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Shabnam Salehi‐Rad
Observed names:
S. Salehi-Rad,
Shabnam Salehi-Rad,
Shabnam Salehi-rad
Institution:
University Health Network
Observed institutions:
National Institutes of Health,
University Health Network,
University of Toronto,
Toronto Western Hospital,
Toronto General Hospital,
National Institute on Aging,
Instituto de Biomedicina de Valencia
show all 7
OpenAlex ID:
A5113666948
Wild-type PINK1 Prevents Basal and Induced Neuronal Apoptosis, a Protective Effect Abrogated by Parkinson Disease-related Mutations
2005
·
Agnes Petit
, Toshitaka Kawarai
, et al.
·
Journal of Biological Chemistry
·
331
Analysis of the PINK1 Gene in a Large Cohort of Cases With Parkinson Disease
2004
·
Ekaterina Rogaeva
, Janel Johnson
, et al.
·
Archives of Neurology
·
200
LRRK2 gene in Parkinson disease
2005
·
C. Paisán-Ruíz
, A. E. Lang
, et al.
·
Neurology
·
178
Analysis of the glucocerebrosidase gene in Parkinson's disease
2004
·
Christine Sato
, Angharad Morgan
, et al.
·
Movement Disorders
·
125
Genetic Variability in CHMP2B and Frontotemporal Dementia
2006
·
Parastoo Momeni
, Ekaterina Rogaeva
, et al.
·
Neurodegenerative Diseases
·
51
Homozygous and heterozygous PINK1 mutations: Considerations for diagnosis and care of Parkinson's disease patients
2006
·
Cindy Zadikoff
, Ekaterina Rogaeva
, et al.
·
Movement Disorders
·
33
Genetic association study of PINK1 coding polymorphisms in Parkinson's disease
2004
·
Justus L. Groen
, Toshitaka Kawarai
, et al.
·
Neuroscience Letters
·
33
Childhood Onset in Familial Prion Disease With a Novel Mutation in the PRNP Gene
2006
·
Ekaterina Rogaeva
, Cindy Zadikoff
, et al.
·
Archives of Neurology
·
24
Novel SPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia
2006
·
Satoshi Kaneko
, Toshitaka Kawarai
, et al.
·
Movement Disorders
·
21
Clinical Findings in a Large Family With a Parkin Ex3Δ40 Mutation
2004
·
Renato P. Munhoz
, Daniel S. Sa
, et al.
·
Archives of Neurology
·
19
Genomic Characterization of Partial Tandem Duplication Involving the KMT2A Gene in Adult Acute Myeloid Leukemia
2024
·
Andrew Seto
, Gregory Downs
, et al.
·
Cancers
·
17
PDF
ETV6 /FLT3 fusion in a mixed-phenotype acute leukemia arising in lymph nodes in a patient with myeloproliferative neoplasm with eosinophilia
2014
·
Niloufar Hosseini
, Kenneth J. Craddock
, et al.
·
Journal of Hematopathology
·
16
PDF
Novel PS1 mutation in a Bavarian kindred with familial Alzheimer disease.
2004
·
Hans H Klünemann
, Ekaterina Rogaeva
, et al.
·
PubMed
·
15
Characterization of a cyclooxygenase-2-765G???C promoter polymorphism in human neural cells
2005
·
Jian-Guo Cui
, Shabnam Salehi-Rad
, et al.
·
Neuroreport
·
8
63. Comparative analysis of testing methods used for the detection of internal tandem duplications in the KMT2A/MLL gene
2022
·
José-Mario Capo-Chichi
, Andrew Seto
, et al.
·
Cancer Genetics
O2–02–06: Results of fine mapping of a late–onset Alzheimer disease locus on chromosome 12: Linkage and association studies
2006
·
Ekaterina Rogaeva
, Joseph Lee
, et al.
·
Alzheimer s & Dementia
P4-076 Polymorphism in the cyclooxygenase-2 (COX-2) and presenilin 2 (PS2) gene promoters: impact on inflammatory signaling and potential contribution to the etiopathology of Alzheimer's disease (AD)
2004
·
J.G. Cui
, P.K. Mukherjee
, et al.
·
Neurobiology of Aging
S2-01-03 Genetic studies in late-onset Alzheimer disease: loci on chromosomes 12 and 10
2004
·
Ekaterina Rogaeva
, Yan Meng
, et al.
·
Neurobiology of Aging
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Works count:
18
Citation count:
1,071
H-index:
13
I10-index:
13
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