Namik Kaya

2.7k citations

83 papers · 1.6k indexed · h-index 23

Molecular Biology top 10%
Nutrition and Dietetics top 5%
Genetics top 10%
Sensory Systems top 1%
Cellular and Molecular Neuroscience top 10%

Co-authors: Dilek Çolak Tiansheng Shen Scott Herness Fangli Zhao Shao‐gang Lu Albandary AlBakheet Mohammed Al‐Owain Brian F. Meyer
Topics: Genetics and Neurodevelopmental Disorders (21 papers)Genomics and Rare Diseases (11 papers)Metabolism and Genetic Disorders (11 papers)
Cited by: Sensory Systems Nutrition and Dietetics Endocrine and Autonomic Systems
Journals: Proceedings of the National Academy of Sciences Journal of Biological Chemistry Journal of Neuroscience
Partner nations: Saudi Arabia United States United Kingdom

In The Last Decade

Namik Kaya

78 papers receiving 1.6k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	A novel missense mutation in ISCA2 causes aberrant splicing and leads to multiple mitochondrial dysfunctions syndrome 4 2024 ·Frontiers in Psychiatry ·Zuhair N. Al‐Hassnan,Mazhor Aldosary,(unknown),(unknown),Rawan Almass,(unknown),Saif Alshahrani,Albandary AlBakheet,Mohammad A. Al–Muhaizea,Robert W. Taylor,Dilek Çolak,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	SHQ1-associated neurodevelopmental disorder: Report of the first homozygous variant in unrelated patients and review of the literature 2023 ·Human Genome Variation ·(unknown),(unknown),Rawan Almass,Ali H. Alwadei,Maha H. Daghestani,Stefan T. Arold,Namik Kaya	3
4	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
5	Detailed genetic and clinical analysis of a novel de novo variant in HPRT1: Case report of a female patient from Saudi Arabia with Lesch–Nyhan syndrome 2023 ·Frontiers in Genetics ·Albandary AlBakheet,(unknown),(unknown),(unknown),Namik Kaya,Zuhair Rahbeeni	4
6	Clinical, genetic, and functional characterization of the glycine receptor β-subunit A455P variant in a family affected by hyperekplexia syndrome 2022 ·Journal of Biological Chemistry ·(unknown),Maha Al‐Rasheed,(unknown),(unknown),(unknown),Mustafa A. Salih,(unknown),Futwan Al‐Mohanna,Dilek Çolak,Victoria L. Harvey,Kirsten Harvey,Stefan T. Arold,Namik Kaya,Arnaud Ruiz	2
7	A Novel Homozygous Founder Variant of RTN4IP1 in Two Consanguineous Saudi Families 2022 ·Cells ·Mazhor Aldosary,Maysoon Alsagob,(unknown),(unknown),Stefan T. Arold,(unknown),(unknown),Rawan Almass,Albandary AlBakheet,(unknown),Alya Qari,Mysoon M. Al‐Ansari,Monika Oláhová,Saif Alshahrani,Moeenaldeen AlSayed,Dilek Çolak,Robert W. Taylor,Mohammed Al‐Owain,Namik Kaya	0
8	Exome Sequencing Reveals Novel TTN Variants in Saudi Patients with Congenital Titinopathies 2021 ·Genetic Testing and Molecular Biomarkers ·Mustafa A. Salih,Muddathir H. Hamad,Marco Savarese,Ibrahim A. Alorainy,(unknown),Hisham Alkhalidi,(unknown),Anoud Albader,(unknown),Maysoon Alsagob,Albandary AlBakheet,Dilek Çolak,Bjarne Udd,Namik Kaya	5
9	Novel homozygous DEAF1 variant suspected in causing white matter disease, intellectual disability, and microcephaly 2014 ·American Journal of Medical Genetics Part A ·Eissa Faqeih,Mohammed Al‐Owain,Dilek Çolak,(unknown),Yusra Alyafee,Mazhor Aldosary,Abdulaziz Alsaman,(unknown),(unknown),(unknown),Maha H. Daghestani,Namik Kaya	12
