Theo dõi
Verena Heinrich
Verena Heinrich
Email được xác minh tại molgen.mpg.de
Tiêu đề
Trích dẫn bởi
Trích dẫn bởi
Năm
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
20752015
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
6752016
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
5802013
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
190*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
1702018
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
1392019
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
1372017
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
1272020
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
1172019
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
1062020
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
892021
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
552012
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
512014
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
512013
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
462020
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
362014
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
322013
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
262015
Strategisches Umweltcontrolling mit Hilfe der Balanced Scorecard
M Fahrbach, V Heinrich, R Pfitzner
UmweltWirtschaftsForum 8 (2), 41-44, 2000
262000
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
252019
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