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JM Gilchrist

Research Profile

Disorders

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Publications

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Michael A Hauser; stephen horrigan; Paula Salmikangas; U M Torian; Kristi D Viles; R Dancel; RW Tim; Anu Taivainen; L Bartoloni; JM Gilchrist; Jeffrey M Stajich; Perry C Gaskell; John Gilbert; Jeffery Vance; Margaret Pericak-Vance; Olli Carpen; Carol A Westbrook; Marcy C Speer
Myotilin is mutated in limb girdle muscular dystrophy 1A.
L Bartoloni; stephen horrigan; Kristi D Viles; JM Gilchrist; Jeffrey M Stajich; Jeffery Vance; LH Yamaoka; Margaret Pericak-Vance; Carol A Westbrook; Marcy C Speer
Use of a CEPH meiotic breakpoint panel to refine the locus of limb-girdle muscular dystrophy type 1A (LGMD1A) to a 2-Mb interval on 5q31.
Marcy C Speer; Jeffery Vance; F Lennon-Graham; Jeffrey M Stajich; Kristi D Viles; JM Gilchrist; V Nigro; R McMichael; J G Chutkow; L Bartoloni; stephen horrigan; Carol A Westbrook; Margaret Pericak-Vance
Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy families.

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All Publications

2000: Michael A Hauser; stephen horrigan; Paula Salmikangas; U M Torian; Kristi D Viles; R Dancel; RW Tim; Anu Taivainen; L Bartoloni; JM Gilchrist; Jeffrey M Stajich; Perry C Gaskell; John Gilbert; Jeffery Vance; Margaret Pericak-Vance; Olli Carpen; Carol A Westbrook; Marcy C Speer
Myotilin is mutated in limb girdle muscular dystrophy 1A.
Human molecular genetics 2000;9(14):2141-7.
1998: L Bartoloni; stephen horrigan; Kristi D Viles; JM Gilchrist; Jeffrey M Stajich; Jeffery Vance; LH Yamaoka; Margaret Pericak-Vance; Carol A Westbrook; Marcy C Speer
Use of a CEPH meiotic breakpoint panel to refine the locus of limb-girdle muscular dystrophy type 1A (LGMD1A) to a 2-Mb interval on 5q31.
Genomics 1998;54(2):250-5.
1998: Marcy C Speer; Jeffery Vance; F Lennon-Graham; Jeffrey M Stajich; Kristi D Viles; JM Gilchrist; V Nigro; R McMichael; J G Chutkow; L Bartoloni; stephen horrigan; Carol A Westbrook; Margaret Pericak-Vance
Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy families.
Human heredity 1998;48(4):179-84.
1998: Marcy C Speer; JM Gilchrist; Jeffrey M Stajich; Perry C Gaskell; Carol A Westbrook; stephen horrigan; L Bartoloni; LH Yamaoka; William Scott; Margaret Pericak-Vance
Evidence for anticipation in autosomal dominant limb-girdle muscular dystrophy.
Journal of medical genetics 1998;35(4):305-8.
1998: Catherine T Falk; JM Gilchrist; Margaret Pericak-Vance; Marcy C Speer
Using neural networks as an aid in the determination of disease status: comparison of clinical diagnosis to neural-network predictions in a pedigree with autosomal dominant limb-girdle muscular dystrophy.
American journal of human genetics 1998;62(4):941-9.
1997: Jeffrey M Stajich; JM Gilchrist; F Lennon; A Lee; LH Yamaoka; B Rosi; Perry C Gaskell; M Pritchard; L Donald; Allen D Roses; Jeffery Vance; Margaret Pericak-Vance
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13 in American families suggests the existence of a second causal mutation.
Neuromuscular disorders : NMD 1997;7 Suppl 1():S75-81.
1996: Jeffrey M Stajich; JM Gilchrist; F Lennon; A Lee; LH Yamaoka; B Helms; Perry C Gaskell; L Donald; Allen D Roses; Jeffery Vance; Margaret Pericak-Vance
