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European Journal of Human Genetics : EJHG|December 24, 2010
A candidate gene study of the type I interferon pathway implicates IKBKE and IL8 as risk loci for SLEJohanna K Sandling, Sophie Garnier, Snaevar Sigurdsson, et al.
European Journal of Human Genetics : EJHG|January 6, 2011
Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sampleAndrew McQuillin, Nicholas Bass, Adebayo Anjorin, et al.
European Journal of Human Genetics : EJHG|October 7, 2010
Gene-based interaction analysis by incorporating external linkage disequilibrium informationJing He, Kai Wang, Andrew C Edmondson, et al.
European Journal of Human Genetics : EJHG|February 24, 2011
Identification of ACOX2 as a shared genetic risk factor for preeclampsia and cardiovascular diseaseAsa Johansson, Joanne E Curran, Matthew P Johnson, et al.
European Journal of Human Genetics : EJHG|March 3, 2011
Intellectual disability without epilepsy associated with STXBP1 disruptionFadi F Hamdan, Julie Gauthier, Sylvia Dobrzeniecka, et al.
European Journal of Human Genetics : EJHG|November 18, 2010
Discriminative accuracy of genomic profiling comparing multiplicative and additive risk modelsRamal Moonesinghe, Muin J Khoury, Tiebin Liu, et al.
European Journal of Human Genetics : EJHG|November 25, 2010
Family-based association study of ITGB3 in autism spectrum disorder and its endophenotypesValerio Napolioni, Federica Lombardi, Roberto Sacco, et al.
European Journal of Human Genetics : EJHG|November 25, 2010
A large homozygous deletion in the SAMHD1 gene causes atypical Aicardi-Goutiéres syndrome associated with mtDNA deletionsEsther Leshinsky-Silver, Gustavo Malinger, Liat Ben-Sira, et al.
European Journal of Human Genetics : EJHG|November 25, 2010
Experiences with array-based sequence capture; toward clinical applicationsRowida Almomani, Jaap van der Heijden, Yavuz Ariyurek, et al.
European Journal of Human Genetics : EJHG|January 13, 2011
Dutch myotonic dystrophy type 2 patients and a North-African DM2 family carry the common European founder haplotypeMarieke J H Coenen, Alide A Tieleman, Mascha M V A P Schijvenaars, et al.
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