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Dominique Campion

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Gaël Nicolas; Jérémie Pariente; Cyril Pottier; Stéphane Rousseau; Anne Rovelet-Lecrux; Yvan Vaschalde; Jérôme Augustin; Xavier Ayrignac; Michel Clanet; Sophie Coutant; Luc Defebvre; Thierry Frébourg; Lucie Guyant-Maréchal; Didier Hannequin; Pierre Krystkowiak; Pierre Labauge; Isabelle Le Ber; Romain Lefaucheur; Solenn Legallic; David Maltête; Olivier Martinaud; Dominique Campion
Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcification.
Cyril Pottier; Anne-Claire Richard; Adeline Rollin-Sillaire; Stephane Rousseau; Anne Rovelet-Lecrux; David Wallon; Dominique Campion; Thierry Frebourg; Didier Hannequin
TREM2 R47H variant as a risk factor for early-onset Alzheimer's disease.
Anne Rovelet-Lecrux; Dominique Campion
Copy number variations involving the microtubule-associated protein tau in human diseases.

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2013: Gaël Nicolas; Jérémie Pariente; Cyril Pottier; Stéphane Rousseau; Anne Rovelet-Lecrux; Yvan Vaschalde; Jérôme Augustin; Xavier Ayrignac; Michel Clanet; Sophie Coutant; Luc Defebvre; Thierry Frébourg; Lucie Guyant-Maréchal; Didier Hannequin; Pierre Krystkowiak; Pierre Labauge; Isabelle Le Ber; Romain Lefaucheur; Solenn Legallic; David Maltête; Olivier Martinaud; Dominique Campion
Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcification.
Neurology 2013;80(2):181-7.
2013: Cyril Pottier; Anne-Claire Richard; Adeline Rollin-Sillaire; Stephane Rousseau; Anne Rovelet-Lecrux; David Wallon; Dominique Campion; Thierry Frebourg; Didier Hannequin
TREM2 R47H variant as a risk factor for early-onset Alzheimer's disease.
Journal of Alzheimer's disease : JAD 2013;35(1):45-9.
2012: Anne Rovelet-Lecrux; Dominique Campion
Copy number variations involving the microtubule-associated protein tau in human diseases.
Biochemical Society transactions 2012;40(4):672-6.
2012: Anne Rovelet-Lecrux; Catherine Thomas-Antérion; Martine Vercelletto; David Wallon; Stéphanie Bombois; Dominique Campion; Bernard Croisile; Jean-Michel Flaman; Thierry Frébourg; Didier Hannequin; Isabelle Le Ber; Solenn Legallic; Richard Lévy; Olivier Martinaud; A Michon; Claire Paquet; Jérémie Pariente; Michèle Puel; Adeline Rollin-Sillaire
A genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer disease.
European journal of human genetics : EJHG 2012;20(6):613-7.
2012: Laetitia Miguel; Tracey Avequin; Dominique Campion; Morgane Delarue; Sébastien Feuillette; Thierry Frébourg; Magalie Lecourtois
Accumulation of insoluble forms of FUS protein correlates with toxicity in Drosophila.
Neurobiology of aging 2012;33(5):1008.e1-15.
2012: Sophie Coutant; Chloé Cabot; Dominique Campion; Thierry Lecroq; Arnaud Lefebvre; Martine Léonard; Elise Prieur-Gaston; Hélène Dauchel
EVA: Exome Variation Analyzer, an efficient and versatile tool for filtering strategies in medical genomics.
BMC bioinformatics 2012;13 Suppl 14():S9.
2012: David Wallon; Sophie Auriacombe; Dominique Campion; Vincent Deramecourt; Isabelle Le Ber; Jérémie Pariente; Florence Pasquier; Anne Rovelet-Lecrux; Suzanna Schraen; Didier Hannequin
Definite behavioral variant of frontotemporal dementia with C9ORF72 expansions despite positive Alzheimer's disease cerebrospinal fluid biomarkers.
Journal of Alzheimer's disease : JAD 2012;32(1):19-22.
2012: David Wallon; Claire Boutoleau-Bretonnière; Dominique Campion; Bernard Croisile; Marie-Bernadette Delisle; Charles Duyckaerts; Thierry Frebourg; Audrey Gabelle; Lucie Guyant-Maréchal; Didier Hannequin; Béatrice Lannes; Annie Laquerrière; Isabelle Le Ber; Olivier Martinaud; Olivier Moreaud; Claire Paquet; Jérémie Pariente; Florence Pasquier; Michèle Puel; Muriel Quillard-Muraine; Adeline Rollin-Sillaire; Stéphane Rousseau; Anne Rovelet-Lecrux; Marie Sarazin; Mathilde Sauvée; François Sellal; Nathalie Streichenberger; Catherine Thomas-Antérion
The French series of autosomal dominant early onset Alzheimer's disease cases: mutation spectrum and cerebrospinal fluid biomarkers.
Journal of Alzheimer's disease : JAD 2012;30(4):847-56.
2011: Emmanuelle Cousin; Jean-François Deleuze; Colette Dib; Emmanuelle Génin; Didier Hannequin; Sandrine Macé; Gaëlle Muzard; Laurent Pradier; Corinne Rocher; Alexis Brice; Dominique Campion
No replication of genetic association between candidate polymorphisms and Alzheimer's disease.
Neurobiology of aging 2011;32(8):1443-51.
2011: Laetitia Miguel; Thierry Frébourg; Dominique Campion; Magalie Lecourtois
Both cytoplasmic and nuclear accumulations of the protein are neurotoxic in Drosophila models of TDP-43 proteinopathies.
Neurobiology of disease 2011;41(2):398-406.
2010: Audrey Guilmatre; Solenn Legallic; Gary Steel; Alecia Willis; Gabriella Di Rosa; Alice Goldenberg; Valérie Drouin-Garraud; Agnès Guet; Cyril Mignot; Vincent des Portes; Vassili Valayannopoulos; Lionel Van Maldergem; Jodi D Hoffman; Claudia Izzi; Caroline Espil-Taris; Simona Orcesi; Luisa Bonafé; Eric Le Galloudec; Hélène Maurey; Christine Ioos; Alexandra Afenjar; Patricia Blanchet; Bernard Echenne; Agathe Roubertie; Thierry Frebourg; David Valle; Dominique Campion
Type I hyperprolinemia: genotype/phenotype correlations.
Human mutation 2010;31(8):961-5.
