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

Job-related exhaustion risk variant in UST is associated with dementia and DNA methylation

UST基因中与工作相关的疲劳风险变异与痴呆和DNA甲基化有关

Sulkava, Sonja; Haukka, Jari; Kaivola, Karri; Doagu, Fatma; Lahtinen, Alexandra; Kantojärvi, Katri; Pärn, Kalle; Palta, Priit; Myllykangas, Liisa; Sulkava, Raimo; Laatikainen, Tiina; Tienari, Pentti J; Paunio, Tiina

Association Between Psychological Distress and Incident Dementia in a Population-Based Cohort in Finland

芬兰一项基于人群队列的研究中,心理困扰与痴呆症发病率之间的关联

Sulkava, Sonja; Haukka, Jari; Sulkava, Raimo; Laatikainen, Tiina; Paunio, Tiina

Melatonin receptor type 1A gene linked to Alzheimer's disease in old age.

褪黑素受体1A型基因与老年阿尔茨海默病有关

Sulkava Sonja, Muggalla Pranuthi, Sulkava Raimo, Ollila Hanna M, Peuralinna Terhi, Myllykangas Liisa, Kaivola Karri, Stone David J, Traynor Bryan J, Renton Alan E, Rivera Alberto M, Helisalmi Seppo, Soininen Hilkka, Polvikoski Tuomo, Hiltunen Mikko, Tienari Pentti J, Huttunen Henri J, Paunio Tiina

Genome-wide association study of neocortical Lewy-related pathology

新皮质路易氏病相关病理的全基因组关联研究

Peuralinna, Terhi; Myllykangas, Liisa; Oinas, Minna; Nalls, Mike A; Keage, Hannah A D; Isoviita, Veli-Matti; Valori, Miko; Polvikoski, Tuomo; Paetau, Anders; Sulkava, Raimo; Ince, Paul G; Zaccai, Julia; Brayne, Carol; Traynor, Bryan J; Hardy, John; Singleton, Andrew B; Tienari, Pentti J

Plasma homocysteine, Alzheimer and cerebrovascular pathology: a population-based autopsy study

血浆同型半胱氨酸、阿尔茨海默病和脑血管病理:一项基于人群的尸检研究

Hooshmand, Babak; Polvikoski, Tuomo; Kivipelto, Miia; Tanskanen, Maarit; Myllykangas, Liisa; Erkinjuntti, Timo; Mäkelä, Mira; Oinas, Minna; Paetau, Anders; Scheltens, Philip; van Straaten, Elizabeth C W; Sulkava, Raimo; Solomon, Alina

Delirium is a strong risk factor for dementia in the oldest-old: a population-based cohort study

谵妄是高龄老人发生痴呆症的一个重要危险因素:一项基于人群的队列研究

Davis, Daniel H J; Muniz Terrera, Graciela; Keage, Hannah; Rahkonen, Terhi; Oinas, Minna; Matthews, Fiona E; Cunningham, Colm; Polvikoski, Tuomo; Sulkava, Raimo; MacLullich, Alasdair M J; Brayne, Carol

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

C9ORF72基因中六核苷酸重复序列的扩增是9p21染色体连锁的ALS-FTD的病因。

Renton, Alan E; Majounie, Elisa; Waite, Adrian; Simón-Sánchez, Javier; Rollinson, Sara; Gibbs, J Raphael; Schymick, Jennifer C; Laaksovirta, Hannu; van Swieten, John C; Myllykangas, Liisa; Kalimo, Hannu; Paetau, Anders; Abramzon, Yevgeniya; Remes, Anne M; Kaganovich, Alice; Scholz, Sonja W; Duckworth, Jamie; Ding, Jinhui; Harmer, Daniel W; Hernandez, Dena G; Johnson, Janel O; Mok, Kin; Ryten, Mina; Trabzuni, Danyah; Guerreiro, Rita J; Orrell, Richard W; Neal, James; Murray, Alex; Pearson, Justin; Jansen, Iris E; Sondervan, David; Seelaar, Harro; Blake, Derek; Young, Kate; Halliwell, Nicola; Callister, Janis Bennion; Toulson, Greg; Richardson, Anna; Gerhard, Alex; Snowden, Julie; Mann, David; Neary, David; Nalls, Michael A; Peuralinna, Terhi; Jansson, Lilja; Isoviita, Veli-Matti; Kaivorinne, Anna-Lotta; Hölttä-Vuori, Maarit; Ikonen, Elina; Sulkava, Raimo; Benatar, Michael; Wuu, Joanne; Chiò, Adriano; Restagno, Gabriella; Borghero, Giuseppe; Sabatelli, Mario; Heckerman, David; Rogaeva, Ekaterina; Zinman, Lorne; Rothstein, Jeffrey D; Sendtner, Michael; Drepper, Carsten; Eichler, Evan E; Alkan, Can; Abdullaev, Ziedulla; Pack, Svetlana D; Dutra, Amalia; Pak, Evgenia; Hardy, John; Singleton, Andrew; Williams, Nigel M; Heutink, Peter; Pickering-Brown, Stuart; Morris, Huw R; Tienari, Pentti J; Traynor, Bryan J

APOE and AβPP gene variation in cortical and cerebrovascular amyloid-β pathology and Alzheimer's disease: a population-based analysis

APOE 和 AβPP 基因变异与皮质和脑血管淀粉样蛋白β病理及阿尔茨海默病的关系:一项基于人群的分析

Peuralinna, Terhi; Tanskanen, Maarit; Mäkelä, Mira; Polvikoski, Tuomo; Paetau, Anders; Kalimo, Hannu; Sulkava, Raimo; Hardy, John; Lai, Shiao-Lin; Arepalli, Sampath; Hernandez, Dena; Traynor, Bryan J; Singleton, Andrew; Tienari, Pentti J; Myllykangas, Liisa

Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

芬兰肌萎缩侧索硬化症中9p21染色体:一项全基因组关联研究

Laaksovirta, Hannu; Peuralinna, Terhi; Schymick, Jennifer C; Scholz, Sonja W; Lai, Shaoi-Lin; Myllykangas, Liisa; Sulkava, Raimo; Jansson, Lilja; Hernandez, Dena G; Gibbs, J Raphael; Nalls, Michael A; Heckerman, David; Tienari, Pentti J; Traynor, Bryan J

Neurofibrillary tau pathology modulated by genetic variation of alpha-synuclein

α-突触核蛋白基因变异调控神经原纤维缠结tau蛋白病理

Peuralinna, Terhi; Oinas, Minna; Polvikoski, Tuomo; Paetau, Anders; Sulkava, Raimo; Niinistö, Leena; Kalimo, Hannu; Hernandez, Dena; Hardy, John; Singleton, Andrew; Tienari, Pentti J; Myllykangas, Liisa