Nature Genetics
Journal Abbreviation: NAT GENET
ISSN: 1061-4036
eISSN: 1546-1718
Publisher: Nature Publishing Group
Publications (57)
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder (2019)
Demontis D, Walters RK, Martin J, Mattheisen M, Als TD, Agerbo E, Baldursson G, et al.
Journal article
Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (Nature Genetics, (2019), 51, 3, (414-430), 10.1038/s41588-019-0358-2) (2019)
Kunkle BW, Grenier-Boley B, Sims R, Bis JC, Damotte V, Naj AC, Boland A, et al.
Journal article, Erratum
Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (Nature Genetics, (2019), 51, 4, (659-674), 10.1038/s41588-019-0364-4) (2019)
Huckins LM, Dobbyn A, Hoffman G, Wang W, Pardiñas AF, T. Nguyen H, Girdhar K, et al.
Journal article, Erratum
A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer (2018)
Wu L, Shi W, Long J, Guo X, Michailidou K, Beesley J, Bolla MK, et al.
Journal article
De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation (2018)
Basilicata MF, Bruel AL, Semplicio G, Valsecchi CIK, Aktas T, Duffourd Y, Rumpf T, et al.
Journal article
UTX-mediated enhancer and chromatin remodeling suppresses myeloid leukemogenesis through noncatalytic inverse regulation of ETS and GATA programs (2018)
Gozdecka M, Meduri E, Mazan M, Tzelepis K, Dudek M, Knights AJ, Pardo M, et al.
Journal article
Mutations in KEOPS-complex genes cause nephritic syndrome with primary microcephaly (2017)
Braun DA, Rao J, Mollet G, Schapiro D, Daugeron MC, Tan W, Gribouval O, et al.
Journal article
Chromatin-remodeling factor SMARCD2 regulates transcriptional networks controlling differentiation of neutrophil granulocytes (2017)
Witzel M, Petersheim D, Fan Y, Bahrami E, Racek T, Rohlfs M, Puchalka J, et al.
Journal article
Titin-truncating variants affect heart function in disease cohorts and the general population (2017)
Schafer S, De Marvao A, Adami E, Fiedler LR, Ng B, Khin E, Rackham OJL, et al.
Journal article
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk (2017)
Day FR, Thompson DJ, Helgason H, Chasman DI, Finucane H, Sulem P, Ruth KS, et al.
Journal article