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Michel Satya Naslavsky

Professor Doutor

Universidade de Sao Paulo

Sao Paulo, Brasil

Population medical genomics, bioinformatics applied in human genome analysis and bioethics are my main research lines. I am exploring the effect of ancestry admixture in pathogenicity interpretation of variants and its potential impact in healthcare

Professor Doutor Full Time

UNIVERSIDADE DE SAO PAULO

Instituto de Biociencias

Sao Paulo, Brasil

2018 - A la fecha

Professor (Medical School) Part Time

Universidade Nove de Julho

Sao Pauilo, Brasil

2017 - 2018


Extreme phenotypes approach to investigate host genetics and COVID-19 outcomes Naslavsky, Michel Satya; Vidigal, Mateus; Matos, Larissa do Rêgo Barros; Cória, Vivian Romanholi; Batista Junior, Pedro Benedito; Razuk, Álvaro; Dolhnikoff, Marisa; Schidlowski, Laire; Prando, Carolina; Cunha-Neto, Edécio; et al. Article ISI Genetics and Molecular Biology (2021)
Avaliação quantitativa do volume cerebral em um grupo de idosos de São Paulo, Brasil: um estudo de base populacional Rodrigues, Mariana Athaniel Silva; Rodrigues, Thiago Pereira; Nascimento, Felipe Barjud Pereira do; Amaro Junior, Edson Article ISI Radiologia Brasileira (2019)
Discordant congenital Zika syndrome twins show differential in vitro viral susceptibility of neural progenitor cells (vol 9, 2018) Caires-Junior, Luiz Carlos; Goulart, Ernesto; Melo, Uira Souto; Silva Araujo, Bruno Henrique; Alvizi, Lucas; Soares-Schanoski, Alessandra; de Oliveira, Danyllo Felipe; Kobayashi, Gerson Shigeru; Griesi-Oliveira, Karina; Musso, Camila Manso; et al. Article ISI NATURE COMMUNICATIONS (2018)
IHH Gene Mutations Causing Short Stature With Nonspecific Skeletal Abnormalities and Response to Growth Hormone Therapy Vasques, Gabriela A.; Funari, Mariana F. A.; Ferreira, Frederico M.; Aza-Carmona, Miriam; Sentchordi-Montane, Lucia; Barraza-Garcia, Jimena; Lerario, Antonio M.; Yamamoto, Guilherme L.; Duarte, Yeda A. O.; Bertola, Debora R.; et al. Article ISI JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2018)
Diabetes is Not Associated with Alzheimer's Disease Neuropathology Pimentel dos Santos Matioli, Maria Niures; Rodriguez, Roberta Diehl; Farias, Daniela Souza; da Silva, Magnolia Moreira; Lucena Ferretti-Rebustini, Renata Eloah; Pasqualucci, Carlos Augusto; Jacob Filho, Wilson; Arvanitakis, Zoe; Naslaysky, Michel Satya Article ISI JOURNAL OF ALZHEIMERS DISEASE (2017)
Exomic variants of an elderly cohort of Brazilians in the ABraOM database de Almeida, Tatiana Ferreira; Ezquina, Suzana A. M.; Sunaga, Daniele Yumi; Pho, Nam; Bozoklian, Daniel; Milkewitz Sandberg, Tatiana Orli; Brito, Luciano Abreu; Lazar, Monize; Bernardo, Danilo Vicensotto; Amaro, Edson, Jr. Article ISI HUMAN MUTATION (2017)
High phenotypic variability in Gerstmann-Straussler-Scheinker disease Smid, Jerusa; Neto, Adalberto Studart; Landemberger, Michele Christine; Machado, Cleiton Fagundes; Nobrega, Paulo Ribeiro; Silva Canedo, Nathalie Henriques; Schultz, Rodrigo Rizek; Rosemberg, Sergio; Chimelli, Leila; Martins, Vilma Regina Article ISI ARQUIVOS DE NEURO-PSIQUIATRIA (2017)
Neuropathological diagnoses and clinical correlates in older adults in Brazil: A cross-sectional study Suemoto, Claudia K.; Ferretti-Rebustini, Renata E. L.; Rodriguez, Roberta D.; Leite, Renata E. P.; Soterio, Luciana; Brucki, Sonia M. D.; Spera, Raphael R.; Cippiciani, Tarcila M.; Farfel, Jose M.; Chiavegatto Filho, Alexandre; et al. Article ISI PLOS MEDICINE (2017)
Chronic Traumatic Encephalopathy Presenting as Alzheimer's Disease in a Retired Soccer Player Anghinah, Renato; Nascimento, Camila Fernandes; Leite, Renata P.; Martin, Maria da Graca M.; Takada, Leonel T. Article ISI JOURNAL OF ALZHEIMERS DISEASE (2016)
