Liena E O Elsayed (Liena Elsayed)

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 5

Top Venues

BMC neurology

European journal of human genetics : EJHG

BMC medical genetics

Human genetics

Princess Nourah Bint Abdulrahman University

UPMC (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Princess Nourah Bint Abdulrahman University Nov 18 2018

Saudi Arabia

Assistant Professor :: College of Medicine, Department of Basic Sciences

University of Khartoum Faculty of Medicine

Sudan

Assistant Professor :: Biochemistry

University of Khartoum Faculty of Medicine

Sudan

Lecturer :: Biochemistry

University of Khartoum Faculty of Medicine

Sudan

Teaching assistant :: Biochemistry

Education History

UPMC

France

PHD :: ICM

University of Khartoum

Sudan

MSC :: Institute of Endemic diseases

Publications

Mahmoud E Koko, Maha A Elseed, Inaam N Mohammed, Ahlam A Hamed, Amal S I Abd Allah, Ashraf Yahia, Rayan A Siddig, Janine Altmüller, Mohammad Reza Toliat, Esra O Elmahdi, Mutaz Amin, Elhami A Ahmed, Isra Z M Eltazi, Fatima A Elmugadam, Wasma A Abdelgadir, Esraa Eltaraifee, Mohamed O M Ibrahim, Nabila M H Ali, Hiba M Malik, Arwa M Babai, Yousuf H Bakhit, Peter Nürnberg, Muntaser E Ibrahim, Mustafa A Salih, Julian Schubert, Liena E O Elsayed, Holger Lerche
Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy. European journal of human genetics : EJHG (2024)
Sandra Martins, Ashraf Yahia, Inês P D Costa, Hassab E Siddig, Rayan Abubaker, Mahmoud E Koko, Marc Corral-Juan, Antoni Matilla-Dueñas, Alexis Brice, Alexandra Dürr, Eric Leguern, Laura P W Ranum, Antonio Amorim, Liena E O Elsayed, Giovanni Stevanin, Leonor Correia Guedes
Machado-Joseph disease in a Sudanese family links East Africa to Portuguese families and allows reestimation of ancestral age of the Machado lineage. Human genetics (2023)
Ashraf Yahia, Zhefan Stephen Chen, Ammar E Ahmed, Sara Emad, Rawaa Adil, Rayan Abubaker, Shaimaa Omer M A Taha, Mustafa A Salih, Liena E O Elsayed, Ho Yin Edwin Chan, Giovanni Stevanin
A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic paraplegia: a case report. BMC neurology 21 (1) (2021)
Liena E O Elsayed, Inaam N Mohammed, Ahlam A A Hamed, Maha A Elseed, Mustafa A M Salih, Ashraf Yahia, Rayan A Siddig, Mutaz Amin, Mahmoud Koko, Mustafa I Elbashir, Muntaser E Ibrahim, Alexis Brice, Ammar E Ahmed, Giovanni Stevanin
Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family. BMC medical genetics 19 (1) (2018)
Ashraf Yahia, Liena E O Elsayed, Arwa Babai, Mustafa A Salih, Sarah Misbah El-Sadig, Mutaz Amin, Mahmoud Koko, Rayan Abubakr, Razaz Idris, Shaimaa Omer M A Taha, Salah A Elmalik, Alexis Brice, Ammar Eltahir Ahmed, Giovanni Stevanin
Intra-familial phenotypic heterogeneity in a Sudanese family with DARS2-related leukoencephalopathy, brainstem and spinal cord involvement and lactate elevation: a case report. BMC neurology 18 (1) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Liena E O Elsayed (Liena Elsayed)