| An integrated genetic linkage map of the soybean genome PB Cregan, T Jarvik, AL Bush, RC Shoemaker, KG Lark, AL Kahler, ... Crop science 39 (5), 1464-1490, 1999 | 1332 | 1999 |
| Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families AM Alazami, N Patel, HE Shamseldin, S Anazi, MS Al-Dosari, F Alzahrani, ... Cell reports 10 (2), 148-161, 2015 | 478 | 2015 |
| Age-specific gene expression signatures for breast tumors and cross-species conserved potential cancer progression markers in young women D Colak, A Nofal, AB AlBakheet, M Nirmal, H Jeprel, A Eldali, ... PloS one 8 (5), e63204, 2013 | 177 | 2013 |
| Mutations in C2orf37, encoding a nucleolar protein, cause hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome AM Alazami, A Al-Saif, A Al-Semari, S Bohlega, S Zlitni, F Alzahrani, ... The American Journal of Human Genetics 83 (6), 684-691, 2008 | 154 | 2008 |
| Comprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases Saudi Mendeliome Group falkuaya@ kfshrc. edu. sa Genome biology 16, 1-14, 2015 | 142 | 2015 |
| Expression and physiological actions of cholecystokinin in rat taste receptor cells S Herness, F Zhao, S Lu, N Kaya, T Shen Journal of Neuroscience 22 (22), 10018-10029, 2002 | 138 | 2002 |
| Expression, physiological action, and coexpression patterns of neuropeptide Y in rat taste-bud cells F Zhao, T Shen, N Kaya, S Lu, Y Cao, S Herness Proceedings of the National Academy of Sciences 102 (31), 11100-11105, 2005 | 130 | 2005 |
| A paracrine signaling role for serotonin in rat taste buds: expression and localization of serotonin receptor subtypes N Kaya, T Shen, S Lu, F Zhao, S Herness American Journal of Physiology-Regulatory, Integrative and Comparative …, 2004 | 124 | 2004 |
| Expression and localization of serotonin receptor subtypes in rat taste buds N Kaya, T Shen, SG Lu, FL Zhao, S Herness Am J Physiol 286, R649-R658, 2004 | 124* | 2004 |
| ISCA2 mutation causes infantile neurodegenerative mitochondrial disorder ZN Al-Hassnan, M Al-Dosary, M Alfadhel, EA Faqeih, M Alsagob, ... Journal of medical genetics 52 (3), 186-194, 2015 | 119 | 2015 |
| Mutations in NALCN cause an autosomal-recessive syndrome with severe hypotonia, speech impairment, and cognitive delay MD Al-Sayed, H Al-Zaidan, AB Albakheet, H Hakami, R Kenana, ... The American Journal of Human Genetics 93 (4), 721-726, 2013 | 114 | 2013 |
| Co-expression patterns of the neuropeptides vasoactive intestinal peptide and cholecystokinin with the transduction molecules α-gustducin and T1R2 in rat taste receptor cells T Shen, N Kaya, FL Zhao, SG Lu, Y Cao, S Herness Neuroscience 130 (1), 229-238, 2005 | 104 | 2005 |
| Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the CA8 gene, encoding carbonic anhydrase (CA) VIII N Kaya, H Aldhalaan, B Al‐Younes, D Colak, T Shuaib, F Al‐Mohaileb, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 …, 2011 | 73 | 2011 |
| An integrated genetic linkage map of the soybean genome N Kaya, TT VanToai, DG Lohnes, J Chung, JE Specht Crop Sci 39, 14641490Cregan, 1999 | 73 | 1999 |
| Autism spectrum disorder in a child with propionic acidemia M Al-Owain, N Kaya, H Al-Shamrani, A Al-Bakheet, A Qari, S Al-Muaigl, ... JIMD reports-case and research reports, 2012/4, 63-66, 2013 | 72 | 2013 |
| Adrenergic signalling between rat taste receptor cells S Herness, F Zhao, N Kaya, S Lu, T Shen, XD Sun The Journal of physiology 543 (2), 601-614, 2002 | 66 | 2002 |
| Left ventricular global transcriptional profiling in human end-stage dilated cardiomyopathy D Colak, N Kaya, J Al-Zahrani, A Al Bakheet, P Muiya, E Andres, ... Genomics 94 (1), 20-31, 2009 | 62 | 2009 |
| p16INK4A Positively Regulates Cyclin D1 and E2F1 through Negative Control of AUF1 HH Al-Khalaf, D Colak, M Al-Saif, A Al-Bakheet, SF Hendrayani, ... PloS one 6 (7), e21111, 2011 | 60 | 2011 |
| Comparison of two dependent within subject coefficients of variation to evaluate the reproducibility of measurement devices MM Shoukri, D Colak, N Kaya, A Donner BMC medical research methodology 8, 1-11, 2008 | 59 | 2008 |
| 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 E Perenthaler, A Nikoncuk, S Yousefi, WM Berdowski, M Alsagob, I Capo, ... Acta neuropathologica 139, 415-442, 2020 | 58 | 2020 |
Dilek Colak,PhDSenior Scientist, KFSHRCVerified email at kfshrc.edu.sa