2010: Sébastien Feuillette; Vincent Deramecourt; Annie Laquerriere; Charles Duyckaerts; Marie-Bernadette Delisle; Claude-Alain Maurage; David Blum; Luc BUEE; Thierry Frébourg; Dominique Campion; Magalie Lecourtois
Filamin-A and Myosin VI colocalize with fibrillary Tau protein in Alzheimer's disease and FTDP-17 brains.
Brain research 2010;1345():182-9.
2010: Delphine Schoder; Didier Hannequin; Olivier Martinaud; Gaëlle Opolczynski; Lucie Guyant-Maréchal; Isabelle Le Ber; Dominique Campion
Morbid risk for schizophrenia in first-degree relatives of people with frontotemporal dementia.
The British journal of psychiatry : the journal of mental science 2010;197(1):28-35.
2010: Sébastien Feuillette; Laetitia Miguel; Thierry Frébourg; Dominique Campion; Magalie Lecourtois
Drosophila models of human tauopathies indicate that Tau protein toxicity in vivo is mediated by soluble cytosolic phosphorylated forms of the protein.
Journal of neurochemistry 2010;113(4):895-903.
2010: Anne Rovelet-Lecrux; Didier Hannequin; Olivier Guillin; Solenn Legallic; Snejana Jurici; David Wallon; Thierry Frebourg; Dominique Campion
Frontotemporal dementia phenotype associated with MAPT gene duplication.
Journal of Alzheimer's disease : JAD 2010;21(3):897-902.
2009: Audrey Guilmatre; Christèle Dubourg; Anne-Laure Mosca; Solenn Legallic; Alice Goldenberg; Valérie Drouin-Garraud; Valérie Layet; Antoine Rosier; Sylvain Briault; Frédérique Bonnet-Brilhault; Frédéric Laumonnier; Sylvie Odent; Gael Le Vacon; Géraldine Joly-Helas; Véronique David; Claude Bendavid; Jean-Michel Pinoit; Céline Henry; Caterina Impallomeni; Eva Germano; Gaetano Tortorella; Gabriella Di Rosa; Catherine Barthelemy; Christian Andres; Laurence Faivre; Thierry Frébourg; Pascale Saugier-Veber; Dominique Campion
Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation.
Archives of general psychiatry 2009;66(9):947-56.
2009: Lina Benajiba; Isabelle Le Ber; Agnès Camuzat; Mathieu Lacoste; Catherine Thomas-Anterion; Philippe Couratier; Solenn Legallic; François Salachas; Didier Hannequin; Marielle Decousus; Lucette Lacomblez; Eric Guedj; Véronique Golfier; William Camu; Bruno Dubois; Dominique Campion; Vincent Meininger; Alexis Brice
TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration.
Annals of neurology 2009;65(4):470-3.
2009: Anne Rovelet-Lecrux; Magalie Lecourtois; Catherine Thomas-Anterion; Isabelle Le Ber; Alexis Brice; Thierry Frebourg; Didier Hannequin; Dominique Campion
Partial deletion of the MAPT gene: a novel mechanism of FTDP-17.
Human mutation 2009;30(4):E591-602.
2009: Solenn Legallic; Jacqueline Bou; Sadeq Haouzir; Gabrielle Allio; Caroline Demily; Michel Petit; Thierry Frebourg; Florence Thibaut; Dominique Campion
No pathogenic rearrangement within the DISC 1 gene in psychosis.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009;150B(1):148-50.
2008: I Guyant-Marechal; E Berger; Annie Laquerrière; A Rovelet-Lecrux; G Viennet; Thierry Frebourg; L Rumbach; Dominique Campion; Didier Hannequin
Intrafamilial diversity of phenotype associated with app duplication.
Neurology 2008;71(23):1925-6.
2008: Anne Rovelet-Lecrux; Vincent Deramecourt; Solenn Legallic; Claude-Alain Maurage; Isabelle Le Ber; Alexis Brice; jean-charles lambert; Thierry Frébourg; Didier Hannequin; Florence Pasquier; Dominique Campion
Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease.
Neurobiology of disease 2008;31(1):41-5.
2008: Ute Dreses-Werringloer; jean-charles lambert; Valérie Vingtdeux; Haitian Zhao; Horia Vais; Adam Siebert; Ankit Jain; Jeremy Koppel; Anne Rovelet-Lecrux; Didier Hannequin; Florence Pasquier; Daniela Galimberti; Elio Scarpini; D M A Mann; Corinne Lendon; Dominique Campion; Philippe Amouyel; Peter Davies; J Kevin Foskett; Fabien Campagne; Philippe Marambaud
A polymorphism in CALHM1 influences Ca2+ homeostasis, Abeta levels, and Alzheimer's disease risk.
Cell 2008;133(7):1149-61.
2008: Isabelle Le Ber; Agnès Camuzat; Didier Hannequin; Florence Pasquier; Eric Guedj; Anne Rovelet-Lecrux; Valerie Hahn-Barma; Julie van der Zee; Fabienne Clot; Serge Bakchine; Michèle Puel; Mustapha Ghanim; Lucette Lacomblez; Jacqueline Mikol; Vincent Deramecourt; Pascal Lejeune; Vincent de La Sayette; Serge Belliard; Martine Vercelletto; Christian Meyrignac; Christine Van Broeckhoven; jean-charles lambert; Patrice Verpillat; Dominique Campion; Marie-Odile Habert; Bruno Dubois; Alexis Brice
Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study.
Brain : a journal of neurology 2008;131(Pt 3):732-46.
2008: Gabriella Di Rosa; Giuseppina Pustorino; Maria Spano; Dominique Campion; Marilena Calabrò; Mohammed Aguennouz; Daniela Caccamo; Solenn Legallic; Domenica Lucia Sgro; Maria Bonsignore; Gaetano Tortorella
Type I hyperprolinemia and proline dehydrogenase (PRODH) mutations in four Italian children with epilepsy and mental retardation.
Psychiatric genetics 2008;18(1):40-2.
2007: Caroline Demily; Solenn Legallic; Jacqueline Bou; Emmanuelle Houy-Durand; Therese van Amelsvoort; Janneke Zinkstok; Sylvie Manouvrier-Hanue; Annick Vogels; Valérie Drouin-Garraud; Nicole Philip; Anne Philippe; Delphine Héron; Pierre Sarda; Michel Petit; Florence Thibaut; Thierry Frébourg; Dominique Campion
ZDHHC8 single nucleotide polymorphism rs175174 is not associated with psychiatric features of the 22q11 deletion syndrome or schizophrenia.
