Saima Riazuddin

584 total citations
3 papers, 449 citations indexed

About

Saima Riazuddin is a scholar working on Sensory Systems, Neurology and Molecular Biology. According to data from OpenAlex, Saima Riazuddin has authored 3 papers receiving a total of 449 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Sensory Systems, 2 papers in Neurology and 1 paper in Molecular Biology. Recurrent topics in Saima Riazuddin's work include Hearing, Cochlea, Tinnitus, Genetics (2 papers), Barrier Structure and Function Studies (1 paper) and Cancer-related molecular mechanisms research (1 paper). Saima Riazuddin is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (2 papers), Barrier Structure and Function Studies (1 paper) and Cancer-related molecular mechanisms research (1 paper). Saima Riazuddin collaborates with scholars based in Pakistan and United States. Saima Riazuddin's co-authors include Andrew J. Griffith, Sadaf Naz, Edward R. Wilcox, Tenesha N. Smith, Tamar Ben‐Yosef, Doris K. Wu, Sheikh Riazuddin, Thomas B. Friedman, Barbara Ploplis and Robert J. Morell and has published in prestigious journals such as Cell, Nature Genetics and Molecular Genetics & Genomic Medicine.

In The Last Decade

Saima Riazuddin

3 papers receiving 439 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Saima Riazuddin Pakistan	2	275	248	168	50	42	3	449
Xiuhong Pang China	13	185 0.7×	71 0.3×	203 1.2×	21 0.4×	47 1.1×	25	323
Graham Atkin United States	9	180 0.7×	65 0.3×	167 1.0×	36 0.7×	40 1.0×	12	409
Zippora Brownstein Israel	14	363 1.3×	125 0.5×	327 1.9×	33 0.7×	60 1.4×	25	620
Liang Zong China	12	302 1.1×	108 0.4×	337 2.0×	52 1.0×	10 0.2×	23	468
Mariem Ben Saïd Tunisia	11	174 0.6×	101 0.4×	214 1.3×	16 0.3×	17 0.4×	26	369
Hong-Joon Park South Korea	16	303 1.1×	143 0.6×	374 2.2×	25 0.5×	25 0.6×	28	553
Éric Lecain France	12	138 0.5×	156 0.6×	92 0.5×	16 0.3×	18 0.4×	20	426
Leenamaija Pakarinen Finland	7	334 1.2×	72 0.3×	299 1.8×	17 0.3×	67 1.6×	9	463
Aki Oshima Japan	8	149 0.5×	91 0.4×	187 1.1×	14 0.3×	17 0.4×	12	306
Allan Kachelmeier United States	10	116 0.4×	166 0.7×	207 1.2×	44 0.9×	15 0.4×	12	363

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-authorship network of co-authors of Saima Riazuddin

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

All Works

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3 of 3 papers shown

1.

Riazuddin, Saima, et al.. (2024). Identification of rare missense variants in the BSN gene co‐segregating with chronic otitis media in a consanguineous Pakistani family. Molecular Genetics & Genomic Medicine. 12(9). e2478–e2478. 1 indexed citations

2.

Wilcox, Edward R., Sadaf Naz, Saima Riazuddin, et al.. (2001). Mutations in the Gene Encoding Tight Junction Claudin-14 Cause Autosomal Recessive Deafness DFNB29. Cell. 104(1). 165–172. 344 indexed citations

3.

Riazuddin, Saima, Zubair M. Ahmed, Anil K. Lalwani, et al.. (2000). Dominant modifier DFNM1 suppresses recessive deafness DFNB26. Nature Genetics. 26(4). 431–434. 104 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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