Atteeq U. Rehman

1.9k total citations
19 papers, 588 citations indexed

About

Atteeq U. Rehman is a scholar working on Molecular Biology, Sensory Systems and Cognitive Neuroscience. According to data from OpenAlex, Atteeq U. Rehman has authored 19 papers receiving a total of 588 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Sensory Systems and 3 papers in Cognitive Neuroscience. Recurrent topics in Atteeq U. Rehman's work include Hearing, Cochlea, Tinnitus, Genetics (9 papers), RNA regulation and disease (4 papers) and Hearing Loss and Rehabilitation (3 papers). Atteeq U. Rehman is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (9 papers), RNA regulation and disease (4 papers) and Hearing Loss and Rehabilitation (3 papers). Atteeq U. Rehman collaborates with scholars based in United States, Pakistan and United Kingdom. Atteeq U. Rehman's co-authors include Thomas B. Friedman, Robert J. Morell, Saima Riazuddin, Sheikh Riazuddin, Zubair M. Ahmed, Shaheen N. Khan, Erich T. Boger, Mohsin Shahzad, Inna A. Belyantseva and Shahid Y. Khan and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and PLoS ONE.

In The Last Decade

Atteeq U. Rehman

17 papers receiving 576 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Atteeq U. Rehman United States 12 373 315 118 93 71 19 588
Valérie Faugère France 14 438 1.2× 277 0.9× 83 0.7× 85 0.9× 38 0.5× 21 550
Sigrid Wayne United States 11 344 0.9× 364 1.2× 115 1.0× 55 0.6× 55 0.8× 19 543
Trent Fowler United States 8 533 1.4× 371 1.2× 120 1.0× 41 0.4× 42 0.6× 10 779
Xiao Mei Ouyang United States 10 353 0.9× 414 1.3× 143 1.2× 57 0.6× 74 1.0× 13 557
Anna Sczaniecka United States 7 311 0.8× 367 1.2× 102 0.9× 44 0.5× 38 0.5× 7 622
Steve D.M. Brown United Kingdom 7 354 0.9× 316 1.0× 106 0.9× 68 0.7× 42 0.6× 8 522
Robert Esterberg United States 11 285 0.8× 301 1.0× 89 0.8× 34 0.4× 39 0.5× 13 600
Sedigheh Delmaghani France 10 479 1.3× 498 1.6× 200 1.7× 52 0.6× 101 1.4× 13 764
Meghan C. Drummond United States 8 242 0.6× 271 0.9× 72 0.6× 48 0.5× 47 0.7× 10 409
Kevin Isgrig United States 11 303 0.8× 395 1.3× 91 0.8× 75 0.8× 50 0.7× 16 520

Countries citing papers authored by Atteeq U. Rehman

Since Specialization
Citations

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

Fields of papers citing papers by Atteeq U. Rehman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Atteeq U. Rehman. 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 Atteeq U. Rehman. The network helps show where Atteeq U. Rehman may publish in the future.

