Mubeen Khan

1.3k total citations
18 papers, 540 citations indexed

About

Mubeen Khan is a scholar working on Molecular Biology, Cell Biology and Immunology. According to data from OpenAlex, Mubeen Khan has authored 18 papers receiving a total of 540 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 3 papers in Cell Biology and 3 papers in Immunology. Recurrent topics in Mubeen Khan's work include Retinal Development and Disorders (14 papers), CRISPR and Genetic Engineering (4 papers) and Advanced biosensing and bioanalysis techniques (4 papers). Mubeen Khan is often cited by papers focused on Retinal Development and Disorders (14 papers), CRISPR and Genetic Engineering (4 papers) and Advanced biosensing and bioanalysis techniques (4 papers). Mubeen Khan collaborates with scholars based in Netherlands, United States and France. Mubeen Khan's co-authors include Frans P.M. Cremers, Rob W.J. Collin, Sílvia Albert, Alejandro Garanto, Riccardo Sangermano, Stéphanie S. Cornelis, Susanne Roosing, Carel B. Hoyng, Nathalie M. Bax and Peter A.C. ’t Hoen and has published in prestigious journals such as Scientific Reports, International Journal of Molecular Sciences and Genome Research.

In The Last Decade

Mubeen Khan

17 papers receiving 537 citations

Peers

Countries citing papers authored by Mubeen Khan

Since Specialization

Citations

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

Fields of papers citing papers by Mubeen Khan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mubeen Khan

