Author details

Full Name

Dandi Qiao

Affiliation

ORCID

Career Start Year

2012

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37046083	Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.	Nature	2023
37126548	The genetic determinants of recurrent somatic mutations in 43,693 blood genomes.	Sci Adv	2023
34996830	<i>C</i> <i>FTR</i> variants are associated with chronic bronchitis in smokers.	Eur Respir J	2022
35766891	Assessing the contribution of rare genetic variants to phenotypes of chronic obstructive pulmonary disease using whole-genome sequence data.	Hum Mol Genet	2022
35649102	Machine Learning Prediction of Progression in Forced Expiratory Volume in 1 Second in the COPDGeneÂ® Study.	Chronic Obstr Pulm Dis	2022
35385699	Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program.	Am J Hum Genet	2022
35385311	Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential.	Sci Adv	2022
36220609	A statistical physics approach for disease module detection.	Genome Res	2022
35927319	Rare genetic variants explain missing heritability in smoking.	Nat Hum Behav	2022
36058164	Clinical outcomes of digital health in adults with cystic fibrosis.	Respiratory Medicine	2022
36383614	A robust and adaptive framework for interaction testing in quantitative traits between multiple genetic loci and exposure variables.	PLoS Genet	2022
34855941	Association of clonal hematopoiesis with chronic obstructive pulmonary disease.	Blood	2022
35115341	A polygenic risk score and age of diagnosis of COPD.	Eur Respir J	2022
35115336	Interstitial lung abnormalities are associated with decreased mean telomere length.	Eur Respir J	2022
34536413	Multiethnic genome-wide and HLA association study of total serum IgE level.	J Allergy Clin Immunol	2021
34166600	Connecting COPD GWAS Genes: FAM13A Controls TGFÎ²2 Secretion by Modulating AP-3 Transport.	Am J Respir Cell Mol Biol	2021
34224973	Tempo-spatial regulation of the Wnt pathway by FAM13A modulates the stemness of alveolar epithelial progenitors.	eBioMedicine	2021
34159627	Genome-wide association analysis of COVID-19 mortality risk in SARS-CoV-2 genomes identifies mutation in the SARS-CoV-2 spike protein that colocalizes with P.1 of the Brazilian strain.	Genet Epidemiol	2021
33720349	Robust, flexible, and scalable tests for Hardy-Weinberg equilibrium across diverse ancestries.	Genetics	2021
34913977	Interaction of Cigarette Smoking and Polygenic Risk Score on Reduced Lung Function.	JAMA Netw Open	2021
34430780	Heterozygosity of the Alpha 1-Antitrypsin Pi*Z Allele and Risk of Liver Disease.	Hepatol Commun	2021
33057025	Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants.	Nat Commun	2020
32353417	Machine Learning and Prediction of All-Cause Mortality in COPD.	Chest	2020
32151973	FAM13A Represses AMPK Activity and Regulates Hepatic Glucose and Lipid Metabolism.	iScience	2020
33039714	A linear prognostic score based on the ratio of interleukin-6 to interleukin-10 predicts outcomes in COVID-19.	EBioMedicine	2020
33181463	Corrigendum to 'A linear prognostic score based on the ratio of interleukin-6 to interleukin-10 predicts outcomes in COVID-19'.	EBioMedicine	2020
32681690	Statistical considerations for the analysis of massively parallel reporter assays data.	Genet Epidemiol	2020
30804560	New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.	Nat Genet	2019
30079747	Identification of Functional Variants in the FAM13A Chronic Obstructive Pulmonary Disease Genome-Wide Association Study Locus by Massively Parallel Reporter Assays.	Am J Respir Crit Care Med	2019
31275357	metaFARVAT: An Efficient Tool for Meta-Analysis of Family-Based, Case-Control, and Population-Based Rare Variant Association Studies.	Front Genet	2019
29725345	A Genome-Wide Linkage Study for Chronic Obstructive Pulmonary Disease in a Dutch Genetic Isolate Identifies Novel Rare Candidate Variants.	Front Genet	2018
29981437	Rare Variants in Known Susceptibility Loci and Their Contribution to Risk of Lung Cancer.	J Thorac Oncol	2018
30060175	Whole exome sequencing analysis in severe chronic obstructive pulmonary disease.	Hum Mol Genet	2018
29915320	Genome-wide assessment of gene-by-smoking interactions in COPD.	Sci Rep	2018
29949718	Whole-Genome Sequencing in Severe Chronic Obstructive Pulmonary Disease.	Am J Respir Cell Mol Biol	2018
29697360	WISARD: workbench for integrated superfast association studies for related datasets.	BMC Med Genomics	2018
28191685	Gene-based segregation method for identifying rare variants in family-based sequencing studies.	Genet Epidemiol	2017
28222494	Selecting cases and controls for DNA sequencing studies using family histories of disease.	Stat Med	2017
28166215	Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis.	Nat Genet	2017
27666371	Increasing Generality and Power of Rare-Variant Tests by Utilizing Extended Pedigrees.	Am J Hum Genet	2016
26736064	Exome Sequencing Analysis in Severe, Early-Onset Chronic Obstructive Pulmonary Disease.	Am J Respir Crit Care Med	2016
27325607	FARVATX: Family-Based Rare Variant Association Test for X-Linked Genes.	Genet Epidemiol	2016
26771213	Exome Array Analysis Identifies a Common Variant in IL27 Associated with Chronic Obstructive Pulmonary Disease.	Am J Respir Crit Care Med	2016
27312886	Family-Based Rare Variant Association Analysis: A Fast and Efficient Method of Multivariate Phenotype Association Analysis.	Genet Epidemiol	2016
27646141	Boosting Gene Mapping Power and Efficiency with Efficient Exact Variance Component Tests of Single Nucleotide Polymorphism Sets.	Genetics	2016
25832413	PLD3 gene variants and Alzheimer's disease.	Nature	2015
25186855	The rare TREM2 R47H variant exerts only a modest effect on Alzheimer disease risk.	Neurology	2014
25439724	PRIMUS: rapid reconstruction of pedigrees from genome-wide estimates of identity by descent.	Am J Hum Genet	2014
25519381	A comparative analysis of family-based and population-based association tests using whole genome sequence data.	BMC Proc	2014
24262215	On the simultaneous association analysis of large genomic regions: a massive multi-locus association test.	Bioinformatics	2014