Saima Riazuddin

9.7k citations

104 papers · 4.3k · h-index 35

Impact in

Sensory Systems top 0.05%
- Hearing, Cochlea, Tinnitus, Genetics
Neurology top 0.5%
- Vestibular and auditory disorders

Papers in

Molecular Biology 60
- Connexins and lens biology 22
- RNA regulation and disease 13
- RNA and protein synthesis mechanisms 10
- Retinal Development and Disorders 10
Sensory Systems 60
- Hearing, Cochlea, Tinnitus, Genetics 58

Co-authors: Zubair M. Ahmed (73 shared papers)Sheikh Riazuddin (42 shared papers)Thomas B. Friedman (42 shared papers)Shaheen N. Khan (28 shared papers)Edward R. Wilcox (14 shared papers)Andrew J. Griffith (12 shared papers)Robert J. Morell (12 shared papers)Inna A. Belyantseva (13 shared papers)
Journals: Human Genetics (12 papers)The American Journal of Human Genetics (10 papers)Genes (6 papers)Clinical Genetics (5 papers)Human Mutation (5 papers)
Partner nations: United States Pakistan United Kingdom

In The Last Decade

Saima Riazuddin

101 papers receiving 4.2k citations

Peers

Countries citing papers authored by Saima Riazuddin

Since Specialization

Citations

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

Fields of papers citing papers by Saima Riazuddin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Saima Riazuddin, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Saima Riazuddin Line = papers co-authored together Saima Riazuddin links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 104 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F The American Journal of Human Genetics ·Zubair M. Ahmed, Saima Riazuddin, Steven L. Bernstein, Zahoor Ahmed, Shaheen Khan, Andrew J. Griffith, Robert J. Morell, Thomas B. Friedman, Sheikh Riazuddin, Edward R. Wilcox	2001	341
2	The Tip-Link Antigen, a Protein Associated with the Transduction Complex of Sensory Hair Cells, Is Protocadherin-15 Journal of Neuroscience ·Zubair M. Ahmed, Richard J. Goodyear, Saima Riazuddin, Ayala Lagziel, P. Kevin Legan, Martine Behra, Shawn M. Burgess, Kathryn S. Lilley, Edward R. Wilcox, Sheikh Riazuddin, Andrew J. Griffith, Gregory I. Frolenkov, Inna A. Belyantseva, Guy P. Richardson, Thomas B. Friedman	2006	235
3	Tricellulin Is a Tight-Junction Protein Necessary for Hearing The American Journal of Human Genetics ·Saima Riazuddin, Zubair M. Ahmed, Alan S. Fanning, Ayala Lagziel, Shin‐ichiro Kitajiri, Khushnooda Ramzan, Shaheen N. Khan, Parna Chattaraj, Penelope L. Friedman, James M. Anderson, Inna A. Belyantseva, Andrew Forge, Sheikh Riazuddin, Thomas B. Friedman	2006	228
4	Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37 The American Journal of Human Genetics ·Zubair M. Ahmed, Robert J. Morell, Saima Riazuddin, Andrea Gropman, Shahzad Shaukat, Mussaber M. Ahmad, Saidi Mohiddin, Lameh Fananapazir, Rafael C. Caruso, Tayyab Husnaın, Shaheen N. Khan, Sheikh Riazuddin, Andrew J. Griffith, Thomas B. Friedman, Edward R. Wilcox	2003	163
5	Increasing the complexity: new genes and new types of albinism Pigment Cell & Melanoma Research ·Lluı́s Montoliu, Karen Grønskov, Aihua Wei, Mónica Mártinez‐García, Almudena Fernández, Benoı̂t Arveiler, Fanny Morice‐Picard, Saima Riazuddin, Tamio Suzuki, Zubair M. Ahmed, Thomas Rosenberg, Wei Li	2013	161