Psychiatric genetics 2007;17(5):311-2.
2007: Anne Rovelet-Lecrux; Thierry Frebourg; Hannu Tuominen; Kari Majamaa; Dominique Campion; Anne M Remes
APP locus duplication in a Finnish family with dementia and intracerebral haemorrhage.
Journal of neurology, neurosurgery, and psychiatry 2007;78(10):1158-9.
2007: Isabelle Le Ber; Julie van der Zee; Didier Hannequin; Ilse Gijselinck; Dominique Campion; Michèle Puel; Annie Laquerrière; Tim De Pooter; Agnès Camuzat; Marleen Van den Broeck; Bruno Dubois; François Sellal; Lucette Lacomblez; Martine Vercelletto; Catherine Thomas-Antérion; Bernard-François Michel; Véronique Golfier; Mira Didic; François Salachas; Charles Duyckaerts; Marc Cruts; Patrice Verpillat; Christine Van Broeckhoven; Alexis Brice
Progranulin null mutations in both sporadic and familial frontotemporal dementia.
Human mutation 2007;28(9):846-55.
2007: Julie van der Zee; Isabelle Le Ber; Sebastian Maurer-Stroh; Sebastiaan Engelborghs; Ilse Gijselinck; Agnès Camuzat; Nathalie Brouwers; Rik Vandenberghe; Kristel Sleegers; Didier Hannequin; Bart Dermaut; Joost Schymkowitz; Dominique Campion; Patrick Santens; Jean-Jacques Martin; Lucette Lacomblez; Tim De Pooter; Karin Peeters; Maria Mattheijssens; Martine Vercelletto; Marleen Van den Broeck; Marc Cruts; Peter Paul De Deyn; Frederic Rousseau; Alexis Brice; Christine Van Broeckhoven
Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia.
Human mutation 2007;28(4):416.
2007: Olivier Blard; Sébastien Feuillette; Jacqueline Bou; Boris Chaumette; Thierry Frébourg; Dominique Campion; Magalie Lecourtois
Cytoskeleton proteins are modulators of mutant tau-induced neurodegeneration in Drosophila.
Human molecular genetics 2007;16(5):555-66.
2007: Lucie Guyant-Maréchal; Anne Rovelet-Lecrux; L Goumidi; Emmanuelle Cousin; Didier Hannequin; Gregory RAUX; C Penet; Sylvain Ricard; Sandrine Macé; Philippe Amouyel; Jean-François Deleuze; Thierry Frebourg; Alexis Brice; jean-charles lambert; Dominique Campion
Variations in the APP gene promoter region and risk of Alzheimer disease.
Neurology 2007;68(9):684-7.
2006: Lucie Cabrejo; Lucie Guyant-Maréchal; Annie Laquerrière; Martine Vercelletto; François De la Fournière; Catherine Thomas-Antérion; Christophe Verny; franck letournel; Florence Pasquier; Anne Vital; Frédéric Checler; Thierry Frebourg; Dominique Campion; Didier Hannequin
Phenotype associated with APP duplication in five families.
Brain : a journal of neurology 2006;129(Pt 11):2966-76.
2006: Cécile Dumanchin; Isabelle Tournier; Cosette Martin; Mira Didic; Serge Belliard; Bertrand Carlander; François Rouhart; Charles Duyckaerts; Jean-François Pellissier; Jean Baptiste Latouche; Didier Hannequin; Thierry Frebourg; Mario Tosi; Dominique Campion
Biological effects of four PSEN1 gene mutations causing Alzheimer disease with spastic paraparesis and cotton wool plaques.
Human mutation 2006;27(10):1063.
2006: Olivier Blard; Thierry Frébourg; Dominique Campion; Magalie Lecourtois
Inhibition of proteasome and Shaggy/Glycogen synthase kinase-3beta kinase prevents clearance of phosphorylated tau in Drosophila.
Journal of neuroscience research 2006;84(5):1107-15.
2006: Lucie Guyant-Maréchal; Annie Laquerrière; Charles Duyckaerts; Cécile Dumanchin; Jacqueline Bou; F Dugny; Isabelle Le Ber; Thierry Frébourg; Didier Hannequin; Dominique Campion
Valosin-containing protein gene mutations: clinical and neuropathologic features.
Neurology 2006;67(4):644-51.
2006: Hélène Jacquet; Judy Rapoport; Bernadette Hecketsweiler; Aaron Bobb; Florence Thibaut; Thierry Frébourg; Dominique Campion
Hyperprolinemia is not associated with childhood onset schizophrenia.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2006;141B(2):192.
2006: Anne Rovelet-Lecrux; Didier Hannequin; Gregory RAUX; Nathalie Le Meur; Annie Laquerrière; Anne Vital; Cécile Dumanchin; Sébastien Feuillette; Alexis Brice; Martine Vercelletto; Frédéric Dubas; Thierry Frebourg; Dominique Campion
APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy.
Nature genetics 2006;38(1):24-6.
2005: Lucie Guyant-Maréchal; Aad Verrips; Carole Girard; Ron A Wevers; Fokje Zijlstra; Erik A Sistermans; Pierre Vera; Dominique Campion; Didier Hannequin
Unusual cerebrotendinous xanthomatosis with fronto-temporal dementia phenotype.
American journal of medical genetics. Part A 2005;139A(2):114-7.
2005: Gregory RAUX; Lucie Guyant-Maréchal; Cosette Martin; Jacqueline Bou; C Penet; Alexis Brice; Didier Hannequin; Thierry Frebourg; Dominique Campion
Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: an update.
Journal of medical genetics 2005;42(10):793-5.
2005: Sandrine Louchart-de la Chapelle; Daniel Levillain; Jean-François Ménard; Alexis Van der Elst; Gabrielle Allio; Sadeq Haouzir; Sonia Dollfus; Dominique Campion; Florence Thibaut
P50 inhibitory gating deficit is correlated with the negative symptomatology of schizophrenia.
Psychiatry research 2005;136(1):27-34.
2005: Olivier Martinaud; Annie Laquerrière; Lucie Guyant-Maréchal; P Ahtoy; Pierre Vera; Nicolas Sergeant; Agnès Camuzat; P Bourgeois; JEAN-JACQUES HAUW; Dominique Campion; Didier Hannequin
Frontotemporal dementia, motor neuron disease and tauopathy: clinical and neuropathological study in a family.
