Lama AlAbdi

5PUBLICATIONS
36CO-AUTHORS
NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Pacific Peoples medicine and treatmentsNeurology and neuromuscular diseasesOptical technology
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Publications (5)

|Jul 15, 2026
MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

|Feb 17, 2025
RNA methyltransferase SPOUT1/CENP-32 links mitotic spindle organization with the neurodevelopmental disorder SpADMiSS.

Avinash V Dharmadhikari, Maria Alba Abad, Sheraz Khan

|Oct 18, 2023
Clinical utility of polygenic scores for cardiometabolic disease in Arabs.

Injeong Shim, Hiroyuki Kuwahara, NingNing Chen

|Oct 06, 2022
Loss-of-function variants in MYCBP2 cause neurobehavioural phenotypes and corpus callosum defects.

Lama AlAbdi, Muriel Desbois, Domniţa-Valeria Rusnac

|Sep 27, 2022
PMEL is mutated in oculocutaneous albinism.

Lama AlAbdi, Muneera Alshammari, Rana Helaby

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Frequent Collaborators

4 joint publications

Fowzan Sami Alkuraya

1 joint publications

Muriel Desbois

1 joint publications

Theresa Brunet

1 joint publications

Ning Zheng