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

Year Number of Results
1998 40
1999 87
2000 182
2001 221
2002 154
2003 167
2004 261
2005 181
2006 188
2007 207
2008 237
2009 222
2010 278
2011 329
2012 330
2013 336
2014 324
2015 264
2016 239
2017 246
2018 292
2019 180
2020 9
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4,464 results
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Page 1
A homozygous missense mutation in SLC25A16 associated with autosomal recessive isolated fingernail dysplasia in a Pakistani family.
Khan S, Ansar M, Khan AK, Shah K, Muhammad N, Shahzad S, Nickerson DA, Bamshad MJ, Santos-Cortez RLP, Leal SM, Ahmad W. Khan S, et al. Br J Dermatol. 2018 Feb;178(2):556-558. doi: 10.1111/bjd.15661. Epub 2017 Dec 1. Br J Dermatol. 2018. PMID: 28504827 Free PMC article. No abstract available.
Genetics of Parkinson's disease.
Klein C, Westenberger A. Klein C, et al. Cold Spring Harb Perspect Med. 2012 Jan;2(1):a008888. doi: 10.1101/cshperspect.a008888. Cold Spring Harb Perspect Med. 2012. PMID: 22315721 Free PMC article. Review.
Missense CACNA1A mutation causing episodic ataxia type 2.
Denier C, Ducros A, Durr A, Eymard B, Chassande B, Tournier-Lasserve E. Denier C, et al. Arch Neurol. 2001 Feb;58(2):292-5. doi: 10.1001/archneur.58.2.292. Arch Neurol. 2001. PMID: 11176968
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