Fuad Al Mutairi

3.0k citations

47 papers · 674 indexed · h-index 16

Co-authors: Majid Alfadhel Ahmed Alfares Wafaa Eyaid Fowzan S. Alkuraya Mohammed Al Balwi Abdulrahman Alswaid Eissa Faqeih Brahim Tabarki
Topics: Metabolism and Genetic Disorders (15 papers)Mitochondrial Function and Pathology (9 papers)Genomics and Rare Diseases (8 papers)
Cited by: Clinical Biochemistry Genetics Rheumatology
Journals: The Journal of Experimental MedicineSHILAP Revista de lepidopterologíaBioinformatics
Partner nations: Saudi Arabia United States Qatar

In The Last Decade

Fuad Al Mutairi

42 papers receiving 666 citations

Peers

Countries citing papers authored by Fuad Al Mutairi

Since Specialization

Citations

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

Fields of papers citing papers by Fuad Al Mutairi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fuad Al Mutairi

This figure shows the co-authorship network connecting the top 25 collaborators of Fuad Al Mutairi. A scholar is included among the top collaborators of Fuad Al Mutairi 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 Fuad Al Mutairi. Fuad Al Mutairi 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

#	Work	Indexed citations
1	Consanguinity and Occurrence of Monogenic Diseases in a Single Tertiary Centre in Riyadh, Saudi Arabia: A 2 Years Cross-Sectional Study 2024 ·The Application of Clinical Genetics ·(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Mohammed Almannai,(unknown),(unknown),(unknown),Abdulrahman Alswaid,Wafaa Eyaid,Fuad Al Mutairi,Muhammad Umair,Majid Alfadhel	0
2	A founder DBR1 variant causes a lethal form of congenital ichthyosis 2023 ·Human Genetics ·Hanan E. Shamseldin,(unknown),(unknown),Ruslan Al‐Ali,(unknown),(unknown),(unknown),Zuhair Rahbeeni,Fuad Al Mutairi,(unknown),(unknown),Firdous Abdulwahab,(unknown),Peter Bauer,Aida M. Bertoli‐Avella,Fowzan S. Alkuraya	6
3	Case Report: Clinical delineation of CACNA1D mutation: New cases and literature review 2023 ·Frontiers in Neurology ·(unknown),(unknown),(unknown),(unknown),(unknown),Fuad Al Mutairi	3
4	A Patient with Coarse Facial Features and Molecular Odyssey: Lessons Learned and Best Practice 2023 ·Clinical Chemistry ·Majid Alfadhel,Muhammad Umair,Abeer Al Tuwaijri,Fuad Al Mutairi	1
5	DeepSVP: integration of genotype and phenotype for structural variant prioritization using deep learning 2021 ·Bioinformatics ·(unknown),Lamia Alsubaie,Nagarajan Kathiresan,Katsuhiko Mineta,(unknown),Fuad Al Mutairi,Majid Alfadhel,Takashi Gojobori,(unknown),Robert Hoehndorf	9
6	Long-term effectiveness of carglumic acid in patients with propionic acidemia (PA) and methylmalonic acidemia (MMA): a randomized clinical trial 2021 ·Orphanet Journal of Rare Diseases ·Majid Alfadhel,Marwan Nashabat,(unknown),(unknown),Ahmed Alfares,(unknown),Muhammad Umair,(unknown),(unknown),Fuad Al Mutairi,Wafaa Eyaid,Abdulrahman Alswaid,(unknown),Eissa Faqeih,Mohammed Almannai,(unknown),(unknown),Mohamed Hussein,Zuhair Rahbeeni,Ali Alasmari	18
7	The phenotypic spectrum of dihydrolipoamide dehydrogenase deficiency in Saudi Arabia 2021 ·Molecular Genetics and Metabolism Reports ·(unknown),Majid Alfadhel,Seham Alameer,Amal Alhashem,Brahim Tabarki,(unknown),(unknown),Fuad Al Mutairi	9
8	Evaluation of long-term effectiveness of the use of carglumic acid in patients with propionic acidemia (PA) or methylmalonic acidemia (MMA): study protocol for a randomized controlled trial 2019 ·BMC Pediatrics ·Marwan Nashabat,(unknown),Fuad Al Mutairi,(unknown),(unknown),(unknown),(unknown),Wafaa Eyaid,Abdulrahman Alswaid,(unknown),Eissa Faqeih,(unknown),Mohamed Hussein,Ali Alasmari,Majid Alfadhel	9
