Abdulrahman Alswaid

3.1k citations

29 papers · 1.1k indexed · h-index 16

Co-authors: Mohammed Al Balwi Laurence Faivre André Mégarbané Arnold Münnich Valérie Cormier‐Daire Hélène Dollfus Yves Alembik Shawna M. Pyott
Topics: Connective tissue disorders research (6 papers)Metabolism and Genetic Disorders (5 papers)Genomics and Rare Diseases (4 papers)
Cited by: Genetics Cancer Research Immunology and Allergy
Journals: SHILAP Revista de lepidopterologíaThe American Journal of Human Genetics Atherosclerosis
Partner nations: Saudi Arabia United States United Kingdom

In The Last Decade

Abdulrahman Alswaid

27 papers receiving 1.1k citations

Peers

Countries citing papers authored by Abdulrahman Alswaid

Since Specialization

Citations

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

Fields of papers citing papers by Abdulrahman Alswaid

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Abdulrahman Alswaid

This figure shows the co-authorship network connecting the top 25 collaborators of Abdulrahman Alswaid. A scholar is included among the top collaborators of Abdulrahman Alswaid 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 Abdulrahman Alswaid. Abdulrahman Alswaid 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	The variant artificial intelligence easy scoring (VARIES) system 2022 ·Computers in Biology and Medicine ·(unknown),(unknown),(unknown),Wardah Alharbi,Lamia Alsubaie,(unknown),(unknown),Abdulrahman Alswaid,(unknown),Fuad Al Mutairi,(unknown),Majid Alfadhel,Ahmed Alfares	2
3	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
4	Genetic carrier screening for disorders included in newborn screening in the Saudi population 2021 ·SHILAP Revista de lepidopterología ·Mariam Al Eissa,(unknown),Lamia Alsubaie,Abdulrahman Alswaid,(unknown),Fuad Al Mutairi,(unknown),Majid Alfadhel,Ahmed Alfares	7
5	The rate of secondary genomic findings in the Saudi population 2021 ·American Journal of Medical Genetics Part A ·(unknown),Lamia Alsubaie,(unknown),(unknown),Abdulrahman Alswaid,(unknown),Fuad Al Mutairi,(unknown),Majid Alfadhel,Ahmed Alfares	7
6	Incidental discovery of an interstitial emphysematous cystitis with liver abscess: A report of hematogenous spread of infection 2020 ·Urology Case Reports ·(unknown),(unknown),(unknown),(unknown),Abdulrahman Alswaid,(unknown)	1
7	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
8	Tetrasomy 18p: case report and review of literature 2018 ·The Application of Clinical Genetics ·(unknown),(unknown),(unknown),(unknown),Mohammed Al Balwi,Abdulrahman Alswaid,Majid Alfadhel	11
9	Whole-genome sequencing offers additional but limited clinical utility compared with reanalysis of whole-exome sequencing 2018 ·Genetics in Medicine ·Ahmed Alfares,(unknown),(unknown),(unknown),(unknown),(unknown),Fuad Al Mutairi,Abdulrahman Alswaid,Ali Alothaim,Wafaa Eyaid,Mohammed Al Balwi,Saeed Al-Turki,Majid Alfadhel	99
10	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
11	Recurrent variants in OTOF are significant contributors to prelingual nonsydromic hearing loss in Saudi patients 2017 ·Genetics in Medicine ·Naif A. M. Almontashiri,Abdulrahman Alswaid,Andrea M. Oza,Khalid A. Al-Mazrou,(unknown),Ahmad Abou Tayoun,Heidi L. Rehm,Sami S. Amr	19
12	Hereditary deletion of the entire FAM20C gene in a patient with Raine syndrome 2013 ·American Journal of Medical Genetics Part A ·(unknown),Abdulrahman Alswaid,(unknown),(unknown),Andrew H. Crosby,Mohammed Al Balwi	33
