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Showing results (641-650 of 915) with videos related to

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Nature Genetics|May 27, 2014
Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorderMohammed Uddin, Kristiina Tammimies, Giovanna Pellecchia, et al.
Plos Genetics|September 15, 2010
Identifying signatures of natural selection in Tibetan and Andean populations using dense genome scan dataAbigail Bigham, Marc Bauchet, Dalila Pinto, et al.
Nature Genetics|June 16, 1999
The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier proteinK Kobayashi, D S Sinasac, M Iijima, et al.
BMC Genomics|October 22, 2016
The Third International Genomic Medicine Conference (3rd IGMC, 2015): overall activities and outcome highlightsMuhammad Abu-Elmagd, Mourad Assidi, Ashraf Dallol, et al.
Genomics|May 18, 1999
A physical and transcriptional map of the preaxial polydactyly locus on chromosome 7q36H C Heus, A Hing, M J van Baren, et al.
Nature Communications|August 4, 2015
Clinically relevant copy number variations detected in cerebral palsyMaryam Oskoui, Matthew J Gazzellone, Bhooma Thiruvahindrapuram, et al.
Springerplus|July 8, 2016
Ankrd11 is a chromatin regulator involved in autism that is essential for neural developmentAnastassia Voronova, Denis Gallagher, Mark Zander, et al.
Blood|January 8, 2017
Biallelic mutations in <i>DNAJC21</i> cause Shwachman-Diamond syndromeSanthosh Dhanraj, Anna Matveev, Hongbing Li, et al.
Molecular Genetics and Genomics : MGG|October 18, 2006
Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndromeErwin Petek, Thomas Schwarzbraun, Abdul Noor, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 28, 2025
Rare variants in <i>BMAL1</i> are associated with a neurodevelopmental syndromeVishnu Anand Cuddapah, Dechun Chen, Bumsik Cho, et al.
Pageof 92

Showing results (641-650 of 915) with videos related to

Sort By:
Pageof 92
Nature Genetics|May 27, 2014
Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorderMohammed Uddin, Kristiina Tammimies, Giovanna Pellecchia, et al.
Plos Genetics|September 15, 2010
Identifying signatures of natural selection in Tibetan and Andean populations using dense genome scan dataAbigail Bigham, Marc Bauchet, Dalila Pinto, et al.
Nature Genetics|June 16, 1999
The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier proteinK Kobayashi, D S Sinasac, M Iijima, et al.
BMC Genomics|October 22, 2016
The Third International Genomic Medicine Conference (3rd IGMC, 2015): overall activities and outcome highlightsMuhammad Abu-Elmagd, Mourad Assidi, Ashraf Dallol, et al.
Genomics|May 18, 1999
A physical and transcriptional map of the preaxial polydactyly locus on chromosome 7q36H C Heus, A Hing, M J van Baren, et al.
Nature Communications|August 4, 2015
Clinically relevant copy number variations detected in cerebral palsyMaryam Oskoui, Matthew J Gazzellone, Bhooma Thiruvahindrapuram, et al.
Springerplus|July 8, 2016
Ankrd11 is a chromatin regulator involved in autism that is essential for neural developmentAnastassia Voronova, Denis Gallagher, Mark Zander, et al.
Blood|January 8, 2017
Biallelic mutations in <i>DNAJC21</i> cause Shwachman-Diamond syndromeSanthosh Dhanraj, Anna Matveev, Hongbing Li, et al.
Molecular Genetics and Genomics : MGG|October 18, 2006
Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndromeErwin Petek, Thomas Schwarzbraun, Abdul Noor, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 28, 2025
Rare variants in <i>BMAL1</i> are associated with a neurodevelopmental syndromeVishnu Anand Cuddapah, Dechun Chen, Bumsik Cho, et al.
Pageof 92