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Elizabeth Pugh

Showing results (11-20 of 42) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|November 8, 2019
Genetic Modifiers of Cystic Fibrosis-Related Diabetes Have Extensive Overlap With Type 2 Diabetes and Related TraitsMelis A Aksit, Rhonda G Pace, Briana Vecchio-Pagán, et al.
Nature Genetics|August 17, 2010
Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's diseaseTaye H Hamza, Cyrus P Zabetian, Albert Tenesa, et al.
Frontiers in Genetics|January 8, 2015
Imputation and quality control steps for combining multiple genome-wide datasetsShefali S Verma, Mariza de Andrade, Gerard Tromp, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 11, 2024
The clinical utility of sequencing the entirety of CFTRMolly B Sheridan, Melis A Aksit, Kymberleigh Pagel, 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|October 7, 2022
Pleiotropic modifiers of age-related diabetes and neonatal intestinal obstruction in cystic fibrosisMelis A Aksit, Hua Ling, Rhonda G Pace, et al.
Human Heredity|June 13, 2009
Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association resultsMary L Marazita, Andrew C Lidral, Jeffrey C Murray, et al.
Science (New York, N.Y.)|November 19, 2005
Epidemiology. DNA identifications after the 9/11 World Trade Center attackLeslie G Biesecker, Joan E Bailey-Wilson, Jack Ballantyne, et al.
Pediatric Research|August 21, 2012
No observed association for mitochondrial SNPs with preterm delivery and related outcomesBrandon W Alleman, Solveig Myking, Kelli K Ryckman, et al.
BMC Proceedings|March 1, 2012
Identifying rare variants from exome scans: the GAW17 experienceSaurabh Ghosh, Heike Bickeböller, Julia Bailey, et al.
Pageof 5

Showing results (11-20 of 42) with videos related to

Sort By:
Pageof 5
The Journal of Clinical Endocrinology and Metabolism|November 8, 2019
Genetic Modifiers of Cystic Fibrosis-Related Diabetes Have Extensive Overlap With Type 2 Diabetes and Related TraitsMelis A Aksit, Rhonda G Pace, Briana Vecchio-Pagán, et al.
Nature Genetics|August 17, 2010
Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's diseaseTaye H Hamza, Cyrus P Zabetian, Albert Tenesa, et al.
Frontiers in Genetics|January 8, 2015
Imputation and quality control steps for combining multiple genome-wide datasetsShefali S Verma, Mariza de Andrade, Gerard Tromp, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 11, 2024
The clinical utility of sequencing the entirety of CFTRMolly B Sheridan, Melis A Aksit, Kymberleigh Pagel, 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|October 7, 2022
Pleiotropic modifiers of age-related diabetes and neonatal intestinal obstruction in cystic fibrosisMelis A Aksit, Hua Ling, Rhonda G Pace, et al.
Human Heredity|June 13, 2009
Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association resultsMary L Marazita, Andrew C Lidral, Jeffrey C Murray, et al.
Science (New York, N.Y.)|November 19, 2005
Epidemiology. DNA identifications after the 9/11 World Trade Center attackLeslie G Biesecker, Joan E Bailey-Wilson, Jack Ballantyne, et al.
Pediatric Research|August 21, 2012
No observed association for mitochondrial SNPs with preterm delivery and related outcomesBrandon W Alleman, Solveig Myking, Kelli K Ryckman, et al.
BMC Proceedings|March 1, 2012
Identifying rare variants from exome scans: the GAW17 experienceSaurabh Ghosh, Heike Bickeböller, Julia Bailey, et al.
Pageof 5