Yamamoto Guilherme L - University of São Paulo, University of São Paulo School of Medicine;amp;Laboratory of Epidemiology and Population SciencesNational Institute on Aging, Santa Casa Hospital;University of São Paulo, University of São Paulo School of Medicine

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论文共 97 篇作者统计合作学者相似作者

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Understanding Rare Variant Contributions to Autism: Lessons from Dystrophin-Deficient Model

Claudia Ismania Samogy Costa, Luciana Madanelo,Jaqueline Yu Ting Wang,Gabriele da Silva Campos, Ana Cristina De Sanctis Girardi,Marília Scliar,Frederico Monfardini, Rita de Cássia Mingroni Pavanello,Vivian Romanholi Cória, Maria Dulcetti Vibranovski, Ana Cristina Krepischi,Naila Cristina Vilaça Lourenço,Mayana Zatz,Guilherme Lopes Yamamoto,Elaine Cristina Zachi,Maria Rita Passos-Bueno

NPJ genomic medicineno. 1 (2025): 18-18

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Low-pass Whole Genome Sequencing As a Cost-Effective Alternative to Chromosomal Microarray Analysis for Low- and Middle-Income Countries

Patricia C. Mazzonetto,Darine Villela,Ana C. V. Krepischi,Paulo M. Pierry,Adriano Bonaldi,Luiz Gustavo D. Almeida,Marcelo G. Paula, Matheus Carvalho Burger, Ana Gabriela de Oliveira, Gustavo G. G. Fonseca,Roberto Giugliani, Mariluce Riegel-Giugliani,Debora Bertola,Guilherme Lopes Yamamoto,Maria Rita Passos-Bueno,Gabriele da Silva Campos, Ana Claudia Dantas Machado,Juliana F. Mazzeu,Eduardo Perrone,Roseli M. Zechi-Ceide,Nancy M. Kokitsu-Nakata,Tarsis Paiva Vieira,Carlos Eduardo Steiner,Vera Lucia Gil-da-Silva-Lopes, Daniela Koeller Rodrigues Vieira,Raquel Boy,Joao Monteiro de Pina-Neto,Cristovam Scapulatempo-Neto,Fernanda Milanezi,Carla Rosenberg

American Journal of Medical Genetics Part A（2024）

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Genetic Variation in NOTCH1 is Associated with Overweight and Obesity in Brazilian Elderly

Estevao Carlos Silva Barcelos,Michel Satya Naslavsky,Izadora Silveira Fernandes,Marilia Oliveira Scliar,Guilherme Lopes Yamamoto,Jaqueline Yu Ting Wang, Lais Bride,Valdemir Pereira de Sousa,Lucia Helena Sagrillo Pimassoni,Paolo Sportoletti,Flavia de Paula,Sandra Ventorin von Zeidler,Yeda Aparecida Oliveira Duarte,Maria Rita Passos-Bueno,Mayana Zatz,Flavia Imbroisi Valle Errera

Scientific Reportsno. 1 (2024)

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W54. USE OF HOMOGENIZED COHORT TO DISSECT THE GENETIC ARCHITECTURE OF AUTISM: LESSONS FROM DYSTROPHIN-DEFICIENT MODEL

Claudia Samogy-Costa, Luciana Mandanelo,Jaqueline Wang,Gabriele Campos,Ana Cristina Girardi,Marilia Scliar,Frederico Monfardini, Vivian Coria, Maria Vibranovski, Naila Lourenco,Mayana Zatz,Guilherme Yamamoto, Rita Pavanello, Elaine Zachi,Maria Rita Passos-Bueno

EUROPEAN NEUROPSYCHOPHARMACOLOGY (2024): 130-130

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Split Hand-Foot Malformations-Unveiling Unique Molecular Diagnosis from a Brazilian Cohort

