Társis Antonio Paiva Vieira (Társis P Vieira, Tarsis P Vieira, T P Vieira, Tarsis Paiva Vieira, Társis Paiva Vieira)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 33

Top Venues

Genes

American journal of medical genetics. Part A

American journal of medical genetics. Part C, Seminars in medical genetics

Sao Paulo medical journal = Revista paulista de medicina

State University of Campinas

State University of Campinas (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

State University of Campinas Dec 01 2014

Brazil

Professor :: Department of Medical Genetics - Faculty of Medical Sciences

Universidade Federal de Alfenas Oct 01 2013 - Nov 30 2014

Brazil

Professor :: Natural Sciences Institute

Brazilian National Cancer Institute Apr 14 2011 - Sep 30 2013

Brazil

Biologist - Cytogeneticist :: Center for Bone Morrow Transplatation (CEMO)

State University of Campinas Apr 10 2009 - Apr 01 2011

Brazil

Biologist - Cytogeneticist :: Department of Medical Genetics - Faculty of Medical Sciences

Education History

State University of Campinas Mar 01 2007 - Feb 28 2012

Brazil

PHD :: Department of Medical Genetics - Faculty of Medical Sciences

State University of Campinas Mar 01 2005 - Feb 28 2007

Brazil

MSC :: Department of Medical Genetics - Faculty of Medical Sciences

Centro Universitário Herminio Ometto de Araras Feb 01 2000 - Nov 30 2003

Brazil

BSC

Publications

Melissa Bittencourt de Wallau, Ana Carolina Xavier, Carolina Araújo Moreno, Chong Ae Kim, Elaine Lustosa Mendes, Erlane Marques Ribeiro, Amanda Oliveira, Têmis Maria Félix, Agnes Cristina Fett-Conte, Luciana Cardoso Bonadia, Gabriela Roldão Correia-Costa, Isabella Lopes Monlleó, Vera Lúcia Gil-da-Silva-Lopes, Társis Antonio Paiva Vieira
22q11.2 Deletion Syndrome: Influence of Parental Origin on Clinical Heterogeneity. Genes 15 (4) (2024)
Henrique Garcia Silveira, Carlos Eduardo Steiner, Giovana Toccoli, Luise Longo Angeloni, Júlia Lôndero Heleno, Samira Spineli-Silva, Ana Mondadori Dos Santos, Társis Antonio Paiva Vieira, Maria Isabel Melaragno, Vera Lúcia Gil-da-Silva-Lopes
Variants in KMT2A in Three Individuals with Previous Suspicion of 22q11.2 Deletion Syndrome. Genes 15 (2) (2024)
Patricia C Mazzonetto, Darine Villela, Ana C V Krepischi, Paulo M Pierry, Adriano Bonaldi, Luiz Gustavo D Almeida, Marcelo G Paula, Matheus Carvalho Bürger, Ana Gabriela de Oliveira, Gustavo G G Fonseca, Roberto Giugliani, Mariluce Riegel, Débora Bertola, Guilherme Lopes Yamamoto, Maria Rita Passos-Bueno, Gabriele da Silva Campos, Ana Claudia Dantas Machado, Juliana Forte Mazzeu, Eduardo Perrone, Roseli M Zechi-Ceide, Nancy Mizue Kokitsu-Nakata, Társis Antonio Paiva Vieira, Carlos Eduardo Steiner, Vera Lúcia Gil-da-Silva-Lopes, Daniela Koeller Rodrigues Vieira, Raquel Boy, João Monteiro de Pina-Neto, Cristovam Scapulatempo-Neto, Fernanda Milanezi, Carla Rosenberg
Low-pass whole genome sequencing as a cost-effective alternative to chromosomal microarray analysis for low- and middle-income countries. American journal of medical genetics. Part A (2024)
Henrique Garcia Silveira, Carlos Eduardo Steiner, Giovana Toccoli, Luise Longo Angeloni, Júlia Lôndero Heleno, Samira Spineli-Silva, Ana Mondadori Dos Santos, Társis Antonio Paiva Vieira, Maria Isabel Melaragno, Vera Lúcia Gil-da-Silva-Lopes
Variants in KMT2A in Three Individuals with Previous Suspicion of 22q11.2 Deletion Syndrome. Genes 15 (2) (2024)
Melissa Bittencourt de Wallau, Ana Carolina Xavier, Carolina Araújo Moreno, Chong Ae Kim, Elaine Lustosa Mendes, Erlane Marques Ribeiro, Amanda Oliveira, Têmis Maria Félix, Agnes Cristina Fett-Conte, Luciana Cardoso Bonadia, Gabriela Roldão Correia-Costa, Isabella Lopes Monlleó, Vera Lúcia Gil-da-Silva-Lopes, Társis Antonio Paiva Vieira
