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

Steven Gazal

Showing results (71-80 of 98) with videos related to

Pageof 10
Sort By:
American Journal of Human Genetics|May 21, 2011
Loss of BRCC3 deubiquitinating enzyme leads to abnormal angiogenesis and is associated with syndromic moyamoyaSnaigune Miskinyte, Matthew G Butler, Dominique Hervé, et al.
Plos One|August 14, 2013
The MUC5B variant is associated with idiopathic pulmonary fibrosis but not with systemic sclerosis interstitial lung disease in the European Caucasian populationRaphael Borie, Bruno Crestani, Philippe Dieude, et al.
Brain : a Journal of Neurology|June 12, 2015
Heterozygous HTRA1 mutations are associated with autosomal dominant cerebral small vessel diseaseEdgard Verdura, Dominique Hervé, Eva Scharrer, et al.
The Journal of Allergy and Clinical Immunology|November 1, 2019
Shared genetic and experimental links between obesity-related traits and asthma subtypes in UK BiobankZhaozhong Zhu, Yanjun Guo, Huwenbo Shi, et al.
European Journal of Human Genetics : EJHG|August 9, 2018
Association of modifiers and other genetic factors explain Marfan syndrome clinical variabilityMelodie Aubart, Steven Gazal, Pauline Arnaud, et al.
Brain : a Journal of Neurology|March 26, 2026
SCN2A variants are associated with familial and sporadic hemiplegic migraineFlorence Riant, Christopher H Thompson, Syed M A Wafa, et al.
Journal of Medical Genetics|August 7, 2014
Juvenile myelomonocytic leukaemia and Noonan syndromeMarion Strullu, Aurélie Caye, Julie Lachenaud, et al.
International Journal of Cancer|October 11, 2014
Genes involved in the WNT and vesicular trafficking pathways are associated with melanoma predispositionMaider Ibarrola-Villava, Rajiv Kumar, Eduardo Nagore, et al.
Nature Genetics|September 5, 2018
Detecting genome-wide directional effects of transcription factor binding on polygenic disease riskYakir A Reshef, Hilary K Finucane, David R Kelley, et al.
Nature Genetics|April 11, 2018
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell typesHilary K Finucane, Yakir A Reshef, Verneri Anttila, et al.
Pageof 10

Showing results (71-80 of 98) with videos related to

Sort By:
Pageof 10
American Journal of Human Genetics|May 21, 2011
Loss of BRCC3 deubiquitinating enzyme leads to abnormal angiogenesis and is associated with syndromic moyamoyaSnaigune Miskinyte, Matthew G Butler, Dominique Hervé, et al.
Plos One|August 14, 2013
The MUC5B variant is associated with idiopathic pulmonary fibrosis but not with systemic sclerosis interstitial lung disease in the European Caucasian populationRaphael Borie, Bruno Crestani, Philippe Dieude, et al.
Brain : a Journal of Neurology|June 12, 2015
Heterozygous HTRA1 mutations are associated with autosomal dominant cerebral small vessel diseaseEdgard Verdura, Dominique Hervé, Eva Scharrer, et al.
The Journal of Allergy and Clinical Immunology|November 1, 2019
Shared genetic and experimental links between obesity-related traits and asthma subtypes in UK BiobankZhaozhong Zhu, Yanjun Guo, Huwenbo Shi, et al.
European Journal of Human Genetics : EJHG|August 9, 2018
Association of modifiers and other genetic factors explain Marfan syndrome clinical variabilityMelodie Aubart, Steven Gazal, Pauline Arnaud, et al.
Brain : a Journal of Neurology|March 26, 2026
SCN2A variants are associated with familial and sporadic hemiplegic migraineFlorence Riant, Christopher H Thompson, Syed M A Wafa, et al.
Journal of Medical Genetics|August 7, 2014
Juvenile myelomonocytic leukaemia and Noonan syndromeMarion Strullu, Aurélie Caye, Julie Lachenaud, et al.
International Journal of Cancer|October 11, 2014
Genes involved in the WNT and vesicular trafficking pathways are associated with melanoma predispositionMaider Ibarrola-Villava, Rajiv Kumar, Eduardo Nagore, et al.
Nature Genetics|September 5, 2018
Detecting genome-wide directional effects of transcription factor binding on polygenic disease riskYakir A Reshef, Hilary K Finucane, David R Kelley, et al.
Nature Genetics|April 11, 2018
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell typesHilary K Finucane, Yakir A Reshef, Verneri Anttila, et al.
Pageof 10