Kai Wang

发表

Common genetic variants on 5p14.1 associate with autism spectrum disorders

Robert T. Schultz, Margaret A. Pericak-Vance, Takeshi Sakurai, 2009, Nature.

Examination of Type 2 Diabetes Loci Implicates CDKAL1 as a Birth Weight Gene

Joseph T. Glessner, Hakon Hakonarson, Patrick Sleiman, 2009, Diabetes.

A genome-wide study reveals copy number variants exclusive to childhood obesity cases.

Hakon Hakonarson, Cuiping Hou, J. Glessner, 2010, American journal of human genetics.

Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects.

Constantin Polychronakos, David C Wilson, Joseph T. Glessner, 2010, Human molecular genetics.

Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes

John A. Sweeney, Geraldine Dawson, Daniel H. Geschwind, 2009, PLoS genetics.

A Genome-Wide Association Study on Obesity and Obesity-Related Traits

Hongyu Zhao, Struan F. A. Grant, Joseph T. Glessner, 2011, PloS one.

Rare Variants Create Synthetic Genome-Wide Associations

David B. Goldstein, Samuel P. Dickson, Hakon Hakonarson, 2010, PLoS biology.

Convergent mechanisms of somatic mutations in polycythemia vera.

Hakon Hakonarson, H. Hakonarson, Kai Wang, 2010, Discovery medicine.

Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications.

Jianxin Shi, Pablo V Gejman, Frank Dudbridge, 2011, The American journal of psychiatry.

Integrative genomics identifies LMO1 as a neuroblastoma oncogene

Nazneen Rahman, Sharon J. Diskin, John M. Maris, 2011, Nature.

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

Susanne Walitza, Aribert Rothenberger, Takeshi Sakurai, 2011, Nature Genetics.

Genome-wide association study of multiplex schizophrenia pedigrees.

Jianxin Shi, Stephan Ripke, Pablo V Gejman, 2012, The American journal of psychiatry.

Population-based study of genetic variation in individuals with autism spectrum disorders from Croatia

Li-San Wang, Hakon Hakonarson, Maja Bucan, 2010, BMC Medical Genetics.

Modeling genetic inheritance of copy number variations

Mahlet G. Tadesse, Struan F. A. Grant, Joseph T. Glessner, 2008, Nucleic acids research.

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

Tariq Ahmad, Albert Cohen, Judy H Cho, 2010, Nature Genetics.

A Genome-Wide Meta-Analysis of Six Type 1 Diabetes Cohorts Identifies Multiple Associated Loci

Constantin Polychronakos, Struan F. A. Grant, Joseph T. Glessner, 2011, PLoS genetics.

Ranking causal variants and associated regions in genome-wide association studies by the support vector machine and random forest

Satish Chikkagoudar, Hakon Hakonarson, Usman Roshan, 2011, Nucleic acids research.

Interpretation of association signals and identification of causal variants from genome-wide association studies.

Samuel P. Dickson, Hakon Hakonarson, David B Goldstein, 2010, American journal of human genetics.

Copy number variation at 1q21.1 associated with neuroblastoma

Sharon J. Diskin, John M. Maris, Struan F. A. Grant, 2009, Nature.

Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms

Sharon J. Diskin, John M. Maris, Joseph T. Glessner, 2008, Nucleic acids research.

Long-read sequencing identified intronic repeat expansions in SAMD12 from Chinese pedigrees affected with familial cortical myoclonic tremor with epilepsy

Nan Li, Li Fang, Qian Liu, 2018, Journal of Medical Genetics.

Variants of DENND1B associated with asthma in children.

Ingo Ruczinski, James Flory, Terri H Beaty, 2010, The New England journal of medicine.

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Robert T. Schultz, Takeshi Sakurai, Joseph Piven, 2009, Nature.

A genome-wide association study identifies a locus for nonsyndromic cleft lip with or without cleft palate on 8q24.

Joseph T. Glessner, Hakon Hakonarson, J. Glessner, 2009, The Journal of pediatrics.

Association between a high-risk autism locus on 5p14 and social communication spectrum phenotypes in the general population.

Joseph T. Glessner, Hakon Hakonarson, Jean Golding, 2010, The American journal of psychiatry.

Duplication of the SLIT3 Locus on 5q35.1 Predisposes to Major Depressive Disorder

Struan F. A. Grant, Joseph T. Glessner, Hakon Hakonarson, 2010, PloS one.

Large Copy-Number Variations Are Enriched in Cases With Moderate to Extreme Obesity

Joseph T. Glessner, Hakon Hakonarson, J. Glessner, 2010, Diabetes.

Common variants at five new loci associated with early-onset inflammatory bowel disease

Johan Van Limbergen, David C Wilson, David C. Wilson, 2009, Nature Genetics.

A genome-wide scan for common alleles affecting risk for autism

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2010, Human molecular genetics.

Gene-based interaction analysis by incorporating external linkage disequilibrium information

Jing He, Chun Li, Kai Wang, 2010, European Journal of Human Genetics.

A genome wide association study of plasma uric acid levels in obese cases and never-overweight controls

Hongyu Zhao, Joseph T. Glessner, Hakon Hakonarson, 2013, Obesity.