FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Richard Delorme

Research Profile

Disorders

Physiology

Concepts & Ideas

Procedures

Activities & Behaviors

Family

Chemicals & Drugs

Co-author Network

Publications

TOP 3
AC Tabet; Alain Verloes; Frédérique Amsellem; Brigitte Benzacken; Richard Delorme; Marion Leboyer; Marion Pilorge; Jean-Marc Pinard; Catalina Betancur
Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother.
Samuele Cortese; Richard Delorme; Robin Azoulay; Bernardo Dalla Bernardina; F Xavier Castellanos; François Chalard; David Chechin; Michel Lecendreux; Marie-Christine Mouren; Andrea Sbarbati; Guy Sebag; Eric Konofal
Brain iron levels in attention-deficit/hyperactivity disorder: a pilot MRI study.
Pauline Chaste; Anne Bargiacchi; Catalina Betancur; Thomas Bourgeron; Séverine Drunat; Marion Gérard-Blanluet; Suzanne Kuzbari; Marion Leboyer; Richard Delorme
High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Richard Delorme (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2012: AC Tabet; Alain Verloes; Frédérique Amsellem; Brigitte Benzacken; Richard Delorme; Marion Leboyer; Marion Pilorge; Jean-Marc Pinard; Catalina Betancur
Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother.
European journal of human genetics : EJHG 2012;20(5):540-6.
2012: Samuele Cortese; Richard Delorme; Robin Azoulay; Bernardo Dalla Bernardina; F Xavier Castellanos; François Chalard; David Chechin; Michel Lecendreux; Marie-Christine Mouren; Andrea Sbarbati; Guy Sebag; Eric Konofal
Brain iron levels in attention-deficit/hyperactivity disorder: a pilot MRI study.
The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2012;13(3):223-31.
2012: Pauline Chaste; Anne Bargiacchi; Catalina Betancur; Thomas Bourgeron; Séverine Drunat; Marion Gérard-Blanluet; Suzanne Kuzbari; Marion Leboyer; Richard Delorme
High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters.
Molecular autism 2012;3(1):5.
2011: Pauline Chaste; Nathalie Clement; Richard Delorme; Christelle Durand; Fabien Fauchereau; Christopher Gillberg; I Carina Gillberg; Jean-Luc Guillaume; Guillaume Huguet; Ralf JOckers; Marina Konyukh; Jean Marie Launay; Claire Leblond; Marion Leboyer; Nathalie Lemière; Jonas Melke; Gudrun Nygren; Cécile Pagan; Maria Rastam; Isabelle Scheid; Emilie Serrano; Ola Ståhlberg; Roberto Toro; Henrik Anckarsäter; Hany Goubran Botros; Lydia Boudarene; Thomas Bourgeron
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders.
Journal of pineal research 2011;51(4):394-9.
2011: Aline S Sampaio; Jacquelyn Crane; Richard Delorme; Jesen Fagerness; Marion Leboyer; David L Pauls; S Evelyn Stewart
Association between polymorphisms in GRIK2 gene and obsessive-compulsive disorder: a family-based study.
CNS neuroscience & therapeutics 2011;17(3):141-7.
2011: Marina Konyukh; Richard Delorme; Pauline Chaste; Claire Leblond; Nathalie Lemière; Gudrun Nygren; Henrik Anckarsäter; Maria Rastam; Ola Ståhlberg; Frederique Amsellem; I Carina Gillberg; Marie-Christine Mouren-Simeoni; Evelyn Herbrecht; Fabien Fauchereau; Roberto Toro; Christopher Gillberg; Marion Leboyer; Thomas Bourgeron
Variations of the candidate SEZ6L2 gene on Chromosome 16p11.2 in patients with autism spectrum disorders and in human populations.
PloS one 2011;6(3):e17289.
2011: Cecile Pagan; Hany Goubran Botros; Karine Poirier; Anne Dumaine; Stéphane Jamain; Sarah Moreno; Arjan de Brouwer; Hilde Van Esch; Richard Delorme; Jean-Marie Launay; Andreas Tzschach; Vera Kalscheuer; Didier Lacombe; Sylvain Briault; Frédéric Laumonnier; Martine Raynaud; Bregje W van Bon; Marjolein H Willemsen; Marion Leboyer; Jamel Chelly; Thomas Bourgeron
Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with intellectual disability.
BMC medical genetics 2011;12():17.
2010: Roberto Toro; Marina Konyukh; Richard Delorme; Claire Leblond; Pauline Chaste; Fabien Fauchereau; Mary Coleman; Marion Leboyer; Christopher Gillberg; Thomas Bourgeron
Key role for gene dosage and synaptic homeostasis in autism spectrum disorders.
Trends in genetics : TIG 2010;26(8):363-72.
2010: M Schiff; Richard Delorme; Jean-François Benoist; Hélène Ogier de Baulny
[Should a metabolic work-up be performed in autism?].
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 2010;17(6):802-3.
2010: Richard Delorme; Pauline Chaste; Isabelle Scheid; Samuel Cortese; Marie-Christine Mouren
Using videotaped vignettes to improve the teaching quality in child and adolescent psychiatry.
Medical teacher 2010;32(8):703-4.
2010: Pauline Chaste; Nathalie Clement; Oriane Mercati; Jean-Luc Guillaume; Richard Delorme; Hany Goubran Botros; Cécile Pagan; Samuel Périvier; Isabelle Scheid; Gudrun Nygren; Henrik Anckarsäter; Maria Rastam; Ola Ståhlberg; Christopher Gillberg; Emilie Serrano; Nathalie Lemière; Jean-Marie Launay; Marie-Christine Mouren-Simeoni; Marion Leboyer; Christopher Gillberg; Ralf JOckers; Thomas Bourgeron
Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general population.
PloS one 2010;5(7):e11495.
2010: Richard Delorme; Catalina Betancur; Isabelle Scheid; Henrik Anckarsäter; Pauline Chaste; Stéphane Jamain; Franck Schuroff; Gudrun Nygren; Evelyn Herbrecht; Anne Dumaine; Marie Christine Mouren; Maria Råstam; Marion Leboyer; Christopher Gillberg; Thomas Bourgeron
Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls.
BMC medical genetics 2010;11():108.
2010: Richard Delorme; Daniel Moreno-De-Luca; Aurélie Gennetier; Wolfgang Maier; Pauline Chaste; Rainald Mössner; Hans Jörgen Grabe; Stephan Ruhrmann; Peter Falkai; Marie-Christine Mouren; Marion Leboyer; Michael Wagner; Catalina Betancur
Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder.
BMC medical genetics 2010;11():100.
2009: Christel Depienne; Daniel Moreno-De-Luca; Delphine Heron; Delphine Bouteiller; Aurélie Gennetier; Richard Delorme; Pauline Chaste; Jean-Pierre Siffroi; Sandra Chantot-Bastaraud; Baya Benyahia; Oriane Trouillard; Gudrun Nygren; Svenny Kopp; Maria Johansson; Maria Rastam; Lydie Burglen; Eric LeGuern; Alain Verloes; Marion Leboyer; Alexis Brice; Christopher Gillberg; Catalina Betancur
Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.
Biological psychiatry 2009;66(4):349-59.
2009: Thomas Bourgeron; Marion Leboyer; Richard Delorme
[Autism: more evidence of a genetic cause].
Bulletin de l'Académie nationale de médecine 2009;193(2):299-304; discussion 304-5.
2009: Xiaohong Gong; Richard Delorme; Fabien Fauchereau; Christelle M Durand; Pauline Chaste; Catalina Betancur; Hany Goubran-Botros; Gudrun Maria Nygren; Henrik Anckarsäter; Maria Rastam; I Carina Gillberg; Svenny Kopp; Marie-Christine Mouren-Simeoni; Christopher Gillberg; Marion Leboyer; Thomas Bourgeron
An investigation of ribosomal protein L10 gene in autism spectrum disorders.
BMC medical genetics 2009;10():7.
2008: Xiaohong Gong; Elena Bacchelli; Francesca Blasi; Claudio Toma; Catalina Betancur; Pauline Chaste; Richard Delorme; Christelle M Durand; Fabien Fauchereau; Hany Goubran Botros; Marion Leboyer; Marie-Christine Mouren-Simeoni; Gudrun Nygren; Henrik Anckarsäter; Maria Rastam; I Carina Gillberg; Christopher Gillberg; Daniel Moreno-De-Luca; Simona Carone; Ilona Nummela; Mari Rossi; Agatino Battaglia; Irma Jarvela; Elena Maestrini; Thomas Bourgeron
Analysis of X chromosome inactivation in autism spectrum disorders.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008;147B(6):830-5.
