Wasim Shah

531 total citations
29 papers, 189 citations indexed

About

Wasim Shah is a scholar working on Reproductive Medicine, Public Health, Environmental and Occupational Health and Genetics. According to data from OpenAlex, Wasim Shah has authored 29 papers receiving a total of 189 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Reproductive Medicine, 17 papers in Public Health, Environmental and Occupational Health and 16 papers in Genetics. Recurrent topics in Wasim Shah's work include Sperm and Testicular Function (18 papers), Reproductive Biology and Fertility (17 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers). Wasim Shah is often cited by papers focused on Sperm and Testicular Function (18 papers), Reproductive Biology and Fertility (17 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers). Wasim Shah collaborates with scholars based in China, Pakistan and Bangladesh. Wasim Shah's co-authors include Ranjha Khan, Xiaohua Jiang, Sobia Dil, Qinghua Shi, Asad Khan, Wei Liu, Muhammad Zubair, Jie Wen, Jianteng Zhou and Ihsan Khan and has published in prestigious journals such as Human Molecular Genetics, Gene and Clinica Chimica Acta.

In The Last Decade

Wasim Shah

27 papers receiving 185 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Wasim Shah China 9 100 80 75 73 15 29 189
Zeng‐Ming Yang China 11 138 1.4× 77 1.0× 72 1.0× 55 0.8× 21 1.4× 22 323
Sobia Dil China 7 98 1.0× 54 0.7× 65 0.9× 64 0.9× 17 1.1× 17 153
Mayo Kodani Japan 7 114 1.1× 74 0.9× 83 1.1× 64 0.9× 3 0.2× 9 201
Huiru Cheng China 9 97 1.0× 119 1.5× 82 1.1× 109 1.5× 42 2.8× 25 273
Rachel J. Mann United States 4 96 1.0× 64 0.8× 111 1.5× 59 0.8× 15 1.0× 6 216
Hanwei Jiang China 10 30 0.3× 133 1.7× 41 0.5× 63 0.9× 14 0.9× 19 202
Yunna Ning China 8 118 1.2× 80 1.0× 109 1.5× 45 0.6× 20 1.3× 16 228
Angela H. Weller United States 7 56 0.6× 206 2.6× 39 0.5× 77 1.1× 24 1.6× 11 277
Jaye Adams United States 3 180 1.8× 108 1.4× 173 2.3× 61 0.8× 14 0.9× 3 310
Pauline Sararols Switzerland 6 38 0.4× 103 1.3× 28 0.4× 69 0.9× 12 0.8× 6 136

Countries citing papers authored by Wasim Shah

Since Specialization
Citations

This map shows the geographic impact of Wasim Shah'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 Wasim Shah with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Wasim Shah more than expected).

Fields of papers citing papers by Wasim Shah

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wasim Shah. 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 Wasim Shah. The network helps show where Wasim Shah may publish in the future.

