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

Year Number of Results
2001 1
2002 4
2003 8
2004 5
2005 14
2006 16
2007 15
2008 19
2009 9
2010 11
2011 3
2012 4
2013 1
2015 1
2018 1
2024 0

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100 results

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Page 1
The implications of ENCODE for diagnostics.
Fratkin E, Bercovici S, Stephan DA. Fratkin E, et al. Among authors: stephan da. Nat Biotechnol. 2012 Nov;30(11):1064-5. doi: 10.1038/nbt.2418. Nat Biotechnol. 2012. PMID: 23138302 No abstract available.
Why life science needs its own Silicon Valley.
Ghadar F, Sviokla J, Stephan DA. Ghadar F, et al. Among authors: stephan da. Harv Bus Rev. 2012 Jul-Aug;90(7-8):25-7. Harv Bus Rev. 2012. PMID: 22852449 No abstract available.
Genetic determinants of athletic performance.
Stephan DA. Stephan DA. Recent Pat DNA Gene Seq. 2012 Dec;6(3):175-9. doi: 10.2174/187221512802717376. Recent Pat DNA Gene Seq. 2012. PMID: 22827596
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study.
Majounie E, Renton AE, Mok K, Dopper EG, Waite A, Rollinson S, Chiò A, Restagno G, Nicolaou N, Simon-Sanchez J, van Swieten JC, Abramzon Y, Johnson JO, Sendtner M, Pamphlett R, Orrell RW, Mead S, Sidle KC, Houlden H, Rohrer JD, Morrison KE, Pall H, Talbot K, Ansorge O; Chromosome 9-ALS/FTD Consortium; French research network on FTLD/FTLD/ALS; ITALSGEN Consortium; Hernandez DG, Arepalli S, Sabatelli M, Mora G, Corbo M, Giannini F, Calvo A, Englund E, Borghero G, Floris GL, Remes AM, Laaksovirta H, McCluskey L, Trojanowski JQ, Van Deerlin VM, Schellenberg GD, Nalls MA, Drory VE, Lu CS, Yeh TH, Ishiura H, Takahashi Y, Tsuji S, Le Ber I, Brice A, Drepper C, Williams N, Kirby J, Shaw P, Hardy J, Tienari PJ, Heutink P, Morris HR, Pickering-Brown S, Traynor BJ. Majounie E, et al. Lancet Neurol. 2012 Apr;11(4):323-30. doi: 10.1016/S1474-4422(12)70043-1. Epub 2012 Mar 9. Lancet Neurol. 2012. PMID: 22406228 Free PMC article.
Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42.
Borck G, Ur Rehman A, Lee K, Pogoda HM, Kakar N, von Ameln S, Grillet N, Hildebrand MS, Ahmed ZM, Nürnberg G, Ansar M, Basit S, Javed Q, Morell RJ, Nasreen N, Shearer AE, Ahmad A, Kahrizi K, Shaikh RS, Ali RA, Khan SN, Goebel I, Meyer NC, Kimberling WJ, Webster JA, Stephan DA, Schiller MR, Bahlo M, Najmabadi H, Gillespie PG, Nürnberg P, Wollnik B, Riazuddin S, Smith RJ, Ahmad W, Müller U, Hammerschmidt M, Friedman TB, Riazuddin S, Leal SM, Ahmad J, Kubisch C. Borck G, et al. Among authors: stephan da. Am J Hum Genet. 2011 Feb 11;88(2):127-37. doi: 10.1016/j.ajhg.2010.12.011. Epub 2011 Jan 20. Am J Hum Genet. 2011. PMID: 21255762 Free PMC article.
Presymptomatic risk assessment for chronic non-communicable diseases.
Padhukasahasram B, Halperin E, Wessel J, Thomas DJ, Silver E, Trumbower H, Cargill M, Stephan DA. Padhukasahasram B, et al. Among authors: stephan da. PLoS One. 2010 Dec 31;5(12):e14338. doi: 10.1371/journal.pone.0014338. PLoS One. 2010. PMID: 21217814 Free PMC article.
100 results