Max Planck Publications of Herrmann Lab

The following publications were published exclusively under the affiliation of the Max Planck Society. For publications by the principal investigator outside of the Max Planck Society, see the links on the lower left.

Journal Article (5)

Journal Article

Kragesteen , B. K.; Spielmann, M.; Paliou, C.; Heinrich, V.; Schöpflin, R.; Esposito, A.; Annunziatella, C.; Bianco , S.; Chiariello, A. M.; Jerković , I. et al.; Harabula, I.; Guckelberger, P.; Pechstein, M.; Wittler, L.; Chan, W.-L.; Franke, M.; Lupiáñez , D. G.; Kraft, K.; Timmermann, B.; Vingron, M.; Visel, A.; Nicodemi, M.; Mundlos, S.; Andrey, G.: Dynamic 3D chromatin architecture determines enhancer specificity and morphogenetic identity in limb development. Nature Genetics 50 (10), pp. 1463 - 1473 (2018)

MPG.PuRe

DOI

publisher-version

supplementary-material

Journal Article

Flöttmann, R.; Kragesteen, B. K.; Geuer, S.; Socha, M.; Allou, L.; Sowińska-Seidler, A.; Bosquillon de Jarcy, L.; Wagner, J.; Jamsheer, A.; Oehl-Jaschkowitz, B. et al.; Wittler, L.; de Silva, D.; Kurth, I.; Maya, I.; Santos-Simarro, F.; Hülsemann, W.; Klopocki, E.; Mountford, R.; Fryer, A.; Borck, G.; Horn, D.; Lapunzina, P.; Wilson, M.; Mascrez, B.; Duboule, D.; Mundlos, S.; Spielmann, M.: Noncoding copy-number variations are associated with congenital limb malformation. GENETICS IN MEDICINE 20 (6), pp. 599 - 607 (2018)

MPG.PuRe

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publisher-version

Journal Article

Bianco, S.; Lupiáñez, D. G.; Chiariello, A. M.; Annunziatella, C.; Kraft, K.; Schöpflin, R.; Wittler, L.; Andrey, G.; Vingron, M.; Pombo, A. et al.; Mundlos, S.; Nicodemi, M.: Polymer physics predicts the effects of structural variants on chromatin architecture. Nature Genetics 50 (5), pp. 662 - 667 (2018)

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publisher-version

Journal Article

Weitensteiner, V.; Zhang, R.; Bungenberg, J.; Marks, M.; Gehlen, J.; Ralser, D. J.; Hilger, A. C.; Sharma, A.; Schumacher , J.; Gembruch, U. et al.; Merz, W. M.; Becker, A.; Altmüller, J.; Thiele, H.; Herrmann, B. G.; Odermatt , B.; Ludwig, M.; Reutter, H.: Exome sequencing in syndromic brain malformations identifies novel mutations in ACTB, and SLC9A6, and suggests BAZ1A as a new candidate gene. Birth Defects Research 110 (7), pp. 587 - 597 (2018)

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Journal Article

Beisaw, A.; Tsaytler, P.; Koch, F.; Schmitz, S. U.; Melissari, M.-T.; Senf, A. D.; Wittler, L.; Pennimpede, T.; Macura, K.; Herrmann, B. G. et al.; Grote, P.: BRACHYURY directs histone acetylation to target loci during mesoderm development. EMBO Reports 19 (1), pp. 118 - 134 (2018)

MPG.PuRe

DOI

publisher-version