Detection of small copy number variations (CNVs) in autism spectrum disorder (ASD) by custom array comparative genomic hybridization (aCGH) Moreira, Eloisa S.; Silva, Isabela M. W.; Lourenco, Naila; Moreira, Danielle P.; Ribeiro, Cintia M.; Martins, Ana Luiza B.; Costa, Silvia S.; Rocha, Katia M.; Aguena, Meire; Fett-Conte, Agnes C.; et al. Article ISI RESEARCH IN AUTISM SPECTRUM DISORDERS (2016)
Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility Toledo, Rodrigo A.; Hatakana, Roxanne; Lourenco, Delmar M., Jr.; Lindsey, Susan C.; Camacho, Cleber P.; Almeida, Marcio; Lima, Jose V., Jr.; Sekiya, Tomoko; Meirelles, Osorio; Blangero, John; et al. Article ISI ENDOCRINE-RELATED CANCER (2015)
Factors associated with lower gait speed among the elderly living in a developing country: a cross-sectional population-based study Busch, Telma de Almeida; Duarte, Yeda Aparecida; Nunes, Daniella Pires; Rodrigues, Anelise dos Santos Article ISI BMC GERIATRICS (2015)
Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome Gos, Monika; Hung, Christina; Pilch, Jacek; Fahiminiya, Somayyeh; Abramowicz, Anna; Cristian, Ingrid; Buscarilli, Michelle; Malaquias, Alexsandra C.; Majewski, Jacek; Kim, Chong Ae; et al. Article ISI JOURNAL OF MEDICAL GENETICS (2015)
Rare Variants in the Epithelial Cadherin Gene Underlying the Genetic Etiology of Nonsyndromic Cleft Lip with or without Cleft Palate Melo, Soraia; Malcher, Carolina; Ferreira, Simone Gomes; Figueiredo, Joana; Alonso, Nivaldo; Felix, Temis Maria; Seruca, Raquel Article ISI HUMAN MUTATION (2015)
Schinzel-Giedion Syndrome in Two Brazilian Patients: Report of a Novel Mutation in SETBP1 and Literature Review of the Clinical Features Carvalho, Ellaine; Honjo, Rachel; Magalhaes, Monize; Yamamoto, Guilherme; Rocha, Katia; Naslavsky, Michel; Kim, Chong; Bertola, Debora Article ISI AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2015)
A defect in the RNA-processing protein HNRPDL causes limb-girdle muscular dystrophy 1G (LGMD1G) Vieira, Natassia M.; Licinio, Luciana; Vainzof, Mariz; Sanchez, Nury; Kitajima, Joao Paulo; Gal, Lihi; Cavacana, Natale; Serafini, Peter R.; Chuartzman, Silvia; Vasquez, Cristina; et al. Article ISI HUMAN MOLECULAR GENETICS (2014)
Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations Longuini, Viviane C.; Goncalves, Tatiana D.; Coutinho, Flavia L.; Francisco, Guilherme; Osaki, Luciana H.; Chammas, Roger; Alves, Venancio A. F.; Siqueira, Sheila A. C.; Schlesinger, David; Gama, Patricia; et al. Article ISI EUROPEAN JOURNAL OF ENDOCRINOLOGY (2014)
Does germ-line deletion of the PIP gene constitute a widespread risk for cancer? Silva, Amanda G.; Krepischi, Ana C. V.; Torrezan, Giovana T.; Capelli, Leonardo P.; Carraro, Dirce M.; D'Angelo, Carla S.; Koiffmann, Celia P.; Masotti, Cibele; Otto, Paulo A.; Achatz, Maria I. W.; et al. Article ISI EUROPEAN JOURNAL OF HUMAN GENETICS (2014)
p27 variant and corticotropinoma susceptibility: a genetic and in vitro study Benfini, Katiuscia; Machado, Marcio C.; Higashi, Leonardo; Viana-, Jose, Jr.; Kater, Claudio Article ISI ENDOCRINE-RELATED CANCER (2014)
African ancestry protects against Alzheimer's disease-related neuropathology Schlesinger, D.; Grinberg, L. T.; Alba, J. G.; Naslavsky, M. S.; Licinio, L.; Farfel, J. M.; Suemoto, C. K.; de Lucena Ferretti, R. E.; Leite, R. E. P.; de Andrade, M. P.; et al. Article ISI MOLECULAR PSYCHIATRY (2013)
The sound of silence: Human beta-defensin-1 gene untranslated SNPs change the predicted mRNA secondary structure in a length-dependent manner Crovella, S.; Lima Filho, J. L.; Rocha, C. R. C. Article ISI IMMUNOLOGY LETTERS (2010)
Functional polymorphisms of DEFB1 gene in type 1 diabetes Brazilian children Guimaraes, R. L.; Segat, L.; Brandao, L. A. C.; Zanin, V.; De Lima Filho, J. L. Article ISI AUTOIMMUNITY (2009)
Predicting alternative candidates as binding sites to DEFB1 668 (-44) SNP: A long way from statistical association with multifactorial diseases Article ISI INFECTION GENETICS AND EVOLUTION (2009)

