Tarsis Paiva Vieira - Department of Medical Genetics, University of Campinas

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论文共 79 篇作者统计合作学者相似作者

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Variants in KMT2A in Three Individuals with Previous Suspicion of 22q11.2 Deletion Syndrome

Henrique Garcia Silveira,Carlos Eduardo Steiner, Giovana Toccoli, Luise Longo Angeloni, Julia Londero Heleno,Samira Spineli-Silva, Ana Mondadori dos Santos,Tarsis Paiva Vieira,Maria Isabel Melaragno,Vera Lucia Gil-da-Silva-Lopes

GENESno. 2 (2024)

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Microdeletion 1p32p31 Presenting with Moyamoya Disease and Incomplete Hippocampal Inversion

Ruy Pires de Oliveira-Sobrinho, Luciana Mota Bispo, Julia Londero Heleno, Fernanda Rocha Rojas Ayala, Fabiano Reis,Tarsis Paiva Vieira,Carlos Eduardo Steiner

Molecular syndromologyno. 3 (2024): 225-231

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22Q11.2 Deletion Syndrome: Influence of Parental Origin on Clinical Heterogeneity

Melissa Bittencourt de Wallau,Ana Carolina Xavier,Carolina Araujo Moreno,Chong Ae Kim,Elaine Lustosa Mendes,Erlane Marques Ribeiro, Amanda Oliveira,Temis Maria Felix,Agnes Cristina Fett-Conte,Luciana Cardoso Bonadia,Gabriela Roldao Correia-Costa,Isabella Lopes Monlleo,Vera Lucia Gil-da-Silva-Lopes,Tarsis Paiva Vieira

Genes（2024）

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Growth Charts of Brazilian Girls with Turner Syndrome Without the Use of GH or Oxandrolone

Stela Carpini-Dantas, Gil Guerra-Junior,Andréa Trevas Maciel-Guerra,Denise Barbieri Marmo,Tarsis Paiva Vieira, Carolina Paniago Lopes,Maria Tereza Matias Baptista, André Moreno Morcillo,Sofia Helena Valente de Lemos-Marini

Jornal de pediatria (2024)

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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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Multiple Aneuploidy: First Report of a Patient Presenting with a Karyotype 45,X/48,XXX,+21

Gabriela Roldao Correia Costa, Josep Jorente, Larissa Bretanha Pontes,Nilma Lucia Viguetti Campos,Antonia Paula Marques-de-Faria,Tarsis Paiva Vieira,Carlos Eduardo Steiner

CYTOGENETIC AND GENOME RESEARCHno. 2 (2024): 103-109

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Patients with Genital Ambiguity Referred Without a Sex Definition: the Relationship Between Clinical Picture and Defined Sex of Rearing

Henrique C. Santos,Beatriz A. Barros, Mayra S. El-Beck,Marcio L. Miranda,Mara S. Guaragna,Helena Fabbri-Scallet,Tais N. Mazzola,Tarsis P. Vieira,Maricilda P. Mello,Antonia P. Marques-de-Faria,Andrea T. Maciel-Guerra,Gil Guerra-Junior

JORNAL DE PEDIATRIAno. 6 (2024): 609-613

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Novel Variants in the SOX11 Gene: Clinical Description of Seven New Patients

Beatriz Schincariol-Manhe, Erica Campagnolo,Samira Spineli-Silva,Nicole de Leeuw,Gabriela Roldao Correia-Costa,Andre Pessoa, Carolina Fischinger Moura de Souza,Cathy Stevens, Poupak Javaher,Helena Fabbri Scallet,Julia Mohr,Saskia Biskup,Johanna C. Herkert,Rolph Pfundt,Lakshmi Mehta, Aisha Rekab,Houda Zghal Elloumi,May Sanyoura,Andrea Trevas Maciel-Guerra,Vera Lucia Gil-da-Silva-Lopes, Ana Mondadori dos Santos,Tarsis Paiva Vieira

EUROPEAN JOURNAL OF HUMAN GENETICS (2024)

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Microdeletion 3q13.2q21.2 in a Patient Previously Diagnosed with MOMO Syndrome

Ruy Pires de Oliveira-Sobrinho,Tarsis Paiva Vieira,Carlos Eduardo Steiner

MOLECULAR SYNDROMOLOGY (2024)

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Genome Sequencing in an Individual Presenting with 22q11.2 Deletion Syndrome and Juvenile Idiopathic Arthritis

Ruy Pires de Oliveira-Sobrinho,Simone Appenzeller, Ianne Pessoa Holanda, Julia Londero Heleno, Josep Jorente,Tarsis Paiva Vieira,Carlos Eduardo Steiner

Genesno. 4 (2024): 513-513

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