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Andre Franke

Showing results (591-600 of 678) with videos related to

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Plos Genetics|May 26, 2018
Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish populationManuel A Rivas, Brandon E Avila, Jukka Koskela, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|August 28, 2024
Blood-based multivariate methylation risk score for cognitive impairment and dementiaJarno Koetsier, Rachel Cavill, Rick Reijnders, et al.
Science Translational Medicine|September 17, 2010
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disabilityAbdul Noor, Annabel Whibley, Christian R Marshall, et al.
Scientific Reports|November 11, 2015
Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal CancerMaria N Timofeeva, Ben Kinnersley, Susan M Farrington, et al.
Gastroenterology|April 30, 2013
Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studiesDavid Ellinghaus, Hu Zhang, Sebastian Zeissig, et al.
Gut|January 21, 2019
Genome-wide association analysis of diverticular disease points towards neuromuscular, connective tissue and epithelial pathomechanismsClemens Schafmayer, James William Harrison, Stephan Buch, et al.
The Journal of Allergy and Clinical Immunology|September 1, 2018
Hypomorphic caspase activation and recruitment domain 11 (CARD11) mutations associated with diverse immunologic phenotypes with or without atopic diseaseBatsukh Dorjbal, Jeffrey R Stinson, Chi A Ma, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 17, 2024
Genetic Risk Factors in Isolated Dystonia Escape Genome-Wide Association StudiesBjörn-Hergen Laabs, Katja Lohmann, Eva-Juliane Vollstedt, et al.
Gut|July 26, 2022
GWAS meta-analysis of 16 790 patients with Barrett's oesophagus and oesophageal adenocarcinoma identifies 16 novel genetic risk loci and provides insights into disease aetiology beyond the single marker levelJulia Schröder, Laura Chegwidden, Carlo Maj, et al.
Immunity|December 9, 2020
Longitudinal Multi-omics Analyses Identify Responses of Megakaryocytes, Erythroid Cells, and Plasmablasts as Hallmarks of Severe COVID-19Joana P Bernardes, Neha Mishra, Florian Tran, et al.
Pageof 68

Showing results (591-600 of 678) with videos related to

Sort By:
Pageof 68
Plos Genetics|May 26, 2018
Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish populationManuel A Rivas, Brandon E Avila, Jukka Koskela, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|August 28, 2024
Blood-based multivariate methylation risk score for cognitive impairment and dementiaJarno Koetsier, Rachel Cavill, Rick Reijnders, et al.
Science Translational Medicine|September 17, 2010
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disabilityAbdul Noor, Annabel Whibley, Christian R Marshall, et al.
Scientific Reports|November 11, 2015
Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal CancerMaria N Timofeeva, Ben Kinnersley, Susan M Farrington, et al.
Gastroenterology|April 30, 2013
Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studiesDavid Ellinghaus, Hu Zhang, Sebastian Zeissig, et al.
Gut|January 21, 2019
Genome-wide association analysis of diverticular disease points towards neuromuscular, connective tissue and epithelial pathomechanismsClemens Schafmayer, James William Harrison, Stephan Buch, et al.
The Journal of Allergy and Clinical Immunology|September 1, 2018
Hypomorphic caspase activation and recruitment domain 11 (CARD11) mutations associated with diverse immunologic phenotypes with or without atopic diseaseBatsukh Dorjbal, Jeffrey R Stinson, Chi A Ma, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 17, 2024
Genetic Risk Factors in Isolated Dystonia Escape Genome-Wide Association StudiesBjörn-Hergen Laabs, Katja Lohmann, Eva-Juliane Vollstedt, et al.
Gut|July 26, 2022
GWAS meta-analysis of 16 790 patients with Barrett's oesophagus and oesophageal adenocarcinoma identifies 16 novel genetic risk loci and provides insights into disease aetiology beyond the single marker levelJulia Schröder, Laura Chegwidden, Carlo Maj, et al.
Immunity|December 9, 2020
Longitudinal Multi-omics Analyses Identify Responses of Megakaryocytes, Erythroid Cells, and Plasmablasts as Hallmarks of Severe COVID-19Joana P Bernardes, Neha Mishra, Florian Tran, et al.
Pageof 68