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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:

Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice
Chaofeng Tu, Jiangshan Cong, Victor Wei Zhang, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 8, pp. 1466-1477
Open Access | Times Cited: 89

Showing 1-25 of 89 citing articles:

Bi-allelic variants in DNAH3 cause male infertility with asthenoteratozoospermia in humans and mice
Guiquan Meng, Yaling Wang, Chen Luo, et al.
Human Reproduction Open (2024) Vol. 2024, Iss. 1
Open Access | Times Cited: 16
DNALI1 deficiency causes male infertility with severe asthenozoospermia in humans and mice by disrupting the assembly of the flagellar inner dynein arms and fibrous sheath
Huan Wu, Yiyuan Liu, Yuqian Li, et al.
Cell Death and Disease (2023) Vol. 14, Iss. 2
Open Access | Times Cited: 35
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: 27
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: 23
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
Genetic Causes of Qualitative Sperm Defects: A Narrative Review of Clinical Evidence
Andrea Graziani, Maria Santa Rocca, Cinzia Vinanzi, et al.
Genes (2024) Vol. 15, Iss. 5, pp. 600-600
Open Access | Times Cited: 8
Development of functional spermatozoa in mammalian spermiogenesis
Haruhiko Miyata, Keisuke Shimada, Yuki Kaneda, et al.
Development (2024) Vol. 151, Iss. 14
Closed Access | Times Cited: 8
The Effect of Edaravone Supplementation Prior to Cryopreservation on Sperm Parameters, DNA Integrity, Apoptosis, Lipid Peroxidation, and Mitochondrial Membrane Potential in Infertile Men with Asthenoteratozoospermia
Maryam Ghasemi, Hamid Nazarian, Zahra Shams Mofarahe, et al.
Reproductive Sciences (2025)
Closed Access | Times Cited: 1
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: 44
Bi-allelic variants in human WDR63 cause male infertility via abnormal inner dynein arms assembly
Shuai Lü, Yayun Gu, Yifei Wu, et al.
Cell Discovery (2021) Vol. 7, Iss. 1
Open Access | Times Cited: 41
Clinical detection, diagnosis and treatment of morphological abnormalities of sperm flagella: A review of literature
Jiaxiong Wang, Weizhuo Wang, Liyan Shen, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 31
Mitochondrial regulation during male germ cell development
Xiaoli Wang, Lisha Yin, Yujiao Wen, et al.
Cellular and Molecular Life Sciences (2022) Vol. 79, Iss. 2
Open Access | Times Cited: 28
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
How exome sequencing improves the diagnostics and management of men with non‐syndromic infertility
Birgit Stallmeyer, Ann‐Kristin Dicke, Frank Tüttelmann
Andrology (2024)
Open Access | Times Cited: 6
BiallelicCFAP61variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia
Tongyao Hu, Lanlan Meng, Chen Tan, et al.
Journal of Medical Genetics (2022) Vol. 60, Iss. 2, pp. 144-153
Open Access | Times Cited: 23
The human sperm proteome—Toward a panel for male fertility testing
Thomas Greither, Mario Dejung, Hermann M. Behre, et al.
Andrology (2023) Vol. 11, Iss. 7, pp. 1418-1436
Open Access | Times Cited: 14
Fat mass and obesity-associated factor (FTO)-mediated N6-methyladenosine regulates spermatogenesis in an age-dependent manner
Yifei Wu, Jincheng Li, Chenmeijie Li, et al.
Journal of Biological Chemistry (2023) Vol. 299, Iss. 6, pp. 104783-104783
Open Access | Times Cited: 13
Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice
Chen Tan, Lanlan Meng, Mingrong Lv, et al.
The American Journal of Human Genetics (2021) Vol. 109, Iss. 1, pp. 157-171
Open Access | Times Cited: 32
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: 28
Multiomics analysis of male infertility
Xiaolong Wu, Liwei Zhou, Jie Shi, et al.
Biology of Reproduction (2022) Vol. 107, Iss. 1, pp. 118-134
Closed Access | Times Cited: 22
Molecular basis of the morphogenesis of sperm head and tail in mice
Keiichiro Yogo
Reproductive Medicine and Biology (2022) Vol. 21, Iss. 1
Open Access | Times Cited: 21
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
CCDC146 is required for sperm flagellum biogenesis and male fertility in mice
Yanjie Ma, Bingbing Wu, Yinghong Chen, et al.
Cellular and Molecular Life Sciences (2023) Vol. 81, Iss. 1
Open Access | Times Cited: 12
Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia
Weili Wang, Lilan Su, Lanlan Meng, et al.
Human Reproduction (2023) Vol. 38, Iss. 7, pp. 1399-1411
Closed Access | Times Cited: 11
A novel frameshift mutation in DNAH6 associated with male infertility and asthenoteratozoospermia
Fei Huang, Jun Zeng, Dan Liu, et al.
Frontiers in Endocrinology (2023) Vol. 14
Open Access | Times Cited: 11
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