Saima Anwar

581 total citations
6 papers, 236 citations indexed

About

Saima Anwar is a scholar working on Sensory Systems, Neurology and Small Animals. According to data from OpenAlex, Saima Anwar has authored 6 papers receiving a total of 236 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Sensory Systems, 3 papers in Neurology and 1 paper in Small Animals. Recurrent topics in Saima Anwar's work include Hearing, Cochlea, Tinnitus, Genetics (5 papers), Vestibular and auditory disorders (3 papers) and Cardiac electrophysiology and arrhythmias (1 paper). Saima Anwar is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (5 papers), Vestibular and auditory disorders (3 papers) and Cardiac electrophysiology and arrhythmias (1 paper). Saima Anwar collaborates with scholars based in Pakistan, United States and Slovakia. Saima Anwar's co-authors include Saima Riazuddin, Zubair M. Ahmed, Sheikh Riazuddin, Thomas B. Friedman, Shahid Y. Khan, Andrew J. Griffith, Muhammad Qasim, Hanka Venselaar, Tayyab Husnaın and Penelope L. Friedman and has published in prestigious journals such as PLoS ONE, The American Journal of Human Genetics and Human Genetics.

In The Last Decade

Saima Anwar

5 papers receiving 231 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Saima Anwar Pakistan 5 155 134 82 52 23 6 236
Marta Gandía Spain 7 197 1.3× 147 1.1× 100 1.2× 63 1.2× 23 1.0× 8 277
Khadijeh Jalalvand Iran 8 145 0.9× 101 0.8× 70 0.9× 37 0.7× 17 0.7× 10 169
Małgorzata Mueller‐Malesińska Poland 6 117 0.8× 111 0.8× 47 0.6× 29 0.6× 11 0.5× 11 173
Payman Jamali Iran 8 62 0.4× 131 1.0× 33 0.4× 20 0.4× 47 2.0× 19 285
Yang Wei–yan China 10 254 1.6× 80 0.6× 121 1.5× 34 0.7× 9 0.4× 24 319
Jaime Gallo‐Terán Spain 7 202 1.3× 74 0.6× 108 1.3× 45 0.9× 6 0.3× 18 229
Judith Löffler Austria 7 152 1.0× 179 1.3× 54 0.7× 15 0.3× 52 2.3× 8 275
Birgit Haack Germany 6 126 0.8× 119 0.9× 39 0.5× 26 0.5× 9 0.4× 9 163
Graça Fialho Portugal 9 111 0.7× 93 0.7× 40 0.5× 15 0.3× 10 0.4× 17 159
M. Cruz Tapia Spain 2 148 1.0× 46 0.3× 78 1.0× 27 0.5× 5 0.2× 3 158

Countries citing papers authored by Saima Anwar

Since Specialization
Citations

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

Fields of papers citing papers by Saima Anwar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Saima Anwar

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

All Works

6 of 6 papers shown
2.
Šoltýsová, Andrea, Lukáš Varga, Andrej Ficek, et al.. (2015). MARVELD2 (DFNB49) Mutations in the Hearing Impaired Central European Roma Population - Prevalence, Clinical Impact and the Common Origin. PLoS ONE. 10(4). e0124232–e0124232. 16 indexed citations
3.
Riazuddin, Saima, Saima Anwar, Martin Fischer, et al.. (2009). Molecular Basis of DFNB73: Mutations of BSND Can Cause Nonsyndromic Deafness or Bartter Syndrome. The American Journal of Human Genetics. 85(2). 273–280. 60 indexed citations
4.
Anwar, Saima, Saima Riazuddin, Zubair M. Ahmed, et al.. (2009). SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis. Journal of Human Genetics. 54(5). 266–270. 69 indexed citations
5.
Ahmed, Zubair M., Saima Riazuddin, Hanka Venselaar, et al.. (2008). Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome. Human Genetics. 124(3). 215–223. 71 indexed citations
6.
Khan, Shahid Y., Saima Riazuddin, Muhammad Tariq, et al.. (2006). Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2–q13.3. Human Genetics. 120(6). 789–793. 20 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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