Ekaterina Rogaeva

发表

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease

Ming Zhang, Lorne Zinman, Sandra E. Black, 2018, Journal of visualized experiments : JoVE.

The Project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public

Naomi R. Wray, Mamede de Carvalho, Blaz Koritnik, 2018, bioRxiv.

Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease

Aldo Quattrone, Nobutaka Hattori, Anthony E. Lang, 2011, Neurobiology of Aging.

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Eden R Martin, Seth Love, Brian Lawlor, 2019, Nature Genetics.

Conversion to Dementia among Two Groups with Cognitive Impairment

Ranjan Duara, David A. Loewenstein, Ekaterina Rogaeva, 2004, Dementia and Geriatric Cognitive Disorders.

Drug Repositioning for Alzheimer’s Disease Based on Systematic ‘omics’ Data Mining

Gerold Schmitt-Ulms, Christine Sato, Ekaterina Rogaeva, 2016, PloS one.

Frontotemporal dementia and its subtypes: a genome-wide association study

Alexander Gerhard, Adrian Danek, Luigi Ferrucci, 2014, The Lancet Neurology.

Exceptionally low likelihood of Alzheimer’s dementia in APOE2 homozygotes from a 5,000-person neuropathological study

Robert C. Green, Andrew J. Saykin, Liana G. Apostolova, 2020, Nature Communications.

Microbleed topography, leukoaraiosis, and cognition in probable Alzheimer disease from the Sunnybrook dementia study.

Gregory M. Szilagyi, Sandra E Black, Ekaterina Rogaeva, 2008, Archives of neurology.

Cerebral perfusion changes in presymptomatic genetic frontotemporal dementia: a GENFI study

Veronica Redaelli, Sebastien Ourselin, Martina Bocchetta, 2019, Brain : a journal of neurology.

Association between early-onset Parkinson disease and 22q11.2 deletion syndrome: identification of a novel genetic form of Parkinson disease and its clinical implications.

Ekaterina Rogaeva, Tim-Rasmus Kiehl, T. Kiehl, 2013, JAMA neurology.

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

Sandro Sorbi, Masatoshi Takeda, Eng King Tan, 2011, Archives of neurology.

Drug Repositioning for Diabetes Based on 'Omics' Data Mining

Ekaterina Rogaeva, E. Rogaeva, Ming Zhang, 2015, PloS one.

Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis

Veronica Redaelli, Sebastien Ourselin, Martina Bocchetta, 2015, The Lancet Neurology.

Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis

Lorne Zinman, Adriano Chiò, Richard W. Orrell, 2014, Nature Neuroscience.

A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

David Heckerman, Lorne Zinman, Joanne Wuu, 2011, Neuron.

Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia.

Nick C. Fox, Pietro Pietrini, Alexander Gerhard, 2018, Nature Medicine.

The association between genetic variants in SORL1 and Alzheimer disease in an urban, multiethnic, community-based cohort.

Yaakov Stern, Richard Mayeux, Ekaterina Rogaeva, 2007, Archives of neurology.

Nicastrin modulates presenilin-mediated notch/glp-1 signal transduction and βAPP processing

Ruedi Aebersold, You-Qiang Song, Sandro Sorbi, 2000, Nature.

Early‐onset Parkinson's disease caused by a compound heterozygous DJ‐1 mutation

Vincenzo Bonifati, John Hardy, Peter Heutink, 2003, Annals of neurology.