13	Genomic analysis of pediatric cataract in Saudi Arabia reveals novel candidate disease genes 2012 ·Genetics in Medicine ·Mohammed A. Aldahmesh,Arif O. Khan,Jawahir Y. Mohamed,Hadia Hijazi,Mohammed Al‐Owain,Abdulrahman Alswaid,Fowzan S. Alkuraya	47
14	Axial spondylometaphyseal dysplasia: Additional reports 2011 ·American Journal of Medical Genetics Part A ·Shigeru Suzuki,Ok‐Hwa Kim,Yoshio Makita,Tetsuya Saito,Gye‐Yeon Lim,Tae‐Joon Cho,Abdulrahman Alswaid,(unknown),(unknown),Osamu Miyazaki,Sachiko Nishina,Andrea Superti‐Furga,Sheila Unger,Kenji Fujieda,Shiro Ikegawa,Gen Nishimura	8
15	Homozygosity for a Missense Mutation in SERPINH1, which Encodes the Collagen Chaperone Protein HSP47, Results in Severe Recessive Osteogenesis Imperfecta 2010 ·The American Journal of Human Genetics ·Helena E. Christiansen,Ulrike Schwarze,Shawna M. Pyott,Abdulrahman Alswaid,Mohammed Al Balwi,(unknown),Melanie Pepin,Mary Ann Weis,David R. Eyre,Peter H. Byers	228
16	A novel missense and a recurrent mutation in SLC2A10 gene of patients affected with arterial tortuosity syndrome 2008 ·Atherosclerosis ·Muhammad Faiyaz‐Ul‐Haque,Syed Hassan Ejaz Zaidi,(unknown),Abdulrahman Alswaid,(unknown),Namik Kaya,Fouad Al‐Dayel,(unknown),(unknown),Lap‐Chee Tsui,Ahmad S. Teebi	23
17	LC‐MS/MS determination of dibasic amino acids for the diagnosis of cystinuria. Application in a family affected by a novel splice‐acceptor site mutation in the SLC7A9 gene 2007 ·Journal of Inherited Metabolic Disease ·(unknown),Khaled K. Abu‐Amero,Abdulrahman Alswaid,G. F. Hoffmann,(unknown),M. S. Rashed	10
18	ADAMTS10 Mutations in Autosomal Recessive Weill-Marchesani Syndrome 2004 ·The American Journal of Human Genetics ·Nathalie Dagoneau,Catherine Benoist-Lasselin,Céline Huber,Laurence Faivre,André Mégarbané,Abdulrahman Alswaid,Hélène Dollfus,Yves Alembik,Arnold Münnich,Laurence Legeai‐Mallet,Valérie Cormier‐Daire	207
19	Protein-Truncating Mutations in ASPM Cause Variable Reduction in Brain Size 2003 ·The American Journal of Human Genetics ·Jacquelyn Bond,(unknown),Daniel J. Hampshire,Kelly Springell,Peter Corry,Marc Abramowicz,Ganeshwaran H. Mochida,Raoul C. M. Hennekam,Eamonn R. Maher,Jean‐Pierre Fryns,Abdulrahman Alswaid,Hussain Jafri,Yasmin Abdul Rashid,Ammar F. Mubaidin,Christopher A. Walsh,Emma Roberts,C. Geoffrey Woods	133
20	Searching for evidence of DFNB2 2002 ·American Journal of Medical Genetics ·(unknown),Philip M. Kelley,James W. Askew,Michael D. Weston,Richard J. Smith,Abdulrahman Alswaid,(unknown),William J. Kimberling	21

About Abdulrahman Alswaid

Abdulrahman Alswaid is a scholar working on Health Informatics, Clinical Biochemistry and Genetics, having authored 29 papers that have together received 1.1k indexed citations. Recurring topics across this work include Connective tissue disorders research (6 papers), Metabolism and Genetic Disorders (5 papers) and Genomics and Rare Diseases (4 papers). The work is most often cited by research in Genetics (698 citations), Cancer Research (195 citations) and Immunology and Allergy (67 citations). Abdulrahman Alswaid has collaborated with scholars based in Saudi Arabia, United States and United Kingdom. Frequent co-authors include Mohammed Al Balwi, Laurence Faivre, André Mégarbané, Arnold Münnich, Valérie Cormier‐Daire, Hélène Dollfus, Yves Alembik, Shawna M. Pyott, Melanie Pepin and Ulrike Schwarze. Their work appears in journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Atherosclerosis.

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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