22q11.2 Deletion Syndrome: Influence of Parental Origin on Clinical Heterogeneity. Genes 15 (4) (2024)
Henrique Garcia Silveira, Carlos Eduardo Steiner, Giovana Toccoli, Luise Longo Angeloni, Júlia Lôndero Heleno, Samira Spineli-Silva, Ana Mondadori Dos Santos, Társis Antonio Paiva Vieira, Maria Isabel Melaragno, Vera Lúcia Gil-da-Silva-Lopes
Variants in KMT2A in Three Individuals with Previous Suspicion of 22q11.2 Deletion Syndrome. Genes 15 (2) (2024)
Ruy Pires de Oliveira-Sobrinho, Simone Appenzeller, Ianne Pessoa Holanda, Júlia Lôndero Heleno, Josep Jorente, null On Behalf Of The Rare Genomes Project Consortium, Társis Antonio Paiva Vieira, Carlos Eduardo Steiner
Genome Sequencing in an Individual Presenting with 22q11.2 Deletion Syndrome and Juvenile Idiopathic Arthritis. Genes 15 (4) (2024)
Ruy Pires de Oliveira-Sobrinho, Simone Appenzeller, Ianne Pessoa Holanda, Júlia Lôndero Heleno, Josep Jorente, null On Behalf Of The Rare Genomes Project Consortium, Társis Antonio Paiva Vieira, Carlos Eduardo Steiner
Genome Sequencing in an Individual Presenting with 22q11.2 Deletion Syndrome and Juvenile Idiopathic Arthritis. Genes 15 (4) (2024)
Henrique Garcia Silveira, Carlos Eduardo Steiner, Giovana Toccoli, Luise Longo Angeloni, Júlia Lôndero Heleno, Samira Spineli-Silva, Ana Mondadori Dos Santos, Társis Antonio Paiva Vieira, Maria Isabel Melaragno, Vera Lúcia Gil-da-Silva-Lopes
Variants in KMT2A in Three Individuals with Previous Suspicion of 22q11.2 Deletion Syndrome. Genes 15 (2) (2024)
Melissa Bittencourt de Wallau, Ana Carolina Xavier, Carolina Araújo Moreno, Chong Ae Kim, Elaine Lustosa Mendes, Erlane Marques Ribeiro, Amanda Oliveira, Têmis Maria Félix, Agnes Cristina Fett-Conte, Luciana Cardoso Bonadia, Gabriela Roldão Correia-Costa, Isabella Lopes Monlleó, Vera Lúcia Gil-da-Silva-Lopes, Társis Antonio Paiva Vieira
22q11.2 Deletion Syndrome: Influence of Parental Origin on Clinical Heterogeneity. Genes 15 (4) (2024)
Henrique Garcia Silveira, Carlos Eduardo Steiner, Giovana Toccoli, Luise Longo Angeloni, Júlia Lôndero Heleno, Samira Spineli-Silva, Ana Mondadori Dos Santos, Társis Antonio Paiva Vieira, Maria Isabel Melaragno, Vera Lúcia Gil-da-Silva-Lopes
Variants in KMT2A in Three Individuals with Previous Suspicion of 22q11.2 Deletion Syndrome. Genes 15 (2) (2024)
Ruy Pires de Oliveira-Sobrinho, Simone Appenzeller, Ianne Pessoa Holanda, Júlia Lôndero Heleno, Josep Jorente, null On Behalf Of The Rare Genomes Project Consortium, Társis Antonio Paiva Vieira, Carlos Eduardo Steiner
Genome Sequencing in an Individual Presenting with 22q11.2 Deletion Syndrome and Juvenile Idiopathic Arthritis. Genes 15 (4) (2024)
Matheus de Mello Copelli, Eleonore Pairet, Milena Atique Tacla, Társis Antonio Paiva Vieira, Simone Appenzeller, Raphaël Helaers, Miikka Vikkula, Vera Lúcia Gil-da-Silva-Lopes
SATB2 -Associated Syndrome Due to a c.715C>T:p(Arg239*) Variant in Adulthood: Natural History and Literature Review. Genes 14 (4) (2023)
Carolina Gama Nascimento, Joana Rosa Marques Prota, Ilária Cristina Sgardioli, Samira Spineli-Silva, Nilma Lúcia Viguetti Campos, Vera Lúcia Gil-da-Silva-Lopes, Társis Antonio Paiva Vieira
Rare 15q21.1q22.31 Duplication Due to a Familial Chromosomal Insertion and Diagnostic Investigation in a Carrier of Balanced Chromosomal Rearrangement and Intellectual Disability. Genes 14 (4) (2023)
