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Author Details

Jinchuan Xing
The State University of New Jersey
2003
108
43
PMIDPaper TitleJournal TitlePublished Year
36251081Common genetic risk factors in ASD and ADHD co-occurring families.Hum Genet2023
37546814Identifying risk genes for embryo aneuploidy using ultra-low coverage whole-genome sequencing.medRxiv2023
37686052Structural Variations Contribute to the Genetic Etiology of Autism Spectrum Disorder and Language Impairments.Int J Mol Sci2023
37372423Transposable Elements Shape the Genome Diversity and the Evolution of Noctuidae Species.Genes (Basel)2023
36013369Transposable Elements in Bats Show Differential Accumulation Patterns Determined by Class and Functionality.Life (Basel)2022
35347416Predicting embryonic aneuploidy rate in IVF patients using whole-exome sequencing.Hum Genet2022
36131352Genomics and epigenetics guided identification of tissue-specific genomic safe harbors.Genome Biol2022
35893067MicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders.Genes (Basel)2022
33070169Analysis of DNA variants in miRNAs and miRNA 3'UTR binding sites in female infertility patients.Lab Invest2021
33787868PrecisionProDB: improving the proteomics performance for precision medicine.Bioinformatics2021
33616445Development and Characterization of a Modular CRISPR and RNA Aptamer Mediated Base Editing System.CRISPR J2021
33860956Origins and mechanisms leading to aneuploidy in human eggs.Prenat Diagn2021
34965893Correction to: Whole exome sequencing identifies novel candidate genes that modify chronic obstructive pulmonary disease susceptibility.Hum Genomics2021
34453124SMAD4 is critical in suppression of BRAF-V600E serrated tumorigenesis.Oncogene2021
33170803Meiosis interrupted: the genetics of female infertility via meiotic failure.Reproduction2021
33098347Alternative genomic diagnoses for individuals with a clinical diagnosis of Dubowitz syndrome.Am J Med Genet A2021
32350135Mathematical modeling of human oocyte aneuploidy.Proc Natl Acad Sci U S A2020
31673123Mutations in ASH1L confer susceptibility to Tourette syndrome.Mol Psychiatry2020
31860080Whole Genome Sequencing and Assembly of the Asian Honey Bee Apis dorsata.Genome Biol Evol2020
32718348Polymorphic mobile element insertions contribute to gene expression and alternative splicing in human tissues.Genome Biol2020
32772081Exome sequencing links CEP120 mutation to maternally derived aneuploid conception risk.Hum Reprod2020
32110248Integrated Mobile Element Scanning (ME-Scan) method for identifying multiple types of polymorphic mobile element insertions.Mob DNA2020
32564135Characterization of the primate TRIM gene family reveals the recent evolution in primates.Mol Genet Genomics2020
30745430The lineage-specific transcription factor CDX2 navigates dynamic chromatin to control distinct stages of intestine development.Development2019
31727126Evaluating nanopore sequencing data processing pipelines for structural variation identification.Genome Biol2019
31575651Pedigree-based estimation of human mobile element retrotransposition rates.Genome Res2019
31226208SIRT7 mediates L1 elements transcriptional repression and their association with the nuclear lamina.Nucleic Acids Res2019
28894297The PNKD gene is associated with Tourette Disorder or Tic disorder in a multiplex family.Mol Psychiatry2018
29986996SMAD4 Suppresses WNT-Driven Dedifferentiation and Oncogenesis in the Differentiated Gut Epithelium.Cancer Res2018
30257206De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis.Cell Rep2018
30455747Can-SINE dynamics in the giant panda and three other Caniformia genomes.Mob DNA2018
30279509Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects.Nat Commun2018
29614345Ancient hybridization and admixture in macaques (genus Macaca) inferred from whole genome sequences.Mol Phylogenet Evol2018
29186378PipelineDog: a simple and flexible graphic pipeline construction and maintenance tool.Bioinformatics2018
26025622Library Construction for High-Throughput Mobile Element Identification and Genotyping.Methods Mol Biol2017
