D. Ge

发表

Large recurrent microdeletions associated with schizophrenia

Thomas W. Mühleisen, Bjarni V. Halldórsson, P. Matthews, 2008, Nature.

Common variants conferring risk of schizophrenia

Pall I. Olason, P. Matthews, H. Stefánsson, 2009, Nature.

Using ERDS to infer copy-number variants in high-coverage genomes.

K. Shianna, D. Ge, A. Need, 2012, American journal of human genetics.

Screening the human exome: a comparison of whole genome and whole transcriptome sequencing

David B Goldstein, James J Goedert, Jason P Smith, 2010, Genome Biology.

Mutation in TECPR2 reveals a role for autophagy in hereditary spastic paraparesis.

K. Shianna, D. Ge, D. Goldstein, 2012, American journal of human genetics.

Long-range LD can confound genome scans in admixed populations.

K. Shianna, D. Ge, A. Need, 2008, American journal of human genetics.

Tissue-Specific Genetic Control of Splicing: Implications for the Study of Complex Traits

K. Shianna, D. Ge, D. Goldstein, 2008, PLoS biology.

A Genome-Wide Association Study in Chronic Obstructive Pulmonary Disease (COPD): Identification of Two Major Susceptibility Loci

K. Shianna, D. Ge, A. Need, 2009, PLoS genetics.

The Characterization of Twenty Sequenced Human Genomes

Elizabeth T. Cirulli, Jacques Fellay, David B. Goldstein, 2010, PLoS genetics.

Whole-Genome Sequencing of a Single Proband Together with Linkage Analysis Identifies a Mendelian Disease Gene

Elizabeth T. Cirulli, Jonathan Pevsner, David B. Goldstein, 2010, PLoS genetics.

A Whole-Genome Association Study of Major Determinants for Host Control of HIV-1

Jacques Fellay, David B. Goldstein, Stylianos E. Antonarakis, 2007, Science.

Common Genetic Variation and the Control of HIV-1 in Humans

Elizabeth T. Cirulli, Huldrych F. Günthard, Jacques Fellay, 2009, PLoS genetics.

A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.

Gail Clement, Gail P. Clement, Greg Gibson, 2009, Human molecular genetics.

Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy.

K. Shianna, D. Ge, A. Need, 2012, American journal of human genetics.

Haplotypic analyses of the aldosterone synthase gene CYP11B2 associated with stage‐2 hypertension in northern Han Chinese

D. Ge, D. Gu, J. He, 2004, Clinical genetics.

A genome-wide comparison of the functional properties of rare and common genetic variants in humans.

Qianqian Zhu, Slave Petrovski, Samuel P. Dickson, 2011, American journal of human genetics.

Differential Serum Cytokine Profiles in Patients with Chronic Hepatitis B, C, and Hepatocellular Carcinoma

D. Ge, Zhaoshi Jiang, O. Podlaha, 2017, Scientific Reports.

Stress-Induced Sodium Excretion: A New Intermediate Phenotype to Study the Early Genetic Etiology of Hypertension?

D. Ge, H. Snieder, S. Su, 2009, Hypertension.

Variation near the region of the lipoprotein lipase gene and hypertension or blood pressure levels in Chinese.

D. Ge, Yan Shen, R. Hui, 2003, Hypertension research : official journal of the Japanese Society of Hypertension.

Interleukin-28B polymorphism improves viral kinetics and is the strongest pretreatment predictor of sustained virologic response in genotype 1 hepatitis C virus.

William M. Lee, K. Shianna, D. Ge, 2010, Gastroenterology.

Change of genetic determinants of left ventricular structure in adolescence: longitudinal evidence from the Georgia cardiovascular twin study.

D. Ge, H. Snieder, G. Harshfield, 2008, American journal of hypertension.

genetic analysis Association of Common JAK 2 Variants With Body Fat , Insulin Sensitivity and Lipid Profile

T. Spector, D. Ge, H. Snieder, 2008 .

Association of Common JAK2 Variants With Body Fat, Insulin Sensitivity and Lipid Profile

T. Spector, D. Ge, H. Snieder, 2008, Obesity.

normal females associated with total-, ldl-and hdl-cholesterol in Amp-kinase alpha 2 subunit gene prkaa 2 variants are

T. Spector, D. Ge, H. Snieder, 2006 .

Year : 2010 Genome-wide mRNA expression correlates of viral control in CD 4 + T-cells from HIV-1-infected individuals

Kristen K. Dang, K. Shianna, D. Ge, 2011 .

Variants in the ITPA gene protect against ribavirin-induced hemolytic anemia and decrease the need for ribavirin dose reduction.

