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

Epigenetic insights into neuropsychiatric and cognitive symptoms in Parkinson's disease: A DNA co-methylation network analysis

帕金森病神经精神和认知症状的表观遗传学见解:DNA共甲基化网络分析

Harvey, Joshua; Smith, Adam R; Weymouth, Luke S; Smith, Rebecca G; Castanho, Isabel; Hubbard, Leon; Creese, Byron; Bresner, Catherine; Williams, Nigel; Pishva, Ehsan; Lunnon, Katie

Penetrance of Neurodevelopmental Copy Number Variants Is Associated With Variations in Cortical Morphology

神经发育拷贝数变异的穿透率与皮质形态变异相关

Silva, Ana I; Sønderby, Ida E; Kirov, George; Abdellaoui, Abdel; Agartz, Ingrid; Ames, David; Armstrong, Nicola J; Artiges, Eric; Banaschewski, Tobias; Bassett, Anne S; Bearden, Carrie E; Blangero, John; Boen, Rune; Boomsma, Dorret I; Bülow, Robin; Butcher, Nancy J; Calhoun, Vince; Campbell, Linda E; Chow, Eva W C; Ciufolini, Simone; Craig, Michael C; Crespo-Farroco, Benedicto; Cunningham, Adam C; Dalvie, Shareefa; Daly, Eileen; Dazzan, Paola; de Geus, Eco J C; de Zubicaray, Greig I; Doherty, Joanne L; Donohoe, Gary; Drakesmith, Mark; Espeseth, Thomas; Frouin, Vincent; Garavan, Hugh; Glahn, David C; Goodrich-Hunsaker, Naomi J; Gowland, Penny A; Grabe, Hans J; Grigis, Antoine; Gudbrandsen, Maria; Gutman, Boris A; Haavik, Jan; Håberg, Asta K; Hall, Jeremy; Heinz, Andreas; Hohmann, Sarah; Hottenga, Jouke-Jan; Jacquemont, Sébastien; Jahanshad, Neda; Jonas, Rachel K; Jones, Derek K; Jönsson, Erik G; Koops, Sanne; Kumar, Kuldeep; Le Hellard, Stephanie; Lemaitre, Herve; Liu, Jingyu; Lundervold, Astri J; Martinot, Jean-Luc; Mather, Karen A; McDonald-McGinn, Donna M; McMahon, Katie L; McRae, Allan F; Medland, Sarah E; Moreau, Clara A; Murphy, Kieran C; Murphy, Declan; Murray, Robin M; Nees, Frauke; Owen, Michael J; Paillère Martinot, Marie-Laure; Orfanos, Diimitri Papadopoulos; Paus, Tomas; Poustka, Luise; Marques, Tiago Reis; Roalf, David R; Sachdev, Perminder S; Scheffler, Freda; Schmitt, J Eric; Schumann, Gunter; Steen, Vidar M; Stein, Dan J; Strike, Lachlan T; Teumer, Alexander; Thalamuthu, Anbupalam; Thomopoulos, Sophia I; Tordesillas-Gutiérrez, Diana; Trollor, Julian N; Uhlmann, Anne; Vajdi, Ariana; van 't Ent, Dennis; van Amelsvoort, Therese; van den Bree, Marianne B M; van der Meer, Dennis; Vázquez-Bourgon, Javier; Villalón-Reina, Julio E; Völker, Uwe; Völzke, Henry; Vorstman, Jacob A S; Westlye, Lars T; Williams, Nigel; Wittfeld, Katharina; Wright, Margaret J; Thompson, Paul M; Andreassen, Ole A; Linden, David E J

Polygenic scores for disease risk are not associated with clinical outcomes in Parkinson's disease

帕金森病疾病风险的多基因评分与临床结果无关

Tan, Manuela Mx; Iwaki, Hirotaka; Bandres-Ciga, Sara; Sosero, Yuri; Shoai, Maryam; Brockmann, Kathrin; Williams, Nigel M; Alcalay, Roy N; Maple-Grødem, Jodi; Alves, Guido; Tysnes, Ole-Bjørn; Auinger, Peggy; Eberly, Shirley; Heutink, Peter; Simon, David K; Kieburtz, Karl; Hardy, John; Williams-Gray, Caroline H; Grosset, Donald G; Corvol, Jean-Christophe; Gan-Or, Ziv; Toft, Mathias; Pihlstrøm, Lasse

Lightweight Carbon-Metal-Based Fabric Anode for Lithium-Ion Batteries

用于锂离子电池的轻质碳金属基织物阳极

Barun Kumar Chakrabarti, Gerard Bree, Anh Dao, Guillaume Remy, Mengzheng Ouyang, Koray Bahadır Dönmez, Billy Wu, Mark Williams, Nigel P Brandon, Chandramohan George, Chee Tong John Low

