| A murine ESC-like state facilitates transgenesis and homologous recombination in human pluripotent stem cells C Buecker, HH Chen, JM Polo, L Daheron, L Bu, TS Barakat, P Okwieka, ... Cell stem cell 6 (6), 535-546, 2010 | 275 | 2010 |
| RNF12 is an X-Encoded dose-dependent activator of X chromosome inactivation I Jonkers, TS Barakat, EM Achame, K Monkhorst, A Kenter, ... Cell 139 (5), 999-1011, 2009 | 264 | 2009 |
| RNF12 initiates X-chromosome inactivation by targeting REX1 for degradation C Gontan, EM Achame, J Demmers, TS Barakat, E Rentmeester, ... Nature 485 (7398), 386-390, 2012 | 231 | 2012 |
| Functional dissection of the enhancer repertoire in human embryonic stem cells TS Barakat, F Halbritter, M Zhang, AF Rendeiro, E Perenthaler, C Bock, ... Cell stem cell 23 (2), 276-288. e8, 2018 | 181 | 2018 |
| RNF12 Activates Xist and Is Essential for X Chromosome Inactivation TS Barakat, N Gunhanlar, C Gontan Pardo, EM Achame, M Ghazvini, ... PLoS genetics 7 (1), e1002001, 2011 | 175 | 2011 |
| Dynamics of gene silencing during X inactivation using allele-specific RNA-seq H Marks, HHD Kerstens, TS Barakat, E Splinter, RAM Dirks, G van Mierlo, ... Genome biology 16, 1-20, 2015 | 130 | 2015 |
| The why of YY1: mechanisms of transcriptional regulation by Yin Yang 1 TCJ Verheul, L van Hijfte, E Perenthaler, TS Barakat Frontiers in cell and developmental biology 8, 592164, 2020 | 104 | 2020 |
| RNF12 controls embryonic stem cell fate and morphogenesis in zebrafish embryos by targeting Smad7 for degradation L Zhang, H Huang, FF Zhou, J Schimmel, CG Pardo, T Zhang, TS Barakat, ... Molecular cell 46 (5), 650-661, 2012 | 95 | 2012 |
| The trans-activator RNF12 and cis-acting elements effectuate X chromosome inactivation independent of X-pairing TS Barakat, F Loos, S van Staveren, E Myronova, M Ghazvini, ... Molecular cell 53 (6), 965-978, 2014 | 85 | 2014 |
| International consensus recommendations on the diagnostic work-up for malformations of cortical development R Oegema, TS Barakat, M Wilke, K Stouffs, D Amrom, E Aronica, ... Nature Reviews Neurology 16 (11), 618-635, 2020 | 80 | 2020 |
| Beyond the exome: the non-coding genome and enhancers in neurodevelopmental disorders and malformations of cortical development E Perenthaler, S Yousefi, E Niggl, TS Barakat Frontiers in cellular neuroscience 13, 352, 2019 | 79 | 2019 |
| X-changing information on X inactivation TS Barakat, I Jonkers, K Monkhorst, J Gribnau Experimental cell research 316 (5), 679-687, 2010 | 68 | 2010 |
| X chromosome inactivation in the cycle of life TS Barakat, J Gribnau Development 139 (12), 2085-2089, 2012 | 66 | 2012 |
| Exome sequencing of a primary ovarian insufficiency cohort reveals common molecular etiologies for a spectrum of disease A Jolly, Y Bayram, S Turan, Z Aycan, T Tos, ZY Abali, B Hacihamdioglu, ... The Journal of Clinical Endocrinology & Metabolism 104 (8), 3049-3067, 2019 | 64 | 2019 |
| Stable X chromosome reactivation in female human induced pluripotent stem cells TS Barakat, M Ghazvini, B de Hoon, T Li, B Eussen, H Douben, ... Stem cell reports 4 (2), 199-208, 2015 | 64 | 2015 |
| SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females FC Radio, K Pang, A Ciolfi, MA Levy, A Hernández-García, L Pedace, ... The American Journal of Human Genetics 108 (3), 502-516, 2021 | 63 | 2021 |
| The pluripotency factor-bound intron 1 of Xist is dispensable for X chromosome inactivation and reactivation in vitro and in vivo A Minkovsky, TS Barakat, N Sellami, MH Chin, N Gunhanlar, J Gribnau, ... Cell reports 3 (3), 905-918, 2013 | 57 | 2013 |
| Defects in KCNJ16 cause a novel tubulopathy with hypokalemia, salt wasting, disturbed acid-base homeostasis, and sensorineural deafness KP Schlingmann, A Renigunta, EJ Hoorn, AL Forst, V Renigunta, ... Journal of the American Society of Nephrology 32 (6), 1498-1512, 2021 | 54 | 2021 |
| 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 | 51 | 2020 |
| REX1 is the critical target of RNF12 in imprinted X chromosome inactivation in mice C Gontan, H Mira-Bontenbal, A Magaraki, C Dupont, TS Barakat, ... Nature communications 9 (1), 4752, 2018 | 42 | 2018 |
