Showing results (171-180 of 229) with videos related to
Sort By:
Pageof 23
Human Mutation|April 14, 2025
A Palindrome-Like Structure on 16p13.3 Is Associated with the Formation of Complex Structural Variations and SRRM2 HaploinsufficiencyAlistair T Pagnamenta, Jing Yu, Tracey A Willis, et al.Journal of Attention Disorders|July 11, 2022
Associations Between ADHD Symptoms and Maternal and Birth Outcomes: An Exploratory Analysis in a Multi-Country Cohort of Expectant MothersAja Louise Murray, Diana Taut, Adriana Baban, et al.Journal of Neurodevelopmental Disorders|October 26, 2016
Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variationMatthew J Gazzellone, Mehdi Zarrei, Christie L Burton, et al.Clinical & Translational Immunology|May 1, 2026
High-dimensional multiomics reveals perturbations to IL-6/IL-6R axis and RUNX3 in CD4+ T cells during third-trimester pregnancyJennifer R Habel, Thi H O Nguyen, Natasha de Alwis, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2018
De novo missense variants in RAC3 cause a novel neurodevelopmental syndromeGregory Costain, Bert Callewaert, Heinz Gabriel, et al.Neurology. Genetics|June 8, 2017
ARHGEF9 disease: Phenotype clarification and genotype-phenotype correlationMichael Alber, Vera M Kalscheuer, Elysa Marco, et al.Journal of Medical Genetics|September 26, 2024
Rare disease genomic testing in the UK and Ireland: promoting timely and equitable accessSian Ellard, Sian Morgan, Sarah L Wynn, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 21, 2018
Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of FallotMiriam S Reuter, Rebekah Jobling, Rajiv R Chaturvedi, et al.Nature Communications|November 27, 2025
Mutations in the β-tubulin TUBB impair ciliogenesis and are associated with ciliopathy-like phenotypesAntonio Mollica, Safia Omer, Georgiana Forguson, et al.Molecular Autism|April 12, 2014
Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disordersCatarina T Correia, Inês C Conceição, Bárbara Oliveira, et al.Pageof 23