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Jing Du

Fudan University · CN
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Area of research
Obstetrics and Gynecology · Reproductive Medicine
Research interest
Research interests include Biology, Medicine, Genetics, Oocyte, DNA methylation, and Internal medicine.
h-index
citations
1,598
works
23
NIH funding
primary concept
email

Recent publications

Genome-wide association study unravels mechanisms of brain glymphatic activity
Nature Communications 2025cited by 16position: middledoi
The genetic architecture of the human hypothalamus and its involvement in neuropsychiatric behaviours and disorders
Nature Human Behaviour 2024cited by 16position: middledoi
Integrated analyses of 5 mC, 5hmC methylation and gene expression reveal pathology-associated AKT3 gene and potential biomarkers for Alzheimer's disease
Journal of Psychiatric Research 2024cited by 6position: lastdoi
Caregivers’ understanding of childhood influenza vaccination during the epidemic in China. A mixed-methods study
Frontiers in Public Health 2023cited by 3position: middledoi
Soil bacterial communities triggered by organic matter inputs associates with a high-yielding pear production
SOIL 2022cited by 21position: middledoi
Placental DNA methylation changes in gestational diabetes mellitus
Epigenetics 2022cited by 16position: lastdoi
Childhood Influenza Vaccination and Its Determinants during 2020–2021 Flu Seasons in China: A Cross-Sectional Survey
Vaccines 2022cited by 9position: middledoi
Predictive plasma biomarker for gestational diabetes: A case-control study in China
Journal of Proteomics 2022cited by 4position: lastdoi
The Chinese mitten crab genome provides insights into adaptive plasticity and developmental regulation
Nature Communications 2021cited by 87position: middledoi
<i>FBXO43</i> variants in patients with female infertility characterized by early embryonic arrest
Human Reproduction 2021cited by 54position: middledoi
Novel biallelic mutations in <i>MEI1:</i> expanding the phenotypic spectrum to human embryonic arrest and recurrent implantation failure
Human Reproduction 2021cited by 50position: middledoi
Bi-allelic Missense Pathogenic Variants in TRIP13 Cause Female Infertility Characterized by Oocyte Maturation Arrest
The American Journal of Human Genetics 2020cited by 136position: middledoi
Biallelic mutations in CDC20 cause female infertility characterized by abnormalities in oocyte maturation and early embryonic development
Protein & Cell 2020cited by 87position: middledoi
Identification novel mutations in TUBB8 in female infertility and a novel phenotype of large polar body in oocytes with TUBB8 mutations
Journal of Assisted Reproduction and Genetics 2020cited by 61position: middledoi
Epigenetic alternations of microRNAs and DNA methylation contribute to gestational diabetes mellitus
Journal of Cellular and Molecular Medicine 2020cited by 60position: lastdoi
A pannexin 1 channelopathy causes human oocyte death
Science Translational Medicine 2019cited by 98position: middledoi
Homozygous mutations in <i>REC114</i> cause female infertility characterised by multiple pronuclei formation and early embryonic arrest
Journal of Medical Genetics 2019cited by 69position: middledoi
Discovery of sex-related genes from embryonic development stage based on transcriptome analysis in Eriocheir sinensis
Gene 2019cited by 22position: firstdoi
DNA methylation levels of imprinted and nonimprinted genes DMRs associated with defective human spermatozoa
Andrologia 2016cited by 43position: lastdoi
Ruxolitinib in corticosteroid-refractory graft-versus-host disease after allogeneic stem cell transplantation: a multicenter survey
Leukemia 2015cited by 538position: middledoi
Association of VEGF Genetic Polymorphisms with Recurrent Spontaneous Abortion Risk: A Systematic Review and Meta-Analysis
PLoS ONE 2015cited by 49position: middledoi
The Ser680Asn polymorphism in the follicle‐stimulating hormone receptor gene is associated with the ovarian response in controlled ovarian hyperstimulation
Clinical Endocrinology 2014cited by 49position: lastdoi
A Possible New Mechanism in the Pathophysiology of Polycystic Ovary Syndrome (PCOS): The Discovery That Leukocyte Telomere Length Is Strongly Associated With PCOS
The Journal of Clinical Endocrinology & Metabolism 2013cited by 67position: middledoi
Association study between methylenetetrahydrofolate reductase polymorphisms and unexplained recurrent pregnancy loss: A meta-analysis
Gene 2012cited by 86position: lastdoi

Grants

No grants ingested yet.

Frequent collaborators

Lei Wang · Fudan University7 papers (2013–2021)Lin He · Fudan University7 papers (2016–2021)Xiaoxi Sun · Fudan University7 papers (2014–2021)Qing Sang · Fudan University7 papers (2013–2021)Zhihua Zhang · Fudan University6 papers (2019–2021)Jian Mu · Liaocheng University6 papers (2019–2021)Biaobang Chen · Fudan University6 papers (2019–2021)Qiaoli Li · Guangxi Medical University5 papers (2019–2021)Jin Li · Xinjiang University5 papers (2013–2021)Wenjing Wang · Shandong University5 papers (2019–2021)Jing Fu · Kunming Medical University5 papers (2019–2021)Ling Wu · Xuzhou Medical College5 papers (2019–2021) · 5 papers (2019–2021)Zhou Zhou · Jiangnan University4 papers (2019–2021)Bin Li · Fudan University4 papers (2019–2020)Jie Dong · National Institutes of Health4 papers (2019–2021)Zhaofeng Zhang · Fudan University4 papers (2012–2022)Jianhua Xu · Fudan University4 papers (2012–2022)Yupei Shen · Fudan University4 papers (2020–2024)Zheng Yan · Fudan University4 papers (2019–2020)
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