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Matthew E Hurles

Showing results (81-90 of 188) with videos related to

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American Journal of Human Genetics|June 26, 2012
Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disordersRui Luo, Stephan J Sanders, Yuan Tian, et al.
Genome Medicine|October 31, 2025
Investigating the interplay between prematurity and genetic variation in the context of rare developmental disordersOlivia Wootton, Patrick Campbell, Sarah Richardson, et al.
Genome Biology|October 27, 2007
Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridizationJohn C Marioni, Natalie P Thorne, Armand Valsesia, et al.
Nature Communications|August 23, 2017
Estimating the human mutation rate from autozygous segments reveals population differences in human mutational processesVagheesh M Narasimhan, Raheleh Rahbari, Aylwyn Scally, et al.
Nature Genetics|April 9, 2013
Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesityEleanor Wheeler, Ni Huang, Elena G Bochukova, et al.
Genome Research|July 1, 2006
Copy number variation: new insights in genome diversityJennifer L Freeman, George H Perry, Lars Feuk, et al.
Genome Biology|May 21, 2010
Towards a comprehensive structural variation map of an individual human genomeAndy W Pang, Jeffrey R MacDonald, Dalila Pinto, et al.
Human Mutation|September 11, 2018
Analysis of novel missense ATR mutations reveals new splicing defects underlying Seckel syndromeMarta Llorens-Agost, Janna Luessing, Amandine van Beneden, et al.
Genome Research|September 9, 2008
Copy number variation and evolution in humans and chimpanzeesGeorge H Perry, Fengtang Yang, Tomas Marques-Bonet, et al.
Genome Research|November 24, 2006
Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arraysDaisuke Komura, Fan Shen, Shumpei Ishikawa, et al.
Pageof 19

Showing results (81-90 of 188) with videos related to

Sort By:
Pageof 19
American Journal of Human Genetics|June 26, 2012
Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disordersRui Luo, Stephan J Sanders, Yuan Tian, et al.
Genome Medicine|October 31, 2025
Investigating the interplay between prematurity and genetic variation in the context of rare developmental disordersOlivia Wootton, Patrick Campbell, Sarah Richardson, et al.
Genome Biology|October 27, 2007
Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridizationJohn C Marioni, Natalie P Thorne, Armand Valsesia, et al.
Nature Communications|August 23, 2017
Estimating the human mutation rate from autozygous segments reveals population differences in human mutational processesVagheesh M Narasimhan, Raheleh Rahbari, Aylwyn Scally, et al.
Nature Genetics|April 9, 2013
Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesityEleanor Wheeler, Ni Huang, Elena G Bochukova, et al.
Genome Research|July 1, 2006
Copy number variation: new insights in genome diversityJennifer L Freeman, George H Perry, Lars Feuk, et al.
Genome Biology|May 21, 2010
Towards a comprehensive structural variation map of an individual human genomeAndy W Pang, Jeffrey R MacDonald, Dalila Pinto, et al.
Human Mutation|September 11, 2018
Analysis of novel missense ATR mutations reveals new splicing defects underlying Seckel syndromeMarta Llorens-Agost, Janna Luessing, Amandine van Beneden, et al.
Genome Research|September 9, 2008
Copy number variation and evolution in humans and chimpanzeesGeorge H Perry, Fengtang Yang, Tomas Marques-Bonet, et al.
Genome Research|November 24, 2006
Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arraysDaisuke Komura, Fan Shen, Shumpei Ishikawa, et al.
Pageof 19