| Clusters of iron-rich cells in the upper beak of pigeons are macrophages not magnetosensitive neurons CD Treiber, MC Salzer, J Riegler, N Edelman, C Sugar, M Breuss, ... Nature 484 (7394), 367-370, 2012 | 216 | 2012 |
| Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities M Breuss*, JIT Heng*, K Poirier, G Tian, XH Jaglin, Z Qu, A Braun, ... Cell reports 2 (6), 1554-1562, 2012 | 198 | 2012 |
| Autism risk in offspring can be assessed through quantification of male sperm mosaicism MW Breuss, D Antaki, RD George, M Kleiber, KN James, LL Ball, O Hong, ... Nature Medicine 26 (1), 143-150, 2020 | 93 | 2020 |
| Tubulins and brain development–The origins of functional specification MW Breuss, I Leca, T Gstrein, AH Hansen, DA Keays Molecular and Cellular Neuroscience 84, 58-67, 2017 | 86 | 2017 |
| Mutations in either TUBB or MAPRE2 cause circumferential skin creases Kunze type M Isrie, M Breuss, G Tian, AH Hansen, F Cristofoli, J Morandell, ... The American Journal of Human Genetics 97 (6), 790-800, 2015 | 83 | 2015 |
| Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration AE Schaffer, MW Breuss, AO Caglayan, N Al-Sanaa, HY Al-Abdulwahed, ... Nature genetics 50 (8), 1093-1101, 2018 | 70 | 2018 |
| Microtubules and neurodevelopmental disease: the movers and the makers M Breuss, DA Keays Cellular and molecular control of neuronal migration, 75-96, 2014 | 70 | 2014 |
| Autosomal-recessive mutations in the tRNA splicing endonuclease subunit TSEN15 cause pontocerebellar hypoplasia and progressive microcephaly MW Breuss, T Sultan, KN James, RO Rosti, E Scott, D Musaev, B Furia, ... The American Journal of Human Genetics 99 (1), 228-235, 2016 | 66 | 2016 |
| Mutations in MAST1 cause mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations R Tripathy, I Leca, T van Dijk, J Weiss, BW van Bon, MC Sergaki, ... Neuron 100 (6), 1354-1368. e5, 2018 | 44 | 2018 |
| Tuba8 is expressed at low levels in the developing mouse and human brain A Braun, M Breuss, MC Salzer, J Flint, NJ Cowan, DA Keays The American Journal of Human Genetics 86 (5), 819-822, 2010 | 42 | 2010 |
| Somatic mosaicism reveals clonal distributions of neocortical development MW Breuss*, X Yang*, JCM Schlachetzki*, D Antaki*, AJ Lana, X Xu, ... Nature 604 (7907), 689-696, 2022 | 40* | 2022 |
| TUBB5 and its disease-associated mutations influence the terminal differentiation and dendritic spine densities of cerebral cortical neurons L Ngo, M Haas, Z Qu, SS Li, J Zenker, KSL Teng, JM Gunnersen, ... Human molecular genetics 23 (19), 5147-5158, 2014 | 40 | 2014 |
| Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans T Gstrein, A Edwards, A Přistoupilová, I Leca, M Breuss, S Pilat-Carotta, ... Nature neuroscience 21 (2), 207-217, 2018 | 39 | 2018 |
| Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development C Chung, X Yang, T Bae, KI Vong, S Mittal, C Donkels, H Westley Phillips, ... Nature genetics 55 (2), 209-220, 2023 | 38 | 2023 |
| Mutations in the murine homologue of TUBB5 cause microcephaly by perturbing cell cycle progression and inducing p53-associated apoptosis M Breuss, T Fritz, T Gstrein, K Chan, L Ushakova, N Yu, FW Vonberg, ... Development 143 (7), 1126-1133, 2016 | 35 | 2016 |
| Developmental and temporal characteristics of clonal sperm mosaicism X Yang*, MW Breuss*, X Xu, D Antaki, KN James, V Stanley, LL Ball, ... Cell 184 (18), 4772-4783. e15, 2021 | 34 | 2021 |
| High resolution anatomical mapping confirms the absence of a magnetic sense system in the rostral upper beak of pigeons CD Treiber, M Salzer, M Breuss, L Ushakova, M Lauwers, N Edelman, ... Communicative & integrative biology 6 (4), e24859, 2013 | 34 | 2013 |
| Mutations in spliceosomal genes PPIL1 and PRP17 cause neurodegenerative pontocerebellar hypoplasia with microcephaly G Chai, A Webb, C Li, D Antaki, S Lee, MW Breuss, N Lang, V Stanley, ... Neuron 109 (2), 241-256. e9, 2021 | 33 | 2021 |
| The expression of Tubb2b undergoes a developmental transition in murine cortical neurons M Breuss*$, J Morandell*, S Nimpf, T Gstrein, M Lauwers, T Hochstoeger, ... Journal of Comparative Neurology 523 (15), 2161-2186, 2015 | 28 | 2015 |
| Mutations in LNPK, encoding the endoplasmic reticulum junction stabilizer lunapark, cause a recessive neurodevelopmental syndrome MW Breuss, A Nguyen, Q Song, T Nguyen, V Stanley, KN James, ... The American Journal of Human Genetics 103 (2), 296-304, 2018 | 26 | 2018 |
David KeaysProfessor of Neurobiology, LMU, Munich. Principal Research Associate, PDN, University of Cambridge.Verified email at bio.lmu.de
