Chong Ae Kim

Dados pessoais

Publicações

Total: 988

Área temática ASJC

Percentual das publicações classificadas

  • HS Ciências da Saúde
  • LS Ciências da Vida
  • MU Multidisciplinar
  • PS Ciências Físicas
  • SH Ciências Sociais e Humanidades

Categoria ASJC

Categorias ASJC mais frequentes

Termos frequentes nas publicações

Nuvem de termos dos títulos das publicações
Nome Vínculo Links Grande área de atuação Área de atuação
Carla Gentile MATAS Ciências da Saúde Fonoaudiologia
Carlos Augusto Galvão BARBOZA Ciências Biológicas Morfologia
Celia Priszkulnik KOIFFMANN Ciências Biológicas Genética
Claudia Berlim De MELLO Ciências Humanas Psicologia
Dafne Dain Gandelman HOROVITZ Ciências da Saúde Medicina
Débora Gusmão MELO Ciências da Saúde Medicina
Débora Maria Befi LOPES Membro Ciências da Saúde Fonoaudiologia
Decio BRUNONI Ciências Biológicas Genética
Erasmo Barbante CASELLA Ciências da Saúde Medicina
Fernanda Tebexreni ORSATI Ciências Humanas Psicologia
Juan Clinton Llerena JUNIOR Ciências da Saúde Medicina
Luiz Renato Rodrigues CARREIRO Ciências Humanas Psicologia
Márcia Helena Da Silva MELO Ciências Humanas Psicologia
Milena Coelho Fernandes CALDATO Ciências da Saúde Medicina
Paulo Ricardo Gazzola ZEN Ciências da Saúde Medicina
Paulo Sérgio BOGGIO Membro Ciências Biológicas Fisiologia
Roberto GIUGLIANI Membro Ciências Biológicas Genética
Vânia D ALMEIDA Membro Ciências Biológicas Bioquímica
Figura 1

Número de publicações por ano e por tipo

Todas as publicações do perfil

Figura 2

Categorias ASJC mais frequentes por ano

A cor dos pontos identifica a categoria predominante

Figura 3

Mapa de calor das categorias ASJC por ano

Frequências absolutas; cores mais escuras indicam mais publicações. Todas as categorias ASJC e anos disponíveis, sem aplicar os filtros da página.

