Author details

Full Name

Dajiang J Liu

Affiliation

ORCID

Career Start Year

2010

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37693466	The pivotal role of the X-chromosome in the genetic architecture of the human brain.	medRxiv	2024
37244961	Future trends in incidence and long-term survival of metastatic cancer in the United States.	Commun Med (Lond)	2023
36702996	Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing.	Nat Genet	2023
36750564	Multi-ancestry and multi-trait genome-wide association meta-analyses inform clinical risk prediction for systemic lupus erythematosus.		2023
35099546	Association of Spinal Cord Stimulator Implantation With Persistent Opioid Use in Patients With Postlaminectomy Syndrome.	JAMA Netw Open	2022
35903101	Hydrophilic But Not Hydrophobic Surfactant Protein Genetic Variants Are Associated With Severe Acute Respiratory Syncytial Virus Infection in Children.	Front Immunol	2022
35833142	Construction and Application of Polygenic Risk Scores in Autoimmune Diseases.	Frontiers in Immunology	2022
36002830	Analysis of KIR gene variants in The Cancer Genome Atlas and UK Biobank using KIRCLE.	BMC Biol	2022
35927319	Rare genetic variants explain missing heritability in smoking.	Nat Hum Behav	2022
35672318	Integrating 3D genomic and epigenomic data to enhance target gene discovery and drug repurposing in transcriptome-wide association studies.	Nature Communications	2022
35777465	MB-SupCon: Microbiome-based Predictive Models via Supervised Contrastive Learning.	J Mol Biol	2022
36477530	Genetic diversity fuels gene discovery for tobacco and alcohol use.	Nature	2022
32762793	Genetic correlation, pleiotropy, and causal associations between substance use and psychiatric disorder.	Psychological Medicine	2022
35259044	Circular RNA hsa_circ_0011324 is involved in endometrial cancer progression and the evolution of its mechanism.	Bioengineered	2022
34426515	Inferring genes that escape X-Chromosome inactivation reveals important contribution of variable escape genes to sex-biased diseases.	Genome Res	2021
33543271	MB-GAN: Microbiome Simulation via Generative Adversarial Network.	Gigascience	2021
34050687	Prothrombotic variants as modifiers of clinical phenotype in four related individuals with haemophilia A.	Haemophilia	2021
33727701	Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Nat Genet	2021
33713107	MetaPrism: A versatile toolkit for joint taxa/gene analysis of metagenomic sequencing data.	G3 (Bethesda)	2021
33385400	Causal Relationship and Shared Genetic Loci between Psoriasis and Type 2 Diabetes through Trans-Disease Meta-Analysis.		2021
32939058	METTL3-mediated maturation of miR-126-5p promotes ovarian cancer progression via PTEN-mediated PI3K/Akt/mTOR pathway.	Cancer Gene Therapy	2021
34613403	Medical Service Use and Charges for Cancer Care in 2018 for Privately Insured Patients Younger Than 65 Years in the US.	JAMA Netw Open	2021
34497267	METTL3 promotes the initiation and metastasis of ovarian cancer by inhibiting CCNG2 expression via promoting the maturation of pri-microRNA-1246.	Cell Death Discovery	2021
30617275	Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci.	Mol Psychiatry	2020
32021280	SPOCD1 accelerates ovarian cancer progression and inhibits cell apoptosis via the PI3K/AKT pathway.	OncoTargets and Therapy	2020
32246825	Prioritizing genetic variants in GWAS with lasso using permutation-assisted tuning.		2020
32291117	A novel laparoscopic technique for retro-aortic and retro-caval lymphadenectomy.	Gynecologic Oncology	2020
32466134	Association Analysis and Meta-Analysis of Multi-Allelic Variants for Large-Scale Sequence Data.	Genes (Basel)	2020
32756942	Seqminer2: an efficient tool to query and retrieve genotypes for statistical genetics analyses from biobank scale sequence dataset.	Bioinformatics	2020
32521332	Investigation of discordant phenotype in mild Hemophilia A using whole exome sequencing.	Thrombosis Research	2020
33230300	Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Nat Genet	2020
33105540	Soluble Compounds Released by Hypoxic Stroma Confer Invasive Properties to Pancreatic Ductal Adenocarcinoma.	Biomedicines	2020
30849219	Methods for the Analysis and Interpretation for Rare Variants Associated with Complex Traits.	Current Protocols in Human Genetics	2019
31856248	Impact of HFE variants and sex in lung cancer.	PLoS ONE	2019
31160809	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2019
29273807	Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
30214655	ADAPTIVE-WEIGHT BURDEN TEST FOR ASSOCIATIONS BETWEEN QUANTITATIVE TRAITS AND GENOTYPE DATA WITH COMPLEX CORRELATIONS.	Annals of Applied Statistics	2018
30024495	Clinical significance of matrix metalloproteinase-2 in endometrial cancer: A systematic review and meta-analysis.	Medicine (United States)	2018
30016313	Proper conditional analysis in the presence of missing data: Application to large scale meta-analysis of tobacco use phenotypes.	PLoS Genet	2018
30275531	Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program.	Nat Genet	2018
29549330	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29595187	Inhibition of Expression of the S100A8 Gene Encoding the S100 Calcium-Binding Protein A8 Promotes Apoptosis by Suppressing the Phosphorylation of Protein Kinase B (Akt) in Endometrial Carcinoma and HEC-1A Cells.	Medical Science Monitor	2018
29549329	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29632382	Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.	Nat Genet	2018
28115622	Robust and rapid algorithms facilitate large-scale whole genome sequencing downstream analysis in an integrative framework.	Nucleic Acids Res	2017
28669402	SEQSpark: A Complete Analysis Tool for Large-Scale Rare Variant Association Studies Using Whole-Genome and Exome Sequence Data.	Am J Hum Genet	2017
28712776	Clonal evolution in paired endometrial intraepithelial neoplasia/atypical hyperplasia and endometrioid adenocarcinoma.	Human Pathology	2017
28358914	Analysis of single nucleotide variants of HFE gene and association to survival in The Cancer Genome Atlas GBM data.	PLoS ONE	2017
29083408	Exome-wide association study of plasma lipids in >300,000 individuals.	Nat Genet	2017
29083407	Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease.	Nat Genet	2017