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Author Details

Candace Guiducci
Broad Institute of MIT and Harvard
2006
58
48
PMIDPaper TitleJournal TitlePublished Year
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
25646566The evolution of drug resistance in clinical isolates of Candida albicans.Elife2015
25646566The evolution of drug resistance in clinical isolates of Candida albicans.Elife2015
24471563The influence of rare genetic variation in SLC30A8 on diabetes incidence and β-cell function.J Clin Endocrinol Metab2014
24471563The influence of rare genetic variation in SLC30A8 on diabetes incidence and β-cell function.J Clin Endocrinol Metab2014
24509480Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.Nat Genet2014
24509480Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.Nat Genet2014
22933432Personalized genetic risk counseling to motivate diabetes prevention: a randomized trial.Diabetes Care2013
22933432Personalized genetic risk counseling to motivate diabetes prevention: a randomized trial.Diabetes Care2013
23525077Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity.Nat Genet2013
23261300Rare, low-frequency, and common variants in the protein-coding sequence of biological candidate genes from GWASs contribute to risk of rheumatoid arthritis.Am J Hum Genet2013
23622249Punctuated evolution of prostate cancer genomes.Cell2013
23622249Punctuated evolution of prostate cancer genomes.Cell2013
23525077Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity.Nat Genet2013
23261300Rare, low-frequency, and common variants in the protein-coding sequence of biological candidate genes from GWASs contribute to risk of rheumatoid arthritis.Am J Hum Genet2013
22238593A genome-wide association search for type 2 diabetes genes in African Americans.PLoS One2012
22479202Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.PLoS Genet2012
22885922Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes.Nat Genet2012
22721967Association testing of previously reported variants in a large case-control meta-analysis of diabetic nephropathy.Diabetes2012
22610119Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer.Nat Genet2012
22607825Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study.Lancet2012
23028342New susceptibility loci associated with kidney disease in type 1 diabetes.PLoS Genet2012
22238593A genome-wide association search for type 2 diabetes genes in African Americans.PLoS One2012
23028342New susceptibility loci associated with kidney disease in type 1 diabetes.PLoS Genet2012
22721967Association testing of previously reported variants in a large case-control meta-analysis of diabetic nephropathy.Diabetes2012
22885922Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes.Nat Genet2012
22479202Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.PLoS Genet2012
22610119Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer.Nat Genet2012
22607825Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study.Lancet2012
21424828The efficacy of detecting variants with small effects on the Affymetrix 6.0 platform using pooled DNA.Hum Genet2011
21424828The efficacy of detecting variants with small effects on the Affymetrix 6.0 platform using pooled DNA.Hum Genet2011
21798893The mutational landscape of head and neck squamous cell carcinoma.Science2011
21706003Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile.Nat Genet2011
21597964Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers.Hum Genet2011
21775993Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction.Nat Genet2011
21775993Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction.Nat Genet2011
21798893The mutational landscape of head and neck squamous cell carcinoma.Science2011
21597964Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers.Hum Genet2011
21706003Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile.Nat Genet2011
19847392Genetic association analysis of LARS2 with type 2 diabetes.Diabetologia2010
20852631A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population.Nat Genet2010
20703447Expression analysis of loci associated with type 2 diabetes in human tissues.Diabetologia2010
20942659Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia.N Engl J Med2010
20839009Association of common DNA sequence variants at 33 genetic loci with blood lipids in individuals of African ancestry from Jamaica.Hum Genet2010
20935630Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.Nat Genet2010
20686565Biological, clinical and population relevance of 95 loci for blood lipids.Nature2010
20935629Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.Nat Genet2010
21060860Common genetic variants and modification of penetrance of BRCA2-associated breast cancer.PLoS Genet2010
20971364A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses.Lancet2010
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University of Michigan ann arbor
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