Jia-Ning Gu

Fudan University — China

Medicine · Health Sciences

16h-index637citations34works1.82yr avg
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Research Topics

Atrial Fibrillation Management and Outcomes(13), Cardiac Arrhythmias and Treatments(12), Congenital heart defects research(7), Cardiac pacing and defibrillation studies(5), Cardiomyopathy and Myosin Studies(4)

Publications34 total

Discovery of ETS1 as a New Gene Predisposing to Dilated Cardiomyopathy
Diagnostics·2025· 1 citedOpen Access
Discovery of <em>ETS1</em> as a New Gene Predisposing to Dilated Cardiomyopathy
Preprints.org·2025· 1 citedOpen Access
Effects of P-AKK on glucose and lipid metabolism and immunity of Micropterus salmoides induced by high starch diet
Aquaculture·2025· 2 cited
Design, synthesis and antitumor evaluation of a novel nectin-4 targeting bicyclic toxin conjugate
Bioorganic & Medicinal Chemistry Letters·2025
Multi-omics identifies OSM-OSMR as a key receptor-ligand in the tumor environment of endometrial adenocarcinoma
International Immunopharmacology·2025Open Access
Dietary Fermented Chicory Root Waste Modulates Growth, Chemical Composition, Lipid Metabolism, and Intestinal Barrier Pathways in Common Carp ( <i>Cyprinus carpio</i> L.) Fed With High‐Fat Diets
Aquaculture Nutrition·2025· 1 citedOpen Access
Identification, Expression, Characteristic Analysis, and Immune Function of Two Akirin Genes in Grass Carp (Ctenopharyngodon idella)
Animals·2024· 2 citedOpen Access
Somatic <i>GATA4</i> mutation contributes to tetralogy of Fallot
Experimental and Therapeutic Medicine·2024· 7 citedOpen Access
Analysis of seismic damage phenomena and causes of frame structures with external verandah
2023
VEZF1 loss-of-function mutation underlying familial dilated cardiomyopathy
European Journal of Medical Genetics·2023· 3 cited
Identification of BMP10 as a Novel Gene Contributing to Dilated Cardiomyopathy
Diagnostics·2023· 16 citedOpen Access
Association Between METS-IR and Prehypertension or Hypertension Among Normoglycemia Subjects in Japan: A Retrospective Study
Frontiers in Endocrinology·2022· 55 citedOpen Access
SOX7 loss-of-function variation as a cause of familial congenital heart disease.
PubMed·2022· 11 citedOpen Access
Complex renal cysts combined with hemorrhage during crizotinib treatment for ALK-rearranged lung adenocarcinoma
Cancer Treatment and Research Communications·2021· 3 citedOpen Access
Detection and functional characterization of a novel <i>MEF2A</i> variation responsible for familial dilated cardiomyopathy
Clinical Chemistry and Laboratory Medicine (CCLM)·2020· 12 cited
ISL1 loss-of-function variation causes familial atrial fibrillation
European Journal of Medical Genetics·2020· 16 cited
A New &lt;i&gt;TBX5&lt;/i&gt; Loss-of-Function Mutation Contributes to Congenital Heart Defect and Atrioventricular Block
International Heart Journal·2020· 20 citedOpen Access
Identification and functional characterization of KLF5 as a novel disease gene responsible for familial dilated cardiomyopathy
European Journal of Medical Genetics·2019· 20 cited
Promoting Growth of Keratocyte from Femtosecond Laser lntrastromal Lenticules Using PDMS Substrate and Cocktail Medium
2019
Identification and Functional Characterization of an ISL1 Mutation Predisposing to Dilated Cardiomyopathy
Journal of Cardiovascular Translational Research·2018· 16 cited
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Frequent Co-authors

Yi‐Qing Yang(11), Xu Liu(10), Ying‐Jia Xu(10), Chenxi Yang(9), Xinhua Wang(7), Li Zhou(6), Weifeng Jiang(6), Hong‐Wei Tan(5), Yuhan Guo(5), Qi Qiao(5), Haifeng Shi(4), Yugang Liu(4), Li Zhou(4), Ruo‐Min Di(4), Xing‐Biao Qiu(4), Yu‐Min Sun(3), Jun Gu(3), Yuanlong Wang(3), Chenxi Yang(3), Cuimei Zhao(3)