K. Shianna, D. Ge, D. Goldstein, 2010, Gastroenterology.

The SH2B Gene is Associated with Serum Leptin and Body Fat in Normal Female Twins

T. Spector, D. Ge, H. Snieder, 2007, Obesity.

Waist-to-height ratio is an accurate and easier index for evaluating obesity in children and adolescents.

D. Ge, Yan Weili, J. Dai, 2007, Obesity.

Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.

Michael R. Johnson, Josemir W Sander, P. Matthews, 2010, American journal of human genetics.

A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia

David B. Goldstein, Lefkos T. Middleton, Hans-Jürgen Möller, 2009, PLoS genetics.

The metabolic syndrome in Uygur and Kazak populations.

D. Ge, Weili Yan, Yuanming Zhang, 2005, Diabetes care.

Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance

Jacques Fellay, David B. Goldstein, Kevin V. Shianna, 2009, Nature.

Genetic variation in IL28B and spontaneous clearance of hepatitis C virus

David B. Goldstein, Michael P. Busch, Gregory D. Kirk, 2009, Nature.

Baseline interpatient hepatitis B viral diversity differentiates HBsAg outcomes in patients treated with tenofovir disoproxil fumarate.

D. Ge, F. Zoulim, P. Hengen, 2015, Journal of hepatology.

Interleukin 28B polymorphisms are the only common genetic variants associated with low‐density lipoprotein cholesterol (LDL‐C) in genotype‐1 chronic hepatitis C and determine the association between LDL‐C and treatment response

K. Shianna, D. Ge, D. Goldstein, 2012, Journal of viral hepatitis.

Genome-wide association study of interferon-related cytopenia in chronic hepatitis C patients.

K. Shianna, D. Ge, D. Goldstein, 2012, Journal of hepatology.

ITPA gene variants protect against anaemia in patients treated for chronic hepatitis C

Jacques Fellay, David B. Goldstein, Kevin V. Shianna, 2010, Nature.

HLA-C cell surface expression and control of HIV / AIDS correlate with a variant upstream of HLA-C

D. Ge, J. Goedert, M. Carrington, 2009 .

Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia.

Jari Tiihonen, Herbert Y Meltzer, David B Goldstein, 2012, American journal of human genetics.

Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease

Chong Shen, Lin Yu, Runsheng Chen, 2012, Nature Genetics.

SVA: software for annotating and visualizing sequenced human genomes

Elizabeth T. Cirulli, Min He, Dongliang Ge, 2011, Bioinform..

Limited contribution of common genetic variants to risk for liver injury due to a variety of drugs

K. Shianna, D. Ge, D. Goldstein, 2012, Pharmacogenetics and genomics.

Host determinants of HIV-1 control in African Americans.

K. Shianna, D. Ge, D. Goldstein, 2010, The Journal of infectious diseases.

Genetic Regulation of α-Synuclein mRNA Expression in Various Human Brain Tissues

Jeffrey N. Browndyke, D. Ge, K. Welsh-Bohmer, 2009, PloS one.

Soluble intercellular adhesion molecule-1 is associated with hepatocellular carcinoma risk: multiplex analysis of serum markers

D. Ge, Zhaoshi Jiang, O. Podlaha, 2017, Scientific Reports.

Heritability of QT Interval: How Much Is Explained by Genes for Resting Heart Rate?

T. Spector, D. Ge, H. Snieder, 2008, Journal of cardiovascular electrophysiology.

Multilocus Analyses of Renin–Angiotensin–Aldosterone System Gene Variants on Blood Pressure at Rest and During Behavioral Stress in Young Normotensive Subjects

D. Ge, H. Snieder, Yanbin Dong, 2007, Hypertension.

Genome-Wide mRNA Expression Correlates of Viral Control in CD4+ T-Cells from HIV-1-Infected Individuals

Kristen K. Dang, K. Shianna, D. Ge, 2010, PLoS pathogens.

Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study

I. Scheffer, K. Shianna, D. Ge, 2007, The Lancet Neurology.

Copy Number Variation of KIR Genes Influences HIV-1 Control

K. Shianna, D. Ge, A. Need, 2011, PLoS biology.

Prioritizing genetic variants for causality on the basis of preferential linkage disequilibrium.

Qianqian Zhu, David B Goldstein, K. Shianna, 2012, American journal of human genetics.

Joint Linkage and Association of Six Single-Nucleotide Polymorphisms in the Factor XIII-A Subunit Gene Point to V34L As the Main Functional Locus

T. Spector, D. Ge, H. Snieder, 2006, Arteriosclerosis, thrombosis, and vascular biology.

Correction: A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia

D. Rujescu, P. Muglia, C. Francks, 2009, PLoS Genetics.

WGAViewer: software for genomic annotation of whole genome association studies.

