Verena Heinrich
Verena Heinrich
Verified email at
Cited by
Cited by
Disruptions of topological chromatin domains cause pathogenic rewiring of gene-enhancer interactions
DG Lupiáñez, K Kraft, V Heinrich, P Krawitz, F Brancati, E Klopocki, ...
Cell 161 (5), 1012-1025, 2015
Formation of new chromatin domains determines pathogenicity of genomic duplications
M Franke, DM Ibrahim, G Andrey, W Schwarzer, V Heinrich, R Schöpflin, ...
Nature 538 (7624), 265-269, 2016
Efficient CRISPR/Cas9 genome editing with low off-target effects in zebrafish
A Hruscha, P Krawitz, A Rechenberg, V Heinrich, J Hecht, C Haass, ...
Development 140 (24), 4982-4987, 2013
Composition and dosage of a multipartite enhancer cluster control developmental expression of Ihh (Indian hedgehog)
AJ Will, G Cova, M Osterwalder, WL Chan, L Wittler, N Brieske, V Heinrich, ...
Nature genetics 49 (10), 1539-1545, 2017
Dynamic 3D chromatin architecture contributes to enhancer specificity and limb morphogenesis
BK Kragesteen, M Spielmann, C Paliou, V Heinrich, R Schöpflin, ...
Nature genetics 50 (10), 1463-1473, 2018
Preformed chromatin topology assists transcriptional robustness of Shh during limb development
C Paliou, P Guckelberger, R Schöpflin, V Heinrich, A Esposito, ...
Proceedings of the National Academy of Sciences 116 (25), 12390-12399, 2019
Characterization of hundreds of regulatory landscapes in developing limbs reveals two regimes of chromatin folding
G Andrey, R Schöpflin, I Jerković, V Heinrich, DM Ibrahim, C Paliou, ...
Genome research 27 (2), 223-233, 2017
Enhancer hijacking determines extrachromosomal circular MYCN amplicon architecture in neuroblastoma
K Helmsauer, ME Valieva, S Ali, R Chamorro González, R Schöpflin, ...
Nature communications 11 (1), 5823, 2020
Serial genomic inversions induce tissue-specific architectural stripes, gene misexpression and congenital malformations
K Kraft, A Magg, V Heinrich, C Riemenschneider, R Schöpflin, ...
Nature cell biology 21 (3), 305-310, 2019
Hi-C identifies complex genomic rearrangements and TAD-shuffling in developmental diseases
US Melo, R Schöpflin, R Acuna-Hidalgo, MA Mensah, B Fischer-Zirnsak, ...
The American Journal of Human Genetics 106 (6), 872-884, 2020
Non-coding deletions identify Maenli lncRNA as a limb-specific En1 regulator
L Allou, S Balzano, A Magg, M Quinodoz, B Royer-Bertrand, R Schöpflin, ...
Nature 592 (7852), 93-98, 2021
The allele distribution in next-generation sequencing data sets is accurately described as the result of a stochastic branching process
V Heinrich, J Stange, T Dickhaus, P Imkeller, U Krüger, S Bauer, ...
Nucleic acids research 40 (6), 2426-2431, 2012
Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndrome
N Ehmke, A Caliebe, R Koenig, SG Kant, Z Stark, V Cormier-Daire, ...
The American Journal of Human Genetics 95 (6), 763-770, 2014
Filtering for compound heterozygous sequence variants in non-consanguineous pedigrees
T Kamphans, P Sabri, N Zhu, V Heinrich, S Mundlos, PN Robinson, ...
PLoS One 8 (8), e70151, 2013
The mole genome reveals regulatory rearrangements associated with adaptive intersexuality
F M. Real, SA Haas, P Franchini, P Xiong, O Simakov, H Kuhl, R Schöpflin, ...
Science 370 (6513), 208-214, 2020
Screening for single nucleotide variants, small indels and exon deletions with a next‐generation sequencing based gene panel approach for U sher syndrome
PM Krawitz, D Schiska, U Krüger, S Appelt, V Heinrich, D Parkhomchuk, ...
Molecular genetics & genomic medicine 2 (5), 393-401, 2014
Estimating exome genotyping accuracy by comparing to data from large scale sequencing projects
V Heinrich, T Kamphans, J Stange, D Parkhomchuk, J Hecht, T Dickhaus, ...
Genome Medicine 5, 1-11, 2013
Somatic neurofibromatosis type 1 (NF1) inactivation events in cutaneous neurofibromas of a single NF1 patient
D Emmerich, T Zemojtel, J Hecht, P Krawitz, M Spielmann, J Kühnisch, ...
European Journal of Human Genetics 23 (6), 870-873, 2015
Strategisches Umweltcontrolling mit Hilfe der Balanced Scorecard
M Fahrbach, V Heinrich, R Pfitzner
UmweltWirtschaftsForum 8 (2), 41-44, 2000
CRUP: a comprehensive framework to predict condition-specific regulatory units
A Ramisch, V Heinrich, LV Glaser, A Fuchs, X Yang, P Benner, ...
Genome biology 20, 1-23, 2019
The system can't perform the operation now. Try again later.
Articles 1–20