Jose Ricardo Magliocco Ceroni - Laboratório Clínico, Hospital Israelita Albert Einstein

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论文共 20 篇作者统计合作学者相似作者

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Genomic study of non-syndromic hearing loss in unaffected individuals: frequency of pathogenic and likely pathogenic variants in a Brazilian cohort of 2097 genomes

Caio Robledo Quaio,Antonio Victor Campos Coelho,Livia Maria Silva Moura,Rafael Lucas Muniz Guedes,Kelin Chen,Jose Ricardo Magliocco Ceroni,Renata Moldenhauer Minillo,Marcel Pinheiro Caraciolo,Rodrigo de Souza Reis,Murilo Cervato,Tatiana Ferreira de Almeida,Joao Bosco de Oliveira Filho

EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 114-114

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The Hospital Israelita Albert Einstein Standards for Constitutional Sequence Variants Classification: Version 2023

Caio Robledo D’Angioli Costa Quaio,José Ricardo Magliocco Ceroni,Michele Araújo Pereira,Anne Caroline Barbosa Teixeira,Renata Yoshiko Yamada,Vivian Pedigone Cintra,Eduardo Perrone,Marina De França,Kelin Chen,Renata Moldenhauer Minillo,Cheysa Arielly Biondo,Mariana Rezende Bandeira de Mello,Lais Rodrigues Moura,Amanda Thamires Batista do Nascimento,Karla de Oliveira Pelegrino,Larissa Barbosa de Lima,Luiza do Amaral Virmond,Carolina Araujo Moreno,Joana Rosa Marques Prota,Jessica Grasiela de Araujo Espolaor,Thiago Yoshinaga Tonholo Silva,Gabriel Hideki Izuka Moraes,Gustavo Santos de Oliveira,Livia Maria Silva Moura,Marcel Pinheiro Caraciolo,Rafael Lucas Muniz Guedes,Michel Chieregato Gretschischkin,Pedro Lui Nigro Chazanas,Carolina Naomi Izo Nakamura,Rodrigo de Souza Reis,Carmen Melo Toledo,Fernanda Stussi Duarte Lage,Giovanna Bloise de Almeida,José Bandeira do Nascimento Júnior,Milena Andreuzo Cardoso,Victor de Paula Azevedo,Tatiana Ferreira de Almeida,Murilo Castro Cervato,Joao Bosco de Oliveira Filho

Human genomics（2023）

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Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil

Michel S. Naslavsky,Marilia O. Scliar,Guilherme L. Yamamoto,Jaqueline Yu Ting Wang,Stepanka Zverinova,Tatiana Karp,Kelly Nunes,José Ricardo Magliocco Ceroni,Diego Lima de Carvalho,Carlos Eduardo da Silva Simões,Daniel Bozoklian,Ricardo Nonaka,Nayane dos Santos Brito Silva,Andreia da Silva Souza,Heloísa de Souza Andrade,Marília Rodrigues Silva Passos,Camila Ferreira Bannwart Castro,Celso T. Mendes-Junior,Rafael L. V. Mercuri,Thiago L. A. Miller,Jose Leonel Buzzo,Fernanda O. Rego,Nathalia M. Araújo,Wagner C. S. Magalhães,Regina Célia Mingroni-Netto,Victor Borda,Heinner Guio,Carlos P. Rojas,Cesar Sanchez,Omar Caceres,Michael Dean,Mauricio L. Barreto,Maria Fernanda Lima-Costa,Bernardo L. Horta,Eduardo Tarazona-Santos,Diogo Meyer,Pedro A. F. Galante,Victor Guryev,Erick C. Castelli,Yeda A. O. Duarte,Maria Rita Passos-Bueno,Mayana Zatz

Nature Communicationsno. 1 (2022)

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Parental Segregation Study Reveals Rare Benign and Likely Benign Variants in a Brazilian Cohort of Rare Diseases