Acta neuropathologica 2005;110(1):84-92.
2005: Sébastien Feuillette; Olivier Blard; Magalie Lecourtois; Thierry Frébourg; Dominique Campion; Cécile Dumanchin
Tau is not normally degraded by the proteasome.
Journal of neuroscience research 2005;80(3):400-5.
2005: Hélène Jacquet; Caroline Demily; Emmanuelle Houy; Bernadette Hecketsweiler; Jacqueline Bou; Gregory RAUX; Jérôme Lerond; Gabrielle Allio; Sadeq Haouzir; A Tillaux; C Bellegou; Gaël Fouldrin; Pascal Delamillieure; Jean-François Ménard; Sonia Dollfus; T D'Amato; Michel Petit; Florence Thibaut; Thierry Frébourg; Dominique Campion
Hyperprolinemia is a risk factor for schizoaffective disorder.
Molecular psychiatry 2005;10(5):479-85.
2005: Sandrine Louchart-de la Chapelle; Irène Nkam; Emmanuelle Houy; Angelique Belmont; Jean-François Ménard; Anne-Claire Roussignol; Ophélie Siwek; Mustapha Mezerai; Marion Guillermou; Gaël Fouldrin; Daniel Levillain; Sonia Dollfus; Dominique Campion; Florence Thibaut
A concordance study of three electrophysiological measures in schizophrenia.
The American journal of psychiatry 2005;162(3):466-74.
2005: Sandrine Macé; Emmanuelle Cousin; Sylvain Ricard; Emmanuelle Génin; Emmanuel Spanakis; Carole Lafargue-Soubigou; Bérengère Génin; Raphaël Fournel; Sandrine Roche; Gilles Haussy; Florence Massey; Stéphane Soubigou; Georges Bréfort; Patrick Benoit; Alexis Brice; Dominique Campion; Melvyn Hollis; Laurent Pradier; Jesus Benavides; Jean-François Deleuze
ABCA2 is a strong genetic risk factor for early-onset Alzheimer's disease.
Neurobiology of disease 2005;18(1):119-25.
2004: Isabelle Le Ber; Maria Martinez; Dominique Campion; Annie Laquerrière; Christine Bétard; guillaume bassez; Carol Girard; Pascale Saugier-Veber; Gregory RAUX; Nicolas Sergeant; Patrick Magnier; Thierry Maisonobe; Bruno Eymard; Charles Duyckaerts; André Delacourte; Thierry Frebourg; Didier Hannequin
A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24.
Brain : a journal of neurology 2004;127(Pt 9):1979-92.
2004: Emmanuelle Houy; Gregory RAUX; Florence Thibaut; Angelique Belmont; Caroline Demily; Gabrielle Allio; Sadeq Haouzir; Gaël Fouldrin; Michel Petit; Thierry Frebourg; Dominique Campion
The promoter -194 C polymorphism of the nicotinic alpha 7 receptor gene has a protective effect against the P50 sensory gating deficit.
Molecular psychiatry 2004;9(3):320-2.
2003: Emmanuelle Cousin; Didier Hannequin; Sandrine Macé; Bruno Dubois; Sylvain Ricard; Emmanuelle Génin; Christophe Brun; Céline Chansac; Laurent Pradier; Thierry Frebourg; Alexis Brice; Dominique Campion; Jean-François Deleuze
No replication of the association between the Nicastrin gene and familial early-onset Alzheimer's disease.
Neuroscience letters 2003;353(2):153-5.
2003: Robert P Erickson; Steve Skinner; Hélène Jacquet; Dominique Campion; Patrick Buckley; Kiran K Mantripragada; Jan P Dumanski
Does chromosome 22 have anything to do with sex determination: further studies on a 46,XX,22q11.2 del male.
American journal of medical genetics. Part A 2003;123A(1):64-7.
2003: Florence Portet; Yves Dauvilliers; Dominique Campion; Gregory RAUX; JEAN-JACQUES HAUW; O Lyon-Caen; W Camu; Jacques Touchon
Very early onset AD with a de novo mutation in the presenilin 1 gene (Met 233 Leu).
Neurology 2003;61(8):1136-7.
2003: Emmanuelle Cousin; Didier Hannequin; Sylvain Ricard; Sandrine Macé; Emmanuelle Génin; Céline Chansac; Alexis Brice; Bruno Dubois; Thierry Frebourg; Luc Mercken; Jesus Benavides; Laurent Pradier; Dominique Campion; Jean-François Deleuze
A risk for early-onset Alzheimer's disease associated with the APBB1 gene (FE65) intron 13 polymorphism.
Neuroscience letters 2003;342(1-2):5-8.
2003: Lucie Maréchal; Gregory RAUX; Cécile Dumanchin; Guillaume Lefebvre; Emmanuelle Deslandre; Carole Girard; Dominique Campion; Dominique Parain; Thierry Frebourg; Didier Hannequin
Severe myoclonus-dystonia syndrome associated with a novel epsilon-sarcoglycan gene truncating mutation.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003;119B(1):114-7.
2003: Lucie Maréchal; Dominique Campion; Didier Hannequin
[Familial forms of Alzheimer's disease].
Presse médicale (Paris, France : 1983) 2003;32(16):756-63.
2003: Hélène Jacquet; J Berthelot; C Bonnemains; Gilles Simard; Pascale Saugier-Veber; Gregory RAUX; Dominique Campion; Dominique Bonneau; Thierry Frebourg
The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH gene.
Journal of medical genetics 2003;40(1):e7.
2002: Patrice Verpillat; Sylvain Ricard; Didier Hannequin; Bruno Dubois; Jacqueline Bou; Agnès Camuzat; Laurent Pradier; Thierry Frebourg; Alexis Brice; Françoise Clerget-Darpoux; Jean-François Deleuze; Dominique Campion
Is the saitohin gene involved in neurodegenerative diseases?
Annals of neurology 2002;52(6):829-32.
2002: Hélène Jacquet; Gregory RAUX; Florence Thibaut; Bernadette Hecketsweiler; Emmanuelle Houy; Caroline Demilly; Sadeq Haouzir; Gabrielle Allio; Gaël Fouldrin; Valérie Drouin; Jacqueline Bou; Michel Petit; Dominique Campion; Thierry Frébourg
PRODH mutations and hyperprolinemia in a subset of schizophrenic patients.