Genotype-phenotype correlation in PRKN-associated Parkinson's disease

PRKN相关帕金森病中的基因型-表型相关性

Menon, Poornima Jayadev; Sambin, Sara; Criniere-Boizet, Baptiste; Courtin, Thomas; Tesson, Christelle; Casse, Fanny; Ferrien, Melanie; Mariani, Louise-Laure; Carvalho, Stephanie; Lejeune, Francois-Xavier; Rebbah, Sana; Martet, Gaspard; Houot, Marion; Lanore, Aymeric; Mangone, Graziella; Roze, Emmanuel; Vidailhet, Marie; Aasly, Jan; Gan Or, Ziv; Yu, Eric; Dauvilliers, Yves; Zimprich, Alexander; Tomantschger, Volker; Pirker, Walter; Álvarez, Ignacio; Pastor, Pau; Di Fonzo, Alessio; Bhatia, Kailash P; Magrinelli, Francesca; Houlden, Henry; Real, Raquel; Quattrone, Andrea; Limousin, Patricia; Korlipara, Prasad; Foltynie, Thomas; Grosset, Donald; Williams, Nigel; Narendra, Derek; Lin, Hsin-Pin; Jovanovic, Carna; Svetel, Marina; Lynch, Timothy; Gallagher, Amy; Vandenberghe, Wim; Gasser, Thomas; Brockmann, Kathrin; Morris, Huw R; Borsche, Max; Klein, Christine; Corti, Olga; Brice, Alexis; Lesage, Suzanne; Corvol, Jean Christophe

Investigation of the genetic aetiology of Lewy body diseases with and without dementia

对伴有和不伴有痴呆的路易体病遗传病因的研究

Wu, Lesley Yue; Real, Raquel; Martinez-Carrasco, Alejandro; Chia, Ruth; Lawton, Michael A; Shoai, Maryam; Bresner, Catherine; Blauwendraat, Cornelis; Singleton, Andrew B; Ryten, Mina; Scholz, Sonja W; Traynor, Bryan J; Williams, Nigel M; Hu, Michele T M; Ben-Shlomo, Yoav; Grosset, Donald G; Hardy, John; Morris, Huw R

Bile acid diarrhoea and metabolic changes after cholecystectomy: a prospective case-control study

胆囊切除术后胆汁酸腹泻和代谢变化:一项前瞻性病例对照研究

Farrugia, Alexia; Williams, Nigel; Khan, Saboor; P Arasaradnam, Ramesh

Association between the LRP1B and APOE loci and the development of Parkinson's disease dementia

LRP1B 和 APOE 基因位点与帕金森病痴呆症发展之间的关联

Real, Raquel; Martinez-Carrasco, Alejandro; Reynolds, Regina H; Lawton, Michael A; Tan, Manuela M X; Shoai, Maryam; Corvol, Jean-Christophe; Ryten, Mina; Bresner, Catherine; Hubbard, Leon; Brice, Alexis; Lesage, Suzanne; Faouzi, Johann; Elbaz, Alexis; Artaud, Fanny; Williams, Nigel; Hu, Michele T M; Ben-Shlomo, Yoav; Grosset, Donald G; Hardy, John; Morris, Huw R

Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia

罕见编码变异作为 22q11.2 缺失的风险修饰因子,提示出生后皮质发育与综合征型精神分裂症有关

Lin, Jhih-Rong; Zhao, Yingjie; Jabalameli, M Reza; Nguyen, Nha; Mitra, Joydeep; Swillen, Ann; Vorstman, Jacob A S; Chow, Eva W C; van den Bree, Marianne; Emanuel, Beverly S; Vermeesch, Joris R; Owen, Michael J; Williams, Nigel M; Bassett, Anne S; McDonald-McGinn, Donna M; Gur, Raquel E; Bearden, Carrie E; Morrow, Bernice E; Lachman, Herbert M; Zhang, Zhengdong D

Psychopathology without Borders: Transcultural psychiatry and implications in clinical presentation and practice

无国界精神病理学:跨文化精神病学及其在临床表现和实践中的应用

Jones, Hannah J; Hubbard, Leon; Mitchell, Ruth E; Jones, Simon A; Williams, Nigel M; Zammit, Stanley; Hall, Jeremy; Garg, S; Afroz, O; Patil, V; Jesus, S; Costa, A R; Simões, G; Gomes, A I; Tarelho, A; Garrido, P