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/vufind/Search/Results?lookfor=%22O%27Callaghan%2C+Benjamin%22&type=Person&sort=year
/vufind/Search/Results?lookfor=%22O%27Callaghan%2C+Benjamin%22&type=Person&sort=year
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PubPharm (18)
1
Common genetic risk for Parkinson's disease and dysfunction of the endo-lysosomal system
enthalten in:
Philosophical transactions of the Royal Society of London. Series B, Biological sciences
| 2024
von
Bhore, N.
|
Bogacki, E.
|
O'Callaghan, B.
| +3
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2
KAT8 compound inhibition inhibits the initial steps of PINK1-dependant mitophagy
enthalten in:
bioRxiv.org
| 2024
von
de Talhouët, C.
|
Esteras Gallego, N.
|
Soutar, M.
| +2
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3
The non-specific lethal complex regulates genes and pathways genetically linked to Parkinson's disease
enthalten in:
Brain : a journal of neurology
| 2023
von
Hicks, A.
|
Reynolds, R.
|
O'Callaghan, B.
| +5
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4
PINK1 : From Parkinson's disease to mitophagy and back again
enthalten in:
PLoS biology
| 2023
von
O'Callaghan, B.
|
Hardy, J.
|
Plun-Favreau, H.
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5
Pathophysiology of Dyt1-Tor1a dystonia in mice is mediated by spinal neural circuit dysfunction
enthalten in:
Science translational medicine
| 2023
von
Pocratsky, A.
|
Nascimento, F.
|
Özyurt, M.
| +7
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6
Regulation of mitophagy by the NSL complex underlies genetic risk for Parkinson's disease at 16q11.2 and MAPT H1 loci
enthalten in:
Brain : a journal of neurology
| 2022
von
Soutar, M.
|
Melandri, D.
|
O'Callaghan, B.
| +26
CommentIn: Brain. 2022 Nov 02;:. - PMID 36319596
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7
Pathophysiology of Dyt1 dystonia is mediated by spinal cord dysfunction
enthalten in:
bioRxiv.org
| 2022
von
Pocratsky, A.
|
Nascimento, F.
|
Özyurt, M.
| +7
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8
Regulation of mitophagy by the NSL complex underlies genetic risk for Parkinson’s disease at Chr16q11.2 and on the MAPT H1 allele
enthalten in:
bioRxiv.org
| 2021
von
Soutar, M.
|
Melandri, D.
|
O’Callaghan, B.
| +24
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9
Brown-Vialetto-Van Laere and Fazio-Londe syndromes : SLC52A3 mutations with puzzling phenotypes and inheritance
enthalten in:
European journal of neurology
| 2021
von
Gayathri, S.
|
Gowda, V.
|
Udhayabanu, T.
| +6
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10
ANGPTL6 Genetic Variants Are an Underlying Cause of Familial Intracranial Aneurysms
enthalten in:
Neurology
| 2021
von
Hostettler, I.
|
O'Callaghan, B.
|
Bugiardini, E.
| +27
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18
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18
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18
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Zeitschriftentitel
3
Brain : a journal of neurology
3
bioRxiv.org
1
American journal of human genetics
1
European Journal of Neurology
1
European journal of neurology
1
Journal of Inherited Metabolic Disease
1
Journal of inherited metabolic disease
1
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1
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1
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1
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1
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1
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1
The Journal of physiology
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Thema
12
Journal Article
11
Research Support, Non-U.S. Gov't
2
570
2
Biology
2
EC 2.7.-
2
GWAS
2
Membrane Transport Proteins
2
Parkinson’s disease
2
Protein Kinases
2
Receptors, G-Protein-Coupled
2
Review
2
SLC52A2
2
SLC52A3
2
SLC52A3 protein, human
1
ANGPTL6 protein, human
1
ATP1A2 protein, human
1
Angiopoietin-Like Protein 6
1
Angiopoietin-like Proteins
1
Autosomal pseudodominance
1
Brown−Vialetto−Van Laere syndrome
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Erscheinungszeitraum
14
2020-
4
2010-2019
Erscheinungsjahr(e)
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Sprache
15
Englisch
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