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

Genetic variants for head size share genes and pathways with cancer

头部大小相关的基因变异与癌症共享基因和通路。

Knol, Maria J; Poot, Raymond A; Evans, Tavia E; Satizabal, Claudia L; Mishra, Aniket; Sargurupremraj, Muralidharan; van der Auwera, Sandra; Duperron, Marie-Gabrielle; Jian, Xueqiu; Hostettler, Isabel C; van Dam-Nolen, Dianne H K; Lamballais, Sander; Pawlak, Mikolaj A; Lewis, Cora E; Carrion-Castillo, Amaia; van Erp, Theo G M; Reinbold, Céline S; Shin, Jean; Scholz, Markus; Håberg, Asta K; Kämpe, Anders; Li, Gloria H Y; Avinun, Reut; Atkins, Joshua R; Hsu, Fang-Chi; Amod, Alyssa R; Lam, Max; Tsuchida, Ami; Teunissen, Mariël W A; Aygün, Nil; Patel, Yash; Liang, Dan; Beiser, Alexa S; Beyer, Frauke; Bis, Joshua C; Bos, Daniel; Bryan, R Nick; Bülow, Robin; Caspers, Svenja; Catheline, Gwenaëlle; Cecil, Charlotte A M; Dalvie, Shareefa; Dartigues, Jean-François; DeCarli, Charles; Enlund-Cerullo, Maria; Ford, Judith M; Franke, Barbara; Freedman, Barry I; Friedrich, Nele; Green, Melissa J; Haworth, Simon; Helmer, Catherine; Hoffmann, Per; Homuth, Georg; Ikram, M Kamran; Jack, Clifford R Jr; Jahanshad, Neda; Jockwitz, Christiane; Kamatani, Yoichiro; Knodt, Annchen R; Li, Shuo; Lim, Keane; Longstreth, W T; Macciardi, Fabio; Mäkitie, Outi; Mazoyer, Bernard; Medland, Sarah E; Miyamoto, Susumu; Moebus, Susanne; Mosley, Thomas H; Muetzel, Ryan; Mühleisen, Thomas W; Nagata, Manabu; Nakahara, Soichiro; Palmer, Nicholette D; Pausova, Zdenka; Preda, Adrian; Quidé, Yann; Reay, William R; Roshchupkin, Gennady V; Schmidt, Reinhold; Schreiner, Pamela J; Setoh, Kazuya; Shapland, Chin Yang; Sidney, Stephen; St Pourcain, Beate; Stein, Jason L; Tabara, Yasuharu; Teumer, Alexander; Uhlmann, Anne; van der Lugt, Aad; Vernooij, Meike W; Werring, David J; Windham, B Gwen; Witte, A Veronica; Wittfeld, Katharina; Yang, Qiong; Yoshida, Kazumichi; Brunner, Han G; Le Grand, Quentin; Sim, Kang; Stein, Dan J; Bowden, Donald W; Cairns, Murray J; Hariri, Ahmad R; Cheung, Ching-Lung; Andersson, Sture; Villringer, Arno; Paus, Tomas; Cichon, Sven; Calhoun, Vince D; Crivello, Fabrice; Launer, Lenore J; White, Tonya; Koudstaal, Peter J; Houlden, Henry; Fornage, Myriam; Matsuda, Fumihiko; Grabe, Hans J; Ikram, M Arfan; Debette, Stéphanie; Thompson, Paul M; Seshadri, Sudha; Adams, Hieab H H

The genetic architecture of structural left-right asymmetry of the human brain

人类大脑结构左右不对称的遗传架构

Sha, Zhiqiang; Schijven, Dick; Carrion-Castillo, Amaia; Joliot, Marc; Mazoyer, Bernard; Fisher, Simon E; Crivello, Fabrice; Francks, Clyde

Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family

全基因组测序发现SEMA3C基因中存在功能性非编码变异,该变异与多代家族中的阅读障碍共分离。

Carrion-Castillo, Amaia; Estruch, Sara B; Maassen, Ben; Franke, Barbara; Francks, Clyde; Fisher, Simon E

The genetics of situs inversus without primary ciliary dyskinesia

无原发性纤毛运动障碍的内脏反位遗传学

Postema, Merel C; Carrion-Castillo, Amaia; Fisher, Simon E; Vingerhoets, Guy; Francks, Clyde

Global and Regional Development of the Human Cerebral Cortex: Molecular Architecture and Occupational Aptitudes

人类大脑皮层的全球和区域发育:分子结构和职业适应性

Shin, Jean; Ma, Shaojie; Hofer, Edith; Patel, Yash; Vosberg, Daniel E; Tilley, Steven; Roshchupkin, Gennady V; Sousa, André M M; Jian, Xueqiu; Gottesman, Rebecca; Mosley, Thomas H; Fornage, Myriam; Saba, Yasaman; Pirpamer, Lukas; Schmidt, Reinhold; Schmidt, Helena; Carrion-Castillo, Amaia; Crivello, Fabrice; Mazoyer, Bernard; Bis, Joshua C; Li, Shuo; Yang, Qiong; Luciano, Michelle; Karama, Sherif; Lewis, Lindsay; Bastin, Mark E; Harris, Mathew A; Wardlaw, Joanna M; Deary, Ian E; Scholz, Markus; Loeffler, Markus; Witte, A Veronica; Beyer, Frauke; Villringer, Arno; Armstrong, Nicola J; Mather, Karen A; Ames, David; Jiang, Jiyang; Kwok, John B; Schofield, Peter R; Thalamuthu, Anbupalam; Trollor, Julian N; Wright, Margaret J; Brodaty, Henry; Wen, Wei; Sachdev, Perminder S; Terzikhan, Natalie; Evans, Tavia E; Adams, Hieab H H H; Ikram, M Arfan; Frenzel, Stefan; Auwera-Palitschka, Sandra van der; Wittfeld, Katharina; Bülow, Robin; Grabe, Hans Jörgen; Tzourio, Christophe; Mishra, Aniket; Maingault, Sophie; Debette, Stephanie; Gillespie, Nathan A; Franz, Carol E; Kremen, William S; Ding, Linda; Jahanshad, Neda; Sestan, Nenad; Pausova, Zdenka; Seshadri, Sudha; Paus, Tomas

A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development

一组在人类胚胎大脑中共同表达的调控基因与语言发育障碍有关

Eising, Else; Carrion-Castillo, Amaia; Vino, Arianna; Strand, Edythe A; Jakielski, Kathy J; Scerri, Thomas S; Hildebrand, Michael S; Webster, Richard; Ma, Alan; Mazoyer, Bernard; Francks, Clyde; Bahlo, Melanie; Scheffer, Ingrid E; Morgan, Angela T; Shriberg, Lawrence D; Fisher, Simon E

Genome sequencing for rightward hemispheric language dominance

右脑语言优势的基因组测序

Carrion-Castillo, Amaia; Van der Haegen, Lise; Tzourio-Mazoyer, Nathalie; Kavaklioglu, Tulya; Badillo, Solveig; Chavent, Marie; Saracco, Jérôme; Brysbaert, Marc; Fisher, Simon E; Mazoyer, Bernard; Francks, Clyde

Association analysis of dyslexia candidate genes in a Dutch longitudinal sample

荷兰纵向样本中阅读障碍候选基因的关联分析

Carrion-Castillo, Amaia; Maassen, Ben; Franke, Barbara; Heister, Angelien; Naber, Marlies; van der Leij, Aryan; Francks, Clyde; Fisher, Simon E