Ashraf Yahia
1 – 10 of 25
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=""
width=""
height=""
allowtransparency="true"
frameborder="0">
</iframe>
- 2026
-
Mark
The RAB3A hot spot variant R83W causes spasticity as part of the ataxia-spasticity spectrum
Roller, Johanna R. ; Yahia, Ashraf LU
; Stevanin, Giovanni
; Ahmed, Ammar E.
; Alawadhi, Amna M.T.
; Almannai, Mohammed
; Busehail, Maryam Y.
; Choi, Alexander H.
; Elhassan, Ali A.
and Elsayed, Liena E.O.
, et al.
(2026)
In Brain
149(4).
p.36-38
- Contribution to journal › Letter
-
Mark
Genetic and environmental influences on sleep quality, ability to settle, and crying duration in 2- and 5-month-old infants : A longitudinal twin study
Viktorsson, Charlotte ; Yahia, Ashraf LU
; Taylor, Mark J.
; Ronald, Angelica
; Tammimies, Kristiina
and Falck-Ytter, Terje
(2026)
In JCPP advances
6(1).
p.1-11
- Contribution to journal › Article
- 2025
-
Mark
Consanguinity and willingness to perform premarital genetic screening in Sudan
Elhadi, Yasir Ahmed Mohammed ; Alrawa, Salma S. ; Alfadul, Esraa S.A. ; Mahgoub, Esra Abdallah Abdalwahed ; El-Osta, Austen ; Belal, Safaa Abdalazeem ; Lucero-Prisno, Don Eliseo ; El Dabbah, Noha Ahmed and Yahia, Ashraf LU
(2025)
In European Journal of Human Genetics
33(12).
p.1655-1662
- Contribution to journal › Article
-
Mark
Prematurity and genetic liability for autism spectrum disorder
Zhang, Yali ; Yahia, Ashraf LU
; Sandin, Sven
; Åden, Ulrika
LU
and Tammimies, Kristiina
(2025)
In Genome Medicine
17(1).
- Contribution to journal › Article
- 2024
-
Mark
Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations
Yahia, Ashraf LU
; Hamed, Ahlam A.A.
; Mohamed, Inaam N.
; Elseed, Maha A.
; Salih, Mustafa A.
; El-sadig, Sarah M.
; Siddig, Hassab Elrasoul
; Nasreldien, Ali Elsir Musa
; Abdullah, Mohamed Ahmed
and Elzubair, Maha
, et al.
(2024)
In European Journal of Human Genetics
32(10).
p.1214-1226
- Contribution to journal › Article
-
Mark
A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changes
- Contribution to journal › Article
-
Mark
Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy
Koko, Mahmoud ; Elseed, Maha A. ; Mohammed, Inaam N. ; Hamed, Ahlam A. ; Abd Allah, Amal S.I. ; Yahia, Ashraf LU
; Siddig, Rayan A.
; Altmüller, Janine
; Toliat, Mohammad Reza
and Elmahdi, Esra O.
, et al.
(2024)
In European Journal of Human Genetics
32(10).
p.1338-1342
- Contribution to journal › Article
-
Mark
Machine Learning Prediction of Autism Spectrum Disorder from a Minimal Set of Medical and Background Information
Rajagopalan, Shyam Sundar ; Zhang, Yali ; Yahia, Ashraf LU
and Tammimies, Kristiina
(2024)
In JAMA Network Open
7(8).
p.1-13
- Contribution to journal › Article
-
Mark
Whole exome sequencing and polygenic assessment of a Swedish cohort with severe developmental language disorder
Yahia, Ashraf LU
; Li, Danyang
; Lejerkrans, Sanna
; Rajagopalan, Shyam
; Kalnak, Nelli
LU
and Tammimies, Kristiina
(2024)
In Human Genetics
143(2).
p.169-183
- Contribution to journal › Article
- 2023
-
Mark
Machado-Joseph disease in a Sudanese family links East Africa to Portuguese families and allows reestimation of ancestral age of the Machado lineage
Martins, Sandra ; Yahia, Ashraf LU
; Costa, Inês P.D.
; Siddig, Hassab E.
; Abubaker, Rayan
; Koko, Mahmoud
; Corral-Juan, Marc
; Matilla-Dueñas, Antoni
; Brice, Alexis
and Durr, Alexandra
, et al.
(2023)
In Human Genetics
142(12).
p.1747-1754
- Contribution to journal › Article