Jinchuan Xing

ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 25

Top Venues

Rutgers The State University of New Jersey

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Rutgers The State University of New Jersey

United States

Associate Professor :: Genetics

Rutgers The State University of New Jersey

United States

Full Member :: Human Genetics Institue of New Jersey

Publications

Smrithi Prem, Bharati Dev, Cynthia Peng, Monal Mehta, Rohan Alibutud, Robert J Connacher, Madeline St Thomas, Xiaofeng Zhou, Paul Matteson, Jinchuan Xing, James H Millonig, Emanuel DiCicco-Bloom
Dysregulation of mTOR signaling mediates common neurite and migration defects in both idiopathic and 16p11.2 deletion autism neural precursor cells. eLife 13 (2024)
Smrithi Prem, Bharati Dev, Cynthia Peng, Monal Mehta, Rohan Alibutud, Robert J Connacher, Madeline St Thomas, Xiaofeng Zhou, Paul Matteson, Jinchuan Xing, James H Millonig, Emanuel DiCicco-Bloom
Dysregulation of mTOR signaling mediates common neurite and migration defects in both idiopathic and 16p11.2 deletion autism neural precursor cells. eLife 13 (2024)
Smrithi Prem, Bharati Dev, Cynthia Peng, Monal Mehta, Rohan Alibutud, Robert J Connacher, Madeline St Thomas, Xiaofeng Zhou, Paul Matteson, Jinchuan Xing, James H Millonig, Emanuel DiCicco-Bloom
Dysregulation of mTOR signaling mediates common neurite and migration defects in both idiopathic and 16p11.2 deletion autism neural precursor cells. eLife 13 (2024)
Smrithi Prem, Bharati Dev, Cynthia Peng, Monal Mehta, Rohan Alibutud, Robert J Connacher, Madeline St Thomas, Xiaofeng Zhou, Paul Matteson, Jinchuan Xing, James H Millonig, Emanuel DiCicco-Bloom
Dysregulation of mTOR signaling mediates common neurite and migration defects in both idiopathic and 16p11.2 deletion autism neural precursor cells. eLife 13 (2024)
Smrithi Prem, Bharati Dev, Cynthia Peng, Monal Mehta, Rohan Alibutud, Robert J Connacher, Madeline St Thomas, Xiaofeng Zhou, Paul Matteson, Jinchuan Xing, James H Millonig, Emanuel DiCicco-Bloom
Dysregulation of mTOR signaling mediates common neurite and migration defects in both idiopathic and 16p11.2 deletion autism neural precursor cells. eLife 13 (2024)
Karleena Rybacki, Mingyi Xia, Mian Umair Ahsan, Jinchuan Xing, Kai Wang
Assessing the Expression of Long INterspersed Elements (LINEs) via Long-Read Sequencing in Diverse Human Tissues and Cell Lines. Genes 14 (10) (2023)
Chunhui Zhang, Lei Wang, Liang Dou, Bisong Yue, Jinchuan Xing, Jing Li
Transposable Elements Shape the Genome Diversity and the Evolution of Noctuidae Species. Genes 14 (6) (2023)
Chunhui Zhang, Lei Wang, Liang Dou, Bisong Yue, Jinchuan Xing, Jing Li
Transposable Elements Shape the Genome Diversity and the Evolution of Noctuidae Species. Genes 14 (6) (2023)
Sheng Wang, Belinda Wang, Vanessa Drury, Sam Drake, Nawei Sun, Hasan Alkhairo, Juan Arbelaez, Clif Duhn, null null, Vanessa H Bal, Kate Langley, Joanna Martin, Pieter J Hoekstra, Andrea Dietrich, Jinchuan Xing, Gary A Heiman, Jay A Tischfield, Thomas V Fernandez, Michael J Owen, Michael C O'Donovan, Anita Thapar, Matthew W State, A Jeremy Willsey
Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD. Nature communications 14 (1) (2023)
Chunhui Zhang, Lei Wang, Liang Dou, Bisong Yue, Jinchuan Xing, Jing Li
Transposable Elements Shape the Genome Diversity and the Evolution of Noctuidae Species. Genes 14 (6) (2023)
Rohan Alibutud, Sammy Hansali, Xiaolong Cao, Anbo Zhou, Vaidhyanathan Mahaganapathy, Marco Azaro, Christine Gwin, Sherri Wilson, Steven Buyske, Christopher W Bartlett, Judy F Flax, Linda M Brzustowicz, Jinchuan Xing
Structural Variations Contribute to the Genetic Etiology of Autism Spectrum Disorder and Language Impairments. International journal of molecular sciences 24 (17) (2023)
Nicole S Paulat, Erin McGuire, Krishnamurthy Subramanian, Austin B Osmanski, Diana D Moreno-Santillán, David A Ray, Jinchuan Xing
Transposable Elements in Bats Show Differential Accumulation Patterns Determined by Class and Functionality. Life (Basel, Switzerland) 12 (8) (2022)
