M A Pericak-Vance

发表

Using neural networks as an aid in the determination of disease status: comparison of clinical diagnosis to neural-network predictions in a pedigree with autosomal dominant limb-girdle muscular dystrophy.

C T Falk, J M Gilchrist, M A Pericak-Vance, 1998, American journal of human genetics.

Life After the Screen: Making Sense of Many P‐Values

E R Martin, M A Pericak-Vance, M C Speer, 2001, Genetic epidemiology.

Multifactor dimensionality reduction reveals gene–gene interactions associated with multiple sclerosis susceptibility in African Americans

J L Haines, M A Pericak-Vance, S Schmidt, 2006, Genes and Immunity.

A NOVEL ALZHEIMER DISEASE LOCUS LOCATED NEAR THE GENE ENCODING TAU PROTEIN

Magda Tsolaki, A Hofman, D A Bennett, 2015, Molecular Psychiatry.

Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism.

E R Martin, M A Pericak-Vance, J. Gilbert, 2005, American journal of human genetics.

An Analysis Paradigm for Investigating Multi‐locus Effects in Complex Disease: Examination of Three GABAA Receptor Subunit Genes on 15q11‐q13 as Risk Factors for Autistic Disorder.

E R Martin, M A Pericak-Vance, J. Gilbert, 2006, Annals of human genetics.

Association Analysis of Chromosome 15 GABAA Receptor Subunit Genes in Autistic Disorder

E R Martin, M A Pericak-Vance, J. Gilbert, 2001, Journal of neurogenetics.

Association of apolipoprotein E allele epsilon 4 with late-onset familial and sporadic Alzheimer's disease.

M A Pericak-Vance, M. Pericak-Vance, J. Gusella, 1993, Neurology.

Genetic Analysis of Complex Diseases

J L Haines, M A Pericak-Vance, W K Scott, 1997, Science.

Genome-wide association study of Alzheimer's disease

M A Pericak-Vance, O L Lopez, E Feingold, 2012, Translational Psychiatry.

Association of the apolipoprotein E gene with age-related macular degeneration: possible effect modification by family history, age, and gender.

J L Haines, M A Pericak-Vance, S Schmidt, 2000, Molecular vision.

Supporting Online Material Materials and Methods Figs. S1 to S7 Tables S1 to S4 References Mutations in the Fus/tls Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

J L Haines, M A Pericak-Vance, J. Haines, 2022 .

Fine mapping of autistic disorder to chromosome 15q11‐q13 by use of phenotypic subtypes.

M A Pericak-Vance, J. Gilbert, M. Cuccaro, 2003, American journal of human genetics.

Linkage analysis of familial Alzheimer disease, using chromosome 21 markers.

E M Wijsman, M A Pericak-Vance, M. Pericak-Vance, 1991, American journal of human genetics.

Association and gene–gene interaction of SLC6A4 and ITGB3 in autism

E R Martin, M A Pericak-Vance, J. Gilbert, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Increased amyloid beta-peptide deposition in cerebral cortex as a consequence of apolipoprotein E genotype in late-onset Alzheimer disease.

A D Roses, M A Pericak-Vance, M. Pericak-Vance, 1993, Proceedings of the National Academy of Sciences of the United States of America.

Genotype‐based association test for general pedigrees: The genotype‐PDT

E R Martin, M A Pericak-Vance, J. Gilbert, 2003, Genetic epidemiology.

Genetic overlap between Alzheimer’s disease and Parkinson’s disease at the MAPT locus

A Smith, M A Pericak-Vance, L A Farrer, 2015, Molecular Psychiatry.