A. Malafosse

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.

Family studies in narcolepsy.

A. Malafosse, A. Besset, M. Billiard, 1994, Sleep.

Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) Report

Naomi R. Wray, Mark A. Frye, Alessio Squassina, 2013, PloS one.

A pocket of very high suicide rates in a non-violent, egalitarian and cooperative population of South-East Asia

A. Malafosse, F. Jollant, R. Docto, 2014, Psychological Medicine.

Distribution of mRNA for the α4 subunit of the nicotinic acetylcholine receptor in the human fetal brain

D. Bertrand, A. Malafosse, P. Vallet, 1998 .

Distribution of mRNA for the alpha4 subunit of the nicotinic acetylcholine receptor in the human fetal brain.

D. Bertrand, A. Malafosse, P. Vallet, 1998, Brain research. Molecular brain research.

A nonsense mutation in the α4 subunit of the nicotinic acetylcholine receptor (CHRNA4) cosegregates with 20q-linked benign neonatal familial convulsions (EBNI)

A. Malafosse, L. Vallée, O. Steinlein, 1994, Neurobiology of Disease.

A history of major depressive disorder influences intent to die in violent suicide attempters.

P. Courtet, A. Malafosse, F. Jollant, 2004, The Journal of clinical psychiatry.

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

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

Prevalence of DSM ^ IV psychiatric disorder in the French elderly population

J. Boulenger, A. Malafosse, K. Ritchie, 2022 .

No association between DUP25 and anxiety disorders

R. Delorme, M. Leboyer, C. N. Henrichsen, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

EEG anomalies in adult ADHD subjects performing a working memory task

P. Baud, A. Malafosse, J. Richiardi, 2013, Neuroscience.

Naturally Occurring Carboxypeptidase A6 Mutations

A. Malafosse, A. Crespel, L. Fricker, 2012, The Journal of Biological Chemistry.

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 .

Short Report on DNA Marker at Candidate Locus

A. Malafosse, M. Guipponi, M. Baldy‐Moulinier, 1997 .

Genetic association of the Phosphoinositide-3 kinase in schizophrenia and bipolar disorder and interaction with a BDNF gene polymorphism

A. Malafosse, F. Karege, N. Perroud, 2011, Brain and behavior.

Distinguishing the relevant features of frequent suicide attempters.

J. Leiva-Murillo, E. Baca-García, P. Courtet, 2011, Journal of psychiatric research.

Association of AKT1 gene variants and protein expression in both schizophrenia and bipolar disorder

M. Leboyer, A. Malafosse, F. Schürhoff, 2010, Genes, brain, and behavior.

Title: Distinguishing the relevant features of frequent suicide attempters Running title: Features of frequent suicide attempters

J. Leiva-Murillo, E. Baca-García, P. Courtet, 2010 .

Lithium and Haloperidol Treatments Differently Affect the Mononuclear Leukocyte Gαs Protein Levels in Bipolar Affective Disorder

J. Golaz, A. Malafosse, M. Schwald, 1999, Neuropsychobiology.

Identification of Six Novel SOD1 Gene Mutations in Familial Amyotrophic Lateral Sclerosis

A. Malafosse, V. Meininger, F. Salachas, 1998, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Coexistence of dominant and recessive familial amyotrophic lateral sclerosis with the D90A Cu,Zn superoxide dismutase mutation within the same country

A. Malafosse, G. Rouleau, G. Rouleau, 2000, European journal of neurology.

Somatic markers and explicit knowledge are both involved in decision-making

P. Courtet, A. Malafosse, I. Jaussent, 2009, Neuropsychologia.

in bipolar disorder NR3C1 receptor gene Childhood maltreatment and methylation of the glucocorticoid

A. Malafosse, J. Aubry, A. Dayer, 2014 .

Childhood maltreatment and methylation of the glucocorticoid receptor gene NR 3 C 1 in bipolar disorder

A. Malafosse, J. Aubry, A. Dayer, 2014 .

Childhood maltreatment and methylation of the glucocorticoid receptor gene NR3C1 in bipolar disorder.

A. Malafosse, J. Aubry, A. Dayer, 2014, The British journal of psychiatry : the journal of mental science.

Genetic linkage study of an autosomal recessive form of juvenile myoclonic epilepsy in a consanguineous Tunisian family

D. Mouthon, A. Malafosse, M. Dogui, 2010, Epilepsy Research.

Dimorphism of TAP‐1 gene in Caucasian with juvenile myoclonic epilepsy and in Tunisian with idiopathic generalized epilepsies

A. Malafosse, M. Dogui, L. Chouchane, 2010, International journal of immunogenetics.

Lack of association between juvenile myoclonic epilepsy and GABRA5 and GABRB3 genes.

