Atteeq U. Rehman

1.9k citations

19 papers · 588 indexed · h-index 12

Co-authors: Thomas B. Friedman Robert J. Morell Saima Riazuddin Sheikh Riazuddin Zubair M. Ahmed Shaheen N. Khan Erich T. Boger Mohsin Shahzad
Topics: Hearing, Cochlea, Tinnitus, Genetics (9 papers)RNA regulation and disease (4 papers)Hearing Loss and Rehabilitation (3 papers)
Cited by: Sensory Systems Otorhinolaryngology Neurology
Journals: Cell Proceedings of the National Academy of Sciences PLoS ONE
Partner nations: United States Pakistan United Kingdom

In The Last Decade

Atteeq U. Rehman

17 papers receiving 576 citations

Peers

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

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

19 of 19 papers shown

#	Work	Indexed citations
1	Rare variants in BMAL1 are associated with a neurodevelopmental syndrome 2025 ·Proceedings of the National Academy of Sciences ·Vishnu Anand Cuddapah,Dechun Chen,Bumsik Cho,Rebecca S. Moore,(unknown),(unknown),Frédéric Tran Mau‐Them,Ashley Wilson,Jacqueline A. Odgis,Atteeq U. Rehman,(unknown),Shiva Ganesan,Vaidehi Jobanputra,Stephen W. Scherer,Ingo Helbig,Amita Sehgal	0
2	Implementation of Rapid Genome Sequencing for Critically Ill Infants With Complex Congenital Heart Disease 2023 ·Circulation Genomic and Precision Medicine ·Thomas Hays,Rebecca Hernan,(unknown),(unknown),(unknown),(unknown),Ganga Krishnamurthy,(unknown),Atteeq U. Rehman,Amanda Thomas‐Wilson,Saurav Guha,(unknown),Volkan Okur,(unknown),Vanessa Felice,Avinash Abhyankar,Vaidehi Jobanputra,Wendy K. Chung	11
3	A de novo variant in the human HIST1H4J gene causes a syndrome analogous to the HIST1H4C-associated neurodevelopmental disorder 2019 ·European Journal of Human Genetics ·Federico Tessadori,Atteeq U. Rehman,Jacques C. Giltay,Fan Xia,Haley Streff,Karen Duran,Jeroen Bakkers,Seema R. Lalani,Gijs van Haaften	11
4	Mutational and phenotypic spectra of KCNE1 deficiency in Jervell and Lange‐Nielsen Syndrome and Romano‐Ward Syndrome 2018 ·Human Mutation ·Rabia Faridi,Risa Tona,Alessandra Brofferio,Michael Hoa,Rafal T. Olszewski,Isabelle Schrauwen,Muhammad Zaman Khan Assir,(unknown),Asma Ali Khan,Atteeq U. Rehman,Carmen C. Brewer,(unknown),Suzanne M. Leal,Sheikh Riazuddin,Steven E. Boyden,Thomas B. Friedman	27
5	Defects in the Alternative Splicing-Dependent Regulation of REST Cause Deafness 2018 ·Cell ·Yoko Nakano,Michael C. Kelly,Atteeq U. Rehman,Erich T. Boger,Robert J. Morell,Matthew W. Kelley,Thomas B. Friedman,Botond Bánfi	57
6	Grxcr2 is required for stereocilia morphogenesis in the cochlea 2018 ·PLoS ONE ·Matthew R. Avenarius,(unknown),Charles Askew,Sherri M. Jones,Kristina L. Hunker,Héla Azaiez,Atteeq U. Rehman,Margit Schraders,Hossein Najmabadi,Hannie Kremer,Richard J. Smith,Gwenaëlle S. G. Géléoc,David F. Dolan,Yehoash Raphael,David C. Kohrman	11
7	First report of the molecular detection of Ancylostoma caninum in Lahore, Pakistan: the threat from pets 2017 ·Veterinární Medicína ·Atteeq U. Rehman,(unknown),Haroon Akbar,Farooq Riaz,Imran Rashid,Wasim Shehzad,(unknown),(unknown),(unknown)	6
8	Harnessing molecular motors for nanoscale pulldown in live cells 2016 ·Molecular Biology of the Cell ·Jonathan E. Bird,Melanie Barzik,Meghan C. Drummond,(unknown),Spencer Goodman,Eva L. Morozko,(unknown),(unknown),Jennifer Skidmore,(unknown),Elizabeth Wilson,Tracy S. Fitzgerald,Atteeq U. Rehman,Donna M. Martin,Erich T. Boger,Inna A. Belyantseva,Thomas B. Friedman	18
9	Mutational Spectrum ofMYO15Aand the Molecular Mechanisms of DFNB3 Human Deafness 2016 ·Human Mutation ·Atteeq U. Rehman,Jonathan E. Bird,Rabia Faridi,Mohsin Shahzad,Sujay Shah,Kwanghyuk Lee,Shaheen N. Khan,Ayesha Imtiaz,Zubair M. Ahmed,Saima Riazuddin,Regie Lyn P. Santos‐Cortez,Wasim Ahmad,Suzanne M. Leal,Sheikh Riazuddin,Thomas B. Friedman	55
