Wenbin He

1.5k citations

58 papers · 917 indexed · h-index 16

Molecular Biology
Genetics top 10%
Reproductive Medicine top 2%
Public Health, Environmental and Occupational Health top 10%
Epidemiology

Co-authors: Nai‐Hong Chen Yue‐Qiu Tan Juan Du Guangxiu Lu Wei Zuo Lanlan Meng Xiaofeng Guo Ge Lin
Topics: Reproductive Biology and Fertility (12 papers)Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers)Sperm and Testicular Function (9 papers)
Cited by: Reproductive Medicine Neurology Genetics
Journals: Scientific Reports European Heart Journal The American Journal of Human Genetics
Partner nations: China Australia Italy

In The Last Decade

Wenbin He

54 papers receiving 904 citations

Peers

Countries citing papers authored by Wenbin He

Since Specialization

Citations

This map shows the geographic impact of Wenbin He's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Wenbin He with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Wenbin He more than expected).

Fields of papers citing papers by Wenbin He

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wenbin He. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Wenbin He. The network helps show where Wenbin He may publish in the future.

Co-authorship network of co-authors of Wenbin He

This figure shows the co-authorship network connecting the top 25 collaborators of Wenbin He. A scholar is included among the top collaborators of Wenbin He based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Wenbin He. Wenbin He is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Integration of serum pharmacochemistry, chromatographic fingerprint, and network pharmacology to identify chemical markers for quality makers of Di Huang Yin Zi 2025 ·Journal of Pharmaceutical and Biomedical Analysis ·(unknown),Xiaoqin Ma,(unknown),Jing Yang,(unknown),Wenbin He,Junlong Zhang	2
2	A hemizygous loss‐of‐function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia 2024 ·Clinical Genetics ·(unknown),(unknown),Lanlan Meng,Chen Tan,Wenbin He,Chaofeng Tu,Juan Du,Guangxiu Lu,Ge Lin,Yue‐Qiu Tan,(unknown)	1
3	Genetic Analysis and Reproductive Interventions for Two Rare Families Affected by Severe Haemophilia A 2024 ·Haemophilia ·Shi‐Min Yuan,Liang Hu,Jim Zhong,(unknown),(unknown),(unknown),Sicong Zeng,Wenbin He,Feng Gu,(unknown),Guangxiu Lu,Ge Lin,Juan Du	1
4	Bi-allelic variants in DNAH3 cause male infertility with asthenoteratozoospermia in humans and mice 2024 ·Human Reproduction Open ·(unknown),Yaling Wang,(unknown),(unknown),Yong Li,Chen Tan,Chaofeng Tu,Victor Wei Zhang,Liang Hu,Huan Zhang,Lanlan Meng,Chunyu Liu,(unknown),Guangxiu Lu,Ge Lin,Juan Du,Yue‐Qiu Tan,Yanwei Sha,Lingbo Wang,Wenbin He	13
5	Impact of Codonopsis decoction on cerebral blood flow and cognitive function in rats with chronic cerebral ischemia 2023 ·Journal of Ethnopharmacology ·Jie Wang,(unknown),Shifeng Chu,Xin Liu,(unknown),Wenbin He	8
6	A richer and more diverse future for microglia phenotypes 2023 ·Heliyon ·Jie Wang,Wenbin He,(unknown)	57
7	Identification of a missense variant of MND1 in meiotic arrest and non-obstructive azoospermia 2023 ·Journal of Human Genetics ·(unknown),Zhiyong Ji,(unknown),Jiaqiang Luo,Yuxiang Zhang,(unknown),(unknown),Ruhui Tian,Erlei Zhi,Yuhua Huang,Nachuan Liu,Wenbin He,Yue‐Qiu Tan,Zheng Li,Chencheng Yao,Peng Li	2
8	Clinical Utility of Medical Exome Sequencing: Expanded Carrier Screening for Patients Seeking Assisted Reproductive Technology in China 2022 ·Frontiers in Genetics ·(unknown),Wenbin He,(unknown),Xiurong Li,Liang Hu,Hao Hu,Guangxiu Lu,Ge Lin,Chang‐Zhi Dong,Victor Wei Zhang,Juan Du,(unknown)	10
9	Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia 2022 ·Frontiers in Genetics ·Yurong Wang,Ling Liu,Chen Tan,(unknown),Lanlan Meng,Hongchuan Nie,Juan Du,Guangxiu Lu,Ge Lin,Wenbin He,Yue‐Qiu Tan	13
