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

Stephen W Scherer

Showing results (71-80 of 499) with videos related to

Pageof 50
Sort By:
Genes|December 23, 2023
Complex Autism Spectrum Disorder in a Patient with a Novel De Novo Heterozygous <i>MYT1L</i> VariantSilas Yip, Kristina Calli, Ying Qiao, et al.
Bioinformatics (Oxford, England)|October 4, 2019
VikNGS: a C++ variant integration kit for next generation sequencing association analysisZeynep Baskurt, Scott Mastromatteo, Jiafen Gong, et al.
Pediatric Research|June 18, 2009
Whole genome scanning: resolving clinical diagnosis and management amidst complex dataSarah E Ali-Khan, Abdallah S Daar, Cheryl Shuman, et al.
BMC Medical Genomics|March 19, 2015
Performance of case-control rare copy number variation annotation in classification of autismWorrawat Engchuan, Kiret Dhindsa, Anath C Lionel, et al.
Neurology. Genetics|September 29, 2017
Hyperventilation-athetosis in <i>ASXL3</i> deficiency (Bainbridge-Ropers) syndromeRubina Dad, Susan Walker, Stephen W Scherer, et al.
Scientific Reports|May 19, 2015
Integrated genomics identifies convergence of ankylosing spondylitis with global immune mediated disease pathwaysMohammed Uddin, Dianne Codner, S M Mahmud Hasan, et al.
International Journal of Cancer|December 21, 2004
Altered expression and deletion of RMO1 in osteosarcomaKolja Eppert, Jay S Wunder, Vicky Aneliunas, et al.
American Journal of Medical Genetics. Part A|February 5, 2003
Molecular characterization of a 12q22-q24 deletion associated with congenital deafness: confirmation and refinement of the DFNA25 locusErwin Petek, Christian Windpassinger, Monika Mach, et al.
Genomics|September 6, 2002
The RAY1/ST7 tumor-suppressor locus on chromosome 7q31 represents a complex multi-transcript systemJohn B Vincent, Erwin Petek, Sandy Thevarkunnel, et al.
The Journal of Biological Chemistry|March 10, 2005
Endothelial nitric-oxide synthase antisense (NOS3AS) gene encodes an autophagy-related protein (APG9-like2) highly expressed in trophoblastTakahiro Yamada, Andrew R Carson, Isabella Caniggia, et al.
Pageof 50

Showing results (71-80 of 499) with videos related to

Sort By:
Pageof 50
Genes|December 23, 2023
Complex Autism Spectrum Disorder in a Patient with a Novel De Novo Heterozygous <i>MYT1L</i> VariantSilas Yip, Kristina Calli, Ying Qiao, et al.
Bioinformatics (Oxford, England)|October 4, 2019
VikNGS: a C++ variant integration kit for next generation sequencing association analysisZeynep Baskurt, Scott Mastromatteo, Jiafen Gong, et al.
Pediatric Research|June 18, 2009
Whole genome scanning: resolving clinical diagnosis and management amidst complex dataSarah E Ali-Khan, Abdallah S Daar, Cheryl Shuman, et al.
BMC Medical Genomics|March 19, 2015
Performance of case-control rare copy number variation annotation in classification of autismWorrawat Engchuan, Kiret Dhindsa, Anath C Lionel, et al.
Neurology. Genetics|September 29, 2017
Hyperventilation-athetosis in <i>ASXL3</i> deficiency (Bainbridge-Ropers) syndromeRubina Dad, Susan Walker, Stephen W Scherer, et al.
Scientific Reports|May 19, 2015
Integrated genomics identifies convergence of ankylosing spondylitis with global immune mediated disease pathwaysMohammed Uddin, Dianne Codner, S M Mahmud Hasan, et al.
International Journal of Cancer|December 21, 2004
Altered expression and deletion of RMO1 in osteosarcomaKolja Eppert, Jay S Wunder, Vicky Aneliunas, et al.
American Journal of Medical Genetics. Part A|February 5, 2003
Molecular characterization of a 12q22-q24 deletion associated with congenital deafness: confirmation and refinement of the DFNA25 locusErwin Petek, Christian Windpassinger, Monika Mach, et al.
Genomics|September 6, 2002
The RAY1/ST7 tumor-suppressor locus on chromosome 7q31 represents a complex multi-transcript systemJohn B Vincent, Erwin Petek, Sandy Thevarkunnel, et al.
The Journal of Biological Chemistry|March 10, 2005
Endothelial nitric-oxide synthase antisense (NOS3AS) gene encodes an autophagy-related protein (APG9-like2) highly expressed in trophoblastTakahiro Yamada, Andrew R Carson, Isabella Caniggia, et al.
Pageof 50