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The single-cell transcriptional landscape of mammalian organogenesis J Cao, M Spielmann, X Qiu, X Huang, DM Ibrahim, AJ Hill, F Zhang, ... Nature 566 (7745), 496-502, 2019 | 2864 | 2019 |
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 | 2187 | 2015 |
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Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13 Y Muragaki, S Mundlos, J Upton, BR Olsen Science 272 (5261), 548-551, 1996 | 704 | 1996 |
A high-resolution anatomical atlas of the transcriptome in the mouse embryo G Diez-Roux, S Banfi, M Sultan, L Geffers, S Anand, D Rozado, A Magen, ... PLoS biology 9 (1), e1000582, 2011 | 680 | 2011 |
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Structural variation in the 3D genome M Spielmann, DG Lupiáñez, S Mundlos Nature Reviews Genetics 19 (7), 453-467, 2018 | 659 | 2018 |
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Clinical diagnostics in human genetics with semantic similarity searches in ontologies S Köhler, MH Schulz, P Krawitz, S Bauer, S Dölken, CE Ott, C Mundlos, ... The American Journal of Human Genetics 85 (4), 457-464, 2009 | 564 | 2009 |
Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1 FS Kaplan, M Xu, P Seemann, JM Connor, DL Glaser, L Carroll, P Delai, ... Human mutation 30 (3), 379-390, 2009 | 487 | 2009 |
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Glucose/galactose malabsorption caused by a defect in the Na+/glucose cotransporter E Turk, B Zabel, S Mundlos, J Dyer, EM Wright Nature 350 (6316), 354-356, 1991 | 451 | 1991 |