Muhammad Imran Khan

2.5k total citations
66 papers, 1.0k citations indexed

About

Muhammad Imran Khan is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Muhammad Imran Khan has authored 66 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 33 papers in Ophthalmology and 14 papers in Genetics. Recurrent topics in Muhammad Imran Khan's work include Retinal Development and Disorders (26 papers), Retinal Diseases and Treatments (23 papers) and Glaucoma and retinal disorders (19 papers). Muhammad Imran Khan is often cited by papers focused on Retinal Development and Disorders (26 papers), Retinal Diseases and Treatments (23 papers) and Glaucoma and retinal disorders (19 papers). Muhammad Imran Khan collaborates with scholars based in Netherlands, Pakistan and United States. Muhammad Imran Khan's co-authors include Raheel Qamar, Shazia Micheal, Anneke I. den Hollander, Frans P.M. Cremers, Farah Akhtar, Rob W.J. Collin, Sorath Noorani Siddiqui, Saemah Nuzhat Zafar, Muhammad Ajmal and Maleeha Azam and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Scientific Reports.

In The Last Decade

Muhammad Imran Khan

62 papers receiving 983 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Muhammad Imran Khan Netherlands 20 663 496 242 151 90 66 1.0k
Saskia D. van der Velde-Visser Netherlands 15 874 1.3× 350 0.7× 190 0.8× 134 0.9× 173 1.9× 17 1.0k
Angela M. Hales Australia 11 760 1.1× 503 1.0× 132 0.5× 234 1.5× 118 1.3× 12 1.0k
Jacqueline Siegel‐Bartelt Canada 8 820 1.2× 111 0.2× 477 2.0× 95 0.6× 44 0.5× 10 1.1k
Valerie Greger Germany 18 830 1.3× 224 0.5× 498 2.1× 47 0.3× 22 0.2× 26 1.2k
Konstantinos Nikopoulos Switzerland 12 623 0.9× 143 0.3× 214 0.9× 118 0.8× 106 1.2× 20 802
Carmen Ramos Spain 15 450 0.7× 125 0.3× 268 1.1× 66 0.4× 74 0.8× 32 720
Christel Kockx Netherlands 20 1.3k 1.9× 168 0.3× 227 0.9× 53 0.4× 98 1.1× 28 1.7k
Joanne Sutherland Canada 11 492 0.7× 315 0.6× 264 1.1× 56 0.4× 38 0.4× 16 874
James M. Dunn Canada 14 749 1.1× 420 0.8× 145 0.6× 69 0.5× 52 0.6× 29 1.3k
Rebecca C. Tyler United States 13 375 0.6× 144 0.3× 334 1.4× 115 0.8× 59 0.7× 19 624

Countries citing papers authored by Muhammad Imran Khan

Since Specialization
Citations

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

Fields of papers citing papers by Muhammad Imran Khan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Muhammad Imran Khan

This figure shows the co-authorship network connecting the top 25 collaborators of Muhammad Imran Khan. A scholar is included among the top collaborators of Muhammad Imran 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 Muhammad Imran Khan. Muhammad Imran Khan 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.
Zafar, Imran, et al.. (2024). Whole-exome sequencing identifies rare recessive variants in azoospermia patients from consanguineous Pakistani families. Molecular Genetics and Genomics. 299(1). 111–111. 1 indexed citations
2.
3.
Yahalom, Claudia, Oded Volovelsky, Mor Hanany, et al.. (2021). SENIOR–LØKEN SYNDROME. Retina. 41(10). 2179–2187. 11 indexed citations
4.
Kuehlewein, Laura, Ditta Zobor, Katarína Štingl, et al.. (2021). Clinical Phenotype of PDE6B-Associated Retinitis Pigmentosa. International Journal of Molecular Sciences. 22(5). 2374–2374. 18 indexed citations
5.
Khan, Muhammad Imran, Maria M. van Genderen, J. Schuil, et al.. (2020). LONGITUDINAL STUDY OF RPE65-ASSOCIATED INHERITED RETINAL DEGENERATIONS. Retina. 40(9). 1812–1828. 11 indexed citations
6.
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Beryozkin, Avigail, Samer Khateb, Muhammad Imran Khan, et al.. (2020). Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations. Scientific Reports. 10(1). 15156–15156. 15 indexed citations
8.
Khan, Mubeen, Stéphanie S. Cornelis, Muhammad Imran Khan, et al.. (2019). Cost‐effective molecular inversion probe‐based ABCA4 sequencing reveals deep‐intronic variants in Stargardt disease. Human Mutation. 40(10). 1749–1759. 37 indexed citations
9.
10.
Khan, Muhammad Imran, et al.. (2017). The Impact of Social Media on Teacher's Performance: A Case of Higher Educational Institutions of Pakistan. European Online Journal of Natural and Social Sciences. 6(2). 206–220. 6 indexed citations
11.
Micheal, Shazia, Sorath Noorani Siddiqui, Saemah Nuzhat Zafar, et al.. (2016). A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma. PLoS ONE. 11(7). e0160016–e0160016. 20 indexed citations
12.
Lamers, Ideke J.C., Miriam Schmidts, Muhammad Ajmal, et al.. (2016). Genetic and clinical characterization of Pakistani families with Bardet-Biedl syndrome extends the genetic and phenotypic spectrum. Scientific Reports. 6(1). 34764–34764. 31 indexed citations
13.
Micheal, Shazia, Humaira Ayub, Farrah Islam, et al.. (2015). Variants in the ASB10 Gene Are Associated with Primary Open Angle Glaucoma. PLoS ONE. 10(12). e0145005–e0145005. 9 indexed citations
14.
Micheal, Shazia, Humaira Ayub, Muhammad Imran Khan, et al.. (2014). Association of known common genetic variants with primary open angle, primary angle closure, and pseudoexfoliation glaucoma in Pakistani cohorts.. PubMed. 20. 1471–9. 29 indexed citations
15.
Ayub, Humaira, Shazia Micheal, Farah Akhtar, et al.. (2014). Association of a Polymorphism in the BIRC6 Gene with Pseudoexfoliative Glaucoma. PLoS ONE. 9(8). e105023–e105023. 11 indexed citations
16.
Cortón, Marta, Almudena Ávila‐Fernández, Elena Vallespín, et al.. (2013). Involvement of LCA5 in Leber Congenital Amaurosis and Retinitis Pigmentosa in the Spanish Population. Ophthalmology. 121(1). 399–407. 14 indexed citations
17.
Mustafa, Farah, Muhammad Imran Khan, Muhammad Zubair, et al.. (2012). Prevalence of Hepatitis C Virus in urban ghettos of twin cities.. Pakistan Journal of Zoology. 44(4). 937–943. 7 indexed citations
18.
Micheal, Shazia, Muhammad Imran Khan, Farah Akhtar, et al.. (2012). Identification of a novel FBN1 gene mutation in a large Pakistani family with Marfan syndrome.. PubMed. 18. 1918–26. 14 indexed citations
19.
Khan, Muhammad Imran, Ferry F.J. Kersten, Maleeha Azam, et al.. (2011). CLRN1 Mutations Cause Nonsyndromic Retinitis Pigmentosa. Ophthalmology. 118(7). 1444–1448.
20.
Micheal, Shazia, et al.. (2009). MTHFR gene C677T and A1298C polymorphisms and homocysteine levels in primary open angle and primary closed angle glaucoma.. PubMed. 15. 2268–78. 54 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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