos LIMA; Manoela Marques ORTEGA; Hélvia NASCIMENTO; Mônica Barbosa De MELO; M T TEORI et al. 2002. A polymorphism in endostatin; an angiogenesis inhibitor on multiple myeloma. In: 48o congresso nacional de genética. Brasil.
  108. Life Sciences Genetics
    Ivao STOILOV; Vital Paulino COSTA; José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO; A J BETINJANE et al. 2001. Mutation screening of the cyp1b1 gene and phenotype-genotype correlation in primary congenital glaucoma cases from brazil. In: Annual meeting of the association for research in vision and ophthalmology. Estados Unidos.
  109. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO; Vital Paulino COSTA; Rui SCHIMITI; Fernando Ferreira COSTA. 2001. Phenotype/genothype correlation in a family pedigree with the cys433arg mutation in the myoc gene. In: 3rd international glaucoma symposium. República Tcheca.
  110. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO; Rui SCHIMITI; Vital Paulino COSTA; Fernando Ferreira COSTA. 2001. Genotype/phenotype correlation in a family with poag harboring the cys433arg mutation in the myoc gene. In: Xxiii congreso panamericano de oftalmología. Argentina.
  111. Life Sciences Genetics
    Manoela Marques ORTEGA; Adriana Silva Santos DUARTE; Mônica Barbosa De MELO; Irene Lorand METZE; Fernando Ferreira COSTA et al. 2001. P53 gene mutations are rare in brazilian patients with multiple myeloma. In: 47o congresso nacional de genética. Brasil.
  112. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Simone Bordignon De JORGE; Mônica Barbosa De MELO; Fernando Ferreira COSTA; Maria De Fátima SONATI. 2001. Optimization of single-strand conformation polymorphism-sscp for screening mutations in fragments of human alpha-globin genes. In: 47o congresso nacional de genética. Brasil.
  113. Life Sciences Clinical Biochemistry
    Manoela Marques ORTEGA; Hélvia NASCIMENTO; Mônica Barbosa De MELO; Fernando Ferreira COSTA; Carmen Sílvia Passos LIMA. 2001. Glutathione s-transferase m1 and t1 polymorphisms: no influence for the risk of multiple myeloma in brazilian patients. In: Xviii congresso nacional do colégio brasileiro de hematologia. Brasil.
  114. Health Sciences Medicine (miscellaneous)
    Manoela Marques ORTEGA; Adriana Silva Santos DUARTE; Mônica Barbosa De MELO; Irene Lorand METZE; Fernando Ferreira COSTA et al. 2001. Low frequency of p53 gene mutations in brazilian patients with multiple myeloma. In: Xviii congresso nacional do colégio brasileiro de hematologia. Brasil.
  115. Life Sciences Genetics
    Edson SHITARA; Mônica Barbosa De MELO; Fernando Ferreira COSTA. 2001. Freqüência de mutações do oncogene n-ras; codons 12; 13 em pacientes com mieloma múltiplo. In: Xviii congresso nacional do colégio brasileiro de hematologia. Brasil.
  116. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Simone Bordignon De JORGE; Mônica Barbosa De MELO; Edna Maria KIMURA; Fernando Ferreira COSTA; Maria De Fátima SONATI. 2001. Optimization of single-strand conformation polymorphism-sscp for screening mutations in fragments of human alpha-globin genes. In: Xviii congresso nacional do colégio brasileiro de hematologia. Brasil.
  117. Life Sciences Agricultural and Biological Sciences (miscellaneous)
    Mônica Barbosa De MELO; Silvana BORDIN; Adriana Silva Santos DUARTE; André VETTORE; Edson Luís KEMPER et al. 2001. Molecular characterization of hemoglobin alpha-d chains of geochelone carbonaria and geochelone denticulata lans turtles. In: Xviii congresso nacional do colégio brasileiro de hematologia. Brasil.
  118. Health Sciences Genetics (clinical)
    Manoela Marques ORTEGA; Hélvia NASCIMENTO; Mônica Barbosa De MELO; M T TEORI; Fernando Ferreira COSTA et al. 2001. High frequency of glutathione s-transferase mu1 (gstm1) null genotype in brazilian patients with advanced multiple myeloma. In: 43 annual meeting of the american society of hematology. Estados Unidos.
  119. Health Sciences Medicine (miscellaneous)
    Manoela Marques ORTEGA; Hélvia NASCIMENTO; Mônica Barbosa De MELO; Fernando Ferreira COSTA; Carmen Sílvia Passos LIMA. 2000. Polimorfismos dos genes mu1 e theta 1 do sistema da glutationa s-transferase em pacientes com mieloma múltiplo. In: 46º congresso nacional de genética. Brasil.
  120. Life Sciences Genetics
    Mônica Barbosa De MELO; José Paulo Cabral De VASCONCELLOS; Vital Paulino COSTA; Rui SCHIMITI; Fernando Ferreira COSTA. 2000. Estudo da mutação cys433arg em família com glaucoma primário de ângulo aberto. In: 46º congresso nacional de genética. Brasil.
  121. Health Sciences Genetics (clinical)
    Carmen Sílvia Passos LIMA; Valder Roberval ARRUDA; Carlos Roberto Escrivão GRIGNOLI; Mônica Barbosa De MELO; Irene Lorand METZE et al. 2000. Increased risk for acute myeloid leukemia in individuals with glutathione s-transferase mu1 (gstm1) and theta (gstt1) gene defects. In: 28th world congress of the international society of hematology. Canadá.
  122. Health Sciences Genetics (clinical)
    Valder Roberval ARRUDA; Carmen Sílvia Passos LIMA; Carlos Roberto Escrivão GRIGNOLI; Mônica Barbosa De MELO; Irene Lorand METZE et al. 2000. Increased risk for acute myeloid leukemia in individuals with glutathione s-transferase mu1 (gstm1) and theta (gstt1) gene defects. In: 5th annual meeting of the european haematology association. Inglaterra.
