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Page 1
Population distribution and ancestry of the cancer protective MDM2 SNP285 (rs117039649).
Knappskog S, Gansmo LB, Dibirova K, Metspalu A, Cybulski C, Peterlongo P, Aaltonen L, Vatten L, Romundstad P, Hveem K, Devilee P, Evans GD, Lin D, Van Camp G, Manolopoulos VG, Osorio A, Milani L, Ozcelik T, Zalloua P, Mouzaya F, Bliznetz E, Balanovska E, Pocheshkova E, Kučinskas V, Atramentova L, Nymadawa P, Titov K, Lavryashina M, Yusupov Y, Bogdanova N, Koshel S, Zamora J, Wedge DC, Charlesworth D, Dörk T, Balanovsky O, Lønning PE. Knappskog S, et al. Among authors: van camp g. Oncotarget. 2014 Sep 30;5(18):8223-34. doi: 10.18632/oncotarget.1910. Oncotarget. 2014. PMID: 25327560 Free PMC article.
Large-scale copy number analysis reveals variations in genes not previously associated with malignant pleural mesothelioma.
Hylebos M, Van Camp G, Vandeweyer G, Fransen E, Beyens M, Cornelissen R, Suls A, Pauwels P, van Meerbeeck JP, Op de Beeck K. Hylebos M, et al. Among authors: van meerbeeck jp, van camp g. Oncotarget. 2017 Dec 1;8(69):113673-113686. doi: 10.18632/oncotarget.22817. eCollection 2017 Dec 26. Oncotarget. 2017. PMID: 29371938 Free PMC article.
Genome-wide SNP analysis reveals no gain in power for association studies of common variants in the Finnish Saami.
Huyghe JR, Fransen E, Hannula S, Van Laer L, Van Eyken E, Mäki-Torkko E, Lysholm-Bernacchi A, Aikio P, Stephan DA, Sorri M, Huentelman MJ, Van Camp G. Huyghe JR, et al. Among authors: van eyken e, van laer l, van camp g. Eur J Hum Genet. 2010 May;18(5):569-74. doi: 10.1038/ejhg.2009.210. Epub 2009 Nov 25. Eur J Hum Genet. 2010. PMID: 19935831 Free PMC article.
DFNA5 promoter methylation a marker for breast tumorigenesis.
Croes L, de Beeck KO, Pauwels P, Vanden Berghe W, Peeters M, Fransen E, Van Camp G. Croes L, et al. Among authors: van camp g. Oncotarget. 2017 May 9;8(19):31948-31958. doi: 10.18632/oncotarget.16654. Oncotarget. 2017. PMID: 28404884 Free PMC article.
Association between variations in CAT and noise-induced hearing loss in two independent noise-exposed populations.
Konings A, Van Laer L, Pawelczyk M, Carlsson PI, Bondeson ML, Rajkowska E, Dudarewicz A, Vandevelde A, Fransen E, Huyghe J, Borg E, Sliwinska-Kowalska M, Van Camp G. Konings A, et al. Among authors: van laer l, van camp g. Hum Mol Genet. 2007 Aug 1;16(15):1872-83. doi: 10.1093/hmg/ddm135. Epub 2007 Jun 13. Hum Mol Genet. 2007. PMID: 17567781
Inherited mitochondrial variants are not a major cause of age-related hearing impairment in the European population.
Bonneux S, Fransen E, Van Eyken E, Van Laer L, Huyghe J, Van de Heyning P, Voets A, Gerards M, Stassen AP, Hendrickx AT, Smeets HJ, Van Camp G. Bonneux S, et al. Among authors: van eyken e, van laer l, van de heyning p, van camp g. Mitochondrion. 2011 Sep;11(5):729-34. doi: 10.1016/j.mito.2011.05.008. Epub 2011 May 30. Mitochondrion. 2011. PMID: 21645648
The coding polymorphism T263I in TGF-beta1 is associated with otosclerosis in two independent populations.
Thys M, Schrauwen I, Vanderstraeten K, Janssens K, Dieltjens N, Van Den Bogaert K, Fransen E, Chen W, Ealy M, Claustres M, Cremers CR, Dhooge I, Declau F, Claes J, Van de Heyning P, Vincent R, Somers T, Offeciers E, Smith RJ, Van Camp G. Thys M, et al. Among authors: van den bogaert k, van de heyning p, van camp g. Hum Mol Genet. 2007 Sep 1;16(17):2021-30. doi: 10.1093/hmg/ddm150. Epub 2007 Jun 22. Hum Mol Genet. 2007. PMID: 17588962
The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment.
Van Laer L, Van Eyken E, Fransen E, Huyghe JR, Topsakal V, Hendrickx JJ, Hannula S, Mäki-Torkko E, Jensen M, Demeester K, Baur M, Bonaconsa A, Mazzoli M, Espeso A, Verbruggen K, Huyghe J, Huygen P, Kunst S, Manninen M, Konings A, Diaz-Lacava AN, Steffens M, Wienker TF, Pyykkö I, Cremers CW, Kremer H, Dhooge I, Stephens D, Orzan E, Pfister M, Bille M, Parving A, Sorri M, Van de Heyning PH, Van Camp G. Van Laer L, et al. Among authors: van de heyning ph, van eyken e, van camp g. Hum Mol Genet. 2008 Jan 15;17(2):159-69. doi: 10.1093/hmg/ddm292. Epub 2007 Oct 6. Hum Mol Genet. 2008. PMID: 17921507
545 results