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Human Genomics|October 27, 2022
DUSP5 and PHLDA1 mutations in mature cystic teratomas of the ovary identified on whole-exome sequencing may explain teratoma characteristicsWen-Chung Wang, Yen-Chein LaiHuman Genomics|November 6, 2015
Genomics is changing personal healthcare and medicine: the dawn of iPH (individualized preventive healthcare)Ruty Mehrian-Shai, Juergen K V ReichardtHuman Genomics|June 23, 2016
AMD and the alternative complement pathway: genetics and functional implicationsPerciliz L Tan, Catherine Bowes Rickman, Nicholas KatsanisHuman Genomics|November 19, 2014
Exome sequencing identifies novel and recurrent mutations in GJA8 and CRYGD associated with inherited cataractDonna S Mackay, Thomas M Bennett, Susan M Culican, et al.Human Genomics|August 20, 2015
Performance evaluation of indel calling tools using real short-read dataMohammad Shabbir Hasan, Xiaowei Wu, Liqing ZhangHuman Genomics|January 9, 2016
Whole exome sequencing identifies novel candidate genes that modify chronic obstructive pulmonary disease susceptibilityShannon Bruse, Michael Moreau, Yana Bromberg, et al.Human Genomics|February 5, 2016
A review of the new HGNC gene family resourceKristian A Gray, Ruth L Seal, Susan Tweedie, et al.Human Genomics|June 3, 2016
Systematic analysis of the molecular mechanism underlying atherosclerosis using a text mining approachDan Xi, Jinzhen Zhao, Wenyan Lai, et al.Human Genomics|July 28, 2016
Association of six CpG-SNPs in the inflammation-related genes with coronary heart diseaseXiaomin Chen, Xiaoying Chen, Yan Xu, et al.Human Genomics|July 22, 2015
Fine-scale population structure of Malays in Peninsular Malaysia and Singapore and implications for association studiesBoon-Peng Hoh, Lian Deng, Mat Jusoh Julia-Ashazila, et al.Pageof 112