Saud Alsahli

834 total citations
11 papers, 128 citations indexed

About

Saud Alsahli is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Saud Alsahli has authored 11 papers receiving a total of 128 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Surgery. Recurrent topics in Saud Alsahli's work include Genetics and Neurodevelopmental Disorders (3 papers), Eosinophilic Esophagitis (2 papers) and Lysosomal Storage Disorders Research (2 papers). Saud Alsahli is often cited by papers focused on Genetics and Neurodevelopmental Disorders (3 papers), Eosinophilic Esophagitis (2 papers) and Lysosomal Storage Disorders Research (2 papers). Saud Alsahli collaborates with scholars based in Saudi Arabia, United States and Netherlands. Saud Alsahli's co-authors include Majid Alfadhel, Fuad Al Mutairi, Emad Masuadi, Saeed Al Tala, Muhammad Talal Alrifai, Fowzan S. Alkuraya, Amal Alhashem, Eissa Faqeih, Khalid Hundallah and Brahim Tabarki and has published in prestigious journals such as SHILAP Revista de lepidopterología, Hepatology and Molecules.

In The Last Decade

Saud Alsahli

11 papers receiving 125 citations

Peers

Countries citing papers authored by Saud Alsahli

Since Specialization

Citations

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

Fields of papers citing papers by Saud Alsahli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Saud Alsahli

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

All Works

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11 of 11 papers shown

#	Work	Indexed citations
1	Advanced Photoelectrochemical Hydrogen Generation by CdO-g-C3N4 in Aqueous Medium under Visible Light 2022 ·Molecules ·Naseer Iqbal, Muhammad Shahzeb Khan, Muhammad Zubair, Safyan Akram Khan, Asghar Ali, (unknown), Saud Alsahli, (unknown), (unknown), (unknown), (unknown)	6
2	Truncating biallelic variant in DNAJA1, encoding the co-chaperone Hsp40, is associated with intellectual disability and seizures 2019 ·Neurogenetics ·Saud Alsahli, Ahmed Alfares, Francisco J. Guzmán‐Vega, Stefan T. Arold, (unknown), Fuad Al Mutairi	3
3	Biallelic Mutations in Tetratricopeptide Repeat Domain 26 (Intraflagellar Transport 56) Cause Severe Biliary Ciliopathy in Humans 2019 ·Hepatology ·Ranad Shaheen, Saud Alsahli, Nour Ewida, Fatema Alzahrani, Hanan E. Shamseldin, Nisha Patel, (unknown), (unknown), Amal Alhashem, Tarfa Al‐Sheddi, Rana Alomar, Eman Alobeid, Mohamed Abouelhoda, Dorota Monies, Abdulrahman Al‐Hussaini, (unknown), Mohammad Shagrani, Eissa Faqeih, Fowzan S. Alkuraya	23
4	Severe Crohnʼs Disease Manifestations in a Child with Cystathionine β-Synthase Deficiency 2018 ·ACG Case Reports Journal ·Saud Alsahli, (unknown), (unknown), (unknown), (unknown), Majid Alfadhel, Fuad Al Mutairi	4
5	KIF16B is a candidate gene for a novel autosomal‐recessive intellectual disability syndrome 2018 ·American Journal of Medical Genetics Part A ·Saud Alsahli, Stefan T. Arold, Ahmed Alfares, Bader Alhaddad, Mohammed Al Balwi, Erik‐Jan Kamsteeg, Waleed Altwaijri, Majid Alfadhel	7
6	Further Delineation of the Clinical Phenotype of Cerebellar Ataxia, Mental Retardation, and Disequilibrium Syndrome Type 4 2018 ·SHILAP Revista de lepidopterología ·Saud Alsahli, Muhammad Talal Alrifai, Saeed Al Tala, Fuad Al Mutairi, Majid Alfadhel	16
7	Aortic calcification in Gaucher disease: a case report 2018 ·The Application of Clinical Genetics ·Saud Alsahli, Dalal Bubshait, Zuhair Rahbeeni, Majid Alfadhel	7
8	Confirming the pathogenicity of NECAP1 in early onset epileptic encephalopathy 2018 ·Epilepsia Open ·Saud Alsahli, Waleed Altwaijri, Fuad Al Mutairi	4
9	Severe Crohnʼs Disease Manifestations in a Child with Cystathionine β-Synthase Deficiency 2018 ·ACG Case Reports Journal ·Saud Alsahli, (unknown), (unknown), (unknown), (unknown), Majid Alfadhel, Fuad Al Mutairi	3
10	Congenital disorders of glycosylation: The Saudi experience 2017 ·American Journal of Medical Genetics Part A ·(unknown), Amal Alhashem, Eissa Faqeih, Majid Alfadhel, Abdullah Alfaifi, (unknown), Saud Alsahli, Hesham Aldhalaan, Fowzan S. Alkuraya, Khalid Hundallah, Adel Mahmoud, Ali Alasmari, Fuad Al Mutairi, (unknown), (unknown), Saad AlShahwan, Brahim Tabarki	29
11	Seasonal variations of respiratory viruses detected from children with respiratory tract infections in Riyadh, Saudi Arabia 2017 ·Journal of Infection and Public Health ·(unknown), (unknown), Saud Alsahli, Emad Masuadi, (unknown)	26

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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