2008: Jonas Melke; Hany Goubran-Botros; Pauline Chaste; Catalina Betancur; Gudrun Nygren; Henrik Anckarsäter; Maria Rastam; Ola Ståhlberg; I Carina Gillberg; Richard Delorme; Nadia Chabane; Marie-Christine Mouren-Simeoni; Fabien Fauchereau; Christelle M Durand; F Chevalier; X Drouot; C Collet; Jean-Marie Launay; Marion Leboyer; Christopher Gillberg; Thomas Bourgeron
Abnormal melatonin synthesis in autism spectrum disorders.
Molecular psychiatry 2008;13(1):90-8.
2007: S Evelyn Stewart; Jesen Fagerness; Jill Platko; Jordan W Smoller; Jeremiah M Scharf; Cornelia Illmann; Eric Jenike; Nadia Chabane; Marion Leboyer; Richard Delorme; Michael A Jenike; David L Pauls
Association of the SLC1A1 glutamate transporter gene and obsessive-compulsive disorder.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007;144B(8):1027-33.
2007: S Evelyn Stewart; Jill Platko; Jesen Fagerness; Julie Birns; Eric Jenike; Jordan W Smoller; Roy H Perlis; Marion Leboyer; Richard Delorme; Nadia Chabane; Scott L Rauch; Michael A Jenike; David L Pauls
A genetic family-based association study of OLIG2 in obsessive-compulsive disorder.
Archives of general psychiatry 2007;64(2):209-14.
2007: Nadia Chabane; Richard Delorme
[Obsessive-compulsive disorder in children and adolescents].
La Revue du praticien 2007;57(1):45-51.
2007: Joseph Buxbaum; Guiqing Cai; Gudrun Nygren; Pauline Chaste; Richard Delorme; Juliet Goldsmith; Maria Råstam; Jeremy Silverman; Eric Hollander; Christopher Gillberg; Marion Leboyer; Catalina Betancur
Mutation analysis of the NSD1 gene in patients with autism spectrum disorders and macrocephaly.
BMC medical genetics 2007;8():68.
2007: Christelle M Durand; Catalina Betancur; Tobias M Boeckers; Jürgen Bockmann; Pauline Chaste; Fabien Fauchereau; Gudrun Nygren; Maria Rastam; I Carina Gillberg; Henrik Anckarsäter; Eili Sponheim; Hany Goubran-Botros; Richard Delorme; Nadia Chabane; Marie-Christine Mouren-Simeoni; Philippe De Mas; Eric Bieth; Bernadette Rogé; Delphine Héron; Lydie Burglen; Christopher Gillberg; Marion Leboyer; Thomas Bourgeron
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.
Nature genetics 2007;39(1):25-7.
2007: Richard Delorme; Véronique Goussé; Isabelle Roy; Anca Trandafir; Flavie MATHIEU; Marie-Christine Mouren-Siméoni; Catalina Betancur; Marion Leboyer
Shared executive dysfunctions in unaffected relatives of patients with autism and obsessive-compulsive disorder.
European psychiatry : the journal of the Association of European Psychiatrists 2007;22(1):32-8.
2006: Marie-Christine Mouren; Richard Delorme
[School phobia or school refusal: controversial concepts].
Bulletin de l'Académie nationale de médecine 2006;190(8):1629-39; discussion 1639-41.
2006: Richard Delorme; Christelle M Durand; Catalina Betancur; Michael Wagner; Stephan Ruhrmann; Hans-Juergen Grabe; Gudrun Nygren; Christopher Gillberg; Marion Leboyer; Thomas Bourgeron; Philippe Courtet; Fabrice Jollant; Catherine Buresi; Jean-Michel Aubry; Patrick Baud; Guido Bondolfi; Gilles Bertschy; Nader Perroud; Alain Malafosse
No human tryptophan hydroxylase-2 gene R441H mutation in a large cohort of psychiatric patients and control subjects.
Biological psychiatry 2006;60(2):202-3.
2006: Christelle M Durand; Caroline Kappeler; Catalina Betancur; Richard Delorme; Hélène Quach; Hany Goubran-Botros; Jonas Melke; Gudrun Nygren; Nadia Chabane; Frank Bellivier; Andrei Szoke; Franck Schurhoff; Maria Rastam; Henrik Anckarsäter; Christopher Gillberg; Marion Leboyer; Thomas Bourgeron
Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disorders.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2006;141B(1):67-70.
