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Page 1
TLR4 polymorphisms, infectious diseases, and evolutionary pressure during migration of modern humans.
Ferwerda B, McCall MB, Alonso S, Giamarellos-Bourboulis EJ, Mouktaroudi M, Izagirre N, Syafruddin D, Kibiki G, Cristea T, Hijmans A, Hamann L, Israel S, ElGhazali G, Troye-Blomberg M, Kumpf O, Maiga B, Dolo A, Doumbo O, Hermsen CC, Stalenhoef AF, van Crevel R, Brunner HG, Oh DY, Schumann RR, de la Rúa C, Sauerwein R, Kullberg BJ, van der Ven AJ, van der Meer JW, Netea MG. Ferwerda B, et al. Among authors: brunner hg. Proc Natl Acad Sci U S A. 2007 Oct 16;104(42):16645-50. doi: 10.1073/pnas.0704828104. Epub 2007 Oct 9. Proc Natl Acad Sci U S A. 2007. PMID: 17925445 Free PMC article.
Presence of Genetic Variants Among Young Men With Severe COVID-19.
van der Made CI, Simons A, Schuurs-Hoeijmakers J, van den Heuvel G, Mantere T, Kersten S, van Deuren RC, Steehouwer M, van Reijmersdal SV, Jaeger M, Hofste T, Astuti G, Corominas Galbany J, van der Schoot V, van der Hoeven H, Hagmolen Of Ten Have W, Klijn E, van den Meer C, Fiddelaers J, de Mast Q, Bleeker-Rovers CP, Joosten LAB, Yntema HG, Gilissen C, Nelen M, van der Meer JWM, Brunner HG, Netea MG, van de Veerdonk FL, Hoischen A. van der Made CI, et al. Among authors: brunner hg. JAMA. 2020 Aug 18;324(7):663-673. doi: 10.1001/jama.2020.13719. JAMA. 2020. PMID: 32706371 Free PMC article.
The modular nature of genetic diseases.
Oti M, Brunner HG. Oti M, et al. Among authors: brunner hg. Clin Genet. 2007 Jan;71(1):1-11. doi: 10.1111/j.1399-0004.2006.00708.x. Clin Genet. 2007. PMID: 17204041 Review.
Molecular genetics of X-linked hearing impairment.
Brunner HG, Smeets B, Smeets D, Nelen M, Cremers CW, Ropers HH. Brunner HG, et al. Ann N Y Acad Sci. 1991;630:176-90. doi: 10.1111/j.1749-6632.1991.tb19586.x. Ann N Y Acad Sci. 1991. PMID: 1683204 Review. No abstract available.
Phenome connections.
Oti M, Huynen MA, Brunner HG. Oti M, et al. Among authors: brunner hg. Trends Genet. 2008 Mar;24(3):103-6. doi: 10.1016/j.tig.2007.12.005. Epub 2008 Feb 19. Trends Genet. 2008. PMID: 18243400
A de novo paradigm for mental retardation.
Vissers LE, de Ligt J, Gilissen C, Janssen I, Steehouwer M, de Vries P, van Lier B, Arts P, Wieskamp N, del Rosario M, van Bon BW, Hoischen A, de Vries BB, Brunner HG, Veltman JA. Vissers LE, et al. Among authors: brunner hg. Nat Genet. 2010 Dec;42(12):1109-12. doi: 10.1038/ng.712. Epub 2010 Nov 14. Nat Genet. 2010. PMID: 21076407
Unlocking Mendelian disease using exome sequencing.
Gilissen C, Hoischen A, Brunner HG, Veltman JA. Gilissen C, et al. Among authors: brunner hg. Genome Biol. 2011 Sep 14;12(9):228. doi: 10.1186/gb-2011-12-9-228. Genome Biol. 2011. PMID: 21920049 Free PMC article. Review.
499 results