Jehan AlRayahi

5PUBLICATIONS
39CO-AUTHORS
Genome structure and regulationNeonatologyGenomicsPaediatrics not elsewhere classified
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Publications (5)

|Jul 02, 2025
Ritscher-Schinzel syndrome can be characterized as an endosomal recyclinopathy.

Kohji Kato, Yosuke Nishio, Kirsty J McMillan

|Jun 13, 2025
Biallelic Loss-of-Function Variant in MINPP1 Causes Pontocerebellar Hypoplasia with Characteristic Severe Neurodevelopmental Disorder.

Aljazi Al-Maraghi, Rulan Shaath, Katherine Ford

|Mar 27, 2024
Integrating Genome Sequencing and Untargeted Metabolomics in Monozygotic Twins with a Rare Complex Neurological Disorder.

Rulan Shaath, Aljazi Al-Maraghi, Haytham Ali

|Jul 31, 2020
PGAP3 Associated with Hyperphosphatasia with Mental Retardation Plays a Novel Role in Brain Morphogenesis and Neuronal Wiring at Early Development.

Sahar I Da'as, Waleed Aamer, Waseem Hasan

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Frequent Collaborators

3 joint publications

Waleed Aamer

3 joint publications

Khalid A Fakhro

2 joint publications

Elbay Aliyev

1 joint publications

Haytham Ali