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DNA methylation within melatonin receptor 1A (MTNR1A) mediates paternally transmitted genetic variant effect on asthma plus rhinitis
Chloé Sarnowski
,
Catherine Laprise
,
Giovanni Malerba
,
Miriam F. Moffatt
,
Marie-Hélène Dizier
et al.
Journal articles
hal-01872256v1
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A genome-wide association study identifies susceptibility loci for primary central nervous system lymphoma at 6p25.3 and 3p22.1: a LOC Network study
Karim Labreche
,
Mailys Daniau
,
Amit Sud
,
Philip J Law
,
Louis Royer-Perron
et al.
Journal articles
hal-02328989v1
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Genomic binding of Pol III transcription machinery and relationship with TFIIS transcription factor distribution in mouse embryonic stem cells
Lucie Carrière
,
Sébastien Graziani
,
Olivier Alibert
,
Yad Ghavi-Helm
,
Fayçal Boussouar
et al.
Journal articles
hal-02349009v1
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Effect of 17q21 variants and smoking exposure in early-onset asthma.
Emmanuelle Bouzigon
,
Eve Corda
,
Hugues Aschard
,
Marie-Hélène Dizier
,
Anne Boland
et al.
Journal articles
inserm-00335307v1
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Bivariate association analysis in selected samples: Application to a GWAS of two Bone Mineral Density phenotypes in males with high or low BMD
Aude Saint Pierre
,
Jean-Marc Kaufman
,
Agnes Ostertag
,
Martine Cohen-Solal
,
Anne Boland
et al.
Journal articles
hal-00625932v1
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Quantifying the heritability of glioma using genome-wide complex trait analysis
Ben Kinnersley
,
Jonathan S. Mitchell
,
Konstantinos Gousias
,
Johannes Schramm
,
Ahmed Idbaih
et al.
Journal articles
hal-01271785v1
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Evidence for a pleiotropic QTL on chromosome 5q13 influencing both time to asthma onset and asthma score in French EGEA families.
Emmanuelle Bouzigon
,
Ayse Ulgen
,
Marie-Hélène Dizier
,
Valérie Siroux
,
Mark Lathrop
et al.
Journal articles
inserm-00139064v1
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Genetic association analyses highlight biological pathways underlying mitral valve prolapse
Christian Dina
,
Nabila Bouatia-Naji
,
Nathan Tucker
,
Francesca N. Delling
,
Katelynn Toomer
et al.
Journal articles
hal-01191656v1
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AP1S2 is mutated in X-linked Dandy–Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome)
Pierre Cacciagli
,
Jean-Pierre Desvignes
,
Nadine Girard
,
Marc Délépine
,
Diana Zelenika
et al.
Journal articles
hal-01668667v1
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Human genetic of premature ovarian failure: a mendelian and candidate genes approach
Sandrine Caburet
,
Frank Batista
,
Paul Laissue
,
A. Veitia Reiner
,
Marc Fellous
et al.
"The First Seven days: from gametes to blastocysts and stem cell". Serono Symposium, Apr 2006, Tampa, United States. 1 p., 2006
Conference poster
hal-02816892v1
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Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks
Florence Demenais
,
Patricia Margaritte-Jeannin
,
Kathleen Barnes
,
William O. C. M. Cookson
,
Janine Altmüller
et al.
Journal articles
inserm-02874534v1
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Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.
Claire S. Leblond
,
Jutta Heinrich
,
Richard Delorme
,
Christian Proepper
,
Catalina Betancur
et al.
Journal articles
inserm-00834560v1
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A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25
Rayjean J. Hung
,
James D. Mckay
,
Valerie Gaborieau
,
Paolo Boffetta
,
Mia Hashibe
et al.
Journal articles
cea-00944415v1
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Dominant gut Prevotella copri in gastrectomised non-obese diabetic Goto–Kakizaki rats improves glucose homeostasis through enhanced FXR signalling
Noémie Péan
,
Aurelie Le Lay
,
Francois Brial
,
Jessica Wasserscheid
,
Claude Rouch
et al.
Journal articles
hal-03089346v1
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Evidence for gene x smoking exposure interactions in a genome-wide linkage screen of asthma and bronchial hyper-responsiveness in EGEA families.
Marie-Hélène Dizier
,
Emmanuelle Bouzigon
,
Michel Guilloud-Bataille
,
Valérie Siroux
,
Arnaud Lemainque
et al.