Co-authorship network of co-authors of Wasim Shah

This figure shows the co-authorship network connecting the top 25 collaborators of Wasim Shah. A scholar is included among the top collaborators of Wasim Shah 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 Wasim Shah. Wasim Shah is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Abbas, Tanveer, Huan Zhang, Hao Yin, et al.. (2025). A novel mutation in CFAP58 leads to MMAF in humans and mice by disrupting CP assembly. Human Molecular Genetics. 34(18). 1575–1583. 1 indexed citations
2.
Zubair, Muhammad, Wasim Shah, Ghulam Mustafa, et al.. (2025). Novel bi-allelic variants in DNAH10 lead to multiple morphological abnormalities of sperm flagella and male infertility. Asian Journal of Andrology. 27(4). 516–523. 1 indexed citations
3.
Ali, Haider, Aurang Zeb, Nisar Ahmad, et al.. (2025). A novel frameshift variant in AXDND1 may cause multiple morphological abnormalities of the sperm flagella in a consanguineous Pakistani family. Asian Journal of Andrology. 27(6). 691–696. 1 indexed citations
4.
Liu, Tao, Aurang Zeb, Ihsan Khan, et al.. (2024). A homozygous ARMC3 splicing variant causes asthenozoospermia and flagellar disorganization in a consanguineous family. Clinical Genetics. 106(4). 437–447. 3 indexed citations
5.
Liu, Tao, Jingwei Ye, Asad Khan, et al.. (2024). Novel homozygous SPAG17 variants cause human male infertility through multiple morphological abnormalities of spermatozoal flagella related to axonemal microtubule doublets. Asian Journal of Andrology. 27(2). 245–253. 2 indexed citations
6.
Zhang, Huan, Muhammad Zubair, Nisar Ahmad, et al.. (2024). A novel missense mutation in <i>QRICH2</i> causes male infertility due to multiple morphological abnormalities of the sperm flagella. JUSTC. 54(9). 904–904. 1 indexed citations
7.
Li, Ming, Yue Wang, Jianteng Zhou, et al.. (2024). A homozygous nonsense variant in HENMT1 causes male infertility in humans and mice. Andrology. 13(6). 1439–1450. 1 indexed citations
8.
Zhang, Xiangjun, Sobia Dil, Ihsan Khan, et al.. (2024). A novel homozygous TSGA10 missense variant causes acephalic spermatozoa syndrome in a Pakistani family. Basic and Clinical Andrology. 34(1). 4–4. 1 indexed citations
9.
Ahmad, Nisar, Aurang Zeb, Jianteng Zhou, et al.. (2024). A novel missense mutation of CCDC34 causes male infertility with oligoasthenoteratozoospermia in a consanguineous Pakistani family. Asian Journal of Andrology. 26(6). 605–609. 4 indexed citations
10.
Zeb, Aurang, Huan Zhang, Wasim Shah, et al.. (2024). Novel biallelic ADCY10 variants cause asthenozoospermia with excessive residual cytoplasm and hydronephrosis in humans. Reproductive BioMedicine Online. 50(3). 104481–104481. 4 indexed citations
11.
Zhang, Huan, Muhammad Zubair, Wasim Shah, et al.. (2024). A novel homozygous splicing mutation in AK7 causes multiple morphological abnormalities of sperm flagella in patients from consanguineous Pakistani families. Asian Journal of Andrology. 27(2). 189–195. 2 indexed citations
12.
Dil, Sobia, Jianteng Zhou, Huan Zhang, et al.. (2023). A homozygous KASH5 frameshift mutation causes diminished ovarian reserve, recurrent miscarriage, and non-obstructive azoospermia in humans. Frontiers in Endocrinology. 14. 1128362–1128362. 8 indexed citations
13.
Zubair, Muhammad, Ranjha Khan, Uzma Hameed, et al.. (2022). A recurrent homozygous missense mutation in CCDC103 causes asthenoteratozoospermia due to disorganized dynein arms. Asian Journal of Andrology. 24(3). 255–259. 12 indexed citations
14.
Khan, Ranjha, Jing Chen, Manan Khan, et al.. (2021). Novel Loss-of-Function Mutations in DNAH1 Displayed Different Phenotypic Spectrum in Humans and Mice. Frontiers in Endocrinology. 12. 765639–765639. 11 indexed citations
15.
Khan, Asad, et al.. (2021). The evolutionarily conserved gene, Fam114a2, is dispensable for fertility in mouse. Reproductive Biology. 21(3). 100531–100531. 4 indexed citations
16.
Khan, Ranjha, et al.. (2021). Inactivation of testis-specific gene C4orf46 is dispensable for spermatogenesis and fertility in mouse. Mammalian Genome. 32(5). 364–370. 4 indexed citations
17.
Shah, Wasim, Ranjha Khan, Asad Khan, et al.. (2021). The Molecular Mechanism of Sex Hormones on Sertoli Cell Development and Proliferation. Frontiers in Endocrinology. 12. 648141–648141. 47 indexed citations
18.
Dil, Sobia, Jianteng Zhou, Yuanwei Zhang, et al.. (2021). Novel biallelic loss-of-function mutations in CFAP43 cause multiple morphological abnormalities of the sperm flagellum in Pakistani families. Asian Journal of Andrology. 23(6). 627–632. 14 indexed citations
19.
Wu, Yufan, Ranjha Khan, Wasim Shah, et al.. (2020). Normal spermatogenesis and fertility in Ddi1 (DNA damage inducible 1) mutant mice. Reproductive Biology. 20(4). 520–524. 9 indexed citations
20.
Khan, Ranjha, Jingwei Ye, Wasim Shah, et al.. (2020). Evolutionarily conserved and testis-specific gene, 4930524B15Rik, is not essential for mouse spermatogenesis and fertility. Molecular Biology Reports. 47(7). 5207–5213. 11 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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