Anthony Wong, Anbo Zhou, Xiaolong Cao, Vaidhyanathan Mahaganapathy, Marco Azaro, Christine Gwin, Sherri Wilson, Steven Buyske, Christopher W Bartlett, Judy F Flax, Linda M Brzustowicz, Jinchuan Xing
MicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders. Genes 13 (8) (2022)
Siqi Sun, Maximilian Miller, Yanran Wang, Katarzyna M Tyc, Xiaolong Cao, Richard T Scott, Xin Tao, Yana Bromberg, Karen Schindler, Jinchuan Xing
Predicting embryonic aneuploidy rate in IVF patients using whole-exome sequencing. Human genetics 141 (10) (2022)
Anbo Zhou, Xiaolong Cao, Vaidhyanathan Mahaganapathy, Marco Azaro, Christine Gwin, Sherri Wilson, Steven Buyske, Christopher W Bartlett, Judy F Flax, Linda M Brzustowicz, Jinchuan Xing
Common genetic risk factors in ASD and ADHD co-occurring families. Human genetics (2022)
Lena Wartosch, Karen Schindler, Melina Schuh, Jennifer R Gruhn, Eva R Hoffman, Rajiv C McCoy, Jinchuan Xing
Origins and mechanisms leading to aneuploidy in human eggs. Prenatal diagnosis 41 (5) (2021)
Xiaolong Cao, Yeting Zhang, Mohamed Abdulkadir, Li Deng, Thomas V Fernandez, Blanca Garcia-Delgar, Julie Hagstrøm, Pieter J Hoekstra, Robert A King, Justin Koesterich, Samuel Kuperman, Astrid Morer, Cara Nasello, Kerstin J Plessen, Joshua K Thackray, Lisheng Zhou, null null, Andrea Dietrich, Jay A Tischfield, Gary A Heiman, Jinchuan Xing
Whole-exome sequencing identifies genes associated with Tourette's disorder in multiplex families. Molecular psychiatry (2021)
Xiaolong Cao, Yeting Zhang, Lindsay M Payer, Hannah Lords, Jared P Steranka, Kathleen H Burns, Jinchuan Xing
Polymorphic mobile element insertions contribute to gene expression and alternative splicing in human tissues. Genome biology 21 (1) (2020)
Jui Wan Loh, Hongseok Ha, Timothy Lin, Nawei Sun, Kathleen H Burns, Jinchuan Xing
Integrated Mobile Element Scanning (ME-Scan) method for identifying multiple types of polymorphic mobile element insertions. Mobile DNA 11 (2020)
Katarzyna M Tyc, Rajiv C McCoy, Karen Schindler, Jinchuan Xing
Mathematical modeling of human oocyte aneuploidy. Proceedings of the National Academy of Sciences of the United States of America 117 (19) (2020)
Anbo Zhou, Timothy Lin, Jinchuan Xing
Evaluating nanopore sequencing data processing pipelines for structural variation identification. Genome biology 20 (1) (2019)
Shiguo Liu, Miaomiao Tian, Fan He, Jiani Li, Hong Xie, Wenmiao Liu, Yeting Zhang, Ru Zhang, Mingji Yi, Fengyuan Che, Xu Ma, Yi Zheng, Hao Deng, Guiju Wang, Lang Chen, Xue Sun, Yinglei Xu, Jingli Wang, Yucui Zang, Mengmeng Han, Xiuhai Wang, Hongzai Guan, Yinlin Ge, Chunmei Wu, Haiyan Wang, Hui Liang, Hui Li, Ni Ran, Zhaochuan Yang, Huanhuan Huang, Yanzhao Wei, Xueping Zheng, Xiangrong Sun, Xueying Feng, Lanlan Zheng, Tao Zhu, Wenhan Luo, Qinan Chen, Yuze Yan, Zuzhou Huang, Zhongcui Jing, Yixia Guo, Xuzhan Zhang, Christian Patrick Schaaf, Jinchuan Xing, Chuanyue Wang, Fuli Yu, Ji-Song Guan
Mutations in ASH1L confer susceptibility to Tourette syndrome. Molecular psychiatry 25 (2) (2019)
Allison A Regier, Yossi Farjoun, David E Larson, Olga Krasheninina, Hyun Min Kang, Daniel P Howrigan, Bo-Juen Chen, Manisha Kher, Eric Banks, Darren C Ames, Adam C English, Heng Li, Jinchuan Xing, Yeting Zhang, Tara C Matise, Goncalo R Abecasis, Will Salerno, Michael C Zody, Benjamin M Neale, Ira M Hall
Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects. Nature communications 9 (1) (2018)
Nan Wang, Yeting Zhang, Erika Gedvilaite, Jui Wan Loh, Timothy Lin, Xiuping Liu, Chang-Gong Liu, Dibyendu Kumar, Robert Donnelly, Kimiyo Raymond, Edward H Schuchman, David E Sleat, Peter Lobel, Jinchuan Xing
Using whole-exome sequencing to investigate the genetic bases of lysosomal storage diseases of unknown etiology. Human mutation 38 (11) (2017)
Hongseok Ha, Jui Wan Loh, Jinchuan Xing
Identification of polymorphic SVA retrotransposons using a mobile element scanning method for SVA (ME-Scan-SVA). Mobile DNA 7 (2016)

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Publication Activity (10 Years)

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Jinchuan Xing