Author details

Full Name

Todd Green

Affiliation

ORCID

Career Start Year

1994

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
29360107	Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.	Sci Data	2018
29257133	Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.	Sci Data	2017
28341696	A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.	Diabetes	2017
27398621	The genetic architecture of type 2 diabetes.	Nature	2016
26551672	Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.	Nat Genet	2015
23396133	Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing.	Nat Genet	2013
22238593	A genome-wide association search for type 2 diabetes genes in African Americans.	PLoS One	2012
22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	PLoS Genet	2012
22693455	Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases.	PLoS Genet	2012
22038522	Common genetic variants differentially influence the transition from clinically defined states of fasting glucose metabolism.	Diabetologia	2012
21597964	Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers.	Hum Genet	2011
21298027	A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac disease.	PLoS Genet	2011
21873659	Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: the Candidate gene Association Resource (CARe).	Invest Ophthalmol Vis Sci	2011
21983784	Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease.	Nat Genet	2011
20228799	Genome-wide association identifies multiple ulcerative colitis susceptibility loci.	Nat Genet	2010
21060860	Common genetic variants and modification of penetrance of BRCA2-associated breast cancer.	PLoS Genet	2010
21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Nat Genet	2010
20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Nat Genet	2010
19915574	Common variants at five new loci associated with early-onset inflammatory bowel disease.	Nat Genet	2009
19846760	Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases.	Proc Natl Acad Sci U S A	2009
18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Nat Genet	2008
18184952	Association between microdeletion and microduplication at 16p11.2 and autism.	N Engl J Med	2008
18650832	MAST3: a novel IBD risk factor that modulates TLR4 signaling.	Genes Immun	2008
17435756	Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.	Nat Genet	2007
17997607	Identification of two independent risk factors for lupus within the MHC in United Kingdom families.	PLoS Genet	2007
17252545	A second major histocompatibility complex susceptibility locus for multiple sclerosis.	Ann Neurol	2007
16825666	A molecular-properties-based approach to understanding PDZ domain proteins and PDZ ligands.	Genome Res	2006
16809782	Ca2+/calmodulin-dependent protein kinase II is a modulator of CARMA1-mediated NF-kappaB activation.	Mol Cell Biol	2006
16998491	A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.	Nat Genet	2006
11326283	A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population.	Nat Genet	2001
11586304	Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease.	Nat Genet	2001
10777714	Genomewide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci.	Am J Hum Genet	2000
9758611	Familial eosinophilia maps to the cytokine gene cluster on human chromosomal region 5q31-q33.	Am J Hum Genet	1998
9797358	Absence of linkage between inflammatory bowel disease and selected loci on chromosomes 3, 7, 12, and 16.	Gastroenterology	1998
7904552	Report of the First International Workshop on Human Chromosome 20 Mapping 1993.	Cytogenet Cell Genet	1994