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Human Genetics|October 19, 2011
Recombination networks as genetic markers in a human variation study of the Old WorldAsif Javed, Marta Melé, Marc Pybus, et al.Human Genetics|October 19, 2011
Integrating pathway analysis and genetics of gene expression for genome-wide association study of basal cell carcinomaMingfeng Zhang, Liming Liang, Nilesh Morar, et al.Human Genetics|November 9, 2011
A global view of the OCA2-HERC2 region and pigmentationMichael P Donnelly, Peristera Paschou, Elena Grigorenko, et al.Human Genetics|November 9, 2011
A novel locus for autosomal dominant congenital motor nystagmus mapped to 1q31-q32.2 between D1S2816 and D1S2692Xueshan Xiao, Shiqiang Li, Xiangming Guo, et al.Human Genetics|October 18, 2011
Increased prevalence of seizures in boys who were probands with the FMR1 premutation and co-morbid autism spectrum disorderWeerasak Chonchaiya, Jacky Au, Andrea Schneider, et al.Human Genetics|December 23, 2011
Utility of genetically modified mice for understanding the neurobiology of substance use disordersChristie D Fowler, Paul J KennyHuman Genetics|May 26, 2009
Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiencyMaria C Pintao, A A Garcia, D Borgel, et al.Human Genetics|June 11, 2009
Megakaryoblastic leukemia factor-1 gene in the susceptibility to coronary artery diseaseKunihiko Hinohara, Toshiaki Nakajima, Michio Yasunami, et al.Human Genetics|February 25, 2009
The genomic basis of cerebral palsy: a HuGE systematic literature reviewM E O'Callaghan, A H MacLennan, E A Haan, et al.Pageof 959