C. Buresi

发表

Association between bipolar disorder and monoamine oxidase A gene polymorphisms: results of a multicenter study.

M. Leboyer, M. Preisig, F. Bellivier, 2000, The American journal of psychiatry.

The Role of Recent Admixture in Forming the Contemporary West Eurasian Genomic Landscape

Igor Rudan, Paolo Anagnostou, Simon Myers, 2015, Current Biology.

Identification of mutations in cystatin B, the gene responsible for the Unverricht-Lundborg type of progressive myoclonus epilepsy (EPM1).

M C Peitsch, M Mirotsou, M. Peitsch, 1997, American journal of human genetics.

Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy

Alain Malafosse, S. Antonarakis, C. Buresi, 1997, Nature.

Lack of association between 5HT2A receptor gene haplotype, bipolar disorder and its clinical subtypes in a West European sample

M. Leboyer, M. Preisig, F. Bellivier, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Antidepressant-induced mania, rapid cycling and the serotonin transporter gene polymorphism

M. Leboyer, F. Bellivier, P. Baud, 2005, The Pharmacogenomics Journal.

Identification and analysis of new sequence variants in the human tryptophan hydroxylase (TpH) gene

D. Mouthon, C. Buresi, A. Malafosse, 2000, Molecular Psychiatry.

No Human Tryptophan Hydroxylase-2 Gene R441H Mutation in a Large Cohort of Psychiatric Patients and Control Subjects

T. Bourgeron, R. Delorme, M. Leboyer, 2006, Biological Psychiatry.

GABAB Receptor 1 Polymorphism (G1465A) and Temporal Lobe Epilepsy

C. Buresi, A. Malafosse, A. Crespel, 2005 .

Structural analysis of the minisatellite present at the 3' end of the human apolipoprotein B gene: new definition of the alleles and evolutionary implications.

C. Buresi, F. Cambien, N. Smaoui, 1996, Human molecular genetics.

Exon duplication and triplication in the human T-cell receptor gamma constant region genes and RFLP in French, Lebanese, Tunisian, and Black African populations

C. Buresi, M. Lefranc, G. Lefranc, 2004, Immunogenetics.

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

Stéphanie Baulac, Andrew Escayg, Miriam H. Meisler, 2000, Nature Genetics.

DNA polymorphisms in linkage disequilibrium at the 3‘ end of the human APO AII gene: relationships with lipids, apolipoproteins and coronary heart disease

C. Buresi, D. Arveiler, G. Luc, 1996, Clinical genetics.

Polymorphism at VNTR Locus 3′ to the apolipoprotein B gene in a tunisian population: Difference from other ethnic groups

C. Buresi, G. Roizes, E. Desmarais, 1995, Genetic epidemiology.

The Role of Recent Admixture in Forming the Contemporary West Eurasian Genomic Landscape

R. J. Herrera, S. Myers, C. Buresi, 2015, Current Biology.

Defective, deleted or converted CYP21B gene and negative association with a rare restriction fragment length polymorphism allele of the factor B gene in congenital adrenal hyperplasia

C. Buresi, J. Lobaccaro, C. Sultan, 1990, Human Genetics.

Carboxypeptidase A6 gene (CPA6) mutations in a recessive familial form of febrile seizures and temporal lobe epilepsy and in sporadic temporal lobe epilepsy

C. Buresi, A. Malafosse, A. Crespel, 2012, Human mutation.

Suicidal behavior: Relationship between phenotype and serotonergic genotype

P. Courtet, C. Buresi, A. Malafosse, 2005, American journal of medical genetics. Part C, Seminars in medical genetics.

[Implication of genes of the serotonergic system on vulnerability to suicidal behavior].

P. Courtet, C. Buresi, A. Malafosse, 2004, Journal of psychiatry & neuroscience : JPN.

The Role of Recent Admix ture in Forming the Contemporary West Eurasian Genomic Landscape Highlights

R. J. Herrera, S. Myers, C. Buresi, 2015 .

Erratum: The role of recent admixture in forming the contemporary west Eurasian genomic landscape (Current Biology (2015) 25 (2518-2526))

R. J. Herrera, S. Myers, C. Buresi, 2015 .

The influence of four serotonin‐related genes on decision‐making in suicide attempters

M. Leboyer, F. Bellivier, P. Courtet, 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

The monoamine oxidase A gene may influence the means used in suicide attempts

P. Courtet, D. Mouthon, C. Buresi, 2005, Psychiatric genetics.

Association between the tryptophan hydroxylase gene and manic-depressive illness.

