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Clara M Lajonchere

Showing results (1-10 of 10) with videos related to

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Neuron|October 20, 2010
Changing the landscape of autism research: the autism genetic resource exchangeClara M Lajonchere,
Vision Research|March 10, 2006
Attentional modulation of the gap effectJay Pratt, Clara M Lajonchere, Richard A Abrams
Journal of Autism and Developmental Disorders|November 14, 2015
Strategies for Disseminating Information on Biomedical Research on Autism to Hispanic ParentsClara M Lajonchere, Barbara Y Wheeler, Thomas W Valente, 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.
Proceedings of the National Academy of Sciences of the United States of America|April 6, 2026
Toward the simultaneous detection of multiple diseases with a highly cost-effective cell-free DNA methylome testWeihua Zeng, Chun-Chi Liu, Shuo Li, 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 Genetics|October 27, 2009
Microduplications of 16p11.2 are associated with schizophreniaShane E McCarthy, Vladimir Makarov, George Kirov, et al.
Human Molecular Genetics|July 31, 2012
Individual common variants exert weak effects on the risk for autism spectrum disordersRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Human Molecular Genetics|July 29, 2010
A genome-wide scan for common alleles affecting risk for autismRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Nature|June 10, 2010
Functional impact of global rare copy number variation in autism spectrum disordersDalila Pinto, Alistair T Pagnamenta, Lambertus Klei, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Neuron|October 20, 2010
Changing the landscape of autism research: the autism genetic resource exchangeClara M Lajonchere,
Vision Research|March 10, 2006
Attentional modulation of the gap effectJay Pratt, Clara M Lajonchere, Richard A Abrams
Journal of Autism and Developmental Disorders|November 14, 2015
Strategies for Disseminating Information on Biomedical Research on Autism to Hispanic ParentsClara M Lajonchere, Barbara Y Wheeler, Thomas W Valente, 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.
Proceedings of the National Academy of Sciences of the United States of America|April 6, 2026
Toward the simultaneous detection of multiple diseases with a highly cost-effective cell-free DNA methylome testWeihua Zeng, Chun-Chi Liu, Shuo Li, 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 Genetics|October 27, 2009
Microduplications of 16p11.2 are associated with schizophreniaShane E McCarthy, Vladimir Makarov, George Kirov, et al.
Human Molecular Genetics|July 31, 2012
Individual common variants exert weak effects on the risk for autism spectrum disordersRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Human Molecular Genetics|July 29, 2010
A genome-wide scan for common alleles affecting risk for autismRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Nature|June 10, 2010
Functional impact of global rare copy number variation in autism spectrum disordersDalila Pinto, Alistair T Pagnamenta, Lambertus Klei, et al.
Pageof 1