Escala: 0 → 17

Mapa de calor das categorias ASJC por ano
Categoria ASJC19801983198419851986198719881989199119921993199419951996199719981999200020012002200320042005200620072008200920102011201220132014201520162017201820192020202120222023202420252026
1311 · Genetics0101200061142924176442613118756128111071110352481171
2716 · Genetics (clinical)1000001220011753111091191512233611083557837458101042
2701 · Medicine (miscellaneous)211011022556014546777204105571563256460250000
2735 · Pediatrics; Perinatology and Child Health10120002023632132225122031120111212100123101
3201 · Psychology (miscellaneous)01000000133542511002111001121121000220040000
2728 · Neurology (clinical)10001100001231101203213301100311132031112000
2808 · Neurology00000001100121212551020110412300002400200000
2801 · Neuroscience (miscellaneous)00000100002001110130010111101051032101000000
1301 · Biochemistry; Genetics and Molecular Biology (miscellaneous)00000000000010011001000010202211000301001000
1312 · Molecular Biology00000000000000101000000010110001100000101001
2710 · Embryology00000001001001012100110000010000000000000000
2712 · Endocrinology; Diabetes and Metabolism00000000001000000000000001020000000001003100
2741 · Radiology; Nuclear Medicine and Imaging00000000000100001000040011000000001000000000
1309 · Developmental Biology00000000000000000001000000020000000021000110
2705 · Cardiology and Cardiovascular Medicine00000000000000000010101000000020100000110000
2738 · Psychiatry and Mental Health00000000101000000000100000021010000000010000
3304 · Education00000001000110000001001000000010001000000000
2725 · Infectious Diseases00000000000000000011001000002000010000000000
1308 · Clinical Biochemistry00000000001000000010001100000000100000000000
2700 · General Medicine00000000100001010000000000000000001000000100
2734 · Pathology and Forensic Medicine00000000000000002000200000000000000000000100
1203 · Language and Linguistics10000000001100000000000000000000000000100000
3616 · Speech and Hearing00000000110000001000000000000000000100000000
1103 · Animal Science and Zoology00000000000000020000000000000001000000000000
1702 · Artificial Intelligence00000000001000000000000000000010000000100000
2723 · Immunology and Allergy00000000000000001000000000000101000000000000
2204 · Biomedical Engineering00000000000000000010000000000100000000000000
2708 · Dermatology00000000000000000000000000100000000000000100
2713 · Epidemiology00000000000000000000000000000000000000010100
2715 · Gastroenterology00000000000000000000000000000000000000000020
2724 · Internal Medicine00000000000000000100000000001000000000000000
2731 · Ophthalmology00000000000000000000000000000100000000000010
2732 · Orthopedics and Sports Medicine00000000000000000001000000000100000000000000
2736 · Pharmacology (medical)00000000000000100000000000010000000000000000
3310 · Linguistics and Language00000000000101000000000000000000000000000000
1300 · General Biochemistry; Genetics and Molecular Biology00000000000000000000000000000100000000000000
1302 · Aging00000000000000000000000000010000000000000000
1303 · Biochemistry00000000000000000001000000000000000000000000
1310 · Endocrinology00000000000000000000000010000000000000000000
1313 · Molecular Medicine00000000000000000000000000000000000000100000
1314 · Physiology00000000000000000000010000000000000000000000
1402 · Accounting00000000000000000000000000000000000000001000
2301 · Environmental Science (miscellaneous)00000000000000000100000000000000000000000000
2401 · Immunology and Microbiology (miscellaneous)00000000000000000000000000000001000000000000
2405 · Parasitology00000000000100000000000000000000000000000000
2702 · Anatomy00000000000000000000000000000000000010000000
2704 · Biochemistry (medical)00000000000000000000000000100000000000000000
2720 · Hematology00000000000000000000100000000000000000000000
2722 · Histology00000000000000000000000000010000000000000000
2727 · Nephrology00000000000000000000010000000000000000000000
2730 · Oncology00000000000000000000001000000000000000000000
2733 · Otorhinolaryngology00000000000000000000000000000000000000000100
