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Francis Rousseau

Observed names: F Rousseau, F. Rousseau, Rousseau Francis, Rousseau, Francis
Observed institutions: Hôpital Necker-Enfants Malades, Centre National de la Recherche Scientifique, Inserm, Commissariat à l'Énergie Atomique et aux Énergies Alternatives, Université Paris-Saclay, Centre National de Recherche en Génomique Humaine, Institut Necker Enfants Malades, Sorbonne Paris Cité, Assistance Publique – Hôpitaux de Paris, Hospices Civils de Lyon, Hôpital Saint-Antoine, Pitié-Salpêtrière Hospital, Genopole (France), Eurofins (France), Institut de Génomique Fonctionnelle, IntegraGen (France), Université Pierre-et-Marie-Curie
ORCID: 0009-0002-5831-1322
Observed ORCID: 0009-0002-5831-1322
OpenAlex ID: A5110270513
Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia
1994 · Francis Rousseau, Jacky Bonaventure, et al. · Nature · 933
A Hepatocellular Carcinoma 5-Gene Score Associated With Survival of Patients After Liver Resection
2013 · Jean–Charles Nault, Aurélien De Reyniès, et al. · Gastroenterology · 347
Association of TALS Developmental Disorder with Defect in Minor Splicing Component U4atac snRNA
2011 · Patrick Edery, Charles Marcaillou, et al. · Science · 238
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Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1
2008 · L Palmieri, V Papaleo, et al. · Molecular Psychiatry · 215
Stop codon FGFR3 mutations in thanatophoric dwarfism type 1
1995 · Francis Rousseau, Pascale Saugier, et al. · Nature Genetics · 200
Missense FGFR3 mutations create cysteine residues in thanatophoric dwarfism type I (TD1)
1996 · F Rousseau · Human Molecular Genetics · 174
A gene for achondroplasia–hypochondroplasia maps to chromosome 4p
1994 · Martine Le Merrer, Francis Rousseau, et al. · Nature Genetics · 139
Common mutations in the fibroblast growth factor receptor 3 (FGFR3) gene account for achondroplasia, hypochondroplasia, and thanatophoric dwarfism
1996 · J. Bonaventure, F. Rousseau, et al. · American Journal of Medical Genetics · 136
Clinical and genetic heterogeneity of hypochondroplasia.
1996 · F Rousseau, J Bonaventure, et al. · Journal of Medical Genetics · 135
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Hsa-miR-31-3p Expression Is Linked to Progression-free Survival in Patients with KRAS Wild-type Metastatic Colorectal Cancer Treated with Anti-EGFR Therapy
2014 · Gilles Manceau, Sandrine Imbeaud, et al. · Clinical Cancer Research · 104
Convergent evidence identifying MAP/microtubule affinity-regulating kinase 1 (MARK1) as a susceptibility gene for autism
2008 · G. Maussion, J. Carayol, et al. · Human Molecular Genetics · 88
Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism
2005 · A Philippi, E Roschmann, et al. · Molecular Psychiatry · 80
Converging Evidence for an Association of ATP2B2 Allelic Variants with Autism in Male Subjects
2011 · Jérôme Carayol, Roberto Sacco, et al. · Biological Psychiatry · 60
Genome-Wide Association Study in a Lebanese Cohort Confirms PHACTR1 as a Major Determinant of Coronary Artery Stenosis
2012 · Jörg Hager, Yoichiro Kamatani, et al. · PLoS ONE · 59
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Case-control and family-based association studies of candidate genes in autistic disorder and its endophenotypes: TPH2 and GLO1
2007 · Roberto Sacco, Veruska Papaleo, et al. · BMC Medical Genetics · 59
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Family-based association study of ITGB3 in autism spectrum disorder and its endophenotypes
2010 · Valerio Napolioni, Federica Lombardi, et al. · European Journal of Human Genetics · 58
Association between miR-31-3p expression and cetuximab efficacy in patients with KRAS wild-type metastatic colorectal cancer: a post-hoc analysis of the New EPOC trial
2017 · Siân Pugh, Raphaële Thiébaut, et al. · Oncotarget · 54
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Mutations of the Fibroblast Growth Factor Receptor-3 Gene in Achondroplasia
2008 · Francis Rousseau, Jacky Bonaventure, et al. · Hormone Research · 53
Exome sequencing as a first-tier test for copy number variant detection: retrospective evaluation and prospective screening in 2418 cases
2022 · Quentin Testard, Xavier Vanhoye, et al. · Journal of Medical Genetics · 48
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Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis
2007 · Anne Philippi, Frédéric Tores, et al. · BMC Medical Genetics · 43
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Common mutations in the gene encoding fibroblast growth factor receptor 3 account for achondroplasia, hypochondroplasia and thanatophoric dysplasia
1996 · J Bonaventure, F Rousseau, et al. · Acta Paediatrica · 43
TFAP2B Influences the Effect of Dietary Fat on Weight Loss under Energy Restriction
2012 · Tanja Stocks, Lars Ängquist, et al. · PLoS ONE · 41
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Association Study of Polymorphisms in the Human Estrogen Receptor Alpha Gene and Prostate Cancer Risk
2003 · Géraldine Cancel-Tassin, Alain Latil, et al. · European Urology · 33
Promoter adiponectin polymorphisms and waist/hip ratio variation in a prospective French adults study
2007 · G Dolley, S Bertrais, et al. · International Journal of Obesity · 28
The GLO1 C332 (Ala111) allele confers autism vulnerability: Family-based genetic association and functional correlates
2014 · Stefano Gabriele, Federica Lombardi, et al. · Journal of Psychiatric Research · 26
Works count: 73
Citation count: 3,559
H-index: 25
I10-index: 33
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