9	Spectrum of mutations underlying Propionic acidemia and further insight into a genotype-phenotype correlation for the common mutation in Saudi Arabia 2019 ·Molecular Genetics and Metabolism Reports ·Mohamed H. Al‐Hamed,Faiqa Imtiaz,Zuhair N. Al‐Hassnan,Mohammed Al‐Owain,Hamad Alzaidan,Mohamed Al‐Amoudi,Eissa Faqeih,Majid Alfadhel,Ali Alasmari,Mohammed M. Saleh,Fuad Al Mutairi,Nabil Moghrabi,Moeenaldeen AlSayed	12
10	Coexistence of genetic conditions: Exploring a possible relationship 2019 ·PubMed ·(unknown),(unknown),Fuad Al Mutairi,(unknown)	0
11	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
12	hCALCRL mutation causes autosomal recessive nonimmune hydrops fetalis with lymphatic dysplasia 2018 ·The Journal of Experimental Medicine ·(unknown),Fuad Al Mutairi,Reema B. Davis,Daniel O. Kechele,(unknown),Joshua C. Snyder,Marc G. Caron,Harvey J. Kliman,Jonathan S. Berg,John Simms,David R. Poyner,Kathleen M. Caron	29
13	Expanding the phenotype of SLC25A42‐associated mitochondrial encephalomyopathy 2018 ·Clinical Genetics ·Mohammed Almannai,Ali Alasmari,(unknown),Eissa Faqeih,Fuad Al Mutairi,Maha Alotaibi,(unknown),Wafaa Eyaid,(unknown),(unknown),(unknown),Fowzan S. Alkuraya	24
14	Novel homozygous mutation in CYP27B1 gene of vitamin D dependent rickets type 1A: a case report 2018 ·(unknown),(unknown),(unknown),Fuad Al Mutairi,Amir Babiker	2
15	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
16	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
17	Clinical, Biochemical, and Molecular Features in 37 Saudi Patients with Very Long Chain Acyl CoA Dehydrogenase Deficiency 2017 ·JIMD Reports ·(unknown),Marwan Nashabat,Majid Alfadhel,Ali Alasmari,Fuad Al Mutairi,Abdulrahman Alswaid,Eissa Faqeih,(unknown),(unknown),(unknown),Deborah Marsden,Wafaa Eyaid	16
18	Further delineation of the phenotypic spectrum of ISCA2 defect: A report of ten new cases 2017 ·European Journal of Paediatric Neurology ·Majid Alfadhel,Marwan Nashabat,Muhammad Talal Alrifai,(unknown),Fuad Al Mutairi,Saif Alshahrani,Barbara Plecko,Rawan Almass,Maysoon Alsagob,(unknown),Ahmed Al‐Rumayyan,Waleed Altwaijri,Mohammed Al‐Owain,Robert W. Taylor,Namik Kaya	22
19	Guidelines for acute management of hyperammonemia in the Middle East region 2016 ·Therapeutics and Clinical Risk Management ·Majid Alfadhel,Fuad Al Mutairi,Nawal Makhseed,Fatma Al Jasmi,Khalid Al‐Thihli,(unknown),Moeen Al-Sayed,Zuhair N. Al‐Hassnan,(unknown),Johannes Häberle,Tawfeg Ben‐Omran	29
20	Thirteen year retrospective review of the spectrum of inborn errors of metabolism presenting in a tertiary center in Saudi Arabia 2016 ·Orphanet Journal of Rare Diseases ·Majid Alfadhel,(unknown),Mohammad Arif Hossain,Fuad Al Mutairi,(unknown),Ahmed Alfares,Mohammed Al Balwi,(unknown),Wafaa Eyaid	56

About Fuad Al Mutairi

Fuad Al Mutairi is a scholar working on Clinical Biochemistry, Genetics and Health Informatics, having authored 47 papers that have together received 674 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (15 papers), Mitochondrial Function and Pathology (9 papers) and Genomics and Rare Diseases (8 papers). The work is most often cited by research in Clinical Biochemistry (195 citations), Genetics (225 citations) and Rheumatology (110 citations). Fuad Al Mutairi has collaborated with scholars based in Saudi Arabia, United States and Qatar. Frequent co-authors include Majid Alfadhel, Ahmed Alfares, Wafaa Eyaid, Fowzan S. Alkuraya, Mohammed Al Balwi, Abdulrahman Alswaid, Eissa Faqeih, Brahim Tabarki, Ali Alasmari and Muhammad Talal Alrifai. Their work appears in journals such as The Journal of Experimental Medicine, SHILAP Revista de lepidopterología and Bioinformatics.

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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