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Lila Allou, PhD - Publications

Affiliations: 
2015- Max Planck Institute for Molecular Genetics, Berlin, Berlin, Germany 
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6 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Allou L, Mundlos S. Disruption of regulatory domains and novel transcripts as disease-causing mechanisms. Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. e2300010. PMID 37381881 DOI: 10.1002/bies.202300010  0.575
2023 Castilla-Ibeas A, Zdral S, Galán L, Haro E, Allou L, Campa VM, Icardo JM, Mundlos S, Oberg KC, Ros MA. Failure of digit tip regeneration in the absence of Lmx1b suggests Lmx1b functions disparate from dorsoventral polarity. Cell Reports. 42: 111975. PMID 36641754 DOI: 10.1016/j.celrep.2022.111975  0.418
2021 Allou L, Balzano S, Magg A, Quinodoz M, Royer-Bertrand B, Schöpflin R, Chan WL, Speck-Martins CE, Carvalho DR, Farage L, Lourenço CM, Albuquerque R, Rajagopal S, Nampoothiri S, Campos-Xavier B, et al. Non-coding deletions identify Maenli lncRNA as a limb-specific En1 regulator. Nature. PMID 33568816 DOI: 10.1038/s41586-021-03208-9  0.367
2017 Flöttmann R, Kragesteen BK, Geuer S, Socha M, Allou L, Sowińska-Seidler A, Bosquillon de Jarcy L, Wagner J, Jamsheer A, Oehl-Jaschkowitz B, Wittler L, de Silva D, Kurth I, Maya I, Santos-Simarro F, et al. Noncoding copy-number variations are associated with congenital limb malformation. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 29236091 DOI: 10.1038/Gim.2017.154  0.616
2015 Mignot C, Lambert L, Pasquier L, Bienvenu T, Delahaye-Duriez A, Keren B, Lefranc J, Saunier A, Allou L, Roth V, Valduga M, Moustaïne A, Auvin S, Barrey C, Chantot-Bastaraud S, et al. WWOX-related encephalopathies: delineation of the phenotypical spectrum and emerging genotype-phenotype correlation. Journal of Medical Genetics. 52: 61-70. PMID 25411445 DOI: 10.1136/Jmedgenet-2014-102748  0.536
2012 Allou L, Lambert L, Amsallem D, Bieth E, Edery P, Destrée A, Rivier F, Amor D, Thompson E, Nicholl J, Harbord M, Nemos C, Saunier A, Moustaïne A, Vigouroux A, et al. 14q12 and severe Rett-like phenotypes: new clinical insights and physical mapping of FOXG1-regulatory elements. European Journal of Human Genetics : Ejhg. 20: 1216-23. PMID 22739344 DOI: 10.1038/ejhg.2012.127  0.412
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