Michel Naslavsky

Professor Doutor

Genetics and Evolutionary Biology

Universidade de Sao Paulo

Sao Paulo, Brasil

Michel Satya Naslavsky

Líneas de Investigación

Experiencia Académica

Professor Doutor Full Time

Experiencia Profesional

Professor (Medical School) Part Time

Article (23)

Extreme phenotypes approach to investigate host genetics and COVID-19 outcomes

Avaliação quantitativa do volume cerebral em um grupo de idosos de São Paulo, Brasil: um estudo de base populacional

Discordant congenital Zika syndrome twins show differential in vitro viral susceptibility of neural progenitor cells (vol 9, 2018)

IHH Gene Mutations Causing Short Stature With Nonspecific Skeletal Abnormalities and Response to Growth Hormone Therapy

Diabetes is Not Associated with Alzheimer's Disease Neuropathology

Exomic variants of an elderly cohort of Brazilians in the ABraOM database

High phenotypic variability in Gerstmann-Straussler-Scheinker disease

Neuropathological diagnoses and clinical correlates in older adults in Brazil: A cross-sectional study

Chronic Traumatic Encephalopathy Presenting as Alzheimer's Disease in a Retired Soccer Player

Detection of small copy number variations (CNVs) in autism spectrum disorder (ASD) by custom array comparative genomic hybridization (aCGH)

Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility

Factors associated with lower gait speed among the elderly living in a developing country: a cross-sectional population-based study

Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome

Rare Variants in the Epithelial Cadherin Gene Underlying the Genetic Etiology of Nonsyndromic Cleft Lip with or without Cleft Palate

Schinzel-Giedion Syndrome in Two Brazilian Patients: Report of a Novel Mutation in SETBP1 and Literature Review of the Clinical Features

A defect in the RNA-processing protein HNRPDL causes limb-girdle muscular dystrophy 1G (LGMD1G)

Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations

Does germ-line deletion of the PIP gene constitute a widespread risk for cancer?

p27 variant and corticotropinoma susceptibility: a genetic and in vitro study

African ancestry protects against Alzheimer's disease-related neuropathology

The sound of silence: Human beta-defensin-1 gene untranslated SNPs change the predicted mRNA secondary structure in a length-dependent manner

Functional polymorphisms of DEFB1 gene in type 1 diabetes Brazilian children

Predicting alternative candidates as binding sites to DEFB1 668 (-44) SNP: A long way from statistical association with multifactorial diseases

Michel Naslavsky