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Author Details
Full Name
Dakai Zhu
Affiliation
The Institute for Clinical and Translational Research, Baylor College of Medicine
ORCID
Career Start Year
1995
Papers
43
H Index
20
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35915169
Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer.
Nat Genet
2022
35500836
A Large-Scale Genome-Wide Gene-Gene Interaction Study of Lung Cancer Susceptibility in Europeans With a Trans-Ethnic Validation in Asians.
J Thorac Oncol
2022
34368847
False positive findings during genome-wide association studies with imputation: influence of allele frequency and imputation accuracy.
Hum Mol Genet
2021
33594163
Rare deleterious germline variants and risk of lung cancer.
NPJ Precis Oncol
2021
34002017
A multi-omics study links TNS3 and SEPT7 to long-term former smoking NSCLC survival.
NPJ Precis Oncol
2021
32393777
Protein-altering germline mutations implicate novel genes related to lung cancer development.
Nat Commun
2020
33126877
A new efficient method to detect genetic interactions for lung cancer GWAS.
BMC Med Genomics
2020
30700444
Elevated Platelet Count Appears to Be Causally Associated with Increased Risk of Lung Cancer: A Mendelian Randomization Analysis.
Cancer Epidemiol Biomarkers Prev
2019
30734280
Genetic variants in ELOVL2 and HSD17B12 predict melanoma-specific survival.
Int J Cancer
2019
30596980
Genetic variants in the calcium signaling pathway genes are associated with cutaneous melanoma-specific survival.
Carcinogenesis
2019
28796414
Genetic variants in the metzincin metallopeptidase family genes predict melanoma survival.
Mol Carcinog
2018
30104567
Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk.
Nat Commun
2018
30254314
Fine mapping of MHC region in lung cancer highlights independent susceptibility loci by ethnicity.
Nat Commun
2018
29981437
Rare Variants in Known Susceptibility Loci and Their Contribution to Risk of Lung Cancer.
J Thorac Oncol
2018
29313974
Genetic variants in RORA and DNMT1 associated with cutaneous melanoma survival.
Int J Cancer
2018
27914105
Genetic variants in the integrin signaling pathway genes predict cutaneous melanoma survival.
Int J Cancer
2017
28499756
Genetic Variants in WNT2B and BTRC Predict Melanoma Survival.
J Invest Dermatol
2017
29088810
Genetic variants of PDGF signaling pathway genes predict cutaneous melanoma survival.
Oncotarget
2017
28510328
Genetic variants in the genes encoding rho GTPases and related regulators predict cutaneous melanoma-specific survival.
Int J Cancer
2017
28604730
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes.
Nat Genet
2017
27578485
Genetic variants in the PIWI-piRNA pathway gene DCP1A predict melanoma disease-specific survival.
Int J Cancer
2016
25243787
Genetic variants in fanconi anemia pathway genes BRCA2 and FANCA predict melanoma survival.
J Invest Dermatol
2015
26394269
International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways.
Nat Commun
2015
26576671
Prediction of the gene expression in normal lung tissue by the gene expression in blood.
BMC Med Genomics
2015
25953768
Functional Variants in Notch Pathway Genes NCOR2, NCSTN, and MAML2 Predict Survival of Patients with Cutaneous Melanoma.
Cancer Epidemiol Biomarkers Prev
2015
25628125
Genetic variants in Hippo pathway genes YAP1, TEAD1 and TEAD4 are associated with melanoma-specific survival.
Int J Cancer
2015
25329654
Role of a genetic variant on the 15q25.1 lung cancer susceptibility locus in smoking-associated nasopharyngeal carcinoma.
PLoS One
2014
23407396
Polymorphisms of nucleotide excision repair genes predict melanoma survival.
J Invest Dermatol
2013
24260271
Findings from the Peutz-Jeghers syndrome registry of uruguay.
PLoS One
2013
22899653
Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls.
Hum Mol Genet
2012
21152100
Association between acquired uniparental disomy and homozygous mutations and HER2/ER/PR status in breast cancer.
PLoS One
2010
18639390
Trends in prevalence of prognostic factors and survival in lung cancer patients from 1985 to 2004 at a tertiary care center.
Cancer Detect Prev
2008
17562082
Imprinting detection by extending a regression-based QTL analysis method.
Hum Genet
2007
12485473
Power of a simplified multivariate test for genetic linkage.
Ann Hum Genet
2002
11173964
Comparison of multivariate tests for genetic linkage.
Hum Hered
2001
11592777
Contrasting molecular pathology of colorectal carcinoma in Egyptian and Western patients.
Br J Cancer
2001
11393661
Tumour necrosis factor 5' promoter single nucleotide polymorphisms influence susceptibility to rheumatoid arthritis (RA) in immunogenetically defined multiplex RA families.
Genes Immun
2001
11197302
Genetic analysis of multiplex rheumatoid arthritis families.
Genes Immun
1999
9433571
Comparison of model-free linkage mapping strategies for the study of a complex trait.
Genet Epidemiol
1997
8839128
Assessing genetic linkage and association with robust components of variance approaches.
Ann Hum Genet
1996
8751869
Genetic variability in the tumor necrosis factor-lymphotoxin region influences susceptibility to rheumatoid arthritis.
Am J Hum Genet
1996
8788007
Association and linkage with quantitative traits.
Genet Epidemiol
1995
9815964
Prognostic significance of p53 immunoreactivity in patients with glioma.
Clin Cancer Res
1995
1 - 43 of 43
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