[Genetic aspects of alcoholic behavior]

Follow-up study of patients treated with olanzapine pamoate in France in real-life treatment situation.

L'Encephale·2017

Attention-deficit/hyperactivity disorder symptoms and psychological comorbidity in eating disorder patients.

Eating and weight disorders : EWD·2017

[Reflection on the psychiatric financial allocation in France].

L'Encephale·2016

[Vigilance level for cardiovascular risk factors in schizophrenic patients].

L'Encephale·2015

Depression comorbid with anxiety or medical illness: The role of paroxetine.

International journal of psychiatry in clinical practice·2014

[Patterns of alcohol consumption in France and their medical and social consequences as seen through the family circle and friends and general practitioners].

L'Encephale·2014

[Ultrasonic prenatal diagnosis of the Jarcho-Levin syndrome].

Journal de genetique humaine·1989

[Genetic mapping of chromosome X: known localizations].

Journal de genetique humaine·1989

[Animal models of gene therapy].

Journal de genetique humaine·1989

[Frontonasal dysplasia or the median cleft face syndrome: a case report].

Journal de genetique humaine·1989

[Linkage disequilibrium and DNA markers associated with the gene for cystic fibrosis].

Journal de genetique humaine·1989

[F.G. syndrome: a rare and/or extremely polymorphic syndrome?].

Journal de genetique humaine·1989

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

Scientific reports·2026

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

The Lancet. Microbe·2026

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

Frontiers in genetics·2026

A Novel <i>FN1</i> Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

Journal of clinical medicine·2026

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

HLA·2026

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Molecular syndromology·2026

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[Genetic aspects of alcoholic behavior]

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Follow-up study of patients treated with olanzapine pamoate in France in real-life treatment situation.

Attention-deficit/hyperactivity disorder symptoms and psychological comorbidity in eating disorder patients.

[Reflection on the psychiatric financial allocation in France].

[Vigilance level for cardiovascular risk factors in schizophrenic patients].

Depression comorbid with anxiety or medical illness: The role of paroxetine.

[Patterns of alcohol consumption in France and their medical and social consequences as seen through the family circle and friends and general practitioners].

[Ultrasonic prenatal diagnosis of the Jarcho-Levin syndrome].

[Genetic mapping of chromosome X: known localizations].

[Animal models of gene therapy].

[Frontonasal dysplasia or the median cleft face syndrome: a case report].

[Linkage disequilibrium and DNA markers associated with the gene for cystic fibrosis].

[F.G. syndrome: a rare and/or extremely polymorphic syndrome?].

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

A Novel <i>FN1</i> Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

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