Nadia Soussi‐Yanicostas

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

Catherine Dodé, Jacqueline Levilliers, Jean‐Michel Dupont et al. · Nature Genetics · 2003 · 825 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +3

Anosmin-1, Defective in the X-Linked Form of Kallmann Syndrome, Promotes Axonal Branch Formation from Olfactory Bulb Output Neurons

Nadia Soussi‐Yanicostas, Fernando de Castro, A Julliard et al. · Cell · 2002 · 212 citations · Full text

Developmental Biology, Neurophysiology, Neuroanatomy +13

Anosmin-1 is a regionally restricted component of basement membranes and interstitial matrices during organogenesis: Implications for the developmental anomalies of X chromosome-linked Kallmann syndrome

Jean‐Pierre Hardelin, A Julliard, Brigitte Moniot et al. · Developmental Dynamics · 1999 · 145 citations · Full text

Decreased microglial Wnt/β-catenin signalling drives microglial pro-inflammatory activation in the developing brain

Juliette Van Steenwinckel, Anne‐Laure Schang, Michelle L. Krishnan et al. · Brain · 2019 · 136 citations · Full text

Glial Biology, Brain Development, Immunology +23

Initial characterization of anosmin-1, a putative extracellular matrix protein synthesized by definite neuronal cell populations in the central nervous system

Nadia Soussi‐Yanicostas, Jean‐Pierre Hardelin, María del Mar Arroyo Jiménez et al. · Journal of Cell Science · 1996 · 119 citations