受强制性开放获取政策约束的文章 - Verena Heinrich了解详情
可在其他位置公开访问的文章：22 篇
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
强制性开放获取政策： US Department of Energy, Swiss National Science Foundation, US National …
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
强制性开放获取政策： German Research Foundation
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
强制性开放获取政策： European Commission
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
强制性开放获取政策： Swiss National Science Foundation, US National Institutes of Health, German …
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
强制性开放获取政策： US Department of Energy, Swiss National Science Foundation, US National …
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
强制性开放获取政策： Swiss National Science Foundation, US National Institutes of Health, German …
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
强制性开放获取政策： US National Institutes of Health, German Research Foundation, Wellcome Trust
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
强制性开放获取政策： Swiss National Science Foundation, German Research Foundation
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
强制性开放获取政策： German Research Foundation
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
强制性开放获取政策： German Research Foundation
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
强制性开放获取政策： Swiss National Science Foundation, German Research Foundation, Wellcome Trust
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
强制性开放获取政策： US Department of Energy, Swiss National Science Foundation, US National …
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
强制性开放获取政策： German Research Foundation
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
强制性开放获取政策： US National Institutes of Health, German Research Foundation
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
强制性开放获取政策： US National Institutes of Health, German Research Foundation
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
强制性开放获取政策： German Research Foundation
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
强制性开放获取政策： German Research Foundation
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
强制性开放获取政策： Federal Ministry of Education and Research, Germany
A likelihood ratio-based method to predict exact pedigrees for complex families from next-generation sequencing data
V Heinrich, T Kamphans, S Mundlos, PN Robinson, PM Krawitz
Bioinformatics 33 (1), 72-78, 2017
强制性开放获取政策： German Research Foundation
Position effects at the FGF8 locus are associated with femoral hypoplasia
M Socha, A Sowińska-Seidler, US Melo, BK Kragesteen, M Franke, ...
The American Journal of Human Genetics 108 (9), 1725-1734, 2021
强制性开放获取政策： German Research Foundation, European Commission, Government of Spain …
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