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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

Molecular psychiatry, 2006-07, Vol.11 (7), p.685-694

2006

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Genome-wide Linkage Analysis for Severe Obesity in French Caucasians Finds Significant Susceptibility Locus on Chromosome 19q

Diabetes (New York, N.Y.), 2004-07, Vol.53 (7), p.1857-1865

2004

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Scores of asthma and asthma severity reveal new regions of linkage in EGEA study families

The European respiratory journal, 2007-08, Vol.30 (2), p.253-259

2007

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Estimation of the Inbreeding Coefficient through Use of Genomic Data

American journal of human genetics, 2003-09, Vol.73 (3), p.516-523

2003

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Genome screen in the French EGEA study: detection of linked regions shared or not shared by allergic rhinitis and asthma

Genes and immunity, 2005-03, Vol.6 (2), p.95-102

2005

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Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families

Annals of human genetics, 2001-01, Vol.65 (1), p.35-41

2001

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A novel immunodeficiency associated with hypomorphic RAG1 mutations and CMV infection

The Journal of clinical investigation, 2005-11, Vol.115 (11), p.3291-3299

2005

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Recessive mutations in PTHR1 cause contrasting skeletal dysplasias in Eiken and Blomstrand syndromes

Human molecular genetics, 2005-01, Vol.14 (1), p.1-5

2005

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Invasions Toolkit :Current Methods for Tracking the Spread and Impact of Invasive Species

Networks of Invasion: A Synthesis of Concepts, 2017, Vol.56, p.85-182

2017

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A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene

Annals of neurology, 2002-06, Vol.51 (6), p.750-759

2002

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Paget Disease of Bone: Mapping of Two Loci at 5q35-qter and 5q31

American journal of human genetics, 2001-09, Vol.69 (3), p.528-543

2001

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Linkage of Benign Familial Infantile Convulsions to Chromosome 16p12-q12 Suggests Allelism to the Infantile Convulsions and Choreoathetosis Syndrome

American journal of human genetics, 2001-03, Vol.68 (3), p.788-794

2001

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A novel X-linked recessive form of Mendelian susceptibility to mycobaterial disease

Journal of medical genetics, 2007-02, Vol.44 (2), p.e65-e65

2007

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A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7p21.3-p15.1

Annals of neurology, 2002-11, Vol.52 (5), p.666-670

2002

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A Major Susceptibility Locus on Chromosome 22q12 Plays a Critical Role in the Control of Kala-Azar

American journal of human genetics, 2003-11, Vol.73 (5), p.1052-1060

2003

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Identification of the first gene locus (SSNS1) for steroid-sensitive nephrotic syndrome on chromosome 2p

Journal of the American Society of Nephrology, 2003-07, Vol.14 (7), p.1897-1900

2003

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Evidence for linkage of a new region (11p14) to eczema and allergic diseases

Human genetics, 2008-01, Vol.122 (6), p.605-614

2008

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Clustering patterns of LOD scores for asthma-related phenotypes revealed by a genome-wide screen in 295 French EGEA families

Human molecular genetics, 2004-12, Vol.13 (24), p.3103-3113

2004

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Amish brittle hair syndrome gene maps to 7p14.1

American journal of medical genetics. Part A, 2005-04, Vol.134A (3), p.290-294

2005

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DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34

European journal of human genetics : EJHG, 2002-03, Vol.10 (3), p.210-212

2002

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DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1

European journal of human genetics : EJHG, 2003-10, Vol.11 (10), p.816-818

2003

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Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1

European journal of human genetics : EJHG, 2003-02, Vol.11 (2), p.185-188

2003

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Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14

Archives of neurology (Chicago), 2004-08, Vol.61 (8), p.1242

2004

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Influence of polymerization of D-amino acid oxidase on the behavior of the enzyme immobilized on chitosan by covalent fixation

European journal of biochemistry, 1988-05, Vol.174 (1), p.171-176

1988

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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

Genome-wide Linkage Analysis for Severe Obesity in French Caucasians Finds Significant Susceptibility Locus on Chromosome 19q

Scores of asthma and asthma severity reveal new regions of linkage in EGEA study families

Estimation of the Inbreeding Coefficient through Use of Genomic Data

Genome screen in the French EGEA study: detection of linked regions shared or not shared by allergic rhinitis and asthma

SRPX2 mutations in disorders of language cortex and cognition

Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families

A novel immunodeficiency associated with hypomorphic RAG1 mutations and CMV infection

Recessive mutations in PTHR1 cause contrasting skeletal dysplasias in Eiken and Blomstrand syndromes

Invasions Toolkit :Current Methods for Tracking the Spread and Impact of Invasive Species

A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene

Paget Disease of Bone: Mapping of Two Loci at 5q35-qter and 5q31

Linkage of Benign Familial Infantile Convulsions to Chromosome 16p12-q12 Suggests Allelism to the Infantile Convulsions and Choreoathetosis Syndrome

A novel X-linked recessive form of Mendelian susceptibility to mycobaterial disease

A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7p21.3-p15.1

A Major Susceptibility Locus on Chromosome 22q12 Plays a Critical Role in the Control of Kala-Azar

Identification of the first gene locus (SSNS1) for steroid-sensitive nephrotic syndrome on chromosome 2p

Evidence for linkage of a new region (11p14) to eczema and allergic diseases

Clustering patterns of LOD scores for asthma-related phenotypes revealed by a genome-wide screen in 295 French EGEA families

Amish brittle hair syndrome gene maps to 7p14.1

DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34

DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1

Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1

Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14

Influence of polymerization of D-amino acid oxidase on the behavior of the enzyme immobilized on chitosan by covalent fixation

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