Nada Al Tassan

5.3k total citations · 1 hit paper
58 papers, 2.4k citations indexed

About

Nada Al Tassan is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, Nada Al Tassan has authored 58 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 21 papers in Pathology and Forensic Medicine and 21 papers in Genetics. Recurrent topics in Nada Al Tassan's work include Genetic factors in colorectal cancer (12 papers), Ophthalmology and Eye Disorders (9 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Nada Al Tassan is often cited by papers focused on Genetic factors in colorectal cancer (12 papers), Ophthalmology and Eye Disorders (9 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Nada Al Tassan collaborates with scholars based in Saudi Arabia, United States and United Kingdom. Nada Al Tassan's co-authors include Jeremy P. Cheadle, Angela Hodges, Julian R. Sampson, Nicholas I. Fleming, Julie Maynard, Geraint T. Williams, Sheila S. David, Alison L. Livingston, D. Rhodri Davies and Nikolas H. Chmiel and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and PLoS ONE.

In The Last Decade

Nada Al Tassan

57 papers receiving 2.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Inherited variants of MYH associated with somatic G:C→T:A mutations in colorectal tumors

2002 980 citations Nada Al Tassan, Jeremy P. Cheadle et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nada Al Tassan Saudi Arabia	22	1.1k	962	657	582	496	58	2.4k
Maria Grazia Tibiletti Italy	29	838 0.8×	810 0.8×	812 1.2×	503 0.9×	469 0.9×	93	2.3k
Conxi Lázaro Spain	35	1.5k 1.4×	838 0.9×	631 1.0×	1.0k 1.8×	673 1.4×	147	3.6k
Aaron Theisen United States	19	761 0.7×	875 0.9×	637 1.0×	1.4k 2.4×	520 1.0×	31	2.4k
Friedel Nollet Belgium	23	2.1k 2.0×	661 0.7×	691 1.1×	306 0.5×	389 0.8×	55	3.4k
Nicoletta Resta Italy	27	887 0.8×	540 0.6×	382 0.6×	408 0.7×	288 0.6×	115	2.0k
Ronald J. deLeeuw Canada	19	795 0.8×	362 0.4×	956 1.5×	745 1.3×	342 0.7×	22	2.5k
Steven Mumm United States	35	2.2k 2.1×	425 0.4×	1.1k 1.6×	1.2k 2.1×	160 0.3×	126	5.2k
Ye-Guang Chen United States	14	2.9k 2.8×	274 0.3×	628 1.0×	333 0.6×	288 0.6×	16	3.6k
Dina Ruano Netherlands	21	483 0.5×	575 0.6×	657 1.0×	234 0.4×	502 1.0×	51	1.7k
Monique Losekoot Netherlands	34	1.4k 1.3×	349 0.4×	226 0.3×	1.3k 2.2×	259 0.5×	125	3.1k

Countries citing papers authored by Nada Al Tassan

Since Specialization

Citations

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

Fields of papers citing papers by Nada Al Tassan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nada Al Tassan

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

All Works

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20 of 20 papers shown

Wills, Christopher, Tim Maughan, David I. Fisher, et al.. (2025). Relationship between inherited genetic variation and survival from colorectal cancer stratified by tumour location. Scientific Reports. 15(1). 2423–2423.

Ghaziuddin, Mohammad, et al.. (2022). Autism and ADHD in the Era of Big Data; An Overview of Digital Resources for Patient, Genetic and Clinical Trials Information. Genes. 13(9). 1551–1551. 2 indexed citations

Baz, Batoul, Mohamed Abouelhoda, Tarek Owaidah, et al.. (2021). Molecular classification of blood and bleeding disorder genes. npj Genomic Medicine. 6(1). 62–62. 2 indexed citations

Tassan, Nada Al, et al.. (2020). A Comprehensive Analysis of Unique and Recurrent Copy Number Variations in Alzheimer’s Disease and its Related Disorders. Current Alzheimer Research. 17(10). 926–938. 1 indexed citations