Co-authorship network of co-authors of Atteeq U. Rehman

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

All Works

19 of 19 papers shown
1.
Cuddapah, Vishnu Anand, Dechun Chen, Bumsik Cho, et al.. (2025). Rare variants in BMAL1 are associated with a neurodevelopmental syndrome. Proceedings of the National Academy of Sciences. 122(31). e2427085122–e2427085122.
2.
Hays, Thomas, Rebecca Hernan, Ganga Krishnamurthy, et al.. (2023). Implementation of Rapid Genome Sequencing for Critically Ill Infants With Complex Congenital Heart Disease. Circulation Genomic and Precision Medicine. 16(5). 415–420. 11 indexed citations
3.
Tessadori, Federico, Atteeq U. Rehman, Jacques C. Giltay, et al.. (2019). A de novo variant in the human HIST1H4J gene causes a syndrome analogous to the HIST1H4C-associated neurodevelopmental disorder. European Journal of Human Genetics. 28(5). 674–678. 11 indexed citations
4.
Faridi, Rabia, Risa Tona, Alessandra Brofferio, et al.. (2018). Mutational and phenotypic spectra of KCNE1 deficiency in Jervell and Lange‐Nielsen Syndrome and Romano‐Ward Syndrome. Human Mutation. 40(2). 162–176. 27 indexed citations
5.
Avenarius, Matthew R., Charles Askew, Sherri M. Jones, et al.. (2018). Grxcr2 is required for stereocilia morphogenesis in the cochlea. PLoS ONE. 13(8). e0201713–e0201713. 11 indexed citations
6.
Nakano, Yoko, Michael C. Kelly, Atteeq U. Rehman, et al.. (2018). Defects in the Alternative Splicing-Dependent Regulation of REST Cause Deafness. Cell. 174(3). 536–548.e21. 57 indexed citations
7.
Rehman, Atteeq U., et al.. (2017). First report of the molecular detection of Ancylostoma caninum in Lahore, Pakistan: the threat from pets. Veterinární Medicína. 62(10). 559–564. 6 indexed citations
8.
Bird, Jonathan E., Melanie Barzik, Meghan C. Drummond, et al.. (2016). Harnessing molecular motors for nanoscale pulldown in live cells. Molecular Biology of the Cell. 28(3). 463–475. 18 indexed citations
9.
Rehman, Atteeq U., Jonathan E. Bird, Rabia Faridi, et al.. (2016). Mutational Spectrum ofMYO15Aand the Molecular Mechanisms of DFNB3 Human Deafness. Human Mutation. 37(10). 991–1003. 55 indexed citations
10.
Imtiaz, Ayesha, Atteeq U. Rehman, Robert J. Morell, et al.. (2016). Recessive mutations of TMC1 associated with moderate to severe hearing loss. Neurogenetics. 17(2). 115–123. 28 indexed citations
11.
Naz, Sadaf, Imtiaz Ahmed, Ghulam Mujtaba, et al.. (2016). Genetic causes of moderate to severe hearing loss point to modifiers. Clinical Genetics. 91(4). 589–598. 36 indexed citations
12.
Faridi, Rabia, Atteeq U. Rehman, Robert J. Morell, et al.. (2016). Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome. Clinical Genetics. 91(2). 328–332. 35 indexed citations
13.
Ijaz, Muhammad, et al.. (2014). PREVALENCE AND CHEMOTHERAPY OF COCCIDIOSIS IN DOGS IN AND AROUND LAHORE- PAKISTAN. The Journal of Animal and Plant Sciences. 24(1). 350–353.
14.
Zein, Wadih M., Benedetto Falsini, Ekaterini Tsilou, et al.. (2014). Cone Responses in Usher Syndrome Types 1 and 2 by Microvolt Electroretinography. Investigative Ophthalmology & Visual Science. 56(1). 107–114. 13 indexed citations
15.
Gong, Zhen‐Hui, et al.. (2012). Construction of the intermediate vector pVBG2307 by incorporating vital elements of expression vectors pBI121 and pBI221. Genetics and Molecular Research. 11(3). 3091–3104. 20 indexed citations
16.
Rehman, Atteeq U., Robert J. Morell, Kwanghyuk Lee, et al.. (2011). Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p. Human Genetics. 130(6). 759–765. 34 indexed citations
17.
Rehman, Atteeq U., Robert J. Morell, Inna A. Belyantseva, et al.. (2010). Targeted Capture and Next-Generation Sequencing Identifies C9orf75, Encoding Taperin, as the Mutated Gene in Nonsyndromic Deafness DFNB79. The American Journal of Human Genetics. 86(3). 378–388. 145 indexed citations
18.
Ahmed, Zubair M., Rizwan Yousaf, Byung Cheon Lee, et al.. (2010). Functional Null Mutations of MSRB3 Encoding Methionine Sulfoxide Reductase Are Associated with Human Deafness DFNB74. The American Journal of Human Genetics. 88(1). 19–29. 73 indexed citations
19.
Khan, Shahid Y., Saima Riazuddin, Mohsin Shahzad, et al.. (2009). DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3. European Journal of Human Genetics. 18(1). 125–129. 8 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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