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Maja Bucan

Showing results (41-50 of 51) with videos related to

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Molecular Psychiatry|June 30, 2018
Rediscovering the value of families for psychiatric genetics researchDavid C Glahn, Vishwajit L Nimgaonkar, Henriette Raventós, et al.
Nature|February 22, 2008
Genotype, haplotype and copy-number variation in worldwide human populationsMattias Jakobsson, Sonja W Scholz, Paul Scheet, et al.
Science (New York, N.Y.)|September 11, 2020
Transcriptomic signatures across human tissues identify functional rare genetic variationNicole M Ferraro, Benjamin J Strober, Jonah Einson, et al.
Plos Genetics|June 27, 2009
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genesMaja Bucan, Brett S Abrahams, Kai Wang, et al.
Nature Genetics|September 2, 2004
The knockout mouse projectChristopher P Austin, James F Battey, Allan Bradley, et al.
Nature Communications|February 2, 2020
Human and mouse essentiality screens as a resource for disease gene discoveryPilar Cacheiro, Violeta Muñoz-Fuentes, Stephen A Murray, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 8, 2018
Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variantsLucilla Pizzo, Matthew Jensen, Andrew Polyak, et al.
Nature|May 1, 2009
Common genetic variants on 5p14.1 associate with autism spectrum disordersKai Wang, Haitao Zhang, Deqiong Ma, et al.
Nature|May 1, 2009
Autism genome-wide copy number variation reveals ubiquitin and neuronal genesJoseph T Glessner, Kai Wang, Guiqing Cai, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 8, 2026
Characterization of the genotypic and phenotypic spectrum of TCF7L2-related neurodevelopmental disorder (TRND)Sally Nijim, Mimi Kim, Melissa Denish, et al.
Pageof 6

Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
Molecular Psychiatry|June 30, 2018
Rediscovering the value of families for psychiatric genetics researchDavid C Glahn, Vishwajit L Nimgaonkar, Henriette Raventós, et al.
Nature|February 22, 2008
Genotype, haplotype and copy-number variation in worldwide human populationsMattias Jakobsson, Sonja W Scholz, Paul Scheet, et al.
Science (New York, N.Y.)|September 11, 2020
Transcriptomic signatures across human tissues identify functional rare genetic variationNicole M Ferraro, Benjamin J Strober, Jonah Einson, et al.
Plos Genetics|June 27, 2009
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genesMaja Bucan, Brett S Abrahams, Kai Wang, et al.
Nature Genetics|September 2, 2004
The knockout mouse projectChristopher P Austin, James F Battey, Allan Bradley, et al.
Nature Communications|February 2, 2020
Human and mouse essentiality screens as a resource for disease gene discoveryPilar Cacheiro, Violeta Muñoz-Fuentes, Stephen A Murray, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 8, 2018
Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variantsLucilla Pizzo, Matthew Jensen, Andrew Polyak, et al.
Nature|May 1, 2009
Common genetic variants on 5p14.1 associate with autism spectrum disordersKai Wang, Haitao Zhang, Deqiong Ma, et al.
Nature|May 1, 2009
Autism genome-wide copy number variation reveals ubiquitin and neuronal genesJoseph T Glessner, Kai Wang, Guiqing Cai, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 8, 2026
Characterization of the genotypic and phenotypic spectrum of TCF7L2-related neurodevelopmental disorder (TRND)Sally Nijim, Mimi Kim, Melissa Denish, et al.
Pageof 6