Stefan Mundlos

Stefan Mundlos

Max-Planck-Institut für molekulare Genetik - La Palma / Germany
Medical and Health Sciences / Medical Genetics
AD Scientific Index ID: 4431384
Max Planck Institute for Molecular Genetics
person_outline Stefan Mundlos's MOST POPULAR ARTICLES
1-) Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone developmentF Otto, AP Thornell, T Crompton, A Denzel, KC Gilmour, IR Rosewell, ...Cell 89 (5), 765-771, 199734421997
2-) The single-cell transcriptional landscape of mammalian organogenesisJ Cao, M Spielmann, X Qiu, X Huang, DM Ibrahim, AJ Hill, F Zhang, ...Nature 566 (7745), 496-502, 201919072019
3-) Disruptions of topological chromatin domains cause pathogenic rewiring of gene-enhancer interactionsDG Lupiáñez, K Kraft, V Heinrich, P Krawitz, F Brancati, E Klopocki, ...Cell 161 (5), 1012-1025, 201518982015
4-) Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasiaS Mundlos, F Otto, C Mundlos, JB Mulliken, AS Aylsworth, S Albright, ...Cell 89 (5), 773-779, 199719181997
5-) The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary diseasePN Robinson, S Köhler, S Bauer, D Seelow, D Horn, S MundlosThe American Journal of Human Genetics 83 (5), 610-615, 200810662008