28472652De Novo Coding Variants Are Strongly Associated with Tourette Disorder.Neuron2017
28369513Identification and characterization of Aurora kinase B and C variants associated with maternal aneuploidy.Mol Hum Reprod2017
29281831Degree of Tissue Differentiation Dictates Susceptibility to BRAF-Driven Colorectal Cancer.Cell Rep2017
28703315Using whole-exome sequencing to investigate the genetic bases of lysosomal storage diseases of unknown etiology.Hum Mutat2017
28532386Extremely low-coverage whole genome sequencing in South Asians captures population genomics information.BMC Genomics2017
27923875Accounting for Protein Subcellular Localization: A Compartmental Map of the Rat Liver Proteome.Mol Cell Proteomics2017
26680994Worldwide patterns of genomic variation and admixture in gray wolves.Genome Res2016
27867939A Rare Variant in <i>CACNA1D</i> Segregates with 7 Bipolar I Disorder Cases in a Large Pedigree.Mol Neuropsychiatry2016
27802136A YY1-dependent increase in aerobic metabolism is indispensable for intestinal organogenesis.Development2016
27708560Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology.Front Neurosci2016
27478512Identification of polymorphic SVA retrotransposons using a mobile element scanning method for SVA (ME-Scan-SVA).Mob DNA2016
27553520Analysis of large-scale whole exome sequencing data to determine the prevalence of genetically-distinct forms of neuronal ceroid lipofuscinosis.Gene2016
26744305Whole exome sequencing identifies novel candidate genes that modify chronic obstructive pulmonary disease susceptibility.Hum Genomics2016
26014613Targeted Capture of Phylogenetically Informative Ves SINE Insertions in Genus Myotis.Genome Biol Evol2015
26283688piRNAs derived from ancient viral processed pseudogenes as transgenerational sequence-specific immune memory in mammals.RNA2015
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Collaborators

Lynn B Jorde
University of Utah School of Medicine
Co-authored papers 35
Mark A Batzer
Louisiana State University
Co-authored papers 27
Chad D Huff
University of Texas M.D. Anderson Cancer Center
Co-authored papers 18
Yuhua Zhang
Pingjin Hospital
Co-authored papers 15
David A Ray
Co-authored papers 10
Hui Wang
Center for BioModular Multi-Scale Systems, Louisiana State University
Co-authored papers 9
Kyudong Han
Dankook University
Co-authored papers 8
Richard Cordaux
Universite de Poitiers, UMR CNRS 7267
Co-authored papers 6
Katarzyna M Tyc
and Massey Cancer Center, Virginia Commonwealth University
Co-authored papers 6
Abdel Halim Salem
Deanship of College of Medicine & Medical Sciences, Arabian Gulf University
Co-authored papers 5
Jay A Tischfield
Co-authored papers 5
Mark Yandell
University of Utah
Co-authored papers 4
Michael J Bamshad
University of Washington
Co-authored papers 4
Steven Buyske
The State University of New Jersey
Co-authored papers 4
Barry Moore
Utah Center for Genetic Discovery, University of Utah
Co-authored papers 4
Linda M Brzustowicz
The State University of New Jersey
Co-authored papers 3
Hakon Hakonarson
The Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 3
Christopher W Bartlett
College of Medicine, The Ohio State University
Co-authored papers 3
Oliver A Ryder
Co-authored papers 3
Nawei Sun
University of California san francisco
Co-authored papers 3
Richard A Gibbs
Baylor College of Medicine
Co-authored papers 3
Tara C Matise
Co-authored papers 3
Yana Bromberg
Rutgers University
Co-authored papers 3
Pauline A Callinan
Center for BioModular Multi-Scale Systems, Louisiana State University
Co-authored papers 3
Benjamin M Neale
Massachusetts General Hospital
Co-authored papers 3
Miriam K Konkel
Clemson University
Co-authored papers 3
Donna M Muzny
Baylor College of Medicine
Co-authored papers 3
Fuli Yu
East China University of Science and Technology
Co-authored papers 3
Marco A Azaro
The State University of New Jersey
Co-authored papers 3
Shalini N Jhangiani
Baylor College of Medicine
Co-authored papers 2
Release 1.2