Ali Al‐Odaib

1.5k total citations
34 papers, 574 citations indexed

About

Ali Al‐Odaib is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Ali Al‐Odaib has authored 34 papers receiving a total of 574 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 16 papers in Genetics and 12 papers in Clinical Biochemistry. Recurrent topics in Ali Al‐Odaib's work include Metabolism and Genetic Disorders (12 papers), Genomics and Rare Diseases (8 papers) and Genomic variations and chromosomal abnormalities (6 papers). Ali Al‐Odaib is often cited by papers focused on Metabolism and Genetic Disorders (12 papers), Genomics and Rare Diseases (8 papers) and Genomic variations and chromosomal abnormalities (6 papers). Ali Al‐Odaib collaborates with scholars based in Saudi Arabia, United States and France. Ali Al‐Odaib's co-authors include Pinar T. Ozand, Serdar Coşkun, Nadia Sakati, Ali Hellani, Khaled K. Abu‐Amero, Moncef Benkhalifa, Piero Rinaldo, Kimiyo Raymond, Michael J. Bennett and Hesham Aldhalaan and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Gene and Fertility and Sterility.

In The Last Decade

Ali Al‐Odaib

32 papers receiving 553 citations

Peers

Countries citing papers authored by Ali Al‐Odaib

Since Specialization

Citations

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

Fields of papers citing papers by Ali Al‐Odaib

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ali Al‐Odaib. 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 Ali Al‐Odaib. The network helps show where Ali Al‐Odaib may publish in the future.

