Author details

Full Name

Kelly Thomas

Affiliation

ORCID

Career Start Year

2008

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36696440	The fidelity of transcription in human cells.		2023
27693347	Genome-Wide Association Study Identifies African-Specific Susceptibility Loci in African Americans With Inflammatory Bowel Disease.	Gastroenterology	2017
28630421	A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling.	Sci Rep	2017
28924153	Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk.	Nat Commun	2017
28827695	Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling.	Sci Rep	2017
27677580	Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing gene.	Nat Commun	2016
27005825	Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility.	BMC Med Genet	2016
26450413	Genetic sharing and heritability of paediatric age of onset autoimmune diseases.	Nat Commun	2015
25678086	Rare variants at 16p11.2 are associated with common variable immunodeficiency.	J Allergy Clin Immunol	2015
26188062	Copy Number Variations in CTNNA3 and RBFOX1 Associate with Pediatric Food Allergy.	J Immunol	2015
26301688	Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases.	Nat Med	2015
26423053	Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies.	Genome Med	2015
24927284	The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism.	Nat Commun	2014
24467814	Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population.	Mol Autism	2014
23382853	Copy number variations in alternative splicing gene networks impact lifespan.	PLoS One	2013
23889995	Whole-genome DNA/RNA sequencing identifies truncating mutations in RBCK1 in a novel Mendelian disease with neuromuscular and cardiac involvement.	Genome Med	2013
23263863	GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.	Hum Mol 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
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
20934710	Variation over time in medical conditions and health service utilization of children with Down syndrome.	Journal of Pediatrics	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
20950786	A genome-wide study reveals copy number variants exclusive to childhood obesity cases.	Am J Hum Genet	2010
21057500	Large intergenic non-coding RNA-RoR modulates reprogramming of human induced pluripotent stem cells.	Nat 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
20546612	The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.	BMC Med Genet	2010
19656524	A genome-wide association study identifies a locus for nonsyndromic cleft lip with or without cleft palate on 8q24.	J Pediatr	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
19478790	The role of obesity-associated loci identified in genome-wide association studies in the determination of pediatric BMI.	Obesity (Silver Spring)	2009
19571010	Many human large intergenic noncoding RNAs associate with chromatin-modifying complexes and affect gene expression.	Proc Natl Acad Sci U S A	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
18760456	ORMDL3 variants associated with asthma susceptibility in North Americans of European ancestry.	J Allergy Clin Immunol	2008