Alya Qari

1.4k total citations
17 papers, 244 citations indexed

About

Alya Qari is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Alya Qari has authored 17 papers receiving a total of 244 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Clinical Biochemistry and 8 papers in Genetics. Recurrent topics in Alya Qari's work include Metabolism and Genetic Disorders (8 papers), Mitochondrial Function and Pathology (3 papers) and Genomics and Rare Diseases (2 papers). Alya Qari is often cited by papers focused on Metabolism and Genetic Disorders (8 papers), Mitochondrial Function and Pathology (3 papers) and Genomics and Rare Diseases (2 papers). Alya Qari collaborates with scholars based in Saudi Arabia, United Kingdom and United States. Alya Qari's co-authors include Hamad Alzaidan, Albandary AlBakheet, Namik Kaya, Mohammed Al‐Owain, Mohammad Ghaziuddin, Malak Abedalthagafi, Moeenaldeen AlSayed, Mazhor Aldosary, Dilek Çolak and Tarfa Al‐Sheddi and has published in prestigious journals such as The American Journal of Human Genetics, Cells and Proceedings of The Nutrition Society.

In The Last Decade

Alya Qari

15 papers receiving 240 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Alya Qari Saudi Arabia	8	106	76	56	30	27	17	244
Enrico Alfei Italy	11	140 1.3×	160 2.1×	39 0.7×	58 1.9×	24 0.9×	25	333
Göran Brandberg Sweden	8	244 2.3×	116 1.5×	74 1.3×	71 2.4×	23 0.9×	10	442
Silvia Masnada Italy	10	99 0.9×	49 0.6×	80 1.4×	20 0.7×	20 0.7×	24	257
Emily Tuttle United States	7	211 2.0×	113 1.5×	29 0.5×	19 0.6×	8 0.3×	10	314
Alfonso Oyarzábal Spain	11	242 2.3×	79 1.0×	156 2.8×	20 0.7×	25 0.9×	18	452
Clara DM van Karnebeek Canada	7	190 1.8×	105 1.4×	78 1.4×	32 1.1×	13 0.5×	7	349
Maura Ruzhnikov United States	9	96 0.9×	73 1.0×	29 0.5×	26 0.9×	12 0.4×	21	213
Francisca Millan United States	11	261 2.5×	250 3.3×	34 0.6×	49 1.6×	33 1.2×	19	479
Elżbieta Szczepanik Poland	9	113 1.1×	48 0.6×	29 0.5×	24 0.8×	5 0.2×	32	208

Countries citing papers authored by Alya Qari

Since Specialization

Citations

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

Fields of papers citing papers by Alya Qari

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alya Qari

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

All Works

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17 of 17 papers shown

Al‐Hamed, Mohamed H., Alya Qari, Mohammed Alotaibi, et al.. (2025). Genetics of Primary Adrenal Insufficiency Beyond CAH in Saudi Arabian Population. Molecular Genetics & Genomic Medicine. 13(1). e70052–e70052. 2 indexed citations

Qari, Alya, et al.. (2024). Evaluation of the use of telehealth in Dietetics’ practice during the COVID-19 pandemic in the Kingdom of Saudi Arabia. Proceedings of The Nutrition Society. 83(OCE2).

AlBakheet, Albandary, Rawan Almass, Alya Qari, et al.. (2024). Novel UBE3B mutations: report of eight patients with Kaufman oculocerebrofacial syndrome with additional clinical findings from a highly consanguineous population. Clinical Dysmorphology. 33(2). 55–62. 1 indexed citations

Aldosary, Mazhor, Maysoon Alsagob, Stefan T. Arold, et al.. (2022). A Novel Homozygous Founder Variant of RTN4IP1 in Two Consanguineous Saudi Families. Cells. 11(19). 3154–3154.

Aldosary, Mazhor, Rawan Almass, Maysoon Alsagob, et al.. (2021). SLC25A42‐associated mitochondrial encephalomyopathy: Report of additional founder cases and functional characterization of a novel deletion. JIMD Reports. 60(1). 75–87. 12 indexed citations

Qari, Alya, et al.. (2020). Familial/inherited cancer syndrome: a focus on the highly consanguineous Arab population. npj Genomic Medicine. 5(1). 3–3. 24 indexed citations

Al‐Hamed, Mohamed H., Hamad Alzaidan, Maged H. Hussein, et al.. (2020). Novel pathogenic MAPKBP1 variant in a family with nephronophthisis. Clinical Kidney Journal. 14(2). 728–730. 1 indexed citations

Al‐Ashwal, Abdullah, Afaf Alsagheir, Khushnooda Ramzan, et al.. (2017). Clinical, Endocrine, and Molecular Genetic Analysis of a Large Cohort of Saudi Arabian Patients with Laron Syndrome. Hormone Research in Paediatrics. 88(2). 119–126. 3 indexed citations

Imtiaz, Faiqa, Khushnooda Ramzan, Nada Al Tassan, et al.. (2017). Twenty novel mutations in BCKDHA, BCKDHB and DBT genes in a cohort of 52 Saudi Arabian patients with maple syrup urine disease. Molecular Genetics and Metabolism Reports. 11. 17–23. 17 indexed citations

10.

Qari, Alya, et al.. (2017). Juvenile idiopathic arthritis in multiplex families: longitudinal follow-up. International Journal of Rheumatic Diseases. 20(7). 898–902. 4 indexed citations

11.

Qari, Alya, et al.. (2016). Genetic counselors’ scope of practice and challenges in genetic counseling services in Saudi Arabia. International Journal of Pediatrics and Adolescent Medicine. 3(1). 1–6. 20 indexed citations

12.

Imtiaz, Faiqa, Mohamed H. Al‐Hamed, Zuhair N. Al‐Hassnan, et al.. (2014). Spectrum of Mutations in 60 Saudi Patients with Mut Methylmalonic Acidemia. JIMD Reports. 29. 39–46. 5 indexed citations

13.

AlSayed, Moeenaldeen, Hamad Alzaidan, Albandary AlBakheet, et al.. (2013). Mutations in NALCN Cause an Autosomal-Recessive Syndrome with Severe Hypotonia, Speech Impairment, and Cognitive Delay. The American Journal of Human Genetics. 93(4). 721–726. 69 indexed citations

14.

Qari, Alya, et al.. (2013). The Development of Genetic Counseling Services and Training Program in Saudi Arabia. Journal of Genetic Counseling. 22(6). 835–838. 16 indexed citations

15.

Al‐Owain, Mohammed, et al.. (2012). Autism Spectrum Disorder in a Child with Propionic Acidemia. JIMD Reports. 7. 63–66. 51 indexed citations

16.

Imtiaz, Faiqa, Mohamed S. Rashed, Bashayer Al‐Mubarak, et al.. (2011). Identification of mutations causing hereditary tyrosinemia type I in patients of Middle Eastern origin. Molecular Genetics and Metabolism. 104(4). 688–690. 16 indexed citations

17.

Shamseldin, Hanan E., Mohammed S. Al‐Dosari, Zuhair Rahbeeni, et al.. (2010). Study of consanguineous populations can improve the annotation of SNP databases. European Journal of Medical Genetics. 54(2). 118–120. 3 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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