A. Malafosse, M. Guipponi, C. Girard-Reydet, 1997, American journal of medical genetics.

Apolipoprotein E genotyping in sporadic amyotrophic lateral sclerosis: evidence for a major influence on the clinical presentation and prognosis

A. Malafosse, W. Camu, A. Sefiani, 1996, Journal of the Neurological Sciences.

Lack of Association Between Juvenile Myoclonic Epilepsy and HLA‐DR13

E. Neidhart, A. Malafosse, S. Hellard, 1999, Epilepsia.

Brief Communication Lack of Association Between Juvenile Myoclon and HLA-DR 13 c Epi

E. Neidhart, A. Malafosse, S. Hellard, 1999 .

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

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

Ion channel variation causes epilepsies

D. Bertrand, A. Malafosse, S. Hellard, 2001, Brain Research Reviews.

Angiotensin I‐converting enzyme I/D polymorphism and suicidal behaviors

M. Leboyer, D. Sparks, D. Sparks, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Facilitation of olfactory bulb kindling after specific destruction of serotoninergic terminals in the olfactory bulb of the rat

A. Malafosse, G. Rondouin, A. Privat, 1986, Neuroscience Letters.

Protein levels of β-catenin and activation state of glycogen synthase kinase-3β in major depression. A study with postmortem prefrontal cortex.

A. Malafosse, F. Karege, N. Perroud, 2012, Journal of affective disorders.

Alterations in Phosphatidylinositol 3-Kinase Activity and PTEN Phosphatase in the Prefrontal Cortex of Depressed Suicide Victims

A. Malafosse, F. Karege, N. Perroud, 2011, Neuropsychobiology.

Increased CPA6 promoter methylation in focal epilepsy and in febrile seizures

A. Malafosse, F. Karege, N. Belhedi, 2014, Epilepsy Research.

The effect of clinical outcome on platelet G proteins of major depressed patients

A. Malafosse, F. Karege, P. Bovier, 1998, European Neuropsychopharmacology.

The Tutsi genocide and transgenerational transmission of maternal stress: epigenetics and biology of the HPA axis

A. Malafosse, F. Karege, L. Stenz, 2014, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

Reproductive Technologies and Genomic Selection in Cattle

A. Malafosse, Y. Heyman, S. Fritz, 2010, Veterinary medicine international.

Localization of mRNA for CHRNA7 in human fetal brain.

D. Bertrand, A. Malafosse, C. Agulhon, 1999, Neuroreport.

Electroclinical signs of benign neonatal familial convulsions

A. Malafosse, C. Marescaux, B. Maton, 1993, Annals of neurology.

Suicide attempt characteristics may orientate toward a bipolar disorder in attempters with recurrent depression.

P. Courtet, A. Malafosse, I. Jaussent, 2010, Journal of affective disorders.

Impaired decision making in suicide attempters.

M. Leboyer, F. Bellivier, P. Courtet, 2005, The American journal of psychiatry.

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

Christian E Elger, Holger Lerche, Ulrich Stephani, 2009, Nature Genetics.

A new locus on chromosome 22q13.31 linked to recessive genetic epilepsy with febrile seizures plus (GEFS+) in a Tunisian consanguineous family

A. Malafosse, F. Béna, M. Guipponi, 2013, BMC Genetics.

Genetics of Temporal Lobe Epilepsy: A Review

A. Malafosse, A. Salzmann, 2012, Epilepsy research and treatment.

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.

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.

C. Gieger, I. Scheffer, T. Wienker, 2012, Human molecular genetics.

correlation with sleep quality Blood and brain magnesium in inbred mice and their

A. Malafosse, P. Franken, D. Chollet, 2012 .

Magnesium Involvement in Sleep: Genetic and Nutritional Models

A. Malafosse, P. Franken, D. Chollet, 2001, Behavior genetics.

Blood and brain magnesium in inbred mice and their correlation with sleep quality.

A. Malafosse, M. Tafti, P. Franken, 2000, American journal of physiology. Regulatory, integrative and comparative physiology.

Idiopathic generalized epilepsies : clinical, experimental and genetic aspects

A. Malafosse, 1994 .

Genetic and epigenetic analysis of SSAT gene dysregulation in suicidal behavior

S. Deutsch, P. Baud, P. Courtet, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Absence of linkage between chromosome 11p15 markers and manic-depressive illness in a Belgian pedigree.

