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

On the procurement of physical risk assessments for climate-related disclosures: guidance from a climate science perspective

关于获取与气候相关信息披露相关的物理风险评估:来自气候科学视角的指导

Harrington, Luke J; Gibson, Peter B; Fauchereau, Nicolas; Lewis, Hamish; Frame, Dave; Rosier, Suzanne M

Firing of Replication Origins Is Disturbed by a CDK4/6 Inhibitor in a pRb-Independent Manner

CDK4/6抑制剂以pRb非依赖的方式干扰复制起始点的激活

Su-Jung Kim ,Chrystelle Maric ,Lina-Marie Briu ,Fabien Fauchereau ,Giuseppe Baldacci ,Michelle Debatisse ,Stéphane Koundrioukoff ,Jean-Charles Cadoret

Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia

全基因组关联研究揭示了发育性阅读障碍的遗传性和遗传相关性的新见解

Gialluisi, Alessandro; Andlauer, Till F M; Mirza-Schreiber, Nazanin; Moll, Kristina; Becker, Jessica; Hoffmann, Per; Ludwig, Kerstin U; Czamara, Darina; Pourcain, Beate St; Honbolygó, Ferenc; Tóth, Dénes; Csépe, Valéria; Huguet, Guillaume; Chaix, Yves; Iannuzzi, Stephanie; Demonet, Jean-Francois; Morris, Andrew P; Hulslander, Jacqueline; Willcutt, Erik G; DeFries, John C; Olson, Richard K; Smith, Shelley D; Pennington, Bruce F; Vaessen, Anniek; Maurer, Urs; Lyytinen, Heikki; Peyrard-Janvid, Myriam; Leppänen, Paavo H T; Brandeis, Daniel; Bonte, Milene; Stein, John F; Talcott, Joel B; Fauchereau, Fabien; Wilcke, Arndt; Kirsten, Holger; Müller, Bent; Francks, Clyde; Bourgeron, Thomas; Monaco, Anthony P; Ramus, Franck; Landerl, Karin; Kere, Juha; Scerri, Thomas S; Paracchini, Silvia; Fisher, Simon E; Schumacher, Johannes; Nöthen, Markus M; Müller-Myhsok, Bertram; Schulte-Körne, Gerd

Efficient, quick and easy-to-use DNA replication timing analysis with START-R suite

START-R 套件可实现高效、快速且易于使用的 DNA 复制时间分析。

Hadjadj, Djihad; Denecker, Thomas; Guérin, Eva; Kim, Su-Jung; Fauchereau, Fabien; Baldacci, Giuseppe; Maric, Chrystelle; Cadoret, Jean-Charles

Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia

全基因组关联扫描发现了与阅读障碍认知预测因子相关的新变异

Gialluisi, Alessandro; Andlauer, Till F M; Mirza-Schreiber, Nazanin; Moll, Kristina; Becker, Jessica; Hoffmann, Per; Ludwig, Kerstin U; Czamara, Darina; St Pourcain, Beate; Brandler, William; Honbolygó, Ferenc; Tóth, Dénes; Csépe, Valéria; Huguet, Guillaume; Morris, Andrew P; Hulslander, Jacqueline; Willcutt, Erik G; DeFries, John C; Olson, Richard K; Smith, Shelley D; Pennington, Bruce F; Vaessen, Anniek; Maurer, Urs; Lyytinen, Heikki; Peyrard-Janvid, Myriam; Leppänen, Paavo H T; Brandeis, Daniel; Bonte, Milene; Stein, John F; Talcott, Joel B; Fauchereau, Fabien; Wilcke, Arndt; Francks, Clyde; Bourgeron, Thomas; Monaco, Anthony P; Ramus, Franck; Landerl, Karin; Kere, Juha; Scerri, Thomas S; Paracchini, Silvia; Fisher, Simon E; Schumacher, Johannes; Nöthen, Markus M; Müller-Myhsok, Bertram; Schulte-Körne, Gerd

Disruption of melatonin synthesis is associated with impaired 14-3-3 and miR-451 levels in patients with autism spectrum disorders

褪黑激素合成中断与自闭症谱系障碍患者的 14-3-3 和 miR-451 水平受损有关

Cécile Pagan, Hany Goubran-Botros, Richard Delorme, Marion Benabou, Nathalie Lemière, Kerren Murray, Frédérique Amsellem, Jacques Callebert, Pauline Chaste, Stéphane Jamain, Fabien Fauchereau, Guillaume Huguet, Erik Maronde, Marion Leboyer, Jean-Marie Launay, Thomas Bourgeron8

A hypothesis-driven approach identifies CDK4 and CDK6 inhibitors as candidate drugs for treatments of adrenocortical carcinomas

通过假设驱动的方法,确定 CDK4 和 CDK6 抑制剂是治疗肾上腺皮质癌的候选药物

Djihad Hadjadj, Su-Jung Kim, Thomas Denecker, Laura Ben Driss, Jean-Charles Cadoret, Chrystelle Maric, Giuseppe Baldacci, Fabien Fauchereau

Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort

欧洲跨语言NeuroDys队列中阅读障碍候选基因的遗传分析

Becker, Jessica; Czamara, Darina; Scerri, Tom S; Ramus, Franck; Csépe, Valéria; Talcott, Joel B; Stein, John; Morris, Andrew; Ludwig, Kerstin U; Hoffmann, Per; Honbolygó, Ferenc; Tóth, Dénes; Fauchereau, Fabien; Bogliotti, Caroline; Iannuzzi, Stéphanie; Chaix, Yves; Valdois, Sylviane; Billard, Catherine; George, Florence; Soares-Boucaud, Isabelle; Gérard, Christophe-Loïc; van der Mark, Sanne; Schulz, Enrico; Vaessen, Anniek; Maurer, Urs; Lohvansuu, Kaisa; Lyytinen, Heikki; Zucchelli, Marco; Brandeis, Daniel; Blomert, Leo; Leppänen, Paavo H T; Bruder, Jennifer; Monaco, Anthony P; Müller-Myhsok, Bertram; Kere, Juha; Landerl, Karin; Nöthen, Markus M; Schulte-Körne, Gerd; Paracchini, Silvia; Peyrard-Janvid, Myriam; Schumacher, Johannes

Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions

FOXP2 和 KIAA0319/TTRAP/THEM2 基因座的遗传变异与特定语言相关脑区的激活改变有关

Pinel, Philippe; Fauchereau, Fabien; Moreno, Antonio; Barbot, Alexis; Lathrop, Mark; Zelenika, Diana; Le Bihan, Denis; Poline, Jean-Baptiste; Bourgeron, Thomas; Dehaene, Stanislas

Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders

SHANK2 突变的遗传和功能分析表明自闭症谱系障碍存在多重打击模型

Claire S Leblond, Jutta Heinrich, Richard Delorme, Christian Proepper, Catalina Betancur, Guillaume Huguet, Marina Konyukh, Pauline Chaste, Elodie Ey, Maria Rastam, Henrik Anckarsäter, Gudrun Nygren, I Carina Gillberg, Jonas Melke, Roberto Toro, Beatrice Regnault, Fabien Fauchereau, Oriane Mercati,