Jacques Fellay, Amalio Telenti, Kunlin Zhang, 2008, Genome research.

Common genetic variation and performance on standardized cognitive tests

Greg Gibson, David B Goldstein, D. Ge, 2010, European Journal of Human Genetics.

Evidence for linkage and association of the markers near the LPL gene with hypertension in Chinese families

D. Ge, R. Hui, D. Gu, 2003, Journal of medical genetics.

Expansion of the Parkinson disease-associated SNCA-Rep1 allele upregulates human α-synuclein in transgenic mouse brain

D. Ge, R. Nussbaum, C. Linnertz, 2009, Human molecular genetics.

β2‐Adrenergic Receptor Gene Variations Associated with Stage‐2 Hypertension in Northern Han Chinese

D. Ge, D. Gu, Biao Li, 2005, Annals of human genetics.

Pharmacogenetics of antipsychotic response in the CATIE trial: a candidate gene analysis

D. Ge, A. Need, D. Goldstein, 2009, European Journal of Human Genetics.

The state of genome-wide association studies in pulmonary disease: a new perspective.

D. Ge, D. Goldstein, J. Christie, 2011, American journal of respiratory and critical care medicine.

Genome-wide association scan identifies a prostaglandin-endoperoxide synthase 2 variant involved in risk of knee osteoarthritis.

A. Hofman, A. Uitterlinden, T. Spector, 2008, American journal of human genetics.

The Association of Genetic Variants with Hepatic Steatosis in Patients with Genotype 1 Chronic Hepatitis C Infection

K. Shianna, D. Ge, D. Goldstein, 2012, Digestive Diseases and Sciences.

Association Study With 33 Single-Nucleotide Polymorphisms in 11 Candidate Genes for Hypertension in Chinese

Runsheng Chen, Shaoyong Su, Shufeng Chen, 2006, Hypertension.

Cardiovascular characteristics in American youth with prehypertension.

D. Ge, H. Snieder, Weili Yan, 2007, American journal of hypertension.

Emergence of Novel Genetic Effects on Blood Pressure and Hemodynamics in Adolescence: The Georgia Cardiovascular Twin Study

D. Ge, H. Snieder, N. Kupper, 2006, Hypertension.

Linkage and linkage disequilibrium analysis of the lipoprotein lipase gene with lipid profiles in Chinese hypertensive families.

D. Ge, Jianfeng Huang, D. Gu, 2005, Clinical science.

The Duffy antigen receptor for chemokines null promoter variant does not influence HIV-1 acquisition or disease progression.

K. Shianna, D. Ge, D. Goldstein, 2009, Cell host & microbe.

The inheritance of peripapillary atrophy.

Paul Mitchell, Harold Snieder, T. Spector, 2007, Investigative ophthalmology & visual science.

Heritability of Strabismus: Genetic Influence Is Specific to Eso-Deviation and Independent of Refractive Error

T. Spector, D. Ge, N. Martin, 2012, Twin Research and Human Genetics.

Ethnic differences in the association of birth weight and blood pressure: the Georgia cardiovascular twin study.

D. Ge, H. Snieder, A. Iliadou, 2007, American journal of hypertension.

Genome-Wide Association Study to Characterize Serum Bilirubin Elevations in Patients with HCV Treated with Gs-9256, An HCV Ns3 Serine Protease Inhibitor

D. Ge, P. Pang, P. Hengen, 2014, Antiviral therapy.

CLINICAL ADVANCES IN LIVER, PANCREAS, AND BILIARY TRACT Interleukin-28B Polymorphism Improves Viral Kinetics and Is the Strongest Pretreatment Predictor of Sustained Virologic Response in Genotype 1 Hepatitis C Virus

William M. Lee, K. Shianna, D. Ge, 2010 .

Association of α1A adrenergic receptor gene variants on chromosome 8p21 with human stage 2 hypertension

D. Ge, Jianfeng Huang, D. Gu, 2006, Journal of hypertension.

Relationships of Cardiovascular Phenotypes With Healthy Weight, at Risk of Overweight, and Overweight in US Youths

D. Ge, H. Snieder, Weili Yan, 2008, Pediatrics.

Heritability of arterial stiffness in black and white American youth and young adults.

D. Ge, H. Snieder, Xiaoling Wang, 2007, American journal of hypertension.

Lipoprotein lipase gene polymorphisms and blood pressure levels in the Northern Chinese Han population.

D. Ge, D. Gu, Runsheng Chen, 2004, Hypertension research : official journal of the Japanese Society of Hypertension.

A functional intronic variant in the tyrosine hydroxylase (TH) gene confers risk of essential hypertension in the Northern Chinese Han population.