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

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	Pathogenic SATB2 missense variants affecting p.Gly392 have variable functional implications and result in diverse clinical phenotypes 2024 ·Journal of Medical Genetics ·Joery den Hoed, H Hashimoto, Mubeen Khan, (unknown), Katherine A. Bosanko, (unknown), Eiji Nakagawa, Hanka Venselaar, Nada Quercia, Lauren Chad, Hiroshi Kurosaka, Stéphane Rondeau, Simon E. Fisher, Shinya Yamamoto, Yuri A. Zárate	1
2	ABCA4 Variant c.5714+5G>A in Trans With Null Alleles Results in Primary RPE Damage 2023 ·Investigative Ophthalmology & Visual Science ·(unknown), Andrej Meglič, (unknown), Mubeen Khan, Aleš Maver, (unknown), Marko Hawlina, Frans P.M. Cremers, Ana Fakin	1
3	Detailed analysis of an enriched deep intronic ABCA4 variant in Irish Stargardt disease patients 2023 ·Scientific Reports ·Laura Whelan, Adrian Dockery, Kirk Stephenson, Julia Zhu, (unknown), (unknown), Mubeen Khan, (unknown), (unknown), (unknown), Emma Duignan, Giuliana Silvestri, Susanne Roosing, Frans P.M. Cremers, David Keegan, Paul F. Kenna, G. Jane Farrar	3
4	Targeted sequencing and in vitro splice assays shed light on ABCA4-associated retinopathies missing heritability 2023 ·Human Genetics and Genomics Advances ·(unknown), Mubeen Khan, (unknown), Ketan Mishra, Laura Whelan, Stéphanie S. Cornelis, Carel B. Hoyng, Kati Kämpjärvi, Caroline C. W. Klaver, Petra Lišková, Heidi Stöhr, Bernhard H. F. Weber, Sandro Banfi, G. Jane Farrar, Dror Sharon, Jana Zernant, Rando Allikmets, Claire‐Marie Dhaenens, Frans P.M. Cremers	7
5	Using single molecule Molecular Inversion Probes as a cost‐effective, high‐throughput sequencing approach to target all genes and loci associated with macular diseases 2022 ·Human Mutation ·(unknown), Claire‐Marie Dhaenens, (unknown), (unknown), Mubeen Khan, Anneke I. den Hollander, (unknown), (unknown), Alexander Hoischen, Maartje van de Vorst, (unknown), (unknown), (unknown), (unknown), Susanne Roosing, Frans P.M. Cremers	14
6	ABCA4c.859-25A>G, a Frequent Palestinian Founder Mutation Affecting the Intron 7 Branchpoint, Is Associated With Early-Onset Stargardt Disease 2022 ·Investigative Ophthalmology & Visual Science ·(unknown), (unknown), Mubeen Khan, Elise Héon, Ketan Mishra, (unknown), (unknown), (unknown), Eyal Banin, Brian P. Brooks, Wadih M. Zein, Robert B. Hufnagel, Susanne Roosing, Claire‐Marie Dhaenens, Dror Sharon, Frans P.M. Cremers, (unknown)	6
7	Benchmarking deep learning splice prediction tools using functional splice assays 2021 ·Human Mutation ·(unknown), Mubeen Khan, Susanne Roosing, Frans P.M. Cremers, Peter A.C. ’t Hoen	65
8	PRPH2 mutation update: In silico assessment of 245 reported and 7 novel variants in patients with retinal disease 2021 ·Human Mutation ·(unknown), Mubeen Khan, (unknown), (unknown), Lonneke Haer‐Wigman, Camiel J.F. Boon, Caroline C. W. Klaver, (unknown), Carel B. Hoyng, Frans P.M. Cremers, Anneke I. den Hollander, Claire‐Marie Dhaenens, Rob W.J. Collin	21
9	In or Out? New Insights on Exon Recognition through Splice-Site Interdependency 2020 ·International Journal of Molecular Sciences ·Mubeen Khan, Stéphanie S. Cornelis, Riccardo Sangermano, (unknown), (unknown), (unknown), Christian Gilissen, Alejandro Garanto, Rob W.J. Collin, Frans P.M. Cremers	9
10	Detailed Phenotyping and Therapeutic Strategies for Intronic ABCA4 Variants in Stargardt Disease 2020 ·Molecular Therapy — Nucleic Acids ·Mubeen Khan, Gavin Arno, Ana Fakin, David A. Parfitt, (unknown), Sílvia Albert, Nathalie M. Bax, Lonneke Duijkers, Michael Niblock, (unknown), Edward Bloch, Elena Schiff, (unknown), (unknown), Carel B. Hoyng, Andrew R. Webster, Frans P.M. Cremers, Michael E. Cheetham, Alejandro Garanto, Rob W.J. Collin	57
11	ABCA4-Associated Stargardt Disease 2020 ·Klinische Monatsblätter für Augenheilkunde ·Mubeen Khan, Frans P.M. Cremers	19
12	Identification of splice defects due to noncanonical splice site or deep-intronic variants in ABCA4. 2019 ·eScholarship (California Digital Library) ·(unknown), Mubeen Khan, Marta Del Pozo‐Valero, Stéphanie S. Cornelis, Carmen Ayuso, Frans P.M. Cremers, Susanne Roosing, (unknown)	0
13	Cost‐effective molecular inversion probe‐based ABCA4 sequencing reveals deep‐intronic variants in Stargardt disease 2019 ·Human Mutation ·Mubeen Khan, Stéphanie S. Cornelis, Muhammad Imran Khan, (unknown), (unknown), (unknown), Ronny Derks, Kornelia Neveling, Maartje van de Vorst, Christian Gilissen, Isabelle Meunier, Sabine Defoort, Bernard Puech, Aurore Devos, Heidi L. Schulz, Heidi Stöhr, Felix Graßmann, Bernhard H. F. Weber, Claire‐Marie Dhaenens, Frans P.M. Cremers	37
14	Identification of splice defects due to noncanonical splice site or deep‐intronic variants in ABCA4 2019 ·Human Mutation ·(unknown), Mubeen Khan, Marta Del Pozo‐Valero, Stéphanie S. Cornelis, Carmen Ayuso, Frans P.M. Cremers, Susanne Roosing, (unknown)	37
15	Late-Onset Stargardt Disease Due to Mild, Deep-Intronic ABCA4 Alleles 2019 ·Investigative Ophthalmology & Visual Science ·Esmee H. Runhart, (unknown), Stéphanie S. Cornelis, Mubeen Khan, Riccardo Sangermano, Sílvia Albert, Nathalie M. Bax, Galuh Astuti, Christian Gilissen, Jan-Willem R. Pott, Joanne Verheij, Ellen A.W. Blokland, Frans P.M. Cremers, L. Ingeborgh van den Born, Carel B. Hoyng	27
16	Identification and Analysis of Genes Associated with Inherited Retinal Diseases 2018 ·Methods in molecular biology ·Mubeen Khan, (unknown), Stéphanie S. Cornelis, Frans P.M. Cremers, Susanne Roosing	12
17	Identification and Rescue of Splice Defects Caused by Two Neighboring Deep-Intronic ABCA4 Mutations Underlying Stargardt Disease 2018 ·The American Journal of Human Genetics ·Sílvia Albert, Alejandro Garanto, Riccardo Sangermano, Mubeen Khan, Nathalie M. Bax, Carel B. Hoyng, Jana Zernant, Winston Lee, Rando Allikmets, Rob W.J. Collin, Frans P.M. Cremers	100
18	ABCA4midigenes reveal the full splice spectrum of all reported noncanonical splice site variants in Stargardt disease 2017 ·Genome Research ·Riccardo Sangermano, Mubeen Khan, Stéphanie S. Cornelis, (unknown), Sílvia Albert, Alejandro Garanto, (unknown), Raheel Qamar, Dorien Lugtenberg, L. Ingeborgh van den Born, Rob W.J. Collin, Frans P.M. Cremers	124

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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