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Jeffrey M. Stajich

Duke University

69

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4498

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Linkage of familial essential tremor to chromosome 5q35.

2016 Movement Disorders
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Stratified Whole Genome Linkage Analysis of Chiari Type I Malformation Implicates Known Klippel-Feil Syndrome Genes as Putative Disease Candidates

2013 PLOS ONE
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Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy

2012 Nature Genetics
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Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.

2010 Annals of Human Genetics
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Novel congenital myopathy locus identified in Native American Indians at 12q13.13-14.1

2008 Neurology
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Native American myopathy: congenital myopathy with cleft palate, skeletal anomalies, and susceptibility to malignant hyperthermia.

2008 American Journal of Medical Genetics Part A
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Pesticide exposure and risk of Parkinson's disease: a family-based case-control study.

2008 BMC Neurology
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Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4.

2007 Neurology
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Smoking, caffeine, and nonsteroidal anti-inflammatory drugs in families with Parkinson disease.

2007 JAMA Neurology
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NOS2A and the modulating effect of cigarette smoking in Parkinson's disease

2006 Annals of Neurology
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Citations (33)