Journal articles
inserm-00136338v1
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Global Genetic Variations Predict Brain Response to Faces
Erin W Dickie
,
Amir Tahmasebi
,
Leon French
,
Natasa Kovacevic
,
Tobias Banaschewski
et al.
Journal articles
pasteur-01967184v1
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Contribution to Alzheimer's disease risk of rare variants in TREM_2, SORL_1, and ABCA_7 in 1779 cases and 1273 controls
Céline Bellenguez
,
Camille Charbonnier
,
Benjamin Grenier-Boley
,
Olivier Quenez
,
Kilan Le Guennec
et al.
Journal articles
hal-01760388v1
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Association of variants in HTRA1 and NOTCH3 with MRI-defined extremes of cerebral small vessel disease in older subjects
Aniket Mishra
,
Ganesh Chauhan
,
Marie-Helene Violleau
,
Dina Vojinovic
,
Xueqiu Jian
et al.
Journal articles
hal-03162406v1
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Evidence for linkage of a new region (11p14) to eczema and allergic diseases.
Michel Guilloud-Bataille
,
Emmanuelle Bouzigon
,
Isabella Annesi-Maesano
,
Jean Bousquet
,
Denis Charpin
et al.
Journal articles
inserm-00324031v1
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PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humans.
Anaïs Grall
,
Eric Guaguère
,
Sandrine Planchais
,
Susanne Grond
,
Emmanuelle Bourrat
et al.
Journal articles
inserm-00662852v1
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Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors
Beatrice S. Melin
,
Jill S. Barnholtz-Sloan
,
Margaret R. Wrensch
,
Christoffer Johansen
,
Dora Il'Yasova
et al.
Journal articles
hal-01602681v1
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Genome-wide association study identifies multiple susceptibility loci for glioma
Ben Kinnersley
,
Marianne Labussière
,
Amy Holroyd
,
Anna-Luisa Di Stefano
,
Peter Broderick
et al.
Journal articles
hal-01316579v1
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Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
Ashley Beecham
,
Nikolaos Patsopoulos
,
Dionysia Xifara
,
Mary Davis
,
Anu Kemppinen
et al.
Journal articles
hal-02565210v1
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New susceptibility loci for cutaneous melanoma risk and progression revealed using a porcine model
Emmanuelle E. Bourneuf
,
Jordi Estellé
,
Amandine Blin
,
Francoise Créchet
,
Maria-Del-Pilar M.-D.-P. Schneider
et al.
Journal articles
hal-02628158v1
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Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
Hong S. Lee
,
Stephan Ripke
,
Benjamin M. Neale
,
Stephen V. Faraone
,
Shaun M. Purcell
et al.
Journal articles
inserm-00864642v1
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Mutations in BCAP31 Cause a Severe X-Linked Phenotype with Deafness, Dystonia, and Central Hypomyelination and Disorganize the Golgi Apparatus
Pierre Cacciagli
,
Julie Sutera-Sardo
,
Ana Borges-Correia
,
Jean-Christophe Roux
,
Imen Dorboz
et al.
Journal articles
hal-01668665v1
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Clustering patterns of LOD scores for asthma-related phenotypes revealed by a genome-wide screen in 295 French EGEA families.
Emmanuelle Bouzigon
,
Marie-Hélène Dizier
,
Christine Krähenbühl
,
Arnaud Lemainque
,
Isabella Annesi-Maesano
et al.
Journal articles
hal-00595818v1
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The International Human Epigenome Consortium: A Blueprint for Scientific Collaboration and Discovery
Eileen Furlong
,
Sitanshu Gakkhar
,
Nina Gasparoni
,
Gilles Gasparoni
,
Daniel H. Geschwind
et al.
Journal articles
hal-01614945v1
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The gene encoding adipose triglyceride lipase (PNPLA2) is mutated in neutral lipid storage disease with myopathy.
Judith Fischer
,
Caroline Lefèvre
,
Eva Morava
,
Jean-Marie Mussini
,
Pascal Laforêt
et al.
Journal articles
inserm-00409618v1
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Variants in DNA double-strand break repair and DNA damage-response genes and susceptibility to lung and head and neck cancers.
Patrick Danoy
,
Stefan Michiels
,
Philippe Dessen
,
Cécile Pignat
,
Thomas Boulet
et al.
Journal articles
hal-00282469v1
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