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TALIF measurements of oxygen atom density in the afterglow of a capillary nanosecond discharge

Plasma sources science & technology, 2015-04, Vol.24 (2), p.25010-13

2015

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Controlled growth of core@shell heterostructures based on Prussian blue analogues

New journal of chemistry, 2011, Vol.35 (6), p.1296

2011

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Lifespan prolonging mechanisms and insulin upregulation without fat accumulation in long-lived reproductives of a higher termite

Communications biology, 2022-01, Vol.5 (1), p.44-16, Article 44

2022

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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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De novo assembly and annotation of three Leptosphaeria genomes using Oxford Nanopore MinION sequencing

Scientific data, 2018-11, Vol.5 (1), p.180235-180235, Article 180235

2018

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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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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 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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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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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 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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Lifespan prolonging mechanisms and insulin upregulation without fat accumulation in long-lived reproductives of a higher termite

Communications biology, 2022-01, Vol.5 (5)

2022

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WFS1 mutations are frequent monogenic causes of juvenile-onset diabetes mellitus in Lebanon

Human molecular genetics, 2008-12, Vol.17 (24), p.4012-4021

2008

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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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Fokus : La scia del monte — Montagne magique

Kunst Bulletin, 2024-06 (6)

Dubach-Lemainque, Ingrid

2024

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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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Fokus : Mirage : la BCV ouvre son horizon à Lausanne

Kunst Bulletin, 2023-10 (10), p.60-63

Dubach-Lemainque, Ingrid

2023

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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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Fokus : Francis Baudevin : langue des signes

Kunst Bulletin, 2023-03 (3), p.66-69

Dubach-Lemainque, Ingrid

2023

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Fokus : Denis Savary : carambolages enchantés

Kunst Bulletin, 2023-01 (1/2), p.56-59

Dubach-Lemainque, Ingrid

2023

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Fokus : Barbezat-Villetard : au gré de nos humeurs

Kunst Bulletin, 2022-11 (11)

Dubach-Lemainque, Ingrid

2022

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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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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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TALIF measurements of oxygen atom density in the afterglow of a capillary nanosecond discharge

Controlled growth of core@shell heterostructures based on Prussian blue analogues

Lifespan prolonging mechanisms and insulin upregulation without fat accumulation in long-lived reproductives of a higher termite

A novel immunodeficiency associated with hypomorphic RAG1 mutations and CMV infection

De novo assembly and annotation of three Leptosphaeria genomes using Oxford Nanopore MinION sequencing

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

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

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

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

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

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

Lifespan prolonging mechanisms and insulin upregulation without fat accumulation in long-lived reproductives of a higher termite

WFS1 mutations are frequent monogenic causes of juvenile-onset diabetes mellitus in Lebanon

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

Fokus : La scia del monte — Montagne magique

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

Fokus : Mirage : la BCV ouvre son horizon à Lausanne

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

Fokus : Francis Baudevin : langue des signes

Fokus : Denis Savary : carambolages enchantés

Fokus : Barbezat-Villetard : au gré de nos humeurs

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

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

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