Lila Allou, PhD

2015-

Jean-louis Guéant	grad student	2010-2015	(BME Tree)
Stefan Mundlos	post-doc		(DevTree)

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Allou L, Mundlos S. (2023) Disruption of regulatory domains and novel transcripts as disease-causing mechanisms. Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. e2300010
Castilla-Ibeas A, Zdral S, Galán L, et al. (2023) Failure of digit tip regeneration in the absence of Lmx1b suggests Lmx1b functions disparate from dorsoventral polarity. Cell Reports. 42: 111975
Allou L, Balzano S, Magg A, et al. (2021) Non-coding deletions identify Maenli lncRNA as a limb-specific En1 regulator. Nature
Flöttmann R, Kragesteen BK, Geuer S, et al. (2017) Noncoding copy-number variations are associated with congenital limb malformation. Genetics in Medicine : Official Journal of the American College of Medical Genetics
Mignot C, Lambert L, Pasquier L, et al. (2015) WWOX-related encephalopathies: delineation of the phenotypical spectrum and emerging genotype-phenotype correlation. Journal of Medical Genetics. 52: 61-70
Allou L, Lambert L, Amsallem D, et al. (2012) 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