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U Ludwig

Showing results (181-190 of 204) with videos related to

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Molecular Genetics & Genomic Medicine|December 5, 2022
Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scoresNina Ishorst, Leonie Henschel, Frederic Thieme, et al.
Nature Genetics|March 10, 2009
Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24Stefanie Birnbaum, Kerstin U Ludwig, Heiko Reutter, et al.
HGG Advances|June 30, 2024
Stratified analyses refine association between TLR7 rare variants and severe COVID-19Jannik Boos, Caspar I van der Made, Gayatri Ramakrishnan, et al.
Human Genetics|December 10, 2021
Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severityChiara Fallerini, Nicola Picchiotti, Margherita Baldassarri, et al.
Plos One|January 1, 2020
Identification of loci of functional relevance to Barrett's esophagus and esophageal adenocarcinoma: Cross-referencing of expression quantitative trait loci data from disease-relevant tissues with genetic association dataJulia Schröder, Vitalia Schüller, Andrea May, et al.
Nature Genetics|August 7, 2012
Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk lociKerstin U Ludwig, Elisabeth Mangold, Stefan Herms, et al.
Nature Genetics|December 22, 2009
Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palateElisabeth Mangold, Kerstin U Ludwig, Stefanie Birnbaum, et al.
Nature Biotechnology|July 19, 2022
Author Correction: LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcodingKerstin U Ludwig, Ricarda M Schmithausen, David Li, et al.
Nature Biotechnology|June 30, 2021
LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcodingKerstin U Ludwig, Ricarda M Schmithausen, David Li, et al.
European Journal of Human Genetics : EJHG|September 12, 2013
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohortJessica Becker, Darina Czamara, Tom S Scerri, et al.
Pageof 21

Showing results (181-190 of 204) with videos related to

Sort By:
Pageof 21
Molecular Genetics & Genomic Medicine|December 5, 2022
Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scoresNina Ishorst, Leonie Henschel, Frederic Thieme, et al.
Nature Genetics|March 10, 2009
Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24Stefanie Birnbaum, Kerstin U Ludwig, Heiko Reutter, et al.
HGG Advances|June 30, 2024
Stratified analyses refine association between TLR7 rare variants and severe COVID-19Jannik Boos, Caspar I van der Made, Gayatri Ramakrishnan, et al.
Human Genetics|December 10, 2021
Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severityChiara Fallerini, Nicola Picchiotti, Margherita Baldassarri, et al.
Plos One|January 1, 2020
Identification of loci of functional relevance to Barrett's esophagus and esophageal adenocarcinoma: Cross-referencing of expression quantitative trait loci data from disease-relevant tissues with genetic association dataJulia Schröder, Vitalia Schüller, Andrea May, et al.
Nature Genetics|August 7, 2012
Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk lociKerstin U Ludwig, Elisabeth Mangold, Stefan Herms, et al.
Nature Genetics|December 22, 2009
Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palateElisabeth Mangold, Kerstin U Ludwig, Stefanie Birnbaum, et al.
Nature Biotechnology|July 19, 2022
Author Correction: LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcodingKerstin U Ludwig, Ricarda M Schmithausen, David Li, et al.
Nature Biotechnology|June 30, 2021
LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcodingKerstin U Ludwig, Ricarda M Schmithausen, David Li, et al.
European Journal of Human Genetics : EJHG|September 12, 2013
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohortJessica Becker, Darina Czamara, Tom S Scerri, et al.
Pageof 21