2739 · Public Health; Environmental and Occupational Health00000000000001000000000000000000000000000000
2746 · Surgery00000000000000000000000000000000010000000000
2803 · Biological Psychiatry00000000000000000000000000000100000000000000
2806 · Developmental Neuroscience00000000000000000000100000000000000000000000
2809 · Sensory Systems00000000000000000000000000000000000000001000
2919 · Pediatrics00000000000000000000000000000000000010000000
3001 · Pharmacology; Toxicology and Pharmaceutics (miscellaneous)00000000000000000000000000000000000100000000
3203 · Clinical Psychology00000000000000000000000000100000000000000000
3204 · Developmental and Educational Psychology00000000000000000000000000000000001000000000
3206 · Neuropsychology and Physiological Psychology00000000000000000000000000001000000000000000
3300 · General Social Sciences00000000000000000000000000000000000000010000
3607 · Medical Laboratory Technology00000000000000001000000000000000000000000000
988 publicação(ões)
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Ano Tipo Registro Área temática e categoria ASJC
2012 Capítulo de livro
Displasias esqueléticas Chong Ae KIM; Israel GOMY; Debora Romeo BERTOLA Diagnóstico por Imagem ISBN 9788520429
HS Orthopedics and Sports Medicine
2012 Capítulo de livro
Principais Síndromes Genéticas Associadas a transtornos Psiquiátricos na Infância e na Adolescência Chong Ae KIM; D R BERTOLA; Leslie Domenioci KULIKOWSKI; F PIAZZON Tratado de Psiquiatria da Infância e da Adolescência ISBN 9788538803300
LS Biological Psychiatry
2012 Trabalho em evento
Characterizing pervasive somatic mosaicism in pos-mortem tissues samples A T DIAS; Roberta Lelis DUTRA; E A ZANARDO; F B PIAZZON; M B MOREIRA et al II Encontro Pauslista de Citogenética (EPACITO)
HS Medicine (miscellaneous)
2012 Trabalho em evento
Complex genomic reorganization in 1p36 and molecular mechanisms for formation E A ZANARDO; F PIAZZON; Roberta Lelis DUTRA; A T DIAS; M M OLIVEIRA et al II Encontro paulista de Citogenética (EPACITO)
LS Biochemistry; Genetics and Molecular Biology (miscellaneous)
2012 Trabalho em evento
Importante papel dos genes SNA29; LZTR1 e P2RXL1 na regulação da resposta imune de portadora de deleção atípica da região 22q11.2 Diogo Cordeiro De Queiroz SOARES; Leuridan Cavalcante TORRES; L D KULIKOWSKI; Debora Romeo BERTOLA; Chong Ae KIM 12o Congresso Brasileiro de Alergia e Imunologia em Pediatria
LS Biochemistry; Genetics and Molecular Biology (miscellaneous)
2012 Trabalho em evento
External validation of the Bartholdi clinical acoring system for Silver Russell syndrome: a report of a Brazilian cohort G L YAMAMOTO; A BONALDI; A M Vianna MORGANTE; I GOMMY; Chong Ae KIM et al 62nd Annual Meeting of the American Society of Human Genetics
LS Neurology
2012 Trabalho em evento
Severe CHST3 mutations in two Brazilian families with spondyloepiphyseal dysplasia with congenital joint dislocations W A R BARATELA; T F ALMEIDA; G L YAMAMOTO; J H MARQUES; O LETAIL et al 62nd Annual Meeting of the American Society of Human Genetics
LS Genetics
2012 Trabalho em evento
Tegumentary manifestations in RASopathies are common and deserve special attentionO C QUAIO; A S BRASIL; A C PEREIRA; Chong Ae KIM; Debora Romeo BERTOLA 62nd Annual Meeting of the American Society of Human Genetics
SH Psychology (miscellaneous)
2012 Trabalho em evento
Schinzel-Giedion syndrome in two Brazilian patients: report of a novel mutation in SETBP1 E D F CARVALHO; M LAZAR; T F ALMEIDA; C R D C QUAIO; G L YAMAMOTO et al 62nd Annual Meeting of the American Society of Human Genetics
HS Genetics (clinical)
2012 Trabalho em evento
Patterns of genetic expression in mental retardation associated or not with microcephaly T F ALMEIDA; D V BERNARDO; C R D C QUAIO; G L YAMAMOTO; E D F CARVALHO et al 62nd Annual Meeting of the American Society of Human Genetics
HS Neurology (clinical)
2012 Trabalho em evento
