Examining the role of common variants in rare neurodevelopmental conditions

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: Examining the role of common variants in rare neurodevelopmental conditions ; volume:636 ; number:8042 ; day:20 ; month:11 ; year:2024 ; pages:404-411 ; date:12.2024
Nature ; 636, Heft 8042 (20.11.2024), 404-411, 12.2024

Creator: Huang, Qin Qin
Wigdor, Emilie M.
Malawsky, Daniel S.
Campbell, Patrick
Samocha, Kaitlin E.
Chundru, V. Kartik
Danecek, Petr
Lindsay, Sarah
Marchant, Thomas
Koko, Mahmoud
Amanat, Sana
Bonfanti, Davide
Sheridan, Eamonn
Radford, Elizabeth J.
Barrett, Jeffrey C.
Wright, Caroline F.
Firth, Helen V.
Warrier, Varun
Strudwick Young, Alexander
Hurles, Matthew E.
Martin, Hilary C.

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41586-024-08217-y

URN: urn:nbn:de:101:1-2502242120562.227278098543

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:28 AM CEST

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Huang, Qin Qin
Wigdor, Emilie M.
Malawsky, Daniel S.
Campbell, Patrick
Samocha, Kaitlin E.
Chundru, V. Kartik
Danecek, Petr
Lindsay, Sarah
Marchant, Thomas
Koko, Mahmoud
Amanat, Sana
Bonfanti, Davide
Sheridan, Eamonn
Radford, Elizabeth J.
Barrett, Jeffrey C.
Wright, Caroline F.
Firth, Helen V.
Warrier, Varun
Strudwick Young, Alexander
Hurles, Matthew E.
Martin, Hilary C.
SpringerLink (Online service)

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Examining the role of common variants in rare neurodevelopmental conditions

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Other Objects (12)

Functional characterization of rare FOXP2 variants in neurodevelopmental disorder

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A pathway-based association analysis model using common and rare variants

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