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Zain Awamleh · SciRah

Researcher profile · Semantic Scholar

Zain Awamleh

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Zain Awamleh — researcher profile on SciRah

h-index: 12
Works: 26
Citations: 458

Most-cited papers

Placental microRNAs in pregnancies with early onset intrauterine growth restriction and preeclampsia: potential impact on gene expression and pathophysiology
Zain Awamleh, G. Gloor, V. Han
2019BMC Medical Genomics119 citations Open access
Semantic Scholar
Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature
D. Rots, Eric J Chater-Diehl, A. Dingemans, S. Goodman +84 more
2021American Journal of Human Genetics64 citations Open access
Semantic Scholar
Exposure to Gestational Diabetes Mellitus (GDM) Alters DNA Methylation in Placenta and Fetal Cord Blood.
Zain Awamleh, D. Butcher, A. Hanley, R. Retnakaran +4 more
2021Diabetes Research and Clinical Practice48 citations
Semantic Scholar
Copy Number Variation Distribution in Six Monozygotic Twin Pairs Discordant for Schizophrenia
C. Castellani, Zain Awamleh, M. G. Melka, R. O'Reilly +1 more
2014Twin Research and Human Genetics41 citations Open access
Semantic Scholar
DNA methylation signature associated with Bohring-Opitz syndrome: a new tool for functional classification of variants in ASXL genes
Zain Awamleh, Eric J Chater-Diehl, S. Choufani, Elizabeth Wei +9 more
2022European Journal of Human Genetics24 citations Open access
Semantic Scholar
Identification of miR-210-5p in human placentae from pregnancies complicated by preeclampsia and intrauterine growth restriction, and its potential role in the pregnancy complications.
Zain Awamleh, V. Han
2020Pregnancy Hypertension23 citations
Semantic Scholar
Biological relevance of CNV calling methods using familial relatedness including monozygotic twins
C. Castellani, M. G. Melka, Andrea E. Wishart, M. E. O. Locke +3 more
2014BMC Bioinformatics21 citations Open access
Semantic Scholar
ANKRD11 pathogenic variants and 16q24.3 microdeletions share an altered DNA methylation signature in patients with KBG syndrome
Zain Awamleh, S. Choufani, C. Cytrynbaum, F. Alkuraya +8 more
2022Human Molecular Genetics20 citations Open access
Semantic Scholar
Generation of DNA Methylation Signatures and Classification of Variants in Rare Neurodevelopmental Disorders Using EpigenCentral
Zain Awamleh, S. Goodman, Prajkta S. Kallurkar, Wendy Wu +4 more
2022Current Protocols15 citations
Semantic Scholar
Multiomics of Bohring-Opitz syndrome truncating ASXL1 mutations identify canonical and noncanonical Wnt signaling dysregulation
Isabella Lin, Angela Wei, Zain Awamleh, Meghna Singh +5 more
2023JCI Insight14 citations Open access
Semantic Scholar
Creation of Matrix Protein Gene Variants of Two Serotypes of Vesicular Stomatitis Virus as Prime-Boost Vaccine Vectors
G. Kim, Kun-Yu Wu, Jiho Hong, Zain Awamleh +1 more
2015Journal of Virology14 citations Open access
Semantic Scholar
Potential pathophysiological role of microRNA 193b-5p in human placentae from pregnancies complicated by preeclampsia and intrauterine growth restriction
Zain Awamleh, V. Han
2020Molecular Biology Reports12 citations
Semantic Scholar
DNA methylation signatures for chromatinopathies: current challenges and future applications
Zain Awamleh, S. Goodman, S. Choufani, R. Weksberg
2023Human Genetics11 citations Open access
Semantic Scholar
A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells
Zain Awamleh, S. Choufani, Wendy Wu, D. Rots +13 more
2024European Journal of Human Genetics10 citations Open access
Semantic Scholar
Suleiman-El-Hattab syndrome: a histone modification disorder caused by TASP1 deficiency.
K. Riedhammer, A. Burgemeister, Vincent Cantagrel, J. Amiel +17 more
2022Human Molecular Genetics8 citations Open access
Semantic Scholar
The utility of DNA methylation signatures in directing genome sequencing workflow: Kabuki syndrome and CDK13‐related disorder
Ashish Marwaha, G. Costain, C. Cytrynbaum, R. Mendoza-Londono +5 more
2022American Journal of Medical Genetics. Part A6 citations Open access
Semantic Scholar
ASXL1 truncating variants in BOS and myeloid leukemia drive shared disruption of Wnt-signaling pathways but have differential isoform usage of RUNX3
Isabella Lin, Zain Awamleh, Mili Sinvhal, Andrew Wan +5 more
2024BMC Medical Genomics5 citations Open access
Semantic Scholar
Transforming blood-derived episignatures into cell-type-agnostic classifiers: A shortcut to prenatal episignatures.
Nikola Reko, Arteen Torabi-Marashi, Prajkta S. Kallurkar, S. Goodman +13 more
2026American Journal of Human Genetics1 citations Open access
Semantic Scholar
ASXL1 mutations that cause Bohring Opitz Syndrome (BOS) or acute myeloid leukemia share epigenomic and transcriptomic signatures
Isabella Lin, Zain Awamleh, Angela Wei, Bianca E. Russell +2 more
2023bioRxiv1 citations Open access
Semantic Scholar
Multi-omics on truncating ASXL1 mutations in Bohring Opitz syndrome identify dysregulation of canonical and non-canonical Wnt signaling
Isabella Lin, Angela Wei, Zain Awamleh, Meghna Singh +5 more
2022bioRxiv1 citations Open access
Semantic Scholar
KMT2A and KMT2B episignatures address diagnostic challenges associated with rare neurodevelopmental disorders.
Zain Awamleh, Anthony Chen, S. Choufani, D. Rots +21 more
2026Genetics in Medicine0 citations
Semantic Scholar
P637: A newly derived DNA methylation signature for Koolen de Vries syndrome addresses the diagnostic challenges of the 17q21.31 locus
Zain Awamleh, S. Choufani, D. Rots, A. Dingemans +4 more
2024Genetics in Medicine Open0 citations Open access
Semantic Scholar
Correction: A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells
Zain Awamleh, S. Choufani, Wendy Wu, D. Rots +13 more
2024European Journal of Human Genetics0 citations Open access
Semantic Scholar
P192: Deep neurologic phenotyping and biomarker development in Bohring-Opitz syndrome using EEGs, neurodevelopmental assessments, and DNA methylation signature
Bianca E. Russell, J. Sloan, H. Nariai, Natasha N. Ludwig +6 more
2024Genetics in Medicine Open0 citations Open access
Semantic Scholar
Fetal and Placental Growth Physiology and Pathophysiology
V. Han, Bethany N. Radford, Zain Awamleh
20200 citations
Semantic Scholar
Placental MicroRNA Expression in Pregnancies Complicated with Preeclampsia and Intrauterine Growth Restriction
Zain Awamleh
20190 citations
Semantic Scholar

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R. Weksberg×13
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S. Choufani×11
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