John D Overton
Overview
Explore the profile of John D Overton including associated specialties, affiliations and a list of published articles.
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69
Citations
7122
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Recent Articles
1.
Kessler M, Damask A, OKeeffe S, Banerjee N, Li D, Watanabe K, et al.
Nature
. 2025 Jan;
637(8047):E27.
PMID: 39779868
No abstract available.
2.
Sun K, Bai X, Chen S, Bao S, Zhang C, Kapoor M, et al.
Nature
. 2025 Jan;
637(8047):E26.
PMID: 39779867
No abstract available.
3.
Gaynor S, Joseph T, Bai X, Zou Y, Boutkov B, Maxwell E, et al.
Nat Genet
. 2024 Sep;
56(11):2345-2351.
PMID: 39322778
Whole-genome sequencing (WGS), whole-exome sequencing (WES) and array genotyping with imputation (IMP) are common strategies for assessing genetic variation and its association with medically relevant phenotypes. To date, there has...
4.
Deficiency of Peptidylglycine-alpha-amidating Monooxygenase, a Cause of Sarcopenic Diabetes Mellitus
Giontella A, Akerlund M, Bronton K, Fava C, Lotta L, Baras A, et al.
J Clin Endocrinol Metab
. 2024 Aug;
110(3):820-829.
PMID: 39137152
Context: Peptidylglycine-α-amidating monooxygenase (PAM) is a critical enzyme in the endocrine system responsible for activation, by amidation, of bioactive peptides. Objective: To define the clinical phenotype of carriers of genetic...
5.
Kosmicki J, Marcketta A, Sharma D, Di Gioia S, Batista S, Yang X, et al.
Nat Genet
. 2024 Aug;
56(8):1592-1596.
PMID: 39103650
Coronavirus disease 2019 (COVID-19) and influenza are respiratory illnesses caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and influenza viruses, respectively. Both diseases share symptoms and clinical risk...
6.
Sun K, Bai X, Chen S, Bao S, Zhang C, Kapoor M, et al.
Nature
. 2024 May;
631(8021):583-592.
PMID: 38768635
Rare coding variants that substantially affect function provide insights into the biology of a gene. However, ascertaining the frequency of such variants requires large sample sizes. Here we present a...
7.
Zhou S, Sosina O, Bovijn J, Laurent L, Sharma V, Akbari P, et al.
Nat Genet
. 2023 Aug;
55(8):1277-1287.
PMID: 37558884
In this study, we leveraged the combined evidence of rare coding variants and common alleles to identify therapeutic targets for osteoporosis. We undertook a large-scale multiancestry exome-wide association study for...
8.
Kessler M, Damask A, OKeeffe S, Banerjee N, Li D, Watanabe K, et al.
Nature
. 2023 Feb;
615(7950):E3.
PMID: 36807635
No abstract available.
9.
Kessler M, Damask A, OKeeffe S, Banerjee N, Li D, Watanabe K, et al.
Nature
. 2022 Nov;
612(7939):301-309.
PMID: 36450978
Clonal haematopoiesis involves the expansion of certain blood cell lineages and has been associated with ageing and adverse health outcomes. Here we use exome sequence data on 628,388 individuals to...
10.
Akbari P, Sosina O, Bovijn J, Landheer K, Nielsen J, Kim M, et al.
Nat Commun
. 2022 Aug;
13(1):4844.
PMID: 35999217
Body fat distribution is a major, heritable risk factor for cardiometabolic disease, independent of overall adiposity. Using exome-sequencing in 618,375 individuals (including 160,058 non-Europeans) from the UK, Sweden and Mexico,...