Claudia A L Ruivenkamp

Years Active: 2017-2023
Publications (10 Years): 3

This page only lists publications with an associated author ORCID identifier.

Publications

Michelle van Slobbe, Arie van Haeringen, Lisenka E L M Vissers, Emilia K Bijlsma, Julie W Rutten, Manon Suerink, Esther A R Nibbeling, Claudia A L Ruivenkamp, Saskia Koene
Reanalysis of whole-exome sequencing (WES) data of children with neurodevelopmental disorders in a standard patient care context. European journal of pediatrics (2023)
Aikaterini Vezyroglou, Rhoda Akilapa, Katy Barwick, Saskia Koene, Catherine A Brownstein, Muriel Holder-Espinasse, Andrew E Fry, Andrea H Németh, George K Tofaris, Eleanor Hay, Imelda Hughes, Sahar Mansour, Santosh R Mordekar, Miranda Splitt, Peter D Turnpenny, Demetria Demetriou, Tamara T Koopmann, Claudia A L Ruivenkamp, Pankaj B Agrawal, Lucinda Carr, Virginia Clowes, Neeti Ghali, Susan Elizabeth Holder, Jessica Radley, Alison Male, Sanjay M Sisodiya, Manju A Kurian, Judith Helen Cross, Meena Balasubramanian
The Phenotypic Continuum of ATP1A3 -Related Disorders. Neurology 99 (14) (2022)
Elliot Sollis, Pelagia Deriziotis, Hirotomo Saitsu, Noriko Miyake, Naomichi Matsumoto, Mariette J V Hoffer, Claudia A L Ruivenkamp, Mariëlle Alders, Nobuhiko Okamoto, Emilia K Bijlsma, Astrid S Plomp, Simon E Fisher
Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders. Human mutation 38 (11) (2017)

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