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BOOST: A Fast Approach to Detecting Gene-Gene Interactions in Genome-wide Case-Control Studies

American journal of human genetics, 2010-09, Vol.87 (3), p.325-340

2010

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Predictive rule inference for epistatic interaction detection in genome-wide association studies

Bioinformatics, 2010-01, Vol.26 (1), p.30-37

2010

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The association of liver function and quality of life of patients with liver cancer

BMC gastroenterology, 2019-05, Vol.19 (1), p.66-66, Article 66

2019

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Chemotherapy-Related Amenorrhea and Menopause in Young Chinese Breast Cancer Patients: Analysis on Incidence, Risk Factors and Serum Hormone Profiles

PloS one, 2015-10, Vol.10 (10), p.e0140842

2015

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Nonsense-Mediated Decay Targeted RNA (ntRNA): Proposal of a ntRNA–miRNA–lncRNA Triple Regulatory Network Usable as Biomarker of Prognostic Risk in Patients with Kidney Cancer

Genes, 2022-09, Vol.13 (9), p.1656

2022

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Promoter polymorphism of matrilin-1 gene predisposes to adolescent idiopathic scoliosis in a Chinese population

European journal of human genetics : EJHG, 2009-04, Vol.17 (4), p.525-532

2009

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MegaSNPHunter: a learning approach to detect disease predisposition SNPs and high level interactions in genome wide association study

BMC bioinformatics, 2009-01, Vol.10 (1), p.13-13, Article 13

2009

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Genes Regulate Blood Pressure, but “Environments” Cause Hypertension

Frontiers in genetics, 2020-11, Vol.11, p.580443-580443

2020

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Molecular evolution in the CREB1 signal pathway and a rare haplotype in CREB1 with genetic predisposition to schizophrenia

Journal of psychiatric research, 2014-10, Vol.57, p.84-89

2014

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Profiles of lipids, blood pressure and weight changes among premenopausal Chinese breast cancer patients after adjuvant chemotherapy

BMC women's health, 2017-07, Vol.17 (1), p.55-11, Article 55

2017

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Melatonin receptor 1B (MTNR1B) gene polymorphism is associated with the occurrence of adolescent idiopathic scoliosis

Spine (Philadelphia, Pa. 1976), 2007-07, Vol.32 (16), p.1748-1753

2007

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Role of pharmacogenetics on adjuvant chemotherapy-induced neutropenia in Chinese breast cancer patients

Journal of cancer research and clinical oncology, 2013-03, Vol.139 (3), p.419-427

2013

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Genetic adaptation of the hypoxia-inducible factor pathway to oxygen pressure among eurasian human populations

Molecular biology and evolution, 2012-11, Vol.29 (11), p.3359-3370

2012

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Detecting two-locus associations allowing for interactions in genome-wide association studies

Bioinformatics, 2010-10, Vol.26 (20), p.2517-2525

2010

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Natural Selection of ATP2B1 Underlies Susceptibility to Essential Hypertension

Frontiers in genetics, 2021-03, Vol.12, p.628516-628516

2021

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The mechanism of transactivation regulation due to polymorphic short tandem repeats (STRs) using IGF1 promoter as a model

Scientific reports, 2016-12, Vol.6 (1), p.38225-38225, Article 38225

2016

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An upregulation in the expression of vanilloid transient potential channels 2 enhances hypotonicity-induced cytosolic Ca²⁺ rise in human induced pluripotent stem cell model of Hutchinson-Gillford Progeria

PloS one, 2014, Vol.9 (1), p.e87273-e87273

2014

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Genome-wide Association and Replication Studies Identified TRHR as an Important Gene for Lean Body Mass

American journal of human genetics, 2009-03, Vol.84 (3), p.418-423

2009

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Direct Measurement of B Lymphocyte Gene Expression Biomarkers in Peripheral Blood Transcriptomics Enables Early Prediction of Vaccine Seroconversion

Genes, 2021-06, Vol.12 (7), p.971

2021

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Lack of Association Between the Promoter Polymorphisms of MMP-3 and IL-6 Genes and Adolescent Idiopathic Scoliosis: A Case-Control Study in a Chinese Han Population

