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Guiqing Cai

Showing results (21-30 of 34) with videos related to

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Genomics|June 8, 2013
Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNAChad M Schafer, Nicholas G Campbell, Guiqing Cai, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 12, 2009
Association between methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and age of onset in schizophreniaMaria Vares, Peter Saetre, Hong Deng, et al.
BMC Medical Genomics|October 18, 2008
Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: efficient identification of known microduplications and identification of a novel microduplication in ASMTGuiqing Cai, Lisa Edelmann, Juliet E Goldsmith, et al.
Molecular Autism|June 14, 2013
Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiencyLatha Soorya, Alexander Kolevzon, Jessica Zweifach, et al.
Plos One|August 31, 2013
Characterization of SLITRK1 variation in obsessive-compulsive disorderUzoezi Ozomaro, Guiqing Cai, Yuji Kajiwara, et al.
Molecular Genetics & Genomic Medicine|December 28, 2019
Lessons learned from expanded reproductive carrier screening in self-reported Ashkenazi, Sephardi, and Mizrahi Jewish patientsGidon Akler, Ashley H Birch, Nicole Schreiber-Agus, et al.
Human Molecular Genetics|April 18, 2015
Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesisRobert A Kozol, Holly N Cukier, Bing Zou, et al.
Plos Genetics|October 2, 2010
Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalitiesAdam C Naj, Gary W Beecham, Eden R Martin, et al.
American Journal of Human Genetics|February 8, 2011
Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosaStephan Züchner, Julia Dallman, Rong Wen, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 9, 2012
A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autismPatrícia B S Celestino-Soper, Sara Violante, Emily L Crawford, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Genomics|June 8, 2013
Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNAChad M Schafer, Nicholas G Campbell, Guiqing Cai, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 12, 2009
Association between methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and age of onset in schizophreniaMaria Vares, Peter Saetre, Hong Deng, et al.
BMC Medical Genomics|October 18, 2008
Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: efficient identification of known microduplications and identification of a novel microduplication in ASMTGuiqing Cai, Lisa Edelmann, Juliet E Goldsmith, et al.
Molecular Autism|June 14, 2013
Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiencyLatha Soorya, Alexander Kolevzon, Jessica Zweifach, et al.
Plos One|August 31, 2013
Characterization of SLITRK1 variation in obsessive-compulsive disorderUzoezi Ozomaro, Guiqing Cai, Yuji Kajiwara, et al.
Molecular Genetics & Genomic Medicine|December 28, 2019
Lessons learned from expanded reproductive carrier screening in self-reported Ashkenazi, Sephardi, and Mizrahi Jewish patientsGidon Akler, Ashley H Birch, Nicole Schreiber-Agus, et al.
Human Molecular Genetics|April 18, 2015
Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesisRobert A Kozol, Holly N Cukier, Bing Zou, et al.
Plos Genetics|October 2, 2010
Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalitiesAdam C Naj, Gary W Beecham, Eden R Martin, et al.
American Journal of Human Genetics|February 8, 2011
Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosaStephan Züchner, Julia Dallman, Rong Wen, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 9, 2012
A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autismPatrícia B S Celestino-Soper, Sara Violante, Emily L Crawford, et al.
Pageof 4