10	Recessive mutations of TMC1 associated with moderate to severe hearing loss 2016 ·Neurogenetics ·Ayesha Imtiaz,(unknown),Atteeq U. Rehman,Robert J. Morell,Jeffrey R. Holt,Thomas B. Friedman,Sadaf Naz	28
11	Genetic causes of moderate to severe hearing loss point to modifiers 2016 ·Clinical Genetics ·Sadaf Naz,Imtiaz Ahmed,Ghulam Mujtaba,Arfa Maqsood,Rasheeda Bashir,Ihtisham Bukhari,Muhammad Riaz Khan,Memoona Ramzan,(unknown),Atteeq U. Rehman,Muhammad Faisal Iqbal,(unknown),(unknown),Carmen C. Brewer,Robert J. Morell,Thomas B. Friedman	36
12	Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome 2016 ·Clinical Genetics ·Rabia Faridi,Atteeq U. Rehman,Robert J. Morell,Penelope L. Friedman,Leigh Demain,(unknown),Asma Ali Khan,(unknown),Muhammad Zaman Khan Assir,Glenda M. Beaman,S. N. Khan,William G. Newman,Saima Riazuddin,Thomas B. Friedman	35
13	PREVALENCE AND CHEMOTHERAPY OF COCCIDIOSIS IN DOGS IN AND AROUND LAHORE- PAKISTAN 2014 ·The Journal of Animal and Plant Sciences ·(unknown),(unknown),Muhammad Ijaz,Kamran Ashraf,Muhammad Muddassir Ali,Iahtasham Khan,Atteeq U. Rehman	0
14	Cone Responses in Usher Syndrome Types 1 and 2 by Microvolt Electroretinography 2014 ·Investigative Ophthalmology & Visual Science ·Wadih M. Zein,Benedetto Falsini,Ekaterini Tsilou,Amy Turriff,Julie M. Schultz,Thomas B. Friedman,Carmen C. Brewer,Christopher Zalewski,Kathryn A. King,Julie Muskett,Atteeq U. Rehman,Robert J. Morell,Andrew J. Griffith,Paul A. Sieving	13
15	Construction of the intermediate vector pVBG2307 by incorporating vital elements of expression vectors pBI121 and pBI221 2012 ·Genetics and Molecular Research ·(unknown),Zhen‐Hui Gong,(unknown),Yue-Qi Yin,(unknown),Muhammad Azam Khan,Atteeq U. Rehman,Ibrahim A. Ahmad	20
16	Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p 2011 ·Human Genetics ·Atteeq U. Rehman,(unknown),Robert J. Morell,Kwanghyuk Lee,Zubair M. Ahmed,Saima Riazuddin,(unknown),Mohsin Shahzad,(unknown),(unknown),Shaheen N. Khan,Saadullah Khan,Carmen C. Brewer,Wasim Ahmad,Suzanne M. Leal,Sheikh Riazuddin,Thomas B. Friedman	34
17	Targeted Capture and Next-Generation Sequencing Identifies C9orf75, Encoding Taperin, as the Mutated Gene in Nonsyndromic Deafness DFNB79 2010 ·The American Journal of Human Genetics ·Atteeq U. Rehman,Robert J. Morell,Inna A. Belyantseva,Shahid Y. Khan,Erich T. Boger,Mohsin Shahzad,Zubair M. Ahmed,Saima Riazuddin,Shaheen N. Khan,Sheikh Riazuddin,Thomas B. Friedman	145
18	Functional Null Mutations of MSRB3 Encoding Methionine Sulfoxide Reductase Are Associated with Human Deafness DFNB74 2010 ·The American Journal of Human Genetics ·Zubair M. Ahmed,Rizwan Yousaf,Byung Cheon Lee,Shaheen N. Khan,Sue Lee,Kwanghyuk Lee,Tayyab Husnaın,Atteeq U. Rehman,(unknown),Muhammad Ansar,Wasim Ahmad,Suzanne M. Leal,Vadim N. Gladyshev,Inna A. Belyantseva,Guy Van Camp,Sheikh Riazuddin,Thomas B. Friedman,Saima Riazuddin	73
19	DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3 2009 ·European Journal of Human Genetics ·Shahid Y. Khan,Saima Riazuddin,Mohsin Shahzad,Nazir Ahmed,Ahmad Usman Zafar,Atteeq U. Rehman,Robert J. Morell,Andrew J. Griffith,Zubair M. Ahmed,Sheikh Riazuddin,Thomas B. Friedman	8

About Atteeq U. Rehman

Atteeq U. Rehman is a scholar working on Sensory Systems, Aging and Otorhinolaryngology, having authored 19 papers that have together received 588 indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (9 papers), RNA regulation and disease (4 papers) and Hearing Loss and Rehabilitation (3 papers). The work is most often cited by research in Sensory Systems (315 citations), Otorhinolaryngology (71 citations) and Neurology (118 citations). Atteeq U. Rehman has collaborated with scholars based in United States, Pakistan and United Kingdom. Frequent 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. Their work appears in journals such as Cell, Proceedings of the National Academy of Sciences and PLoS ONE.

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