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Papers authored by Christine Lonjou

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2021 Héctor Climente-González, Sushmita Roy, Christine Lonjou

ORCID

, Fabienne Lesueur, Dominique Stoppa-Lyonnet, Nadine Andrieu, Chloé-Agathe Azencott

Boosting GWAS using biological networks: A study on susceptibility to familial breast cancer

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Christine Lonjou

ORCID

, Séverine Eon‐Marchais, Thérèse Truong

ORCID

, Marie‐Gabrielle Dondon

ORCID

, Mojgan Karimi, Yue Jiao, Francesca Damiola

ORCID

, Laure Barjhoux, Dorothée Le Gal, Juana Beauvallet, Noura Mebirouk, Eve Cavaciuti, Jean Chiesa, Anne Floquet, Séverine Audebert‐Bellanger and 33 other authors

Gene‐ and pathway‐level analyses of iCOGS variants highlight novel signaling pathways underlying familial breast cancer susceptibility

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2020 Héctor Climente-González, Christine Lonjou

ORCID

, Fabienne Lesueur, Dominique Stoppa-Lyonnet, Nadine Andrieu, Chloé-Agathe Azencott

Biological networks and GWAS: comparing and combining network methods to understand the genetics of familial breast cancer susceptibility in the GENESIS study

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2017 Christine Lonjou

ORCID

, Francesca Damiola

ORCID

, Monika Moissonnier, Geoffroy Durand, Irina Malakhova, Vladimir Masyakin, Florence Le Calvez-Kelm

ORCID

, Elisabeth Cardis, Graham Byrnes, Ausrele Kesminiene, Fabienne Lesueur

ORCID

Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation

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2014 Kinga M. Bujakowska, Qi Zhang, Anna M. Siemiatkowska, Qin Liu, Emily Place, Marni J. Falk, Mark Consugar, Marie-Elise Lancelot, Aline Antonio, Christine Lonjou

ORCID

, Wassila Carpentier, Saddek Mohand-Said, Anneke I. den Hollander, Frans P. M. Cremers, Bart P. Leroy and 7 other authors

Mutations in IFT172 cause isolated retinal degeneration and Bardet-Biedl syndrome

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2013 Mélanie Eyries, David Montani

ORCID

, Barbara Girerd, Claire Perret, Anne Leroy, Christine Lonjou

ORCID

, Nadjim Chelghoum, Florence Coulet, Damien Bonnet, Peter Dorfmüller, Elie Fadel, Olivier Sitbon, Gérald Simonneau, David-Alexandre Tregouët, Marc Humbert and 1 other authors

EIF2AK4 mutations cause pulmonary veno-occlusive disease, a recessive form of pulmonary hypertension

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Laure Ségurel, Frederic Austerlitz, Bruno Toupance, Mathieu Gautier, Joanna L. Kelley, Patrick Pasquet, Christine Lonjou

ORCID

, Myriam Georges, Sarah Voisin, Corinne Cruaud, Arnaud Couloux, Tatyana Hegay, Almaz Aldashev, Renaud Vitalis, Evelyne Heyer

Positive selection of protective variants for type 2 diabetes from the Neolithic onward: a case study in Central Asia

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2011 Kinga Bujakowska, Isabelle Audo, Saddek Mohand-Saïd, Marie-Elise Lancelot, Aline Antonio, Aurore Germain, Thierry Léveillard, Mélanie Letexier, Jean-Paul Saraiva, Christine Lonjou

ORCID

, Wassila Carpentier, José-Alain Sahel, Shomi S. Bhattacharya, Christina Zeitz

CRB1 mutations in inherited retinal dystrophies.

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Isabelle Audo, Saddek Mohand-Saïd, Sophie Tronche, José-Alain Sahel, Kinga Bujakowska, Christina Zeitz, Marie-Elise Lancelot, Aline Antonio, Aurore Germain, Wassila Carpentier, Christine Lonjou

ORCID

, Shomi Bhattacharya

A novel DFNB31 mutation associated with Usher type 2 syndrome showing variable degrees of auditory loss in a consanguineous Portuguese family.

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2008 Z. G. Vitezica, P. Wolkenstein, C. Lonjou

ORCID

, M. Eliaszewicz, X. Sicard, J.-C. Roujeau, A. Hovnanian

ORCID

No association between HLA-B and cutaneous reactions to sulphonamides in human immunodeficiency virus-infected patients

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Zulma G. Vitezica, Brigitte Milpied, Christine Lonjou

ORCID

, Nicolas Borot, Terence Niel Ledger, Anne Lefebvre, Alain Hovnanian

HLA-DRB1 * 01 associated with cutaneous hypersensitivity induced by nevirapine and efavirenz

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Christine Lonjou

ORCID

, Nicolas Borot, Peggy Sekula, Neil Ledger, Laure Thomas, Sima Halevy, Luigi Naldi, Jan-Nico Bouwes-Bavinck, Alexis Sidoroff, Claudia de Toma, Martin Schumacher, Jean-Claude Roujeau, Alain Hovnanian, Maja Mockenhaupt

A European study of HLA-B in Stevens–Johnson syndrome and toxic epidermal necrolysis related to five high-risk drugs

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2006 L. Thomas, C. de Toma, M. Schumacher, M. Mockenhaupt, J.-C. Roujeau, N. Borot, N. Ledger, H. LeLouet, E. Graf, Christine Lonjou

ORCID

ORCID

, Roujeau Jc, RegiSCAR Group

A marker for Stevens-Johnson syndrome ...: Ethnicity matters

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2003 Christine Lonjou

ORCID

, Weihua Zhang, Andrew Collins

ORCID

, William J. Tapper, Eiram Elahi, Nikolas Maniatis, Newton E. Morton

Linkage disequilibrium in human populations

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2002 W. Zhang, A. Collins

ORCID

, C. Lonjou

ORCID

, N. E. E. Morton

A linkage tournament: Affection status, parametric analysis, multivariate traits, and enhancements to variance components and relative pairs

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2001 L. J. Palmer, C. Lonjou

ORCID

, K. Barnes, H. Chen, W. O. C. M. Cookson, K. A. Deichmann, J. W. Holloway, T. Laitinen, M. Wjst, N. E. Morton

A retrospective collaboration on chromosome 5 by the International Consortium on Asthma Genetics (COAG)

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Jw W. Holloway, Holloway Jw, C. Lonjou

ORCID

, B. Beghe, Q. Peng, Q. Penq, Tr R. Gaunt

ORCID

, Gaunt Tr, I. Gomes, Ip P. Hall, Hall Ip, Jc C. Dewar, Dewar Jc, J. Wilkinson, Thomas Ns and 5 other authors

Linkage analysis of the 5q31-33 candidate region for asthma in 240 UK families

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2000 N. Simon Thomas, Jane Wilkinson, Christine Lonjou

ORCID

, Newton E. Morton, Stephen T. Holgate

Linkage Analysis of Markers on Chromosome 11q13 with Asthma and Atopy in a United Kingdom Population

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C. Lonjou

ORCID

, K. Barnes, H. Chen, W. O. C. M. Cookson, K. A. Deichmann, Deichmann Ka, I. P. Hall, J. W. Holloway, T. Laitinen, L. J. Palmer, M. Wjst, N. E. Morton

A first trial of retrospective collaboration for positional cloning in complex inheritance : Assay of the cytokine region on chromosome 5 by the Consortium on Asthma Genetics (COAG).

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1999 A. Collins

ORCID

, C. Lonjou

ORCID

, Ne E. Morton

Genetic epidemiology of single-nucleotide polymorphisms

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