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Genetics

D-Index
64
Citations
59168
World Ranking
2725
National Ranking
1194

Overview

Jinchuan Xing is affiliated with Rutgers, The State University of New Jersey in the United States. Their research primarily focuses on the field of Biochemistry, Genetics, and Molecular Biology, with a significant body of work spanning 95 publications. Key subfields of study include Molecular Biology, Genetics, Plant Science, Pediatrics, Perinatology and Child Health, and Cognitive Neuroscience.

The scientist's work covers multiple topics related to genetics and developmental biology. These topics include:

  • Prenatal Screening and Diagnostics
  • Machine Learning in Bioinformatics
  • Genetics and Neurodevelopmental Disorders
  • Genetic Syndromes and Imprinting
  • Autism Spectrum Disorder Research
  • Chromosomal and Genetic Variations
  • Genetics, Bioinformatics, and Biomedical Research

Among Jinchuan Xing's recent publications, there are several notable research articles:

  • "Meiosis interrupted: the genetics of female infertility via meiotic failure," 2020, published in Reproduction
  • "Origins and mechanisms leading to aneuploidy in human eggs," 2021, published in Prenatal Diagnosis
  • "Polymorphic mobile element insertions contribute to gene expression and alternative splicing in human tissues," 2020, published in Genome Biology
  • "Whole-exome sequencing identifies genes associated with Tourette's disorder in multiplex families," 2021, published in Molecular Psychiatry
  • "Mathematical modeling of human oocyte aneuploidy," 2020, published in Proceedings of the National Academy of Sciences

Jinchuan Xing has frequently published in several academic venues, with recurring contributions to:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Zenodo (CERN European Organization for Nuclear Research)
  • Genes
  • Prenatal Diagnosis
  • Genome Biology

The scientist collaborates regularly with a number of co-authors, including:

  • Xiaolong Cao
  • Siqi Sun
  • Karen Schindler
  • Katarzyna M. Tyc
  • Yeting Zhang

Best Publications

  • A global reference for human genetic variation.

    Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin

  • An integrated map of genetic variation from 1,092 human genomes

    Goncalo R Abecasis;Adam Auton;Lisa D Brooks

  • Table S2: Trans-factors and trinucleotide repeat instability Trans-factor

    Arturo López Castel;John D Cleary;Christopher E Pearson

  • Evolutionary and biomedical insights from the rhesus macaque genome

    Richard A. Gibbs;Jeffrey Rogers

  • Mapping copy number variation by population-scale genome sequencing

    Ryan E. Mills;Klaudia Walter;Chip Stewart;Robert E. Handsaker

  • Genetic Evidence for High-Altitude Adaptation in Tibet

    Tatum S. Simonson;Yingzhong Yang;Chad D. Huff;Haixia Yun

  • A global reference for human genetic variation

    Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin

  • A map of human genome variation from population-scale sequencing

    Richard M. Durbin;David L. Altshuler;Gonçalo R. Abecasis;David R. Bentley

  • A genetic mechanism for Tibetan high-altitude adaptation

    Felipe R. Lorenzo;Chad Huff;Chad Huff;Mikko Myllymäki;Benjamin Olenchock

  • SVA elements : A hominid-specific retroposon family

    Hui Wang;Jinchuan Xing;Deepak Grover;Dale J. Hedges

  • Mobile elements create structural variation: analysis of a complete human genome.

    Jinchuan Xing;Yuhua Zhang;Kyudong Han;Abdel Halim Salem;Abdel Halim Salem;Abdel Halim Salem

  • A Comprehensive Map of Mobile Element Insertion Polymorphisms in Humans

    Chip Stewart;Deniz Kural;Michael P. Strömberg;Jerilyn A. Walker

  • The common marmoset genome provides insight into primate biology and evolution

    Kim C. Worley;Wesley C. Warren;Jeffrey Rogers;Devin Locke

  • Draft genome sequence of the Tibetan antelope

    Ri Li Ge;Qingle Cai;Yong Yi Shen;Yong Yi Shen;A. San

  • Using VAAST to Identify an X-Linked Disorder Resulting in Lethality in Male Infants Due to N-Terminal Acetyltransferase Deficiency

    Alan F. Rope;Kai Wang;Rune Evjenth;Jinchuan Xing

  • A probabilistic disease-gene finder for personal genomes

    Mark Yandell;Chad D Huff;Hao Hu;Marc Singleton

  • Mapping and Characterization of Structural Variation in 17,795 Human Genomes

    Haley J Abel;David E Larson;Allison A Regier;Colby Chiang

  • Worldwide patterns of genomic variation and admixture in gray wolves.

    Zhenxin Fan;Zhenxin Fan;Pedro Silva;Ilan Gronau;Shuoguo Wang

  • Alu elements and hominid phylogenetics

    Abdel Halim Salem;Abdel Halim Salem;David A. Ray;Jinchuan Xing;Pauline A. Callinan

  • Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects

    Allison A. Regier;Yossi Farjoun;David E. Larson;Olga Krasheninina

Frequent Co-Authors

Lynn B. Jorde
Lynn B. Jorde University of Utah
Mark A. Batzer
Mark A. Batzer Louisiana State University
Chad D. Huff
Chad D. Huff The University of Texas MD Anderson Cancer Center
Dale J. Hedges
Dale J. Hedges University of Miami
David A. Ray
David A. Ray Texas Tech University
Gholson J. Lyon
Gholson J. Lyon Cold Spring Harbor Laboratory
Hui Wang
Hui Wang Salk Institute for Biological Studies
Mark Yandell
Mark Yandell University of Utah
Donna M. Muzny
Donna M. Muzny Baylor College of Medicine
Richard A. Gibbs
Richard A. Gibbs Baylor College of Medicine

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