Christiane Zweier
5PUBLICATIONS
24CO-AUTHORS
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Publications (5)
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|Sep 18, 2024
Complex trait associations in rare diseases and impacts on Mendelian variant interpretation.Craig Smail, Bing Ge, Marissa R Keever-Keigher
|Dec 01, 2023
Gain-of-function and loss-of-function variants in GRIA3 lead to distinct neurodevelopmental phenotypes.Berardo Rinaldi, Allan Bayat, Linda G Zachariassen
|May 04, 2019
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.Lot Snijders Blok, Justine Rousseau, Joanna Twist
|Feb 17, 2019
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.Lot Snijders Blok, Justine Rousseau, Joanna Twist
|Nov 07, 2018
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.Lot Snijders Blok, Justine Rousseau, Joanna Twist
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Frequent Collaborators
3 joint publications
Lot Snijders Blok
3 joint publications
A Micheil Innes
3 joint publications
Hitoshi Kurumizaka
3 joint publications
Paul A Wade
3 joint publications
Simon E Fisher
3 joint publications
Philippe M Campeau
1 joint publications
Craig Smail
1 joint publications
Marissa R Keever-Keigher
1 joint publications
Warren A Cheung
1 joint publications
Jeffrey J Johnston