Complex genomic reorganization in microdeletions/microduplications syndromes and molecular mechanisms for formation L D KULIKOWSKI; F PIAZZON; E ZANARDO; R DUTRA; A DIAS et al 62nd Annual Meeting of the American Society of Human Genetics
LS Genetics
2012 Trabalho em evento
Facing current diagnostic challenges in array copy number analysis F B PIAZZON; R DUTRA; E ZANARDO; A DIAS; M MOREIRA et al 62nd Annual Meeting of the American Society of Human Genetics
PS Biomedical Engineering
2012 Trabalho em evento
Array-based copy number analysis in patients associating Obesity and developmental delay/learning disabilities and additional features. C D ANGELO; I KOHL; C De CASTRO; Chong Ae KIM; D R BERTOLA et al 62nd Annual Meeting of the American Society of Human Genetics
LS Neurology
2012 Trabalho em evento
Novel ROR2 mutations in patients with autosomal recessive Robinow syndrome J MAZZEU; H KAYSERILLI; Chong Ae KIM; D BRUNONI; P C PIERI et al 62nd Annual Meeting of the American Society of Human Genetics
LS Genetics
2012 Trabalho em evento
Hipertensão arterial e distúrbios miccionais em pacientes com síndrome de Williams-Beuren E A FURUZAWA; Rachel S HONJO; C S LANETZKI; R L DUTRA; L D KULIKOWSKI et al XXVI Congresso Brasileiro de Nefrologia
HS Medicine (miscellaneous)
2012 Trabalho em evento
Natural killer cell deficiency in patients with mucopolysaccharidoses Leuridan Cavalcante TORRES; Caio Robledo QUAIO; José FRANCO; Israel GOMY; Debora Romeo BERTOLA et al 15th ESID Biennial Meeting
HS Genetics (clinical)
2012 Trabalho em evento
Mucopolyssaccharidoses type IV: case of a patient with humoral response deficiency Leuridan Cavalcante TORRES; Diogo Cordeiro De Queiroz SOARES; Caio Robledo D C QUAIO; José FRANCO; Leslie Domenici KULIKOWSKI et al 15th ESID Biennial Meeting
HS Medicine (miscellaneous)
2012 Artigo em periódico
Serpentine fibula polycystic kidney syndrome is part of the phenotypic spectrum of Hajdu-Cheney syndrome M J GRAY; Chong Ae KIM; Debora Romeo BERTOLA; P R ARANTES; H STEWART et al European Journal of Human Genetics ISSN 1018-4813
LS Genetics
2012 Artigo em periódico
Ocular manifestations of Noonan syndrome Lenina Rocha Pitta MARIN; Felipe Theodoro Bezerra Gaspar Carvalho Da SILVA; F V M SÁ; A S BRASIL; A PEREIRA et al Ophthalmic Genetics ISSN 1381-6810
HS Ophthalmology
2012 Artigo em periódico
Report of a large Brazilian family with a very attenuated form of Hunter syndrome (MPS II). Caio Robledo D C QUAIO; Henrique GRINBERG; M L C VIEIRA; Ana Carolina PAULA; G N LEAL et al Journal of Inherited Metabolic Disease ISSN 0141-8955
HS Genetics (clinical)
2012 Artigo em periódico
The First Cardiac Transplant Experience in a Patient with Mucopolyssaccharidosis Henrique GRINBERG; Caio Robledo D C QUAIO; Monica Samuel AVILA; Silvia Moreira Ayub FERREIRA; Marcelo Luiz Campos VIEIRA et al Cardiovascular Pathology ISSN 1054-8807
HS Medicine (miscellaneous)
2012 Artigo em periódico
Multiple; diffuse schwannomas in a RASopathy phenotype patient with germline KRAS mutation: a causal relationship Debora Romeo BERTOLA; A C PEREIRA; A S BRASIL; L SUZUKI; C LEITE et al Clinical Genetics ISSN 0009-9163
HS Genetics (clinical)
2012 Artigo em periódico
Copy Number Variation in Williams-Beuren syndrome: Suitable Diagnostic Strategy for Developing Countries Roberta Lelis DUTRA; Rachel Sayuri HONJO; Leslie Domenici KULIKOWSKI; Fernanda Andrade Macaferri FONSECA; Patrícia PIERI et al BMC Research Notes ISSN 1756-0500
LS Genetics
2012 Artigo em periódico
Mutations in SRCAP; SNF2 - related CREBBP activator protein; cause Floating-Harbor Syndrome. Rebecca L HOOD; Matthew A LINES; Sara NIKKEL; Jeremy SCHWARTZENTRUBER; Chandree BEAULIEU et al American Journal of Human Genetics ISSN 0002-9297
HS Genetics (clinical)
2012 Artigo em periódico
Identification of 2 Novel ANTXR 2 Mutations in Brazilian Patients with Hyaline Fibromatosis Syndrome and Proposal of Grading System Rafael DENADAI; Cassio Eduardo Raposo AMARAL; Debora Romeo BERTOLA; Chong Ae KIM; Nivaldo ALONSO et al American Journal of Medical Genetics. Part A ISSN 1552-4825
LS Genetics
2012 Capítulo de livro
HS Orthopedics and Sports Medicine

