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Dilek Colak,PhD
Dilek Colak,PhD
Senior Scientist, KFSHRC
Verified email at kfshrc.edu.sa
Title
Cited by
Cited by
Year
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
3402013
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
2022016
Novel CENPJ mutation causes Seckel syndrome
MS Al-Dosari, R Shaheen, D Colak, FS Alkuraya
Journal of medical genetics 47 (6), 411-414, 2010
1782010
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
1742015
Gene expression profile classification: a review
MH Asyali, D Colak, O Demirkaya, MS Inan
Current Bioinformatics 1 (1), 55-73, 2006
1722006
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
1502017
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
1392013
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
1302008
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
962015
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
962013
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
872014
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
852013
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
672012
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
672011
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
502011
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
462009
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
461993
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
452016
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
442008
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
441995
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