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

Year Number of Results
2001 1
2002 2
2003 3
2004 4
2005 5
2006 6
2007 5
2008 3
2009 7
2010 4
2011 3
2012 6
2013 5
2014 8
2015 16
2016 10
2017 4
2018 5
2019 3
2020 2
2021 1
2022 5
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94 results
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Page 1
Diagnostic Yield and Novel Candidate Genes by Exome Sequencing in 152 Consanguineous Families With Neurodevelopmental Disorders.
Reuter MS, Tawamie H, Buchert R, Hosny Gebril O, Froukh T, Thiel C, Uebe S, Ekici AB, Krumbiegel M, Zweier C, Hoyer J, Eberlein K, Bauer J, Scheller U, Strom TM, Hoffjan S, Abdelraouf ER, Meguid NA, Abboud A, Al Khateeb MA, Fakher M, Hamdan S, Ismael A, Muhammad S, Abdallah E, Sticht H, Wieczorek D, Reis A, Abou Jamra R. Reuter MS, et al. Among authors: hoffjan s. JAMA Psychiatry. 2017 Mar 1;74(3):293-299. doi: 10.1001/jamapsychiatry.2016.3798. JAMA Psychiatry. 2017. PMID: 28097321
Trying to understand the genetics of atopic dermatitis.
Stemmler S, Hoffjan S. Stemmler S, et al. Among authors: hoffjan s. Mol Cell Probes. 2016 Dec;30(6):374-385. doi: 10.1016/j.mcp.2016.10.004. Epub 2016 Oct 8. Mol Cell Probes. 2016. PMID: 27725295 Review.
SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile.
Al-Jawahiri R, Foroutan A, Kerkhof J, McConkey H, Levy M, Haghshenas S, Rooney K, Turner J, Shears D, Holder M, Lefroy H, Castle B, Reis LM, Semina EV; University of Washington Centre for Mendelian Genomics (UW-CMG), Lachlan K, Chandler K, Wright T, Clayton-Smith J, Hug FP, Pitteloud N, Bartoloni L, Hoffjan S, Park SM, Thankamony A, Lees M, Wakeling E, Naik S, Hanker B, Girisha KM, Agolini E, Giuseppe Z, Alban Z, Tessarech M, Keren B, Afenjar A, Zweier C, Reis A, Smol T, Tsurusaki Y, Nobuhiko O, Sekiguchi F, Tsuchida N, Matsumoto N, Kou I, Yonezawa Y, Ikegawa S, Callewaert B, Freeth M; Genomics England Research Consortium, Kleinendorst L, Donaldson A, Alders M, De Paepe A, Sadikovic B, McNeill A. Al-Jawahiri R, et al. Among authors: hoffjan s. Genet Med. 2022 Jun;24(6):1261-1273. doi: 10.1016/j.gim.2022.02.013. Epub 2022 Mar 24. Genet Med. 2022. PMID: 35341651 Free article.
[The genetics of chronic obstructive pulmonary disease].
Arinir U, Hoffjan S, Knoop H, Schultze-Werninghaus G, Epplen JT, Rohde G. Arinir U, et al. Among authors: hoffjan s. Pneumologie. 2009 Jan;63(1):41-8. doi: 10.1055/s-0028-1100824. Epub 2009 Jan 9. Pneumologie. 2009. PMID: 19137504 Free article. Review. German.
The genetics of multiple sclerosis: an update 2010.
Hoffjan S, Akkad DA. Hoffjan S, et al. Mol Cell Probes. 2010 Oct;24(5):237-43. doi: 10.1016/j.mcp.2010.04.006. Epub 2010 May 5. Mol Cell Probes. 2010. PMID: 20450971 Review.
94 results