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Leonard Rappaport

Showing results (11-20 of 18) with videos related to

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Plos One|April 19, 2012
The co-morbidity burden of children and young adults with autism spectrum disordersIsaac S Kohane, Andrew McMurry, Griffin Weber, et al.
The Journal of Clinical Investigation|April 3, 2009
Comment on "Autistic-like phenotypes in Cadps2-knockout mice and aberrant CADPS2 splicing in autistic patients"Alal Eran, Kaitlin R Graham, Kayla Vatalaro, et al.
Plos One|December 11, 2012
Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disordersSek Won Kong, Christin D Collins, Yuko Shimizu-Motohashi, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 14, 2014
Safety, pharmacokinetics, and preliminary assessment of efficacy of mecasermin (recombinant human IGF-1) for the treatment of Rett syndromeOmar S Khwaja, Eugenia Ho, Katherine V Barnes, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 15, 2010
Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disordersMichael S L Ching, Yiping Shen, Wen-Hann Tan, et al.
Pediatrics|March 17, 2010
Clinical genetic testing for patients with autism spectrum disordersYiping Shen, Kira A Dies, Ingrid A Holm, et al.
Neuron|January 29, 2013
Using whole-exome sequencing to identify inherited causes of autismTimothy W Yu, Maria H Chahrour, Michael E Coulter, et al.
American Journal of Human Genetics|October 17, 2024
MARK2 variants cause autism spectrum disorder via the downregulation of WNT/β-catenin signaling pathwayMaolei Gong, Jiayi Li, Zailong Qin, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Plos One|April 19, 2012
The co-morbidity burden of children and young adults with autism spectrum disordersIsaac S Kohane, Andrew McMurry, Griffin Weber, et al.
The Journal of Clinical Investigation|April 3, 2009
Comment on "Autistic-like phenotypes in Cadps2-knockout mice and aberrant CADPS2 splicing in autistic patients"Alal Eran, Kaitlin R Graham, Kayla Vatalaro, et al.
Plos One|December 11, 2012
Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disordersSek Won Kong, Christin D Collins, Yuko Shimizu-Motohashi, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 14, 2014
Safety, pharmacokinetics, and preliminary assessment of efficacy of mecasermin (recombinant human IGF-1) for the treatment of Rett syndromeOmar S Khwaja, Eugenia Ho, Katherine V Barnes, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 15, 2010
Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disordersMichael S L Ching, Yiping Shen, Wen-Hann Tan, et al.
Pediatrics|March 17, 2010
Clinical genetic testing for patients with autism spectrum disordersYiping Shen, Kira A Dies, Ingrid A Holm, et al.
Neuron|January 29, 2013
Using whole-exome sequencing to identify inherited causes of autismTimothy W Yu, Maria H Chahrour, Michael E Coulter, et al.
American Journal of Human Genetics|October 17, 2024
MARK2 variants cause autism spectrum disorder via the downregulation of WNT/β-catenin signaling pathwayMaolei Gong, Jiayi Li, Zailong Qin, et al.
Pageof 2