Nuha Alrayes

Exome analysis identified a novel missense mutation in the CLPP gene in a consanguineous Saudi family expanding the clinical spectrum of Perrault Syndrome type-3

Saleem Ahmed, Musharraf Jelani, Nuha Alrayes et al. · Journal of the Neurological Sciences · 2015 · 45 citations

Life Sciences, Genetics, Molecular Genetics +11

Multilevel systems biology analysis of lung transcriptomics data identifies key miRNAs and potential miRNA target genes for SARS-CoV-2 infection

Babajan Banaganapalli, Nuha Alrayes, Zuhier Awan et al. · Computers in Biology and Medicine · 2021 · 45 citations · Full text

Life Sciences, Molecular Biology, Systems Biology +16

A missense mutation in TRAPPC6A leads to build-up of the protein, in patients with a neurodevelopmental syndrome and dysmorphic features

Hussein Sheikh Ali Mohamoud, Saleem Ahmed, Musharraf Jelani et al. · Scientific Reports · 2018 · 40 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Truncating mutation in intracellular phospholipase A1 gene (DDHD2) in hereditary spastic paraplegia with intellectual disability (SPG54)

Nuha Alrayes, Hussein Sheikh Ali Mohamoud, Musharraf Jelani et al. · BMC Research Notes · 2015 · 23 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

The alkylglycerol monooxygenase (AGMO) gene previously involved in autism also causes a novel syndromic form of primary microcephaly in a consanguineous Saudi family

Nuha Alrayes, Hussein Sheikh Ali Mohamoud, Saleem Ahmed et al. · Journal of the Neurological Sciences · 2016 · 23 citations

Medicine, Genetics, Molecular Genetics +13