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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2000 | 1 |
2007 | 1 |
2010 | 1 |
2011 | 1 |
2012 | 2 |
2013 | 1 |
2015 | 1 |
2024 | 0 |
PubMed for id: 1890272232
7 results
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Page 1
Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes.
Hum Genet. 2015 Oct;134(10):1055-68. doi: 10.1007/s00439-015-1585-y. Epub 2015 Jul 24.
Hum Genet. 2015.
PMID: 26204995
Free PMC article.
Polymorphisms in seizure 6-like gene are associated with bipolar disorder I: evidence of gene × gender interaction.
Xu C, Mullersman JE, Wang L, Bin Su B, Mao C, Posada Y, Camarillo C, Mao Y, Escamilla MA, Wang KS.
Xu C, et al.
J Affect Disord. 2013 Feb 15;145(1):95-9. doi: 10.1016/j.jad.2012.07.017. Epub 2012 Aug 22.
J Affect Disord. 2013.
PMID: 22920719
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Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.
Wilk JB, Shrine NR, Loehr LR, Zhao JH, Manichaikul A, Lopez LM, Smith AV, Heckbert SR, Smolonska J, Tang W, Loth DW, Curjuric I, Hui J, Cho MH, Latourelle JC, Henry AP, Aldrich M, Bakke P, Beaty TH, Bentley AR, Borecki IB, Brusselle GG, Burkart KM, Chen TH, Couper D, Crapo JD, Davies G, Dupuis J, Franceschini N, Gulsvik A, Hancock DB, Harris TB, Hofman A, Imboden M, James AL, Khaw KT, Lahousse L, Launer LJ, Litonjua A, Liu Y, Lohman KK, Lomas DA, Lumley T, Marciante KD, McArdle WL, Meibohm B, Morrison AC, Musk AW, Myers RH, North KE, Postma DS, Psaty BM, Rich SS, Rivadeneira F, Rochat T, Rotter JI, Soler Artigas M, Starr JM, Uitterlinden AG, Wareham NJ, Wijmenga C, Zanen P, Province MA, Silverman EK, Deary IJ, Palmer LJ, Cassano PA, Gudnason V, Barr RG, Loos RJ, Strachan DP, London SJ, Boezen HM, Probst-Hensch N, Gharib SA, Hall IP, O'Connor GT, Tobin MD, Stricker BH.
Wilk JB, et al.
Am J Respir Crit Care Med. 2012 Oct 1;186(7):622-32. doi: 10.1164/rccm.201202-0366OC. Epub 2012 Jul 26.
Am J Respir Crit Care Med. 2012.
PMID: 22837378
Free PMC article.
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Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study.
Irvin MR, Wineinger NE, Rice TK, Pajewski NM, Kabagambe EK, Gu CC, Pankow J, North KE, Wilk JB, Freedman BI, Franceschini N, Broeckel U, Tiwari HK, Arnett DK.
Irvin MR, et al.
PLoS One. 2011;6(8):e24052. doi: 10.1371/journal.pone.0024052. Epub 2011 Aug 25.
PLoS One. 2011.
PMID: 21901158
Free PMC article.
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Incorporation of a genetic factor into an epidemiologic model for prediction of individual risk of lung cancer: the Liverpool Lung Project.
Raji OY, Agbaje OF, Duffy SW, Cassidy A, Field JK.
Raji OY, et al.
Cancer Prev Res (Phila). 2010 May;3(5):664-9. doi: 10.1158/1940-6207.CAPR-09-0141. Epub 2010 Apr 27.
Cancer Prev Res (Phila). 2010.
PMID: 20424129
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Seizure 6-like (SEZ6L) gene and risk for lung cancer.
Gorlov IP, Meyer P, Liloglou T, Myles J, Boettger MB, Cassidy A, Girard L, Minna JD, Fischer R, Duffy S, Spitz MR, Haeussinger K, Kammerer S, Cantor C, Dierkesmann R, Field JK, Amos CI.
Gorlov IP, et al.
Cancer Res. 2007 Sep 1;67(17):8406-11. doi: 10.1158/0008-5472.CAN-06-4784.
Cancer Res. 2007.
PMID: 17804757
Free article.
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Identification of a 428-kb homozygously deleted region disrupting the SEZ6L gene at 22q12.1 in a lung cancer cell line.
Nishioka M, Kohno T, Takahashi M, Niki T, Yamada T, Sone S, Yokota J.
Nishioka M, et al.
Oncogene. 2000 Dec 14;19(54):6251-60. doi: 10.1038/sj.onc.1204031.
Oncogene. 2000.
PMID: 11175339
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