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Author Details
Full Name
Holli H Dilks
Affiliation
Sarah Cannon Research Institute
ORCID
Career Start Year
2001
Papers
38
H Index
21
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
29381148
Trans-ethnic analysis of metabochip data identifies two new loci associated with BMI.
Int J Obes (Lond)
2018
27249515
Evidence for extensive pleiotropy among pharmacogenes.
Pharmacogenomics
2016
27200085
Population Stratification in the Context of Diverse Epidemiologic Surveys Sans Genome-Wide Data.
Front Genet
2016
25435401
Mining diverse small RNA species in the deep transcriptome.
Trends Biochem Sci
2015
25789475
Pleiotropic and sex-specific effects of cancer GWAS SNPs on melanoma risk in the population architecture using genomics and epidemiology (PAGE) study.
PLoS One
2015
23935004
Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia.
Gut
2014
25474351
Detection of pleiotropy through a Phenome-wide association study (PheWAS) of epidemiologic data as part of the Environmental Architecture for Genes Linked to Environment (EAGLE) study.
PLoS Genet
2014
25590050
Replication of <i>SCN5A</i> Associations with Electrocardio-graphic Traits in African Americans from Clinical and Epidemiologic Studies.
Evol Comput Mach Learn Data Min Bioinform
2014
25363704
Rare variant APOC3 R19X is associated with cardio-protective profiles in a diverse population-based survey as part of the Epidemiologic Architecture for Genes Linked to Environment Study.
Circ Cardiovasc Genet
2014
25374661
GWATCH: a web platform for automated gene association discovery analysis.
Gigascience
2014
24896101
Accuracy of administratively-assigned ancestry for diverse populations in an electronic medical record-linked biobank.
PLoS One
2014
24681604
Pleiotropic associations of risk variants identified for other cancers with lung cancer risk: the PAGE and TRICL consortia.
J Natl Cancer Inst
2014
24297552
Utilization of an EMR-biorepository to identify the genetic predictors of calcineurin-inhibitor toxicity in heart transplant recipients.
Pac Symp Biocomput
2014
24480881
Replication of associations between GWAS SNPs and melanoma risk in the Population Architecture Using Genomics and Epidemiology (PAGE) Study.
J Invest Dermatol
2014
23577127
A systematic screen of FDA-approved drugs for inhibitors of biological threat agents.
PLoS One
2013
24094743
Fine Mapping and Identification of BMI Loci in African Americans.
Am J Hum Genet
2013
24063630
Genetic variants associated with fasting glucose and insulin concentrations in an ethnically diverse population: results from the Population Architecture using Genomics and Epidemiology (PAGE) study.
BMC Med Genet
2013
24256507
Lipid trait-associated genetic variation is associated with gallstone disease in the diverse Third National Health and Nutrition Examination Survey (NHANES III).
BMC Med Genet
2013
23651022
Assessment of a pharmacogenomic marker panel in a polypharmacy population identified from electronic medical records.
Pharmacogenomics
2013
23424124
Characterization of the Metabochip in diverse populations from the International HapMap Project in the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) project.
Pac Symp Biocomput
2013
22588608
Operational implementation of prospective genotyping for personalized medicine: the design of the Vanderbilt PREDICT project.
Clin Pharmacol Ther
2012
22688886
Serum vitamins A and E as modifiers of lipid trait genetics in the National Health and Nutrition Examination Surveys as part of the Population Architecture using Genomics and Epidemiology (PAGE) study.
Hum Genet
2012
21234876
Strategies for genotyping.
Curr Protoc Hum Genet
2011
18325640
Detecting AIDS restriction genes: from candidate genes to genome-wide association discovery.
Vaccine
2008
19005266
Mitochondrial DNA haplogroups influence AIDS progression.
AIDS
2008
17006671
Elevated male European and female African contributions to the genomes of African American individuals.
Hum Genet
2007
17590083
Regulatory polymorphisms in the cyclophilin A gene, PPIA, accelerate progression to AIDS.
PLoS Pathog
2007
16362345
Searching for signals of evolutionary selection in 168 genes related to immune function.
Hum Genet
2006
16825163
[Association study of chromosome 4 STRs polymorphisms with nasopharyngeal carcinoma].
Yi Chuan
2006
16848974
Genetic factors leading to chronic Epstein-Barr virus infection and nasopharyngeal carcinoma in South East China: study design, methods and feasibility.
Hum Genomics
2006
16809281
Consistent effects of TSG101 genetic variability on multiple outcomes of exposure to human immunodeficiency virus type 1.
J Virol
2006
16248677
The case for selection at CCR5-Delta32.
PLoS Biol
2005
15128462
Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes.
BMC Med Genet
2004
15564514
Association of DC-SIGN promoter polymorphism with increased risk for parenteral, but not mucosal, acquisition of human immunodeficiency virus type 1 infection.
J Virol
2004
12853138
Characterization of genomic structure and polymorphisms in the human carbamyl phosphate synthetase I gene.
Gene
2003
12555242
Defining the autism minimum candidate gene region on chromosome 7.
Am J Med Genet B Neuropsychiatr Genet
2003
11496372
Incorporating language phenotypes strengthens evidence of linkage to autism.
Am J Med Genet
2001
11543639
Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families.
Genomics
2001
1 - 38 of 38
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The State University of New Jersey
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