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U Ludwig

Showing results (151-160 of 204) with videos related to

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American Journal of Medical Genetics. Part A|February 18, 2020
Nine newly identified individuals refine the phenotype associated with MYT1L mutationsIsabelle C Windheuser, Jessica Becker, Kirsten Cremer, et al.
Annals of Clinical and Translational Neurology|August 5, 2025
The rs10191329 Risk Allele Is Associated With Pronounced Retinal Layer Atrophy in Multiple SclerosisGabriel Bsteh, Ruchi Tanavade, Nik Krajnc, et al.
Molecular Genetics & Genomic Medicine|September 26, 2017
Analysis of sequence data to identify potential risk variants for oral clefts in multiplex familiesEmily R Holzinger, Qing Li, Margaret M Parker, et al.
Biomolecules|July 29, 2023
Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates <i>LZTR1</i> in Disease FormationRicarda Köllges, Jil Stegmann, Sophia Schneider, et al.
Plos Genetics|March 12, 2016
Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative GeneKerstin U Ludwig, Syeda Tasnim Ahmed, Anne C Böhmer, et al.
Genes|December 11, 2019
Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports <i>SH3PXD2A</i> as a Clefting Susceptibility GeneIris Alm van Rooij, Kerstin U Ludwig, Julia Welzenbach, et al.
Plos Genetics|March 13, 2015
Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophyMarkus Draaken, Michael Knapp, Tracie Pennimpede, et al.
European Journal of Human Genetics : EJHG|June 23, 2011
Genetic determination of human facial morphology: links between cleft-lips and normal variationStefan Boehringer, Fedde van der Lijn, Fan Liu, et al.
Schizophrenia Research|April 7, 2009
Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoterJens Treutlein, Thomas W Mühleisen, Josef Frank, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|October 20, 2012
Resequencing of VAX1 in patients with nonsyndromic cleft lip with or without cleft palateEntessar Nasser, Elisabeth Mangold, Daniela C Tradowsky, et al.
Pageof 21

Showing results (151-160 of 204) with videos related to

Sort By:
Pageof 21
American Journal of Medical Genetics. Part A|February 18, 2020
Nine newly identified individuals refine the phenotype associated with MYT1L mutationsIsabelle C Windheuser, Jessica Becker, Kirsten Cremer, et al.
Annals of Clinical and Translational Neurology|August 5, 2025
The rs10191329 Risk Allele Is Associated With Pronounced Retinal Layer Atrophy in Multiple SclerosisGabriel Bsteh, Ruchi Tanavade, Nik Krajnc, et al.
Molecular Genetics & Genomic Medicine|September 26, 2017
Analysis of sequence data to identify potential risk variants for oral clefts in multiplex familiesEmily R Holzinger, Qing Li, Margaret M Parker, et al.
Biomolecules|July 29, 2023
Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates <i>LZTR1</i> in Disease FormationRicarda Köllges, Jil Stegmann, Sophia Schneider, et al.
Plos Genetics|March 12, 2016
Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative GeneKerstin U Ludwig, Syeda Tasnim Ahmed, Anne C Böhmer, et al.
Genes|December 11, 2019
Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports <i>SH3PXD2A</i> as a Clefting Susceptibility GeneIris Alm van Rooij, Kerstin U Ludwig, Julia Welzenbach, et al.
Plos Genetics|March 13, 2015
Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophyMarkus Draaken, Michael Knapp, Tracie Pennimpede, et al.
European Journal of Human Genetics : EJHG|June 23, 2011
Genetic determination of human facial morphology: links between cleft-lips and normal variationStefan Boehringer, Fedde van der Lijn, Fan Liu, et al.
Schizophrenia Research|April 7, 2009
Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoterJens Treutlein, Thomas W Mühleisen, Josef Frank, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|October 20, 2012
Resequencing of VAX1 in patients with nonsyndromic cleft lip with or without cleft palateEntessar Nasser, Elisabeth Mangold, Daniela C Tradowsky, et al.
Pageof 21