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

Sortilin receptor 1 predicts longitudinal cognitive change

Sortilin受体1预测纵向认知变化

Reynolds, Chandra A; Zavala, Catalina; Gatz, Margaret; Vie, Loryana; Johansson, Boo; Malmberg, Bo; Ingelsson, Erik; Prince, Jonathan A; Pedersen, Nancy L

Genome-wide and gene-based association implicates FRMD6 in Alzheimer disease

全基因组和基于基因的关联研究表明FRMD6与阿尔茨海默病有关

Hong, Mun-Gwan; Reynolds, Chandra A; Feldman, Adina L; Kallin, Mikael; Lambert, Jean-Charles; Amouyel, Philippe; Ingelsson, Erik; Pedersen, Nancy L; Prince, Jonathan A

Genetic association of sequence variants near AGER/NOTCH4 and dementia

AGER/NOTCH4附近序列变异与痴呆症的遗传关联

Bennet, Anna M; Reynolds, Chandra A; Eriksson, Ulrika K; Hong, Mun-Gwan; Blennow, Kaj; Gatz, Margaret; Alexeyenko, Andrey; Pedersen, Nancy L; Prince, Jonathan A

Associations of gene sequence variation and serum levels of C-reactive protein and interleukin-6 with Alzheimer's disease and dementia.

基因序列变异与血清 C 反应蛋白和白细胞介素-6 水平和阿尔茨海默病及痴呆症的关联

Eriksson Ulrika K, Pedersen Nancy L, Reynolds Chandra A, Hong Mun-Gwan, Prince Jonathan A, Gatz Margaret, Dickman Paul W, Bennet Anna M

Meta-analysis of the association between variants in SORL1 and Alzheimer disease

对SORL1基因变异与阿尔茨海默病关联的荟萃分析

Reitz, Christiane; Cheng, Rong; Rogaeva, Ekaterina; Lee, Joseph H; Tokuhiro, Shinya; Zou, Fanggeng; Bettens, Karolien; Sleegers, Kristel; Tan, Eng King; Kimura, Ryo; Shibata, Nobuto; Arai, Heii; Kamboh, M Ilyas; Prince, Jonathan A; Maier, Wolfgang; Riemenschneider, Matthias; Owen, Michael; Harold, Denise; Hollingworth, Paul; Cellini, Elena; Sorbi, Sandro; Nacmias, Benedetta; Takeda, Masatoshi; Pericak-Vance, Margaret A; Haines, Jonathan L; Younkin, Steven; Williams, Julie; van Broeckhoven, Christine; Farrer, Lindsay A; St George-Hyslop, Peter H; Mayeux, Richard

Analysis of lipid pathway genes indicates association of sequence variation near SREBF1/TOM1L2/ATPAF2 with dementia risk

脂质代谢通路基因分析表明,SREBF1/TOM1L2/ATPAF2 附近序列变异与痴呆风险相关。

Reynolds, Chandra A; Hong, Mun-Gwan; Eriksson, Ulrika K; Blennow, Kaj; Wiklund, Fredrik; Johansson, Boo; Malmberg, Bo; Berg, Stig; Alexeyenko, Andrey; Grönberg, Henrik; Gatz, Margaret; Pedersen, Nancy L; Prince, Jonathan A

Pleiotropy in the presence of allelic heterogeneity: alternative genetic models for the influence of APOE on serum LDL, CSF amyloid-β42, and dementia

等位基因异质性存在下的多效性:APOE 对血清 LDL、脑脊液淀粉样蛋白-β42 和痴呆症影响的替代遗传模型

Bennet, Anna M; Reynolds, Chandra A; Gatz, Margaret; Blennow, Kaj; Pedersen, Nancy L; Prince, Jonathan A

Sequence variation in SORL1 and dementia risk in Swedes

瑞典人SORL1基因序列变异与痴呆风险

Reynolds, Chandra A; Hong, Mun-Gwan; Eriksson, Ulrika K; Blennow, Kaj; Johansson, Boo; Malmberg, Bo; Berg, Stig; Gatz, Margaret; Pedersen, Nancy L; Bennet, Anna M; Prince, Jonathan A

Serum lipid levels and cognitive change in late life

晚年血脂水平与认知变化

Reynolds, Chandra A; Gatz, Margaret; Prince, Jonathan A; Berg, Stig; Pedersen, Nancy L

A survey of ABCA1 sequence variation confirms association with dementia

ABCA1序列变异调查证实其与痴呆症相关

Reynolds, Chandra A; Hong, Mun-Gwan; Eriksson, Ulrika K; Blennow, Kaj; Bennet, Anna M; Johansson, Boo; Malmberg, Bo; Berg, Stig; Wiklund, Fredrik; Gatz, Margaret; Pedersen, Nancy L; Prince, Jonathan A