Human molecular genetics 2002;11(19):2243-9.
2002: Mekki Boussaha; Didier Hannequin; Patrice Verpillat; Alexis Brice; Thierry Frebourg; Dominique Campion
Polymorphisms of insulin degrading enzyme gene are not associated with Alzheimer's disease.
Neuroscience letters 2002;329(1):121-3.
2002: Patrice Verpillat; Agnès Camuzat; Didier Hannequin; Catherine Thomas-Anterion; Michèle Puel; Serge Belliard; Bruno Dubois; Mira Didic; Lucette Lacomblez; Olivier Moreaud; Véronique Golfier; Dominique Campion; Alexis Brice; Françoise Clerget-Darpoux
Apolipoprotein E gene in frontotemporal dementia: an association study and meta-analysis.
European journal of human genetics : EJHG 2002;10(7):399-405.
2002: Patrice Verpillat; Agnès Camuzat; Didier Hannequin; Catherine Thomas-Anterion; Michèle Puel; Serge Belliard; Bruno Dubois; Mira Didic; Bernard-François Michel; Lucette Lacomblez; Olivier Moreaud; François Sellal; Véronique Golfier; Dominique Campion; Françoise Clerget-Darpoux; Alexis Brice
Association between the extended tau haplotype and frontotemporal dementia.
Archives of neurology 2002;59(6):935-9.
2002: M L Jacquemont; Dominique Campion; Valérie Hahn; C M E Tallaksen; Thierry Frebourg; Alexis Brice; Alexandra Durr
Spastic paraparesis and atypical dementia caused by PSEN1 mutation (P264L), responsible for Alzheimer's disease.
Journal of medical genetics 2002;39(2):E2.
2002: Gregory RAUX; F Bonnet-Brilhault; S Louchart; Emmanuelle Houy; R Gantier; Daniel Levillain; Gabrielle Allio; Sadeq Haouzir; Michel Petit; M Martinez; Thierry Frebourg; Florence Thibaut; Dominique Campion
The -2 bp deletion in exon 6 of the 'alpha 7-like' nicotinic receptor subunit gene is a risk factor for the P50 sensory gating deficit.
Molecular psychiatry 2002;7(9):1006-11.
2001: Patrice Verpillat; S Bouley; Dominique Campion; Didier Hannequin; Bruno Dubois; Serge Belliard; Michèle Puel; Catherine Thomas-Antérion; Yves Agid; Alexis Brice; Françoise Clerget-Darpoux
Use of haplotype information to test involvement of the LRP gene in Alzheimer's disease in the French population.
European journal of human genetics : EJHG 2001;9(6):464-8.
2001: M de Chaldée; M Corbex; Dominique Campion; M Jay; D Samolyk; Michel Petit; Florence Thibaut; Claudine Laurent; Jacques Mallet
No evidence for linkage between COMT and schizophrenia in a French population.
Psychiatry research 2001;102(1):87-90.
2000: Gregory RAUX; R Gantier; Catherine Thomas-Anterion; J Boulliat; Patrice Verpillat; Didier Hannequin; Alexis Brice; Thierry Frebourg; Dominique Campion
Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation.
Neurology 2000;55(10):1577-8.
2000: E Lopez-Perez; Cécile Dumanchin; Christian Czech; Dominique Campion; Bruno Goud; Laurent Pradier; Thierry Frebourg; Frédéric Checler
Overexpression of Rab11 or constitutively active Rab11 does not affect sAPPalpha and Abeta secretions by wild-type and Swedish mutated betaAPP-expressing HEK293 cells.
Biochemical and biophysical research communications 2000;275(3):910-5.
2000: L Zurutuza; Patrice Verpillat; Gregory RAUX; Didier Hannequin; Michèle Puel; Serge Belliard; A Michon; Y Pothin; Agnès Camuzat; C Penet; Cosette Martin; Alexis Brice; Dominique Campion; Françoise Clerget-Darpoux; Thierry Frebourg
APOE promoter polymorphisms do not confer independent risk for Alzheimer's disease in a French population.
European journal of human genetics : EJHG 2000;8(9):713-6.
2000: Patrice Verpillat; S Bouley; Didier Hannequin; Serge Belliard; Michèle Puel; Catherine Thomas-Anterion; Bruno Dubois; Yves Agid; Dominique Campion; Françoise Clerget-Darpoux; Alexis Brice
Alpha2-macroglobulin gene and Alzheimer's disease: confirmation of association by haplotypes analyses.
Annals of neurology 2000;48(3):400-2.
2000: Gregory RAUX; R Gantier; Cosette Martin; Y Pothin; Alexis Brice; Thierry Frebourg; Dominique Campion
A novel presenilin 1 missense mutation (L153V) segregating with early-onset autosomal dominant Alzheimer's disease.
Human mutation 2000;16(1):95.
2000: R Gantier; D Gilbert; Cécile Dumanchin; Dominique Campion; D Davoust; F Toma; Thierry Frébourg
The pathogenic L392V mutation of presenilin 1 decreases the affinity to glycogen synthase kinase-3 beta.
Neuroscience letters 2000;283(3):217-20.
1999: M de Chaldée; Claudine Laurent; Florence Thibaut; M Martinez; D Samolyk; Michel Petit; Dominique Campion; Jacques Mallet
Linkage disequilibrium on the COMT gene in French schizophrenics and controls.
American journal of medical genetics 1999;88(5):452-7.
1999: R Gantier; Cécile Dumanchin; Dominique Campion; C Loutelier; C Lange; J Gagnon; D Davoust; Thierry Frébourg; F Toma
The L392V mutation of presenilin 1 associated with autosomal dominant early-onset Alzheimer's disease alters the secondary structure of the hydrophilic loop.
Neuroreport 1999;10(14):3071-4.
1999: Dominique Campion; Cécile Dumanchin; Didier Hannequin; Bruno Dubois; Serge Belliard; Michèle Puel; Catherine Thomas-Anterion; A Michon; Cosette Martin; Frédéric Charbonnier; Gregory RAUX; Agnès Camuzat; C Penet; V Mesnage; M Martinez; Françoise Clerget-Darpoux; Alexis Brice; Thierry Frebourg
Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum.
American journal of human genetics 1999;65(3):664-70.
