日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Integration of clinical, pathological, radiological, and transcriptomic data improves prediction for first-line immunotherapy outcome in metastatic non-small cell lung cancer

整合临床、病理、放射学和转录组学数据可提高转移性非小细胞肺癌一线免疫治疗疗效的预测准确性

Captier, Nicolas; Lerousseau, Marvin; Orlhac, Fanny; Hovhannisyan-Baghdasarian, Narinée; Luporsi, Marie; Woff, Erwin; Lagha, Sarah; Salamoun Feghali, Paulette; Lonjou, Christine; Beaulaton, Clément; Zinovyev, Andrei; Salmon, Hélène; Walter, Thomas; Buvat, Irène; Girard, Nicolas; Barillot, Emmanuel

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

对 iCOGS 变异的基因和通路水平分析突显了家族性乳腺癌易感性的潜在新信号通路

Lonjou, Christine; Eon-Marchais, Séverine; Truong, Thérèse; Dondon, Marie-Gabrielle; Karimi, Mojgan; Jiao, Yue; Damiola, Francesca; Barjhoux, Laure; Le Gal, Dorothée; Beauvallet, Juana; Mebirouk, Noura; Cavaciuti, Eve; Chiesa, Jean; Floquet, Anne; Audebert-Bellanger, Séverine; Giraud, Sophie; Frebourg, Thierry; Limacher, Jean-Marc; Gladieff, Laurence; Mortemousque, Isabelle; Dreyfus, Hélène; Lejeune-Dumoulin, Sophie; Lasset, Christine; Venat-Bouvet, Laurence; Bignon, Yves-Jean; Pujol, Pascal; Maugard, Christine M; Luporsi, Elisabeth; Bonadona, Valérie; Noguès, Catherine; Berthet, Pascaline; Delnatte, Capucine; Gesta, Paul; Lortholary, Alain; Faivre, Laurence; Buecher, Bruno; Caron, Olivier; Gauthier-Villars, Marion; Coupier, Isabelle; Mazoyer, Sylvie; Monraz, Luis-Cristobal; Kondratova, Maria; Kuperstein, Inna; Guénel, Pascal; Barillot, Emmanuel; Stoppa-Lyonnet, Dominique; Andrieu, Nadine; Lesueur, Fabienne

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

利用生物网络增强全基因组关联研究:一项关于家族性乳腺癌易感性的研究

Climente-González, Héctor; Lonjou, Christine; Lesueur, Fabienne; Stoppa-Lyonnet, Dominique; Andrieu, Nadine; Azencott, Chloé-Agathe

Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing

家族性乳腺癌与DNA修复基因:GENESIS研究揭示的已知和新型易感基因及其对多基因检测的意义

Girard, Elodie; Eon-Marchais, Séverine; Olaso, Robert; Renault, Anne-Laure; Damiola, Francesca; Dondon, Marie-Gabrielle; Barjhoux, Laure; Goidin, Didier; Meyer, Vincent; Le Gal, Dorothée; Beauvallet, Juana; Mebirouk, Noura; Lonjou, Christine; Coignard, Juliette; Marcou, Morgane; Cavaciuti, Eve; Baulard, Céline; Bihoreau, Marie-Thérèse; Cohen-Haguenauer, Odile; Leroux, Dominique; Penet, Clotilde; Fert-Ferrer, Sandra; Colas, Chrystelle; Frebourg, Thierry; Eisinger, François; Adenis, Claude; Fajac, Anne; Gladieff, Laurence; Tinat, Julie; Floquet, Anne; Chiesa, Jean; Giraud, Sophie; Mortemousque, Isabelle; Soubrier, Florent; Audebert-Bellanger, Séverine; Limacher, Jean-Marc; Lasset, Christine; Lejeune-Dumoulin, Sophie; Dreyfus, Hélène; Bignon, Yves-Jean; Longy, Michel; Pujol, Pascal; Venat-Bouvet, Laurence; Bonadona, Valérie; Berthet, Pascaline; Luporsi, Elisabeth; Maugard, Christine M; Noguès, Catherine; Delnatte, Capucine; Fricker, Jean-Pierre; Gesta, Paul; Faivre, Laurence; Lortholary, Alain; Buecher, Bruno; Caron, Olivier; Gauthier-Villars, Marion; Coupier, Isabelle; Servant, Nicolas; Boland, Anne; Mazoyer, Sylvie; Deleuze, Jean-François; Stoppa-Lyonnet, Dominique; Andrieu, Nadine; Lesueur, Fabienne

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

对与乳头状甲状腺癌易感性相关的DNA修复相关单核苷酸多态性(SNP)的研究发现,MGMT是白俄罗斯受辐射儿童中一个新的候选基因。

Lonjou, Christine; Damiola, Francesca; Moissonnier, Monika; Durand, Geoffroy; Malakhova, Irina; Masyakin, Vladimir; Le Calvez-Kelm, Florence; Cardis, Elisabeth; Byrnes, Graham; Kesminiene, Ausrele; Lesueur, Fabienne

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

IFT172 基因突变导致孤立性视网膜变性和 Bardet-Biedl 综合征

Kinga M Bujakowska, Qi Zhang, Anna M Siemiatkowska, Qin Liu, Emily Place, Marni J Falk, Mark Consugar, Marie-Elise Lancelot, Aline Antonio, Christine Lonjou, Wassila Carpentier, Saddek Mohand-Saïd, Anneke I den Hollander, Frans P M Cremers, Bart P Leroy, Xiaowu Gai, José-Alain Sahel, L Ingeborgh van

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

从新石器时代开始,对2型糖尿病具有保护作用的变异基因就得到了正向选择:以中亚为例

Ségurel, Laure; Austerlitz, Frederic; Toupance, Bruno; Gautier, Mathieu; Kelley, Joanna L; Pasquet, Patrick; Lonjou, Christine; Georges, Myriam; Voisin, Sarah; Cruaud, Corinne; Couloux, Arnaud; Hegay, Tatyana; Aldashev, Almaz; Vitalis, Renaud; Heyer, Evelyne

CRB1 mutations in inherited retinal dystrophies

遗传性视网膜营养不良中的CRB1突变

Bujakowska, Kinga; Audo, Isabelle; Mohand-Saïd, Saddek; Lancelot, Marie-Elise; Antonio, Aline; Germain, Aurore; Léveillard, Thierry; Letexier, Mélanie; Saraiva, Jean-Paul; Lonjou, Christine; Carpentier, Wassila; Sahel, José-Alain; Bhattacharya, Shomi S; Zeitz, Christina

Linkage disequilibrium in human populations

人类群体中的连锁不平衡

Lonjou, Christine; Zhang, Weihua; Collins, Andrew; Tapper, William J; Elahi, Eiram; Maniatis, Nikolas; Morton, Newton E

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)

复杂遗传定位克隆的回顾性合作首次尝试:哮喘遗传学联盟 (COAG) 对 5 号染色体上的细胞因子区域进行检测

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