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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1986 2
1987 1
1990 2
1991 2
1992 2
1993 3
1994 2
1995 1
1996 5
1997 3
1998 6
1999 2
2000 1
2001 3
2002 2
2003 4
2004 2
2005 2
2006 1
2007 2
2008 3
2010 1
2012 1
2013 1
2014 1
2016 1
2024 0

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55 results

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Page 1
Linkage of familial essential tremor to chromosome 5q35.
Hicks JE, Konidari I, Scott BL, Stajich JM, Ashley-Koch AE, Gilbert JR, Scott WK. Hicks JE, et al. Among authors: stajich jm. Mov Disord. 2016 Jul;31(7):1059-62. doi: 10.1002/mds.26582. Epub 2016 Feb 26. Mov Disord. 2016. PMID: 26918299
Confirmation of linkage in von Hippel-Lindau disease.
Vance JM, Small KW, Jones MA, Stajich JM, Yamaoka LH, Roses AD, Hung WY, Pericak-Vance MA. Vance JM, et al. Among authors: stajich jm. Genomics. 1990 Mar;6(3):565-7. doi: 10.1016/0888-7543(90)90488-g. Genomics. 1990. PMID: 2328994
Clinical Studies in Non-chromosome 4-Linked Facioscapulohumeral Muscular Dystrophy.
Tim RW, Gilbert JR, Stajich JM, Rampersaud E, Viles KD, Tawil R, Padberg GW, Frants R, van der Maarel S, Bossen EH, Friedman AH, Pericak-Vance MA, Speer MC. Tim RW, et al. Among authors: stajich jm. J Clin Neuromuscul Dis. 2001 Sep;3(1):1-7. doi: 10.1097/00131402-200109000-00001. J Clin Neuromuscul Dis. 2001. PMID: 19078645
Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy.
Sarparanta J, Jonson PH, Golzio C, Sandell S, Luque H, Screen M, McDonald K, Stajich JM, Mahjneh I, Vihola A, Raheem O, Penttilä S, Lehtinen S, Huovinen S, Palmio J, Tasca G, Ricci E, Hackman P, Hauser M, Katsanis N, Udd B. Sarparanta J, et al. Among authors: stajich jm. Nat Genet. 2012 Feb 26;44(4):450-5, S1-2. doi: 10.1038/ng.1103. Nat Genet. 2012. PMID: 22366786 Free PMC article.
Myotilin is mutated in limb girdle muscular dystrophy 1A.
Hauser MA, Horrigan SK, Salmikangas P, Torian UM, Viles KD, Dancel R, Tim RW, Taivainen A, Bartoloni L, Gilchrist JM, Stajich JM, Gaskell PC, Gilbert JR, Vance JM, Pericak-Vance MA, Carpen O, Westbrook CA, Speer MC. Hauser MA, et al. Among authors: stajich jm. Hum Mol Genet. 2000 Sep 1;9(14):2141-7. doi: 10.1093/hmg/9.14.2141. Hum Mol Genet. 2000. PMID: 10958653
Genetic polymorphisms of the N-acetyltransferase genes and risk of Parkinson's disease.
van der Walt JM, Martin ER, Scott WK, Zhang F, Nance MA, Watts RL, Hubble JP, Haines JL, Koller WC, Lyons K, Pahwa R, Stern MB, Colcher A, Hiner BC, Jankovic J, Ondo WG, Allen FH Jr, Goetz CG, Small GW, Mastaglia F, Roses AD, Stajich JM, Booze MW, Fujiwara K, Gibson RA, Middleton LT, Scott BL, Pericak-Vance MA, Vance JM. van der Walt JM, et al. Among authors: stajich jm. Neurology. 2003 Apr 8;60(7):1189-91. doi: 10.1212/01.wnl.0000055929.84668.9a. Neurology. 2003. PMID: 12682333
Age at onset in two common neurodegenerative diseases is genetically controlled.
Li YJ, Scott WK, Hedges DJ, Zhang F, Gaskell PC, Nance MA, Watts RL, Hubble JP, Koller WC, Pahwa R, Stern MB, Hiner BC, Jankovic J, Allen FA Jr, Goetz CG, Mastaglia F, Stajich JM, Gibson RA, Middleton LT, Saunders AM, Scott BL, Small GW, Nicodemus KK, Reed AD, Schmechel DE, Welsh-Bohmer KA, Conneally PM, Roses AD, Gilbert JR, Vance JM, Haines JL, Pericak-Vance MA. Li YJ, et al. Among authors: stajich jm. Am J Hum Genet. 2002 Apr;70(4):985-93. doi: 10.1086/339815. Epub 2002 Mar 1. Am J Hum Genet. 2002. PMID: 11875758 Free PMC article.
55 results