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/vufind/Search/Results?lookfor=%22Zhou%2C+Hufeng%22&type=Person&sort=year
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PubPharm (71)
1
Whole genome association testing in 333,100 individuals across three biobanks identifies rare non-coding single variant and genomic aggregate associations with height
enthalten in:
bioRxiv.org
| 2023
von
Hawkes, G.
|
Beaumont, R.
|
Li, Z.
| +52
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2
A framework for detecting noncoding rare variant associations of large-scale whole-genome sequencing studies
enthalten in:
bioRxiv.org
| 2023
von
Li, Z.
|
Li, X.
|
Zhou, H.
| +58
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3
A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies
enthalten in:
bioRxiv.org
| 2023
von
Li, X.
|
Chen, H.
|
Selvaraj, M.
| +65
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4
A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies
enthalten in:
bioRxiv : the preprint server for biology
| 2023
von
Li, X.
|
Chen, H.
|
Selvaraj, M.
| +66
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5
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies
enthalten in:
Nature genetics
| 2023
von
Li, X.
|
Quick, C.
|
Zhou, H.
| +158
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6
FAVOR : functional annotation of variants online resource and annotator for variation across the human genome
enthalten in:
Nucleic acids research
| 2023
von
Zhou, H.
|
Arapoglou, T.
|
Li, X.
| +22
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7
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies
enthalten in:
Nature methods
| 2022
von
Li, Z.
|
Li, X.
|
Zhou, H.
| +167
CommentIn: Nat Methods. 2022 Dec;19(12):1532-1533. - PMID 36316564
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8
FAVOR: Functional Annotation of Variants Online Resource and Annotator for Variation across the Human Genome
enthalten in:
bioRxiv.org
| 2022
von
Zhou, H.
|
Arapoglou, T.
|
Li, X.
| +21
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9
Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer
enthalten in:
Nature genetics
| 2022
von
Byun, J.
|
Han, Y.
|
Li, Y.
| +82
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10
A multi-dimensional integrative scoring framework for predicting functional variants in the human genome
enthalten in:
bioRxiv.org
| 2022
von
Li, X.
|
Yung, G.
|
Zhou, H.
| +5
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