Jeffrey M. Stajich

Neurology

2100 Erwin Rd
Durham, NC 27705

Last Updated: 09/26/2026

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Found 5 publications

Linkage of familial essential tremor to chromosome 5q35.

Linkage of familial essential tremor to chromosome 5q35.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: October 09, 2013

Genetic evaluation and application of posterior cranial fossa traits as endophenotypes for Chiari type I malformation.

Genetic evaluation and application of posterior cranial fossa traits as endophenotypes for Chiari type I malformation.

Journal: Annals of human genetics

Published: April 04, 2013

Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates.

Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates.

Journal: PloS one

Published: January 12, 2013

Exome analysis of two limb-girdle muscular dystrophy families: mutations identified and challenges encountered.

Exome analysis of two limb-girdle muscular dystrophy families: mutations identified and challenges encountered.

Journal: PloS one

Published: July 23, 2012

Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy.

Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy.

Journal: Nature genetics

Published: October 13, 2011

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Last Updated: 09/26/2026