Arama Sonuçları - Ziv Gan‐Or
- Gösterilen 1 - 20 sonuçlar arası kayıtlar. 76
- Sonraki Sayfaya Git
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1
Autophagy lysosomal pathway dysfunction in Parkinson's disease; evidence from human genetics Yazar: Konstantin Senkevich, Ziv Gan‐Or
Baskı/Yayın Bilgisi 2019Revisão -
2
Binding of Antibiotics to Bovine and Ovine Serum Yazar: Ziv Gan‐Or, F.G. Sulman
Baskı/Yayın Bilgisi 1972Artigo -
3
<scp>LRRK2</scp> and Parkinson's disease: from genetics to targeted therapy Yazar: Yuri L. Sosero, Ziv Gan‐Or
Baskı/Yayın Bilgisi 2023Revisão -
4
Tau and MAPT genetics in tauopathies and synucleinopathies Yazar: Etienne Léveillé, Owen A. Ross, Ziv Gan‐Or
Baskı/Yayın Bilgisi 2021Revisão -
5
Genetic perspective on the role of the autophagy-lysosome pathway in Parkinson disease Yazar: Ziv Gan‐Or, Patrick A. Dion, Guy A. Rouleau
Baskı/Yayın Bilgisi 2015Revisão -
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Sleep disorders and Parkinson disease; lessons from genetics Yazar: Ziv Gan‐Or, Roy N. Alcalay, Guy A. Rouleau, Ronald B. Postuma
Baskı/Yayın Bilgisi 2018Revisão -
8
Neuroanatomical correlates of genetic risk for obesity in children Yazar: Filip Morys, Eric Yu, Mari Shishikura, Casey Paquola, Uku Vainik, Gideon Nave, Philipp Koellinger, Ziv Gan‐Or, Alain Dagher
Baskı/Yayın Bilgisi 2023Artigo -
9
<i>GBA</i>p.T369M substitution in Parkinson disease: Polymorphism or association? A meta-analysis Yazar: Victoria Mallett, Jay P. Ross, Roy N. Alcalay, Amirthagowri Ambalavanan, Ellen Sidransky, Patrick A. Dion, Guy A. Rouleau, Ziv Gan‐Or
Baskı/Yayın Bilgisi 2016Artigo -
10
Type 2 Diabetes as a Determinant of Parkinson's Disease Risk and Progression Yazar: Harneek Chohan, Konstantin Senkevich, Radhika K. Patel, Jonathan P. Bestwick, Benjamin Meir Jacobs, Sara Bandrés‐Ciga, Ziv Gan‐Or, Alastair Noyce
Baskı/Yayın Bilgisi 2021Revisão -
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12
Brain atrophy progression in Parkinson’s disease is shaped by connectivity and local vulnerability Yazar: Christina Tremblay, Shady Rahayel, Andrew Vo, Filip Morys, Golia Shafiei, Nooshin Abbasi, Ross D. Markello, Ziv Gan‐Or, Bratislav Mišić, Alain Dagher
Baskı/Yayın Bilgisi 2021Artigo -
13
Machine learning nominates the inositol pathway and novel genes in Parkinson’s disease Yazar: Eric Yu, Roxanne Larivière, Rhalena A. Thomas, Lang Liu, Konstantin Senkevich, Shady Rahayel, Jean‐François Trempe, Edward A. Fon, Ziv Gan‐Or
Baskı/Yayın Bilgisi 2023Artigo -
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Differential effects of severe vs mild <i>GBA</i> mutations on Parkinson disease Yazar: Ziv Gan‐Or, Idan Amshalom, Laura L. Kilarski, Anat Bar‐Shira, Mali Gana‐Weisz, Anat Mirelman, Karen Marder, Susan Bressman, Nir Giladi, Avi Orr‐Urtreger
Baskı/Yayın Bilgisi 2015Revisão -
16
A homozygous mutation in <i><scp>SLC1A4</scp></i> in siblings with severe intellectual disability and microcephaly Yazar: Myriam Srour, Fadi F. Hamdan, Ziv Gan‐Or, D. Labuda, Christina Nassif, Maryam Oskoui, Mali Gana‐Weisz, Avi Orr‐Urtreger, Guy A. Rouleau, Jacques L. Michaud
Baskı/Yayın Bilgisi 2015Artigo -
17
Common X‐Chromosome Variants Are Associated with Parkinson Disease Risk Yazar: Yann Le Guen, Valerio Napolioni, Michaël E. Belloy, Eric Yu, Lynne Krohn, Jennifer A. Ruskey, Ziv Gan‐Or, Gabriel Kennedy, Sarah J. Eger, Michael D. Greicius
Baskı/Yayın Bilgisi 2021Revisão -
18
Plasma Glucosylsphingosine in <scp><i>GBA1</i></scp> Mutation Carriers with and without Parkinson's Disease Yazar: Matthew Surface, Manisha Balwani, Cheryl Waters, Alexander Haimovich, Ziv Gan‐Or, Karen Marder, Tammy Hsieh, Linxia Song, Shalini Padmanabhan, F. Hsieh, Kalpana Merchant, Roy N. Alcalay
Baskı/Yayın Bilgisi 2021Artigo -
19
Effect Modification between Genes and Environment and Parkinson's Disease Risk Yazar: María Teresa Periñán, Kajsa Brolin, Sara Bandrés‐Ciga, Cornelis Blauwendraat, Christine Klein, Ziv Gan‐Or, Andrew Singleton, Pilar Gómez‐Garre, Maria Swanberg, Pablo Mir, Alastair Noyce
Baskı/Yayın Bilgisi 2022Revisão -
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Arama Araçları:
İlgili Konular
Medicine
Biology
Disease
Genetics
Gene
Parkinson's disease
Internal medicine
Genotype
Single-nucleotide polymorphism
Pathology
Neuroscience
Genome-wide association study
Mutation
LRRK2
Psychology
Genetic association
Bioinformatics
Dementia
Phenotype
Psychiatry
Allele
Cohort
Odds ratio
Biochemistry
Genetic variants
Glucocerebrosidase
Mendelian randomization
Alpha-synuclein
Computational biology
Dementia with Lewy bodies