PubMed Mentions documentation

Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations. posted by NITRC Moderator on Dec 17, 2025

PubMed Mentions documentation

Identification of transcriptional regulatory variants in pig duodenum, liver, and muscle tissues. posted by NITRC Moderator on Dec 17, 2025

PubMed Mentions documentation

Genetic liability for gastrointestinal inflammation disorders and association with gastrointestinal symptoms in children with and without autism. posted by NITRC Moderator on Dec 17, 2025

PubMed Mentions documentation

X-Chromosome Association Study in Latin American Cohorts Identifies New Loci in Parkinson's Disease. posted by NITRC Moderator on Dec 17, 2025

PubMed Mentions documentation

Africa-specific human genetic variation near CHD1L associates with HIV-1 load. posted by NITRC Moderator on Dec 17, 2025

PubMed Mentions documentation

Conserved islands of divergence associated with adaptive variation in sockeye salmon are maintained by multiple mechanisms. posted by NITRC Moderator on Dec 17, 2025

PubMed Mentions documentation

A Genetic Risk Variant for Multiple Sclerosis Severity is Associated with Brain Atrophy. posted by NITRC Moderator on Dec 17, 2025

PubMed Mentions documentation

Do chromosome rearrangements fix by genetic drift or natural selection? Insights from Brenthis butterflies. posted by NITRC Moderator on Dec 17, 2025

PubMed Mentions documentation

Comparative population genomics of manta rays has global implications for management. posted by NITRC Moderator on Dec 17, 2025

PubMed Mentions documentation

HLA-DQA1*05 Not Associated With Ustekinumab Loss of Response and Antidrug Antibodies in Ulcerative Colitis and Crohn's Disease Patients. posted by NITRC Moderator on Dec 17, 2025