M. Leboyer, J. Mallet, A. Malafosse, 1991, The American journal of psychiatry.

Manic Depressive Illness and Tyrosine Hydroxylase Gene: Linkage Heterogeneity and Association

M. Leboyer, J. Mallet, A. Malafosse, 1997, Neurobiology of Disease.

Family Studies of Affective Disorders with 11p15.5 DNA Markers

M. Leboyer, J. Mallet, A. Malafosse, 1992 .

Tyrosine hydroxylase polymorphisms associated with manic-depressive illness

M. Leboyer, J. Mallet, A. Malafosse, 1990, The Lancet.

Failure to replicate linkage between chromosome 5q11-q13 markers and schizophrenia in 28 families

M. Leboyer, J. Mallet, A. Malafosse, 1992, Psychiatry Research.

Evidence for a Pseudoautosomal Locus for Schizophrenia

M. Leboyer, A. Malafosse, D. Campion, 1992, British Journal of Psychiatry.

Contribution of Common Genetic Variants to Antidepressant Response

K. Tansey, P. McGuffin, C. Lewis, 2013, Biological Psychiatry.

Consanguinity, schizophrenia and bipolar disorder

P. Courtet, A. Malafosse, M. Taleb, 2013 .

Identical genetic locus for Baltic and Mediterranean myoclonus

A. Chapelle, A. Malafosse, R. Michelucci, 1992, The Lancet.

Progressive myoclonus epilepsies

A. Malafosse, C. Dravet, 2004 .

Response to psychotherapy in borderline personality disorder and methylation status of the BDNF gene

A. Malafosse, F. Karege, P. Prada, 2013, Translational Psychiatry.

Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage at 3p14

C Henry, S Cichon, B Etain, 2006, Molecular Psychiatry.

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.

Monoamine Oxidase A and Tryptophan Hydroxylase Gene Polymorphisms

M. Preisig, F. Ferrero, A. Malafosse, 2005, American journal of pharmacogenomics : genomics-related research in drug development and clinical practice.

Suicidal behaviors and the tryptophan hydroxylase gene.

P. Courtet, J. Mallet, A. Malafosse, 1995, Archives of general psychiatry.

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.

A case of SUDEP in a patient with Dravet syndrome with SCN1A mutation

A. Malafosse, C. Korff, Michael T. Mund, 2010, Epilepsia.

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.

How Mutations in the nAChRs Can Cause ADNFLE Epilepsy

D. Bertrand, A. Malafosse, S. Berkovic, 2002, Epilepsia.

Linkage mapping of benign familial infantile convulsions (BFIC) to chromosome 19q.

A. Malafosse, F. Rivier, A. Crespel, 1997, Human molecular genetics.

CREB1 modulates the influence of childhood sexual abuse on adult's anger traits

P. Baud, P. Courtet, A. Malafosse, 2012, Genes, brain, and behavior.

Is it valid to measure suicidal ideation by depression rating scales?

M. Desseilles, P. Courtet, A. Malafosse, 2012, Journal of affective disorders.

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.

Genetics of suicidal behavior

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

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

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

Additive effects between prematurity and postnatal risk factors of suicidal behavior.

P. Courtet, A. Malafosse, I. Jaussent, 2013, Journal of psychiatric research.

Childhood trauma as a correlative factor of suicidal behavior – via aggression traits. Similar results in an Italian and in a French sample

A. Roy, P. Courtet, A. Malafosse, 2009, European Psychiatry.

Copy number variants and therapeutic response to antidepressant medication in major depressive disorder

T. Peters, M. Rietschel, K. Tansey, 2014, The Pharmacogenomics Journal.

The HLA-G low expressor genotype confers protection against Bipolar Disorder

A. Malafosse, S. Jamain, B. Étain, 2013 .

The HLA-G low expressor genotype is associated with protection against bipolar disorder.

