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authFullName_s : Mark Lathrop

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 of Allergy and Clinical Immunology, 2016, 138 (3), pp.748 - 753. ⟨10.1016/j.jaci.2015.12.1341⟩
Journal articles hal-01872256v1

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.
Neuro-Oncology, 2019, 21 (8), pp.1039-1048. ⟨10.1093/neuonc/noz088⟩
Journal articles hal-02328989v1

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.
Nucleic Acids Research, 2012, 40 (1), pp.270-283. ⟨10.1093/nar/gkr737⟩
Journal articles hal-02349009v1

Effect of 17q21 variants and smoking exposure in early-onset asthma.

Emmanuelle Bouzigon , Eve Corda , Hugues Aschard , Marie-Hélène Dizier , Anne Boland et al.
New England Journal of Medicine, 2008, 359 (19), pp.1985-94. ⟨10.1056/NEJMoa0806604⟩
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.
European Journal of Human Genetics, 2011, ⟨10.1038/ejhg.2011.22⟩
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.
Scientific Reports, 2015, 5, pp.17267. ⟨10.1038/srep17267⟩
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.
Human Genetics, 2007, 121 (6), pp.711-719. ⟨10.1007/s00439-007-0363-x⟩
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.
Nature Genetics, 2015, 47 (10), pp.1206-1211. ⟨10.1038/ng.3383⟩
Journal articles hal-01191656v1

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.
European Journal of Human Genetics, 2013, 22 (3), pp.363 - 368. ⟨10.1038/ejhg.2013.135⟩
Journal articles hal-01668667v1

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

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.
Nature Genetics, 2018, 50 (1), pp.42-53. ⟨10.1038/s41588-017-0014-7⟩
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.
PLoS Genetics, 2012, 8 (2), pp.e1002521. ⟨10.1371/journal.pgen.1002521⟩
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.
Nature, 2008, 452 (7187), pp.633-637. ⟨10.1038/nature06885⟩
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.
Diabetologia, 2020, 63 (6), pp.1223 - 1235. ⟨10.1007/s00125-020-05122-7⟩
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.
European Journal of Human Genetics, 2007, 15 (7), pp.810-815. ⟨10.1038/sj.ejhg.5201830⟩
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.
PLoS Genetics, 2014, 10 (8), pp.e1004523. ⟨10.1371/journal.pgen.1004523⟩
Journal articles pasteur-01967184v1

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.
Neurobiology of Aging, 2017, 59, pp.220.e1-220.e9. ⟨10.1016/j.neurobiolaging.2017.07.001⟩
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.
Brain - A Journal of Neurology , 2019, 142 (4), pp.1009-1023. ⟨10.1093/brain/awz024⟩
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.
Human Genetics, 2008, 122 (6), pp.605-14. ⟨10.1007/s00439-007-0439-7⟩
Journal articles inserm-00324031v1

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.
Nature Genetics, 2012, 44 (2), pp.140-7. ⟨10.1038/ng.1056⟩
Journal articles inserm-00662852v1

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.
Nature Genetics, 2017, 49 (5), pp.789-794. ⟨10.1038/ng.3823⟩
Journal articles hal-01602681v1

Genome-wide association study identifies multiple susceptibility loci for glioma

Ben Kinnersley , Marianne Labussière , Amy Holroyd , Anna-Luisa Di Stefano , Peter Broderick et al.
Nature Communications, 2015, 6, pp.8559. ⟨10.1038/ncomms9559⟩
Journal articles hal-01316579v1

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.
Nature Genetics, 2013, 45 (11), pp.1353-1360. ⟨10.1038/ng.2770⟩
Journal articles hal-02565210v1

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.
Oncotarget, 2018, 9 (45), pp.27682-27697. ⟨10.18632/oncotarget.25455⟩
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.
Nature Genetics, 2013, 45 (9), pp.984-994. ⟨10.1038/ng.2711⟩
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.
American Journal of Human Genetics, 2013, 93, pp.579-586. ⟨10.1016/j.ajhg.2013.07.023⟩
Journal articles hal-01668665v1

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.
Human Molecular Genetics, 2004, 13 (24), pp.3103-13. ⟨10.1093/hmg/ddh340⟩
Journal articles hal-00595818v1

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.
Cell, 2016, 167 (5), pp.1145--1149. ⟨10.1016/j.cell.2016.11.007⟩
Journal articles hal-01614945v1

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.
Nature Genetics, 2007, 39 (1), pp.28-30. ⟨10.1038/ng1951⟩
Journal articles inserm-00409618v1

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.
International Journal of Cancer, 2008, 123 (2), pp.457-463. ⟨10.1002/ijc.23524⟩
Journal articles hal-00282469v1