Thomas E Ludwig
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Explore the profile of Thomas E Ludwig including associated specialties, affiliations and a list of published articles.
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10
Citations
138
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Recent Articles
1.
Azar Y, Ludwig T, Le Bon H, Strom T, Bluteau O, Di-Filippo M, et al.
Atherosclerosis
. 2024 Nov;
399:118596.
PMID: 39500114
Background And Aims: PCSK9 is a key regulator of LDL-cholesterol levels. PCSK9 gain of function variants (GOFVs) cause autosomal dominant hypercholesterolemia (ADH). The first described PCSK9-GOFV, p.Ser127Arg, almost exclusively reported...
2.
Alves I, Giemza J, Blum M, Bernhardsson C, Chatel S, Karakachoff M, et al.
Nat Commun
. 2024 Aug;
15(1):6710.
PMID: 39112481
The demographical history of France remains largely understudied despite its central role toward understanding modern population structure across Western Europe. Here, by exploring publicly available Europe-wide genotype datasets together with...
3.
Bocher O, Ludwig T, Oglobinsky M, Marenne G, Deleuze J, Suryakant S, et al.
PLoS Genet
. 2022 Sep;
18(9):e1009923.
PMID: 36112662
Rare variant association tests (RVAT) have been developed to study the contribution of rare variants widely accessible through high-throughput sequencing technologies. RVAT require to aggregate rare variants in testing units...
4.
Marenne G, Ludwig T, Bocher O, Herzig A, Aloui C, Tournier-Lasserve E, et al.
Genet Epidemiol
. 2022 Apr;
46(5-6):256-265.
PMID: 35419876
Next-generation sequencing technologies have opened up the possibility to sequence large samples of cases and controls to test for association with rare variants. To limit cost and increase sample sizes,...
5.
Aloui C, Herve D, Marenne G, Savenier F, Le Guennec K, Bergametti F, et al.
Ann Neurol
. 2021 Oct;
90(6):962-975.
PMID: 34606115
Objective: The majority of patients with a familial cerebral small vessel disease (CSVD) referred for molecular screening do not show pathogenic variants in known genes. In this study, we aimed...
6.
Gourhant L, Bocher O, de Saint Martin L, Ludwig T, Boland A, Deleuze J, et al.
Reprod Biomed Online
. 2021 Mar;
42(4):789-798.
PMID: 33658156
Research Question: Are there genetic determinants shared by unrelated women with unexplained recurrent early miscarriage (REM)? Design: Thirty REM cases and 30 controls were selected with extreme phenotype among women...
7.
Bocher O, Marenne G, Saint Pierre A, Ludwig T, Guey S, Tournier-Lasserve E, et al.
Genet Epidemiol
. 2019 May;
43(6):646-656.
PMID: 31087445
Genetic association studies have provided new insights into the genetic variability of human complex traits with a focus mainly on continuous or binary traits. Methods have been proposed to take...
8.
Cuppens T, Ludwig T, Trouve P, Genin E
Bioinformatics
. 2018 Dec;
35(14):2492-2494.
PMID: 30508040
Summary: When analyzing sequence data, genetic variants are considered one by one, taking no account of whether or not they are found in the same individual. However, variant combinations might...
9.
Jossinet F, Ludwig T, Westhof E
Bioinformatics
. 2010 Jun;
26(16):2057-9.
PMID: 20562414
Summary: Assemble is an intuitive graphical interface to analyze, manipulate and build complex 3D RNA architectures. It provides several advanced and unique features within the framework of a semi-automated modeling...
10.
Jossinet F, Ludwig T, Westhof E
Curr Opin Microbiol
. 2007 Jun;
10(3):279-85.
PMID: 17548241
The range of functions ascribed to RNA molecules has grown considerably during recent years. Consequently, the analysis and comparison of RNA sequences have become recurrent tasks in molecular biology. Because...