Tahsin Stefan Barakat

Author

Also Known As

Anna Hau, Barakat, Tahsin Stefan, Grazia M. S. Mancini, Stefan Barakat, T Barakat, T S Barakat, T. Barakat, T.S. Barakat, Tahsin Stefan Barakat, Tahsin Stefan Barakat

155

Publications

3.5K

Citations

H-Index

Concepts

All Affiliations

Erasmus MC Radboud University Nijmegen Radboud University Medical Center Inserm University College London

About

Tahsin Stefan Barakat is an author at Erasmus MC specializing in medicine, genetics, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	24	1.5K
2	Health Sciences	1	1	220
3	Natural Sciences	1	1	13
4	Public Health	1	1	22
5	Social Sciences	1	1	29

Tahsin Stefan Barakat

Publications

2.7K

Citations

H-Index

Page 1

	Year	Citations
RNF12 Is an X-Encoded Dose-Dependent Activator of X Chromosome Inactivation Iris H. Jonkers, Tahsin Stefan Barakat, Eskeatnaf Mulugeta, Cell ChromatinTranscriptional RegulationGenome InstabilityChromosome BiologyX Chromosome Inactivation	2009	229
RNF12 initiates X-chromosome inactivation by targeting REX1 for degradation Cristina Gontan, Eskeatnaf Mulugeta, Jeroen Demmers, Nature Genome InstabilityTranscriptional RegulationGeneticsChromosome BiologyX-chromosome Inactivation	2012	223
Functional Dissection of the Enhancer Repertoire in Human Embryonic Stem Cells Tahsin Stefan Barakat, Florian Halbritter, Man Zhang, Cell stem cell	2018	221
A Murine ESC-like State Facilitates Transgenesis and Homologous Recombination in Human Pluripotent Stem Cells Christa Buecker, Hsu-Hsin Chen, José M. Polo, Cell stem cell Induced Pluripotent Stem CellDevelopmental BiologyMedicineHomologous RecombinationStem Cells	2010	220
RNF12 Activates Xist and Is Essential for X Chromosome Inactivation Tahsin Stefan Barakat, Nilhan Gunhanlar, Cristina Gontan, PLoS Genetics	2011	145
Dynamics of gene silencing during X inactivation using allele-specific RNA-seq Hendrik Marks, Hindrik H. D. Kerstens, Tahsin Stefan Barakat, Genome biology	2015	139
RNF12 Controls Embryonic Stem Cell Fate and Morphogenesis in Zebrafish Embryos by Targeting Smad7 for Degradation Long Zhang, Huizhe Huang, Fangfang Zhou, Molecular Cell Developmental BiologySignaling PathwayMedicineZebrafish EmbryosStem Cell Research	2012	95
SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females Francesca Clementina Radio, Kaifang Pang, Andrea Ciolfi, The American Journal of Human Genetics Down SyndromeDeletion SyndromeDevelopmental BiologyGenetic DisorderGenetics	2021	80
The Trans-Activator RNF12 and Cis-Acting Elements Effectuate X Chromosome Inactivation Independent of X-Pairing Tahsin Stefan Barakat, Friedemann Loos, Selma van Staveren, Molecular Cell ChromatinGenome InstabilityTranscriptional RegulationChromatin StructureGenetics	2014	76
Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease Angad Jolly, Yavuz Bayram, Serap Turan, The Journal of Clinical Endocrinology & Metabolism	2019	75

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