Mao Lin

Zunyi Medical University — China

Biochemistry, Genetics and Molecular Biology · Life Sciences

15h-index876citations59works2.32yr avg
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Research Topics

Connective tissue disorders research(12), Congenital heart defects research(8), Genetic factors in colorectal cancer(7), Hematopoietic Stem Cell Transplantation(6), Cytomegalovirus and herpesvirus research(6)

Publications56 total

Clinical outcomes after surgical treatment of severe congenital spinal deformity in skeletally mature patients: A minimum two-year follow-up study
Journal of Orthopaedic Surgery and Research·2025Open Access
Valine-curcumin complex improves bioavailability and disease resistance in juvenile largemouth bass
Aquaculture Reports·2025Open Access
The aza-Diels-Alder reaction between cyclic imine and aza-ortho-quinone methide precursor to access polycyclic-fused tetrahydroquinazoline
Tetrahedron·2025
Variants in the SOX9 transactivation middle domain induce axial skeleton dysplasia and scoliosis
Proceedings of the National Academy of Sciences·2025· 1 citedOpen Access
[Physiological characteristics of <i>Bacillus thuringiensis</i> subspecies <i>israelensis</i> with double mutations of <i>cwlE</i> and <i>sigK</i> and its activity against larvae of <i>Culex pipiens pallens</i>].
PubMed·2024· 3 cited
[A multicenter study on the effects of congenital cytomegalovirus infection on hearing loss].
PubMed·2024
Core planar cell polarity genes <i>VANGL1</i> and <i>VANGL2</i> in predisposition to congenital vertebral malformations
Proceedings of the National Academy of Sciences·2024· 7 citedOpen Access
Parental Postoperative Pain Management Perceptions, Attitudes, and Practices in Pediatric Limb Fractures
Pain Management Nursing·2023· 13 cited
Mesenchymal Stem/Stromal Cells: AN INVESTIGATION OF INTER- AND INTRA-DONOR VARIABILITY IN BONE MARROW-DERIVED MESENCHYMAL STROMAL CELLS: IMPLICATIONS FOR CLINICAL APPLICATIONS
Cytotherapy·2023
Molecular phylogeny suggests synonymy of Sandalia bridgesi Lorenz, 2009 with S. triticea (Lamarck, 1810) (Gastropoda, Ovulidae)
ZooKeys·2022· 4 citedOpen Access
ADAMTS5 in Osteoarthritis: Biological Functions, Regulatory Network, and Potential Targeting Therapies
Frontiers in Molecular Biosciences·2021· 100 citedOpen Access
Deciphering the mutational signature of congenital limb malformations
Molecular Therapy — Nucleic Acids·2021· 11 citedOpen Access
Phenotypic and genetic spectrum of isolated macrodactyly: somatic mosaicism of PIK3CA and AKT1 oncogenic variants
Orphanet Journal of Rare Diseases·2020· 24 citedOpen Access
Cost-effectiveness analysis of using the TBX6-associated congenital scoliosis risk score (TACScore) in genetic diagnosis of congenital scoliosis
Orphanet Journal of Rare Diseases·2020· 5 citedOpen Access
A novel COMP mutation in a Chinese family with multiple epiphyseal dysplasia
BMC Medical Genetics·2020· 5 citedOpen Access
Diagnostic yield and clinical impact of exome sequencing in early-onset scoliosis (EOS)
Journal of Medical Genetics·2020· 63 citedOpen Access
Cover
Molecular Genetics & Genomic Medicine·2020Open Access
Additional file 1 of Cost-effectiveness analysis of using the TBX6-associated congenital scoliosis risk score (TACScore) in genetic diagnosis of congenital scoliosis
Figshare·2020Open Access
Identification of novel FBN1 variations implicated in congenital scoliosis
Journal of Human Genetics·2019· 29 citedOpen Access
Whole-Genome Methylation Analysis of Phenotype Discordant Monozygotic Twins Reveals Novel Epigenetic Perturbation Contributing to the Pathogenesis of Adolescent Idiopathic Scoliosis
Frontiers in Bioengineering and Biotechnology·2019· 24 citedOpen Access
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Frequent Co-authors

Sen Zhao(26), Nan Wu(26), Guixing Qiu(24), Zhihong Wu(20), Yuchen Niu(19), Zihui Yan(18), Jiaqi Liu(16), Yuanqiang Zhang(15), Shengru Wang(15), Yanxue Zhao(14), Lianlei Wang(14), Xiaoxin Li(13), Zhen Cai(13), Jiachen Lin(12), Wei‐Sheng Chen(12), Gang Liu(12), Yuzhi Zuo(11), Xinzhuang Yang(10), Jianguo Zhang(9), He Huang(9)