J. Stevens

SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease.

J. Gilbert, M. Pericak-Vance, A. Roses, 2000, American journal of human genetics.

Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus

P. O'Connell, R. Wolff, M. Culver, 1990, Cell.

Exome Analysis of a Family With Pleiotropic Congenital Heart Disease

M. Leppert, S. Levy, N. Matsunami, 2012, Circulation. Cardiovascular genetics.

Analysis of high‐risk pedigrees identifies 11 candidate variants for Alzheimer's disease

Lyndsay A. Staley, L. Cannon-Albright, J. Kauwe, 2021, Alzheimer's & dementia : the journal of the Alzheimer's Association.

Genome-wide analysis of high-risk primary brain cancer pedigrees identifies PDXDC1 as a candidate brain cancer predisposition gene.

L. Cannon-Albright, J. Farnham, C. Teerlink, 2020, Neuro-oncology.

Identification and genomic analysis of pedigrees with exceptional longevity identifies candidate rare variants

Lyndsay A. Staley, L. Cannon-Albright, J. Kauwe, 2020, Neurobiology of Disease.

FANCM c5791C>T stopgain mutation (rs144567652) is a familial colorectal cancer risk factor

L. Cannon-Albright, S. Tavtigian, R. Bell, 2020, Molecular genetics & genomic medicine.