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Mona Allouba

Observed names: Allouba, Mona, M Allouba, Mona H. Allouba, mona allouba
ORCID: 0000-0003-0790-8815
Observed ORCID: 0000-0003-0790-8815
OpenAlex ID: A5043301786
Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy
2019 · Roddy Walsh, Francesco Mazzarotto, et al. · Genome Medicine · 127
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Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies
2021 · Francesco Mazzarotto, Megan H. Hawley, et al. · Genetics in Medicine · 88
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The penetrance of rare variants in cardiomyopathy-associated genes: A cross-sectional approach to estimating penetrance for secondary findings
2023 · Kathryn A. McGurk, Xiaolei Zhang, et al. · The American Journal of Human Genetics · 72
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Disease-specific variant pathogenicity prediction significantly improves variant interpretation in inherited cardiac conditions
2020 · Xiaolei Zhang, Roddy Walsh, et al. · Genetics in Medicine · 62
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Ethnicity, consanguinity, and genetic architecture of hypertrophic cardiomyopathy
2023 · Mona Allouba, Roddy Walsh, et al. · European Heart Journal · 50
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Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies
2023 · Alex Lipov, Sean J. Jurgens, et al. · Nature Cardiovascular Research · 39
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An Investigation of Fibulin-2 in Hypertrophic Cardiomyopathy
2020 · Ayman M. Ibrahim, Mohamed Roshdy, et al. · International Journal of Molecular Sciences · 20
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NaNog: A pluripotency homeobox (master) molecule
2015 · Mona H. Allouba, Ahmed M. ElGuindy, et al. · Global Cardiology Science and Practice · 15
The Egyptian Collaborative Cardiac Genomics (ECCO-GEN) Project: defining a healthy volunteer cohort
2020 · Yasmine Aguib, Mona Allouba, et al. · npj Genomic Medicine · 11
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New Variant With a Previously Unrecognized Mechanism of Pathogenicity in Hypertrophic Cardiomyopathy
2021 · Yasmine Aguib, Mona Allouba, et al. · Circulation · 10
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Reprogramming for cardiac regeneration
2014 · Christophe Michel Raynaud, Faizzan Syed Ahmad, et al. · Global Cardiology Science and Practice · 8
Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy
2025 · Michele Nicastro, Alexa M.C. Vermeer, et al. · The American Journal of Human Genetics · 4
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Abstract 14969: Transcriptome Signature of Cardiac Fibroblasts in HCM Patients Identifies Novel Drivers Of ECM Remodeling and Pro-Inflammatory Signaling
2022 · Ayman M Ibrahim, Aya Galal, et al. · Circulation · 1
Pangenomes aid accurate detection of large insertions and deletions from targeted sequencing: the case of cardiomyopathies
2026 · Francesco Mazzarotto, Özem Kalay, et al. · Genome Medicine
Additional file 2 of Pangenomes aid accurate detection of large insertions and deletions from targeted sequencing: the case of cardiomyopathies
2026 · Francesco Mazzarotto, Özem Kalay, et al. · Figshare
Additional file 3 of Pangenomes aid accurate detection of large insertions and deletions from targeted sequencing: the case of cardiomyopathies
2026 · Francesco Mazzarotto, Özem Kalay, et al. · Figshare
Additional file 1 of Pangenomes aid accurate detection of large insertions and deletions from targeted sequencing: the case of cardiomyopathies
2026 · Francesco Mazzarotto, Özem Kalay, et al. · Figshare
Transcriptomic signature of Human Cardiac Fibroblast in Hypertrophic Obstructive Cardiomyopathy
2026 · Ayman M. Ibrahim, Sarah Halawa, et al. · bioRxiv (Cold Spring Harbor Laboratory)
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The mutational spectrum of Jervell and Lange-Nielsen syndrome: insights from highly consanguineous families
2025 · Aya Hataba, Mona Allouba, et al. · medRxiv
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Diagnosis and surgical treatment for a rare cause of arterial tortuosity
2025 · Amr Alsalakawy, Amr Elsawy, et al. · JTCVS Techniques
Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies
2023 · A Lipov, S J Jurgens, et al. · European Heart Journal
PDF
Abstract P2036: Induced Pluripotent Stem Cell- Derived Cardiomyocytes Provide New Insights Of The Pathogenic Consequences Of The Novel Frameshift Variant (c.5769delG) In MYH7 Gene
2023 · Sara Elshorbagy, Ayman M Ibrahim, et al. · Circulation Research
Homozygosity predominantly affects hypertrophic cardiomyopathy minor genes in an Egyptian clinical cohort
2022 · M Allouba, R Walsh, et al. · European Heart Journal
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Additional file 1: of Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy
2019 · Walsh, Roddy, Mazzarotto, Francesco, et al. · Figshare
Works count: 26
Citation count: 507
H-index: 10
I10-index: 10
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