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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
2022 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
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.
A novel mutation in the von Hippel-Lindau gene.
Loeb DB, Pericak-Vance MA, Stajich JM, Vance JM. Loeb DB, et al. Among authors: stajich jm. Hum Mol Genet. 1994 Aug;3(8):1423-4. doi: 10.1093/hmg/3.8.1423. Hum Mol Genet. 1994. PMID: 7987327 No abstract available.
55 results