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Amal M Alhashem

10PUBLICATIONS

29CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)NeonatologyNeurology and neuromuscular diseasesInfant and child healthAdolescent health

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Publications (10)

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|Jun 29, 2025

Congenital glaucoma associated with high hyperopia, an ophthalmic phenotypical manifestation for <i>GLIS3</i> deletion: case report and review of literature.

Faeeqah Almhmoudi, Ghufran Abudawood, Arif O Khan

|Nov 27, 2024

<i>ANKS6</i> Variants Underlie Polycystic Kidneys in Prenatal and Neonatal Cases.

Lama S Almohlesy, Faiqa Imtiaz, Maha Tulbah

|Jul 23, 2024

Multiplex Consanguineous Family Highlights <i>CLASP1</i> as a Candidate Gene for Lissencephaly.

Rawan Alsafh, Amal Alhashem, Aly Elsyed

|Sep 12, 2023

Variable phenotype of a null PPP1R13L allele in children with dilated cardiomyopathy.

Sahar Tulbah, Nadiah Alruwaili, Amal Alhashem

|Oct 21, 2022

De Novo Ring Chromosome 15: Molecular Cytogenetic and Clinical Characterization of First Case from Saudi Arabia.

Amal Alhashem, Saria Alazmeh, Ayla Barakat

|Jul 13, 2022

A Biallelic Variant in <i>FRA10AC1</i> Is Associated With Neurodevelopmental Disorder and Growth Retardation.

Norah Alsaleh, Amal Alhashem, Brahim Tabarki

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Frequent Collaborators

2 joint publications

Faiqa Imtiaz

2 joint publications

Naif Almontashiri

2 joint publications

Fowzan S Alkuraya

1 joint publications

Khushnooda Ramzan

1 joint publications

Rebecca Buchert

1 joint publications

Benjamin Ellezam

1 joint publications

Johannes A Mayr

1 joint publications

Philippe M Campeau

1 joint publications

Nicolas A Dumont

1 joint publications

Christian Beetz

Frequent Collaborators

2 joint publications

Faiqa Imtiaz

2 joint publications

Naif Almontashiri

2 joint publications

Fowzan S Alkuraya

1 joint publications

Khushnooda Ramzan

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