1999: Cécile Dumanchin; Christian Czech; Dominique Campion; Marie-Hélène Cuif; T Poyot; Cosette Martin; Frédéric Charbonnier; Bruno Goud; Laurent Pradier; Thierry Frebourg
Presenilins interact with Rab11, a small GTPase involved in the regulation of vesicular transport.
Human molecular genetics 1999;8(7):1263-9.
1999: Florence Thibaut; Alexis Van der Elst; Dominique Campion; C Martin; B Coron; Sonia Dollfus; Thierry Frebourg; Michel Petit
Apolipoprotein E-varepsilon4 frequency in deficit schizophrenia.
European psychiatry : the journal of the Association of European Psychiatrists 1999;14(3):148-51.
1999: Karine Ancolio; Cécile Dumanchin; H Barelli; J M Warter; Alexis Brice; Dominique Campion; Thierry Frébourg; Frédéric Checler
Unusual phenotypic alteration of beta amyloid precursor protein (betaAPP) maturation by a new Val-715 --> Met betaAPP-770 mutation responsible for probable early-onset Alzheimer's disease.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(7):4119-24.
1999: F Bonnet-Brilhault; Claudine Laurent; Dominique Campion; Florence Thibaut; C Lafargue; Frédéric Charbonnier; Jean-François Deleuze; Jean-François Ménard; M Jay; Michel Petit; Thierry Frebourg; Jacques Mallet
No evidence for involvement of KCNN3 (hSKCa3) potassium channel gene in familial and isolated cases of schizophrenia.
European journal of human genetics : EJHG 1999;7(2):247-50.
1998: Cécile Dumanchin; Agnès Camuzat; Dominique Campion; Patrice Verpillat; D Hannequin; Bruno Dubois; Pascale Saugier-Veber; Cosette Martin; C Penet; Frédéric Charbonnier; Yves Agid; Thierry Frebourg; Alexis Brice
Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism.
Human molecular genetics 1998;7(11):1825-9.
1998: Cécile Dumanchin; Alexis Brice; Dominique Campion; Didier Hannequin; Cosette Martin; V Moreau; Yves Agid; M Martinez; Françoise Clerget-Darpoux; Thierry Frebourg
De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study Group.
Journal of medical genetics 1998;35(8):672-3.
1998: Claudine Laurent; Cecilia Zander; Florence Thibaut; F Bonnet-Brilhault; O Chavand; M Jay; D Samolyk; Michel Petit; M Martinez; Dominique Campion; C Néri; Jacques Mallet; H Cann
Anticipation in schizophrenia: no evidence of expanded CAG/CTG repeat sequences in French families and sporadic cases.
American journal of medical genetics 1998;81(4):342-6.
1998: F Salomon-Nguyen; M Le Coniat-Busson; Roland Heilig; Dominique Campion; Jean Weissenbach; R Berger
Evidence of chromosomal inversion using fluorescence in situ hybridization to stretched DNA.
Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie 1998;321(6):447-52.
1998: M Martinez; Dominique Campion; Alexis Brice; Didier Hannequin; Bruno Dubois; O Didierjean; A Michon; Catherine Thomas-Anterion; Michèle Puel; Thierry Frebourg; Yves Agid; Françoise Clerget-Darpoux
Apolipoprotein E epsilon4 allele and familial aggregation of Alzheimer disease.
Archives of neurology 1998;55(6):810-6.
1998: Florence Thibaut; B Coron; D Hannequin; L Segard; C Martin; Sonia Dollfus; Dominique Campion; Thierry Frebourg; Michel Petit
No association of apolipoprotein epsilon 4 allele with schizophrenia even in cognitively impaired patients.
Schizophrenia research 1998;30(2):149-53.
1998: Didier Hannequin; Dominique Campion; Cécile Dumanchin; M Martinez; Yves Agid; Françoise Clerget-Darpoux; Thierry Frebourg; Alexis Brice
[Genetics of Alzheimer's disease].
Revue neurologique 1998;154 Suppl 2():S65-74.
1997: F Bonnet-Brilhault; Claudine Laurent; Florence Thibaut; Dominique Campion; O Chavand; D Samolyk; M Martinez; Michel Petit; Jacques Mallet
Serotonin transporter gene polymorphism and schizophrenia: an association study.
Biological psychiatry 1997;42(7):634-6.
1997: O Didierjean; M Martinez; Dominique Campion; Didier Hannequin; Bruno Dubois; Cosette Martin; Michèle Puel; Catherine Thomas-Anterion; Florence Pasquier; O Moreau; Marie-Claude Babron; C Penet; Yves Agid; Françoise Clerget-Darpoux; Thierry Frebourg; Alexis Brice
No effect of the alpha1-antichymotrypsin A allele in Alzheimer's disease.
Journal of neurology, neurosurgery, and psychiatry 1997;63(1):103-5.
1997: Florence Thibaut; JM Ribeyre; N Dourmap; R Meloni; C Laurent; Dominique Campion; Jean-François Ménard; Sonia Dollfus; J Mallet; Michel Petit
Association of DNA polymorphism in the first intron of the tyrosine hydroxylase gene with disturbances of the catecholaminergic system in schizophrenia.
Schizophrenia research 1997;23(3):259-64.
1997: H Bickeböller; Dominique Campion; Alexis Brice; Philippe Amouyel; Didier Hannequin; O Didierjean; C Penet; Cosette Martin; Jordi Pérez-Tur; A Michon; Bruno Dubois; F Ledoze; Catherine Thomas-Anterion; Florence Pasquier; Michèle Puel; Jean-Francois Demonet; Olivier Moreaud; Marie-Claude Babron; D Meulien; D Guez; Marie-Christine Chartier-Harlin; Thierry Frebourg; Yves Agid; M Martinez; Françoise Clerget-Darpoux
Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sex.
American journal of human genetics 1997;60(2):439-46.
1997: Alain Malafosse; Marion Leboyer; T d'Amato; S Amadéo; Mocrane Abbar; Dominique Campion; O Canseil; Didier Castelnau; F Gheysen; Bernard GRANGER; B Henrikson; M F Poirier; O Sabaté; D Samolyk; J Feingold; Jacques Mallet
Manic depressive illness and tyrosine hydroxylase gene: linkage heterogeneity and association.
Neurobiology of disease 1997;4(5):337-49.
1997: Claudine Laurent; Florence Thibaut; Philippe Ravassard; Dominique Campion; D Samolyk; C Lafargue; Michel Petit; M Martinez; Jacques Mallet
Detection of two new polymorphic sites in the human interleukin-1 beta gene: lack of association with schizophrenia in a French population.
