Namik Kaya

2.7k total citations
83 papers, 1.6k citations indexed

About

Namik Kaya is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Namik Kaya has authored 83 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 34 papers in Genetics and 11 papers in Clinical Biochemistry. Recurrent topics in Namik Kaya's work include Genetics and Neurodevelopmental Disorders (21 papers), Genomics and Rare Diseases (11 papers) and Metabolism and Genetic Disorders (11 papers). Namik Kaya is often cited by papers focused on Genetics and Neurodevelopmental Disorders (21 papers), Genomics and Rare Diseases (11 papers) and Metabolism and Genetic Disorders (11 papers). Namik Kaya collaborates with scholars based in Saudi Arabia, United States and United Kingdom. Namik Kaya's co-authors include Dilek Çolak, Scott Herness, Shao‐gang Lu, Tiansheng Shen, Fangli Zhao, Albandary AlBakheet, Mohammed Al‐Owain, Brian F. Meyer, Yu Cao and Banan Al‐Younes and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Neuroscience.

In The Last Decade

Namik Kaya

78 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Namik Kaya Saudi Arabia 23 761 327 288 266 202 83 1.6k
Dirk Prawitt Germany 26 1.2k 1.6× 302 0.9× 579 2.0× 393 1.5× 107 0.5× 49 2.0k
Leonardo Guasti United Kingdom 32 1.7k 2.3× 202 0.6× 407 1.4× 76 0.3× 390 1.9× 66 2.9k
Saida Ortolano Spain 22 824 1.1× 70 0.2× 135 0.5× 303 1.1× 178 0.9× 41 1.8k
Jean M. Camden United States 31 1.0k 1.3× 132 0.4× 165 0.6× 94 0.4× 484 2.4× 71 2.5k
Francesca Odoardi Germany 24 630 0.8× 38 0.1× 104 0.4× 116 0.4× 295 1.5× 39 2.9k
Gerald L. Stelmack Canada 23 1.2k 1.5× 53 0.2× 92 0.3× 102 0.4× 409 2.0× 33 1.9k
Xing‐Jun Liu China 18 630 0.8× 50 0.2× 151 0.5× 124 0.5× 279 1.4× 40 1.6k
Gijsbertus J. Pronk Netherlands 17 1.5k 2.0× 68 0.2× 131 0.5× 72 0.3× 290 1.4× 22 2.4k
Keizo Kasono Japan 22 784 1.0× 89 0.3× 214 0.7× 62 0.2× 261 1.3× 66 1.7k
Silvia Murillo‐Cuesta Spain 17 777 1.0× 52 0.2× 74 0.3× 379 1.4× 41 0.2× 31 1.7k

