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

Lack of evidence for an association between UCHL1 S18Y and Parkinson's disease

缺乏证据表明UCHL1 S18Y与帕金森病之间存在关联

Hutter, Carolyn M; Samii, Ali; Factor, Stewart A; Nutt, John G; Higgins, Donald S; Bird, Thomas D; Griffith, Alida; Roberts, John W; Leis, Berta C; Montimurro, Jennifer S; Kay, Denise M; Edwards, Karen L; Payami, Haydeh; Zabetian, Cyrus P

Glucocerebrosidase gene mutations: a risk factor for Lewy body disorders

葡萄糖脑苷脂酶基因突变:路易体病的一个风险因素

Mata, Ignacio F; Samii, Ali; Schneer, Seth H; Roberts, John W; Griffith, Alida; Leis, Berta C; Schellenberg, Gerard D; Sidransky, Ellen; Bird, Thomas D; Leverenz, James B; Tsuang, Debby; Zabetian, Cyrus P

DBH -1021C-->T does not modify risk or age at onset in Parkinson's disease

DBH -1021C-->T 不改变帕金森病的风险或发病年龄

Chun, Lani S; Samii, Ali; Hutter, Carolyn M; Griffith, Alida; Roberts, John W; Leis, Berta C; Mosley, Anthony D; Wander, P Luke; Edwards, Karen L; Payami, Haydeh; Zabetian, Cyrus P

Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease

帕金森病中MAPT H1单倍型和亚单倍型的关联分析

Zabetian, Cyrus P; Hutter, Carolyn M; Factor, Stewart A; Nutt, John G; Higgins, Donald S; Griffith, Alida; Roberts, John W; Leis, Berta C; Kay, Denise M; Yearout, Dora; Montimurro, Jennifer S; Edwards, Karen L; Samii, Ali; Payami, Haydeh

LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago

LRRK2 G2019S 突变存在于起源于欧洲和中东的帕金森病家族中:证据表明,两千年前发生了两次截然不同的起源事件。

Zabetian, Cyrus P; Hutter, Carolyn M; Yearout, Dora; Lopez, Alexis N; Factor, Stewart A; Griffith, Alida; Leis, Berta C; Bird, Thomas D; Nutt, John G; Higgins, Donald S; Roberts, John W; Kay, Denise M; Edwards, Karen L; Samii, Ali; Payami, Haydeh