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W Scott Watkins

Showing results (41-50 of 57) with videos related to

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Genomics|July 21, 2010
Toward a more uniform sampling of human genetic diversity: a survey of worldwide populations by high-density genotypingJinchuan Xing, W Scott Watkins, Adam Shlien, et al.
Biorxiv : the Preprint Server for Biology|December 25, 2025
Human acrocentric chromosome short arm <i>de novo</i> mutation and recombinationJiadong Lin, F Kumara Mastrorosa, Michelle D Noyes, et al.
Plos One|August 6, 2014
Clinical and biochemical function of polymorphic NR0B1 GGAA-microsatellites in Ewing sarcoma: a report from the Children's Oncology GroupMichael J Monument, Kirsten M Johnson, Elizabeth McIlvaine, et al.
Genome Research|June 14, 2003
Genetic variation among world populations: inferences from 100 Alu insertion polymorphismsW Scott Watkins, Alan R Rogers, Christopher T Ostler, et al.
Molecular Biology and Evolution|August 6, 2011
Crohn's disease and genetic hitchhiking at IBD5Chad D Huff, David J Witherspoon, Yuhua Zhang, et al.
The American Journal of Psychiatry|October 3, 2008
Strong evidence for a novel schizophrenia risk locus on chromosome 1p31.1 in homogeneous pedigrees from Tamil Nadu, IndiaElizabeth G Holliday, Dale R Nyholt, Srinivasan Tirupati, et al.
Nature Communications|October 19, 2019
De novo and recessive forms of congenital heart disease have distinct genetic and phenotypic landscapesW Scott Watkins, E Javier Hernandez, Sergiusz Wesolowski, et al.
Medrxiv : the Preprint Server for Health Sciences|May 15, 2024
Genome Sequencing is Critical for Forecasting Outcomes Following Congenital Cardiac SurgeryW Scott Watkins, E Javier Hernandez, Thomas Miller, et al.
Human Genomics|July 12, 2005
Large-scale SNP analysis reveals clustered and continuous patterns of human genetic variationMark D Shriver, Rui Mei, Esteban J Parra, et al.
Nature Communications|July 10, 2025
Genome sequencing is critical for forecasting outcomes following congenital cardiac surgeryW Scott Watkins, Edgar J Hernandez, Thomas A Miller, et al.
Pageof 6

Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
Genomics|July 21, 2010
Toward a more uniform sampling of human genetic diversity: a survey of worldwide populations by high-density genotypingJinchuan Xing, W Scott Watkins, Adam Shlien, et al.
Biorxiv : the Preprint Server for Biology|December 25, 2025
Human acrocentric chromosome short arm <i>de novo</i> mutation and recombinationJiadong Lin, F Kumara Mastrorosa, Michelle D Noyes, et al.
Plos One|August 6, 2014
Clinical and biochemical function of polymorphic NR0B1 GGAA-microsatellites in Ewing sarcoma: a report from the Children's Oncology GroupMichael J Monument, Kirsten M Johnson, Elizabeth McIlvaine, et al.
Genome Research|June 14, 2003
Genetic variation among world populations: inferences from 100 Alu insertion polymorphismsW Scott Watkins, Alan R Rogers, Christopher T Ostler, et al.
Molecular Biology and Evolution|August 6, 2011
Crohn's disease and genetic hitchhiking at IBD5Chad D Huff, David J Witherspoon, Yuhua Zhang, et al.
The American Journal of Psychiatry|October 3, 2008
Strong evidence for a novel schizophrenia risk locus on chromosome 1p31.1 in homogeneous pedigrees from Tamil Nadu, IndiaElizabeth G Holliday, Dale R Nyholt, Srinivasan Tirupati, et al.
Nature Communications|October 19, 2019
De novo and recessive forms of congenital heart disease have distinct genetic and phenotypic landscapesW Scott Watkins, E Javier Hernandez, Sergiusz Wesolowski, et al.
Medrxiv : the Preprint Server for Health Sciences|May 15, 2024
Genome Sequencing is Critical for Forecasting Outcomes Following Congenital Cardiac SurgeryW Scott Watkins, E Javier Hernandez, Thomas Miller, et al.
Human Genomics|July 12, 2005
Large-scale SNP analysis reveals clustered and continuous patterns of human genetic variationMark D Shriver, Rui Mei, Esteban J Parra, et al.
Nature Communications|July 10, 2025
Genome sequencing is critical for forecasting outcomes following congenital cardiac surgeryW Scott Watkins, Edgar J Hernandez, Thomas A Miller, et al.
Pageof 6