Milena Atique Tacla, Matheus de Mello Copelli, Eleonore Pairet, Isabella Lopes Monlleó, Erlane Marques Ribeiro, Elaine Lustosa Mendes, Raphaël Helaers, Társis Antonio Paiva Vieira, Miikka Vikkula, Vera Lúcia Gil-da-Silva-Lopes
Molecular investigation in individuals with orofacial clefts and microphthalmia-anophthalmia-coloboma spectrum. European journal of human genetics : EJHG (2023)
Carolina Gama Nascimento, Joana Rosa Marques Prota, Ilária Cristina Sgardioli, Samira Spineli-Silva, Nilma Lúcia Viguetti Campos, Vera Lúcia Gil-da-Silva-Lopes, Társis Antonio Paiva Vieira
Rare 15q21.1q22.31 Duplication Due to a Familial Chromosomal Insertion and Diagnostic Investigation in a Carrier of Balanced Chromosomal Rearrangement and Intellectual Disability. Genes 14 (4) (2023)
Samira Spineli-Silva, Isabella L Monlleó, Têmis M Félix, Vera L Gil-da-Silva-Lopes, Társis Antonio Paiva Vieira
Overlapping Spectrum of Craniofacial Microsomia Phenotype in Cat-Eye Syndrome. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association (2023)
Matheus de Mello Copelli, Eleonore Pairet, Milena Atique Tacla, Társis Antonio Paiva Vieira, Simone Appenzeller, Raphaël Helaers, Miikka Vikkula, Vera Lúcia Gil-da-Silva-Lopes
SATB2 -Associated Syndrome Due to a c.715C>T:p(Arg239*) Variant in Adulthood: Natural History and Literature Review. Genes 14 (4) (2023)
Matheus de Mello Copelli, Eleonore Pairet, Milena Atique Tacla, Társis Antonio Paiva Vieira, Simone Appenzeller, Raphaël Helaers, Miikka Vikkula, Vera Lúcia Gil-da-Silva-Lopes
SATB2 -Associated Syndrome Due to a c.715C>T:p(Arg239*) Variant in Adulthood: Natural History and Literature Review. Genes 14 (4) (2023)
Matheus de Mello Copelli, Eleonore Pairet, Milena Atique Tacla, Társis Antonio Paiva Vieira, Simone Appenzeller, Raphaël Helaers, Miikka Vikkula, Vera Lúcia Gil-da-Silva-Lopes
SATB2 -Associated Syndrome Due to a c.715C>T:p(Arg239*) Variant in Adulthood: Natural History and Literature Review. Genes 14 (4) (2023)
Carolina Gama Nascimento, Joana Rosa Marques Prota, Ilária Cristina Sgardioli, Samira Spineli-Silva, Nilma Lúcia Viguetti Campos, Vera Lúcia Gil-da-Silva-Lopes, Társis Antonio Paiva Vieira
Rare 15q21.1q22.31 Duplication Due to a Familial Chromosomal Insertion and Diagnostic Investigation in a Carrier of Balanced Chromosomal Rearrangement and Intellectual Disability. Genes 14 (4) (2023)
Carolina Gama Nascimento, Joana Rosa Marques Prota, Ilária Cristina Sgardioli, Samira Spineli-Silva, Nilma Lúcia Viguetti Campos, Vera Lúcia Gil-da-Silva-Lopes, Társis Antonio Paiva Vieira
Rare 15q21.1q22.31 Duplication Due to a Familial Chromosomal Insertion and Diagnostic Investigation in a Carrier of Balanced Chromosomal Rearrangement and Intellectual Disability. Genes 14 (4) (2023)
Gabriela Roldão Correia-Costa, Ana Mondadori Dos Santos, Nicole de Leeuw, Sumara Zuanazi Pinto Rigatto, Vera Maria Santoro Belangero, Carlos Eduardo Steiner, Vera Lúcia Gil-da-Silva-Lopes, Társis Antonio Paiva Vieira
Dual Molecular Diagnoses of Recessive Disorders in a Child from Consanguineous Parents: Case Report and Literature Review. Genes 13 (12) (2022)
Gabriela Roldão Correia-Costa, Ana Mondadori Dos Santos, Nicole de Leeuw, Sumara Zuanazi Pinto Rigatto, Vera Maria Santoro Belangero, Carlos Eduardo Steiner, Vera Lúcia Gil-da-Silva-Lopes, Társis Antonio Paiva Vieira
Dual Molecular Diagnoses of Recessive Disorders in a Child from Consanguineous Parents: Case Report and Literature Review. Genes 13 (12) (2022)
Gabriela Roldão Correia-Costa, Ana Mondadori Dos Santos, Nicole de Leeuw, Sumara Zuanazi Pinto Rigatto, Vera Maria Santoro Belangero, Carlos Eduardo Steiner, Vera Lúcia Gil-da-Silva-Lopes, Társis Antonio Paiva Vieira
