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SumVg: Total Heritability Explained by All Variants in Genome-Wide Association Studies Based on Summary Statistics with Standard Error Estimates

International journal of molecular sciences, 2024-01, Vol.25 (2), p.1347

2024

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Exploring shared genetic bases and causal relationships of schizophrenia and bipolar disorder with 28 cardiovascular and metabolic traits

Psychological medicine, 2019-06, Vol.49 (8), p.1286-1298

2019

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HLA-DP and IL28B Polymorphisms: Influence of Host Genome on Hepatitis B Surface Antigen Seroclearance in Chronic Hepatitis B

Clinical infectious diseases, 2013-06, Vol.56 (12), p.1695-1703

2013

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Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease

Proceedings of the National Academy of Sciences - PNAS, 2009-02, Vol.106 (8), p.2694-2699

2009

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Genetic variant in vitamin D binding protein is associated with serum 25-hydroxyvitamin D and vitamin D insufficiency in southern Chinese

Journal of human genetics, 2013-11, Vol.58 (11), p.749-751

2013

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The support of human genetic evidence for approved drug indications

Nature genetics, 2015-08, Vol.47 (8), p.856-860

2015

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Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease

Scientific reports, 2015-11, Vol.5 (1), p.16473-16473, Article 16473

2015

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Patient complexity and genotype-phenotype correlations in biliary atresia: a cross-sectional analysis

BMC medical genomics, 2017-04, Vol.10 (1), p.22-22, Article 22

2017

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Integrating Clinical Data and Imputed Transcriptome from GWAS to Uncover Complex Disease Subtypes: Applications in Psychiatry and Cardiology

American journal of human genetics, 2019-12, Vol.105 (6), p.1193-1212

2019

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Positive effects of low LDL-C and statins on bone mineral density: an integrated epidemiological observation analysis and Mendelian randomization study

International journal of epidemiology, 2020-08, Vol.49 (4), p.1221-1235

2020

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A joint study of whole exome sequencing and structural MRI analysis in major depressive disorder

Psychological medicine, 2020-02, Vol.50 (3), p.384-395

2020

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A framework to decipher the genetic architecture of combinations of complex diseases: applications in cardiovascular medicine

Bioinformatics (Oxford, England), 2021-11, Vol.37 (22), p.4137-4147

2021

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An autoimmune pleiotropic SNP modulates IRF5 alternative promoter usage through ZBTB3-mediated chromatin looping

Nature communications, 2023-03, Vol.14 (1), p.1208-1208, Article 1208

2023

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Mendelian Randomization Focused Analysis of Vitamin D on the Secondary Prevention of Ischemic Stroke

Stroke (1970), 2021-12, Vol.52 (12), p.3926-3937

2021

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Meta-analysis Followed by Replication Identifies Loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as Associated with Systemic Lupus Erythematosus in Asians

American journal of human genetics, 2013-01, Vol.92 (1), p.41-51

2013

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Pre-B-cell leukemia homeobox 1 (PBX1) shows functional and possible genetic association with bone mineral density variation

Human molecular genetics, 2009-02, Vol.18 (4), p.679-687

2009

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Burden of rare variants in ALS genes influences survival in familial and sporadic ALS

Neurobiology of aging, 2017-10, Vol.58, p.238.e9-238.e15

2017

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Comprehensive and integrative analyses identify TYW5 as a schizophrenia risk gene

BMC medicine, 2022-05, Vol.20 (1), p.169-169, Article 169

2022

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cepip: context-dependent epigenomic weighting for prioritization of regulatory variants and disease-associated genes

Genome Biology, 2017-03, Vol.18 (1), p.52-52, Article 52

2017

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Genetic variant representation, annotation and prioritization in the post-GWAS era

Cell research, 2012-10, Vol.22 (10), p.1505-1508

2012

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Genetically deprived vitamin D exposure predisposes to atrial fibrillation

Europace (London, England), 2017-12, Vol.19 (suppl_4), p.iv25-iv31

2017

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HaploShare: identification of extended haplotypes shared by cases and evaluation against controls

Genome Biology, 2015-05, Vol.16 (1), p.92-92, Article 92

2015

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Predicting the number and sizes of IBD regions among family members and evaluating the family size requirement for linkage studies

European journal of human genetics : EJHG, 2008-12, Vol.16 (12), p.1535-1543

2008

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Common Variants on Xq28 Conferring Risk of Schizophrenia in Han Chinese

Schizophrenia bulletin, 2014-07, Vol.40 (4), p.777-786

2014

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Possible Modifying Effect of Hemoglobin A1c on Genetic Susceptibility to Severe Diabetic Retinopathy in Patients With Type 2 Diabetes

Investigative ophthalmology & visual science, 2020-08, Vol.61 (10), p.7-7

2020

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SumVg: Total Heritability Explained by All Variants in Genome-Wide Association Studies Based on Summary Statistics with Standard Error Estimates

Exploring shared genetic bases and causal relationships of schizophrenia and bipolar disorder with 28 cardiovascular and metabolic traits

HLA-DP and IL28B Polymorphisms: Influence of Host Genome on Hepatitis B Surface Antigen Seroclearance in Chronic Hepatitis B

Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease

Genetic variant in vitamin D binding protein is associated with serum 25-hydroxyvitamin D and vitamin D insufficiency in southern Chinese

The support of human genetic evidence for approved drug indications

Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease

Patient complexity and genotype-phenotype correlations in biliary atresia: a cross-sectional analysis

Integrating Clinical Data and Imputed Transcriptome from GWAS to Uncover Complex Disease Subtypes: Applications in Psychiatry and Cardiology

Positive effects of low LDL-C and statins on bone mineral density: an integrated epidemiological observation analysis and Mendelian randomization study

A joint study of whole exome sequencing and structural MRI analysis in major depressive disorder

A framework to decipher the genetic architecture of combinations of complex diseases: applications in cardiovascular medicine

An autoimmune pleiotropic SNP modulates IRF5 alternative promoter usage through ZBTB3-mediated chromatin looping

Mendelian Randomization Focused Analysis of Vitamin D on the Secondary Prevention of Ischemic Stroke

Meta-analysis Followed by Replication Identifies Loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as Associated with Systemic Lupus Erythematosus in Asians

Pre-B-cell leukemia homeobox 1 (PBX1) shows functional and possible genetic association with bone mineral density variation

Burden of rare variants in ALS genes influences survival in familial and sporadic ALS

Comprehensive and integrative analyses identify TYW5 as a schizophrenia risk gene

cepip: context-dependent epigenomic weighting for prioritization of regulatory variants and disease-associated genes

Genetic variant representation, annotation and prioritization in the post-GWAS era

Genetically deprived vitamin D exposure predisposes to atrial fibrillation

HaploShare: identification of extended haplotypes shared by cases and evaluation against controls

Predicting the number and sizes of IBD regions among family members and evaluating the family size requirement for linkage studies

Common Variants on Xq28 Conferring Risk of Schizophrenia in Han Chinese

Possible Modifying Effect of Hemoglobin A1c on Genetic Susceptibility to Severe Diabetic Retinopathy in Patients With Type 2 Diabetes

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