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Verheijen, Jan
299
results:
Search for persons
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Online (299)
Mediatypes
E-Books (2)
Articles (Online) (135)
Bookchapter (Online) (1)
OpenAccess-fulltext (161)
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1
P348: Agnostic analysis of transcriptome sequencing of pati..:
Verheijen, Jan
;
William, Nancy
;
Figueiral, Marta
...
Genetics in Medicine Open. 2 (2024) - p. 101242 , 2024
Link:
https://doi.org/10.1016/..
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2
De novo and inherited monoallelic variants in TUBA4A cause ..:
Benkirane, Mehdi
;
Bonhomme, Marion
;
Morsy, Heba
...
Brain. , 2024
Link:
https://doi.org/10.1093/..
?
3
P341: Identification of novel variants and phenotypic expan..:
Verheijen, Jan
;
Vanhye, Lotte
;
Shaikh, Ayesha Niaz
...
Genetics in Medicine Open. 1 (2023) 1 - p. 100369 , 2023
Link:
https://doi.org/10.1016/..
?
4
Therapeutic approaches in Congenital Disorders of Glycosyla..:
Verheijen, Jan
;
Tahata, Shawn
;
Kozicz, Tamas
..
Genetics in Medicine. 22 (2020) 2 - p. 268-279 , 2020
Link:
https://doi.org/10.1038/..
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5
Defining a new immune deficiency syndrome: MAN2B2-CDG:
Verheijen, Jan
;
Wong, Sunnie Y.
;
Rowe, Jared H.
...
Journal of Allergy and Clinical Immunology. 145 (2020) 3 - p. 1008-1011 , 2020
Link:
https://doi.org/10.1016/..
?
6
Repurposing the aldose reductase inhibitor and diabetic neu..:
Iyer, Sangeetha
;
Sam, Feba S.
;
DiPrimio, Nina
...
Disease Models & Mechanisms. , 2019
Link:
https://doi.org/10.1242/..
?
7
A novel phosphoglucomutase‐deficient mouse model reveals ab..:
Balakrishnan, Bijina
;
Verheijen, Jan
;
Lupo, Arielle
...
Journal of Inherited Metabolic Disease. 42 (2019) 5 - p. 998-1007 , 2019
Link:
https://doi.org/10.1002/..
?
8
Common and rare TBK1 variants in early-onset Alzheimer dise..:
Verheijen, Jan
;
van der Zee, Julie
;
Gijselinck, Ilse
...
Neurobiology of Aging. 62 (2018) - p. 245.e1-245.e7 , 2018
Link:
https://doi.org/10.1016/..
?
9
Understanding Alzheimer Disease at the Interface between Ge..:
Verheijen, Jan
;
Sleegers, Kristel
Trends in Genetics. 34 (2018) 6 - p. 434-447 , 2018
Link:
https://doi.org/10.1016/..
?
10
[P2–116]: TRANSCRIPTOME ANALYSIS IN BLOOD AND BRAIN IDENTIF..:
Verheijen, Jan
;
Mateiu, Ligia
;
De Roeck, Arne
...
Alzheimer's & Dementia. 13 (2017) 7S_Part_13 - p. , 2017
Link:
https://doi.org/10.1016/..
?
11
Deleterious ABCA7 mutations and transcript rescue mechanism..:
On behalf of the European Early-Onset Dementia (EU EOD) consortium
;
De Roeck, Arne
;
Van den Bossche, Tobi
...
Acta Neuropathologica. 134 (2017) 3 - p. 475-487 , 2017
Link:
https://doi.org/10.1007/..
?
12
[O2–13–05]: DELETERIOUS ABCA7 MUTATIONS CONTRIBUTE TO EARLY..:
De Roeck, Arne
;
Van den Bossche, Tobi
;
Verheijen, Jan
...
Alzheimer's & Dementia. 13 (2017) 7S_Part_11 - p. , 2017
Link:
https://doi.org/10.1016/..
?
13
A comprehensive study of the genetic impact of rare variant..:
Verheijen, Jan
;
Van den Bossche, Tobi
;
van der Zee, Julie
...
Acta Neuropathologica. 132 (2016) 2 - p. 213-224 , 2016
Link:
https://doi.org/10.1007/..
?
14
O3‐13‐06: Targeted re‐sequencing of sorl1 in early‐onset Al..:
Sleegers, Kristel
;
Verheijen, Jan
;
van der Zee, Julie
...
Alzheimer's & Dementia. 11 (2015) 7S_Part_5 - p. , 2015
Link:
https://doi.org/10.1016/..
?
15
A 22‐single nucleotide polymorphism Alzheimer's disease ris..:
Sleegers, Kristel
;
Bettens, Karolien
;
De Roeck, Arne
...
Alzheimer's & Dementia. 11 (2015) 12 - p. 1452-1460 , 2015
Link:
https://doi.org/10.1016/..
1-15