List of works - Qiongshi Lu

A Genome-Wide Association Study to Identify Single-Nucleotide Polymorphisms for Acute Kidney Injury

A Powerful Approach to Estimating Annotation-Stratified Genetic Covariance via GWAS Summary Statistics

scientific article published in December 2017

A quantile integral linear model to quantify genetic effects on phenotypic variability

scientific article published in 2022

A review of study designs and statistical methods for genomic epidemiology studies using next generation sequencing

scientific article

A statistical framework for cross-tissue transcriptome-wide association analysis

scientific article published on 25 February 2019

A statistical framework to predict functional non-coding regions in the human genome through integrated analysis of annotation data

scientific article

An evaluation of noncoding genome annotation tools through enrichment analysis of 15 genome-wide association studies

scientific article

Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations

scientific article published on 12 January 2021

Comparison of methods for estimating genetic correlation between complex traits using GWAS summary statistics

scientific article published in 2021

Computational Genomics in the Era of Precision Medicine: Applications to Variant Analysis and Gene Therapy

scientific article published on 28 January 2022

Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.

scientific article published on 9 October 2017

Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus

scientific article published on 19 October 2020

Genetic variants and functional pathways associated with resilience to Alzheimer's disease

scientific article published on 01 August 2020

GenoWAP: GWAS signal prioritization through integrated analysis of genomic functional annotation.

scientific article

Genome-wide Association Study of Maximum Habitual Alcohol Intake in >140,000 U.S. European and African American Veterans Yields Novel Risk Loci

scientific article published on 08 April 2019

Genome-wide association study of cognitive performance in U.S. veterans with schizophrenia or bipolar disorder

scientific article published on 24 December 2019

Genome-wide association study of post-traumatic stress disorder reexperiencing symptoms in >165,000 US veterans

scientific article published on 29 July 2019

Genome-wide association study reveals sex-specific genetic architecture of facial attractiveness

scientific article published on 04 April 2019

High frequency of mitochondrial DNA mutations in HIV-infected treatment-experienced individuals

scientific article published on 22 June 2016

Integrated analysis of genomics, longitudinal metabolomics, and Alzheimer's risk factors among 1,111 cohort participants

scientific article published on 18 May 2019

Joint modeling of genetically correlated diseases and functional annotations increases accuracy of polygenic risk prediction

scientific article

Leveraging functional annotation to identify genes associated with complex diseases

scientific article published on 02 November 2020

Leveraging functional annotations in genetic risk prediction for human complex diseases

scientific article

Mutations disrupting neuritogenesis genes confer risk for cerebral palsy

scientific article published on 28 September 2020

Mutations in Chromatin Modifier and Ephrin Signaling Genes in Vein of Galen Malformation

scientific article published on 18 December 2018

Post-GWAS Prioritization Through Data Integration Provides Novel Insights on Chronic Obstructive Pulmonary Disease.

scientific article

Systematic tissue-specific functional annotation of the human genome highlights immune-related DNA elements for late-onset Alzheimer's disease

scientific article

The impact of parenting a child with serious mental illness: Accounting for the parent's genetic vulnerability to mental illness

scientific article published on 16 July 2020

Two locus inheritance of non-syndromic midline craniosynostosis via rare SMAD6 and common BMP2 alleles

scientific article

Validating psychosocial pathways of risk between neuroticism and late life depression using a polygenic score approach

scientific article published on 04 March 2019

List of works by Qiongshi Lu

A Genome-Wide Association Study to Identify Single-Nucleotide Polymorphisms for Acute Kidney Injury

A Powerful Approach to Estimating Annotation-Stratified Genetic Covariance via GWAS Summary Statistics

A quantile integral linear model to quantify genetic effects on phenotypic variability

A review of study designs and statistical methods for genomic epidemiology studies using next generation sequencing

A statistical framework for cross-tissue transcriptome-wide association analysis

A statistical framework to predict functional non-coding regions in the human genome through integrated analysis of annotation data

An evaluation of noncoding genome annotation tools through enrichment analysis of 15 genome-wide association studies

Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations

Comparison of methods for estimating genetic correlation between complex traits using GWAS summary statistics

Computational Genomics in the Era of Precision Medicine: Applications to Variant Analysis and Gene Therapy

Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.

Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus

Genetic variants and functional pathways associated with resilience to Alzheimer's disease

GenoWAP: GWAS signal prioritization through integrated analysis of genomic functional annotation.

Genome-wide Association Study of Maximum Habitual Alcohol Intake in >140,000 U.S. European and African American Veterans Yields Novel Risk Loci

Genome-wide association study of cognitive performance in U.S. veterans with schizophrenia or bipolar disorder

Genome-wide association study of post-traumatic stress disorder reexperiencing symptoms in >165,000 US veterans

Genome-wide association study reveals sex-specific genetic architecture of facial attractiveness

High frequency of mitochondrial DNA mutations in HIV-infected treatment-experienced individuals

Integrated analysis of genomics, longitudinal metabolomics, and Alzheimer's risk factors among 1,111 cohort participants

Joint modeling of genetically correlated diseases and functional annotations increases accuracy of polygenic risk prediction

Leveraging functional annotation to identify genes associated with complex diseases

Leveraging functional annotations in genetic risk prediction for human complex diseases

Mutations disrupting neuritogenesis genes confer risk for cerebral palsy

Mutations in Chromatin Modifier and Ephrin Signaling Genes in Vein of Galen Malformation

Post-GWAS Prioritization Through Data Integration Provides Novel Insights on Chronic Obstructive Pulmonary Disease.

Systematic tissue-specific functional annotation of the human genome highlights immune-related DNA elements for late-onset Alzheimer's disease

The impact of parenting a child with serious mental illness: Accounting for the parent's genetic vulnerability to mental illness

Two locus inheritance of non-syndromic midline craniosynostosis via rare SMAD6 and common BMP2 alleles

Validating psychosocial pathways of risk between neuroticism and late life depression using a polygenic score approach