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Liena Elsayed

5PUBLICATIONS

20CO-AUTHORS

Epigenetics (incl. genome methylation and epigenomics)Te hītori ahurea Māori (Māori cultural history)Gene expression (incl. microarray and other genome-wide approaches)Social epidemiologyNeonatology

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Publications (5)

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|Feb 05, 2024

Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy.

Mahmoud Koko, Maha A Elseed, Inaam N Mohammed

|Nov 13, 2023

Machado-Joseph disease in a Sudanese family links East Africa to Portuguese families and allows reestimation of ancestral age of the Machado lineage.

Sandra Martins, Ashraf Yahia, Inês P D Costa

|Feb 19, 2021

A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic paraplegia: a case report.

Ashraf Yahia, Zhefan Stephen Chen, Ammar E Ahmed

|Oct 25, 2018

Intra-familial phenotypic heterogeneity in a Sudanese family with DARS2-related leukoencephalopathy, brainstem and spinal cord involvement and lactate elevation: a case report.

Ashraf Yahia, Liena Elsayed, Arwa Babai

|May 10, 2018

Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family.

Liena E O Elsayed, Inaam N Mohammed, Ahlam A A Hamed

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Frequent Collaborators

2 joint publications

Ashraf Yahia

2 joint publications

Mahmoud Koko

1 joint publications

Sandra Martins

1 joint publications

Inês P D Costa

1 joint publications

Rayan Abubaker

1 joint publications

Marc Corral-Juan

1 joint publications

Antoni Matilla-Dueñas

1 joint publications

Alexis Brice

1 joint publications

Alexandra Durr

1 joint publications

Laura P W Ranum

Frequent Collaborators

2 joint publications

Ashraf Yahia

2 joint publications

Mahmoud Koko

1 joint publications

Sandra Martins

1 joint publications

Inês P D Costa

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