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Namik Kaya

Observed names: Kaya Namik, Kaya, Namik, N Kaya, N. Kaya
ORCID: 0000-0001-8912-7507
Observed ORCID: 0000-0001-8912-7507
OpenAlex ID: A5089367252
Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families
2014 · Anas M. Alazami, Nisha Patel, et al. · Cell Reports · 474
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Age-Specific Gene Expression Signatures for Breast Tumors and Cross-Species Conserved Potential Cancer Progression Markers in Young Women
2013 · Dilek Colak, Asmaa Nofal, et al. · PLoS ONE · 148
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Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome
2008 · Anas M. Alazami, Amr Al-Saif, et al. · The American Journal of Human Genetics · 140
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Expression and Physiological Actions of Cholecystokinin in Rat Taste Receptor Cells
2002 · Scott Herness, Fang-li Zhao, et al. · Journal of Neuroscience · 123
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Mutations in NALCN Cause an Autosomal-Recessive Syndrome with Severe Hypotonia, Speech Impairment, and Cognitive Delay
2013 · Moeenaldeen D. Al-Sayed, Hamad Al-Zaidan, et al. · The American Journal of Human Genetics · 120
A paracrine signaling role for serotonin in rat taste buds: expression and localization of serotonin receptor subtypes
2004 · Namik Kaya, Tiansheng Shen, et al. · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · 112
ISCA2 mutation causes infantile neurodegenerative mitochondrial disorder
2014 · Zuhair N Al-Hassnan, Mazhor Al-Dosary, et al. · Journal of Medical Genetics · 104
A novel X‐linked disorder with developmental delay and autistic features
2011 · Namik Kaya, Dilek Colak, et al. · Annals of Neurology · 77
Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the CA8 gene, encoding carbonic anhydrase (CA) VIII
2011 · Namik Kaya, Hesham Aldhalaan, et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 68
Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases
2019 · Elena Perenthaler, Anita Nikoncuk, et al. · Acta Neuropathologica · 67
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Autism Spectrum Disorder in a Child with Propionic Acidemia
2012 · M. Al-Owain, N. Kaya, et al. · JIMD Reports · 67
Comparison of two dependent within subject coefficients of variation to evaluate the reproducibility of measurement devices
2008 · Mohamed M Shoukri, Dilek Colak, et al. · BMC Medical Research Methodology · 59
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Molecular and clinical spectra of FBXL4 deficiency
2017 · Ayman W. El-Hattab, Hongzheng Dai, et al. · Human Mutation · 57
Integrated Left Ventricular Global Transcriptome and Proteome Profiling in Human End-Stage Dilated Cardiomyopathy
2016 · Dilek Colak, Ayodele A. Alaiya, et al. · PLoS ONE · 57
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p16INK4A Positively Regulates Cyclin D1 and E2F1 through Negative Control of AUF1
2011 · Huda H. Al-Khalaf, Dilek Colak, et al. · PLoS ONE · 54
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Left ventricular global transcriptional profiling in human end-stage dilated cardiomyopathy
2009 · Dilek Colak, Namik Kaya, et al. · Genomics · 54
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Bi-allelic variants in HOPS complex subunit VPS41 cause cerebellar ataxia and abnormal membrane trafficking
2021 · Leslie E Sanderson, Kristina Lanko, et al. · Brain · 53
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METTL23, a transcriptional partner of GABPA, is essential for human cognition
2014 · Rachel E. Reiff, Bassam R. Ali, et al. · Human Molecular Genetics · 46
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Novel intragenic deletion in OPHN1 in a family causing XLMR with cerebellar hypoplasia and distinctive facial appearance
2010 · M Al-Owain, N Kaya, et al. · Clinical Genetics · 40
Clinical and biochemical features associated with BCS1L mutation
2012 · Mohammed Al‐Owain, Dilek Colak, et al. · Journal of Inherited Metabolic Disease · 39
A novel deletion of theMEN1gene in a large family of multiple endocrine neoplasia type 1 (MEN1) with aggressive phenotype: MEN1deletion inMEN1syndrome
2011 · Hussein Raef, Minjing Zou, et al. · Clinical Endocrinology · 37
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Breast stromal fibroblasts from histologically normal surgical margins are pro‐carcinogenic
2013 · Maha A Al‐Rakan, Dilek Colak, et al. · The Journal of Pathology · 36
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Novel mutation in GLRB in a large family with hereditary hyperekplexia
2011 · M Al‐Owain, D Colak, et al. · Clinical Genetics · 36
A novel mutation and first report of dilated cardiomyopathy in ALG6-CDG (CDG-Ic): a case report
2010 · Mohammed Al-Owain, Sarar Mohamed, et al. · Orphanet Journal of Rare Diseases · 36
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Integrative and comparative genomics analysis of early hepatocellular carcinoma differentiated from liver regeneration in young and old
2010 · Dilek Colak, Muhammad A Chishti, et al. · Molecular Cancer · 34
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Works count: 118
Citation count: 3,156
H-index: 30
I10-index: 72
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