  123. Life Sciences Genetics
    Valder Roberval ARRUDA; Carmen Sílvia Passos LIMA; Carlos Roberto Escrivão GRIGNOLI; Mônica Barbosa De MELO; Irene Lorand METZE et al. 1999. Increased risk for acute myeloid leukemia in individuals with glutathione s-transferase mu1 (gstm1) and theta (gstt1) gene defects. In: Xvii congresso nacional do colégio brasileiro de hematologia. Brasil.
  124. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Silvana BORDIN; Fernando Lopes ALBERTO; Vanessa G CRESPI; Adriana Silva Santos DUARTE; Daniela Sanchez BASSÈRES et al. 1998. Dnase i hypersensitive site 3'to the beta globin gene cluster contains a taa insertion specific for beta s-benin haplotype. In: Ish-eha combined haematology congress. Holanda.
  125. Life Sciences Genetics
    Daniela Sanchez BASSÈRES; Dilmara Lopes VICENTIM; Silvana BORDIN; Mônica Barbosa De MELO; Fernando Ferreira COSTA et al. 1998. Beta-spectrin santa barbara: a novel frameshift mutation of the beta-spectrin gene associated with hereditary spherocytosis. In: Ish-eha combined haematology congress. Holanda.
  126. Life Sciences Genetics
    Mônica Barbosa De MELO; Silvana BORDIN; Daniela Sanchez BASSÈRES; Sara Teresinha Ollala SAAD; Irene Lorand METZE et al. 1998. Mutações no gene p53 em pacientes com leucemia mielóide aguda. In: Vii international congress of the world apheresis association - waa e xxiii congresso brasileiro de hematologia e hemoterapia (hemo 98). Brasil.
  127. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO; Vital Paulino COSTA; Newton Kara JOSÉ; Fernando Ferreira COSTA. 1998. Mutações no gene tigr (trabecular meshwork-induced glucocorticoid response protein) em uma população com glaucoma juvenil e glaucoma primário de ângulo aberto. In: Xiii congresso brasileiro de prevenção da cegueira e reabilitação visual. Brasil.
  128. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO; Vital Paulino COSTA; Fernando Ferreira COSTA; Silvana BORDIN et al. 1998. Mutations in the tigr gene in a brazilian population with juvenile glaucoma. In: Annual meeting of the association for research in vision and ophthalmology. Estados Unidos.
  129. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Silvana BORDIN; Vanessa G CRESPI; Daniela Sanchez BASSÈRES; Adriana Silva Santos DUARTE; Mônica Barbosa De MELO et al. 1997. Different rates of recombination among polymorphic short tandem repeats of the beta-globin gene cluster in beta s chromosomes. In: Xxxix annual meeting of the american society of hematology. Estados Unidos.
  130. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Valder Roberval ARRUDA; Carmen Sílvia Passos LIMA; Carlos Roberto Escrivão GRIGNOLI; Mônica Barbosa De MELO; Irene Lorand METZE et al. 1997. High prevalence of the glutathione s-transferase (gst) null genotype in acute myeloblastic leukemia. In: Xxxix annual meeting of the american society of hematology. Estados Unidos.
  131. Life Sciences Genetics
    Daniela Sanchez BASSÈRES; Alessandra C TAVARES; Silvana BORDIN; Dilmara Lopes VICENTIM; Mônica Barbosa De MELO et al. 1997. Novel beta-spectrin variants associated with hereditary spherocytosis in brazil. In: Xxxix annual meeting of the american society of hematology. Estados Unidos.
  132. Health Sciences Genetics (clinical)
    Mônica Barbosa De MELO; Sara Teresinha Ollala SAAD; Nilofer Nina AHMAD; Fernando Ferreira COSTA. 1997. Mutações nos genes supressores de tumores p53 e rb1 em pacientes com leucemia mielóide aguda. In: Xvi congresso nacional do colégio brasileiro de hematologia. Brasil.
  133. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Silvana BORDIN; Vanessa G CRESPI; Daniela Sanchez BASSÈRES; Adriana Silva Santos DUARTE; Mônica Barbosa De MELO et al. 1997. Caracterização molecular das regiões polimórficas de repetição do complexo da globina beta por pcr-sscp. In: Xvi congresso nacional do colégio brasileiro de hematologia. Brasil.
  134. Life Sciences Genetics
    Daniela Sanchez BASSÈRES; Alessandra C TAVARES; Silvana BORDIN; Dilmara Lopes VICENTIM; Mônica Barbosa De MELO et al. 1997. New beta-spectrin variants associated with hereditary spherocytosis in brazil. In: Xvi congresso nacional do colégio brsileiro de hematologia. Brasil.
  135. Life Sciences Genetics
    Fernando Ferreira COSTA; Mônica Barbosa De MELO; Sara Teresinha Ollala SAAD; Nilofer Nina AHMAD. 1997. P53 and rb1 gene mutations in brazilian patients with acute myeloid leukemia. In: Xiv meeting of the international society of haematology - european and african division. Suécia.
  136. Life Sciences Genetics
    Mônica Barbosa De MELO; Sara Teresinha Ollala SAAD; Nilofer Nina AHMAD; Fernando Ferreira COSTA. 1997. Mutações nos genes supressores de tumores p53 e rb1 em pacientes com leucemia mielóide aguda (lma). In: Xii reunião anual da federação de sociedades de biologia experimental - fesbe. Brasil.
  137. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Valder Roberval ARRUDA; Carlos Roberto Escrivão GRIGNOLI; Mônica Barbosa De MELO; Irene Lorand METZE; Sara Teresinha Ollala SAAD et al. 1997. High prevalence of the glutathione s-tranferase (gst) null genotype in acute myeloblastic leukemia. In: Xvi congresso nacional do colégio brasileiro de hematologia. Brasil.
  138. Life Sciences Genetics
    Mônica Barbosa De MELO; Fernando Ferreira COSTA; Nilofer Nina AHMAD. 1996. Conformation sensitive gel electrophoresis (csge) for rapid screening of the retinoblastoma (rb1) gene. In: Annual meeting of the association for research in vision and ophthalmology. Estados Unidos.
