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

B Vincent

Showing results (501-510 of 551) with videos related to

Pageof 56
Sort By:
Molecular Psychiatry|April 12, 2017
Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous familiesR Harripaul, N Vasli, A Mikhailov, et al.
The New England Journal of Medicine|October 18, 2013
Deep dermatophytosis and inherited CARD9 deficiencyFanny Lanternier, Saad Pathan, Quentin B Vincent, et al.
Nature|December 15, 2015
Sublimation in bright spots on (1) CeresA Nathues, M Hoffmann, M Schaefer, et al.
Human Molecular Genetics|February 9, 2013
Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizuresAnath C Lionel, Andrea K Vaags, Daisuke Sato, et al.
Human Molecular Genetics|July 25, 2015
Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disabilityAbolfazl Heidari, Chanakan Tongsook, Reza Najafipour, et al.
American Journal of Human Genetics|February 7, 2008
Structural variation of chromosomes in autism spectrum disorderChristian R Marshall, Abdul Noor, John B Vincent, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 7, 2025
Species introductions shift seed dispersal potential more than extinctions across 120 island plant-frugivore communitiesJulia H Heinen, Donald R Drake, Kim McConkey, et al.
The Journal of Experimental Medicine|September 21, 2016
Dual T cell- and B cell-intrinsic deficiency in humans with biallelic RLTPR mutationsYi Wang, Cindy S Ma, Yun Ling, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 7, 2009
Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestryLaura J Scott, Pierandrea Muglia, Xiangyang Q Kong, et al.
Psychological Medicine|December 15, 2012
Estimating the heritability of reporting stressful life events captured by common genetic variantsR A Power, T Wingenbach, S Cohen-Woods, et al.
Pageof 56

Showing results (501-510 of 551) with videos related to

Sort By:
Pageof 56
Molecular Psychiatry|April 12, 2017
Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous familiesR Harripaul, N Vasli, A Mikhailov, et al.
The New England Journal of Medicine|October 18, 2013
Deep dermatophytosis and inherited CARD9 deficiencyFanny Lanternier, Saad Pathan, Quentin B Vincent, et al.
Nature|December 15, 2015
Sublimation in bright spots on (1) CeresA Nathues, M Hoffmann, M Schaefer, et al.
Human Molecular Genetics|February 9, 2013
Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizuresAnath C Lionel, Andrea K Vaags, Daisuke Sato, et al.
Human Molecular Genetics|July 25, 2015
Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disabilityAbolfazl Heidari, Chanakan Tongsook, Reza Najafipour, et al.
American Journal of Human Genetics|February 7, 2008
Structural variation of chromosomes in autism spectrum disorderChristian R Marshall, Abdul Noor, John B Vincent, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 7, 2025
Species introductions shift seed dispersal potential more than extinctions across 120 island plant-frugivore communitiesJulia H Heinen, Donald R Drake, Kim McConkey, et al.
The Journal of Experimental Medicine|September 21, 2016
Dual T cell- and B cell-intrinsic deficiency in humans with biallelic RLTPR mutationsYi Wang, Cindy S Ma, Yun Ling, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 7, 2009
Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestryLaura J Scott, Pierandrea Muglia, Xiangyang Q Kong, et al.
Psychological Medicine|December 15, 2012
Estimating the heritability of reporting stressful life events captured by common genetic variantsR A Power, T Wingenbach, S Cohen-Woods, et al.
Pageof 56