Selected Publications

High-throughput functional analysis of lncRNA core promoters elucidates rules governing tissue specificity.
Mattioli K, Volders PJ, Gerhardinger C, Lee JC, Maass PG, Melé M, Rinn JL.
Genome Research. 2019 Mar;29(3):344-355.

Interchromosomal interactions: A genomic love story of kissing chromosomes.
Maass PG, Barutcu AR, Rinn JL.
Journal of Cell Biology. 2019 Jan 7;218(1):27-38. Review

Reorganization of inter-chromosomal interactions in the 2q37-deletion syndrome.
Maass PG, Weise A, Rittscher K, Lichtenwald J, Barutcu AR, Liehr T, Aydin A, Wefeld-Neuenfeld Y, Pölsler L, Tinschert S, Rinn JL, Luft FC, Bähring S.
EMBO Journal. 2018 Aug 1;37(15).

Inter-chromosomal Contact Properties in Live-Cell Imaging and in Hi-C.
Maass PG, Barutcu AR, Weiner CL, Rinn JL.
Molecular Cell. 2018 Mar 15;69(6):1039-1045.e3. Erratum in: Mol Cell. 2018 Apr 5;70(1):188-189.

Spatiotemporal allele organization by allele-specific CRISPR live-cell imaging (SNP-CLING).
Maass PG, Barutcu AR, Shechner DM, Weiner CL, Melé M, Rinn JL.
Nature Structure Molecular Biology. 2018 Feb;25(2):176-184.

PDE3A mutations cause autosomal dominant hypertension with brachydactyly.
Maass PG, Aydin A, Luft FC, Schächterle C, Weise A, Stricker S, Lindschau C, Vaegler M, Qadri F, Toka HR, Schulz H, Krawitz PM, Parkhomchuk D, Hecht J, Hollfinger I, Wefeld-Neuenfeld Y, Bartels-Klein E, Mühl A, Kann M, Schuster H, Chitayat D, Bialer MG, Wienker TF, Ott J, Rittscher K, Liehr T, Jordan J, Plessis G, Tank J, Mai K, Naraghi R, Hodge R, Hopp M, Hattenbach LO, Busjahn A, Rauch A, Vandeput F, Gong M, Rüschendorf F, Hübner N, Haller H, Mundlos S, Bilginturan N, Movsesian MA, Klussmann E, Toka O, Bähring S.
Nature Genetics. 2015 Jun;47(6):647-53. 

A misplaced lncRNA causes brachydactyly in humans.
Maass PG, Rump A, Schulz H, Stricker S, Schulze L, Platzer K, Aydin A, Tinschert S, Goldring MB, Luft FC, Bähring S.
Journal of Clinical Investigation. 2012 Nov;122(11):3990-4002.