Stajich J - Search Results

1

Exclusion mapping of chromosomal regions which cross hybridise to FSHD1A associated markers in FSHD1B.

Gilbert JR, Speer MC, Stajich J, Clancy R, Lewis K, Qiu H, Yamaoka L, Kumar A, Vance J, Stewart C, et al. Gilbert JR, et al. Among authors: stajich j. J Med Genet. 1995 Oct;32(10):770-3. doi: 10.1136/jmg.32.10.770. J Med Genet. 1995. PMID: 8558552 Free PMC article.

2

Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5q.

Speer MC, Yamaoka LH, Gilchrist JH, Gaskell CP, Stajich JM, Vance JM, Kazantsev A, Lastra AA, Haynes CS, Beckmann JS, et al. Speer MC, et al. Among authors: stajich jm. Am J Hum Genet. 1992 Jun;50(6):1211-7. Am J Hum Genet. 1992. PMID: 1598902 Free PMC article.

3

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.

4

Genetic mapping of dinucleotide repeat polymorphisms and von Hippel-Lindau disease on chromosome 3p25-26.

Pericak-Vance MA, Nunes KJ, Whisenant E, Loeb DB, Small KW, Stajich JM, Rimmler JB, Yamaoka LH, Smith DI, Drabkin HA, et al. Pericak-Vance MA, et al. Among authors: stajich jm. J Med Genet. 1993 Jun;30(6):487-91. doi: 10.1136/jmg.30.6.487. J Med Genet. 1993. PMID: 8100855 Free PMC article.

5

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.

6

Evidence for locus heterogeneity in the Bethlem myopathy and linkage to 2q37.

Speer MC, Tandan R, Rao PN, Fries T, Stajich JM, Bolhuis PA, Jöbsis GJ, Vance JM, Viles KD, Sheffield K, James C, Kahler SG, Pettenati M, Gilbert JR, Denton PH, Yamaoka LH, Pericak-Vance MA. Speer MC, et al. Among authors: stajich jm. Hum Mol Genet. 1996 Jul;5(7):1043-6. doi: 10.1093/hmg/5.7.1043. Hum Mol Genet. 1996. PMID: 8817344

7

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.

8

Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7.

Speer MC, Vance JM, Grubber JM, Lennon Graham F, Stajich JM, Viles KD, Rogala A, McMichael R, Chutkow J, Goldsmith C, Tim RW, Pericak-Vance MA. Speer MC, et al. Among authors: stajich jm. Am J Hum Genet. 1999 Feb;64(2):556-62. doi: 10.1086/302252. Am J Hum Genet. 1999. PMID: 9973293 Free PMC article.

9

Further exclusion of FSHD1B from the telomeric region of 10q.

Speer MC, Pericak-Vance MA, Stajich JM, Sarrica J, Jordan M, Roses AD, Vance JM, Gilbert JR. Speer MC, et al. Among authors: stajich jm. Neurogenetics. 1997 Sep;1(2):151-2. doi: 10.1007/s100480050023. Neurogenetics. 1997. PMID: 10732819

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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