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Bertoli-Avella, Aida
161
results:
Format
Online (161)
Mediatypes
Articles (Online) (60)
OpenAccess-fulltext (101)
Sorted by: Relevance
Sorted by: Year
?
1
Facing the challenges to shorten the diagnostic odyssey: fi..:
Velasco, Harvy Mauricio
;
Bertoli-Avella, Aida
;
Jaramillo, Carolina Jaramillo
...
European Journal of Human Genetics. , 2024
Link:
https://doi.org/10.1038/..
?
2
Bi-allelic ACBD6 variants lead to a neurodevelopmental synd..:
Kaiyrzhanov, Rauan
;
Rad, Aboulfazl
;
Lin, Sheng-Jia
...
Brain. 147 (2023) 4 - p. 1436-1456 , 2023
Link:
https://doi.org/10.1093/..
?
3
Inactivation of DRG1, encoding a translation factor GTPase,..:
Westrip, Christian A.E.
;
Paul, Franziska
;
Al-Murshedi, Fathiya
...
Genetics in Medicine. 25 (2023) 9 - p. 100893 , 2023
Link:
https://doi.org/10.1016/..
?
4
A founder DBR1 variant causes a lethal form of congenital i..:
Shamseldin, Hanan E.
;
Sadagopan, Mukunth
;
Martini, Javier
...
Human Genetics. 142 (2023) 10 - p. 1491-1498 , 2023
Link:
https://doi.org/10.1007/..
?
5
Biallelic MAD2L1BP (p31comet) mutation is associated with m..:
Abdel-Salam, Ghada M. H.
;
Hellmuth, Susanne
;
Gradhand, Elise
...
JCI Insight. 8 (2023) 22 - p. , 2023
Link:
https://doi.org/10.1172/..
?
6
At a glance: the largest Niemann-Pick type C1 cohort with 6..:
Guatibonza Moreno, Pilar
;
Pardo, Luba M.
;
Pereira, Catarina
...
European Journal of Human Genetics. 31 (2023) 10 - p. 1108-1116 , 2023
Link:
https://doi.org/10.1038/..
?
7
AXIN1 bi-allelic variants disrupting the C-terminal DIX dom..:
Terhal, Paulien
;
Venhuizen, Anton J.
;
Lessel, Davor
...
The American Journal of Human Genetics. 110 (2023) 9 - p. 1470-1481 , 2023
Link:
https://doi.org/10.1016/..
?
8
OP033: An integrated multiomic panel as an excellent tool f..:
Almeida, Ligia
;
Pereira, Catarina
;
Aanicai, Ruxandra
...
Genetics in Medicine. 24 (2022) 3 - p. S361 , 2022
Link:
https://doi.org/10.1016/..
?
9
Alternative splicing of BUD13 determines the severity of a ..:
Kornak, Uwe
;
Saha, Namrata
;
Keren, Boris
...
Genetics in Medicine. 24 (2022) 9 - p. 1927-1940 , 2022
Link:
https://doi.org/10.1016/..
?
10
A novel variant in SMG9 causes intellectual disability, con..:
Rahikkala, Elisa
;
Urpa, Lea
;
Ghimire, Bishwa
...
European Journal of Human Genetics. 30 (2022) 5 - p. 619-627 , 2022
Link:
https://doi.org/10.1038/..
?
11
The Leukodystrophy Spectrum in Saudi Arabia: Epidemiologica..:
Alfadhel, Majid
;
Almuqbil, Mohammed
;
Al Mutairi, Fuad
...
Frontiers in Pediatrics. 9 (2021) - p. , 2021
Link:
https://doi.org/10.3389/..
?
12
A disorder clinically resembling cystic fibrosis caused by ..:
Bertoli-Avella, Aida
;
Hotakainen, Ronja
;
Al Shehhi, Maryam
...
Journal of Medical Genetics. 59 (2021) 10 - p. 993-1001 , 2021
Link:
https://doi.org/10.1136/..
?
13
Novel C19orf12 loss-of-function variant leading to neurodeg..:
Lefter, Antonia
;
Mitrea, Iulia
;
Mitrea, Dan
...
Neurocase. 27 (2021) 6 - p. 481-483 , 2021
Link:
https://doi.org/10.1080/..
?
14
Inherited deficiency of stress granule ZNFX1 in patients wi..:
Le Voyer, Tom
;
Neehus, Anna-Lena
;
Yang, Rui
...
Proceedings of the National Academy of Sciences. 118 (2021) 15 - p. , 2021
Link:
https://doi.org/10.1073/..
?
15
Truncating mutations in YIF1B cause a progressive encephalo..:
AlMuhaizea, Mohammed
;
AlMass, Rawan
;
AlHargan, Aljouhra
...
Acta Neuropathologica. 139 (2020) 4 - p. 791-794 , 2020
Link:
https://doi.org/10.1007/..
1-15