P. S. St. Jean

发表

An Abundance of Rare Functional Variants in 202 Drug Target Genes Sequenced in 14,002 People

Claudio J. Verzilli, Peter M Woollard, G. Abecasis, 2012, Science.

Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease.

A. J. Slater, Rachel L. Taylor, P. Matthews, 2008, Archives of neurology.

Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families

Jennifer Williamson, Bradley F. Boeve, Ramon Diaz-Arrastia, 2012, PloS one.

Diabetes in the Old Order Amish: characterization and heritability analysis of the Amish Family Diabetes Study.

M. Wagner, M. Ehm, W. Knowler, 2000, Diabetes care.

Genetics plays a limited role in predicting chronic obstructive pulmonary disease treatment response and exacerbation.

P. S. St. Jean, D. Fraser, M. Chiano, 2021, Respiratory medicine.

Cognitive Decline in Alzheimer’s Disease: Limited Clinical Utility for GWAS or Polygenic Risk Scores in a Clinical Trial Setting

P. S. St. Jean, D. Pulford, J. Euesden, 2020, Genes.

Ultrasound screening of first-degree relatives of patients with an abdominal aortic aneurysm.

D. Steed, M. Webster, P. Majumder, 1991, Journal of vascular surgery.

Alpha-1-antitrypsin deficiency in aneurysmal disease.

D. Steed, M. Webster, P. S. St. Jean, 1996, Human heredity.

On the inheritance of abdominal aortic aneurysm.

D. Steed, M. Webster, P. Majumder, 1991, American journal of human genetics.

A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia

David B. Goldstein, Lefkos T. Middleton, Hans-Jürgen Möller, 2009, PLoS genetics.

Pharmacogenetic analysis of belimumab fails to identify robust genetic predictors of efficacy in lupus

P. S. St. Jean, L. McCarthy, A. Hughes, 2019, Pharmacogenetics and genomics.

Mapping of both autosomal recessive and dominant variants of pseudoxanthoma elasticum to chromosome 16p13.1.

K. Lindpaintner, P. S. St. Jean, K. Neldner, 1997, Human molecular genetics.