arrow
G

Guy A. Rouleau

mcgill university
H指数:146
被引数:9.7万

个人简介

暂无内容

教育背景

暂无内容

工作经历

暂无内容

荣誉奖项

暂无内容

GBA1 Canada initiative (G-can), a pre-competitive, open science platform for GBA1 research

GBA1加拿大倡议(G-can),一个用于GBA1研究的预竞争、开放科学平台

2026-10-150
PRE
Whole-exome sequencing in individuals with obsessive–compulsive disorder and chronic tic disorders identifies 36 large-effect risk genes

对强迫症和慢性抽动障碍个体进行全外显子组测序鉴定出36个具有大效应的风险基因

2026-09-010
OA
Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis

大规模外显子分析揭示了肌萎缩侧索硬化症中新的罕见变异贡献

2026-03-310
OAAI
The Genetic and Molecular Analyses of Rare Candidate Germline BRIP1/FANCJ Variants Implicated in Hereditary Breast and Ovarian Cancers

罕见候选生殖细胞系BRIP1/FANCJ变异在遗传性乳腺癌和卵巢癌中的遗传与分子分析

2026-03-040
OAAI
A multi-ancestry genetic reference for the Quebec population

魁北克人口的多血统遗传参考

2026-02-030
OAAI
Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic Paraplegia

CPT1C基因中的失活功能变异:不支持其在遗传性痉挛性截瘫中的因果作用

2025-11-010
OAAI
Pathway-Specific Polygenic Scores for Lithium Response for Predicting Clinical Lithium Treatment Response in Patients with Bipolar Disorder

锂反应的通路特异性多基因评分,用于预测双相障碍患者临床锂治疗反应

2025-06-250
OAAI
Genomic and Developmental Models to Predict Cognitive and Adaptive Outcomes in Autistic Children

基因组与发育模型在预测自闭症儿童认知和适应结局中的应用

2025-06-010
PRE
Heterozygous RAB3A variants cause cerebellar ataxia by a partial loss-of-function mechanism

杂合RAB3A变异通过部分失活机制导致小脑共济失调

BRAIN
IF11.7
2025-06-012
PRE
Polygenic Scores and Mood Disorder Onsets in the Context of Family History and Early Psychopathology

多基因评分、心境障碍发作与家族史及早期精神病理学的关系

2025-04-160
OA
The Neurodegenerative Disease Knowledge Portal
2025-04-010
PRE
Insufficient evidence for natural selection associated with the Black Death

与黑死病相关的自然选择证据不足

NATURE
IF48.5
2025-02-190
PRE