World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
70
Citations
19857
World Ranking
2261
National Ranking
1015

Overview

Yong-hui Jiang is a researcher affiliated with the Yale School of Medicine in the United States. Their work predominantly spans the field of Biochemistry, Genetics and Molecular Biology, with a notable focus on subfields including Genetics, Molecular Biology, Cognitive Neuroscience, Plant Science, and Pediatrics, Perinatology and Child Health.

The scientist's research covers several main topics, which include:

  • Genetics and Neurodevelopmental Disorders
  • Autism Spectrum Disorder Research
  • Prenatal Screening and Diagnostics
  • Genomics and Rare Diseases
  • Genetic Syndromes and Imprinting
  • Neurogenesis and neuroplasticity mechanisms
  • Epigenetics and DNA Methylation

Jiang has contributed to a range of studies published in diverse scientific venues. They have multiple publications in outlets such as bioRxiv (Cold Spring Harbor Laboratory), Nature Communications, Pest Management Science, UNC Libraries, and Genetics in Medicine Open.

Selected recent papers by Yong-hui Jiang include:

  • Prevalence of Autism Spectrum Disorder in China: A Nationwide Multi-center Population-based Study Among Children Aged 6 to 12 Years (2020), Neuroscience Bulletin
  • Vitamin C epigenetically controls osteogenesis and bone mineralization (2022), Nature Communications
  • TET1-mediated DNA hydroxymethylation regulates adult remyelination in mice (2021), Nature Communications
  • Exome sequencing analysis on products of conception: a cohort study to evaluate clinical utility and genetic etiology for pregnancy loss (2020), Genetics in Medicine
  • Regulatory roles and mechanisms of alternative RNA splicing in adipogenesis and human metabolic health (2021), Cell & Bioscience

Frequent collaborators in Jiang's research include A. Bale, Peining Li, Suyan Wang, Pedro Laborda, and Yongqing Zhang, reflecting ongoing partnerships across multiple projects.

Best Publications

  • Molecular classification of cutaneous malignant melanoma by gene expression profiling

    M. Bittner;P.S.J. Meltzer;Y.D. Chen;Y. Jiang

  • De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome.

    Toshinobu Matsuura;James S. Sutcliffe;Ping Fang;Robert-Jan Galjaard

  • MUTATION OF THE ANGELMAN UBIQUITIN LIGASE IN MICE CAUSES INCREASED CYTOPLASMIC P53 AND DEFICITS OF CONTEXTUAL LEARNING AND LONG-TERM POTENTIATION

    Y. H. Jiang;D. Armstrong;U. Albrecht;C. M. Atkins

  • Modeling autism by SHANK gene mutations in mice.

    Yong-hui Jiang;Michael D. Ehlers

  • Autism as a disorder of neural information processing: directions for research and targets for therapy

    M K Belmonte;E H Cook;G M Anderson;J L R Rubenstein

  • Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3

    Xiaoming Wang;Portia A. McCoy;Ramona M. Rodriguiz;Yanzhen Pan

  • Mutation of the E6-AP Ubiquitin Ligase Reduces Nuclear Inclusion Frequency While Accelerating Polyglutamine-Induced Pathology in SCA1 Mice

    Christopher J Cummings;Eyal Reinstein;Yaling Sun;Barbara Antalffy

  • Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing

    Yong-hui Jiang;Ryan K.C. Yuen;Xin Jin;Xin Jin;Mingbang Wang

  • EPIGENETICS AND HUMAN DISEASE

    Yong Hui Jiang;Jan Bressler;Arthur L. Beaudet

  • Clinical and Molecular Phenotype of Aicardi-Goutières Syndrome

    Gillian Rice;Teresa Patrick;Rekha Parmar;Claire F Taylor

  • Correction: Corrigendum: Genetic Variants Identified from Epilepsy of Unknown Etiology in Chinese Children by Targeted Exome Sequencing

    Yimin Wang;Xiaonan Du;Rao Bin;Shanshan Yu

  • Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios

    Xiaolin Zhu;Slavé Petrovski;Slavé Petrovski;Pingxing Xie;Pingxing Xie;Elizabeth K. Ruzzo

  • The utility of the traditional medical genetics diagnostic evaluation in the context of next-generation sequencing for undiagnosed genetic disorders

    Vandana Shashi;Allyn McConkie-Rosell;Bruce Rosell;Kelly Schoch

  • Rescue of neurological deficits in a mouse model for Angelman syndrome by reduction of αCaMKII inhibitory phosphorylation

    Geeske M. Van Woerden;Karen D. Harris;Mohammad Reza Hojjati;Richard M. Gustin

  • Derangements of Hippocampal Calcium/Calmodulin-Dependent Protein Kinase II in a Mouse Model for Angelman Mental Retardation Syndrome

    Edwin J. Weeber;Yong-Hui Jiang;Ype Elgersma;Ype Elgersma;Andrew W. Varga

  • Prevalence of Autism Spectrum Disorder in China: A Nationwide Multi-center Population-based Study Among Children Aged 6 to 12 Years

    Hao Zhou;Xiu Xu;Weili Yan;Xiaobing Zou

  • Genetics of Angelman syndrome.

    Yong hui Jiang;Efrat Lev-Lehman;Jan Bressler;Ting Fen Tsai

  • Altered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3.

    Yong-hui Jiang;Yanzhen Pan;Li Zhu;Luis Landa

  • Paternal Deletion from Snrpn to Ube3a in the Mouse Causes Hypotonia, Growth Retardation and Partial Lethality and Provides Evidence for a Gene Contributing to Prader-Willi Syndrome

    Ting Fen Tsai;Yong Hui Jiang;Jan Bressler;Dawna Armstrong

  • Molecular classification of cutaneous malignant melanoma by gene expression profiling

    M. Bittner;P. Meltzer;Y. Chen;Y. Jiang

Frequent Co-Authors

Vandana Shashi
Vandana Shashi Duke University
David Goldstein
David Goldstein University of New South Wales
Arthur L. Beaudet
Arthur L. Beaudet Baylor College of Medicine
Slavé Petrovski
Slavé Petrovski AstraZeneca (United Kingdom)
Brendan Lee
Brendan Lee Baylor College of Medicine
Xiaoming Wang
Xiaoming Wang Florida State University
Michael F. Wangler
Michael F. Wangler Baylor College of Medicine
Teri A. Manolio
Teri A. Manolio National Institutes of Health
Jennifer E. Posey
Jennifer E. Posey Baylor College of Medicine
John H. Postlethwait
John H. Postlethwait University of Oregon

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Related Online Degrees & Career Pathways

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