Maria R. Bueno-Passos
Sao Paulo, SP, Brazil
Last Updated: 09/26/2026
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Found 134 publications
Expanding the phenotypic spectrum associated with ZIC1 variants: A neurodevelopmental disorder with and without craniosynostosis.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: September 16, 2025
Catatonia and regression in an autism spectrum disorder patient harbouring a BRSK2 frameshift mutation.
Journal: Journal of medical genetics
Published: July 29, 2025
IL17RA and IL21R polymorphisms influence type 1 diabetes predisposition and autoimmune phenotypes.
Journal: Frontiers in endocrinology
Published: April 29, 2025
Identifying biomarkers and trajectories of executive functions and language development in the first 3 years of life: Design, methods, and findings of the Germina cohort study.
Journal: Development and psychopathology
Published: March 05, 2025
Guided and unguided neural organoids play complementary roles in studying neurodevelopment and neuroinflammation.
Journal: Einstein (Sao Paulo, Brazil)
Published: March 05, 2025
Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populations.
Journal: medRxiv : the preprint server for health sciences
Published: January 20, 2025
Deleterious coding variation associated with autism is shared across ancestries.
Journal: Nature medicine
Published: December 20, 2024
Psychiatric genetics in the diverse landscape of Latin American populations.
Journal: Nature genetics
Published: September 06, 2024
Van der Woude syndrome and amniotic band sequence: A clue to a common genetic etiology? A case report.
Journal: Genetics and molecular biology
Published: June 24, 2024
Lead contamination in human milk affects infants' language trajectory: results from a prospective cohort study.
Journal: Frontiers in public health
Published: June 17, 2024
Last Updated: 09/26/2026