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Michael Wittig

Showing results (21-30 of 68) with videos related to

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Cell|May 31, 2011
Maternal epigenetic pathways control parental contributions to Arabidopsis early embryogenesisDaphné Autran, Célia Baroux, Michael T Raissig, et al.
Mechanisms of Ageing and Development|July 12, 2011
A genome-wide association study confirms APOE as the major gene influencing survival in long-lived individualsAlmut Nebel, Rabea Kleindorp, Amke Caliebe, et al.
Brain Communications|June 12, 2024
Genome-wide meta-analysis of short-tandem repeats for Parkinson's disease risk using genotype imputationOlena Ohlei, Kimberly Paul, Susan Searles Nielsen, et al.
Frontiers in Immunology|December 12, 2019
Complement Receptor 1 (CR1, CD35) Polymorphisms and Soluble CR1: A Proposed Anti-inflammatory Role to Quench the Fire of "Fogo Selvagem" Pemphigus FoliaceusLuana Caroline Oliveira, Gabriela Canalli Kretzschmar, Andressa Cristina Moraes Dos Santos, et al.
Nucleic Acids Research|September 12, 2012
From next-generation sequencing alignments to accurate comparison and validation of single-nucleotide variants: the pibase softwareMichael Forster, Peter Forster, Abdou Elsharawy, et al.
Annals of Clinical and Translational Neurology|July 16, 2020
Whole-exome and HLA sequencing in Febrile infection-related epilepsy syndromeIngo Helbig, Giulia Barcia, Manuela Pendziwiat, et al.
Epilepsia|January 6, 2011
A duplication in 1q21.3 in a family with early onset and childhood absence epilepsyHiltrud Muhle, Ines Steinich, Sarah von Spiczak, et al.
Human Molecular Genetics|July 14, 2009
Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritanceLeanne M Dibbens, Saul Mullen, Ingo Helbig, et al.
Blood Advances|September 21, 2022
Haplotype sequence collection of ABO blood group alleles by long-read sequencing reveals putative A1-diagnostic variantsMorgan Gueuning, Gian Andri Thun, Michael Wittig, et al.
Gastroenterology|August 30, 2008
Genome-wide association analysis in sarcoidosis and Crohn's disease unravels a common susceptibility locus on 10p12.2Andre Franke, Annegret Fischer, Michael Nothnagel, et al.
Pageof 7

Showing results (21-30 of 68) with videos related to

Sort By:
Pageof 7
Cell|May 31, 2011
Maternal epigenetic pathways control parental contributions to Arabidopsis early embryogenesisDaphné Autran, Célia Baroux, Michael T Raissig, et al.
Mechanisms of Ageing and Development|July 12, 2011
A genome-wide association study confirms APOE as the major gene influencing survival in long-lived individualsAlmut Nebel, Rabea Kleindorp, Amke Caliebe, et al.
Brain Communications|June 12, 2024
Genome-wide meta-analysis of short-tandem repeats for Parkinson's disease risk using genotype imputationOlena Ohlei, Kimberly Paul, Susan Searles Nielsen, et al.
Frontiers in Immunology|December 12, 2019
Complement Receptor 1 (CR1, CD35) Polymorphisms and Soluble CR1: A Proposed Anti-inflammatory Role to Quench the Fire of "Fogo Selvagem" Pemphigus FoliaceusLuana Caroline Oliveira, Gabriela Canalli Kretzschmar, Andressa Cristina Moraes Dos Santos, et al.
Nucleic Acids Research|September 12, 2012
From next-generation sequencing alignments to accurate comparison and validation of single-nucleotide variants: the pibase softwareMichael Forster, Peter Forster, Abdou Elsharawy, et al.
Annals of Clinical and Translational Neurology|July 16, 2020
Whole-exome and HLA sequencing in Febrile infection-related epilepsy syndromeIngo Helbig, Giulia Barcia, Manuela Pendziwiat, et al.
Epilepsia|January 6, 2011
A duplication in 1q21.3 in a family with early onset and childhood absence epilepsyHiltrud Muhle, Ines Steinich, Sarah von Spiczak, et al.
Human Molecular Genetics|July 14, 2009
Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritanceLeanne M Dibbens, Saul Mullen, Ingo Helbig, et al.
Blood Advances|September 21, 2022
Haplotype sequence collection of ABO blood group alleles by long-read sequencing reveals putative A1-diagnostic variantsMorgan Gueuning, Gian Andri Thun, Michael Wittig, et al.
Gastroenterology|August 30, 2008
Genome-wide association analysis in sarcoidosis and Crohn's disease unravels a common susceptibility locus on 10p12.2Andre Franke, Annegret Fischer, Michael Nothnagel, et al.
Pageof 7