  139. Life Sciences Genetics
    Mônica Barbosa De MELO; Nilofer Nina AHMAD; Jerry A SHIELDS; Larry A DONOSO. 1996. Conformation sensitive gel electrophoresis (csge) for rapid detection of mutations in the rb1 gene. In: 48th annual conference - wills eye hospital. Estados Unidos.
  140. Life Sciences Genetics
    Mônica Barbosa De MELO; Carmen Sílvia Passos LIMA; Irene Lorand METZE; Sara Teresinha Ollala SAAD; Fernando Ferreira COSTA. 1994. Mutações no proto-oncogene n-ras em pacientes com leucemia mielóide aguda (lma) estão associadas a mau prognóstico. In: Xxi congresso brasileiro de hematologia e hemoterapia. Brasil.
  141. Health Sciences Genetics (clinical)
    N A BERGAMO; Claudia S RAINHO; Mônica Barbosa De MELO; A MEDEIROS; Sílvia R ROGATTO. 1994. Alterações citogenéticas e do oncogene k-ras em leiomiomas uterinos. In: Ii congresso latinoamericano de genética. México.
  142. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Mônica Vannucci NUNES; Mônica Barbosa De MELO; Fernando Ferreira COSTA; Marileila Varella GARCIA. 1994. Método simples de extração de dna a partir de preparações cromossômicas para citogenética. In: Ix reunião da federação de sociedades de biologia experimental - fesbe. Brasil.
  143. Life Sciences Genetics
    Mônica Barbosa De MELO; Irene Lorand METZE; Fernando Ferreira COSTA. 1992. N-ras mutations in patients with acute leukemia. In: Xx congresso brasileiro de hematologia. Brasil.
  144. Life Sciences Neurology
    Mônica Barbosa De MELO; Sandra Cecília Botelho COSTA; Irene Lorand METZE; Fernando Ferreira COSTA. 1992. Mutações do oncogene n-ras em pacientes com leucemia aguda. In: Vii reunião anual da federação de sociedades de biologia experimental. Brasil.
  145. Health Sciences Medicine (miscellaneous)
    Mônica Barbosa De MELO; Tereza Sueko Ide SALES; Irene Lorand METZE; Fernando Ferreira COSTA. 1991. Dna isolado de esfregaços usados na rotina hematológica pode ser utilizado para detecção de alterações genéticas moleculares pela reação em cadeia da polimerase (pcr). In: Xiii congresso nacional do colégio brasileiro de hematologia. Brasil.
  146. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Mônica Barbosa De MELO; Tereza Sueko Ide SALES; Irene Lorand METZE; Fernando Ferreira COSTA. 1991. Dna isolado de esfregaços usados na rotina hematológica pode ser utilizado para detecção de alterações genéticas moleculares pela pcr. In: Xxxvii congresso nacional de genética. Brasil.
  1. Life Sciences Cell Biology
    Bertozzo Victor De Haidar E; Da Silva Costa Sueli MATILDE; Ito Mirta TOMIE; Cruz Pedro Rodrigues Sousa DA; Souza Bruno BATISTA et al. 2023. Comparative transcriptome analysis of endothelial progenitor cells of hbss patients with and without proliferative retinopathy. Experimental biology and medicine. 1, 153537022311579-.
  2. Life Sciences Genetics
    Rodrigues Thiago Adalton ROSA; De Souza Bruno BATISTA; Bertozzo Victor De Haidar E; De Castro Júlia Nicoliello PEREIRA; Camargo Ana Carolina LIMA et al. 2023. Association of variants in the atxn2</i> (rs7137828); foxc1</i> (rs2745572) and txnrd2</i> (rs35934224) genes as risk factors for primary open-angle glaucoma development in a brazilian cohort. Ophthalmic genetics. 44, 246-252.
  3. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    De Guimarães Juliana ALBANO; Hounpke Bidossessi WILFRIED; Duarte BRUNA; Boso Ana Luiza MYLLA; Viturino Marina Gonçalves MONTEIRO et al. 2022. Transcriptomics and network analysis highlight potential pathways in the pathogenesis of pterygium. Scientific reports. 12, 286-.
  4. Life Sciences Genetics
    Manoel Vinicius Rocha ARAKI; Yuri De Carvalho Oiamore SILVA; Thiago Adalton Rosa RODRIGUES; Flavia Fialho BAJANO; Souza B B et al. 2022. Association of abca1 (rs2472493) and gas7 (rs9913911) gene variants with primary open-angle glaucoma in a brazilian population. Molecular vision. 28, 1-.
  5. Health Sciences Rheumatology
    Rim Priscila H H; De Vasconcellos José Paulo C; Mônica Barbosa De MELO; Medina Flavio M C; Sacconi Daniela P D et al. 2022. Correlation between genetic and environmental risk factors for age-related macular degeneration in brazilian patients. Plos one. 17, e0268795-.
  6. Social Sciences & Humanities Sociology and Political Science
    Da Cruz Pedro Rodrigues SOUSA; Ananina GALINA; Secolin RODRIGO; Gil Da Silva Lopes Vera LÚCIA; Lima Carmen Silvia PASSOS et al. 2022. Demographic history differences between hispanics and brazilians imprint haplotype features. G3-genes genomes genetics. 1, 1-.
  7. Health Sciences Medicine (miscellaneous)
    Gil Gislene PEREIRA; Ananina GALINA; Maschietto MARIANA; Lima Sheila Coelho SOARES; Da Silva Costa Sueli MATILDE et al. 2022. Epigenetic analysis in placentas from sickle cell disease patients reveals a hypermethylation profile. Plos one. 17, e0274762-.
  8. Health Sciences Neurology (clinical)
    Viturino Marina GM; Neto Jamil M; Bajano Flávia F; Costa Sueli MS; Roque Alicia B et al. 2021. Evaluation of polymorphisms and the risk for age-related macular degeneration in a southeastern brazilian population. Experimental biology and medicine. 1, 153537022098546-10.
