Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.


The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page


My NCBI Filters

Results by year

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

Text availability

Article attribute

Article type

Publication date

Search Results

55 results

Results by year

Filters applied: . Clear all
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
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.
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
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
Parkin mutations and susceptibility alleles in late-onset Parkinson's disease.
Oliveira SA, Scott WK, Martin ER, Nance MA, Watts RL, Hubble JP, Koller WC, Pahwa R, Stern MB, Hiner BC, Ondo WG, Allen FH Jr, Scott BL, Goetz CG, Small GW, Mastaglia F, Stajich JM, Zhang F, Booze MW, Winn MP, Middleton LT, Haines JL, Pericak-Vance MA, Vance JM. Oliveira SA, et al. Among authors: stajich jm. Ann Neurol. 2003 May;53(5):624-9. doi: 10.1002/ana.10524. Ann Neurol. 2003. PMID: 12730996
55 results