Spine (Philadelphia, Pa. 1976), 2010-08, Vol.35 (18), p.1701-1705

2010

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A Decade in Review after Idiopathic Scoliosis Was First Called a Complex Trait-A Tribute to the Late Dr. Yves Cotrel for His Support in Studies of Etiology of Scoliosis

Genes, 2021-07, Vol.12 (7), p.1033

2021

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Older men with higher self-rated socioeconomic status have shorter telomeres

Age and ageing, 2009-09, Vol.38 (5), p.553-558

2009

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Functional Interaction Between SNPs and Microsatellite in the Transcriptional Regulation of Insulin-Like Growth Factor 1

Human mutation, 2013-09, Vol.34 (9), p.1289-1297

2013

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Dopamine Receptor D4 Gene −521C/T Polymorphism Is Associated with Opioid Dependence through Cold-Pain Responses

Annals of the New York Academy of Sciences, 2008-10, Vol.1139 (1), p.20-26

2008

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BOOST: A Fast Approach to Detecting Gene-Gene Interactions in Genome-wide Case-Control Studies

Predictive rule inference for epistatic interaction detection in genome-wide association studies

The association of liver function and quality of life of patients with liver cancer

Chemotherapy-Related Amenorrhea and Menopause in Young Chinese Breast Cancer Patients: Analysis on Incidence, Risk Factors and Serum Hormone Profiles

Nonsense-Mediated Decay Targeted RNA (ntRNA): Proposal of a ntRNA–miRNA–lncRNA Triple Regulatory Network Usable as Biomarker of Prognostic Risk in Patients with Kidney Cancer

Promoter polymorphism of matrilin-1 gene predisposes to adolescent idiopathic scoliosis in a Chinese population

MegaSNPHunter: a learning approach to detect disease predisposition SNPs and high level interactions in genome wide association study

Genes Regulate Blood Pressure, but “Environments” Cause Hypertension

Molecular evolution in the CREB1 signal pathway and a rare haplotype in CREB1 with genetic predisposition to schizophrenia

Profiles of lipids, blood pressure and weight changes among premenopausal Chinese breast cancer patients after adjuvant chemotherapy

Melatonin receptor 1B (MTNR1B) gene polymorphism is associated with the occurrence of adolescent idiopathic scoliosis

Role of pharmacogenetics on adjuvant chemotherapy-induced neutropenia in Chinese breast cancer patients

Genetic adaptation of the hypoxia-inducible factor pathway to oxygen pressure among eurasian human populations

Detecting two-locus associations allowing for interactions in genome-wide association studies

Natural Selection of ATP2B1 Underlies Susceptibility to Essential Hypertension

The mechanism of transactivation regulation due to polymorphic short tandem repeats (STRs) using IGF1 promoter as a model

An upregulation in the expression of vanilloid transient potential channels 2 enhances hypotonicity-induced cytosolic Ca²⁺ rise in human induced pluripotent stem cell model of Hutchinson-Gillford Progeria

Genome-wide Association and Replication Studies Identified TRHR as an Important Gene for Lean Body Mass

Direct Measurement of B Lymphocyte Gene Expression Biomarkers in Peripheral Blood Transcriptomics Enables Early Prediction of Vaccine Seroconversion

Lack of Association Between the Promoter Polymorphisms of MMP-3 and IL-6 Genes and Adolescent Idiopathic Scoliosis: A Case-Control Study in a Chinese Han Population

A Decade in Review after Idiopathic Scoliosis Was First Called a Complex Trait-A Tribute to the Late Dr. Yves Cotrel for His Support in Studies of Etiology of Scoliosis

Older men with higher self-rated socioeconomic status have shorter telomeres

Functional Interaction Between SNPs and Microsatellite in the Transcriptional Regulation of Insulin-Like Growth Factor 1

European bone mineral density loci are also associated with BMD in East-Asian populations

Dopamine Receptor D4 Gene −521C/T Polymorphism Is Associated with Opioid Dependence through Cold-Pain Responses

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