Keyue Ding

Dr. Keyue Ding


Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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25 July 2003 in Annals of Neurology
Verified
Journal Article
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YCYucai Chen
Yucai Chen
JLJianjun Lu
Jianjun Lu
HPHong Pan
Hong Pan
YZYuehua Zhang
Yuehua Zhang
HWHusheng Wu
Husheng Wu
XWXiru Wu
Xiru Wu

12 September 2013 in Human Genetics
Verified
Journal Article
Closed access
PDF file
KSKhader Shameer
Khader Shameer
JDJoshua C. Denny
Joshua C. Denny
KDKeyue Ding
Keyue Ding
HJHayan Jouni
Hayan Jouni
DCDavid R. Crosslin
David R. Crosslin
Iftikhar KulloIftikhar Kullo
Iftikhar Kullo

28 September 2010 in PLOS ONE
Verified
Journal Article
Open access
PDF file
Iftikhar KulloIftikhar Kullo
Iftikhar Kullo
KDKeyue Ding
Keyue Ding
HJHayan Jouni
Hayan Jouni
CSCarin Y. Smith
Carin Y. Smith
CCChristopher G. Chute
Christopher G. Chute
The Electronic Medical Record (EMR) is a potential source for high throughput phenotyping to conduct genome-wide association studies (GWAS), including those of medically relevant quantitative traits. We describe use of the Mayo Clinic EMR to conduct a GWAS of red blood cell (RBC) traits in a cohort of patients with peripheral arterial disease (PAD) and controls without PAD. Results for hemoglobin level, hematocrit, RBC count, mean corpuscular volume, mean corpuscular hemoglobin, and mean corpuscular hemoglobin concentration were extracted from the EMR from January 1994 to September 2009. Out of 35,159 RBC trait values in 3,411 patients, we excluded 12,864 values in 1,165 patients that had been measured during hospitalization or in the setting of hematological disease, malignancy, or use of drugs that affect RBC traits, leaving a final genotyped sample of 3,012, 80% of whom had ≥2 measurements. The median of each RBC trait was used in the genetic analyses, which were conducted using an additive model that adjusted for age, sex, and PAD status. We identified four genomic loci that were associated (P<5×10−8) with one or more of the RBC traits (HBLS1/MYB on 6q23.3, TMPRSS6 on 22q12.3, HFE on 6p22.1, and SLC17A1 on 6p22.2). Three of these loci (HBLS1/MYB, TMPRSS6, and HFE) had been identified in recent GWAS and the allele frequencies, effect sizes, and the directions of effects of the replicated SNPs were similar to the prior studies. Our results demonstrate feasibility of using the EMR to conduct high throughput genomic studies of medically relevant quantitative traits.

1 November 2003 in Bioinformatics
Verified
Journal Article
Open access
PDF file
KDKeyue Ding
Keyue Ding
KZKaixin Zhou
Kaixin Zhou
FHFuchu He
Fuchu He
YSYan Shen
Yan Shen
Summary: We describe an integrated java-based program that provides elaborate graphic and plain-text output of pairwise linkage disequilibrium (LD) analysis of single nucleotide polymorphisms genotypic data. It is most suitable for molecular geneticists, who are focusing on LD measures estimation, statistical significance test and extent prediction. Availability: The software is available at: http://www.chgb.org.cn/lda/lda.htm Supplementary information: Detailed tutorials, LDA help system and examples are distributed within LDA software. For Macintosh OS X user, the Jre version 1.4 can be downloaded from http://connect.apple.com

1 October 2007 in Nature Clinical Practice Cardiovascular Medicine
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Journal Article
Closed access
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Iftikhar KulloIftikhar Kullo
Iftikhar Kullo
KDKeyue Ding
Keyue Ding

1 July 2011 in The American Journal of Human Genetics
Verified
Journal Article
Closed access
Iftikhar KulloIftikhar Kullo
Iftikhar Kullo
KDKeyue Ding
Keyue Ding
KSKhader Shameer
Khader Shameer
CMCatherine A. McCarty
Catherine A. McCarty
GJGail P. Jarvik
Gail P. Jarvik
CCChristopher G. Chute
Christopher G. Chute