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13.
Annals of neurology 1996;40(5):801-4.
1996: JM Gilchrist; M Sikirica; Edward G Stopa; S Shanske
Adult-onset MELAS. Evidence for involvement of neurons as well as cerebral vasculature in strokelike episodes.
Stroke; a journal of cerebral circulation 1996;27(8):1420-3.
1995: Marcy C Speer; JM Gilchrist; J G Chutkow; R McMichael; Carol A Westbrook; Jeffrey M Stajich; E M Jorgenson; Perry C Gaskell; B L Rosi; R Ramesar
Evidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy.
American journal of human genetics 1995;57(6):1371-6.
1994: LH Yamaoka; Carol A Westbrook; Marcy C Speer; JM Gilchrist; Ethylin Jabs; E G Schweins; Jeffrey M Stajich; Perry C Gaskell; Allen D Roses; Margaret Pericak-Vance
Development of a microsatellite genetic map spanning 5q31-q33 and subsequent placement of the LGMD1A locus between D5S178 and IL9.
Neuromuscular disorders : NMD 1994;4(5-6):471-5.
1994: JM Gilchrist; Janice M Massey; Donald B Sanders
Single fiber EMG and repetitive stimulation of the same muscle in myasthenia gravis.
Muscle & nerve 1994;17(2):171-5.
1993: JM Gilchrist; Janice M Massey; Donald B Sanders
Single-fiber EMG and repetitive stimulation of the same muscle in myasthenia gravis.
Annals of the New York Academy of Sciences 1993;681():567-9.
1992: Rosalind A Coleman; H S Winter; B Wolf; JM Gilchrist; Yuan-Tsong Chen
Glycogen storage disease type III (glycogen debranching enzyme deficiency): correlation of biochemical defects with myopathy and cardiomyopathy.
Annals of internal medicine 1992;116(11):896-900.
1992: JM Gilchrist; E Dosremedios; G Johnson; J Tornabene
Technical artifact simulating "motor axonopathy".
Muscle & nerve 1992;15(4):442-4.
1991: JM Gilchrist; M Ambler; P Agatiello
Steroid-responsive tubular aggregate myopathy.
Muscle & nerve 1991;14(3):233-6.
1989: Paul E Barkhaus; JM Gilchrist
Duchenne muscular dystrophy manifesting carriers.
Archives of neurology 1989;46(6):673-5.
1989: C R Stewart; S D Nandedkar; Janice M Massey; JM Gilchrist; Paul E Barkhaus; Donald B Sanders
Evaluation of an automatic method of measuring features of motor unit action potentials.
Muscle & nerve 1989;12(2):141-8.
1989: JM Gilchrist; Donald B Sanders
Myasthenic U-shaped decrement in multifocal cervical radiculopathy.
Muscle & nerve 1989;12(1):64-6.
1988: JM Gilchrist; S D Nandedkar; C S Stewart; Janice M Massey; Donald B Sanders; Paul E Barkhaus
Automatic analysis of the electromyographic interference pattern using the turns: amplitude ratio.
Electroencephalography and clinical neurophysiology 1988;70(6):534-40.
1988: C R Stewart; Stephen Kahler; JM Gilchrist
Congenital myopathy with cleft palate and increased susceptibility to malignant hyperthermia: King syndrome?
Pediatric neurology 1988;4(6):371-4.
1988: D A Krendel; JM Gilchrist; E H Bossen
Distal vacuolar myopathy with complete heart block.
Archives of neurology 1988;45(6):698-9.
1988: JM Gilchrist; Margaret Pericak-Vance; L Silverman; Allen D Roses
Clinical and genetic investigation in autosomal dominant limb-girdle muscular dystrophy.
Neurology 1988;38(1):5-9.
1987: D A Krendel; JM Gilchrist; A O Johnson; E H Bossen
Isolated deficiency of vitamin E with progressive neurologic deterioration.
Neurology 1987;37(3):538-40.