6	Actin-Bundling Protein TRIOBP Forms Resilient Rootlets of Hair Cell Stereocilia Essential for Hearing Cell ·Shin‐ichiro Kitajiri, Takeshi Sakamoto, Inna A. Belyantseva, Richard J. Goodyear, Ruben Stepanyan, Ikuko Fujiwara, Jonathan E. Bird, Saima Riazuddin, Sheikh Riazuddin, Zubair M. Ahmed, Jenny E. Hinshaw, James R. Sellers, James R. Bartles, John A. Hammer, Guy P. Richardson, Andrew J. Griffith, Gregory I. Frolenkov, Thomas B. Friedman	2010	158
7	Targeted Capture and Next-Generation Sequencing Identifies C9orf75, Encoding Taperin, as the Mutated Gene in Nonsyndromic Deafness DFNB79 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	2010	156
8	Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC Human Genetics ·Zubair M. Ahmed, Tenesha N. Smith, Saima Riazuddin, Tomoko Makishima, Manju Ghosh, Sirosh Bokhari, P.S.N. Menon, Dilip Deshmukh, Andrew J. Griffith, Sheikh Riazuddin, Thomas B. Friedman, Edward R. Wilcox	2002	131
9	CIB2 interacts with TMC1 and TMC2 and is essential for mechanotransduction in auditory hair cells Nature Communications ·Arnaud P. J. Giese, Yi‐Quan Tang, Ghanshyam P. Sinha, Michael R. Bowl, Adam C. Goldring, Andrew Parker, Mary J Freeman, Steve D. M. Brown, Saima Riazuddin, Robert Fettiplace, William R Schafer, Gregory I. Frolenkov, Zubair M. Ahmed	2017	118
10	Mutations in a Novel Gene, TMIE, Are Associated with Hearing Loss Linked to the DFNB6 Locus The American Journal of Human Genetics ·Sadaf Naz, Chantal Giguère, David C. Kohrman, Kristina L. Mitchem, Saima Riazuddin, Robert J. Morell, Arabandi Ramesh, Srikumari Srisailpathy, Dilip Deshmukh, Sheikh Riazuddin, Andrew J. Griffith, Thomas B. Friedman, Richard J. Smith, Edward R. Wilcox	2002	109
11	Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome Human Genetics ·Nikki Liburd, Manju Ghosh, Saima Riazuddin, Sadaf Naz, Shaheen Khan, Zubair M. Ahmed, Sheikh Riazuddin, Yong Liang, P.S.N. Menon, Tenesha N. Smith, Ann C. M. Smith, Ken‐Shiung Chen, James R. Lupski, Edward R. Wilcox, Lorraine Potocki, Thomas B. Friedman	2001	102
12	Tricellulin deficiency affects tight junction architecture and cochlear hair cells Journal of Clinical Investigation ·Gowri Nayak, Sue I. Lee, Rizwan Yousaf, Stephanie E. Edelmann, Claire E. Trincot, Christina M. Van Itallie, Ghanshyam P. Sinha, Maria Rafeeq, Sherri M. Jones, Inna A. Belyantseva, James M. Anderson, Andrew Forge, Gregory I. Frolenkov, Saima Riazuddin	2013	86
13	Mutations in TRIOBP, Which Encodes a Putative Cytoskeletal-Organizing Protein, Are Associated with Nonsyndromic Recessive Deafness The American Journal of Human Genetics ·Saima Riazuddin, Shaheen N. Khan, Zubair M. Ahmed, Manju Ghosh, Kyle Caution, Sabiha Nazli, Madhulika Kabra, Ahmad Usman Zafar, Kevin Chen, Sadaf Naz, Anthony Antonellis, William J. Pavan, Eric D. Green, Edward R. Wilcox, Penelope L. Friedman, Robert J. Morell, Sheikh Riazuddin, Thomas B. Friedman	2005	85
14	Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan Clinical Genetics ·BY Choi, ZM Ahmed, Saima Riazuddin, MA Bhinder, Mohsin Shahzad, Tayyab Husnaın, AJ Griffith, TB Friedman	2009	83
15	Mutation spectrum ofMYO7Aand evaluation of a novel nonsyndromic deafnessDFNB2allele with residual function Human Mutation ·Saima Riazuddin, Sabiha Nazli, Zubair M. Ahmed, Yi Yang, Fareeha Zulfiqar, Rehan Sadiq Shaikh, Ahmed U. Zafar, Shaheen N. Khan, Farooq Sabar, Fouzia T. Javid, Edward R. Wilcox, Ekaterini Tsilou, Erich T. Boger, James R. Sellers, Inna A. Belyantseva, Sheikh Riazuddin, Thomas B. Friedman	2008	82