10	Case Report: A Novel Heterozygous ZP3 Deletion Associated With Empty Follicle Syndrome and Abnormal Follicular Development 2021 ·Frontiers in Genetics ·Yongzhe Chen,(unknown),(unknown),Wenbin He,Juan Du,Sufen Cai,Fei Gong,Guangxiu Lu,Ge Lin,Can Dai	12
11	Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice 2021 ·The American Journal of Human Genetics ·Chen Tan,Lanlan Meng,Mingrong Lv,Xiaojin He,Yanwei Sha,Dongdong Tang,(unknown),(unknown),Wenbin He,Chaofeng Tu,Hongchuan Nie,Huan Zhang,Juan Du,Guangxiu Lu,Liqing Fan,Yunxia Cao,Ge Lin,Yue‐Qiu Tan	32
12	Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCD 2020 ·Human Genetics ·Chaofeng Tu,Hongchuan Nie,Lanlan Meng,Weili Wang,Haiyu Li,Shi‐Min Yuan,Dehua Cheng,Wenbin He,Gang Liu,Juan Du,Fei Gong,Guangxiu Lu,Ge Lin,Victor Wei Zhang,Yue‐Qiu Tan	57
13	Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagella 2019 ·Scientific Reports ·Chaofeng Tu,Hongchuan Nie,Lanlan Meng,Shi‐Min Yuan,Wenbin He,Aixiang Luo,Haiyu Li,Wen Li,Juan Du,Guangxiu Lu,Ge Lin,Yue‐Qiu Tan	51
14	Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature 2018 ·Molecular Cytogenetics ·Haiyu Li,Juan Du,Wen Li,Dehua Cheng,Wenbin He,(unknown),Bo Xiong,Shi‐Min Yuan,Chaofeng Tu,Lanlan Meng,Aixiang Luo,Ge Lin,Guangxiu Lu,Yue‐Qiu Tan	7
15	Novel mutations of PKD genes in Chinese patients suffering from autosomal dominant polycystic kidney disease and seeking assisted reproduction 2018 ·BMC Medical Genetics ·Wenbin He,Wenjuan Xiao,Yue‐Qiu Tan,(unknown),Wen Li,Victor Wei Zhang,(unknown),Xiurong Li,Liang Hu,Guangxiu Lu,Ge Lin,(unknown)	13
16	Novel inactivating mutations in the FSH receptor cause premature ovarian insufficiency with resistant ovary syndrome 2018 ·Reproductive BioMedicine Online ·Wenbin He,Juan Du,Xiaowen Yang,Wen Li,(unknown),Can Dai,Yongzhe Chen,Yaxin Zhang,Guangxiu Lu,Ge Lin,Fei Gong,Yue‐Qiu Tan	27
17	Expanded carrier screening and preimplantation genetic diagnosis in a couple who delivered a baby affected with congenital factor VII deficiency 2018 ·BMC Medical Genetics ·Wenbin He,Yue‐Qiu Tan,Xiao Hu,Wen Li,Bo Xiong,Keli Luo,Fei Gong,Guangxiu Lu,Ge Lin,(unknown)	2
18	A case of megalencephalic leukoencephalopathy with subcortical cysts type 1 was identified with a novel compound heterozygous alteration (c.135delC; c.423+2dupT) in China 2017 ·Clinical Case Reports ·Cheng Dai,Wenbin He,Juan Du,Yue‐Qiu Tan,Guangxiu Lu,(unknown)	1
19	Causes of Death Among Persons Who Survive an Acute Ischemic Stroke 2014 ·Current Neurology and Neuroscience Reports ·Shuai Zhang,Wenbin He,Nai‐Hong Chen	23
20	Do glial cells play an anti-oxidative role in Huntington's disease? 2014 ·Free Radical Research ·Yan Gao,Shifeng Chu,(unknown),Wei Zuo,(unknown),Wenbin He,Jiaqing Yan,(unknown)	11

About Wenbin He

Wenbin He is a scholar working on Reproductive Medicine, Genetics and Neurology, having authored 58 papers that have together received 917 indexed citations. Recurring topics across this work include Reproductive Biology and Fertility (12 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers) and Sperm and Testicular Function (9 papers). The work is most often cited by research in Reproductive Medicine (257 citations), Neurology (107 citations) and Genetics (293 citations). Wenbin He has collaborated with scholars based in China, Australia and Italy. Frequent co-authors include Nai‐Hong Chen, Yue‐Qiu Tan, Juan Du, Guangxiu Lu, Wei Zuo, Lanlan Meng, Xiaofeng Guo, Ge Lin, Cong‐Yuan Xia and Shuai Zhang. Their work appears in journals such as Scientific Reports, European Heart Journal and The American Journal of Human Genetics.

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