Psychiatric genetics 1997;7(3):103-5.
1997: Florence Thibaut; Dominique Campion; Claudine Laurent; F Bonnet-Brilhault; Michel Petit
[Dynamic DNA mutations, anticipation and schizophrenia].
L'Encéphale 1997;23(1):22-7.
1996: Alexis Brice; Bruno Dubois; Yves Agid; Dominique Campion; M Martinez; F Clerger-Darpoux; M Bellis; J Mallet; Thierry Frebourg; Didier Hannequin; Michèle Puel; F Ledoze; Florence Pasquier; M A Zimmerman; Catherine Thomas-Anterion; O Moreaud; J Y Goas
[Genetics of dominant autosomal forms of Alzheimer disease: 3 genes and one phenotype. Groupe de Recherche Francais sur la Maladie d'Alzheimer].
Revue neurologique 1996;152(12):725-6.
1996: Sonia Dollfus; Dominique Campion; T Vasse; P Preterre; Claudine Laurent; Thierry d'Amato; Florence Thibaut; Jacques Mallet; Michel Petit
Association study between dopamine D1, D2, D3, and D4 receptor genes and schizophrenia defined by several diagnostic systems.
Biological psychiatry 1996;40(5):419-21.
1996: Dominique Campion; Alexis Brice; Didier Hannequin; Frédéric Charbonnier; Bruno Dubois; Cosette Martin; A Michon; C Penet; M Bellis; A Calenda; M Martinez; Yves Agid; Françoise Clerget-Darpoux; Thierry Frebourg
No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study Group.
Journal of medical genetics 1996;33(8):661-4.
1996: Dominique Campion; Alexis Brice; Cécile Dumanchin; Michèle Puel; M Baulac; V De La Sayette; Didier Hannequin; Charles Duyckaerts; A Michon; Cosette Martin; V Moreau; C Penet; M Martinez; Françoise Clerget-Darpoux; Yves Agid; Thierry Frebourg
A novel presenilin 1 mutation resulting in familial Alzheimer's disease with an onset age of 29 years.
Neuroreport 1996;7(10):1582-4.
1996: R Sherrington; S Froelich; Sandro Sorbi; Dominique Campion; H Chi; Ekaterina Rogaeva; Georges Levesque; Evgeny I Rogaev; C Lin; Yan Liang; Masaki Ikeda; L Mar; Alexis Brice; Yves Agid; M E Percy; F Clerget-Darpoux; Silvia Piacentini; Giordana Marcon; Benedetta Nacmias; Luigi Amaducci; Thierry Frebourg; Lars Lannfelt; Johanna M Rommens; Peter St George-Hyslop
Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant.
Human molecular genetics 1996;5(7):985-8.
1996: B Coron; Dominique Campion; Florence Thibaut; Sonia Dollfus; P Preterre; S Langlois; T Vasse; V Moreau; C Martin; Frédéric Charbonnier; Claudine Laurent; Jacques Mallet; Michel Petit; T Frebourg
Association study between schizophrenia and monoamine oxidase A and B DNA polymorphisms.
Psychiatry research 1996;62(3):221-6.
1996: M Martinez; Dominique Campion; Marie-Claude Babron; Didier Hannequin; Yves Agid; M Bellis; Alexis Brice; J Mallet; A Michon; Catherine Thomas-Anterion; Françoise Clerget-Darpoux
Segregation analysis of Alzheimer pedigrees: rare Mendelian dominant mutation(s) explain a minority of early-onset cases. French Alzheimer Collaborative Group.
American journal of medical genetics 1996;67(1):9-12.
1996: Didier Hannequin; Dominique Campion; Alexis Brice; Thierry Frebourg; M Martinez; F Clerget-Darpoux; Yves Agid
[Genetics of Alzheimer's disease].
La Revue de médecine interne / fondée ... par la Société nationale francaise de médecine interne 1996;17(7):545-50.
1995: Jordi Pérez-Tur; Dominique Campion; M Martinez; Alexis Brice; Sandrine Tardieu; Didier Hannequin; Yves Agid; André Delacourte; Françoise Clerget-Darpoux; Marie-Christine Chartier-Harlin
Evidence for apolipoprotein E epsilon 4 association in early-onset Alzheimer's patients with late-onset relatives.
American journal of medical genetics 1995;60(6):550-3.
1995: Didier Hannequin; Dominique Campion; Sandrine Tardieu; Pascal Auzou; M Martinez; Bruno Dubois; Françoise Clerget-Darpoux; Yves Agid; Alexis Brice
[Phenotype of familial forms of early-onset Alzheimer's disease linked to chromosome 14. Clinical and neuropsychological characteristics of a large group].
Revue neurologique 1995;151(12):682-90.
1995: Dominique Campion; Jean-Michel Flaman; Alexis Brice; Didier Hannequin; Bruno Dubois; Cosette Martin; V Moreau; Frédéric Charbonnier; O Didierjean; Sandrine Tardieu
Mutations of the presenilin I gene in families with early-onset Alzheimer's disease.
Human molecular genetics 1995;4(12):2373-7.
1995: Florence Thibaut; M Martinez; Michel Petit; M Jay; Dominique Campion
Further evidence for anticipation in schizophrenia.
Psychiatry research 1995;59(1-2):25-33.
1995: S Bodeau-Péan; Claudine Laurent; Dominique Campion; M Jay; Florence Thibaut; Sonia Dollfus; Michel Petit; D Samolyk; Thierry d'Amato; M Martinez
No evidence for linkage or association between the dopamine transporter gene and schizophrenia in a French population.
Psychiatry research 1995;59(1-2):1-6.
1995: R Meloni; Claudine Laurent; Dominique Campion; B Ben Hadjali; Florence Thibaut; S Dollfus; Michel Petit; D Samolyk; M Martinez; M F Poirier
A rare allele of a microsatellite located in the tyrosine hydroxylase gene found in schizophrenic patients.
Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie 1995;318(7):803-9.
1995: Dominique Campion; M Martinez; Didier Hannequin; Alexis Brice; Catherine Thomas-Anterion; A Michon; Marie-Claude Babron; Bruno Dubois; Y Goas; A Jaillard-Serradt
Characteristics of familial aggregation in early-onset Alzheimer's disease: evidence of subgroups.