M. Leboyer, F. Bellivier, A. Malafosse, 2013, Human immunology.

Naturally Occurring Carboxypeptidase A6 Mutations EFFECT ON ENZYME FUNCTION AND ASSOCIATION WITH EPILEPSY * S

A. Malafosse, A. Crespel, L. Fricker, 2020 .

European collaborative study of early‐onset bipolar disorder: Evidence for genetic heterogeneity on 2q14 according to age at onset

S. Cichon, M. Rietschel, M. Nöthen, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Simultaneous analysis of serotonin transporter, tryptophan hydroxylase 1 and 2 gene expression in the ventral prefrontal cortex of suicide victims

E. Neidhart, A. Malafosse, Brice Petit, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Increased methylation of glucocorticoid receptor gene (NR3C1) in adults with a history of childhood maltreatment: a link with the severity and type of trauma

P. Courtet, D. Mouthon, A. Malafosse, 2011, Translational Psychiatry.

Increased DNA methylation status of the serotonin receptor 5HTR1A gene promoter in schizophrenia and bipolar disorder.

Alain Malafosse, A. Malafosse, F. Karege, 2011, Journal of affective disorders.

Allelic heterogeneity of mediterranean myoclonus and the cystatin B gene

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

Genetic Predictors of Response to Serotonergic and Noradrenergic Antidepressants in Major Depressive Disorder: A Genome-Wide Analysis of Individual-Level Data and a Meta-Analysis

T. Peters, M. Rietschel, K. Tansey, 2012, PLoS medicine.

War exposure, 5-HTTLPR genotype and lifetime risk of depression.

A. Malafosse, J. Touchon, K. Ritchie, 2011, The British journal of psychiatry : the journal of mental science.

Alteration in Kinase Activity But Not in Protein Levels of Protein Kinase B and Glycogen Synthase Kinase-3β in Ventral Prefrontal Cortex of Depressed Suicide Victims

A. Malafosse, M. Schwald, F. Karege, 2007, Biological Psychiatry.

Social phobia is associated with suicide attempt history in bipolar inpatients.

M. Leboyer, M. Preisig, P. Baud, 2007, Bipolar Disorders.

Depression in elderly persons subject to childhood maltreatment is not modulated by corpus callosum and hippocampal loss.

P. Courtet, A. Malafosse, K. Ritchie, 2012, Journal of affective disorders.

COMT but not serotonin‐related genes modulates the influence of childhood abuse on anger traits

M. Leboyer, C. Lewis, F. Bellivier, 2010, Genes, brain, and behavior.

HPA axis genes may modulate the effect of childhood adversities on decision-making in suicide attempters.

P. Courtet, A. Malafosse, I. Jaussent, 2013, Journal of psychiatric research.

Clinical and genetic correlates of suicidal ideation during antidepressant treatment in a depressed outpatient sample.

A. Malafosse, R. Uher, J. Aubry, 2011, Pharmacogenomics.

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.

Decreased activation of lateral orbitofrontal cortex during risky choices under uncertainty is associated with disadvantageous decision-making and suicidal behavior

Natalia S. Lawrence, Mary L. Phillips, Philippe Courtet, 2010, NeuroImage.

Psychiatric diagnoses and personality traits associated with disadvantageous decision-making

M. Leboyer, A. Malafosse, I. Jaussent, 2007, European Psychiatry.

Age at onset in bipolar I affective disorder in the USA and Europe

D. Kupfer, M. Leboyer, E. Frank, 2014, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

Adverse childhood environment and late‐life cognitive functioning

R. Stewart, P. Courtet, A. Malafosse, 2011, International journal of geriatric psychiatry.

Association between the TPH gene A218C polymorphism and suicidal behavior: A meta‐analysis

F. Bellivier, A. Malafosse, P. Chaste, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Propagation of improved breeds: the role of artificial insemination and embryo transfer.

A. Malafosse, 1990, Revue scientifique et technique.

Association between centromeric deletions of the SMN gene and sporadic adult‐onset lower motor neuron disease

A. Malafosse, V. Meininger, F. Salachas, 1998, Annals of neurology.

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

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

Impaired decision-making in suicide attempters may increase the risk of problems in affective relationships.

P. Courtet, A. Malafosse, I. Jaussent, 2007, Journal of affective disorders.

Suicidal phenotypes associated with family history of suicidal behavior and early traumatic experiences.

