| Reactive glia in the injured brain acquire stem cell properties in response to sonic hedgehog S Sirko, G Behrendt, PA Johansson, P Tripathi, MR Costa, S Bek, ... Cell stem cell 12 (4), 426-439, 2013 | 340 | 2013 |
| Treatment of retinitis pigmentosa due to MERTK mutations by ocular subretinal injection of adeno-associated virus gene vector: results of a phase I trial NG Ghazi, EB Abboud, SR Nowilaty, H Alkuraya, A Alhommadi, H Cai, ... Human genetics 135 (3), 327-343, 2016 | 202 | 2016 |
| Novel CENPJ mutation causes Seckel syndrome MS Al-Dosari, R Shaheen, D Colak, FS Alkuraya Journal of medical genetics 47 (6), 411-414, 2010 | 178 | 2010 |
| Bidirectional crosstalk between PD-L1 expression and epithelial to mesenchymal transition: significance in claudin-low breast cancer cells A Alsuliman, D Colak, O Al-Harazi, H Fitwi, A Tulbah, T Al-Tweigeri, ... Molecular cancer 14 (1), 1-13, 2015 | 174 | 2015 |
| Gene expression profile classification: a review MH Asyali, D Colak, O Demirkaya, MS Inan Current Bioinformatics 1 (1), 55-73, 2006 | 172 | 2006 |
| PD‐L1 promotes OCT4 and Nanog expression in breast cancer stem cells by sustaining PI3K/AKT pathway activation S Almozyan, D Colak, F Mansour, A Alaiya, O Al‐Harazi, A Qattan, ... International journal of cancer 141 (7), 1402-1412, 2017 | 150 | 2017 |
| 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 | 139 | 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 | 130 | 2008 |
| 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 | 96 | 2015 |
| Mutation in PHC1 implicates chromatin remodeling in primary microcephaly pathogenesis S Awad, MS Al-Dosari, N Al-Yacoub, D Colak, MA Salih, FS Alkuraya, ... Human molecular genetics 22 (11), 2200-2213, 2013 | 96 | 2013 |
| The DNA replication program is altered at the FMR1 locus in fragile X embryonic stem cells J Gerhardt, MJ Tomishima, N Zaninovic, D Colak, Z Yan, Q Zhan, ... Molecular cell 53 (1), 19-31, 2014 | 87 | 2014 |
| 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 | 85 | 2013 |
| Loss of function mutation in LARP7, chaperone of 7SK ncRNA, causes a syndrome of facial dysmorphism, intellectual disability, and primordial dwarfism AM Alazami, M Al‐Owain, F Alzahrani, T Shuaib, H Al‐Shamrani, ... Human mutation 33 (10), 1429-1434, 2012 | 67 | 2012 |
| 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 | 67 | 2011 |
| 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 | 50 | 2011 |
| 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 | 46 | 2009 |
| Radar cross-section study of cylindrical cavity-backed apertures with outer or inner material coating: The case of E-polarization D Colak, AI Nosich, A Altintas IEEE transactions on antennas and propagation 41 (11), 1551-1559, 1993 | 46 | 1993 |
| Mutations in SMG9, Encoding an Essential Component of Nonsense-Mediated Decay Machinery, Cause a Multiple Congenital Anomaly Syndrome in Humans and … R Shaheen, S Anazi, T Ben-Omran, MZ Seidahmed, LB Caddle, K Palmer, ... The American Journal of Human Genetics 98 (4), 643-652, 2016 | 45 | 2016 |
| 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), 1-11, 2008 | 44 | 2008 |
| Radar cross-section study of cylindrical cavity-backed apertures with outer or inner material coating: the case of H-polarization D Colak, AI Nosich, A Altintas IEEE transactions on antennas and propagation 43 (5), 440-447, 1995 | 44 | 1995 |
