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Genetics

D-Index
51
Citations
13298
World Ranking
3846
National Ranking
1660

Overview

Bai-Lin Wu is affiliated with Claritas Genomics in the United States, where their research activities focus primarily on medicine with a notable emphasis on radiology, nuclear medicine, and imaging. Their work spans several interconnected subfields including genetics, cognitive neuroscience, inorganic chemistry, and artificial intelligence.

Their published research covers key topics such as cardiac imaging and diagnostics, genetics and neurodevelopmental disorders, genomic variations and chromosomal abnormalities, autism spectrum disorder research, radioactive element chemistry and processing, as well as geochemistry and geologic mapping. This multidisciplinary approach highlights the diverse scope of their scientific investigations.

Key publication venues where Bai-Lin Wu has contributed include:

  • Neuroscience Bulletin
  • Ore Geology Reviews
  • PubMed
  • Annals of Noninvasive Electrocardiology
  • Frontiers in Cardiovascular Medicine

Frequent collaborators appearing alongside Bai-Lin Wu in research works comprise Fengyun Zheng, Guoyuan Liu, Ting Dang, Qiaowen Chen, and Yu An.

Among the recent papers authored by Bai-Lin Wu are:

  • "GABA Signaling Pathway-associated Gene PLCL1 Rare Variants May be Associated with Autism Spectrum Disorders," 2021, Neuroscience Bulletin
  • "[Ultrasound features and clinical characteristics of intestinal ischemia secondary to acute mesenteric venous thrombosis]," 2020, PubMed
  • "Compositions of in-situ trace elements, S and Pb isotopes of pyrite in Mengqiguer deposit, Yili basin, NW China: implications for uranium mineralization processes of sandstone − type uranium deposit," 2025, Ore Geology Reviews
  • "SD + SV4 diagnosis of left ventricular hypertrophy, a revaluation of ECG criterion by cardiac magnetic resonance imaging," 2021, Annals of Noninvasive Electrocardiology
  • "Cardiac computer tomography-derived radiomics in assessing myocardial characteristics at the connection between the left atrial appendage and the left atrium in atrial fibrillation patients," 2025, Frontiers in Cardiovascular Medicine

Best Publications

  • Association between Microdeletion and Microduplication at 16p11.2 and Autism

    Lauren A. Weiss;Yiping Shen;Joshua M. Korn;Joshua M. Korn;Dan E. Arking

  • Intracytoplasmic Sperm Injection May Increase the Risk of Imprinting Defects

    Gerald F. Cox;Gerald F. Cox;Joachim Bürger;Va Lip;Ulrike A. Mau

  • Association between microdeletion and microduplication at 16p11.2 and autism

    Lauren A. Weiss;Yiping Shen;Joshua M. Korn;Dan E. Arking

  • Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries

    Michael E. Talkowski;Jill A. Rosenfeld;Ian Blumenthal;Vamsee Pillalamarri

  • Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

    Sébastien Jacquemont;Alexandre Reymond;Flore Zufferey;Louise Harewood

  • Clinical Genetic Testing for Patients With Autism Spectrum Disorders

    Yiping Shen;Kira A. Dies;Ingrid A. Holm;Carolyn Bridgemohan

  • Genomic dissection of population substructure of Han Chinese and its implication in association studies.

    Shuhua Xu;Xianyong Yin;Shilin Li;Wenfei Jin

  • Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders

    David T. Miller;Yiping Shen;Lauren A. Weiss;Joshua Korn

  • Somatic mutations in cerebral cortical malformations

    Saumya S. Jamuar;Anh Thu N Lam;Martin Kircher;Alissa M. D'Gama

  • A Genome-Wide Search for Signals of High Altitude Adaptation in Tibetans

    Shuhua Xu;Shilin Li;Yajun Yang;Jingze Tan

  • Deletions of NRXN1 (Neurexin-1) Predispose to a Wide Spectrum of Developmental Disorders

    Michael S L Ching;Yiping Shen;Yiping Shen;Wen-Hann Tan;Wen-Hann Tan;Shafali S Jeste;Shafali S Jeste

  • GJB2 mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment

    Pu Dai;Fei Yu;Bing Han;Xuezhong Liu

  • High-intensity ras signaling induces premature senescence by activating p38 pathway in primary human fibroblasts

    Qingdong Deng;Rong Liao;Bai-Lin Wu;Peiqing Sun

  • Assessment of 2q23.1 Microdeletion Syndrome Implicates MBD5 as a Single Causal Locus of Intellectual Disability, Epilepsy, and Autism Spectrum Disorder

    Michael E. Talkowski;Sureni V. Mullegama;Jill A. Rosenfeld;Bregje W M Van Bon

  • Copy number variation plays an important role in clinical epilepsy

    Heather Olson;Yiping Shen;Jennifer Avallone;Beth R. Sheidley

  • The Adult Galactosemic Phenotype

    Susan E. Waisbren;Nancy L. Potter;Catherine M. Gordon;Robert C. Green

  • VANGL2 mutations in human cranial neural-tube defects.

    Yunping Lei;Ting Zhang;Hong Li;Bai Lin Wu

  • Connexin 26 studies in patients with sensorineural hearing loss.

    Margaret A. Kenna;Bai-Lin Wu;Douglas A. Cotanche;Bruce R. Korf

  • Exonic Deletions in AUTS2 Cause a Syndromic Form of Intellectual Disability and Suggest a Critical Role for the C Terminus

    Gea Beunders;Els Voorhoeve;Christelle Golzio;Luba M. Pardo

  • Mutations in HFM1 in Recessive Primary Ovarian Insufficiency

    Jian Wang;Wenxiang Zhang;Hong Jiang;Bai-Lin Wu

Frequent Co-Authors

Yiping Shen
Yiping Shen Boston Children's Hospital
James F. Gusella
James F. Gusella Harvard University
Bruce R. Korf
Bruce R. Korf University of Alabama at Birmingham
Cynthia C. Morton
Cynthia C. Morton Brigham and Women's Hospital
Christopher A. Walsh
Christopher A. Walsh Howard Hughes Medical Institute
Michael E. Talkowski
Michael E. Talkowski Harvard University
Douglas M. Ruderfer
Douglas M. Ruderfer Vanderbilt University Medical Center
Christian R. Marshall
Christian R. Marshall University of Toronto
Stephen W. Scherer
Stephen W. Scherer University of Toronto
Seth L. Alper
Seth L. Alper Beth Israel Deaconess Medical Center

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