Physician

Family Medicine

Dr. Andy P. Peiffer, MD

Dr. Andy P. Peiffer practices Family Medicine. Andy Peiffer is also published. He has 15 publications published. The lastest publication: "A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns.'

Publications

Further evidence for the role of genes on chromosome 2 and chromosome 5 in the inheritance of pulmonary function.
Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration.
Genome-wide detection and characterization of positive selection in human populations.
A second generation human haplotype map of over 3.1 million SNPs.
Community engagement and informed consent in the International HapMap project.
Quantitative trait loci on chromosomes 1, 2, 3, 4, 8, 9, 11, 12, and 18 control variation in levels of T and B lymphocyte subpopulations.
A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy.
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns.
Genes for rare idiopathic generalized epilepsies: BFNC.
A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome.
Microcephaly with simplified gyral pattern in six related children.
A locus for febrile seizures (FEB3) maps to chromosome 2q23-24.
AGT genetic variation, plasma AGT, and blood pressure: An analysis of the Utah Genetic Reference Project pedigrees.
Genetic analysis of a complex trait in the Utah Genetic Reference Project: a major locus for PTC taste ability on chromosome 7q and a secondary locus on chromosome 16p.

Doctors Specialties

Family Medicine

Accepted Insurances

Blue Cross Blue Shield
Cigna
Commercial Insurance Company
Humana
Medicare MCR
United Healthcare

Education

University of Laval Faculty of Medicine

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