Search research articles
Contact Us
Filters
Showing results (1-10 of 12) with videos related to
Page
of 2
Sort By:
BMC Medical Genomics
|
October 24, 2020
Noninvasive prenatal paternity determination using microhaplotypes: a pilot study
Jaqueline Yu Ting Wang, Martin R Whittle, Renato David Puga, et al.
Translational Psychiatry
|
June 6, 2022
Rare CACNA1H and RELN variants interact through mTORC1 pathway in oligogenic autism spectrum disorder
André Luíz Teles E Silva, Talita Glaser, Karina Griesi-Oliveira, et al.
Neurology. Genetics
|
October 16, 2020
Manifesting carriers of X-linked myotubular myopathy: Genetic modifiers modulating the phenotype
Lucas Santos Souza, Camila Freitas Almeida, Guilherme Lopes Yamamoto, et al.
European Journal of Human Genetics : EJHG
|
June 6, 2023
Three generation families: Analysis of de novo variants in autism
Claudia I Samogy Costa, Gabriele da Silva Campos, Eduarda Morgana da Silva Montenegro, et al.
NPJ Genomic Medicine
|
March 6, 2025
Understanding rare variant contributions to autism: lessons from dystrophin-deficient model
Claudia Ismania Samogy Costa, Luciana Madanelo, Jaqueline Yu Ting Wang, et al.
Scientific Reports
|
July 24, 2024
Genetic variation in NOTCH1 is associated with overweight and obesity in Brazilian elderly
Estevão Carlos Silva Barcelos, Michel Satya Naslavsky, Izadora Silveira Fernandes, et al.
Clinical Genetics
|
October 19, 2021
Copy number variations in a Brazilian cohort with autism spectrum disorders highlight the contribution of cell adhesion genes
Claudia Ismania Samogy Costa, Eduarda Morgana da Silva Montenegro, Mehdi Zarrei, et al.
Development and Psychopathology
|
March 5, 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
Daniel Fatori, Elizabeth Shephard, Danilo Benette, et al.
Nature Communications
|
March 5, 2022
Whole-genome sequencing of 1,171 elderly admixed individuals from São Paulo, Brazil
Michel S Naslavsky, Marilia O Scliar, Guilherme L Yamamoto, et al.
Nature Communications
|
March 31, 2022
Author Correction: Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil
Michel S Naslavsky, Marilia O Scliar, Guilherme L Yamamoto, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
BMC Medical Genomics
|
October 24, 2020
Noninvasive prenatal paternity determination using microhaplotypes: a pilot study
Jaqueline Yu Ting Wang, Martin R Whittle, Renato David Puga, et al.
Translational Psychiatry
|
June 6, 2022
Rare CACNA1H and RELN variants interact through mTORC1 pathway in oligogenic autism spectrum disorder
André Luíz Teles E Silva, Talita Glaser, Karina Griesi-Oliveira, et al.
Neurology. Genetics
|
October 16, 2020
Manifesting carriers of X-linked myotubular myopathy: Genetic modifiers modulating the phenotype
Lucas Santos Souza, Camila Freitas Almeida, Guilherme Lopes Yamamoto, et al.
European Journal of Human Genetics : EJHG
|
June 6, 2023
Three generation families: Analysis of de novo variants in autism
Claudia I Samogy Costa, Gabriele da Silva Campos, Eduarda Morgana da Silva Montenegro, et al.
NPJ Genomic Medicine
|
March 6, 2025
Understanding rare variant contributions to autism: lessons from dystrophin-deficient model
Claudia Ismania Samogy Costa, Luciana Madanelo, Jaqueline Yu Ting Wang, et al.
Scientific Reports
|
July 24, 2024
Genetic variation in NOTCH1 is associated with overweight and obesity in Brazilian elderly
Estevão Carlos Silva Barcelos, Michel Satya Naslavsky, Izadora Silveira Fernandes, et al.
Clinical Genetics
|
October 19, 2021
Copy number variations in a Brazilian cohort with autism spectrum disorders highlight the contribution of cell adhesion genes
Claudia Ismania Samogy Costa, Eduarda Morgana da Silva Montenegro, Mehdi Zarrei, et al.
Development and Psychopathology
|
March 5, 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
Daniel Fatori, Elizabeth Shephard, Danilo Benette, et al.
Nature Communications
|
March 5, 2022
Whole-genome sequencing of 1,171 elderly admixed individuals from São Paulo, Brazil
Michel S Naslavsky, Marilia O Scliar, Guilherme L Yamamoto, et al.
Nature Communications
|
March 31, 2022
Author Correction: Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil
Michel S Naslavsky, Marilia O Scliar, Guilherme L Yamamoto, et al.
Page
of 2