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/vufind/Search/Results?lookfor=%22Newman%2C+William+G%22&type=Person&sort=year
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PubPharm (414)
1
Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease
enthalten in:
bioRxiv.org
| 2024
von
de Lange, K.
|
Moutsianas, L.
|
Lee, J.
| +29
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2
Exploring the genetic architecture of inflammatory bowel disease by whole genome sequencing identifies association at
ADCY7
enthalten in:
bioRxiv.org
| 2024
von
Luo, Y.
|
de Lange, K.
|
Jostins, L.
| +27
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3
Influence of autozygosity on common disease risk across the phenotypic spectrum
enthalten in:
bioRxiv.org
| 2024
von
Malawsky, D.
|
van Walree, E.
|
Jacobs, B.
| +15
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4
Public preferences for pharmacogenetic testing in the NHS : Embedding a discrete choice experiment within service design to better meet user needs
enthalten in:
British journal of clinical pharmacology
| 2024
von
McDermott, J.
|
Sharma, V.
|
Newman, W.
| +3
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5
Human
HPSE2
gene transfer ameliorates bladder pathophysiology in a mutant mouse model of urofacial syndrome
enthalten in:
bioRxiv.org
| 2024
von
Lopes, F.
|
Grenier, C.
|
Jarvis, B.
| +7
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6
Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome
enthalten in:
Clinical genetics
| 2024
von
Faridi, R.
|
Stratton, P.
|
Salmeri, N.
| +6
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7
Perceived risk of type 2 diabetes: Using linked genomic, clinical and questionnaire data to understand the potential use of genetic risk tools in British South Asians
enthalten in:
bioRxiv.org
| 2024
von
Law, J.
|
Stow, D.
|
Hodgson, S.
| +4
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8
Deep intronic variant causes aberrant splicing of ATP7A in a family with a variable occipital horn syndrome phenotype
enthalten in:
European journal of medical genetics
| 2024
von
Harkness, J.
|
Thomas, H.
|
Urquhart, J.
| +6
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9
Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project data
enthalten in:
bioRxiv.org
| 2023
von
Cipriani, V.
|
Vestito, L.
|
Magavern, E.
| +58
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10
Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project data
enthalten in:
medRxiv : the preprint server for health sciences
| 2023
von
Cipriani, V.
|
Vestito, L.
|
Magavern, E.
| +58
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