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Sara L Pulit

Showing results (41-50 of 63) with videos related to

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Human Molecular Genetics|June 25, 2014
A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathyJonas J W Kuiper, Jessica Van Setten, Stephan Ripke, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|March 8, 2018
Identification of an Amino Acid Motif in HLA-DRβ1 That Distinguishes Uveitis in Patients With Juvenile Idiopathic ArthritisAnne-Mieke J W Haasnoot, Marco W Schilham, Sylvia Kamphuis, et al.
Human Mutation|July 18, 2017
The role of de novo mutations in the development of amyotrophic lateral sclerosisPerry T C van Doormaal, Nicola Ticozzi, Jochen H Weishaupt, et al.
Kidney International|October 22, 2015
Prioritization and burden analysis of rare variants in 208 candidate genes suggest they do not play a major role in CAKUTNayia Nicolaou, Sara L Pulit, Isaac J Nijman, et al.
Circulation. Cardiovascular Genetics|December 15, 2015
Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension RiskBing Yu, Sara L Pulit, Shih-Jen Hwang, et al.
Circulation. Cardiovascular Genetics|June 22, 2014
Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) ConsortiumJared W Magnani, Jennifer A Brody, Bram P Prins, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 14, 2017
Reconsidering the causality of TIA1 mutations in ALSRick A van der Spek, Wouter van Rheenen, Sara L Pulit, et al.
Neurobiology of Aging|October 22, 2018
Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohortGijs H P Tazelaar, Annelot M Dekker, Joke J F A van Vugt, et al.
Heart Rhythm|January 15, 2014
Common variation in fatty acid metabolic genes and risk of incident sudden cardiac arrestRozenn N Lemaitre, Catherine O Johnson, Stephanie Hesselson, et al.
Neurology|March 4, 2016
Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaborationRainer Malik, Matthew Traylor, Sara L Pulit, et al.
Pageof 7

Showing results (41-50 of 63) with videos related to

Sort By:
Pageof 7
Human Molecular Genetics|June 25, 2014
A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathyJonas J W Kuiper, Jessica Van Setten, Stephan Ripke, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|March 8, 2018
Identification of an Amino Acid Motif in HLA-DRβ1 That Distinguishes Uveitis in Patients With Juvenile Idiopathic ArthritisAnne-Mieke J W Haasnoot, Marco W Schilham, Sylvia Kamphuis, et al.
Human Mutation|July 18, 2017
The role of de novo mutations in the development of amyotrophic lateral sclerosisPerry T C van Doormaal, Nicola Ticozzi, Jochen H Weishaupt, et al.
Kidney International|October 22, 2015
Prioritization and burden analysis of rare variants in 208 candidate genes suggest they do not play a major role in CAKUTNayia Nicolaou, Sara L Pulit, Isaac J Nijman, et al.
Circulation. Cardiovascular Genetics|December 15, 2015
Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension RiskBing Yu, Sara L Pulit, Shih-Jen Hwang, et al.
Circulation. Cardiovascular Genetics|June 22, 2014
Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) ConsortiumJared W Magnani, Jennifer A Brody, Bram P Prins, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 14, 2017
Reconsidering the causality of TIA1 mutations in ALSRick A van der Spek, Wouter van Rheenen, Sara L Pulit, et al.
Neurobiology of Aging|October 22, 2018
Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohortGijs H P Tazelaar, Annelot M Dekker, Joke J F A van Vugt, et al.
Heart Rhythm|January 15, 2014
Common variation in fatty acid metabolic genes and risk of incident sudden cardiac arrestRozenn N Lemaitre, Catherine O Johnson, Stephanie Hesselson, et al.
Neurology|March 4, 2016
Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaborationRainer Malik, Matthew Traylor, Sara L Pulit, et al.
Pageof 7