Displasias esqueléticas

Diagnóstico por Imagem

Chong Ae KIM; Israel GOMY; Debora Romeo BERTOLA

ISBN 9788520429
2012 Capítulo de livro
LS Biological Psychiatry

Principais Síndromes Genéticas Associadas a transtornos Psiquiátricos na Infância e na Adolescência

Tratado de Psiquiatria da Infância e da Adolescência

Chong Ae KIM; D R BERTOLA; Leslie Domenioci KULIKOWSKI; F PIAZZON

ISBN 9788538803300
2012 Trabalho em evento
HS Medicine (miscellaneous)

Characterizing pervasive somatic mosaicism in pos-mortem tissues samples

II Encontro Pauslista de Citogenética (EPACITO)

A T DIAS; Roberta Lelis DUTRA; E A ZANARDO; F B PIAZZON; M B MOREIRA et al

2012 Trabalho em evento
LS Biochemistry; Genetics and Molecular Biology (miscellaneous)

Complex genomic reorganization in 1p36 and molecular mechanisms for formation

II Encontro paulista de Citogenética (EPACITO)

E A ZANARDO; F PIAZZON; Roberta Lelis DUTRA; A T DIAS; M M OLIVEIRA et al

2012 Trabalho em evento
LS Biochemistry; Genetics and Molecular Biology (miscellaneous)

Importante papel dos genes SNA29; LZTR1 e P2RXL1 na regulação da resposta imune de portadora de deleção atípica da região 22q11.2

12o Congresso Brasileiro de Alergia e Imunologia em Pediatria

Diogo Cordeiro De Queiroz SOARES; Leuridan Cavalcante TORRES; L D KULIKOWSKI; Debora Romeo BERTOLA; Chong Ae KIM

2012 Trabalho em evento
LS Neurology

External validation of the Bartholdi clinical acoring system for Silver Russell syndrome: a report of a Brazilian cohort

62nd Annual Meeting of the American Society of Human Genetics

G L YAMAMOTO; A BONALDI; A M Vianna MORGANTE; I GOMMY; Chong Ae KIM et al

2012 Trabalho em evento
LS Genetics

Severe CHST3 mutations in two Brazilian families with spondyloepiphyseal dysplasia with congenital joint dislocations

62nd Annual Meeting of the American Society of Human Genetics

W A R BARATELA; T F ALMEIDA; G L YAMAMOTO; J H MARQUES; O LETAIL et al

2012 Trabalho em evento
SH Psychology (miscellaneous)

Tegumentary manifestations in RASopathies are common and deserve special attentionO

62nd Annual Meeting of the American Society of Human Genetics

C QUAIO; A S BRASIL; A C PEREIRA; Chong Ae KIM; Debora Romeo BERTOLA

2012 Trabalho em evento
HS Genetics (clinical)

Schinzel-Giedion syndrome in two Brazilian patients: report of a novel mutation in SETBP1

62nd Annual Meeting of the American Society of Human Genetics

E D F CARVALHO; M LAZAR; T F ALMEIDA; C R D C QUAIO; G L YAMAMOTO et al

2012 Trabalho em evento
HS Neurology (clinical)

Patterns of genetic expression in mental retardation associated or not with microcephaly

62nd Annual Meeting of the American Society of Human Genetics

T F ALMEIDA; D V BERNARDO; C R D C QUAIO; G L YAMAMOTO; E D F CARVALHO et al

2012 Trabalho em evento
LS Genetics

Complex genomic reorganization in microdeletions/microduplications syndromes and molecular mechanisms for formation

62nd Annual Meeting of the American Society of Human Genetics

L D KULIKOWSKI; F PIAZZON; E ZANARDO; R DUTRA; A DIAS et al

2012 Trabalho em evento
PS Biomedical Engineering

Facing current diagnostic challenges in array copy number analysis

62nd Annual Meeting of the American Society of Human Genetics

F B PIAZZON; R DUTRA; E ZANARDO; A DIAS; M MOREIRA et al

2012 Trabalho em evento
LS Neurology

Array-based copy number analysis in patients associating Obesity and developmental delay/learning disabilities and additional features.

