Kelly A. Thomas

发表

Strong synaptic transmission impact by copy number variations in schizophrenia

Raquel E. Gur, Mark Weiser, Muredach P. Reilly, 2010, Proceedings of the National Academy of Sciences.

Copy Number Variations in Alternative Splicing Gene Networks Impact Lifespan

Vilmundur Gudnason, Lenore J. Launer, Tamara B. Harris, 2013, PloS one.

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

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

Copy Number Variations in CTNNA3 and RBFOX1 Associate with Pediatric Food Allergy

Joseph T. Glessner, Frank D. Mentch, Hakon Hakonarson, 2015, The Journal of Immunology.

Whole-genome DNA/RNA sequencing identifies truncating mutations in RBCK1 in a novel Mendelian disease with neuromuscular and cardiac involvement

H. Hakonarson, Cecilia Kim, E. Toskala, 2013, Genome Medicine.

Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk

Joseph T. Glessner, J. Glessner, H. Hakonarson, 2017, Nature Communications.

Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases

Constantin Polychronakos, Yiran Guo, Dong Li, 2016 .

The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

Thomas Bourgeron, Ellen M. Wijsman, Gillian Baird, 2014, Nature Communications.

Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population

Joseph T. Glessner, J. Glessner, H. Hakonarson, 2014, Molecular Autism.

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

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

Identification of Rare Recurrent Copy Number Variants in High-Risk Autism Families and Their Prevalence in a Large ASD Population

H. Hakonarson, Cecilia Kim, D. Hadley, 2013, PloS one.

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.

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height.

Tom R. Gaunt, Tom S. Price, Joseph T. Glessner, 2011, American journal of human genetics.

Role of BMI‐Associated Loci Identified in GWAS Meta‐Analyses in the Context of Common Childhood Obesity in European Americans

Joseph T. Glessner, Hakon Hakonarson, J. Glessner, 2011, Obesity.

The Role of Obesity‐associated Loci Identified in Genome‐wide Association Studies in the Determination of Pediatric BMI

Joseph T. Glessner, Ryan M. Smith, J. Glessner, 2009, Obesity.

GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.

Yiran Guo, Joseph T. Glessner, Hakon Hakonarson, 2013, Human molecular genetics.

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.

Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies

Marylyn D. Ritchie, Shefali S. Verma, Kelly A. Birdwell, 2015, Genome Medicine.

Examination of genetic variants influencing lipid traits in pediatric populations

Joseph T. Glessner, Alexa J Moy, J. Glessner, 2012, Journal of Pediatric Genetics.

Genetic sharing and heritability of paediatric age of onset autoimmune diseases

Hongzhe Li, Constantin Polychronakos, Yiran Guo, 2015, Nature Communications.

Common variants at 5q22 associate with pediatric eosinophilic esophagitis

Joseph T. Glessner, Lisa J. Martin, J. Glessner, 2010, Nature Genetics.

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.

Investigation of the Locus Near MC4R With Childhood Obesity in Americans of European and African Ancestry

Joseph T. Glessner, Ryan M. Smith, J. Glessner, 2009, Obesity.

GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus

Joseph T. Glessner, J. Glessner, H. Hakonarson, 2013, Scientific Reports.

Variants of DENND1B associated with asthma in children.

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

Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing gene

A. Uitterlinden, H. Hakonarson, F. Rivadeneira, 2016, Nature Communications.

Whole-genome DNA/RNA sequencing identifies truncating mutations in RBCK1 in a novel Mendelian disease with neuromuscular and cardiac involvement

H. Hakonarson, Cecilia Kim, J. Bradfield, 2013, Genome Medicine.

Genome-Wide Association Study Identifies African-Specific Susceptibility Loci in African Americans With Inflammatory Bowel Disease.

Judy H. Cho, David T. Okou, Claire L. Simpson, 2017, Gastroenterology.

Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

H. Hakonarson, Cecilia Kim, Yiran Guo, 2017, Scientific Reports.

A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

John J. Connolly, I. Ntalla, E. Zeggini, 2017, Scientific Reports.

Rare variants at 16p11.2 are associated with common variable immunodeficiency.

Joseph T. Glessner, J. Glessner, H. Hakonarson, 2015, The Journal of allergy and clinical immunology.

Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility

Joseph T. Glessner, Debra K. Shivers, J. Glessner, 2016, BMC Medical Genetics.

ORMDL3 variants associated with asthma susceptibility in North Americans of European ancestry.

Ryan M. Smith, J. Glessner, Cecilia Kim, 2008, The Journal of allergy and clinical immunology.

17q12-21 variants interact with smoke exposure as a risk factor for pediatric asthma but are equally associated with early-onset versus late-onset asthma in North Americans of European ancestry.

Joseph T. Glessner, Ryan M. Smith, J. Glessner, 2009, The Journal of allergy and clinical immunology.

Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders

J. Glessner, H. Hakonarson, Cecilia Kim, 2017, Genome Medicine.

Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk

Joseph T. Glessner, J. Glessner, H. Hakonarson, 2017, Nature Communications.

The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature

J. Glessner, H. Hakonarson, Cecilia Kim, 2010, BMC Medical Genetics.

Examination of All Type 2 Diabetes GWAS Loci Reveals HHEX-IDE as a Locus Influencing Pediatric BMI

Joseph T. Glessner, J. Glessner, H. Hakonarson, 2009, Diabetes.

Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders

Joseph T. Glessner, J. Glessner, H. Hakonarson, 2017, Genome Medicine.