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Rachel H. Giles
Rachel H. Giles
University Medical Center Utrecht
Verified email at umcutrecht.nl
Title
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Cited by
Year
Caught up in a Wnt storm: Wnt signaling in cancer
RH Giles, JH Van Es, H Clevers
Biochimica et Biophysica Acta (BBA)-Reviews on Cancer 1653 (1), 1-24, 2003
19382003
Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP
F Petrif, RH Giles, HG Dauwerse, JJ Saris, R Hennekam, M Masuno, ...
Nature 376 (6538), 348-351, 1995
14131995
Mutations in the APC tumour suppressor gene cause chromosomal instability
R Fodde, J Kuipers, C Rosenberg, R Smits, M Kielman, C Gaspar, ...
Nature cell biology 3 (4), 433-438, 2001
9142001
European association of urology guidelines on renal cell carcinoma: the 2019 update
B Ljungberg, L Albiges, Y Abu-Ghanem, K Bensalah, S Dabestani, ...
European urology 75 (5), 799-810, 2019
8972019
Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways
L Sang, JJ Miller, KC Corbit, RH Giles, MJ Brauer, EA Otto, LM Baye, ...
Cell 145 (4), 513-528, 2011
5722011
Conjunction dysfunction: CBP/p300 in human disease
RH Giles, DJM Peters, MH Breuning
Trends in Genetics 14 (5), 178-183, 1998
5331998
Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling
M Chaki, R Airik, AK Ghosh, RH Giles, R Chen, GG Slaats, H Wang, ...
Cell 150 (3), 533-548, 2012
3612012
Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy
EA Otto, TW Hurd, R Airik, M Chaki, W Zhou, C Stoetzel, SB Patil, S Levy, ...
Nature genetics 42 (10), 840-850, 2010
3512010
Genetic analysis of von Hippel‐Lindau disease
M Nordstrom‐O'Brien, RB van der Luijt, E van Rooijen, ...
Human mutation 31 (5), 521-537, 2010
2972010
Genetic, environmental, and epigenetic factors involved in CAKUT
N Nicolaou, KY Renkema, EMHF Bongers, RH Giles, NVAM Knoers
Nature Reviews Nephrology 11 (12), 720-731, 2015
2352015
FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair
W Zhou, EA Otto, A Cluckey, R Airik, TW Hurd, M Chaki, K Diaz, FP Lach, ...
Nature genetics 44 (8), 910-915, 2012
2272012
Human embryonic mesenchymal stem cell-derived conditioned medium rescues kidney function in rats with established chronic kidney disease
A van Koppen, JA Joles, BWM van Balkom, SK Lim, D de Kleijn, RH Giles, ...
PloS one 7 (6), e38746, 2012
2092012
Functional aspects of primary cilia in signaling, cell cycle and tumorigenesis
SG Basten, RH Giles
Cilia 2 (1), 1-23, 2013
1972013
An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes
G Wheway, M Schmidts, DA Mans, K Szymanska, TMT Nguyen, H Racher, ...
Nature cell biology 17 (8), 1074-1087, 2015
1952015
Updated European Association of Urology Guidelines: recommendations for the treatment of first-line metastatic clear cell renal cancer
T Powles, L Albiges, M Staehler, K Bensalah, S Dabestani, RH Giles, ...
European urology 73 (3), 311-315, 2018
1892018
An organelle-specific protein landscape identifies novel diseases and molecular mechanisms
K Boldt, J Van Reeuwijk, Q Lu, K Koutroumpas, TMT Nguyen, Y Texier, ...
Nature communications 7 (1), 1-13, 2016
1882016
The many faces of the tumor suppressor gene APC
JH van Es, RH Giles, HC Clevers
Experimental cell research 264 (1), 126-134, 2001
1822001
EAU guidelines on renal cell carcinoma
B Ljungberg, L Albiges, K Bensalah, A Bex, RH Giles, M Hora, MA Kuczyk, ...
European Association of Urology, 2020
1682020
Updated European Association of Urology guidelines on renal cell carcinoma: immune checkpoint inhibition is the new backbone in first-line treatment of metastatic clear-cell …
L Albiges, T Powles, M Staehler, K Bensalah, RH Giles, M Hora, ...
European urology 76 (2), 151-156, 2019
1642019
Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutations
F Petrij, HG Dauwerse, RI Blough, RH Giles, JJ van der Smagt, ...
Journal of medical genetics 37 (3), 168-176, 2000
1442000
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