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Arts, Peer
93
results:
Search for persons
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Format
Online (92)
Print (1)
Mediatypes
Books (1)
Articles (Online) (33)
OpenAccess-fulltext (59)
Languages
german (1)
english (82)
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Sorted by: Year
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1
Unraveling facets of MECOM-associated syndrome: somatic gen..:
Venugopal, Parvathy
;
Arts, Peer
;
Fox, Lucy C.
...
Blood Advances. 8 (2024) 13 - p. 3437-3443 , 2024
Link:
https://doi.org/10.1182/..
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2
Transcription factor genetics and biology in predisposition..:
Zerella, Jiarna R.
;
Homan, Claire C.
;
Arts, Peer
...
Frontiers in Oncology. 13 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
3
Author Correction: Genomic autopsy to identify underlying c..:
Byrne, Alicia B.
;
Arts, Peer
;
Ha, Thuong T.
...
Nature Medicine. 30 (2023) 1 - p. 302-302 , 2023
Link:
https://doi.org/10.1038/..
?
4
Discovering a new part of the phenotypic spectrum of Coffin..:
van der Sluijs, Pleuntje J.
;
Joosten, Marieke
;
Alby, Caroline
...
Genetics in Medicine. 25 (2023) 2 - p. 100004 , 2023
Link:
https://doi.org/10.1016/..
?
5
Introme accurately predicts the impact of coding and noncod..:
Sullivan, Patricia J.
;
Gayevskiy, Velimir
;
Davis, Ryan L.
...
Genome Biology. 24 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1186/..
?
6
Integrated multi-omics for rapid rare disease diagnosis on ..:
Lunke, Sebastian
;
Bouffler, Sophie E.
;
Patel, Chirag V.
...
Nature Medicine. 29 (2023) 7 - p. 1681-1691 , 2023
Link:
https://doi.org/10.1038/..
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7
Somatic mutational landscape of hereditary hematopoietic ma..:
Homan, Claire C.
;
Drazer, Michael W.
;
Yu, Kai
...
Blood Advances. 7 (2023) 20 - p. 6092-6107 , 2023
Link:
https://doi.org/10.1182/..
?
8
Genomic autopsy to identify underlying causes of pregnancy ..:
Byrne, Alicia B.
;
Arts, Peer
;
Ha, Thuong T.
...
Nature Medicine. 29 (2023) 1 - p. 180-189 , 2023
Link:
https://doi.org/10.1038/..
?
9
Discovering a new part of the phenotypic spectrum of Coffin..:
van der Sluijs, Pleuntje J.
;
Joosten, Marieke
;
Alby, Caroline
...
Genetics in Medicine. 24 (2022) 8 - p. 1753-1760 , 2022
Link:
https://doi.org/10.1016/..
?
10
Human variation in population-wide gene expression data pre..:
Bonaguro, Lorenzo
;
Schulte-Schrepping, Jonas
;
Carraro, Caterina
...
iScience. 25 (2022) 11 - p. 105328 , 2022
Link:
https://doi.org/10.1016/..
?
11
Variable expressivity in a four-generation ACDMPV family wi..:
Yıldız Bölükbaşı, Esra
;
Karolak, Justyna A.
;
Szafranski, Przemyslaw
...
European Journal of Human Genetics. 30 (2022) 10 - p. 1182-1186 , 2022
Link:
https://doi.org/10.1038/..
?
12
GATA2 deficiency syndrome: A decade of discovery:
Homan, Claire C.
;
Venugopal, Parvathy
;
Arts, Peer
...
Human Mutation. 42 (2021) 11 - p. 1399-1421 , 2021
Link:
https://doi.org/10.1002/..
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13
The RUNX1 database (RUNX1db): establishment of an expert cu..:
Homan, Claire C.
;
King-Smith, Sarah L.
;
Lawrence, David M.
...
Haematologica. 106 (2021) 11 - p. 3004-3007 , 2021
Link:
https://doi.org/10.3324/..
?
14
Compound heterozygous variants in LAMC3 in association with..:
De Angelis, Carla
;
Byrne, Alicia B.
;
Morrow, Rebecca
...
BMC Medical Genomics. 14 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1186/..
?
15
Impact of rare and common genetic variation in the interleu..:
van Deuren, Rosanne C.
;
Arts, Peer
;
Cavalli, Giulio
...
Genome Medicine. 13 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1186/..
1-15