Author details

Full Name

Edward C Frackelton

Affiliation

ORCID

Career Start Year

2007

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
30623581	Assessing the utilization of high-resolution 2-field HLA typing in solid organ transplantation.	American Journal of Transplantation	2019
27005825	Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility.	BMC Med Genet	2016
23731541	Large sample size, wide variant spectrum, and advanced machine-learning technique boost risk prediction for inflammatory bowel disease.	Am J Hum Genet	2013
23341896	Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population.	PLoS One	2013
23505181	The missense variation landscape of FTO, MC4R, and TMEM18 in obese children of African Ancestry.	Obesity (Silver Spring)	2013
22454397	Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis.	Hum Mol Genet	2012
27625808	Examination of genetic variants influencing lipid traits in pediatric populations.	J Pediatr Genet	2012
22138692	Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder.	Nat Genet	2011
21212767	BMD-associated variation at the Osterix locus is correlated with childhood obesity in females.	Obesity (Silver Spring)	2011
21124317	Integrative genomics identifies LMO1 as a neuroblastoma oncogene.	Nature	2011
21980299	A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci.	PLoS Genet	2011
21779088	Role of BMI-associated loci identified in GWAS meta-analyses in the context of common childhood obesity in European Americans.	Obesity (Silver Spring)	2011
20489179	Strong synaptic transmission impact by copy number variations in schizophrenia.	Proc Natl Acad Sci U S A	2010
19546859	Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes.	Mol Psychiatry	2010
20950786	A genome-wide study reveals copy number variants exclusive to childhood obesity cases.	Am J Hum Genet	2010
21152026	Duplication of the SLIT3 locus on 5q35.1 predisposes to major depressive disorder.	PLoS One	2010
20176734	Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects.	Hum Mol Genet	2010
20124441	Common variants in HSPB7 and FRMD4B associated with advanced heart failure.	Circ Cardiovasc Genet	2010
19933996	Examination of all type 2 diabetes GWAS loci reveals HHEX-IDE as a locus influencing pediatric BMI.	Diabetes	2010
20208534	Common variants at 5q22 associate with pediatric eosinophilic esophagitis.	Nat Genet	2010
20378605	In silico replication of the genome-wide association results of the Type 1 Diabetes Genetics Consortium.	Hum Mol Genet	2010
20546612	The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.	BMC Med Genet	2010
18840781	Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.	Diabetes	2009
23776345	Association of the BANK 1 R61H variant with systemic lupus erythematosus in Americans of European and African ancestry.	Appl Clin Genet	2009
19592680	High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.	Genome Res	2009
19592620	Examination of type 2 diabetes loci implicates CDKAL1 as a birth weight gene.	Diabetes	2009
19265794	Investigation of the locus near MC4R with childhood obesity in Americans of European and African ancestry.	Obesity (Silver Spring)	2009
19404257	Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.	Nature	2009
19404256	Common genetic variants on 5p14.1 associate with autism spectrum disorders.	Nature	2009
19478790	The role of obesity-associated loci identified in genome-wide association studies in the determination of pediatric BMI.	Obesity (Silver Spring)	2009
19249008	Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease.	Am J Hum Genet	2009
19465406	Association of RASGRP1 with type 1 diabetes is revealed by combined follow-up of two genome-wide studies.	J Med Genet	2009
19660801	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.	J Allergy Clin Immunol	2009
19656524	A genome-wide association study identifies a locus for nonsyndromic cleft lip with or without cleft palate on 8q24.	J Pediatr	2009
19915574	Common variants at five new loci associated with early-onset inflammatory bowel disease.	Nat Genet	2009
18758464	Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease.	Nat Genet	2008
18760456	ORMDL3 variants associated with asthma susceptibility in North Americans of European ancestry.	J Allergy Clin Immunol	2008
18463370	Chromosome 6p22 locus associated with clinically aggressive neuroblastoma.	N Engl J Med	2008
18335027	Association analysis of the FTO gene with obesity in children of Caucasian and African ancestry reveals a common tagging SNP.	PLoS One	2008
18426861	Association analysis of type 2 diabetes Loci in type 1 diabetes.	Diabetes	2008
18464277	Novel, complex interruptions of the GAA repeat in small, expanded alleles of two affected siblings with late-onset Friedreich ataxia.	Movement Disorders	2008
18198356	A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association study.	Diabetes	2008
18576341	Association of the TRAF1-C5 locus on chromosome 9 with juvenile idiopathic arthritis.	Arthritis Rheum	2008
18974833	Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies.	PLoS One	2008
17618837	Association of variants of the interleukin-23 receptor gene with susceptibility to pediatric Crohn's disease.	Clin Gastroenterol Hepatol	2007
17625155	Association of the T300A non-synonymous variant of the ATG16L1 gene with susceptibility to paediatric Crohn's disease.	Gut	2007
17632545	A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.	Nature	2007