E. Baca-García, P. Courtet, A. Malafosse, 2012, Journal of affective disorders.

Validity of Diagnosis Using the French Translation of the Semi‐Structured Interview for Seizure Classification

M. Tricot, A. Malafosse, A. Crespel, 1999, Epilepsia.

Benign infantile familial convulsions are not an allelic form of the benign familial neonatal convulsions gene

A. Malafosse, B. Echenne, O. Dulac, 1994, Annals of neurology.

Benign infantile epilepsy with autosomal dominant inheritance

A. Malafosse, F. Rivier, B. Echenne, 1994, Brain and Development.

Suicidal Behavior Is Associated with Reduced Corpus Callosum Area

P. Courtet, A. Malafosse, K. Ritchie, 2011, Biological Psychiatry.

Confirmation of linkage of benign familial neonatal convulsions to D20S19 and D20S20

M. Leboyer, J. Mallet, A. Malafosse, 1992, Human Genetics.

Collecting Saliva by Mail for Genetic and Cotinine Analyses in Participants Recruited through the Internet

D. Bertrand, J. Etter, E. Neidhart, 2005, European Journal of Epidemiology.

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

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

Modulation of anger control in suicide attempters by TPH‐1

P. Baud, P. Courtet, A. Malafosse, 2009, Genes, brain, and behavior.

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.

[Unverricht-Lündborg disease: clinical and electrophysiologic study of 19 Maghreb families].

A. Malafosse, M. Fredj, R. Gouider, 1998, Revue neurologique.

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.

Genetic susceptibility for bipolar disorder and response to antidepressants in major depressive disorder

M. O’Donovan, K. Tansey, P. McGuffin, 2014, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

BRD2 and TAP-1 genes and juvenile myoclonic epilepsy

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

Temperament personality profiles in suicidal behaviour: an investigation of associated demographic, clinical and genetic factors.

P. Baud, P. Courtet, D. Mouthon, 2013, Journal of affective disorders.

Candidate genes for temporal lobe epilepsy: a replication study

A. Malafosse, A. Crespel, N. Perroud, 2008, Neurological Sciences.

Magnetic resonance imaging correlates of first-episode psychosis in young adult male patients: combined analysis of grey and white matter.

F. Lazeyras, A. Malafosse, S. Haller, 2012, Journal of psychiatry & neuroscience : JPN.

A non-radioactive assay for the cAMP-dependent protein kinase activity in rat brain homogenates and age-related changes in hippocampus and cortex

A. Malafosse, M. Schwald, F. Karege, 2001, Brain Research.

Impulsivity, aggression and suicidal behavior in unipolar and bipolar disorders.

P. Baud, P. Courtet, D. Mouthon, 2011, Journal of affective disorders.

Genes, suicide and decisions

P. Courtet, A. Malafosse, F. Jollant, 2010, European Psychiatry.

[The Esprit Project: a longitudinal general population study of psychiatric disorders in France in subjects over 65 years old].

P. Courtet, A. Malafosse, J. Touchon, 2006, L'Encephale.

Localization of candidate genomic regions influencing paradoxical sleep in mice

K. Kitahama, A. Malafosse, M. Jouvet, 1997, Neuroreport.

Gender and Genotype Modulation of the Association Between Lipid Levels and Depressive Symptomatology in Community-Dwelling Elderly (The ESPRIT Study)

R. Stewart, A. Malafosse, K. Ritchie, 2010, Biological Psychiatry.

Replication of association between a SCN1A splice variant and febrile seizures

A. Malafosse, A. Crespel, A. Salzmann, 2011, Epilepsia.

A novel exon 3 mutation in a Tunisian patient with Lafora's disease

A. Malafosse, G. Lesca, A. Mrabet, 2011, Journal of the Neurological Sciences.

Rare genotype combination of the serotonin transporter gene associated with treatment response in severe personality disorder

E. Baca-García, P. Courtet, D. Mouthon, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genetic overlap between schizophrenia and bipolar disorder: A study with AKT1 gene variants and clinical phenotypes

M. Leboyer, A. Malafosse, F. Karege, 2012, Schizophrenia Research.

Association of adverse childhood environment and 5-HTTLPR Genotype with late-life depression.

R. Stewart, P. Courtet, A. Malafosse, 2009, The Journal of clinical psychiatry.

Genome-wide Association Analysis of Genetic Generalized Epilepsies Implicates Susceptibility Loci at 1q43, 2p16.1, 2q22.3 and 17q21.32 Epicure Consortium

C. Gieger, I. Scheffer, T. Wienker, 2022 .

Linkage Studies on Tuberous Sclerosis with Probes for Chromosome 11q

A. Malafosse, M. Lathrop, C. Julier, 1991 .

Combined analysis of data from two granddaughter designs: A simple strategy for QTL confirmation and increasing experimental power in dairy cattle

A. Malafosse, D. Boichard, S. Hiendleder, 2003, Genetics Selection Evolution.

5-HTTLPR genotype, stressful life events and late-life depression: No evidence of interaction in a French population

R. Stewart, A. Malafosse, T. Power, 2010, Neurobiology of Aging.