Eduardo Da Cas,Jose Ricardo Magliocco Ceroni,Guilherme Lopes Yamamoto,Matheus Augusto Araujo Castro, Edgard Franca Bisneto,Alexander Augusto de Lima Jorge, Joao Bosco Oliveira,Chong Ae Kim, Ana Cristina Vitorino Krepischi,Debora Romeo Bertola

CLINICAL GENETICS（2024）

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Clinical Characterization and Underlying Genetic Findings in Brazilian Patients with Syndromic Microcephaly Associated with Neurodevelopmental Disorders

Giovanna Cantini Tolezano,Giovanna Civitate Bastos,Silvia Souza da Costa,Marília de Oliveira Scliar,Carolina Fischinger Moura de Souza, Hélio Van Der Linden Jr, Walter Luiz Magalhães Fernandes,Paulo Alberto Otto,Angela M. Vianna-Morgante,Luciana Amaral Haddad,Rachel Sayuri Honjo,Guilherme Lopes Yamamoto,Chong Ae Kim,Carla Rosenberg,Alexander Augusto de Lima Jorge,Débora Romeo Bertola,Ana Cristina Victorino Krepischi

Molecular Neurobiologyno. 8 (2024): 5230-5247

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Plastic Bronchitis in Noonan Syndrome: Further Evidence Suggesting a Higher Risk of Lymphatic Abnormalities in Individuals Harboring Variants in PTPN11 Residue P.phe285

Lucas Vieira Lacerda Pires, Eduardo Da Cas, Leticia Cole de Melo, Cleyde Mirian Aversa Nakaie, Vera Dermachi Aiello,Guilherme Lopes Yamamoto,Rachel Sayuri Honjo,Chong Ae Kim,Debora Romeo Bertola

MOLECULAR SYNDROMOLOGY (2024)

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Whole Genome Sequencing As a First-Tier Diagnostic Test for Infants in Neonatal Intensive Care Units: A Pilot Study in Brazil

Michele P. Migliavacca,Joselito Sobreira, Diana Bermeo, Mireille Gomes, Dayse Alencar, Luciane Sussuchi,Camila Alves Souza,Juliana Santos Silva,Jose Eduardo Kroll,Matheus Burger,Rodrigo Guarischi-Sousa,Darine Villela,Guilherme L. Yamamoto,Fernanda Milanezi,Nelson Horigoshi,Regina Grigolli Cesar,Werther Brunow de Carvalho,Rachel Sayuri Honjo,Debora Romeo Bertola,Chong Ae Kim,Lucian de Souza, Renato S. Procianoy, Rita C. Silveria,Carla Rosenberg,Roberto Giugliani,Gustavo Aguiar Campana,Cristovam Scapulatempo-Neto,Nara Sobreira

American Journal of Medical Genetics Part A（2024）

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Burden of Rare Copy Number Variants in Microcephaly: A Brazilian Cohort of 185 Microcephalic Patients and Review of the Literature

Giovanna Cantini Tolezano,Giovanna Civitate Bastos,Silvia Souza da Costa,Bruna Lucheze Freire,Thais Kataoka Homma,Rachel Sayuri Honjo,Guilherme Lopes Yamamoto,Maria Rita Passos-Bueno,Celia Priszkulnik Koiffmann,Chong Ae Kim,Angela Maria Vianna-Morgante,Alexander Augusto de Lima Jorge,Débora Romeo Bertola,Carla Rosenberg,Ana Cristina Victorino Krepischi

Journal of Autism and Developmental Disorders（2024）

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A Dopamine Receptor D2 Genetic Polymorphism Associated with Transition to Mental Disorders in a Cohort of Individuals with At-Risk Mental State for Psychosis

Julia Hatagami Marques,Leda Leme Talib,Lucas Hortencio,Julio Cesar Andrade,Tania Maria Alves,Mauricio Henriques Serpa,Guilherme Lopes Yamamoto,Martinus Theodorus van de Bilt,Wulf Rossler,Wagner Farid Gattaz,Alexandre Andrade Loch

BRAZILIAN JOURNAL OF PSYCHIATRYno. 3 (2023): 268-273

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