M. Leboyer, F. Bellivier, P. Courtet, 1998, Archives of general psychiatry.

Variant mapping of the Apo(B) AT rich minisatellite. Dependence on nucleotide sequence of the copy number variations. Instability of the non-canonical alleles.

C. Buresi, F. Cambien, G. Roizes, 1993, Nucleic acids research.

Study of the voltage‐gated sodium channel β1 subunit gene (SCN1B) in the benign familial infantile convulsions syndrome (BFIC)

C. Buresi, A. Malafosse, A Malafosse, 2000, Human mutation.

Identification of a new locus for generalized epilepsy with febrile seizures plus (GEFS+) on chromosome 2q24-q33.

D. Mouthon, C. Buresi, A. Malafosse, 1999, American journal of human genetics.

Exon duplication and triplication in the human T-cell receptor gamma constant region genes and RFLP in French, Lebanese, Tunisian, and Black African populations

C. Buresi, M. Lefranc, S. Huck, 2006, Immunogenetics.

No association between non‐violent suicidal behavior and the serotonin transporter promoter polymorphism

P. Baud, P. Courtet, D. Mouthon, 2003, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Association between violent suicidal behavior and the low activity allele of the serotonin transporter gene

J. Boulenger, P. Baud, P. Courtet, 2001, Molecular Psychiatry.

Suicide attempts and the tryptophan hydroxylase gene

M. Leboyer, F. Bellivier, P. Courtet, 2001, Molecular Psychiatry.

Serotonin transporter gene may be involved in short-term risk of subsequent suicide attempts

Philippe Courtet, Stephane Torres, Frank Bellivier, 2003, Biological Psychiatry.

Allelic heterogeneity of mediterranean myoclonus and the cystatin B gene

C. Buresi, A. Malafosse, P. Genton, 1997, Annals of neurology.

myoclonic epilepsy Association of the connexin36 gene with juvenile

J. Villemure, S. Antonarakis, S. Deutsch, 2005 .

Association of the connexin36 gene with juvenile myoclonic epilepsy

M Rees, J. Villemure, S. Antonarakis, 2004, Journal of Medical Genetics.

Association of genes coding for the alpha-4, alpha-5, beta-2 and beta-3 subunits of nicotinic receptors with cigarette smoking and nicotine dependence.

D. Bertrand, M. Munafo, J. Etter, 2009, Addictive behaviors.

Interaction between BDNF Val66Met and childhood trauma on adult’s violent suicide attempt

M. Leboyer, F. Bellivier, P. Baud, 2008, Genes, brain, and behavior.

Founder Effect in Patients with Unverricht‐Lundborg Disease on Reunion Island

C. Buresi, A. Malafosse, A. Biraben, 2003, Epilepsia.

Catechol‐O‐methyltransferase polymorphism (COMT) in suicide attempters: A possible gender effect on anger traits

P. Baud, P. Courtet, C. Buresi, 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Haplotype study of West European and North African Unverricht-Lundborg chromosomes: evidence for a few founder mutations

C. Buresi, A. Malafosse, A. Biraben, 2002, Human Genetics.

A PCR amplification method reveals instability of the dodecamer repeat in progressive myoclonus epilepsy (EPM1) and no correlation between the size of the repeat and age at onset.

S. Antonarakis, C. Buresi, A. Malafosse, 1998, American journal of human genetics.

BRD2 and TAP-1 genes and juvenile myoclonic epilepsy

C. Buresi, A. Malafosse, M. Dogui, 2010, Neurological Sciences.

Association between brain-derived neurotrophic factor gene and a severe form of bipolar disorder, but no interaction with the serotonin transporter gene.

M. Leboyer, M. Preisig, F. Bellivier, 2008, Bipolar disorders.

Deletion, insertion, and restriction site polymorphism of the T-cell receptor gamma variable locus in French, Lebanese, Tunisian, and Black African populations

C. Buresi, M. Lefranc, G. Lefranc, 2006, Immunogenetics.

GABA receptor 1 polymorphism (G1465A) and temporal lobe epilepsy.

C. Buresi, A. Malafosse, A. Crespel, 2005, Epilepsia.

Interaction between BDNF Val66Met and childhood trauma on adult’s violent suicide attempt

M. Leboyer, P. Baud, P. Courtet, 2008, Genes, brain, and behavior.

Decreased expression of Gαs mRNA and protein levels in lithium‐treated bipolar affective disorder

J. Golaz, C. Buresi, A. Malafosse, 2000 .