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

Genetics to Improve Outcomes in Schizophrenia (GENios): A within-case molecular genetic study protocol

利用遗传学改善精神分裂症预后(GENios):一项病例内分子遗传学研究方案

Smart, Sophie E; Fenner, Eilidh; Humphreys, Rhys; Wells, Amanda; Fender, Katherine; Bresner, Catherine; Trauzzi, Giulia; Willcocks, Isabella R; Legge, Sophie E; Pardiñas, Antonio F; Rees, Elliott; Escott-Price, Valentina; Holmans, Peter; O'Donovan, Michael C; Owen, Michael J; Walters, James T R

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

Genome-wide determinants of mortality and motor progression in Parkinson's disease

帕金森病死亡率和运动功能进展的全基因组决定因素

Manuela M X Tan ,Michael A Lawton ,Miriam I Pollard ,Emmeline Brown ,Raquel Real ,Alejandro Martinez Carrasco ,Samir Bekadar ,Edwin Jabbari ,Regina H Reynolds ,Hirotaka Iwaki ,Cornelis Blauwendraat ,Sofia Kanavou ,Leon Hubbard ,Naveed Malek ,Katherine A Grosset ,Nin Bajaj ,Roger A Barker ,David J Burn ,Catherine Bresner ,Thomas Foltynie ,Nicholas W Wood ,Caroline H Williams-Gray ,Ole A Andreassen ,Mathias Toft ,Alexis Elbaz ,Fanny Artaud ,Alexis Brice ,Jean-Christophe Corvol ,Jan Aasly ,Matthew J Farrer ,Michael A Nalls ,Andrew B Singleton ,Nigel M Williams ,Yoav Ben-Shlomo ,John Hardy ,Michele T M Hu ,Donald G Grosset ,Maryam Shoai ,Lasse Pihlstrøm ,Huw R Morris

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

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

Identification of a possible proteomic biomarker in Parkinson's disease: discovery and replication in blood, brain and cerebrospinal fluid

帕金森病潜在蛋白质组学生物标志物的鉴定:在血液、脑组织和脑脊液中的发现和验证

Winchester, Laura; Barber, Imelda; Lawton, Michael; Ash, Jessica; Liu, Benjamine; Evetts, Samuel; Hopkins-Jones, Lucinda; Lewis, Suppalak; Bresner, Catherine; Malpartida, Ana Belen; Williams, Nigel; Gentlemen, Steve; Wade-Martins, Richard; Ryan, Brent; Holgado-Nevado, Alejo; Hu, Michele; Ben-Shlomo, Yoav; Grosset, Donald; Lovestone, Simon

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

Genome-Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease

帕金森病认知和运动进展的全基因组关联研究

Tan, Manuela M X; Lawton, Michael A; Jabbari, Edwin; Reynolds, Regina H; Iwaki, Hirotaka; Blauwendraat, Cornelis; Kanavou, Sofia; Pollard, Miriam I; Hubbard, Leon; Malek, Naveed; Grosset, Katherine A; Marrinan, Sarah L; Bajaj, Nin; Barker, Roger A; Burn, David J; Bresner, Catherine; Foltynie, Thomas; Wood, Nicholas W; Williams-Gray, Caroline H; Hardy, John; Nalls, Michael A; Singleton, Andrew B; Williams, Nigel M; Ben-Shlomo, Yoav; Hu, Michele T M; Grosset, Donald G; Shoai, Maryam; Morris, Huw R

Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease study

英国一项大型基于人群的帕金森病研究中孟德尔突变的遗传分析

Tan, Manuela M X; Malek, Naveed; Lawton, Michael A; Hubbard, Leon; Pittman, Alan M; Joseph, Theresita; Hehir, Jason; Swallow, Diane M A; Grosset, Katherine A; Marrinan, Sarah L; Bajaj, Nin; Barker, Roger A; Burn, David J; Bresner, Catherine; Foltynie, Thomas; Hardy, John; Wood, Nicholas; Ben-Shlomo, Yoav; Grosset, Donald G; Williams, Nigel M; Morris, Huw R

Features of GBA-associated Parkinson's disease at presentation in the UK Tracking Parkinson's study

英国帕金森病追踪研究:GBA相关帕金森病在临床表现中的特征

Malek, Naveed; Weil, Rimona S; Bresner, Catherine; Lawton, Michael A; Grosset, Katherine A; Tan, Manuela; Bajaj, Nin; Barker, Roger A; Burn, David J; Foltynie, Thomas; Hardy, John; Wood, Nicholas W; Ben-Shlomo, Yoav; Williams, Nigel W; Grosset, Donald G; Morris, Huw R