Caio Robledo D.’Angioli Costa Quaio,Jose Ricardo Magliocco Ceroni,Murilo Castro Cervato, Helena Strelow Thurow,Caroline Monaco Moreira, Ana Carolina Gomes Trindade,Cintia Reys Furuzawa,Rafaela Rogerio Floriano de Souza,Sandro Felix Perazzio,Aurelio Pimenta Dutra,Christine Hsiaoyun Chung,Chong Ae Kim

Scientific Reports（2022）

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Whole-genome sequencing of 1,171 elderly admixed individuals from São Paulo, Brazil

NATURE COMMUNICATIONS（2022）

引用25浏览0WOSNATURE引用

Author Correction: Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil

Nature Communicationsno. 1 (2022): 1-1

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Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil (vol 13, 1004, 2022)

Michel S. Naslavsky,Marilia O. Scliar,Guilherme L. Yamamoto,Jaqueline Yu Ting Wang,Stepanka Zverinova,Tatiana Karp,Kelly Nunes,Jose Ricardo Magliocco Ceroni,Diego Lima de Carvalho,Carlos Eduardo da Silva Simoes,Daniel Bozoklian,Ricardo Nonaka,Nayane dos Santos Brito Silva,Andreia da Silva Souza,Heloisa de Souza Andrade,Marilia Rodrigues Silva Passos,Camila Ferreira Bannwart Castro,Celso T. Mendes-Junior,Rafael L. V. Mercuri,Thiago L. A. Miller,Jose Leonel Buzzo,Fernanda O. Rego,Nathalia M. Araujo,Wagner C. S. Magalhaes,Regina Celia Mingroni-Netto,Victor Borda,Heinner Guio,Carlos P. Rojas,Cesar Sanchez,Omar Caceres,Michael Dean,Mauricio L. Barreto,Maria Fernanda Lima-Costa,Bernardo L. Horta,Eduardo Tarazona-Santos,Diogo Meyer,Pedro A. F. Galante,Victor Guryev,Erick C. Castelli,Yeda A. O. Duarte,Maria Rita Passos-Bueno,Mayana Zatz

NATURE COMMUNICATIONS（2022）

引用3浏览0引用

Genomic Study of Nonsyndromic Hearing Loss in Unaffected Individuals: Frequency of Pathogenic and Likely Pathogenic Variants in a Brazilian Cohort of 2,097 Genomes

Caio Robledo D' Angioli Costa Quaio,Antonio Victor Campos Coelho,Livia Maria Silva Moura,Rafael Lucas Muniz Guedes,Kelin Chen,Jose Ricardo Magliocco Ceroni,Renata Moldenhauer Minillo,Marcel Pinheiro Caraciolo,Rodrigo de Souza Reis,Bruna Mascaro Cordeiro de Azevedo,Maria Soares Nobrega,Anne Caroline Barbosa Teixeira, Matheus Martinelli Lima,Thamara Rayssa da Mota, Marina Cadena da Matta, Gabriela Borges Cherulli Colichio, Aline Lulho Roncalho, Ana Flavia Martinho Ferreira, Gabriela Pereira Campilongo,Eduardo Perrone,Luiza do Amaral Virmond,Carolina Araujo Moreno,Joana Rosa Marques Prota,Marina de Franca,Murilo Castro Cervato,Tatiana Ferreira de Almeida,Joao Bosco de Oliveira Filho

Frontiers in genetics（2022）

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Congenital limb deficiency: Genetic investigation of 44 individuals presenting mainly longitudinal defects in isolated or syndromic forms

Leticia Alves da Rocha,Lucas Vieira Lacerda Pires,Guilherme Lopes Yamamoto,Jose Ricardo Magliocco Ceroni,Rachel Sayuri Honjo,Edgard de Novaes Franca Bisneto,Luiz Antonio Nunes Oliveira,Carla Rosenberg,Ana Cristina Victorino Krepischi,Maria Rita Passos-Bueno,Chong Ae Kim,Debora Romeo Bertola

Clinical genetics（2021）

引用6浏览0WOS引用

Whole-genome sequencing of 1,171 elderly admixed individuals from the largest Latin American metropolis (São Paulo, Brazil)

Nature Communications (2020)

引用18浏览0引用

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