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Human Molecular Genetics|July 5, 2013
MAP2K3 is associated with body mass index in American Indians and Caucasians and may mediate hypothalamic inflammationLi Bian, Michael Traurig, Robert L Hanson, et al.Human Molecular Genetics|July 12, 2013
Cigarette smoking induces small airway epithelial epigenetic changes with corresponding modulation of gene expressionLauren J Buro-Auriemma, Jacqueline Salit, Neil R Hackett, et al.Human Molecular Genetics|July 13, 2013
Mitochondrial DNA deletions in muscle satellite cells: implications for therapiesSally Spendiff, Mojgan Reza, Julie L Murphy, et al.Human Molecular Genetics|July 13, 2013
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosisMario Sabatelli, Alice Moncada, Amelia Conte, et al.Human Molecular Genetics|July 13, 2013
Molecular modeling indicates distinct classes of missense variants with mild and severe XLRS phenotypesYuri V Sergeev, Susan Vitale, Paul A Sieving, et al.Human Molecular Genetics|July 19, 2013
SCG10 promotes non-amyloidogenic processing of amyloid precursor protein by facilitating its trafficking to the cell surfaceJingjing Wang, Chunyan Shan, Wenyuan Cao, et al.Human Molecular Genetics|July 2, 2013
Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarraysGregory Costain, Anath C Lionel, Daniele Merico, et al.Human Molecular Genetics|July 2, 2013
Mutations in LYRM4, encoding iron-sulfur cluster biogenesis factor ISD11, cause deficiency of multiple respiratory chain complexesSze Chern Lim, Martin Friemel, Justine E Marum, et al.Human Molecular Genetics|December 6, 2012
Evidence of associations of APOBEC3B gene deletion with susceptibility to persistent HBV infection and hepatocellular carcinomaTongwen Zhang, Jianqiang Cai, Jiang Chang, et al.Human Molecular Genetics|December 11, 2012
Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and miceTyler F Beck, Danielle Veenma, Oleg A Shchelochkov, et al.Pageof 1,196