Kerstin U Ludwig
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Explore the profile of Kerstin U Ludwig including associated specialties, affiliations and a list of published articles.
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2648
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Recent Articles
11.
Schmidt A, Roner S, Mai K, Klinkhammer H, Kircher M, Ludwig K
Bioinformatics
. 2023 Apr;
39(5).
PMID: 37084271
Motivation: Missense variants are a frequent class of variation within the coding genome, and some of them cause Mendelian diseases. Despite advances in computational prediction, classifying missense variants into pathogenic...
12.
Kircher M, Ludwig K
Med Genet
. 2023 Apr;
34(4):275-286.
PMID: 37034418
Identification of genetic variation in individual genomes is now a routine procedure in human genetic research and diagnostics. For many variants, however, insufficient evidence is available to establish a pathogenic...
13.
Zieger H, Weinhold L, Schmidt A, Holtgrewe M, Juranek S, Siewert A, et al.
HGG Adv
. 2023 Jan;
4(1):100166.
PMID: 36589413
Non-syndromic cleft lip with/without cleft palate (nsCL/P) is a highly heritable facial disorder. To date, systematic investigations of the contribution of rare variants in non-coding regions to nsCL/P etiology are...
14.
Ishorst N, Henschel L, Thieme F, Drichel D, Sivalingam S, Mehrem S, et al.
Mol Genet Genomic Med
. 2022 Dec;
11(3):e2109.
PMID: 36468602
Background: Nonsyndromic cleft lip with/without cleft palate (nsCL/P) is a congenital malformation of multifactorial etiology. Research has identified >40 genome-wide significant risk loci, which explain less than 40% of nsCL/P...
15.
Mingardo E, Beaman G, Grote P, Nordenskjold A, Newman W, Woolf A, et al.
Commun Biol
. 2022 Nov;
5(1):1203.
PMID: 36352089
Classic bladder exstrophy represents the most severe end of all human congenital anomalies of the kidney and urinary tract and is associated with bladder cancer susceptibility. Previous genetic studies identified...
16.
Butler-Laporte G, Povysil G, Kosmicki J, Cirulli E, Drivas T, Furini S, et al.
PLoS Genet
. 2022 Nov;
18(11):e1010367.
PMID: 36327219
Host genetics is a key determinant of COVID-19 outcomes. Previously, the COVID-19 Host Genetics Initiative genome-wide association study used common variants to identify multiple loci associated with COVID-19 outcomes. However,...
17.
Mathey C, Maj C, Scheer A, Fazaal J, Wedi B, Wieczorek D, et al.
Front Genet
. 2022 Aug;
13:914376.
PMID: 35923707
Angioedema is a relatively rare but potentially life-threatening adverse reaction to angiotensin-converting enzyme inhibitors (ACEi) and angiotensin receptor blockers (ARBs). As with hereditary forms of angioedema (HAE), this adverse reaction...
18.
Ludwig K, Schmithausen R, Li D, Jacobs M, Hollstein R, Blumenstock K, et al.
Nat Biotechnol
. 2022 Jul;
40(8):1295.
PMID: 35851378
No abstract available.
19.
Degenhardt F, Ellinghaus D, Juzenas S, Lerga-Jaso J, Wendorff M, Maya-Miles D, et al.
Hum Mol Genet
. 2022 Jul;
31(23):3945-3966.
PMID: 35848942
Given the highly variable clinical phenotype of Coronavirus disease 2019 (COVID-19), a deeper analysis of the host genetic contribution to severe COVID-19 is important to improve our understanding of underlying...
20.
Cruz R, Diz-de Almeida S, de Heredia M, Quintela I, Ceballos F, Pita G, et al.
Hum Mol Genet
. 2022 Jun;
31(22):3789-3806.
PMID: 35708486
Here, we describe the results of a genome-wide study conducted in 11 939 coronavirus disease 2019 (COVID-19) positive cases with an extensive clinical information that were recruited from 34 hospitals...