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Ruivenkamp, Claudia A.L.
279
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Online (279)
Mediatypes
Articles (Online) (85)
OpenAccess-fulltext (194)
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1
Refining the 9q34.3 microduplication syndrome reveals mild ..:
Rots, Dmitrijs
;
Rooney, Kathleen
;
Relator, Raissa
...
Clinical Genetics. 105 (2024) 6 - p. 655-660 , 2024
Link:
https://doi.org/10.1111/..
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2
Reanalysis of whole-exome sequencing (WES) data of children..:
van Slobbe, Michelle
;
van Haeringen, Arie
;
Vissers, Lisenka E. L. M.
...
European Journal of Pediatrics. 183 (2023) 1 - p. 345-355 , 2023
Link:
https://doi.org/10.1007/..
?
3
The neurodevelopmental and facial phenotype in individuals ..:
Aerden, Mio
;
Denommé-Pichon, Anne-Sophie
;
Bonneau, Dominique
...
European Journal of Human Genetics. 31 (2023) 4 - p. 461-468 , 2023
Link:
https://doi.org/10.1038/..
?
4
PHIP-associated Chung-Jansen syndrome: Report of 23 new ind..:
Kampmeier, Antje
;
Leitão, Elsa
;
Parenti, Ilaria
...
Frontiers in Cell and Developmental Biology. 10 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
5
Variants in PHF8 cause a spectrum of X-linked neurodevelopm..:
Sobering, Andrew K.
;
Bryant, Laura M.
;
Li, Dong
...
Human Genetics and Genomics Advances. 4 (2023) 1 - p. 100168 , 2023
Link:
https://doi.org/10.1016/..
?
6
The Phenotypic Continuum ofATP1A3-Related Disorders:
Vezyroglou, Aikaterini
;
Akilapa, Rhoda
;
Barwick, Katy
...
Neurology. 99 (2022) 14 - p. , 2022
Link:
https://doi.org/10.1212/..
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7
Variants in PHF8 cause a spectrum of X-linked neurodevelopm..:
Sobering, Andrew K.
;
Bryant, Laura M.
;
Li, Dong
...
Human Genetics and Genomics Advances. 3 (2022) 3 - p. 100102 , 2022
Link:
https://doi.org/10.1016/..
?
8
Diagnostic Value of a Protocolized In-Depth Evaluation of P..:
Atmar, Khaled
;
Ruivenkamp, Claudia A. L.
;
Hooimeijer, Louise
...
Frontiers in Immunology. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
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9
Biallelic Variants in the Ectonucleotidase ENTPD1 Cause a C..:
Calame, Daniel G.
;
Herman, Isabella
;
Maroofian, Reza
...
Annals of Neurology. 92 (2022) 2 - p. 304-321 , 2022
Link:
https://doi.org/10.1002/..
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10
Biallelic ADAM22 pathogenic variants cause progressive ence..:
van der Knoop, Marieke M
;
Maroofian, Reza
;
Fukata, Yuko
...
Brain. 145 (2022) 7 - p. 2301-2312 , 2022
Link:
https://doi.org/10.1093/..
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11
Biallelic loss of LDB3 leads to a lethal pediatric dilated ..:
Koopmann, Tamara T.
;
Jamshidi, Yalda
;
Naghibi-Sistani, Mohammad
...
European Journal of Human Genetics. 31 (2022) 1 - p. 97-104 , 2022
Link:
https://doi.org/10.1038/..
?
12
Episignature Mapping of TRIP12 Provides Functional Insight ..:
van der Laan, Liselot
;
Rooney, Kathleen
;
Alders, Mariëlle
...
International Journal of Molecular Sciences. 23 (2022) 22 - p. 13664 , 2022
Link:
https://doi.org/10.3390/..
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13
Expansion and mechanistic insights into de novo DEAF1 varia..:
McGee, Stacey R
;
Rajamanickam, Shivakumar
;
Adhikari, Sandeep
...
Human Molecular Genetics. 32 (2022) 3 - p. 386-401 , 2022
Link:
https://doi.org/10.1093/..
?
14
Recurrent de novo missense variants across multiple histone..:
Tessadori, Federico
;
Duran, Karen
;
Knapp, Karen
...
The American Journal of Human Genetics. 109 (2022) 4 - p. 750-758 , 2022
Link:
https://doi.org/10.1016/..
?
15
Further delineation of phenotypic spectrum of SCN2A‐related..:
Richardson, Ruth
;
Baralle, Diana
;
Bennett, Christopher
...
American Journal of Medical Genetics Part A. 188 (2021) 3 - p. 867-877 , 2021
Link:
https://doi.org/10.1002/..
1-15