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Showing results (831-840 of 915) with videos related to

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Molecular Psychiatry|February 18, 2021
RCL1 copy number variants are associated with a range of neuropsychiatric phenotypesCatherine A Brownstein, Richard S Smith, Lance H Rodan, et al.
Plos Biology|September 7, 2007
The diploid genome sequence of an individual humanSamuel Levy, Granger Sutton, Pauline C Ng, et al.
Nature Genetics|May 1, 1997
Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomasL Schmidt, F M Duh, F Chen, et al.
Molecular Psychiatry|May 12, 2016
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disordersO Mercati, G Huguet, A Danckaert, et al.
American Journal of Human Genetics|July 16, 2013
Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencingYong-hui Jiang, Ryan K C Yuen, Xin Jin, et al.
Nature|February 21, 2012
Clonal selection drives genetic divergence of metastatic medulloblastomaXiaochong Wu, Paul A Northcott, Adrian Dubuc, et al.
NPJ Genomic Medicine|March 15, 2022
Whole genome sequencing delineates regulatory, copy number, and cryptic splice variants in early onset cardiomyopathyRobert Lesurf, Abdelrahman Said, Oyediran Akinrinade, et al.
Human Molecular Genetics|May 17, 2023
ANK2 loss-of-function variants are associated with epilepsy, and lead to impaired axon initial segment plasticity and hyperactive network activity in hiPSC-derived neuronal networksMaria W A Teunissen, Elly Lewerissa, Eline J H van Hugte, et al.
Molecular Psychiatry|July 24, 2024
Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplicationsRuben C Gur, Carrie E Bearden, Sebastien Jacquemont, et al.
Brain : a Journal of Neurology|August 18, 2022
CAPRIN1 haploinsufficiency causes a neurodevelopmental disorder with language impairment, ADHD and ASDLisa Pavinato, Andrea Delle Vedove, Diana Carli, et al.
Pageof 92

Showing results (831-840 of 915) with videos related to

Sort By:
Pageof 92
Molecular Psychiatry|February 18, 2021
RCL1 copy number variants are associated with a range of neuropsychiatric phenotypesCatherine A Brownstein, Richard S Smith, Lance H Rodan, et al.
Plos Biology|September 7, 2007
The diploid genome sequence of an individual humanSamuel Levy, Granger Sutton, Pauline C Ng, et al.
Nature Genetics|May 1, 1997
Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomasL Schmidt, F M Duh, F Chen, et al.
Molecular Psychiatry|May 12, 2016
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disordersO Mercati, G Huguet, A Danckaert, et al.
American Journal of Human Genetics|July 16, 2013
Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencingYong-hui Jiang, Ryan K C Yuen, Xin Jin, et al.
Nature|February 21, 2012
Clonal selection drives genetic divergence of metastatic medulloblastomaXiaochong Wu, Paul A Northcott, Adrian Dubuc, et al.
NPJ Genomic Medicine|March 15, 2022
Whole genome sequencing delineates regulatory, copy number, and cryptic splice variants in early onset cardiomyopathyRobert Lesurf, Abdelrahman Said, Oyediran Akinrinade, et al.
Human Molecular Genetics|May 17, 2023
ANK2 loss-of-function variants are associated with epilepsy, and lead to impaired axon initial segment plasticity and hyperactive network activity in hiPSC-derived neuronal networksMaria W A Teunissen, Elly Lewerissa, Eline J H van Hugte, et al.
Molecular Psychiatry|July 24, 2024
Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplicationsRuben C Gur, Carrie E Bearden, Sebastien Jacquemont, et al.
Brain : a Journal of Neurology|August 18, 2022
CAPRIN1 haploinsufficiency causes a neurodevelopmental disorder with language impairment, ADHD and ASDLisa Pavinato, Andrea Delle Vedove, Diana Carli, et al.
Pageof 92