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Showing results (61-70 of 78) with videos related to

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The New England Journal of Medicine|May 9, 2008
Chromosome 6p22 locus associated with clinically aggressive neuroblastomaJohn M Maris, Yael P Mosse, Jonathan P Bradfield, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 22, 2010
Strong synaptic transmission impact by copy number variations in schizophreniaJoseph T Glessner, Muredach P Reilly, Cecilia E Kim, et al.
American Journal of Human Genetics|June 5, 2013
Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosisJohn A Martignetti, Lifeng Tian, Dong Li, et al.
American Journal of Human Genetics|January 10, 2006
Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sampleBrian K Suarez, Jubao Duan, Alan R Sanders, et al.
Nature|December 3, 2010
Integrative genomics identifies LMO1 as a neuroblastoma oncogeneKai Wang, Sharon J Diskin, Haitao Zhang, et al.
BMC Medical Genetics|March 24, 2016
Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibilityTerri H Finkel, Jin Li, Zhi Wei, et al.
JCI Insight|May 8, 2023
Lymphatic disorders caused by mosaic, activating KRAS variants respond to MEK inhibitionSarah E Sheppard, Michael E March, Christoph Seiler, et al.
Human Molecular Genetics|February 24, 2010
Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effectsKai Wang, Robert Baldassano, Haitao Zhang, et al.
Nature Communications|January 16, 2020
Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associationsYun Rose Li, Joseph T Glessner, Bradley P Coe, et al.
Nature Medicine|June 1, 2023
Genomic profiling informs diagnoses and treatment in vascular anomaliesDong Li, Sarah E Sheppard, Michael E March, et al.
Pageof 8

Showing results (61-70 of 78) with videos related to

Sort By:
Pageof 8
The New England Journal of Medicine|May 9, 2008
Chromosome 6p22 locus associated with clinically aggressive neuroblastomaJohn M Maris, Yael P Mosse, Jonathan P Bradfield, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 22, 2010
Strong synaptic transmission impact by copy number variations in schizophreniaJoseph T Glessner, Muredach P Reilly, Cecilia E Kim, et al.
American Journal of Human Genetics|June 5, 2013
Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosisJohn A Martignetti, Lifeng Tian, Dong Li, et al.
American Journal of Human Genetics|January 10, 2006
Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sampleBrian K Suarez, Jubao Duan, Alan R Sanders, et al.
Nature|December 3, 2010
Integrative genomics identifies LMO1 as a neuroblastoma oncogeneKai Wang, Sharon J Diskin, Haitao Zhang, et al.
BMC Medical Genetics|March 24, 2016
Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibilityTerri H Finkel, Jin Li, Zhi Wei, et al.
JCI Insight|May 8, 2023
Lymphatic disorders caused by mosaic, activating KRAS variants respond to MEK inhibitionSarah E Sheppard, Michael E March, Christoph Seiler, et al.
Human Molecular Genetics|February 24, 2010
Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effectsKai Wang, Robert Baldassano, Haitao Zhang, et al.
Nature Communications|January 16, 2020
Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associationsYun Rose Li, Joseph T Glessner, Bradley P Coe, et al.
Nature Medicine|June 1, 2023
Genomic profiling informs diagnoses and treatment in vascular anomaliesDong Li, Sarah E Sheppard, Michael E March, et al.
Pageof 8