16	Functional Null Mutations of MSRB3 Encoding Methionine Sulfoxide Reductase Are Associated with Human Deafness DFNB74 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, Sarah Bonneux, Muhammad Ansar, Wasim Ahmad, Suzanne M. Leal, Vadim N. Gladyshev, Inna A. Belyantseva, Guy Van Camp, Sheikh Riazuddin, Thomas B. Friedman, Saima Riazuddin	2010	81
17	Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes Journal of Medical Genetics ·Julie M. Schultz, Rashid Bhatti, Anne C. Madeo, Amy Turriff, Julie Muskett, Christopher Zalewski, (unknown), Zubair M. Ahmed, Saima Riazuddin, (unknown), Zawar Hussain, Muhammad Qasim, (unknown), Meira R. Meltzer, X. Z. Liu, Murali Munisamy, Manju Ghosh, Heidi L. Rehm, Ekaterini Tsilou, AJ Griffith, Wadih M. Zein, Carmen C. Brewer, (unknown), Thomas B. Friedman	2011	80
18	Mutations of human TMHS cause recessively inherited non-syndromic hearing loss Journal of Medical Genetics ·Muhammad Imran Shabbir, Zubair M. Ahmed, Shahid Y. Khan, Saima Riazuddin, Ali Muhammad Waryah, Shaheen N. Khan, Reyna D Camps, Manju Ghosh, Madulika Kabra, Inna A. Belyantseva, Thomas B. Friedman, Sheikh Riazuddin	2006	79
19	Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome Human Genetics ·Zubair M. Ahmed, Saima Riazuddin, Sandar Aye, Rana A. Ali, Hanka Venselaar, Saima Anwar, Polina P. Belyantseva, Muhammad Qasim, Sheikh Riazuddin, Thomas B. Friedman	2008	74
20	Mutational spectrum ofMYO15A: the large N-terminal extension of myosin XVA is required for hearing Human Mutation ·N. Nal, Zubair M. Ahmed, Engin Erkal, Özgül M. Alper, Güven Lüleci, Oktay Dinç, Ali Muhammad Waryah, Qurat Ul Ain, Saba Tasneem, Tayyab Husnaın, Parna Chattaraj, Saima Riazuddin, Erich T. Boger, Manju Ghosh, Madhulika Kabra, Sheikh Riazuddin, Robert J. Morell, Thomas B. Friedman	2007	73

About Saima Riazuddin

Saima Riazuddin is a scholar working on Molecular Biology, Sensory Systems, Neurology, Cell Biology and Otorhinolaryngology, having authored 104 papers that have together received 4.3k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (58 papers), Connexins and lens biology (22 papers), RNA regulation and disease (13 papers), Vestibular and auditory disorders (13 papers), RNA and protein synthesis mechanisms (10 papers), Retinal Development and Disorders (10 papers), Ear Surgery and Otitis Media (10 papers) and melanin and skin pigmentation (9 papers). The work is most often cited by research in Sensory Systems (2.4k citations), Neurology (900 citations), Otorhinolaryngology (325 citations), Molecular Biology (2.3k citations) and Cell Biology (524 citations). Saima Riazuddin has collaborated with scholars based in United States, Pakistan and United Kingdom. Frequent co-authors include Zubair M. Ahmed, Sheikh Riazuddin, Thomas B. Friedman, Shaheen N. Khan, Edward R. Wilcox, Andrew J. Griffith, Robert J. Morell, Inna A. Belyantseva, Gregory I. Frolenkov and Tayyab Husnaın. Their work appears in journals such as Human Genetics, The American Journal of Human Genetics, Genes, Clinical Genetics and Human Mutation.

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