Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Panos Deloukas

Showing results (51-60 of 349) with videos related to

Pageof 35
Sort By:
European Journal of Human Genetics : EJHG|October 16, 2008
Mosaic 22q13 deletions: evidence for concurrent mosaic segmental isodisomy and gene conversionMaria Clara Bonaglia, Roberto Giorda, Silvana Beri, et al.
Human Molecular Genetics|January 22, 2004
The impact of SNP density on fine-scale patterns of linkage disequilibriumXiayi Ke, Sarah Hunt, William Tapper, et al.
Plos Genetics|November 1, 2008
Modifier effects between regulatory and protein-coding variationAntigone S Dimas, Barbara E Stranger, Claude Beazley, et al.
Pharmacogenetics and Genomics|December 14, 2011
Association of the GGCX (CAA)16/17 repeat polymorphism with higher warfarin dose requirements in African AmericansLarisa H Cavallari, Minoli Perera, Mia Wadelius, et al.
European Journal of Epidemiology|February 6, 2021
Thyroid function, sex hormones and sexual function: a Mendelian randomization studyAlisa D Kjaergaard, Eirini Marouli, Areti Papadopoulou, et al.
Investigative Ophthalmology & Visual Science|November 24, 2005
Posterior polymorphous corneal dystrophy in Czech families maps to chromosome 20 and excludes the VSX1 geneRhian Gwilliam, Petra Liskova, Martin Filipec, et al.
Genome Medicine|January 8, 2016
A multi-factorial analysis of response to warfarin in a UK prospective cohortStephane Bourgeois, Andrea Jorgensen, Eunice J Zhang, et al.
Plos One|October 11, 2012
High prevalence of posterior polymorphous corneal dystrophy in the Czech Republic; linkage disequilibrium mapping and dating an ancestral mutationPetra Liskova, Rhian Gwilliam, Martin Filipec, et al.
Thyroid : Official Journal of the American Thyroid Association|December 1, 2021
Thyroid Function and the Risk of Alzheimer's Disease: A Mendelian Randomization StudyEirini Marouli, Lina Yusuf, Alisa D Kjaergaard, et al.
Ebiomedicine|December 5, 2021
Genome-Wide association between EYA1 and Aspirin-induced peptic ulcerationStephane Bourgeois, Daniel F Carr, Crispin O Musumba, et al.
Pageof 35

Showing results (51-60 of 349) with videos related to

Sort By:
Pageof 35
European Journal of Human Genetics : EJHG|October 16, 2008
Mosaic 22q13 deletions: evidence for concurrent mosaic segmental isodisomy and gene conversionMaria Clara Bonaglia, Roberto Giorda, Silvana Beri, et al.
Human Molecular Genetics|January 22, 2004
The impact of SNP density on fine-scale patterns of linkage disequilibriumXiayi Ke, Sarah Hunt, William Tapper, et al.
Plos Genetics|November 1, 2008
Modifier effects between regulatory and protein-coding variationAntigone S Dimas, Barbara E Stranger, Claude Beazley, et al.
Pharmacogenetics and Genomics|December 14, 2011
Association of the GGCX (CAA)16/17 repeat polymorphism with higher warfarin dose requirements in African AmericansLarisa H Cavallari, Minoli Perera, Mia Wadelius, et al.
European Journal of Epidemiology|February 6, 2021
Thyroid function, sex hormones and sexual function: a Mendelian randomization studyAlisa D Kjaergaard, Eirini Marouli, Areti Papadopoulou, et al.
Investigative Ophthalmology & Visual Science|November 24, 2005
Posterior polymorphous corneal dystrophy in Czech families maps to chromosome 20 and excludes the VSX1 geneRhian Gwilliam, Petra Liskova, Martin Filipec, et al.
Genome Medicine|January 8, 2016
A multi-factorial analysis of response to warfarin in a UK prospective cohortStephane Bourgeois, Andrea Jorgensen, Eunice J Zhang, et al.
Plos One|October 11, 2012
High prevalence of posterior polymorphous corneal dystrophy in the Czech Republic; linkage disequilibrium mapping and dating an ancestral mutationPetra Liskova, Rhian Gwilliam, Martin Filipec, et al.
Thyroid : Official Journal of the American Thyroid Association|December 1, 2021
Thyroid Function and the Risk of Alzheimer's Disease: A Mendelian Randomization StudyEirini Marouli, Lina Yusuf, Alisa D Kjaergaard, et al.
Ebiomedicine|December 5, 2021
Genome-Wide association between EYA1 and Aspirin-induced peptic ulcerationStephane Bourgeois, Daniel F Carr, Crispin O Musumba, et al.
Pageof 35