| Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly K Poirier, N Lebrun, L Broix, G Tian, Y Saillour, C Boscheron, E Parrini, ... Nature genetics 45 (6), 639-647, 2013 | 518 | 2013 |
| Cerebral cortex development: an outside‐in perspective G Agirman, L Broix, L Nguyen FEBS letters 591 (24), 3978-3992, 2017 | 135 | 2017 |
| Mutations in the HECT domain of NEDD4L lead to AKT–mTOR pathway deregulation and cause periventricular nodular heterotopia L Broix, H Jagline, E L Ivanova, S Schmucker, N Drouot, J Clayton-Smith, ... Nature genetics 48 (11), 1349-1358, 2016 | 119 | 2016 |
| The centrosome protein AKNA regulates neurogenesis via microtubule organization G Camargo Ortega, S Falk, PA Johansson, E Peyre, L Broix, SK Sahu, ... Nature 567 (7746), 113-117, 2019 | 78 | 2019 |
| ATAT1-enriched vesicles promote microtubule acetylation via axonal transport A Even, G Morelli, L Broix, C Scaramuzzino, S Turchetto, I Gladwyn-Ng, ... Science advances 5 (12), eaax2705, 2019 | 72 | 2019 |
| Beta tubulin isoforms are not interchangeable for rescuing impaired radial migration due to Tubb3 knockdown Y Saillour, L Broix, E Bruel-Jungerman, N Lebrun, G Muraca, J Rucci, ... Human molecular genetics 23 (6), 1516-1526, 2014 | 62 | 2014 |
| Mosaic parental germline mutations causing recurrent forms of malformations of cortical development JL Zillhardt, K Poirier, L Broix, N Lebrun, A Elmorjani, J Martinovic, ... European Journal of Human Genetics 24 (4), 611-614, 2016 | 45 | 2016 |
| HOXC4 homeoprotein efficiently expands human hematopoietic stem cells and triggers similar molecular alterations as HOXB4 C Auvray, A Delahaye, F Pflumio, R Haddad, S Amsellem, A Miri-Nezhad, ... Haematologica 97 (2), 168, 2012 | 45 | 2012 |
| Ciliogenesis and cell cycle alterations contribute to KIF2A-related malformations of cortical development L Broix, L Asselin, CG Silva, EL Ivanova, P Tilly, JG Gilet, N Lebrun, ... Human Molecular Genetics 27 (2), 224-238, 2018 | 43 | 2018 |
| TUBG1 missense variants underlying cortical malformations disrupt neuronal locomotion and microtubule dynamics but not neurogenesis EL Ivanova, JG Gilet, V Sulimenko, A Duchon, G Rudolf, K Runge, ... Nature communications 10 (1), 2129, 2019 | 27 | 2019 |
| Coordination between transport and local translation in neurons L Broix, S Turchetto, L Nguyen Trends in cell biology 31 (5), 372-386, 2021 | 18 | 2021 |
| Conditional switching of KIF2A mutation provides new insights into cortical malformation pathogeny JG Gilet, EL Ivanova, D Trofimova, G Rudolf, H Meziane, L Broix, N Drouot, ... Human Molecular Genetics 29 (5), 766-784, 2020 | 17 | 2020 |
| ATP-citrate lyase promotes axonal transport across species A Even, G Morelli, S Turchetto, M Shilian, RL Bail, S Laguesse, N Krusy, ... Nature communications 12 (1), 5878, 2021 | 16 | 2021 |
| Deciphering Developmental Disorders study L Broix, H Jagline, E Ivanova, S Schmucker, N Drouot, J Clayton-Smith, ... Mutations in the HECT domain of NEDD4L lead to Akt-mTOR pathway deregulation …, 2016 | 13 | 2016 |
| Ex vivo recording of axonal transport dynamics on postnatal organotypic cortical slices S Turchetto, L Broix, L Nguyen STAR protocols 1 (3), 100131, 2020 | 5 | 2020 |
| Molecular analysis of axonal transport dynamics upon modulation of microtubule acetylation S Turchetto, R Le Bail, L Broix, L Nguyen Axonal Transport: Methods and Protocols, 207-224, 2022 | 3 | 2022 |
| ATP-Citrate lyase fuels axonal transport across species A Even, G Morelli, R Le Bail, M Shilian, S Turchetto, L Broix, A Brandis, ... bioRxiv, 2020.07. 07.192096, 2020 | | 2020 |
| Understanding the pathophysiological mechanisms of malformations of cortical development associated with mutations in KIF2A and NEDD4L genes L Broix < bound method Organization. get_name_with_acronym of< Organization: TEL …, 2016 | | 2016 |
| Compréhension des mécanismes physiopathologiques des malformations du développement cortical associées à des mutations dans les gènes KIF2A et NEDD4L L Broix Université Sorbonne Paris Cité, 2016 | | 2016 |