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Genome Biology|May 7, 2004
Transcriptional regulation of protein complexes in yeastNicolas Simonis, Jacques van Helden, George N Cohen, et al.Journal of Molecular Biology|September 16, 2006
Modularity of the transcriptional response of protein complexes in yeastNicolas Simonis, Didier Gonze, Chris Orsi, et al.Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|January 12, 2024
An unusual presentation of de novo RAC3 variation in prenatal diagnosisColombine Meunier, Marie Cassart, Karole Kostyla, et al.Neurology. Genetics|September 2, 2016
MME mutation in dominant spinocerebellar ataxia with neuropathy (SCA43)Chantal Depondt, Simona Donatello, Myriam Rai, et al.Neurology|April 11, 2014
Autosomal recessive cerebellar ataxia of adult onset due to STUB1 mutationsChantal Depondt, Simona Donatello, Nicolas Simonis, et al.BMC Developmental Biology|October 24, 2012
Protein interactions of the transcription factor Hoxa1Barbara Lambert, Julie Vandeputte, Sophie Remacle, et al.Journal of Medical Genetics|October 9, 2012
Two novel CCDC88C mutations confirm the role of DAPLE in autosomal recessive congenital hydrocephalusAnais Drielsma, Chaim Jalas, Nicolas Simonis, et al.BMC Cancer|May 28, 2016
Systematic interactome mapping of acute lymphoblastic leukemia cancer gene products reveals EXT-1 tumor suppressor as a Notch1 and FBWX7 common interactorSarah Daakour, Leon Juvenal Hajingabo, Despoina Kerselidou, et al.Molecular Biology of the Cell|October 3, 2014
Predicting interactome network perturbations in human cancer: application to gene fusions in acute lymphoblastic leukemiaLeon Juvenal Hajingabo, Sarah Daakour, Maud Martin, et al.Journal of Medical Genetics|July 2, 2013
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactylyNicolas Simonis, Isabelle Migeotte, Nelle Lambert, et al.Pageof 3