American journal of medical genetics 1995;60(3):221-7.
1995: Alexis Brice; Sandrine Tardieu; Dominique Campion; E Le Guern; M Martinez; A Carpentier; C Penet; Bruno Dubois; M Bellis; Jacques Mallet
Allelic association at the D14S43 locus in early onset Alzheimer's disease. French Alzheimer's Disease Collaborative Study Group.
American journal of medical genetics 1995;60(2):91-3.
1995: Dominique Campion; Cosette Martin; Roland Heilig; Frédéric Charbonnier; V Moreau; Jean-Michel Flaman; JL Petit; Didier Hannequin; Alexis Brice; Thierry Frebourg
The NACP/synuclein gene: chromosomal assignment and screening for alterations in Alzheimer disease.
Genomics 1995;26(2):254-7.
1995: Dominique Campion; Alexis Brice; Didier Hannequin; Sandrine Tardieu; Bruno Dubois; A Calenda; E Brun; C Penet; J Tayot; M Martinez
A large pedigree with early-onset Alzheimer's disease: clinical, neuropathologic, and genetic characterization.
Neurology 1995;45(1):80-5.
1994: Thierry d'Amato; G Waksman; M Martinez; Claudine Laurent; Philip Gorwood; Dominique Campion; M Jay; C Petit; C Savoye; C Bastard
Pseudoautosomal region in schizophrenia: linkage analysis of seven loci by sib-pair and lod-score methods.
Psychiatry research 1994;52(2):135-47.
1994: Claudine Laurent; C Savoye; D Samolyk; R Meloni; Jacques Mallet; Dominique Campion; M Martinez; Thierry d'Amato; C Bastard; Sonia Dollfus
Homozygosity at the dopamine D3 receptor locus is not associated with schizophrenia.
Journal of medical genetics 1994;31(3):260.
1994: Dominique Campion; Thierry d'Amato; C Bastard; Claudine Laurent; F Guedj; M Jay; Sonia Dollfus; Florence Thibaut; Michel Petit; Philip Gorwood
Genetic study of dopamine D1, D2, and D4 receptors in schizophrenia.
Psychiatry research 1994;51(3):215-30.
1994: O Sabaté; Dominique Campion; Thierry d'Amato; M P Martres; Pierre Sokoloff; Bruno GIROS; Marion Leboyer; M Jay; F Guedj; Florence Thibaut
Failure to find evidence for linkage or association between the dopamine D3 receptor gene and schizophrenia.
The American journal of psychiatry 1994;151(1):107-11.
1994: Claudine Laurent; S Bodeau-Péan; Dominique Campion; Thierry d'Amato; M Jay; S Dollfus; F Thibault; Michel Petit; D Samolyk; M Martinez
No major role for the dopamine D2 receptor Ser-->Cys311 mutation in schizophrenia.
Psychiatric genetics 1994;4(4):229-30.
1993: D Carter; Dominique Campion; Thierry d'Amato; M Jay; Alexis Brice; M Bellis; J Mallet; Yves Agid
No mutation in codon 713 of the amyloid precursor gene in schizophrenic patients.
Human molecular genetics 1993;2(3):321.
1993: Alexis Brice; A L Boch; Giovanni Stevanin; C Khati; Bruno Dubois; Yves Agid; Dominique Campion; F Clerget; J Mallet; M Bellis
Absence of the amyloid precursor protein gene mutation (APP717: Val->Ile) in 85 cases of early onset Alzheimer's disease.
Journal of neurology, neurosurgery, and psychiatry 1993;56(1):112-3.
1993: M Martinez; Dominique Campion; Marie-Claude Babron; F Clerget-Darpoux
Is a single mutation at the same locus responsible for all affected cases in a large Alzheimer pedigree (FAD4)?
Genetic epidemiology 1993;10(6):431-5.
1992: Dominique Campion; Thierry d'Amato; H Laklou; O Sabate; M Jay; Marion Leboyer; Alain Malafosse; Philip Gorwood; Marie-Claude Babron; D Hillaire
Failure to replicate linkage between chromosome 5q11-q13 markers and schizophrenia in 28 families.
Psychiatry research 1992;44(3):171-9.
1992: Dominique Campion; Florence Thibaut; Pierre Denise; P Courtin; M Pottier; D Levillain
SPEM impairment in drug-naive schizophrenic patients: evidence for a trait marker.
Biological psychiatry 1992;32(10):891-902.
1992: Marion Leboyer; M J Filteau; M Jay; Dominique Campion; Thierry Rochet; Thierry d'Amato; J Feingold; A Des Lauriers; D Widlöcher
No gender effect on age at onset in familial schizophrenia?
The American journal of psychiatry 1992;149(10):1409.
1992: Thierry d'Amato; Dominique Campion; Philip Gorwood; M Jay; O Sabate; C Petit; M Abbar; Alain Malafosse; Marion Leboyer; D Hillaire
Evidence for a pseudoautosomal locus for schizophrenia. II: Replication of a non-random segregation of alleles at the DXYS14 locus.
The British journal of psychiatry : the journal of mental science 1992;161():59-62.
1992: Philip Gorwood; Marion Leboyer; Thierry d'Amato; M Jay; Dominique Campion; D Hillaire; J Mallet; JOSUE FEINGOLD
Evidence for a pseudoautosomal locus for schizophrenia. I: A replication study using phenotype analysis.
The British journal of psychiatry : the journal of mental science 1992;161():55-8.
1992: Dominique Campion; Marion Leboyer; D Hillaire; L Halle; Philip Gorwood; B Cavelier; M F Soufflet; Thierry d'Amato; B Muller; Cécile Kaplan
Relationship of HLA to schizophrenia not supported in multiplex families.
Psychiatry research 1992;41(2):99-105.
1992: Marion Leboyer; M J Filteau; M Jay; Dominique Campion; Thierry d'Amato; M Guilloud-Bataille; D Hillaire; JOSUE FEINGOLD; A des Lauriers; D Widlöcher
Clinical subtypes and age at onset in schizophrenic siblings.
Psychiatry research 1992;41(2):107-14.
1990: Marion Leboyer; M Jay; Thierry d'Amato; Dominique Campion; M Guilloud-Bataille; D Hillaire; A Drouet; J P Lépine; E Bois; JOSUE FEINGOLD
Subtyping familial schizophrenia: reliability, concordance, and stability.
Psychiatry research 1990;34(1):77-88.