Manan Khan

418 total citations
10 papers, 172 citations indexed

About

Manan Khan is a scholar working on Genetics, Molecular Biology and Reproductive Medicine. According to data from OpenAlex, Manan Khan has authored 10 papers receiving a total of 172 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Molecular Biology and 5 papers in Reproductive Medicine. Recurrent topics in Manan Khan's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Reproductive Biology and Fertility (4 papers) and Sperm and Testicular Function (4 papers). Manan Khan is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Reproductive Biology and Fertility (4 papers) and Sperm and Testicular Function (4 papers). Manan Khan collaborates with scholars based in China, Pakistan and Canada. Manan Khan's co-authors include Qinghua Shi, Xiaohua Jiang, Yuanwei Zhang, Asim Ali, Teka Khan, Nazish Jabeen, Ranjha Khan, Shi Yin, Huan Zhang and Liu Wang and has published in prestigious journals such as Development, Scientific Reports and Biology of Reproduction.

In The Last Decade

Manan Khan

10 papers receiving 172 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Manan Khan China	7	98	71	66	56	11	10	172
Pu-Yao Zhang China	8	184 1.9×	25 0.4×	30 0.5×	64 1.1×	15 1.4×	10	262
Teka Khan China	6	137 1.4×	60 0.8×	71 1.1×	44 0.8×	18 1.6×	8	193
Hanwei Jiang China	10	133 1.4×	30 0.4×	63 1.0×	41 0.7×	14 1.3×	19	202
Gaku Minase Japan	5	66 0.7×	73 1.0×	58 0.9×	45 0.8×	8 0.7×	11	128
Suixing Fan China	8	235 2.4×	58 0.8×	76 1.2×	53 0.9×	19 1.7×	13	293
Christiane Pleuger Germany	7	66 0.7×	108 1.5×	37 0.6×	66 1.2×	4 0.4×	12	192
Bikem Soygur United States	8	109 1.1×	40 0.6×	45 0.7×	65 1.2×	13 1.2×	18	237
Jacob Malte Jensen Denmark	8	112 1.1×	47 0.7×	87 1.3×	24 0.4×	39 3.5×	9	207
Ayako Muraoka Japan	9	63 0.6×	182 2.6×	21 0.3×	48 0.9×	12 1.1×	22	292
Chloé Mayère Switzerland	7	155 1.6×	35 0.5×	95 1.4×	51 0.9×	17 1.5×	12	198

Countries citing papers authored by Manan Khan

Since Specialization

Citations

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

Fields of papers citing papers by Manan Khan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manan Khan

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

All Works

Sort: Min cites: Since: Top N: Style:

10 of 10 papers shown

Ali, Asim, Ahsanullah Unar, Muhammad Zubair, et al.. (2023). A novel NPHP4 homozygous missense variant identified in infertile brothers with multiple morphological abnormalities of the sperm flagella. Journal of Assisted Reproduction and Genetics. 41(1). 109–120. 6 indexed citations

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

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

Huang, Zhu, Manan Khan, Teka Khan, et al.. (2019). The deubiquitinating gene Usp29 is dispensable for fertility in male mice. Science China Life Sciences. 62(4). 544–552. 7 indexed citations

Hussain, Hafiz Muhammad Jafar, Ghulam Murtaza, Xiaohua Jiang, et al.. (2019). Whole Exome Sequencing Revealed a Novel Nonsense Variant in the GNRHR Gene Causing Normosmic Hypogonadotropic Hypogonadism in a Pakistani Family. Hormone Research in Paediatrics. 91(1). 9–16. 5 indexed citations

Khan, Manan, Nazish Jabeen, Teka Khan, et al.. (2018). The evolutionarily conserved genes: Tex37, Ccdc73, Prss55 and Nxt2 are dispensable for fertility in mice. Scientific Reports. 8(1). 4975–4975. 36 indexed citations

Khan, Teka, Manan Khan, Saadullah Khan, et al.. (2018). Whole exome sequencing identifies a novel dominant missense mutation underlying leukonychia in a Pakistani family. Journal of Human Genetics. 63(10). 1071–1076. 5 indexed citations

Yin, Shi, Xiaohua Jiang, Hanwei Jiang, et al.. (2017). Histone acetyltransferase KAT8 is essential for mouse oocyte development by regulating ROS levels. Development. 144(12). 2165–2174. 27 indexed citations

Jiang, Xiaohua, Tieliang Ma, Yuanwei Zhang, et al.. (2015). Specific Deletion of Cdh2 in Sertoli Cells Leads to Altered Meiotic Progression and Subfertility of Mice1. Biology of Reproduction. 92(3). 79–79. 49 indexed citations

10.

LeBlanc, Marissa A., Lynette S. Penney, Daniel Gaston, et al.. (2013). A novel rearrangement of occludin causes brain calcification and renal dysfunction. Human Genetics. 132(11). 1223–1234. 22 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.

Explore authors with similar magnitude of impact