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Patrick Deelen

Showing results (21-30 of 65) with videos related to

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Nature Genetics|October 21, 2018
Author Correction: Individual variations in cardiovascular-disease-related protein levels are driven by genetics and gut microbiomeDaria V Zhernakova, Trang H Le, Alexander Kurilshikov, et al.
Journal of Cardiovascular Translational Research|January 9, 2023
Phenotypic and Genetic Factors Associated with Absence of Cardiomyopathy Symptoms in PLN:c.40_42delAGA CarriersEsteban A Lopera-Maya, Shuang Li, Remco de Brouwer, et al.
Cell Host & Microbe|November 8, 2016
Functional and Genomic Architecture of Borrelia burgdorferi-Induced Cytokine Responses in HumansMarije Oosting, Mariska Kerstholt, Rob Ter Horst, et al.
European Journal of Human Genetics : EJHG|October 9, 2019
Immunochip meta-analysis in European and Argentinian populations identifies two novel genetic loci associated with celiac diseaseIsis Ricaño-Ponce, Javier Gutierrez-Achury, Ana Florencia Costa, et al.
Cell Reports|December 16, 2016
TMEM258 Is a Component of the Oligosaccharyltransferase Complex Controlling ER Stress and Intestinal InflammationDaniel B Graham, Ariel Lefkovith, Patrick Deelen, et al.
European Journal of Human Genetics : EJHG|August 30, 2021
TAB2 deletions and variants cause a highly recognisable syndrome with mitral valve disease, cardiomyopathy, short stature and hypermobilityAafke Engwerda, Erika K S M Leenders, Barbara Frentz, et al.
Plos One|March 25, 2015
Lessons learned from whole exome sequencing in multiplex families affected by a complex genetic disorder, intracranial aneurysmJanice L Farlow, Hai Lin, Laura Sauerbeck, et al.
American Journal of Human Genetics|April 2, 2025
Low-cost generation of clinical-grade, layperson-friendly pharmacogenetic passports using oligonucleotide arraysPauline Lanting, Robert Warmerdam, Jelle Slager, et al.
Genome Medicine|August 25, 2020
CAPICE: a computational method for Consequence-Agnostic Pathogenicity Interpretation of Clinical Exome variationsShuang Li, K Joeri van der Velde, Dick de Ridder, et al.
BMC Genomics|October 6, 2014
Genetic and epigenetic regulation of gene expression in fetal and adult human liversMarc Jan Bonder, Silva Kasela, Mart Kals, et al.
Pageof 7

Showing results (21-30 of 65) with videos related to

Sort By:
Pageof 7
Nature Genetics|October 21, 2018
Author Correction: Individual variations in cardiovascular-disease-related protein levels are driven by genetics and gut microbiomeDaria V Zhernakova, Trang H Le, Alexander Kurilshikov, et al.
Journal of Cardiovascular Translational Research|January 9, 2023
Phenotypic and Genetic Factors Associated with Absence of Cardiomyopathy Symptoms in PLN:c.40_42delAGA CarriersEsteban A Lopera-Maya, Shuang Li, Remco de Brouwer, et al.
Cell Host & Microbe|November 8, 2016
Functional and Genomic Architecture of Borrelia burgdorferi-Induced Cytokine Responses in HumansMarije Oosting, Mariska Kerstholt, Rob Ter Horst, et al.
European Journal of Human Genetics : EJHG|October 9, 2019
Immunochip meta-analysis in European and Argentinian populations identifies two novel genetic loci associated with celiac diseaseIsis Ricaño-Ponce, Javier Gutierrez-Achury, Ana Florencia Costa, et al.
Cell Reports|December 16, 2016
TMEM258 Is a Component of the Oligosaccharyltransferase Complex Controlling ER Stress and Intestinal InflammationDaniel B Graham, Ariel Lefkovith, Patrick Deelen, et al.
European Journal of Human Genetics : EJHG|August 30, 2021
TAB2 deletions and variants cause a highly recognisable syndrome with mitral valve disease, cardiomyopathy, short stature and hypermobilityAafke Engwerda, Erika K S M Leenders, Barbara Frentz, et al.
Plos One|March 25, 2015
Lessons learned from whole exome sequencing in multiplex families affected by a complex genetic disorder, intracranial aneurysmJanice L Farlow, Hai Lin, Laura Sauerbeck, et al.
American Journal of Human Genetics|April 2, 2025
Low-cost generation of clinical-grade, layperson-friendly pharmacogenetic passports using oligonucleotide arraysPauline Lanting, Robert Warmerdam, Jelle Slager, et al.
Genome Medicine|August 25, 2020
CAPICE: a computational method for Consequence-Agnostic Pathogenicity Interpretation of Clinical Exome variationsShuang Li, K Joeri van der Velde, Dick de Ridder, et al.
BMC Genomics|October 6, 2014
Genetic and epigenetic regulation of gene expression in fetal and adult human liversMarc Jan Bonder, Silva Kasela, Mart Kals, et al.
Pageof 7