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Science Advances|April 6, 2022
Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potentialTetsushi Nakao, Alexander G Bick, Margaret A Taub, et al.
Nature Cardiovascular Research|May 31, 2024
Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcificationPaul S de Vries, Matthew P Conomos, Kuldeep Singh, et al.
Blood|September 3, 2024
Whole-genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver rolesJennifer E Huffman, Jayna Nicholas, Julie Hahn, et al.
JAMA Psychiatry|October 31, 2019
Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition, Dennis van der Meer, Ida E Sønderby, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2023
Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver rolesJennifer E Huffman, Jayna Nicolas, Julie Hahn, et al.
Nature|October 15, 2020
Inherited causes of clonal haematopoiesis in 97,691 whole genomesAlexander G Bick, Joshua S Weinstock, Satish K Nandakumar, et al.
Molecular Psychiatry|October 5, 2018
Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal gangliaIda E Sønderby, Ómar Gústafsson, Nhat Trung Doan, et al.
Molecular Psychiatry|February 2, 2019
Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal gangliaIda E Sønderby, Ómar Gústafsson, Nhat Trung Doan, et al.
Cell Genomics|May 9, 2022
Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMedMargaret A Taub, Matthew P Conomos, Rebecca Keener, et al.
Translational Psychiatry|March 23, 2021
1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humansIda E Sønderby, Dennis van der Meer, Clara Moreau, et al.
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