HUMAN MOLECULAR GENETICS

HUMAN MOLECULAR GENETICS Journal

publication venue for

De novo loss-of-function KCNMA1 variants are associated with a new multiple malformation syndrome and a broad spectrum of developmental and neurological phenotypes. 28:2937-2951. 2019
A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration.. 25:358-70. 2016
Trans-ethnic meta-analysis of white blood cell phenotypes.. 23:6944-60. 2014
Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network.. 22:2529-38. 2013
Functional and physical interaction between the mismatch repair and FA-BRCA pathways. 20:4395-4410. 2011

International Standard Serial Number (ISSN)

0964-6906

Electronic International Standard Serial Number (EISSN)

1460-2083