  9. Life Sciences Genetics
    Makita Lana SAYURI; Muniz Bernardo CARVALHO; Da Silva Alícia Buffoni ROQUE; Bajano Flávia FIALHO; Hirata Fábio ENDO et al. 2021. Interleukin-1β-31 (rs1143627) genetic variant and the risk of age-related macular degeneration in the brazilian population. Ophthalmic genetics. 16, 1-6.
  10. Life Sciences Genetics
    Gasparini Matheus S; Dos Santos Leandro M; Hamade Ahmad MA; Gross Luísa G; Favarato Arthur P et al. 2021. Identification of sars-cov-2 on the ocular surface in a cohort of covid-19 patients from brazil. Experimental biology and medicine. 19, 153537022110246-.
  11. Life Sciences Genetics
    Neto Jamil M; Viturino Marina GM; Ananina GALINA; Bajano Flávia F; Costa Sueli M Da S et al. 2021. Association of genetic variants rs641153 ( cfb</i> ); rs2230199 ( c3</i> ); and rs1410996 ( cfh</i> ) with age-related macular degeneration in a brazilian population. Experimental biology and medicine. 7, 153537022110245-.
  12. Life Sciences Genetics
    Occhiutto Marcelo LUÍS; Mônica Barbosa De MELO; Cabral De Vasconcellos José PAULO; Rodrigues Thiago Adalton ROSA; Bajano Flávia FIALHO et al. 2021. -association of apoe</i> gene polymorphisms with primary open angle glaucoma in brazilian patients-. Ophthalmic genetics. 42, 53-61.
  13. Life Sciences Cell Biology
    Ito Mirta T; Da Silva Costa Sueli M; Baptista Letícia C; Carvalho Siqueira Gabriela Q; Albuquerque Dulcinéia M et al. 2020. Angiogenesis-related genes in endothelial progenitor cells may be involved in sickle cell stroke. Journal of the american heart association. 9, e014143-.
  14. Health Sciences Medicine (miscellaneous)
    Domingos Igor F; Pereira Martins Diego A; Borges Medeiros Rayssa L; Falcao Diego A; Hatzlhofer Betania L et al. 2020. Evaluation of oxidative stress-related genetic variants for predicting stroke in patients with sickle cell anemia. Journal of the neurological sciences. 414, 116839-.
  15. Life Sciences Cell Biology
    Baptista Letícia CARVALHO; Costa Maria LAURA; Castro Fernanda GARANHANI; De Souza Rocha CRISTIANE; Cendes Iscia LOPES et al. 2020. Placental transcriptome profile of women with sickle cell disease reveals differentially expressed genes involved in migration; trophoblast differentiation and inflammation. Blood cells molecules and diseases. 84, 102458-.
  16. Life Sciences Genetics
    Baptista Letícia C; Figueira Camilla O; Souza Bruno B; Fertrin Kleber Y; Antolini ARTHUR et al. 2019. Different morphological and gene expression profile in placentas of the same sickle cell anemia patient in pregnancies of opposite outcomes. Experimental biology and medicine. 244, 153537021983430-.
  17. Life Sciences Genetics
    Cruz Pedro R S; Ananina GALINA; Gil Da Silva Lopes Vera LUCIA; Simioni MILENA; Menaa FARID et al. 2019. Genetic comparison of sickle cell anaemia cohorts from brazil and the united states reveals high levels of divergence. Scientific reports. 9, 10896-.
  18. Health Sciences Radiology, Nuclear Medicine and Imaging
    De Carvalho Siqueira Gabriela QUEILA; Ananina GALINA; De Souza Bruno BATISTA; Borges Murilo GUIMARÃES; Ito Mirta TOMIE et al. 2019. Whole-exome sequencing indicates flg</i> 2 variant associated with leg ulcers in brazilian sickle cell anemia patients. Experimental biology and medicine. 244, 153537021984959-.
  19. Life Sciences Genetics
    Hauser Michael A; Allingham R RAND; Aung TIN; Van Der Heide Carly J; Taylor Kent D et al. 2019. Association of genetic variants with primary open-angle glaucoma among individuals with african ancestry. Jama-journal of the american medical association. 322, 1682-.
  20. Life Sciences Immunology and Microbiology (miscellaneous)
    Ana Claudia Viana WANZELER; Italo Antunes França BARBOSA; Bruna DUARTE; Daniel BORGES; Eduardo Buzolin BARBOSA et al. 2019. Mechanisms and biomarker candidates in pterygium development. Arquivos brasileiros de oftalmologia. 82, 528-536.
  21. Health Sciences Neurology (clinical)
    Tamires Prates LANA; Sueli Matilde Da Silva COSTA; Galina ANANINA; Fábio Endo HIRATA; Priscila Hae Hyun RIM et al. 2018. Association of htra1 rs11200638 with age-related macular degeneration (amd) in brazilian patients. Ophthalmic genetics. 39, 46-50.
  22. Life Sciences Genetics
    Marques Ana MARIA; Ananina GALINA; Vital Paulino COSTA; José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO. 2018. Estimating the age of the p.cys433arg variant in the myoc gene in patients with primary open-angle glaucoma. Plos one. 13, e0207409-.
  23. Life Sciences Genetics
    Oliveira Mariana B; De Vasconcellos José Paulo C; Ananina GALINA; Costa Vital P; Mônica Barbosa De MELO. 2018. Association between il1a</i> and il1b</i> polymorphisms and primary open angle glaucoma in a brazilian population. Experimental biology and medicine. 243, 1083-1091.
  24. Health Sciences Infectious Diseases
    Svidnicki Paulo VINICIUS; Braghini Carolina AYUMI; Vital Paulino COSTA; Rui Barroso SCHIMITI; De Vasconcellos José Paulo CABRAL et al. 2018. Occurrence of myoc</i> and cyp1b1</i> variants in juvenile open angle glaucoma brazilian patients. Ophthalmic genetics. 39, 717-724.
  25. Health Sciences Genetics (clinical)
    Medina Flavio Mac CORD; Motta Augusto Alves Lopes DA; Takahashi Walter YUKIHIKO; Carricondo Pedro CARLOS; Motta Mario Martins Dos SANTOS et al. 2017. Association of the cfh</i></b> y402h polymorphism with the 1-year response of exudative amd to intravitreal anti-vegf treatment in the brazilian population. Ophthalmic research. 1, 1-7.