Dual Molecular Diagnoses of Recessive Disorders in a Child from Consanguineous Parents: Case Report and Literature Review. Genes 13 (12) (2022)
Flávia Marcorin de Oliveira, Beatriz Amstalden Barros, Ana Paula Dos Santos, Nilma Lúcia Viguetti Campos, Taís Nitsch Mazzola, Paulo Latuf Filho, Liliana Aparecida Lucci De Angelo Andrade, Mara Sanches Guaragna, Maricilda Palandi de Mello, Gil Guerra-Junior, Társis Antonio Paiva Vieira, Andréa Trevas Maciel-Guerra
SOX3 duplication in a boy with 46,XX ovotesticular disorder of sex development and his 46,XX sister with atypical genitalia: Probable germline mosaicism. American journal of medical genetics. Part A (2022)
Luísa Riccetto, Társis Antonio Paiva Vieira, Nilma Lucia Viguetti-Campos, Taís Nitsch Mazzola, Mara Sanches Guaragna, Helena Fabbri-Scallet, Maricilda Palandi de Mello, Antonia Paula Marques-de-Faria, Andréa Trevas Maciel-Guerra, Gil Guerra Junior
Clinical and laboratory differences between chromosomal and undefined causes of non-obstructive azoospermia: A retrospective study. Sao Paulo medical journal = Revista paulista de medicina (2022)
Gabriela Roldão Correia-Costa, Ilária Cristina Sgardioli, Ana Paula Dos Santos, Tânia Kawasaki de Araujo, Rodrigo Secolin, Iscia Lopes-Cendes, Vera Lúcia Gil-da-Silva-Lopes, Társis Antonio Paiva Vieira
Increased runs of homozygosity in the autosomal genome of Brazilian individuals with neurodevelopmental delay/intellectual disability and/or multiple congenital anomalies investigated by chromosomal microarray analysis. Genetics and molecular biology 45 (1) (2022)
Gabriela Roldão Correia-Costa, Ana Mondadori Dos Santos, Nicole de Leeuw, Sumara Zuanazi Pinto Rigatto, Vera Maria Santoro Belangero, Carlos Eduardo Steiner, Vera Lúcia Gil-da-Silva-Lopes, Társis Antonio Paiva Vieira
Dual Molecular Diagnoses of Recessive Disorders in a Child from Consanguineous Parents: Case Report and Literature Review. Genes 13 (12) (2022)
Vera Lúcia Gil-da-Silva-Lopes, Milena Atique Tacla, Ilária Cristina Sgardioli, Társis Antonio Paiva Vieira, Isabella Lopes Monlleó
Brazil's Craniofacial Project: Different approaches on orofacial clefts and 22q11.2 deletion syndrome. American journal of medical genetics. Part C, Seminars in medical genetics 184 (4) (2020)
Samira Spineli-Silva, Ilária Cristina Sgardioli, Ana P Dos Santos, Luna L Bergamini, Isabella L Monlleó, Marshall I B Fontes, Têmis Maria Félix, Erlane M Ribeiro, Ana C Xavier, Elaine Lustosa-Mendes, Vera Lúcia Gil-da-Silva-Lopes, Társis Antonio Paiva Vieira
Genomic imbalances in craniofacial microsomia. American journal of medical genetics. Part C, Seminars in medical genetics 184 (4) (2020)
L C de Souza, A P Dos Santos, I C Sgardioli, N L Viguetti-Campos, J R Marques Prota, R P de Oliveira-Sobrinho, Társis Antonio Paiva Vieira, V L Gil-da-Silva-Lopes
Phenotype comparison among individuals with developmental delay/intellectual disability with or without genomic imbalances. Journal of intellectual disability research : JIDR 63 (11) (2019)
Laiara Cristina de Souza, Ilária Cristina Sgardioli, Ilária Cristina Sgardioli, Társis Antonio Paiva Vieira
A recognizable phenotype related to 19p13.12 microdeletion. American journal of medical genetics. Part A 176 (8) (2018)

Társis Antonio Paiva Vieira.css-eqlu8i{font-size:small;padding-left:4px;} (Társis P Vieira, Tarsis P Vieira, T P Vieira, Tarsis Paiva Vieira, Társis Paiva Vieira)

Publication Activity (10 Years)

Top Topics

Top Venues

Társis Antonio Paiva Vieira (Társis P Vieira, Tarsis P Vieira, T P Vieira, Tarsis Paiva Vieira, Társis Paiva Vieira)