10	The clinical utility of molecular karyotyping for neurocognitive phenotypes in a consanguineous population 2014 ·Genetics in Medicine ·(unknown),Salma M. Wakil,Shamsa Anazi,Anas M. Alazami,Nisha Patel,Ranad Shaheen,Hanan E. Shamseldin,(unknown),(unknown),Mustafa A. Salih,Heba Y. El Khashab,Amal Y. Kentab,Mohammed N. Al-Nasser,Fahad A. Bashiri,Namik Kaya,Mais Hashem,Fowzan S. Alkuraya	11
11	Mutations in NALCN Cause an Autosomal-Recessive Syndrome with Severe Hypotonia, Speech Impairment, and Cognitive Delay 2013 ·The American Journal of Human Genetics ·Moeenaldeen AlSayed,Hamad Alzaidan,Albandary AlBakheet,(unknown),(unknown),Yusra Alyafee,Mazhor Aldosary,Alya Qari,Tarfa Al‐Sheddi,(unknown),(unknown),(unknown),Hindi Al‐Hindi,(unknown),Dilek Çolak,Namik Kaya	69
12	Induction of cell proliferation in old rat liver can reset certain gene expression levels characteristic of old liver to those associated with young liver 2012 ·AGE ·M. Azhar Chishti,Namik Kaya,(unknown),Falah Almohanna,Malcolm H. Goyns,Dilek Çolak	7
13	Autism Spectrum Disorder in a Child with Propionic Acidemia 2012 ·JIMD Reports ·Mohammed Al‐Owain,Namik Kaya,(unknown),Albandary AlBakheet,Alya Qari,(unknown),Mohammad Ghaziuddin	51
14	Renal Failure Associated with APECED and Terminal 4q Deletion: Evidence of Autoimmune Nephropathy 2010 ·Journal of Immunology Research ·Mohammed Al‐Owain,Namik Kaya,Hamad Alzaidan,Ibrahim Hussain,(unknown),Hindi Al‐Hindi,Shelley Kennedy,M. Anwar Iqbal,Hamad Al‐Mojalli,Albandary AlBakheet,Anne Puel,Jean‐Laurent Casanova,Saleh Al‐Muhsen	12
15	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
16	Left ventricular global transcriptional profiling in human end-stage dilated cardiomyopathy 2009 ·Genomics ·Dilek Çolak,Namik Kaya,(unknown),(unknown),(unknown),Editha Andres,John Quackenbush,Nduna Dzimiri	45
17	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
18	Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome 2008 ·The American Journal of Human Genetics ·Anas M. Alazami,Amr Al‐Saif,Abdulaziz Alsemari,Saeed Bohlega,Soumaya Zlitni,Fatema Alzahrani,Prashant Bavi,Namik Kaya,Dilek Çolak,Hanif Khalak,(unknown),Borut Peterlin,Sumita Danda,Kailash P. Bhatia,Susanne A. Schneider,Nadia Sakati,Christopher A. Walsh,Futwan Al‐Mohanna,Brian F. Meyer,Fowzan S. Alkuraya	94
19	Yeni Geliştirilen Tespit Kabı ile Ergin Arılarda Varroa Enfestasyonunun Belirlenmesi 2006 ·Uludağ Arıcılık Dergisi ·Sırrı Kar,Namik Kaya,Esin Güven,Zafer Karaer	5
20	İzmir ilinde enginarlarda zarar yapan Enginar kurdu Phragmacossia albida (Erschov), (Lepidoptera, Cossidae)'nın savaş yöntemleri üzerinde araştırmalar 1982 ·Turkish Journal of Entomology ·Namik Kaya,(unknown),(unknown)	1

About Namik Kaya

Namik Kaya is a scholar working on Clinical Biochemistry, Genetics and Sensory Systems, having authored 83 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (21 papers), Genomics and Rare Diseases (11 papers) and Metabolism and Genetic Disorders (11 papers). The work is most often cited by research in Sensory Systems (266 citations), Nutrition and Dietetics (327 citations) and Endocrine and Autonomic Systems (120 citations). Namik Kaya has collaborated with scholars based in Saudi Arabia, United States and United Kingdom. Frequent co-authors include Dilek Çolak, Tiansheng Shen, Scott Herness, Fangli Zhao, Shao‐gang Lu, Albandary AlBakheet, Mohammed Al‐Owain, Brian F. Meyer, Yu Cao and Banan Al‐Younes. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Neuroscience.

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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