  26. Health Sciences Radiology, Nuclear Medicine and Imaging
    Souto Fernanda Maria SILVEIRA; De Vasconcellos José Paulo CABRAL; Mônica Barbosa De MELO; Sartorato Edi LÚCIA; Moura Frederico CASTELO. 2017. Differentiating leber hereditary optic neuropathy from normal-tension glaucoma. Neuro-ophthalmology (aeolus press. 1980). 41, 1-4.
  27. Health Sciences Infectious Diseases
    Nunes Hugo FREIRE; Ananina GALINA; Vital Paulino COSTA; Zanchin Nilson Ivo TONIN; De Vasconcellos José Paulo CABRAL et al. 2017. Investigation of cav1/cav2</i> rs4236601 and cdkn2b-as1</i> rs2157719 in primary open-angle glaucoma patients from brazil. Ophthalmic genetics. 7, 1-6.
  28. Life Sciences Genetics
    Daniela Prescila Dezidério SACCONI; Vasconcellos J P C; Hirata Fabio ENDO; Medina Flávio MACCORD; Rim Priscila Hae HYUN et al. 2016. Evaluation of cfh y402h polymorphism and cfhr3/chfr1 deletion in age-related macular degeneration patients from brazil. Ophthalmic genetics. 4, 1-3.
  29. Life Sciences Genetics
    Chiea Chuen KHOR; Tan DO; Hongyan JIA; Masakazu NAKANO; Ronnie GEORGE et al. 2016. Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma. Nature genetics (print). X-X.
  30. Health Sciences Medicine (miscellaneous)
    Baptista Letícia C; Costa Maria LAURA; Ferreira REGIANE; Albuquerque Dulcinéia M; Lanaro CAROLINA et al. 2016. Abnormal expression of inflammatory genes in placentas of women with sickle cell anemia and sickle hemoglobin c disease. Annals of hematology. 95, 1859-1867.
  31. Life Sciences Neuroscience (miscellaneous)
    Cruz P R S; Lira R P C; Pereira Filho S A C; Souza B B; Mitsuushi F N et al. 2015. Increased circulating pedf and low sicam-1 are associated with sickle cell retinopathy. Blood cells; molecules & diseases (print). 54, 33-37.
  32. Life Sciences Genetics
    Mônica Barbosa De MELO; Mandal Anil K; Tavares Ivan M; Ali Mohammed HASNAT; Kabra MEHA et al. 2015. Genotype-phenotype correlations in cyp1b1-associated primary congenital glaucoma patients representing two large cohorts from india and brazil. Plos one. 10, e0127147-.
  33. Life Sciences Genetics
    Medina Flávio MACCORD; Augusto Lopes Alves Da MOTTA; Walter Y TAKAHASHI; Pedro Carlos CARRICONDO; Mario Martins Dos Santos MOTTA et al. 2015. Pharmacogenetic effect of cfh gene polymorphism in response to the initial intravitreal injection of bevacizumab for wet amd. Ophthalmic research. 54, 169-174.
  34. Life Sciences Neuroscience (miscellaneous)
    Mônica Barbosa De MELO. 2014. An eye on sickle cell retinopathy. Revista brasileira de hematologia e hemoterapia (impresso). 36, 319-321.
  35. Life Sciences Genetics
    Hirata Fabio ENDO; José Paulo Cabral De VASCONCELLOS; Medina Flávio MACCORD; Rim Priscila Hae HYUN; Fulco Enzo Augusto MEDEIROS et al. 2014. Association of loc387715/arms2</i> (rs10490924) gene polymorphism with age-related macular degeneration in the brazilian population. Ophthalmic genetics. 1, 1-5.
  36. Life Sciences Genetics
    Gislene Pereira GIL; Galina ANANINA; Mariana B OLIVEIRA; Fernando Ferreira COSTA; Márcio José Da SILVA et al. 2013. Polymorphism in the hmox1 gene is associated with high levels of fetal hemoglobin in brazilian patients with sickle cell anemia. Hemoglobin. 37, 315-324.
  37. Health Sciences Genetics (clinical)
    Braghini Carolina AYUMI; Neshich Izabella Agostinho PENA; Neshich GORAN; Soardi Fernanda CAROLINE; De Mello Maricilda PALANDI et al. 2013. New mutation in the myocilin gene segregates with juvenile-onset open-angle glaucoma in a brazilian family. Gene (amsterdam). 523, 50-57.
  38. Life Sciences Genetics
    Fábio Francisco De Oliveira RODRIGUES; Roberto Euzébio Dos SANTOS; André Lima De OLIVEIRA; Renato De Lima ROZENOWICZ; Mônica Barbosa De MELO et al. 2012. Prognostic assessment of polymorphisms of the mdr-1 and gstp1 genes in patients with stage ii and iii breast cancer submitted to neoadjuvant chemotherapy. The breast journal. 18, 185-187.
  39. Life Sciences Genetics
    Niro KASAHARA; Cristiano Caixeta UMBELINO; Maurício Della PAOLERA; Mylene Neves ROCHA; Flávio RICHETI et al. 2011. Myocilin mt.1 gene promoter single nucleotide polymorphism (-1000c>g) in brazilian patients with primary open angle glaucoma. Ophthalmic genetics. 32, 18-23.
  40. Health Sciences Immunology and Allergy
    Farid MENAA; Carolina Ayumi BRAGHINI; José Paulo Cabral De VASCONCELLOS; Bouzid MENAA; Vital Paulino COSTA et al. 2011. Keeping an eye on myocilin: a complex molecule associated with primary open-angle glaucoma susceptibility. Molecules (basel. online). 16, 5402-5421.
  41. Life Sciences Genetics
    Eugênio Santana De FIGUEIREDO; Giordano GG; Anderson TAVARES; Márcio José Da SILVA; José Paulo Cabral De VASCONCELLOS et al. 2011. Novel human crygd rare variant in a brazilian family with congenital cataract. Molecular vision. 17, 2207-2211.