D. Ge, Xiangfeng Lu, D. Gu, 2008, Clinical science.

Genome Wide-Association Study Identifies Il28B Polymorphism to Be Associated with Baseline Alt and Hepatic Necro-Inflammatory Activity in Chronic Hepatitis C Patients Enrolled in the Ideal Study

D. Ge, D. Goldstein, Qianqian Zhu, 2010 .

Linkage Analysis of Chromosome 1 with Essential Hypertension and Blood Pressure Quantitative Traits in Chinese Families

D. Ge, Yan Shen, Jianfeng Huang, 2005, Annals of human genetics.

Linkage analysis of 2q14-q23 and 5q32 with blood pressure quantitative traits in Chinese sib pairs

D. Ge, Yan Shen, Zhijian Yao, 2003, Journal of hypertension.

A twin study of auditory processing indicates that dichotic listening ability is a strongly heritable trait

D. Ge, H. Snieder, T. Friedman, 2007, Human Genetics.

Urinary norepinephrine and epinephrine excretion rates are heritable, but not associated with office and ambulatory blood pressure

D. Ge, H. Snieder, F. Treiber, 2012, Hypertension Research.

Differential Serum Cytokine Profiles in Patients with Chronic Hepatitis B, C, and Hepatocellular Carcinoma

D. Ge, Zhaoshi Jiang, O. Podlaha, 2017, Scientific Reports.

Linkage analysis of chromosome 14 and essential hypertension in Chinese population.

D. Ge, Jianfeng Huang, Biao Li, 2005, Chinese medical journal.

Genetic susceptibility loci for essential hypertension and blood pressure on chromosome 17 in 147 Chinese pedigrees

D. Ge, Jianfeng Huang, D. Gu, 2004, Journal of hypertension.

Il28B Genetic Polymorphism Has Genome Wide Significant Associations with Serum Low Density Lipoprotein Levels and Hepatic Steatosis in Patients with Genotype 1 Chronic Hepatitis C (Chc)

William M. Lee, D. Ge, D. Goldstein, 2010 .

Hepatitis C trials that combine investigational agents with pegylated interferon should be stratified by interleukin‐28B genotype

D. Ge, D. Goldstein, J. Fellay, 2010, Hepatology.

HEPATITIS C TRIALS THAT COMBINE INVESTIGATIONAL AGENTS WITH PEGYLATED-INTERFERON-alpha SHOULD BE STRATIFIED BY IL28B GENOTYPE

D. Ge, D. Goldstein, J. Fellay, 2010 .

Association analysis of the variant in the regulatory subunit of phosphoinositide 3‐kinase (p85α) with Type 2 diabetes mellitus and hypertension in the Chinese Han population

D. Ge, Jianfeng Huang, D. Gu, 2005, Diabetic medicine : a journal of the British Diabetic Association.

The Georgia Cardiovascular Twin Study: Influence of Genetic Predisposition and Chronic Stress on Risk for Cardiovascular Disease and Type 2 Diabetes

D. Ge, H. Snieder, Yanbin Dong, 2006, Twin Research and Human Genetics.

The Georgia Cardiovascular Twin Study: Influence of Genetic Predisposition and Chronic Stress on Risk for Cardiovascular Disease and Type 2 Diabetes

D. Ge, H. Snieder, Yanbin Dong, 2006, Twin Research and Human Genetics.

Lipoprotein lipase gene is in linkage with blood pressure phenotypes in Chinese pedigrees

D. Ge, Yan Shen, Jianfeng Huang, 2004, Human Genetics.

Randomised clinical trial: a phase 1, dose‐ranging study of the anti‐matrix metalloproteinase‐9 monoclonal antibody GS‐5745 versus placebo for ulcerative colitis

D. Ge, X. Zhao, R. Fogel, 2016, Alimentary pharmacology & therapeutics.

Genetic association analysis of myocardial infarction with thrombospondin-1 N700S variant in a Chinese population.

D. Ge, Jianfeng Huang, D. Gu, 2004, Thrombosis research.

Interleukin-28B polymorphism improves viral kinetics and is the strongest pretreatment predictor of sustained virologic response in genotype 1 hepatitis C virus.

William M. Lee, K. Shianna, D. Ge, 2010, Gastroenterology.

The Duffy antigen receptor for chemokines null promoter variant does not influence HIV-1 acquisition or disease progression.

K. Shianna, D. Ge, M. Carrington, 2009, Cell host & microbe.

Heritability of Strabismus: Genetic Influence Is Specific to Eso-Deviation and Independent of Refractive Error

T. Spector, D. Ge, H. Snieder, 2012, Twin Research and Human Genetics.