Shona M Kerr
Overview
Explore the profile of Shona M Kerr 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
37
Citations
2521
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
11.
Devereux-Cooke A, Leary S, McGrath S, Northwood E, Redshaw A, Shepherd C, et al.
BMC Neurol
. 2022 Jul;
22(1):269.
PMID: 35854226
Background: Myalgic encephalomyelitis / chronic fatigue syndrome (ME/CFS) is a common, long-term condition characterised by post-exertional malaise, often with fatigue that is not significantly relieved by rest. ME/CFS has no...
12.
Winkler T, Rasheed H, Teumer A, Gorski M, Rowan B, Stanzick K, et al.
Commun Biol
. 2022 Jun;
5(1):580.
PMID: 35697829
Reduced glomerular filtration rate (GFR) can progress to kidney failure. Risk factors include genetics and diabetes mellitus (DM), but little is known about their interaction. We conducted genome-wide association meta-analyses...
13.
Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects
Howe L, Nivard M, Morris T, Hansen A, Rasheed H, Cho Y, et al.
Nat Genet
. 2022 May;
54(5):581-592.
PMID: 35534559
Estimates from genome-wide association studies (GWAS) of unrelated individuals capture effects of inherited variation (direct effects), demography (population stratification, assortative mating) and relatives (indirect genetic effects). Family-based GWAS designs can...
14.
He T, Mischak M, Clark A, Campbell R, Delles C, Diez J, et al.
Eur J Heart Fail
. 2021 Apr;
23(11):1875-1887.
PMID: 33881206
Aims: Heart failure (HF) is a major public health concern worldwide. The diversity of HF makes it challenging to decipher the underlying complex pathological processes using single biomarkers. We examined...
15.
Halachev M, Meynert A, Taylor M, Vitart V, Kerr S, Klaric L, et al.
PLoS Genet
. 2019 Nov;
15(11):e1008480.
PMID: 31765389
Human population isolates provide a snapshot of the impact of historical demographic processes on population genetics. Such data facilitate studies of the functional impact of rare sequence variants on biomedical...
16.
Tin A, Marten J, Kuhns V, Li Y, Wuttke M, Kirsten H, et al.
Nat Genet
. 2019 Oct;
51(10):1459-1474.
PMID: 31578528
Elevated serum urate levels cause gout and correlate with cardiometabolic diseases via poorly understood mechanisms. We performed a trans-ancestry genome-wide association study of serum urate in 457,690 individuals, identifying 183...
17.
Gilbert E, OReilly S, Merrigan M, McGettigan D, Vitart V, Joshi P, et al.
Proc Natl Acad Sci U S A
. 2019 Sep;
116(38):19064-19070.
PMID: 31481615
Britain and Ireland are known to show population genetic structure; however, large swathes of Scotland, in particular, have yet to be described. Delineating the structure and ancestry of these populations...
18.
Kerr S, Klaric L, Halachev M, Hayward C, Boutin T, Meynert A, et al.
Sci Rep
. 2019 Jul;
9(1):10964.
PMID: 31358886
The Viking Health Study Shetland is a population-based research cohort of 2,122 volunteer participants with ancestry from the Shetland Isles in northern Scotland. The high kinship and detailed phenotype data...
19.
Wuttke M, Li Y, Li M, Sieber K, Feitosa M, Gorski M, et al.
Nat Genet
. 2019 Jun;
51(6):957-972.
PMID: 31152163
Chronic kidney disease (CKD) is responsible for a public health burden with multi-systemic complications. Through trans-ancestry meta-analysis of genome-wide association studies of estimated glomerular filtration rate (eGFR) and independent replication...
20.
Thormann A, Halachev M, McLaren W, Moore D, Svinti V, Campbell A, et al.
Nat Commun
. 2019 Jun;
10(1):2373.
PMID: 31147538
We aimed to develop an efficient, flexible and scalable approach to diagnostic genome-wide sequence analysis of genetically heterogeneous clinical presentations. Here we present G2P ( www.ebi.ac.uk/gene2phenotype ) as an online...