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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Molecular genetics of infertility: loss-of-function mutations in humans and corresponding knockout/mutated mice
Shi-Ya Jiao, Yihong Yang, Su‐Ren Chen
Human Reproduction Update (2020) Vol. 27, Iss. 1, pp. 154-189
Closed Access | Times Cited: 193

Showing 1-25 of 193 citing articles:

IQUB mutation induces radial spoke 1 deficiency causing asthenozoospermia with normal sperm morphology in humans and mice
Tingwenyi Hu, Xiangrong Tang, Tiechao Ruan, et al.
Cell Communication and Signaling (2025) Vol. 23, Iss. 1
Open Access | Times Cited: 2
Genetic factors as potential molecular markers of human oocyte and embryo quality
Qing Sang, Zhou Zhou, Jian Mu, et al.
Journal of Assisted Reproduction and Genetics (2021) Vol. 38, Iss. 5, pp. 993-1002
Open Access | Times Cited: 77
Meiotic recombination: insights into its mechanisms and its role in human reproduction with a special focus on non-obstructive azoospermia
Chunbo Xie, Weili Wang, Chaofeng Tu, et al.
Human Reproduction Update (2022) Vol. 28, Iss. 6, pp. 763-797
Closed Access | Times Cited: 53
Genetic landscape of a large cohort of Primary Ovarian Insufficiency: New genes and pathways and implications for personalized medicine
Abdelkader Heddar, Çağrı Oğur, Sabrina Corrêa da Costa, et al.
EBioMedicine (2022) Vol. 84, pp. 104246-104246
Open Access | Times Cited: 52
Aging conundrum: A perspective for ovarian aging
Jiachen Wu, Yang Liu, Yinhua Song, et al.
Frontiers in Endocrinology (2022) Vol. 13
Open Access | Times Cited: 43
The perinuclear theca protein Calicin helps shape the sperm head and maintain the nuclear structure in mice
Xiaozhen Zhang, Lin-Lin Wei, Hui-Juan Jin, et al.
Cell Reports (2022) Vol. 40, Iss. 1, pp. 111049-111049
Open Access | Times Cited: 40
Loss-of-function mutations in CFAP57 cause multiple morphological abnormalities of the flagella in humans and mice
Ao Ma, Jianteng Zhou, Haider Ali, et al.
JCI Insight (2023) Vol. 8, Iss. 3
Open Access | Times Cited: 28
CFAP70 is a solid and valuable target for the genetic diagnosis of oligo-astheno-teratozoospermia in infertile men
Hui-Juan Jin, Junli Wang, Xinyan Geng, et al.
EBioMedicine (2023) Vol. 93, pp. 104675-104675
Open Access | Times Cited: 24
Gene-knockout by iSTOP enables rapid reproductive disease modeling and phenotyping in germ cells of the founder generation
Yaling Wang, Jingwen Chen, Xueying Huang, et al.
Science China Life Sciences (2024) Vol. 67, Iss. 5, pp. 1035-1050
Closed Access | Times Cited: 12
CRISPR innovations in tissue engineering and gene editing
ZahraSadat Razavi, M. Soltani, Mohammad Souri, et al.
Life Sciences (2024), pp. 123120-123120
Open Access | Times Cited: 10
Whole-exome sequencing of a cohort of infertile men reveals novel causative genes in teratozoospermia that are chiefly related to sperm head defects
Yaqian Li, Yan Wang, Yuting Wen, et al.
Human Reproduction (2021) Vol. 37, Iss. 1, pp. 152-177
Closed Access | Times Cited: 45
Maternal effect genes: Update and review of evidence for a link with birth defects
Laura E. Mitchell
Human Genetics and Genomics Advances (2021) Vol. 3, Iss. 1, pp. 100067-100067
Open Access | Times Cited: 44
Loss of perinuclear theca ACTRT1 causes acrosome detachment and severe male subfertility in mice
Xiaozhen Zhang, Lin-Lin Wei, Xiaohui Zhang, et al.
Development (2022) Vol. 149, Iss. 12
Open Access | Times Cited: 34
Loss-of-function mutations in CEP78 cause male infertility in humans and mice
Xueguang Zhang, Rui Zheng, Chen Liang, et al.
Science Advances (2022) Vol. 8, Iss. 40
Open Access | Times Cited: 30
Drug development advances in human genetics‐based targets
X. Zhang, Wenjun Yu, Yan Li, et al.
MedComm (2024) Vol. 5, Iss. 2
Open Access | Times Cited: 8
Novel variations in TENT5D lead to teratozoospermia in infertile patients
Ying‐Teng Zhang, Gan Shen, Liang‐Chai Zhuo, et al.
Andrology (2024) Vol. 12, Iss. 6, pp. 1336-1346
Open Access | Times Cited: 7
Betaine alleviates spermatogenic cells apoptosis of oligoasthenozoospermia rat model by up-regulating methyltransferases and affecting DNA methylation
Qiyan Lin, Xiyu Ge, Leilei Gao, et al.
Phytomedicine (2024) Vol. 129, pp. 155713-155713
Closed Access | Times Cited: 7
Emerging biomaterials for reproductive medicine
Xiaocheng Wang, Dan Wu, Wenzhao Li, et al.
Engineered Regeneration (2021) Vol. 2, pp. 230-245
Open Access | Times Cited: 38
CCDC38 is required for sperm flagellum biogenesis and male fertility in mice
Ruidan Zhang, Bingbing Wu, Chao Liu, et al.
Development (2022) Vol. 149, Iss. 11
Open Access | Times Cited: 24
Further evidence from DNAH12 supports favorable fertility outcomes of infertile males with dynein axonemal heavy chain gene family variants
Hao Geng, Kai Wang, Dan Liang, et al.
iScience (2024) Vol. 27, Iss. 7, pp. 110366-110366
Open Access | Times Cited: 6
Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility
Kuokuo Li, Guanxiong Wang, Mingrong Lv, et al.
Journal of Assisted Reproduction and Genetics (2021) Vol. 39, Iss. 1, pp. 251-259
Open Access | Times Cited: 29
Sperm Ion Transporters and Channels in Human Asthenozoospermia: Genetic Etiology, Lessons from Animal Models, and Clinical Perspectives
Emma Cavarocchi, Marjorie Whitfield, Fabrice Saez, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 7, pp. 3926-3926
Open Access | Times Cited: 22
Mutations in CCIN cause teratozoospermia and male infertility
Yong Fan, Chenhui Huang, Juan Chen, et al.
Science Bulletin (2022) Vol. 67, Iss. 20, pp. 2112-2123
Open Access | Times Cited: 22
Biallelic Variants in CFAP61 Cause Multiple Morphological Abnormalities of the Flagella and Male Infertility
Ao Ma, Aurang Zeb, Imtiaz Ali, et al.
Frontiers in Cell and Developmental Biology (2022) Vol. 9
Open Access | Times Cited: 20
Bi‐allelic pathogenic variants in PABPC1L cause oocyte maturation arrest and female infertility
Weijie Wang, Jing Guo, Juanzi Shi, et al.
EMBO Molecular Medicine (2023) Vol. 15, Iss. 6
Open Access | Times Cited: 13
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