Syndrome-informed phenotyping identifies a polygenic background for achondroplasia-like facial variation in the general population
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
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Englisch
- Bibliographic citation
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Syndrome-informed phenotyping identifies a polygenic background for achondroplasia-like facial variation in the general population ; volume:15 ; number:1 ; day:2 ; month:12 ; year:2024 ; pages:1-13 ; date:12.2024
Nature Communications ; 15, Heft 1 (2.12.2024), 1-13, 12.2024
- Creator
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Vanneste, Michiel
Hoskens, Hanne
Goovaerts, Seppe
Matthews, Harold
Devine, Jay
Aponte, Jose D.
Cole, Joanne
Shriver, Mark
Marazita, Mary L.
Weinberg, Seth M.
Walsh, Susan
Richmond, Stephen
Klein, Ophir D.
Spritz, Richard A.
Peeters, Hilde
Hallgrímsson, Benedikt
Claes, Peter
- Contributor
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SpringerLink (Online service)
- DOI
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10.1038/s41467-024-54839-1
- URN
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urn:nbn:de:101:1-2502162211252.200627519468
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:37 AM CEST
Data provider
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Vanneste, Michiel
- Hoskens, Hanne
- Goovaerts, Seppe
- Matthews, Harold
- Devine, Jay
- Aponte, Jose D.
- Cole, Joanne
- Shriver, Mark
- Marazita, Mary L.
- Weinberg, Seth M.
- Walsh, Susan
- Richmond, Stephen
- Klein, Ophir D.
- Spritz, Richard A.
- Peeters, Hilde
- Hallgrímsson, Benedikt
- Claes, Peter
- SpringerLink (Online service)
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KBG syndrome: videoconferencing and use of artificial intelligence driven facial phenotyping in 25 new patients
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Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects
Closing the phenotyping gap with non-invasive belowground field phenotyping
Beyond the polygenic additive model
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Detailed phenotyping identifies genes with pleiotropic effects on body composition
High‐throughput CRISPRi phenotyping identifies new essential genes in Streptococcus pneumoniae
Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease
Polygenic Scores for Cognitive Abilities and Their Association with Different Aspects of General Intelligence—A Deep Phenotyping Approach
A correction for sample overlap in genome-wide association studies in a polygenic pleiotropy-informed framework
Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke
KBG syndrome: videoconferencing and use of artificial intelligence driven facial phenotyping in 25 new patients
Multi-PGS enhances polygenic prediction by combining 937 polygenic scores
Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects
Closing the phenotyping gap with non-invasive belowground field phenotyping
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