  42. Life Sciences Genetics
    Maurício Della PAOLERA; José Paulo Cabral De VASCONCELLOS; Cristiano Caixeta UMBELINO; Niro KASAHARA; Mylene Neves ROCHA et al. 2010. Cyp1b1 gene analysis in primary congenital glaucoma brazilian patients: novel mutations and association with poor prognosis. Journal of glaucoma. 19, 176-182.
  43. Life Sciences Cancer Research
    André Lima De OLIVEIRA; Fábio RODRIGUES; Roberto Euzébio Dos SANTOS; Tsutomo AOKI; Mylene Neves ROCHA et al. 2010. Gstt1; gstm1; and gstp1 polymorphisms and chemotherapy response in locally advanced breast cancer. Genetics and molecular research. 9, 1045-1053.
  44. Life Sciences Genetics
    Cristiano Caixeta UMBELINO; José Paulo Cabral De VASCONCELLOS; Niro KASAHARA; Maurício Della PAOLERA; Geraldo Viecente De ALMEIDA et al. 2009. Lack of association between optineurin gene variants t34t; e50k; m98k; 691_692insag and r545q and primary open angle glaucoma in brazilian patients. Ophthalmic genetics. 30, 13-18.
  45. Life Sciences Genetics
    Alessandro SANTANA; Mauro WAISWOL; Enyr Saran ARCIERI; José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO. 2009. Mutation analysis of cryaa; crygc and crygd genes associated with autosomal dominant congenital cataract in brazilian families. Molecular vision. 15, 793-800.
  46. Life Sciences Developmental Biology
    Anderson Ferreira Da CUNHA; Af BRUGNEROTTO; Ma CORAT; Ee DEVLIN; Ap GIMENES et al. 2009. High levels of human gamma-globin are expressed in adult mice carrying a transgene of the brazilian type of hereditary persistence of fetal hemoglobin ((a)gamma -195). Hemoglobin. 33, 439-447.
  47. Health Sciences Medicine (miscellaneous)
    Andréa Danielle Sant Anna SANTOS; Roberto Adelino De Almeida PRADO; Mônica Barbosa De MELO; Murilo Rezende MELO; Carlos Alberto LONGUI. 2008. Structural evaluation of type 3 dopaminergic receptor gene (drd3) in chronic anovulatory women. Genetics and molecular research. 7, 140-151.
  48. Life Sciences Genetics
    Fábio Francisco De Oliveira RODRIGUES; Roberto Euzébio Dos SANTOS; Mônica Barbosa De MELO; M A L G SILVA; André Lima De OLIVEIRA et al. 2008. Correlation of polymorphism c3435t of the mdr-1 gene and the response of primary chemotherapy in women wityh locally advanced breast cancer. Genetics and molecular research. 7, 177-183.
  49. Health Sciences Genetics (clinical)
    Adriano Namo CURY; Carlos Alberto LONGUI; Cristiane KOCHI; Luís Eduardo Procópio CALLIARI; Nilza SCALISSI et al. 2008. Graves' disease in brazilian children and adults: lack of genetic association with ctla-4 +49a>g polymorphism. Hormone research. 70, 36-41.
  50. Life Sciences Neurology
    Vânia P A WOBETO; E T ROSIM; Mônica Barbosa De MELO; Luís Eduardo Procópio CALLIARI; Maria De Fátima SONATI. 2007. Haptoglobin polymorphism and diabetic retinopathy in brazilian patients. Diabetes research and clinical practice. 77, 385-388.
  51. Health Sciences Pediatrics, Perinatology and Child Health
    Cristiane KOCHI; Carlos Alberto LONGUI; Sofia H V LEMOSMARINI; Gili GUERRAJR; Mônica Barbosa De MELO et al. 2007. The influence of parental origin of x chromosme genes on the stature of patients with 45x turner syndrome; no prelo. Genetics and molecular research. 6, 1-7.
  52. Health Sciences Genetics (clinical)
    Flávio RICHETI; Renata Maria NORONHA; Ricardo Temudo Lessa WAETGE; José Paulo Cabral De VASCONCELLOS; Osías Francisco De SOUZA et al. 2007. Evaluation of ac(n) and c(-106)t polymorphisms of the aldose reductase gene in brazilian patients with dm1 and susceptibility to diabetic retinopathy; aceito para publicação. Molecular vision. 13, 740-745.
  53. Life Sciences Genetics
    Luís Eduardo Procópio CALLIARI; Carlos Alberto LONGUI; Mylene Neves ROCHA; Cláudia Dutra Costantin FARIA; Cristiane KOCHI et al. 2007. A novel mutation in dax1 gene causing different phenotypes in three siblings with adrenal hypoplasia congenita. Genetics and molecular research. 6, 177-183.
  54. Health Sciences Radiology, Nuclear Medicine and Imaging
    Wener CELLA; José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO; Bianca KNEIPP; Fernando Ferreira COSTA et al. 2006. Structural assessment of pitx2; foxc1; cyp1b1 and gja1 genes in patients with axenfeld-rieger syndrome with developmental glaucoma. Investigative ophtalmology & visual science. Estados Unidos. 47, (5) 1803-1809.
  55. Health Sciences Medicine (miscellaneous)
    Mônica Souza Filho MOURA; Mônica Barbosa De MELO; Carlos Alberto LONGUI; Mylene Neves ROCHA; Osmar MONTE. 2006. Triagem de mutações nos receptores de angiotensina ii; agtr1 e agtr2 e avaliação dos polimorfismos c573t e a1166c do gene agtr1 em pacientes com adrenarca precoce idiopática. Arquivos brasileiros de endocrinologia & metabologia. Brasil. 50, (5) 893-900.
  56. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO; Rui Barroso SCHIMITI; Norisvaldo César BRESSANIM; Fernando Ferreira COSTA et al. 2005. A novel mutation in the gja1 gene in a family with oculodentodigital dysplasia. Archives of ophthalmology. Estados Unidos. 123, (10) 1422-1426.
