E. Frackelton

发表

A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene

Joseph T. Glessner, J. Glessner, H. Hakonarson, 2007, Nature.

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

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

Follow-Up Analysis of Genome-Wide Association Data Identifies Novel Loci for Type 1 Diabetes

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

Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease.

David C. Wilson, Joseph T. Glessner, J. Glessner, 2009, American journal of human genetics.

Large sample size, wide variant spectrum, and advanced machine-learning technique boost risk prediction for inflammatory bowel disease.

H. Hakonarson, Cecilia Kim, K. Van Steen, 2013, American journal of human genetics.

Concept, Design and Implementation of a Cardiovascular Gene-Centric 50 K SNP Array for Large-Scale Genomic Association Studies

Mark I. McCarthy, Deborah A. Nickerson, Xiaowu Gai, 2008, PloS one.

Chromosome 6p22 locus associated with clinically aggressive neuroblastoma.

Nazneen Rahman, Joseph T. Glessner, Hakon Hakonarson, 2008, The New England journal of medicine.

Association Analysis of the FTO Gene with Obesity in Children of Caucasian and African Ancestry Reveals a Common Tagging SNP

Struan F. A. Grant, Joseph T. Glessner, Hakon Hakonarson, 2008, PloS one.

A Novel Susceptibility Locus for Type 1 Diabetes on Chr12q13 Identified by a Genome-Wide Association Study

Constantin Polychronakos, Luc Marchand, Margaret L. Lawson, 2008, 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.

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

T. Shaikh, H. Hakonarson, S. Grant, 2010, Molecular Psychiatry.

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.

Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis.

H. Hakonarson, Cecilia Kim, J. Trojanowski, 2012, Human molecular genetics.

Common variants at 5q22 associate with pediatric eosinophilic esophagitis

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

The Children's Hospital of Philadelphia Research Institute Impact Factor Report, FY2008

Cecilia Kim, N. Rahman, K. Cole, 2008 .

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.

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.

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.

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.

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.

Integrative genomics identifies LMO1 as a neuroblastoma oncogene

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

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

T. Shaikh, H. Hakonarson, S. Grant, 2010, Molecular Psychiatry.

Examination of genetic variants influencing lipid traits in pediatric populations

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

Association of HMGA2 Gene Variation with Height in Specific Pediatric Age Categories

Ryan M. Smith, J. Glessner, H. Hakonarson, 2008 .

High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.

Xiaowu Gai, Laura K Conlin, Livija Medne, 2009, Genome research.

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.

The missense variation landscape of FTO, MC4R and TMEM18 in obese children of African ancestry

J. Glessner, H. Hakonarson, Cecilia Kim, 2012, Obesity.

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.

Association of the TRAF1-C5 locus on chromosome 9 with juvenile idiopathic arthritis.

Hakon Hakonarson, J. Glessner, H. Hakonarson, 2008, Arthritis and rheumatism.

Variants of DENND1B associated with asthma in children.

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

Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease

Joseph T. Glessner, Hakon Hakonarson, Ryan M. Smith, 2008, Nature Genetics.

BMD‐Associated Variation at the Osterix Locus Is Correlated With Childhood Obesity in Females

J. Glessner, H. Hakonarson, Cecilia Kim, 2011, Obesity.

Assessing the utilization of high‐resolution 2‐field HLA typing in solid organ transplantation

Deborah Ferriola, Allison Gasiewski, Ryan Morlen, 2019, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

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.

Association of RASGRP1 with type 1 diabetes is revealed by combined follow-up of two genome-wide studies

C Polychronakos, H. Hakonarson, S. Grant, 2009, Journal of Medical Genetics.

Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility

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

Association of the T300A non-synonymous variant of the ATG16L1 gene with susceptibility to paediatric Crohn’s disease

Joseph T. Glessner, Ryan M. Smith, J. Glessner, 2007, Gut.

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.

Novel, complex interruptions of the GAA repeat in small, expanded alleles of two affected siblings with late‐onset Friedreich ataxia

E. Frackelton, Robert B. Wilson, D. Lynch, 2008, Movement disorders : official journal of the Movement Disorder Society.

Common Variants in HSPB7 and FRMD4B Associated With Advanced Heart Failure

Joseph T. Glessner, Hakon Hakonarson, Liming Qu, 2010, Circulation. Cardiovascular genetics.

Association of the BANK 1 R61H variant with systemic lupus erythematosus in Americans of European and African ancestry

Joseph T. Glessner, Ryan M. Smith, J. Glessner, 2008, The application of clinical genetics.

Common Variants in HSPB 7 and FRMD 4 B Associated With Advanced Heart Failure

Joseph T. Glessner, J. Glessner, H. Hakonarson, 2010 .

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

Joseph T. Glessner, T. Shaikh, J. Glessner, 2009, Molecular Psychiatry.

In silico replication of the genome-wide association results of the Type 1 Diabetes Genetics Consortium.

H. Hakonarson, Cecilia Kim, S. Grant, 2010, Human molecular genetics.

Association of variants of the interleukin-23 receptor gene with susceptibility to pediatric Crohn's disease.

Joseph T. Glessner, Ryan M. Smith, J. Glessner, 2007, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

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.

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

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

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.

Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis.

H. Hakonarson, Cecilia Kim, J. Trojanowski, 2012, Human molecular genetics.

Association Analysis of Type 2 Diabetes Loci in Type 1 Diabetes

Constantin Polychronakos, Hakon Hakonarson, Cecilia Kim, 2008, Diabetes.

Characterization of Eosinophilic Esophagitis Murine Models Using Optical Coherence Tomography References and Links

R. D. Ferguson, J. Glessner, H. Hakonarson, 2022 .

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

Ryan M. Smith, J. Glessner, H. Hakonarson, 2009, Obesity.

Association of the BANK 1 R61H variant with systemic lupus erythematosus in Americans of European and African ancestry

Ryan M. Smith, J. Glessner, H. Hakonarson, 2008, The application of clinical genetics.