Stajich JM - Search Results

1

Development of a microsatellite genetic map spanning 5q31-q33 and subsequent placement of the LGMD1A locus between D5S178 and IL9.

Yamaoka LH, Westbrook CA, Speer MC, Gilchrist JM, Jabs EW, Schweins EG, Stajich JM, Gaskell PC, Roses AD, Pericak-Vance MA. Yamaoka LH, et al. Among authors: stajich jm. Neuromuscul Disord. 1994 Sep-Nov;4(5-6):471-5. doi: 10.1016/0960-8966(94)90086-8. Neuromuscul Disord. 1994. PMID: 7881291

2

Linkage studies in facioscapulohumeral muscular dystrophy (FSHD).

Gilbert JR, Stajich JM, Speer MC, Vance JM, Stewart CS, Yamaoka LH, Samson F, Fardeau M, Potter TG, Roses AD, et al. Gilbert JR, et al. Among authors: stajich jm. Am J Hum Genet. 1992 Aug;51(2):424-7. Am J Hum Genet. 1992. PMID: 1642241 Free PMC article.

3

Evidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD).

Gilbert JR, Stajich JM, Wall S, Carter SC, Qiu H, Vance JM, Stewart CS, Speer MC, Pufky J, Yamaoka LH, et al. Gilbert JR, et al. Among authors: stajich jm. Am J Hum Genet. 1993 Aug;53(2):401-8. Am J Hum Genet. 1993. PMID: 8328457 Free PMC article.

4

Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity.

Ben Othmane K, Middleton LT, Loprest LJ, Wilkinson KM, Lennon F, Rozear MP, Stajich JM, Gaskell PC, Roses AD, Pericak-Vance MA, et al. Ben Othmane K, et al. Among authors: stajich jm. Genomics. 1993 Aug;17(2):370-5. doi: 10.1006/geno.1993.1334. Genomics. 1993. PMID: 8406488

5

Evidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy.

Speer MC, Gilchrist JM, Chutkow JG, McMichael R, Westbrook CA, Stajich JM, Jorgenson EM, Gaskell PC, Rosi BL, Ramesar R, et al. Speer MC, et al. Among authors: stajich jm. Am J Hum Genet. 1995 Dec;57(6):1371-6. Am J Hum Genet. 1995. PMID: 8533766 Free PMC article.

6

Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13.

Stajich JM, Gilchrist JM, Lennon F, Lee A, Yamaoka L, Helms B, Gaskell PC, Donald L, Roses AD, Vance JM, Pericak-Vance MA. Stajich JM, et al. Ann Neurol. 1996 Nov;40(5):801-4. doi: 10.1002/ana.410400519. Ann Neurol. 1996. PMID: 8957024

7

Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13 in American families suggests the existence of a second causal mutation.

Stajich JM, Gilchrist JM, Lennon F, Lee A, Yamaoka L, Rosi B, Gaskell PC, Pritchard M, Donald L, Roses AD, Vance JM, Pericak-Vance MA. Stajich JM, et al. Neuromuscul Disord. 1997 Oct;7 Suppl 1:S75-81. doi: 10.1016/s0960-8966(97)00087-4. Neuromuscul Disord. 1997. PMID: 9392021

8

Evidence for anticipation in autosomal dominant limb-girdle muscular dystrophy.

Speer MC, Gilchrist JM, Stajich JM, Gaskell PC, Westbrook CA, Horrigan SK, Bartoloni L, Yamaoka LH, Scott WK, Pericak-Vance MA. Speer MC, et al. Among authors: stajich jm. J Med Genet. 1998 Apr;35(4):305-8. doi: 10.1136/jmg.35.4.305. J Med Genet. 1998. PMID: 9598725 Free PMC article.

9

Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy families.

Speer MC, Vance JM, Lennon-Graham F, Stajich JM, Viles KD, Gilchrist JM, Nigro V, McMichael R, Chutkow JG, Bartoloni L, Horrigan SK, Westbrook CA, Pericak-Vance MA. Speer MC, et al. Among authors: stajich jm. Hum Hered. 1998 Jul-Aug;48(4):179-84. doi: 10.1159/000022799. Hum Hered. 1998. PMID: 9694248

10

The genes encoding for D4Z4 binding proteins HMGB2, YY1, NCL, and MYOD1 are excluded as candidate genes for FSHD1B.

Bastress KL, Stajich JM, Speer MC, Gilbert JR. Bastress KL, et al. Among authors: stajich jm. Neuromuscul Disord. 2005 Apr;15(4):316-20. doi: 10.1016/j.nmd.2004.12.006. Epub 2005 Jan 28. Neuromuscul Disord. 2005. PMID: 15792872

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