  57. Health Sciences Medicine (miscellaneous)
    Carlos Alberto LONGUI; Sofia LEMOSMARINI; Bonald FIGUEIREDO; Berenice Bilharinho MENDONÇA; Margarete De CASTRO et al. 2004. Inhibin alpha-subunit (inha) gene and locus changes in paediatric adrenocortical tumours from tp53 r337h mutation heterozygote carriers. Journal of medical genetics. Inglaterra. 41, 354-359.
  58. Life Sciences Aquatic Science
    Mônica Barbosa De MELO; Silvana BORDIN; Adriana Silva Santos DUARTE; Satie H OGO; Márcio A TORSONI et al. 2003. Molecular characterization of hemoglobin alpha-d chains from geochelone carbonaria and geochelone denticulata land turtles. Comparative biochemistry and physiology. part b: biochemistry & molecular biology (print). 134, 389-395.
  59. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO; Rui Barroso SCHIMITI; Fernando Ferreira COSTA; Vital Paulino COSTA. 2003. Penetrance and phenotype of the cys433arg myocilin mutation in a family pedigree with primary open-angle glaucoma. Journal of glaucoma. Estados Unidos. 12, 104-107.
  60. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Manoela Marques ORTEGA; Hélvia NASCIMENTO; Mônica Barbosa De MELO; M T TEORI; Fernando Ferreira COSTA et al. 2003. Polymorphisms of glutathione s-transferase mu1 (gstm1) and theta 1 (gstt1) genes in multiple myeloma. Acta haematologica. República Tcheca. 109, 108-109.
  61. Health Sciences Medicine (miscellaneous)
    Manoela Marques ORTEGA; Mônica Barbosa De MELO; Cármino Antônio De SOUZA; Irene Lorand METZE; Fernando Ferreira COSTA et al. 2003. A possible role of the p53 gene deletion as a prognostic factor in multiple myeloma. Annals of hematology. Alemanha. 82, 405-409.
  62. Health Sciences Cardiology and Cardiovascular Medicine
    Kleber Y FERTRIN; Mônica Barbosa De MELO; Ângela Maria De ASSIS; Sara Teresinha Olalla SAAD; Fernando Ferreira COSTA. 2003. Udp-glucuronosyltransferase 1 gene promoter polymorphism is associated with increased serum bilirubin levels and cholecystectomy in patients with sickle cell anemia. Clinical genetics. Dinamarca. 64, (2) 160-162.
  63. Health Sciences Medicine (miscellaneous)
    Simone Bordignon De JORGE; Mônica Barbosa De MELO; Fernando Ferreira COSTA; Maria De Fátima SONATI. 2003. Screening for mutations in human alpha-globin genes by nonradioactive single-strand conformation polymorphism. Brazilian journal of medical and biological research. Brasil. 36, (11) 1471-1474.
  64. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Silvana BORDIN; Vanessa G CRESPI; Adriana S S DUARTE; Daniela Sanchez BASSÈRES; Mônica Barbosa De MELO et al. 2002. Dnaase i hypersensitive site 3'to the beta-globin gene cluster contains a taa insertion specific for beta(s)-benin haplotype. Haematologica (roma). Itália. 87, (3) 246-249.
  65. Health Sciences Medicine (miscellaneous)
    Mônica Barbosa De MELO; Nilofer Nina AHMAD; Carmen Sílvia Passos LIMA; Kátia Borgia Barbosa PAGNANO; Silvana BORDIN et al. 2002. Mutations in the p53 gene in acute myeloid leukemia patients correlate with poor prognosis. Hematology. 7, (1) 13-19.
  66. Life Sciences Genetics
    Ivao STOILOV; Vital Paulino COSTA; José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO; Alberto J BETINJANE et al. 2002. Molecular genetics of primary congenital glaucoma in brazil. Investigative ophtalmology & visual science. Estados Unidos. 43, (6) 1820-1827.
  67. Health Sciences General Medicine
    Luís Soares Gouvea HORTA; Carlos Alberto LONGUI; E S SOARES; Antônio Francisco D OSWALDO; C R FULLER et al. 2002. Methylation of the androgen receptor gene in cryptorchid boys. The journal of endocrine genetics. Estados Unidos. 3, 27-31.
  68. Life Sciences Genetics
    Carlos Alberto LONGUI; Mylene Neves ROCHA; Liana Carla Albuquerque Peres MARTINHO; Gustavo Gir GOMES; Ricardo Eustachio De MIRANDA et al. 2002. Molecular detection of x0 - turner syndrome. Genetics and molecular research. Brasil. 1, (3) 266-270.
  69. Life Sciences Clinical Biochemistry
    Valder Roberval ARRUDA; Carmen Sílvia Passos LIMA; Carlos Roberto Escrivão GRIGNOLI; Mônica Barbosa De MELO; Irene Lorand METZE et al. 2001. Increased risk for acute myeloid leukaemia in individuals with glutathione s-transferase mu 1 (gstm1) and theta 1 (gstt1) gene defects. European journal of haematology. Grã-Bretanha. 66, (6) 383-388.
  70. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Anamaria Aranha CAMARGO; Mônica Barbosa De MELO; Et AL. 2001. The contribution of 700;000 orf sequence tags to the definition of the human transcripome. Pnas. proceedings of the national academy of sciences of the united states of america. Estados Unidos. 98, (21) 12103-12108.
  71. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO; Rui SCHIMITI; Vital Paulino COSTA; Fernando Ferreira COSTA. 2001. Estudo da mutação cys433arg no gene myoc em família com glaucoma primário de ângulo aberto. Arquivos brasileiros de oftalmologia. Brasil. 64, (4) 74-.
  72. Health Sciences Immunology and Allergy
    José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO; Vital Paulino COSTA; Daniela Miti Lemos TSUKUMO; Daniela Sanchez BASSÈRES et al. 2000. Novel mutation in the myoc gene in primary open angle glaucoma patients. Journal of medical genetics. Inglaterra. 37, 301-303.
