Author details

Full Name

Xue Zhong

Affiliation

ORCID

Career Start Year

2013

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36703017	A phenome-wide comparative analysis of genetic discordance between obesity and type 2 diabetes.		2023
38055739	Essential role of MFSD1-GLMP-GIMAP5 in lymphocyte survival and liver homeostasis.		2023
38012144	OVOL2 sustains postnatal thymic epithelial cell identity.	Nat Commun	2023
37934820	Essential requirement for IER3IP1 in B cell development.		2023
36750564	Multi-ancestry and multi-trait genome-wide association meta-analyses inform clinical risk prediction for systemic lupus erythematosus.		2023
36169218	A Single Nucleotide Polymorphism in <i>SH2B3/LNK</i> Promotes Hypertension Development and Renal Damage.	Circ Res	2022
35482923	RNPS1 inhibits excessive tumor necrosis factor/tumor necrosis factor receptor signaling to support hematopoiesis in mice.	Proceedings of the National Academy of Sciences of the United States of America	2022
36344522	Discerning asthma endotypes through comorbidity mapping.	Nat Commun	2022
34260399	Thousands of induced germline mutations affecting immune cells identified by automated meiotic mapping coupled with machine learning.	Proceedings of the National Academy of Sciences of the United States of America	2021
33630350	Calcium flux control by Pacs1-Wdr37 promotes lymphocyte quiescence and lymphoproliferative diseases.	EMBO Journal	2021
33357513	Host genetic effects in pneumonia.	Am J Hum Genet	2021
32810290	Dominant atopy risk mutations identified by mouse forward genetic analysis.	Allergy	2021
34715901	Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes.	Genome Med	2021
34582791	Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.	Am J Hum Genet	2021
31883642	Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts.	Am J Hum Genet	2020
33020666	A unified framework for joint-tissue transcriptome-wide association and Mendelian randomization analysis.	Nat Genet	2020
32888493	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Cell	2020
32761233	Adenosine monophosphate deaminase 3 null mutation causes reduction of naive T cells in mouse peripheral blood.	Blood advances	2020
32368286	Plasma exo-hsa_circRNA_0056616: A potential biomarker for lymph node metastasis in lung adenocarcinoma.	Journal of Cancer	2020
32296164	Electronic health record phenotypes associated with genetically regulated expression of CFTR and application to cystic fibrosis.	Genet Med	2020
32220963	Genetic and structural studies of RABL3 reveal an essential role in lymphoid development and function.	Proc Natl Acad Sci U S A	2020
32071239	Essential requirement for nicastrin in marginal zone and B-1 B cell development.	Proceedings of the National Academy of Sciences of the United States of America	2020
31985756	Essential cell-extrinsic requirement for PDIA6 in lymphoid and myeloid development.	Journal of Experimental Medicine	2020
31336988	SCINA: A Semi-Supervised Subtyping Algorithm of Single Cells and Bulk Samples.	Genes (Basel)	2019
31073040	LMBR1L regulates lymphopoiesis through Wnt/Î²-catenin signaling.	Science	2019
30988527	A Bayesian framework that integrates multi-omics data and gene networks predicts risk genes from schizophrenia GWAS data.	Nat Neurosci	2019
30827500	GRIK5 Genetically Regulated Expression Associated with Eye and Vascular Phenomes: Discovery through Iteration among Biobanks, Electronic Health Records, and Zebrafish.	Am J Hum Genet	2019
30307499	Whole genome sequence association with E-selectin levels reveals loss-of-function variant in African Americans.	Hum Mol Genet	2019
30256891	De novo pattern discovery enables robust assessment of functional consequences of non-coding variants.	Bioinformatics	2019
31509211	A Genetic Approach to the Association Between PCSK9 and Sepsis.	JAMA Netw Open	2019
31427773	Syndromic immune disorder caused by a viable hypomorphic allele of spliceosome component Snrnp40.	Nature Immunology	2019
29764838	A common TCN1 loss-of-function variant is associated with lower vitamin B12 concentration in African Americans.	Blood	2018
30442666	Excessive endosomal TLR signaling causes inflammatory disease in mice with defective SMCR8-WDR41-C9ORF72 complex function.	Proceedings of the National Academy of Sciences of the United States of America	2018
30333305	LNK deficiency promotes acute aortic dissection and rupture.	JCI Insight	2018
27797769	Cancer driver gene discovery through an integrative genomics approach in a non-parametric Bayesian framework.	Bioinformatics	2017
28911083	Multiregion whole-exome sequencing of matched primary and metastatic tumors revealed genomic heterogeneity and suggested polyclonal seeding in colorectal cancer metastasis.	Ann Oncol	2017
25535243	A Bayesian framework for de novo mutation calling in parents-offspring trios.	Bioinformatics	2015
26539468	Assessing Computational Steps for CLIP-Seq Data Analysis.	BioMed Research International	2015
26099277	Network-based stratification analysis of 13 major cancer types using mutations in panels of cancer genes.	BMC Genomics	2015
26043085	Leveraging Identity-by-Descent for Accurate Genotype Inference in Family Sequencing Data.	PLoS Genet	2015
25568282	A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis.	Bioinformatics	2015
24878723	A comparison of microRNA sequencing reproducibility and noise reduction using mirVana and TRIzol isolation methods.	International Journal of Computational Biology and Drug Design	2014
25321409	Illumina human exome genotyping array clustering and quality control.	Nat Protoc	2014
24142874	LIN28B promotes growth and tumorigenesis of the intestinal epithelium via Let-7.	Genes and Development	2013