Co-authorship network of co-authors of Ali Al‐Odaib

This figure shows the co-authorship network connecting the top 25 collaborators of Ali Al‐Odaib. A scholar is included among the top collaborators of Ali Al‐Odaib 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 Ali Al‐Odaib. Ali Al‐Odaib 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	Natural history of SPTBN4-related neurodevelopmental disorder with hypotonia, neuropathy, and deafness 2025 ·Orphanet Journal of Rare Diseases ·(unknown), Mohammad A. Al–Muhaizea, (unknown), (unknown), (unknown), (unknown), Anoud Albader, (unknown), Rawan Almass, Albandary AlBakheet, Tarfa Al‐Sheddi, Eman Alobeid, Maha Al‐Rasheed, Ali Al‐Odaib, Hamad Alzaidan, Moeenaldeen AlSayed, Namik Kaya	0
2	Case report: Clinical and genetic characterization of a novel ALDH7A1 variant causing pyridoxine-dependent epilepsy, developmental delay, and intellectual disability in two siblings 2024 ·Frontiers in Psychiatry ·Mustafa A. Salih, Albandary AlBakheet, Rawan Almass, Ahlam A. Hamed, Ali Al‐Odaib, Namik Kaya	2
3	Clinical, radiological, and genetic characterization of SLC13A5 variants in Saudi families: Genotype phenotype correlation and brief review of the literature 2023 ·Frontiers in Pediatrics ·(unknown), Hesham Aldhalaan, (unknown), (unknown), (unknown), (unknown), Albandary AlBakheet, (unknown), (unknown), (unknown), Moeen Al-Sayed, Hamad Alzaidan, Maha Al‐Rasheed, Ali Al‐Odaib, Namik Kaya	2
4	Incidence of newborn screening disorders among 56632 infants in Central Saudi Arabia 2020 ·Saudi Medical Journal ·Sarar Mohamed, W Elsheikh, Aida I. Al‐Aqeel, Amal Alhashem, Ali Al‐Odaib, (unknown), (unknown), (unknown), (unknown), Amer Ammari, (unknown)	17
5	Targeted SLC19A3 gene sequencing of 3000 Saudi newborn: a pilot study toward newborn screening 2019 ·Annals of Clinical and Translational Neurology ·Majid Alfadhel, Muhammad Umair, Bader Almuzzaini, Saif Alsaif, (unknown), (unknown), Wardah Alharbi, (unknown), (unknown), (unknown), (unknown), (unknown), Marwan Nashabat, Ali Al‐Odaib, Waleed Altwaijri, Ahmed Al‐Rumayyan, Muhammad Talal Alrifai, Ahmed Alfares, Mohammed Al Balwi, Brahim Tabarki	39
6	Feasibility of Responsive Teaching With Mothers and Young Children With Autism in Saudi Arabia 2018 ·Journal of Early Intervention ·Turki Alquraini, Ali Al‐Odaib, Hesham Aldhalaan, (unknown), Gerald Mahoney	14
7	A Novel Homozygous Mutation in SPTBN2 Leads to Spinocerebellar Ataxia in a Consanguineous Family: Report of a New Infantile-Onset Case and Brief Review of the Literature 2017 ·The Cerebellum ·Mohammad A. Al–Muhaizea, (unknown), Rawan Almass, (unknown), Mazhor Aldosary, Maysoon Alsagob, Ali Al‐Odaib, Dilek Çolak, Namik Kaya	16
8	An overview of the Prince Salman Center for Disability Research scientific outcomes. 2014 ·PubMed ·Ali Al‐Odaib, Sultan T. Al‐Sedairy	8
9	Arginine 16 Glycine Polymorphism inβ2-Adrenergic Receptor Gene Is Associated with Obesity, Hyperlipidemia, Hyperleptinemia, and Insulin Resistance in Saudis 2012 ·International Journal of Endocrinology ·Maha H. Daghestani, Arjumand S. Warsy, (unknown), (unknown), Ali Al‐Odaib, Abdelmoneim Eldali, (unknown), Sawsan A. Omer, Zeinab Hassan	17
10	Identification of a novel IVD mutation in a consanguineous family with isovaleric acidemia 2012 ·Gene ·Namik Kaya, Dilek Çolak, Albandary AlBakheet, Banan Al‐Younes, (unknown), Maha H. Daghestani, (unknown), (unknown), Ali Al‐Odaib, Aida I. Al‐Aqeel	3
11	Chromosome 12q24.31-q24.33 deletion causes multiple dysmorphic features and developmental delay: First mosaic patient and overview of the phenotype related to 12q24qter defects 2011 ·Molecular Cytogenetics ·(unknown), Naji Aldosari, (unknown), Tarfa Alshidi, Dilek Çolak, (unknown), Ali Al‐Odaib, Nadia Sakati, Brian F. Meyer, Pinar T. Ozand, Namik Kaya	8
12	Genomic and transcriptomic analyses distinguish classic Rett and Rett-like syndrome and reveals shared altered pathways 2010 ·Genomics ·Dilek Çolak, Hesham Aldhalaan, Michael Nester, Albandary AlBakheet, Banan Al‐Younes, (unknown), (unknown), Aziza Chedrawi, (unknown), (unknown), Laila Al‐Alwan, Ali Al‐Odaib, Pinar T. Ozand, Mehmet Sait Inan, Namik Kaya	18
13	The Gln27Glu Polymorphism in β2-Adrenergic receptor gene is linked to hypertriglyceridemia, hyperinsulinemia and hyperleptinemia in Saudis 2010 ·Lipids in Health and Disease ·Maha H. Daghestani, Arjumand S. Warsy, (unknown), Ali Al‐Odaib, Abdelmoneim Eldali, (unknown), (unknown)	9
14	Preimplantation genetic diagnosis in Saudi Arabia: parents' experience and attitudes 2010 ·Prenatal Diagnosis ·(unknown), Ali Al‐Odaib, (unknown), Jenny Hewison	19
15	Molecular genotyping of hemophilia A in Saudi Arabia: report of 2 novel mutations 2009 ·Blood Coagulation & Fibrinolysis ·Tarek Owaidah, (unknown), (unknown), (unknown), (unknown), (unknown), Ali Al‐Odaib, (unknown)	13
16	Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan disease 2008 ·Genetics in Medicine ·Namik Kaya, Faiqa Imtiaz, Dilek Çolak, Moeenaldeen AlSayed, Ali Al‐Odaib, (unknown), Bashayer Al‐Mubarak, Mohammad Al-Owain, Hesham Aldhalaan, Aziza Chedrawi, Zuhair N. Al‐Hassnan, Serdar Coşkun, Nadia Sakati, Pinar T. Ozand, Brian F. Meyer	17
17	Array comparative genomic hybridization (aCGH) reveals the largest novel deletion in PCCA found in a Saudi family with propionic acidemia 2008 ·European Journal of Medical Genetics ·Namik Kaya, Mohammad Al-Owain, Albandary AlBakheet, Dilek Çolak, Ali Al‐Odaib, Faiqa Imtiaz, Serdar Coşkun, (unknown), Zuhair N. Al‐Hassnan, Hamad Alzaidan, Brian F. Meyer, Pinar T. Ozand	14
18	Preimplantation genetic diagnosis for Niemann‐Pick disease type B 2004 ·Prenatal Diagnosis ·Ali Hellani, Edward H. Schuchman, Ali Al‐Odaib, (unknown), Kamal Jaroudi, Pinar T. Ozand, Serdar Coşkun	6
19	Multiple displacement amplification on single cell and possible preimplantation genetic diagnosis applications 2004 ·Fertility and Sterility ·(unknown), Serdar Coşkun, Nadia Sakati, M. Benkhalifa, Ali Al‐Odaib, (unknown)	3
20	Clinical and biochemical features of fatty acid oxidation disorders 1998 ·Current Opinion in Pediatrics ·Piero Rinaldo, Kimiyo Raymond, Ali Al‐Odaib, Michael J. Bennett	51

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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