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Cuiping Hou

Showing results (51-60 of 78) with videos related to

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Human Molecular Genetics|June 16, 2018
Pathogenic variant in EPHB4 results in central conducting lymphatic anomalyDong Li, Tara L Wenger, Christoph Seiler, et al.
The American Journal of Psychiatry|January 17, 2008
No significant association of 14 candidate genes with schizophrenia in a large European ancestry sample: implications for psychiatric geneticsAlan R Sanders, Jubao Duan, Douglas F Levinson, et al.
American Journal of Human Genetics|October 19, 2010
A genome-wide study reveals copy number variants exclusive to childhood obesity casesJoseph T Glessner, Jonathan P Bradfield, Kai Wang, et al.
Scientific Reports|August 23, 2017
Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signalingDong Li, Xiao Chang, John J Connolly, et al.
Scientific Reports|June 21, 2017
A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signalingDong Li, Xiao Chang, John J Connolly, et al.
American Journal of Human Genetics|March 3, 2009
Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn DiseaseKai Wang, Haitao Zhang, Subra Kugathasan, et al.
Nature Genetics|May 5, 2009
Common variations in BARD1 influence susceptibility to high-risk neuroblastomaMario Capasso, Marcella Devoto, Cuiping Hou, et al.
Cancer Research|February 22, 2012
Common variation at BARD1 results in the expression of an oncogenic isoform that influences neuroblastoma susceptibility and oncogenicityKristopher R Bosse, Sharon J Diskin, Kristina A Cole, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|March 29, 2022
Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic AnalysisJin Li, Yun R Li, Joseph T Glessner, et al.
Nature|June 19, 2009
Copy number variation at 1q21.1 associated with neuroblastomaSharon J Diskin, Cuiping Hou, Joseph T Glessner, et al.
Pageof 8

Showing results (51-60 of 78) with videos related to

Sort By:
Pageof 8
Human Molecular Genetics|June 16, 2018
Pathogenic variant in EPHB4 results in central conducting lymphatic anomalyDong Li, Tara L Wenger, Christoph Seiler, et al.
The American Journal of Psychiatry|January 17, 2008
No significant association of 14 candidate genes with schizophrenia in a large European ancestry sample: implications for psychiatric geneticsAlan R Sanders, Jubao Duan, Douglas F Levinson, et al.
American Journal of Human Genetics|October 19, 2010
A genome-wide study reveals copy number variants exclusive to childhood obesity casesJoseph T Glessner, Jonathan P Bradfield, Kai Wang, et al.
Scientific Reports|August 23, 2017
Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signalingDong Li, Xiao Chang, John J Connolly, et al.
Scientific Reports|June 21, 2017
A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signalingDong Li, Xiao Chang, John J Connolly, et al.
American Journal of Human Genetics|March 3, 2009
Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn DiseaseKai Wang, Haitao Zhang, Subra Kugathasan, et al.
Nature Genetics|May 5, 2009
Common variations in BARD1 influence susceptibility to high-risk neuroblastomaMario Capasso, Marcella Devoto, Cuiping Hou, et al.
Cancer Research|February 22, 2012
Common variation at BARD1 results in the expression of an oncogenic isoform that influences neuroblastoma susceptibility and oncogenicityKristopher R Bosse, Sharon J Diskin, Kristina A Cole, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|March 29, 2022
Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic AnalysisJin Li, Yun R Li, Joseph T Glessner, et al.
Nature|June 19, 2009
Copy number variation at 1q21.1 associated with neuroblastomaSharon J Diskin, Cuiping Hou, Joseph T Glessner, et al.
Pageof 8