J. L. Haines

Mutations in the <i>FUS/TLS</i> Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

Thomas J. Kwiatkowski, Daryl A. Bosco, Aurélie Leclerc et al. · Science · 2009 · 2.5K citations

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Somatic Variant +14

A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex

J. L. Haines, Monica Ter‐Minassian, A. Bazyk et al. · Nature Genetics · 1996 · 653 citations

Complete Genomic Screen, Neurological Disorder, Medicine +11

Identification of Novel Genes in Late-Onset Alzheimer's Disease

Jeffery M. Vance, Janet M. Grubber, Lisa Bailey et al. · Experimental Gerontology · 2000 · 198 citations

Alzheimer's Disease, Dementia, Neurochemical Biomarkers +5

Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14

Khemissa Bejaoui, Koichi Hirabayashi, Fayçal Hentati et al. · Neurology · 1995 · 146 citations

Miyoshi Myopathy, Mendelian Disorder, Family Members +13

C3 R102G polymorphism increases risk of age-related macular degeneration

Kylee L. Spencer, Lana M. Olson, B. M. Anderson et al. · Human Molecular Genetics · 2008 · 129 citations · Full text

Inflammation, Complement System, Strong Ld +14