Maha Alotaibi

899 total citations
17 papers, 86 citations indexed

About

Maha Alotaibi is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Maha Alotaibi has authored 17 papers receiving a total of 86 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Clinical Biochemistry. Recurrent topics in Maha Alotaibi's work include Mitochondrial Function and Pathology (3 papers), Metabolism and Genetic Disorders (3 papers) and Connective tissue disorders research (3 papers). Maha Alotaibi is often cited by papers focused on Mitochondrial Function and Pathology (3 papers), Metabolism and Genetic Disorders (3 papers) and Connective tissue disorders research (3 papers). Maha Alotaibi collaborates with scholars based in Saudi Arabia, United Kingdom and United States. Maha Alotaibi's co-authors include Khushnooda Ramzan, Wesam Kurdi, John A. Sayer, Wafaa Eyaid, Nouf S. Al‐Numair, Sarah J. Rice, Nada Alsahan, Mohammed Almannai, Maha Alnemer and Fowzan S. Alkuraya and has published in prestigious journals such as SHILAP Revista de lepidopterología, Human Genetics and Frontiers in Genetics.

In The Last Decade

Maha Alotaibi

12 papers receiving 82 citations

Peers

Maha Alotaibi
Ahlam A. Hamed Sudan
Alan Kwong United States
Danielle Nolan United States
Henrik Åhlman Sweden
Claudio Bruno Italy
Chontelle King New Zealand
Nuria Martí‐Gutiérrez United States
Hanène Benrhouma Tunisia
Meghan Candee United States
Marie‐Aude Spitz France
Ahlam A. Hamed Sudan
Maha Alotaibi
Citations per year, relative to Maha Alotaibi Maha Alotaibi (= 1×) peers Ahlam A. Hamed

Countries citing papers authored by Maha Alotaibi

Since Specialization
Citations

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

Fields of papers citing papers by Maha Alotaibi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maha Alotaibi

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

All Works

17 of 17 papers shown
1.
Alotaibi, Maha. (2024). Parental genetic knowledge and attitudes toward childhood with genetic disorders. Frontiers in Genetics. 15. 1434322–1434322.
2.
Alotaibi, Maha, et al.. (2023). Craniofacial and Dental Manifestations in Pediatric Patients with Achondroplasia: A Case Report and Clinical View. International Journal of Clinical Pediatric Dentistry. 16(2). 409–415.
3.
4.
Almannai, Mohammed, Lama AlAbdi, Sateesh Maddirevula, et al.. (2022). KIF26A is mutated in the syndrome of congenital hydrocephalus with megacolon. Human Genetics. 142(3). 399–405. 3 indexed citations
5.
Alshammari, Bushra, et al.. (2022). Self-Rated Emergency Core Nursing Competencies Among Emergency Nurses in Qassim, Saudi Arabia. Cureus. 14(12). e32416–e32416. 4 indexed citations
6.
Alotaibi, Maha, et al.. (2022). Identification of a New Variant of the MBTPS1 Gene of the Kondo-Fu Type of Spondyloepiphyseal Dysplasia (SEDKF) in a Saudi Patient. SHILAP Revista de lepidopterología. 2022. 1–5. 4 indexed citations
7.
Ramzan, Khushnooda, et al.. (2021). Detection of a Recurrent TMEM38B Gene Deletion Associated with Recessive Osteogenesis Imperfecta. PubMed. 9(1). e124–e124. 4 indexed citations
8.
9.
Alotaibi, Maha, et al.. (2021). A Case of Geroderma Osteodysplasticum Syndrome: Unique Clinical Findings. SHILAP Revista de lepidopterología. 9(2). 175–178. 1 indexed citations
10.
11.
Alotaibi, Maha & Khushnooda Ramzan. (2020). A de novo variant of CHD8 in a patient with autism spectrum disorder. PubMed. 8(1). e107–e107. 12 indexed citations
12.
Westenberger, Ana, Maha Alotaibi, Malak Alghamdi, et al.. (2020). Biallelic loss‐of‐function HACD1 variants are a bona fide cause of congenital myopathy. Clinical Genetics. 99(4). 513–518. 8 indexed citations
13.
Al‐Hamed, Mohamed H., Nada Alsahan, Sarah J. Rice, et al.. (2019). Bialleleic PKD1 mutations underlie early-onset autosomal dominant polycystic kidney disease in Saudi Arabian families. Pediatric Nephrology. 34(9). 1615–1623. 22 indexed citations
14.
Aldosary, Mazhor, et al.. (2019). Involvement of mitochondrial dysfunction in pathogenesis of hemophagocytic lymphohistiocytosis. SHILAP Revista de lepidopterología. 2(1). 81–84. 1 indexed citations
15.
Almannai, Mohammed, Ali Alasmari, Eissa Faqeih, et al.. (2018). Expanding the phenotype of SLC25A42‐associated mitochondrial encephalomyopathy. Clinical Genetics. 93(5). 1097–1102. 24 indexed citations
16.
Alotaibi, Maha, et al.. (2018). Vici syndrome: A rare autosomal recessive syndrome in Yamani infant. 4(1). 1 indexed citations
17.
Alotaibi, Maha, et al.. (2017). New homozygous mutation in ALPL gene in Saudi patient with infantile hypophosphatasia. 2(3). 1 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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