62nd Annual Meeting of the American Society of Human Genetics

C D ANGELO; I KOHL; C De CASTRO; Chong Ae KIM; D R BERTOLA et al

2012 Trabalho em evento
LS Genetics

Novel ROR2 mutations in patients with autosomal recessive Robinow syndrome

62nd Annual Meeting of the American Society of Human Genetics

J MAZZEU; H KAYSERILLI; Chong Ae KIM; D BRUNONI; P C PIERI et al

2012 Trabalho em evento
HS Medicine (miscellaneous)

Hipertensão arterial e distúrbios miccionais em pacientes com síndrome de Williams-Beuren

XXVI Congresso Brasileiro de Nefrologia

E A FURUZAWA; Rachel S HONJO; C S LANETZKI; R L DUTRA; L D KULIKOWSKI et al

2012 Trabalho em evento
HS Genetics (clinical)

Natural killer cell deficiency in patients with mucopolysaccharidoses

15th ESID Biennial Meeting

Leuridan Cavalcante TORRES; Caio Robledo QUAIO; José FRANCO; Israel GOMY; Debora Romeo BERTOLA et al

2012 Trabalho em evento
HS Medicine (miscellaneous)

Mucopolyssaccharidoses type IV: case of a patient with humoral response deficiency

15th ESID Biennial Meeting

Leuridan Cavalcante TORRES; Diogo Cordeiro De Queiroz SOARES; Caio Robledo D C QUAIO; José FRANCO; Leslie Domenici KULIKOWSKI et al

2012 Artigo em periódico
LS Genetics

Serpentine fibula polycystic kidney syndrome is part of the phenotypic spectrum of Hajdu-Cheney syndrome

European Journal of Human Genetics

M J GRAY; Chong Ae KIM; Debora Romeo BERTOLA; P R ARANTES; H STEWART et al

ISSN 1018-4813
2012 Artigo em periódico
HS Ophthalmology

Ocular manifestations of Noonan syndrome

Ophthalmic Genetics

Lenina Rocha Pitta MARIN; Felipe Theodoro Bezerra Gaspar Carvalho Da SILVA; F V M SÁ; A S BRASIL; A PEREIRA et al

ISSN 1381-6810
2012 Artigo em periódico
HS Genetics (clinical)

Report of a large Brazilian family with a very attenuated form of Hunter syndrome (MPS II).

Journal of Inherited Metabolic Disease

Caio Robledo D C QUAIO; Henrique GRINBERG; M L C VIEIRA; Ana Carolina PAULA; G N LEAL et al

ISSN 0141-8955
2012 Artigo em periódico
HS Medicine (miscellaneous)

The First Cardiac Transplant Experience in a Patient with Mucopolyssaccharidosis

Cardiovascular Pathology

Henrique GRINBERG; Caio Robledo D C QUAIO; Monica Samuel AVILA; Silvia Moreira Ayub FERREIRA; Marcelo Luiz Campos VIEIRA et al

ISSN 1054-8807
2012 Artigo em periódico
HS Genetics (clinical)

Multiple; diffuse schwannomas in a RASopathy phenotype patient with germline KRAS mutation: a causal relationship

Clinical Genetics

Debora Romeo BERTOLA; A C PEREIRA; A S BRASIL; L SUZUKI; C LEITE et al

ISSN 0009-9163
2012 Artigo em periódico
LS Genetics

Copy Number Variation in Williams-Beuren syndrome: Suitable Diagnostic Strategy for Developing Countries

BMC Research Notes

Roberta Lelis DUTRA; Rachel Sayuri HONJO; Leslie Domenici KULIKOWSKI; Fernanda Andrade Macaferri FONSECA; Patrícia PIERI et al

ISSN 1756-0500
2012 Artigo em periódico
HS Genetics (clinical)

Mutations in SRCAP; SNF2 - related CREBBP activator protein; cause Floating-Harbor Syndrome.

American Journal of Human Genetics

Rebecca L HOOD; Matthew A LINES; Sara NIKKEL; Jeremy SCHWARTZENTRUBER; Chandree BEAULIEU et al

ISSN 0002-9297
2012 Artigo em periódico
LS Genetics

Identification of 2 Novel ANTXR 2 Mutations in Brazilian Patients with Hyaline Fibromatosis Syndrome and Proposal of Grading System

American Journal of Medical Genetics. Part A

Rafael DENADAI; Cassio Eduardo Raposo AMARAL; Debora Romeo BERTOLA; Chong Ae KIM; Nivaldo ALONSO et al

ISSN 1552-4825