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233 results

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Page 1
Linkage and association analysis of CACNG3 in childhood absence epilepsy.
Everett KV, Chioza B, Aicardi J, Aschauer H, Brouwer O, Callenbach P, Covanis A, Dulac O, Eeg-Olofsson O, Feucht M, Friis M, Goutieres F, Guerrini R, Heils A, Kjeldsen M, Lehesjoki AE, Makoff A, Nabbout R, Olsson I, Sander T, Sirén A, McKeigue P, Robinson R, Taske N, Rees M, Gardiner M. Everett KV, et al. Among authors: mckeigue p. Eur J Hum Genet. 2007 Apr;15(4):463-72. doi: 10.1038/sj.ejhg.5201783. Epub 2007 Jan 31. Eur J Hum Genet. 2007. PMID: 17264864 Free PMC article.
Linkage and mutational analysis of CLCN2 in childhood absence epilepsy.
Everett K, Chioza B, Aicardi J, Aschauer H, Brouwer O, Callenbach P, Covanis A, Dooley J, Dulac O, Durner M, Eeg-Olofsson O, Feucht M, Friis M, Guerrini R, Heils A, Kjeldsen M, Nabbout R, Sander T, Wirrell E, McKeigue P, Robinson R, Taske N, Gardiner M. Everett K, et al. Among authors: mckeigue p. Epilepsy Res. 2007 Jul;75(2-3):145-53. doi: 10.1016/j.eplepsyres.2007.05.004. Epub 2007 Jun 18. Epilepsy Res. 2007. PMID: 17580110 Free article.
Genome-wide high-density SNP-based linkage analysis of infantile hypertrophic pyloric stenosis identifies loci on chromosomes 11q14-q22 and Xq23.
Everett KV, Chioza BA, Georgoula C, Reece A, Capon F, Parker KA, Cord-Udy C, McKeigue P, Mitton S, Pierro A, Puri P, Mitchison HM, Chung EM, Gardiner RM. Everett KV, et al. Among authors: mckeigue p. Am J Hum Genet. 2008 Mar;82(3):756-62. doi: 10.1016/j.ajhg.2007.12.023. Epub 2008 Feb 28. Am J Hum Genet. 2008. PMID: 18308288 Free PMC article.
Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14.
Chioza BA, Aicardi J, Aschauer H, Brouwer O, Callenbach P, Covanis A, Dooley JM, Dulac O, Durner M, Eeg-Olofsson O, Feucht M, Friis ML, Guerrini R, Kjeldsen MJ, Nabbout R, Nashef L, Sander T, Sirén A, Wirrell E, McKeigue P, Robinson R, Gardiner RM, Everett KV. Chioza BA, et al. Among authors: mckeigue p. Epilepsy Res. 2009 Dec;87(2-3):247-55. doi: 10.1016/j.eplepsyres.2009.09.010. Epub 2009 Oct 17. Epilepsy Res. 2009. PMID: 19837565 Free PMC article.
Abundant pleiotropy in human complex diseases and traits.
Sivakumaran S, Agakov F, Theodoratou E, Prendergast JG, Zgaga L, Manolio T, Rudan I, McKeigue P, Wilson JF, Campbell H. Sivakumaran S, et al. Among authors: mckeigue p. Am J Hum Genet. 2011 Nov 11;89(5):607-18. doi: 10.1016/j.ajhg.2011.10.004. Am J Hum Genet. 2011. PMID: 22077970 Free PMC article. Review.
Inference of identity by descent in population isolates and optimal sequencing studies.
Glodzik D, Navarro P, Vitart V, Hayward C, McQuillan R, Wild SH, Dunlop MG, Rudan I, Campbell H, Haley C, Wright AF, Wilson JF, McKeigue P. Glodzik D, et al. Among authors: mckeigue p. Eur J Hum Genet. 2013 Oct;21(10):1140-5. doi: 10.1038/ejhg.2012.307. Epub 2013 Jan 30. Eur J Hum Genet. 2013. PMID: 23361219 Free PMC article.
Malaria susceptibility and CD36 mutation.
Aitman TJ, Cooper LD, Norsworthy PJ, Wahid FN, Gray JK, Curtis BR, McKeigue PM, Kwiatkowski D, Greenwood BM, Snow RW, Hill AV, Scott J. Aitman TJ, et al. Among authors: mckeigue pm. Nature. 2000 Jun 29;405(6790):1015-6. doi: 10.1038/35016636. Nature. 2000. PMID: 10890433 No abstract available.
233 results