Countries citing papers authored by Namik Kaya

Since Specialization
Citations

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

Fields of papers citing papers by Namik Kaya

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Namik Kaya

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

All Works

20 of 20 papers shown
1.
Al‐Hassnan, Zuhair N., Mazhor Aldosary, Rawan Almass, et al.. (2024). A novel missense mutation in ISCA2 causes aberrant splicing and leads to multiple mitochondrial dysfunctions syndrome 4. Frontiers in Psychiatry. 15. 1428175–1428175.
2.
Salih, Mustafa A., Albandary AlBakheet, Rawan Almass, et al.. (2024). Case report: Clinical and genetic characterization of a novel ALDH7A1 variant causing pyridoxine-dependent epilepsy, developmental delay, and intellectual disability in two siblings. Frontiers in Psychiatry. 15. 1501238–1501238. 2 indexed citations
3.
Almass, Rawan, et al.. (2023). SHQ1-associated neurodevelopmental disorder: Report of the first homozygous variant in unrelated patients and review of the literature. Human Genome Variation. 10(1). 7–7. 3 indexed citations
4.
Aldhalaan, Hesham, Albandary AlBakheet, Moeen Al-Sayed, et al.. (2023). Clinical, radiological, and genetic characterization of SLC13A5 variants in Saudi families: Genotype phenotype correlation and brief review of the literature. Frontiers in Pediatrics. 10. 1051534–1051534. 2 indexed citations
5.
Al‐Rasheed, Maha, Mustafa A. Salih, Futwan Al‐Mohanna, et al.. (2022). Clinical, genetic, and functional characterization of the glycine receptor β-subunit A455P variant in a family affected by hyperekplexia syndrome. Journal of Biological Chemistry. 298(7). 102018–102018. 2 indexed citations
6.
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.
7.
8.
Salih, Mustafa A., Muddathir H. Hamad, Marco Savarese, et al.. (2021). Exome Sequencing Reveals Novel TTN Variants in Saudi Patients with Congenital Titinopathies. Genetic Testing and Molecular Biomarkers. 25(12). 757–764. 5 indexed citations
9.
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
10.
Faqeih, Eissa, Mohammed Al‐Owain, Dilek Çolak, et al.. (2014). Novel homozygous DEAF1 variant suspected in causing white matter disease, intellectual disability, and microcephaly. American Journal of Medical Genetics Part A. 164(6). 1565–1570. 12 indexed citations
11.
Kaya, Namik, Hesham Aldhalaan, Banan Al‐Younes, et al.. (2011). Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the CA8 gene, encoding carbonic anhydrase (CA) VIII. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(7). 826–834. 53 indexed citations
12.
Aldosari, Naji, Tarfa Alshidi, Dilek Çolak, et al.. (2011). 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. Molecular Cytogenetics. 4(1). 9–9. 8 indexed citations
13.
Al‐Owain, Mohammed, et al.. (2010). Novel intragenic deletion in OPHN1 in a family causing XLMR with cerebellar hypoplasia and distinctive facial appearance. Clinical Genetics. 79(4). 363–370. 24 indexed citations
14.
Al‐Owain, Mohammed, Namik Kaya, Hamad Alzaidan, et al.. (2010). Renal Failure Associated with APECED and Terminal 4q Deletion: Evidence of Autoimmune Nephropathy. Journal of Immunology Research. 2010(1). 586342–586342. 12 indexed citations
15.
Çolak, Dilek, Hesham Aldhalaan, Michael Nester, et al.. (2010). Genomic and transcriptomic analyses distinguish classic Rett and Rett-like syndrome and reveals shared altered pathways. Genomics. 97(1). 19–28. 18 indexed citations
16.
Al‐Owain, Mohammed, et al.. (2010). A novel mutation and first report of dilated cardiomyopathy in ALG6-CDG (CDG-Ic): a case report. Orphanet Journal of Rare Diseases. 5(1). 7–7. 28 indexed citations
17.
Çolak, Dilek, et al.. (2009). Left ventricular global transcriptional profiling in human end-stage dilated cardiomyopathy. Genomics. 94(1). 20–31. 45 indexed citations
18.
Kaya, Namik, Faiqa Imtiaz, Dilek Çolak, et al.. (2008). Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan disease. Genetics in Medicine. 10(9). 675–684. 17 indexed citations
19.
Kar, Sırrı, Namik Kaya, Esin Güven, & Zafer Karaer. (2006). Yeni Geliştirilen Tespit Kabı ile Ergin Arılarda Varroa Enfestasyonunun Belirlenmesi. Uludağ Arıcılık Dergisi. 2006(2). 5 indexed citations
20.

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Dirk Prawitt Breakdown of academic impact, for papers by Leonardo Guasti Breakdown of academic impact, for papers by Saida Ortolano Breakdown of academic impact, for papers by Jean M. Camden Breakdown of academic impact, for papers by Francesca Odoardi Breakdown of academic impact, for papers by Gerald L. Stelmack Breakdown of academic impact, for papers by Xing‐Jun Liu Breakdown of academic impact, for papers by Gijsbertus J. Pronk Breakdown of academic impact, for papers by Keizo Kasono Breakdown of academic impact, for papers by Silvia Murillo‐Cuesta
Rankless by CCL
2026