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HUMAN MOLECULAR GENETICS
Journal
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Overview
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
Research
category
BIOCHEMISTRY & MOLECULAR BIOLOGY
Web of Science Category
GENETICS & HEREDITY
Web of Science Category
Identity
International Standard Serial Number (ISSN)
0964-6906
Electronic International Standard Serial Number (EISSN)
1460-2083
Other
journal abbreviation
HUM MOL GENET