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Christiane Zweier

5PUBLICATIONS

24CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Digital processor architecturesBiomedical engineering not elsewhere classifiedLinguistic structures (incl. phonology, morphology and syntax)Neurogenetics

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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

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

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