Nada Derar

431 total citations
3 papers, 26 citations indexed

About

Nada Derar is a scholar working on Genetics, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Nada Derar has authored 3 papers receiving a total of 26 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Molecular Biology and 1 paper in Clinical Biochemistry. Recurrent topics in Nada Derar's work include Dermatological and Skeletal Disorders (1 paper), Skin and Cellular Biology Research (1 paper) and Wnt/β-catenin signaling in development and cancer (1 paper). Nada Derar is often cited by papers focused on Dermatological and Skeletal Disorders (1 paper), Skin and Cellular Biology Research (1 paper) and Wnt/β-catenin signaling in development and cancer (1 paper). Nada Derar collaborates with scholars based in Saudi Arabia. Nada Derar's co-authors include Fowzan S. Alkuraya, Brian F. Meyer, Dorota Monies, Mohammed Al‐Owain, Zuhair N. Al‐Hassnan, Nabil Moghrabi, Mohamed Abouelhoda, Hamad Alzaidan, Naif Alhathal and Hanan E. Shamseldin and has published in prestigious journals such as Human Genetics, Genetics in Medicine and European Journal of Medical Genetics.

In The Last Decade

Nada Derar

3 papers receiving 26 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nada Derar Saudi Arabia	2	19	14	4	3	2	3	26
Hannah J. Perrin United States	2	18 0.9×	8 0.6×	6 1.5×	2 0.7×	2 1.0×	3	27
Milena Jakimovska North Macedonia	4	19 1.0×	10 0.7×	5 1.3×	4 1.3×	2 1.0×	7	36
Deirdre Donnelly United Kingdom	3	27 1.4×	7 0.5×	3 0.8×	4 1.3×	2 1.0×	4	38
Friedhelm Hildebrandt United States	3	23 1.2×	18 1.3×	4 1.0×	3 1.0×	1 0.5×	4	29
Sadegheh Haghshenas Canada	4	33 1.7×	16 1.1×	4 1.0×	2 0.7×	3 1.5×	9	45
Erh‐Chan Yeh Taiwan	2	24 1.3×	12 0.9×	6 1.5×	6 2.0×	3 1.5×	3	38
A. Stuckey United Kingdom	3	27 1.4×	23 1.6×	3 0.8×	2 0.7×		3	31
Ikhlas Ben Ayed Tunisia	4	22 1.2×	13 0.9×	4 1.0×	3 1.0×	4 2.0×	12	40
Kayla E. Lawrence United States	1	18 0.9×	16 1.1×	2 0.5×	2 0.7×	2 1.0×	2	32
Neethu Shah United States	1	12 0.6×	16 1.1×	7 1.8×	3 1.0×		2	25

Countries citing papers authored by Nada Derar

Since Specialization

Citations

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

Fields of papers citing papers by Nada Derar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nada Derar

This figure shows the co-authorship network connecting the top 25 collaborators of Nada Derar. A scholar is included among the top collaborators of Nada Derar 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 Nada Derar. Nada Derar 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:

3 of 3 papers shown

1.

Shamseldin, Hanan E., Nada Derar, Hamad Alzaidan, et al.. (2023). PRSS8, encoding prostasin, is mutated in patients with autosomal recessive ichthyosis. Human Genetics. 142(4). 477–482. 4 indexed citations

2.

Altassan, Ruqaiah, Raashda A. Sulaiman, Zuhair N. Al‐Hassnan, et al.. (2022). COVID-19 in Unvaccinated patients with inherited metabolic disorders: A single center experience. European Journal of Medical Genetics. 65(11). 104602–104602. 1 indexed citations

3.

Derar, Nada, Zuhair N. Al‐Hassnan, Mohammed Al‐Owain, et al.. (2018). De novo truncating variants in WHSC1 recapitulate the Wolf–Hirschhorn (4p16.3 microdeletion) syndrome phenotype. Genetics in Medicine. 21(1). 185–188. 21 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.

Explore authors with similar magnitude of impact