Maria Teresa Vieira Sanseverino

Universidade Federal do Rio Grande do Sul — Brazil

Health Professions · Health Sciences

23h-index2.9kcitations293works2.12yr avg
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Research Topics

Health, Medicine and Society(34), Hermeneutics and Narrative Identity(34), Aging, Elder Care, and Social Issues(34), Maternal and Neonatal Healthcare(33), Prenatal Screening and Diagnostics(27)

Publications293 total

Epidemiology of congenital heart defects in live births: findings from a study in Southern Brazil
BMC Cardiovascular Disorders·2026Open Access
Epidemiology of Congenital Heart Defects in Live Births: Findings from a Study in Southern Brazil
2025Open Access
Scientific and Public Health Challenges in Folic Acid Supplementation: Insights from Brazil and Global Implications
Nutrients·2025· 2 citedOpen Access
Congenital Oropouche in Humans: Clinical Characterization of a Possible New Teratogenic Syndrome
Viruses·2025· 14 citedOpen Access
Congenital Oropouche in Humans: Clinical Characterization of a Possible New Teratogenic Syndrome
Preprints.org·2025Open Access
Epidemiological surveillance in congenital anomalies and rare diseases in Brazil: present situation and future challenges
Journal of Community Genetics·2025· 2 citedOpen Access
Home Articles About Contact Toward clarity: why we need to standardize the term 'recurrent pregnancy loss'
JBRA·2025Open Access
Infant Mortality Due to Congenital Anomalies: Brazil, 2000 to 2023
SSRN Electronic Journal·2025Open Access
Potencialidades das inovações tecnológicas no ensino de genética e embriologia: uma revisão narrativa
Cuadernos de Educación y Desarrollo·2024Open Access
Identificando lacunas no currículo médico atual: perspectivas da formação em genética
Cuadernos de Educación y Desarrollo·2024Open Access
<scp><i>CNOT1</i></scp> p.<scp>Arg535Cys</scp> variant in holoprosencephaly with late onset diabetes mellitus
American Journal of Medical Genetics Part A·2024· 2 citedOpen Access
Congenital anomalies in pregnancies with overt and pregestational type 2 diabetes: a gray portrayal from a cohort in Brazil
Diabetology & Metabolic Syndrome·2024· 1 citedOpen Access
Identification of a founder effect involving n.197C&gt;T variant in RMRP gene associated to cartilage-hair hypoplasia syndrome in Brazilian patients
Scientific Reports·2024· 4 citedOpen Access
A germline chimeric KANK1-DMRT1 transcript derived from a complex structural variant is associated with a congenital heart defect segregating across five generations
Chromosome Research·2024· 7 cited
Birth after low-level +20 Aneuploid Mosaic Embryo Transfer: A Case Report
JBRA·2024Open Access
A germline chimeric KANK1-DMRT1 transcript derived from a complex structural variant is associated with a congenital heart defect segregating across five generations
Research Square (Research Square)·2023· 1 citedOpen Access
Caffeine intake during pregnancy and adverse outcomes: An integrative review
Reproductive Toxicology·2023· 12 cited
A New Strategy for the Old Challenge of Thalidomide: Systems Biology Prioritization of Potential Immunomodulatory Drug (IMiD)-Targeted Transcription Factors
International Journal of Molecular Sciences·2023· 3 citedOpen Access
Profile of calls and activities of the first Teratogen Information Service in Latin America through 32 years
Neurotoxicology and Teratology·2023
Expression profiles of meiotic genes in male vs. female gonads and gametes: Insights into fertility issues
Frontiers in Genetics·2023· 2 citedOpen Access
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Frequent Co-authors

Lavínia Schüler‐Faccini(35), Fernanda Sales Luiz Vianna(19), Lucas Rosa Fraga(16), Roberto Giugliani(7), Thayne Woycinck Kowalski(7), André Anjos da Silva(6), Júlio César Loguercio Leite(5), Caroline Gross Dutra(5), Juliano André Boquett(5), Rozana Oliveira Gonçalves(5), José Antônio de Azevedo Magalhães(4), Alberto Mantovani Abeche(4), Erlane Marques Ribeiro(3), Dafne Dain Gandelman Horovitz(3), Denise P. Cavalcanti(3), Maria Juliana R. Doriqui(3), Antonette S. El-Husny(3), Rejane Gus(3), Têmis Maria Félix(3), Tani Ranieri(3)