Stefan F Pinter

Scopus Author ID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2015-2023
Publications (10 Years): 6

Top Topics

Children With Cerebral Palsy

Induced Pluripotent Stem Cells

Top Venues

Proceedings of the National Academy of Sciences of the United States of America

Nature structural & molecular biology

Nature communications

This page only lists publications with an associated author ORCID identifier.

Publications

Darcy T Ahern, Prakhar Bansal, Isaac V Faustino, Heather R Glatt-Deeley, Yuvabharath Kondaveeti, Erin C Banda, Stefan F Pinter
Isogenic hiPSC models of Turner syndrome reveal shared roles of inactive X and Y in the human cranial neural crest network. bioRxiv : the preprint server for biology (2023)
Darcy T Ahern, Prakhar Bansal, Maria K Armillei, Isaac V Faustino, Yuvabharath Kondaveeti, Heather R Glatt-Deeley, Erin C Banda, Stefan F Pinter
Monosomy X in isogenic human iPSC-derived trophoblast model impacts expression modules preserved in human placenta. Proceedings of the National Academy of Sciences of the United States of America 119 (40) (2022)
Moritz Bauer, Enrique Vidal, Eduard Zorita, Nil Üresin, Stefan F Pinter, Guillaume J Filion, Bernhard Payer
Chromosome compartments on the inactive X guide TAD formation independently of transcription during X-reactivation. Nature communications 12 (1) (2021)
Andrej J Savol, Peggy I Wang, Yesu Jeon, David Colognori, Eda Yildirim, Stefan F Pinter, Bernhard Payer, Jeannie T Lee, Ruslan I Sadreyev
Genome-wide identification of autosomal genes with allelic imbalance of chromatin state. PloS one 12 (8) (2017)
Hsueh-Ping Chu, John E Froberg, Barry Kesner, Hyun Jung Oh, Fei Ji, Ruslan Sadreyev, Stefan F Pinter, Jeannie T Lee
PAR-TERRA directs homologous sex chromosome pairing. Nature structural & molecular biology 24 (8) (2017)
Stefan F Pinter, David Colognori, Brian J Beliveau, Ruslan I Sadreyev, Bernhard Payer, Eda Yildirim, Chao-Ting Wu, Jeannie T Lee
Allelic Imbalance Is a Prevalent and Tissue-Specific Feature of the Mouse Transcriptome. Genetics 200 (2) (2015)