Margaret A. Pericak‐Vance

Linkage of Familial Dilated Cardiomyopathy with Conduction Defect and Muscular Dystrophy to Chromosome 6q23

D. Messina, Marcy C. Speer, Margaret A. Pericak‐Vance et al. · The American Journal of Human Genetics · 1997 · 167 citations · Full text

Cardiomyopathy, Mendelian Disorder, Genetic Disorder +8

Migraine with Aura Susceptibility Locus on Chromosome 19p13 Is Distinct from the Familial Hemiplegic Migraine Locus

Keith Jones, Margaret G. Ehm, Margaret A. Pericak‐Vance et al. · Genomics · 2001 · 79 citations

Cluster Headache, Is Distinct, Aura Susceptibility Locus +5

A Novel Long and Unstable CAG/CTG Trinucleotide Repeat on Chromosome 17q

Takeshi Ikeuchi, Kazuhiro Sanpei, Hiroki Takano et al. · Genomics · 1998 · 44 citations

Chromatin, Genome Instability, Dna Sequencing +12

No genetic association between the LRP receptor and sporadic or late-onset familial Alzheimer disease

William K. Scott, Larry H. Yamaoka, Meredyth P. Bass et al. · Neurogenetics · 1998 · 38 citations

Neurodegenerative Diseases, Alzheimer's Disease, Genetics +10

Linkage analysis of candidate myelin genes in familial multiple sclerosis

Eric Seboun, Antony Rombos, Koishiro Usuku et al. · Neurogenetics · 1999 · 27 citations

Neurogenomics, Neurological Disorder, Genetic Disorder +10