2006: Richard Delorme; Arnaud Bille; Catalina Betancur; Flavie MATHIEU; Nadia Chabane; Marie-Christine Mouren-Simeoni; Marion Leboyer
Exploratory analysis of obsessive compulsive symptom dimensions in children and adolescents: a prospective follow-up study.
BMC psychiatry 2006;6():1.
2005: Richard Delorme; Catalina Betancur; M Wagner; Marie-Odile Krebs; Philip Gorwood; P Pearl; Gudrun Nygren; Christelle M Durand; Friederike Buhtz; P Pickering; Jonas Melke; Stephan Ruhrmann; Henrik Anckarsäter; Nadia Chabane; Amélie Kipman; Claudia Reck; Bruno Millet; Isabelle Roy; Marie-Christine Mouren-Simeoni; Wolfgang Maier; Maria Råstam; Christopher Gillberg; Marion Leboyer; Thomas Bourgeron
Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder.
Molecular psychiatry 2005;10(12):1059-61.
2005: Véronique Goussé; Richard Delorme; Nadia Chabane; Fernando Perez-Diaz; M Flavie; Marie-Christine Mouren-Siméoni; Marion Leboyer
[Is age at onset associated with executive dysfunction in obsessive-compulsive disorder?].
L'Encéphale 2005;31(6 Pt 1):666-71.
2005: Nadia Chabane; Richard Delorme; Bruno Millet; Marie-Christine Mouren; Marion Leboyer; David L Pauls
Early-onset obsessive-compulsive disorder: a subgroup with a specific clinical and familial pattern?
Journal of child psychology and psychiatry, and allied disciplines 2005;46(8):881-7.
2005: Richard Delorme; Catalina Betancur; Jacques Callebert; Nadia Chabane; Jean-Louis Laplanche; Marie-Christine Mouren-Simeoni; Jean-Marie Launay; Marion Leboyer
Platelet serotonergic markers as endophenotypes for obsessive-compulsive disorder.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2005;30(8):1539-47.
2005: Richard Delorme; Jean-Louis Golmard; Nadia Chabane; Bruno Millet; Marie-Odile Krebs; Marie-Christine Mouren-Simeoni; Marion Leboyer
Admixture analysis of age at onset in obsessive-compulsive disorder.
Psychological medicine 2005;35(2):237-43.
2004: Charlotte Neergaard Henrichsen; Richard Delorme; Maria Boucherie; Dominique Marelli; Patrick Baud; Frank Bellivier; Philippe Courtet; Nadia Chabane; Chantal Henry; Marion Leboyer; Alain Malafosse; Stylianos E Antonarakis; Sophie Dahoun
No association between DUP25 and anxiety disorders.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004;128B(1):80-3.
2004: Nadia Chabane; Bruno Millet; Richard Delorme; Dirk Lichtermann; Flavie MATHIEU; Jean-Louis Laplanche; Isabelle Roy; Marie-Christine Mouren; Régis Hankard; Wolfgang Maier; Jean-Marie Launay; Marion Leboyer
Lack of evidence for association between serotonin transporter gene (5-HTTLPR) and obsessive-compulsive disorder by case control and family association study in humans.
Neuroscience letters 2004;363(2):154-6.
2004: Richard Delorme; Marie-Odile Krebs; Nadia Chabane; Isabelle Roy; Bruno Millet; Marie-Christine Mouren-Simeoni; Wolfgang Maier; Thomas Bourgeron; Marion Leboyer
Frequency and transmission of glutamate receptors GRIK2 and GRIK3 polymorphisms in patients with obsessive compulsive disorder.
Neuroreport 2004;15(4):699-702.
2004: Richard Delorme; Nadia Chabane; Jacques Callebert; Bruno Falissard; Marie-Christine Mouren-Siméoni; Frédéric Rouillon; Jean-Marie Launay; Marion Leboyer
Platelet serotonergic predictors of clinical improvement in obsessive compulsive disorder.
Journal of clinical psychopharmacology 2004;24(1):18-23.
2003: Bruno Millet; Nadia Chabane; Richard Delorme; Marion Leboyer; Sophie Leroy; Marie-France Poirier; Marie-Chantal Bourdel; Marie-Christine Mouren-Simeoni; Fréderic Rouillon; Henri Loo; Marie-Odile Krebs
Association between the dopamine receptor D4 (DRD4) gene and obsessive-compulsive disorder.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003;116B(1):55-9.