Jay A. Tischfield

Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders

Phil H. Lee, Verneri Anttila, Hyejung Won et al. · Cell · 2019 · 1.4K citations · Full text

Psychiatry, Psychiatric Disorders, Genetic Disorder +15

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

Stephan Sanders, A. Gulhan Ercan‐Sencicek, Vanessa Hus et al. · Neuron · 2011 · 1.3K citations · Full text

Neurodevelopmental Disorders, Williams Syndrome Region, Syndromic Autism +10

Single-nucleotide polymorphism in the human mu opioid receptor gene alters β-endorphin binding and activity: Possible implications for opiate addiction

Cherie E. Bond, K. Steven LaForge, Mingting Tian et al. · Proceedings of the National Academy of Sciences · 1998 · 1.1K citations · Full text

Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A

Isabelle Richard, Odile Broux, Valéerie Allamand et al. · Cell · 1995 · 989 citations · Full text

Molecular Physiology, Skeletal Muscle, Genetics +2

Genome-wide search for genes affecting the risk for alcohol dependence

Theodore Reich, Howard J. Edenberg, Alison Goate et al. · American Journal of Medical Genetics · 1998 · 737 citations

Biology, Premature Death, Genome-wide Association Study +14