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/vufind/Search/Results?lookfor=%22Weedon%2C+Michael+N%22&type=Person&sort=year
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PubPharm (379)
1
Estimating population level disease prevalence using genetic risk scores
enthalten in:
bioRxiv.org
| 2024
von
Evans, B.
|
Słowiński, P.
|
Hattersley, A.
| +7
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2
A genome wide association study of frozen shoulder identifies a common variant of
WNT7B
and diabetes as causal risk factors
enthalten in:
bioRxiv.org
| 2024
von
Green, H.
|
Jones, A.
|
Evans, J.
| +6
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3
The penetrance of age-related monogenic disease depends on ascertainment context
enthalten in:
bioRxiv.org
| 2024
von
Mirshahi, U.
|
Colclough, K.
|
Wright, C.
| +12
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4
A novel disease mechanism leading to the expression of a disallowed gene in the pancreatic beta-cell identified by non-coding, regulatory mutations controlling
HK1
enthalten in:
bioRxiv.org
| 2024
von
Wakeling, M.
|
Owens, N.
|
Hopkinson, J.
| +20
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5
Correlations in sleeping patterns and circadian preference between spouses
enthalten in:
bioRxiv.org
| 2024
von
Richmond, R.
|
Howe, L.
|
Heilbron, K.
| +8
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6
Genetic modifiers of rare variants in monogenic developmental disorder loci
enthalten in:
Nature genetics
| 2024
von
Kingdom, R.
|
Beaumont, R.
|
Wood, A.
| +2
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7
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements
enthalten in:
European journal of human genetics : EJHG
| 2024
von
Laver, T.
|
Wakeling, M.
|
Caswell, R.
| +17
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8
Human inherited PD-L1 deficiency is clinically and immunologically less severe than PD-1 deficiency
enthalten in:
The Journal of experimental medicine
| 2024
von
Johnson, M.
|
Ogishi, M.
|
Domingo-Vila, C.
| +29
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9
Applying a genetic risk score model to enhance prediction of future multiple sclerosis diagnosis at first presentation with optic neuritis
enthalten in:
Nature communications
| 2024
von
Loginovic, P.
|
Wang, F.
|
Li, J.
| +15
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10
Penetrance and expressivity of mitochondrial variants in a large clinically unselected population
enthalten in:
Human molecular genetics
| 2024
von
Cannon, S.
|
Hall, T.
|
Hawkes, G.
| +7
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17
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15
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10
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10
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9
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9
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8
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