Last Updated: 09/26/2026
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Found 6 publications
Rare variants in STAB2 in patients with chronic thromboembolic pulmonary hypertension.
Journal: ERJ open research
Published: December 10, 2024
Analysis of high-risk pedigrees identifies 11 candidate variants for Alzheimer's disease.
Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association
Published: September 16, 2020
Genome-wide analysis of high-risk primary brain cancer pedigrees identifies PDXDC1 as a candidate brain cancer predisposition gene.
Journal: Neuro-oncology
Published: July 10, 2020
FANCM c5791C>T stopgain mutation (rs144567652) is a familial colorectal cancer risk factor.
Journal: Molecular genetics & genomic medicine
Published: June 26, 2020
Identification and genomic analysis of pedigrees with exceptional longevity identifies candidate rare variants.
Journal: Neurobiology of disease
Published: March 02, 2020
Exome analysis of a family with pleiotropic congenital heart disease.
Journal: Circulation. Cardiovascular genetics
Published: February 17, 2012
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Last Updated: 09/26/2026