Saeed Al Turki

6.3k total citations
13 papers, 526 citations indexed

About

Saeed Al Turki is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Saeed Al Turki has authored 13 papers receiving a total of 526 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Cancer Research. Recurrent topics in Saeed Al Turki's work include Genomics and Rare Diseases (3 papers), Cancer Genomics and Diagnostics (3 papers) and Acute Myeloid Leukemia Research (2 papers). Saeed Al Turki is often cited by papers focused on Genomics and Rare Diseases (3 papers), Cancer Genomics and Diagnostics (3 papers) and Acute Myeloid Leukemia Research (2 papers). Saeed Al Turki collaborates with scholars based in Saudi Arabia, United Kingdom and United States. Saeed Al Turki's co-authors include Matthew E. Hurles, Raheleh Rahbari, Blair H. Smith, Michael R. Stratton, Robert J. Hardwick, Ludmil B. Alexandrov, Andrew D. Morris, Sarah Lindsay, Arthur Wüster and Anna F. Dominiczak and has published in prestigious journals such as Cell, Nature Genetics and Journal of Clinical Oncology.

In The Last Decade

Saeed Al Turki

12 papers receiving 522 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Saeed Al Turki Saudi Arabia 7 281 276 122 43 40 13 526
Avni Santani United States 16 405 1.4× 439 1.6× 110 0.9× 43 1.0× 21 0.5× 39 781
Martine Doco‐Fenzy France 15 349 1.2× 302 1.1× 59 0.5× 80 1.9× 37 0.9× 29 690
Véronique Geoffroy France 12 559 2.0× 510 1.8× 70 0.6× 41 1.0× 17 0.4× 17 775
Ruth Charlton United Kingdom 12 240 0.9× 168 0.6× 118 1.0× 23 0.5× 16 0.4× 25 477
Elisa Tassano Italy 15 310 1.1× 272 1.0× 58 0.5× 46 1.1× 10 0.3× 54 596
Prachi Kothiyal United States 7 171 0.6× 211 0.8× 64 0.5× 51 1.2× 28 0.7× 12 373
Elizabeth Wohler United States 13 266 0.9× 338 1.2× 62 0.5× 73 1.7× 8 0.2× 40 603
Nick Warr United Kingdom 14 573 2.0× 431 1.6× 62 0.5× 25 0.6× 20 0.5× 21 756
Arnaud Kress France 9 276 1.0× 202 0.7× 65 0.5× 18 0.4× 12 0.3× 17 437
Pietro Palumbo Italy 15 314 1.1× 325 1.2× 25 0.2× 61 1.4× 16 0.4× 64 620

Countries citing papers authored by Saeed Al Turki

Since Specialization
Citations

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

Fields of papers citing papers by Saeed Al Turki

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Saeed Al Turki

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

All Works

13 of 13 papers shown
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3.
Alosaimi, Bandar, Liliane Okdah, Khaled Alkattan, et al.. (2022). Development and Validation of ScriptTaq COVID PCR: An In-House Multiplex rRT-PCR for Low-Cost Detection. Current Issues in Molecular Biology. 44(12). 6117–6131. 1 indexed citations
4.
Turki, Saeed Al, et al.. (2022). Pathogenic germline mutations prevalence in Saudi patients with pancreatic ductal adenocarcinoma.. Journal of Clinical Oncology. 40(4_suppl). 538–538.
5.
Alzahrani, Musa, Saeed Al Turki, Khadega A. Abuelgasim, et al.. (2022). Pro106Leu MPL mutation is associated with thrombocytosis and a low risk of thrombosis, splenomegaly and marrow fibrosis. Platelets. 33(8). 1220–1227. 1 indexed citations
6.
Almarri, Mohamed A., Marc Haber, Pille Hallast, et al.. (2021). The genomic history of the Middle East. Cell. 184(18). 4612–4625.e14. 33 indexed citations
7.
Turki, Saeed Al, et al.. (2019). Isolated Bone Marrow Non–Langerhans Cell Histiocytosis Preceding RUNX1-Mutated Acute Myeloid Leukemia: Case Report and Literature Review. American Journal of Clinical Pathology. 151(6). 638–646. 3 indexed citations
8.
Amr, Sami S., Saeed Al Turki, Matthew S. Lebo, et al.. (2016). Using large sequencing data sets to refine intragenic disease regions and prioritize clinical variant interpretation. Genetics in Medicine. 19(5). 496–504. 11 indexed citations
9.
Tayoun, Ahmad Abou, Saeed Al Turki, Andrea M. Oza, et al.. (2015). Improving hearing loss gene testing: a systematic review of gene evidence toward more efficient next-generation sequencing–based diagnostic testing and interpretation. Genetics in Medicine. 18(6). 545–553. 45 indexed citations
10.
D’Alessandro, Lisa C.A., Saeed Al Turki, Ashok Kumar Manickaraj, et al.. (2015). Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect. Genetics in Medicine. 18(2). 189–198. 29 indexed citations
11.
Rahbari, Raheleh, Arthur Wüster, Sarah Lindsay, et al.. (2015). Timing, rates and spectra of human germline mutation. Nature Genetics. 48(2). 126–133. 381 indexed citations
12.
Manase, Dorin, Lisa C.A. D’Alessandro, Ashok Kumar Manickaraj, et al.. (2014). High throughput exome coverage of clinically relevant cardiac genes. BMC Medical Genomics. 7(1). 67–67. 8 indexed citations
13.
Raffan, Eleanor, Liam A. Hurst, Saeed Al Turki, et al.. (2011). Early Diagnosis of Werner's Syndrome Using Exome-Wide Sequencing in a Single, Atypical Patient. SHILAP Revista de lepidopterología. 2. 8–8. 9 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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