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

W Scherer

Showing results (751-760 of 915) with videos related to

Pageof 92
Sort By:
JAMA Psychiatry|May 9, 2025
Genetic Architecture and Risk of Childhood Maltreatment Across 5 Psychiatric DiagnosesTrine Tollerup Nielsen, Paraskevi Bali, Jakob Grove, et al.
American Journal of Human Genetics|October 13, 2006
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxiaLars Feuk, Aino Kalervo, Marita Lipsanen-Nyman, et al.
Nature Biotechnology|May 10, 2011
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variantsDalila Pinto, Katayoon Darvishi, Xinghua Shi, et al.
Nature Genetics|October 5, 2001
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2S Hadano, C K Hand, H Osuga, et al.
Nature Communications|December 6, 2019
Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disordersL D'Abate, S Walker, R K C Yuen, et al.
NPJ Genomic Medicine|July 2, 2025
Assessing the diagnostic impact of blood transcriptome profiling in a pediatric cohort previously assessed by genome sequencingHuayun Hou, Kyoko E Yuki, Gregory Costain, et al.
Molecular Autism|April 12, 2014
Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disordersCatarina T Correia, Inês C Conceição, Bárbara Oliveira, et al.
American Journal of Human Genetics|January 13, 2005
Identification of C7orf11 (TTDN1) gene mutations and genetic heterogeneity in nonphotosensitive trichothiodystrophyKazuhiko Nakabayashi, Daniela Amann, Yan Ren, et al.
Clinical Chemistry|October 29, 2005
Population differences in the polyalanine domain and 6 new mutations in HLXB9 in patients with Currarino syndromeMercè Garcia-Barceló, Man-Ting So, Danny Ko-Chun Lau, et al.
Human Mutation|May 27, 2015
Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental RetardationLaura Addis, Joo Wook Ahn, Richard Dobson, et al.
Pageof 92

Showing results (751-760 of 915) with videos related to

Sort By:
Pageof 92
JAMA Psychiatry|May 9, 2025
Genetic Architecture and Risk of Childhood Maltreatment Across 5 Psychiatric DiagnosesTrine Tollerup Nielsen, Paraskevi Bali, Jakob Grove, et al.
American Journal of Human Genetics|October 13, 2006
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxiaLars Feuk, Aino Kalervo, Marita Lipsanen-Nyman, et al.
Nature Biotechnology|May 10, 2011
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variantsDalila Pinto, Katayoon Darvishi, Xinghua Shi, et al.
Nature Genetics|October 5, 2001
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2S Hadano, C K Hand, H Osuga, et al.
Nature Communications|December 6, 2019
Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disordersL D'Abate, S Walker, R K C Yuen, et al.
NPJ Genomic Medicine|July 2, 2025
Assessing the diagnostic impact of blood transcriptome profiling in a pediatric cohort previously assessed by genome sequencingHuayun Hou, Kyoko E Yuki, Gregory Costain, et al.
Molecular Autism|April 12, 2014
Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disordersCatarina T Correia, Inês C Conceição, Bárbara Oliveira, et al.
American Journal of Human Genetics|January 13, 2005
Identification of C7orf11 (TTDN1) gene mutations and genetic heterogeneity in nonphotosensitive trichothiodystrophyKazuhiko Nakabayashi, Daniela Amann, Yan Ren, et al.
Clinical Chemistry|October 29, 2005
Population differences in the polyalanine domain and 6 new mutations in HLXB9 in patients with Currarino syndromeMercè Garcia-Barceló, Man-Ting So, Danny Ko-Chun Lau, et al.
Human Mutation|May 27, 2015
Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental RetardationLaura Addis, Joo Wook Ahn, Richard Dobson, et al.
Pageof 92