Jeffrey G Reid
Overview
Explore the profile of Jeffrey G Reid including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
73
Citations
10353
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
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.
Rodriguez-Flores J, Khalid S, Parikshak N, Rasheed A, Ye B, Kapoor M, et al.
Nat Commun
. 2024 Sep;
15(1):8029.
PMID: 39271666
The genetic factors of stroke in South Asians are largely unexplored. Exome-wide sequencing and association analysis (ExWAS) in 75 K Pakistanis identified NM_000435.3(NOTCH3):c.3691 C > T, encoding the missense amino...
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.
Sun K, Bai X, Chen S, Bao S, Kapoor M, Zhang C, et al.
bioRxiv
. 2023 May;
PMID: 37214792
Coding variants that have significant impact on function can provide insights into the biology of a gene but are typically rare in the population. Identifying and ascertaining the frequency of...
9.
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.
10.
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...