Almohanna, Falah, et al.. (2019). Estimating transfection efficiency in differentiated and undifferentiated neural cells. BMC Research Notes. 12(1). 225–225. 21 indexed citations

Monies, Dorota, Thamer Alkhairallah, Saeed Bohlega, et al.. (2019). Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson’s Disease. Scientific Reports. 9(1). 3344–3344. 28 indexed citations

Alharbi, Musa, Rasha Aljelaify, Lamia Alsubaie, et al.. (2018). Durable Response to Nivolumab in a Pediatric Patient with Refractory Glioblastoma and Constitutional Biallelic Mismatch Repair Deficiency. The Oncologist. 23(12). 1401–1406. 51 indexed citations

Alharbi, Musa, Rasha Aljelaify, Fatimah Alqubaishi, et al.. (2018). Rare TP53 variant associated with Li-Fraumeni syndrome exhibits variable penetrance in a Saudi family. npj Genomic Medicine. 3(1). 35–35. 7 indexed citations

Al‐Mubarak, Bashayer, Mohamed Abouelhoda, Hesham Aldhalaan, et al.. (2017). Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families. Scientific Reports. 7(1). 5679–5679. 66 indexed citations

10.

Shinwari, Jameela, et al.. (2017). Analysis of shared homozygosity regions in Saudi siblings with attention deficit hyperactivity disorder. Psychiatric Genetics. 27(4). 131–138. 8 indexed citations

11.

Monies, Dorota, Hindi Al‐Hindi, Mohamed Abouelhoda, et al.. (2016). A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies. Human Genomics. 10(1). 32–32. 29 indexed citations

12.

Abouelhoda, Mohamed, Mohamed El-Kalioby, Nisha Patel, et al.. (2016). Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burden. Genetics in Medicine. 18(12). 1244–1249. 67 indexed citations

13.

Burkholder, John A., Dieter C. Bröering, Mohamed Abouelhoda, et al.. (2016). Genetic profiling of children with advanced cholestatic liver disease. Clinical Genetics. 92(1). 52–61. 30 indexed citations

14.

Shinwari, Jameela, Arif O. Khan, Salma Awad, et al.. (2014). Recessive Mutations in COL25A1 Are a Cause of Congenital Cranial Dysinnervation Disorder. The American Journal of Human Genetics. 96(1). 147–152. 30 indexed citations

15.

Wakil, Salma M., Asma I. Tahir, Batoul Baz, et al.. (2014). A study of the role of GATA2 gene polymorphism in coronary artery disease risk traits. Gene. 544(2). 152–158. 33 indexed citations

16.

Tassan, Nada Al, et al.. (2013). Interleukin (IL)-17A and IL-17F and asthma in Saudi Arabia: mRNA transcript levels and gene polymorphisms. AFRICAN JOURNAL OF BIOTECHNOLOGY. 12(23). 3615–3621. 7 indexed citations

17.

Tahir, Asma I., Editha Andres, Nejat Mazhar, et al.. (2013). The 3′-UTR of the adiponectin Q gene harbours susceptibility loci for atherosclerosis and its metabolic risk traits. BMC Medical Genetics. 14(1). 127–127. 6 indexed citations

18.

Eldali, Abdelmoneim, Asma Tulbah, Sooad Al-Daihan, et al.. (2011). TP53 genetic alterations in Arab breast cancer patients: Novel mutations, pattern and distribution. Oncology Letters. 2(2). 363–369. 15 indexed citations

19.

Oystreck, Darren T., Arif O. Khan, Nada Al Tassan, et al.. (2009). Synergistic Divergence: A Distinct Ocular Motility Dysinnervation Pattern. Investigative Ophthalmology & Visual Science. 50(11). 5213–5213. 14 indexed citations

20.

Khan, Arif O., Dania S. Khalil, & Nada Al Tassan. (2008). Congential Fibrosis of the Extraocular Muscles Type I (CFEOM1) on the Arabian Peninsula. Ophthalmic Genetics. 29(1). 25–28. 6 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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