Saeed Al-Turki

1.6k total citations
7 papers, 250 citations indexed

About

Saeed Al-Turki is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Saeed Al-Turki has authored 7 papers receiving a total of 250 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Neurology. Recurrent topics in Saeed Al-Turki's work include Genomics and Rare Diseases (3 papers), Mitochondrial Function and Pathology (2 papers) and Neonatal and fetal brain pathology (1 paper). Saeed Al-Turki is often cited by papers focused on Genomics and Rare Diseases (3 papers), Mitochondrial Function and Pathology (2 papers) and Neonatal and fetal brain pathology (1 paper). Saeed Al-Turki collaborates with scholars based in United Kingdom, Saudi Arabia and United States. Saeed Al-Turki's co-authors include Barry A. Chioza, Andrew H. Crosby, Ali Alothaim, Wafaa Eyaid, Majid Alfadhel, Abdulrahman Alswaid, Ahmed Alfares, Fuad Al Mutairi, Mohammed Al Balwi and Matt Hurles and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Neurology.

In The Last Decade

Saeed Al-Turki

7 papers receiving 247 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Saeed Al-Turki United Kingdom	4	114	102	41	36	31	7	250
Emily Tuttle United States	7	211 1.9×	113 1.1×	42 1.0×	62 1.7×	28 0.9×	10	314
Ina Schanze Germany	11	201 1.8×	146 1.4×	26 0.6×	19 0.5×	20 0.6×	19	295
Shinobu Fukumura Japan	11	149 1.3×	55 0.5×	44 1.1×	43 1.2×	12 0.4×	29	272
Laila Mahmoud Qatar	6	100 0.9×	136 1.3×	23 0.6×	35 1.0×	19 0.6×	6	254
Asma I. Tahir Saudi Arabia	11	129 1.1×	90 0.9×	21 0.5×	12 0.3×	28 0.9×	19	294
Cameron Mroske United States	9	156 1.4×	255 2.5×	38 0.9×	39 1.1×	19 0.6×	11	390
Berge A. Minassian Canada	10	130 1.1×	94 0.9×	30 0.7×	29 0.8×	17 0.5×	16	265
Taghreed Shuaib Saudi Arabia	9	133 1.2×	74 0.7×	45 1.1×	27 0.8×	18 0.6×	13	243
Ayelet Zerem Israel	11	180 1.6×	127 1.2×	42 1.0×	26 0.7×	7 0.2×	22	321
Fabíola Paoli Monteiro Brazil	11	198 1.7×	138 1.4×	28 0.7×	12 0.3×	25 0.8×	24	314

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

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7 of 7 papers shown

1.

John, Anne, et al.. (2023). Case report: Birk–Landau–Perez syndrome linked to the SLC30A9 gene—identification of additional cases and expansion of the phenotypic spectrum. Frontiers in Genetics. 14. 1219514–1219514. 2 indexed citations

2.

Aleem, Aamer, et al.. (2022). Clinical and Pathologic Characteristics of Essential Thrombocythemia (ET) Patients Harboring Calreticulin (CALR) Mutations. Blood. 140(Supplement 1). 12282–12283. 1 indexed citations

3.

Alfares, Ahmed, Fuad Al Mutairi, Abdulrahman Alswaid, et al.. (2018). Whole-genome sequencing offers additional but limited clinical utility compared with reanalysis of whole-exome sequencing. Genetics in Medicine. 20(11). 1328–1333. 99 indexed citations

4.

Alsubaie, Lamia, Saeed Al-Turki, Ali Alothaim, & Ahmed Alfares. (2018). Clinical reassessment of post-laboratory variant call format (VCF) files. SHILAP Revista de lepidopterología. 1(1). 31–36. 1 indexed citations

5.

Ahmed, Momin, Barry A. Chioza, Anna Rajab, et al.. (2015). Loss of PCLO function underlies pontocerebellar hypoplasia type III. Neurology. 84(17). 1745–1750. 41 indexed citations

6.

Baple, Emma L., Reza Maroofian, Barry A. Chioza, et al.. (2013). Mutations in KPTN Cause Macrocephaly, Neurodevelopmental Delay, and Seizures. The American Journal of Human Genetics. 94(1). 87–94. 35 indexed citations

7.

Barwick, Katy, Jane Wright, Saeed Al-Turki, et al.. (2012). Defective Presynaptic Choline Transport Underlies Hereditary Motor Neuropathy. The American Journal of Human Genetics. 91(6). 1103–1107. 71 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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