  73. Life Sciences Genetics
    Nilofer Nina AHMAD; Mônica Barbosa De MELO; A D SINGH; Larry A DONOSO; Jerry A SHIELDS. 1999. A possible hot spot in exon 21 of the rb gene predisposing to a low penetrant retinoblastoma phenotype?. Ophthalmic genetics. Holanda. 20, (4) 225-231.
  74. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO; Fernando MENEZES; Daniela Miti Lemos TSUKUMO; Vital Paulino COSTA et al. 1998. Mutações no gene myoc/tigr em uma população brasileira com glaucoma juvenil e glaucoma primário de ângulo aberto. Arquivos brasileiros de oftalmologia. Brasil. 61, (6) 690-694.
  75. Life Sciences Genetics
    Silvana BORDIN; Juliana Touguinha MARTINS; Marilda De Souza GONÇALVES; Mônica Barbosa De MELO; Sara Teresinha Ollala SAAD et al. 1998. Haplotype analysis and gamma a gene polymorphism associated with the brazilian type of hereditary persistence of fetal hemoglobin. American journal of hematology. Estados Unidos. 58, (1) 49-54.
  76. Life Sciences Cell Biology
    Mônica Barbosa De MELO; Fernando Ferreira COSTA; Sara Teresinha Ollala SAAD; Irene Lorand METZE; Silvana BORDIN et al. 1998. Molecular analysis of the retinoblastoma (rb1) gene in acute myeloid leukemia patients. Leukemia research. 22, (9) 787-792.
  77. Health Sciences Genetics (clinical)
    Mônica Barbosa De MELO; Irene Lorand METZE; Carmen Sílvia Passos LIMA; Sara Teresinha Ollala SAAD; Fernando Ferreira COSTA. 1997. N-ras gene point mutations in brazilian acute myelogenous leukemia patients correlate with a poor prognosis. Leukemia & lymphoma. 24, 309-317.
  78. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Mônica Vannucci NUNES; Mônica Barbosa De MELO; Fernando Ferreira COSTA; Marileila VARELLAGARCIA. 1995. A simple technique for isolation of dna suitable for pcr amplification from cytogenetic preparations. Brazilian journal of genetics. Brasil. 18, (3) 489-490.
  79. Physical Sciences Biomedical Engineering
    Mônica Barbosa De MELO; Tereza Sueko Ide SALES; Irene Lorand METZE; Fernando Ferreira COSTA. 1992. Rapid method for isolation of dna from glass slide smears for pcr. Acta haematologica. Inglaterra. 87, 214-215.
  1. Life Sciences Genetics
    Mônica Barbosa De MELO; Cabral De Vasconcellos José PAULO; Paulino Costa VITAL. 2021. Primary congenital glaucoma genetics: the experience in brazil. In: Essentials in ophthalmology. Cingapura.
  2. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO. 2019. Genética relacionada ao glaucoma. In: Glaucoma na infância. Brasil.
  3. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Mônica Barbosa De MELO; Sallum Juliana M F. 2019. Princípios de biologia molecular e padrões de herança. In: Série oftalmologia brasileira - genética ocular. Brasil.
  4. Health Sciences Neurology (clinical)
    Vasconcellos J P C; Mônica Barbosa De MELO; Costa Vital P. 2019. Glaucoma primário de ângulo aberto. In: Série oftalmologia brasileira - genética ocular. Brasil.
  5. Health Sciences Radiology, Nuclear Medicine and Imaging
    José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO; Souza B B. 2019. Glaucoma primário de ângulo fechado. In: Série oftalmologia brasileira - genética ocular. Brasil.
  6. Life Sciences Genetics
    Vasconcellos J P C; Mônica Barbosa De MELO. 2017. Genética do glaucoma congênito primário e de desenvolvimento. In: Oftalmologia pediátrica e estrabismo. Brasil.
  7. Health Sciences Medicine (miscellaneous)
    Eugênio Santana De FIGUEIREDO; Mônica Barbosa De MELO. 2015. Catarata infantil: etiologia; genética e prevenção. In: Catarata. Brasil.
  8. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; Vital Paulino COSTA; Mônica Barbosa De MELO. 2010. Genética e biologia molecular no glaucoma. In: Glaucoma. Brasil.
  9. Social Sciences & Humanities Psychology (miscellaneous)
    José Paulo Cabral De VASCONCELLOS; Vital Paulino COSTA; Mônica Barbosa De MELO. 2010. Tratamento clínico- novas perspectivas clínicas- terapia gênica. In: Glaucoma. Brasil.
  10. Health Sciences Medicine (miscellaneous)
    José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO. 2009. Doenças genéticas. In: Saúde ocular e prevenção da cegueira. Brasil.
  11. Life Sciences Animal Science and Zoology
    José Paulo Cabral De VASCONCELLOS; Vital Paulino COSTA; Mônica Barbosa De MELO. 2007. Terapia gênica. In: Glaucoma. Brasil.
  12. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; Vital Paulino COSTA; Mônica Barbosa De MELO. 2007. Genética e biologia molecular no glaucoma. In: Glaucoma. Brasil.
  13. Life Sciences Physiology
    Mônica Barbosa De MELO. 2006. Endocrinologia molecular - seqüenciamento gênico. In: Endocrinologia para o pediatra. Brasil.
  14. Health Sciences Dentistry (miscellaneous)
    Mônica Barbosa De MELO. 2006. Endocrinologia molecular - diabetes mellitus tipo 2. In: Endocrinologia para o pediatra. Brasil.
  15. Health Sciences Nutrition and Dietetics
    Murilo Rezende MELO; Mônica Barbosa De MELO. 2006. Endocrinologia molecular - southern; northern e western blots. In: Endocrinologia para o pediatra. Brasil.
  16. Life Sciences Endocrinology
    Mônica Barbosa De MELO. 2006. Endocrinologia molecular - diabetes mellitus tipo 1. In: Endocrinologia para o pediatra. Brasil.
  1. Health Sciences Radiology, Nuclear Medicine and Imaging
    Sallum Juliana M F; Maria Fernanda ABALEM; Simone FINZI; Mônica Barbosa De MELO. 2019. Série oftalmologia brasileira - genética ocular. Brasil.