Publications by authors named "Zain Awamleh"

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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, Leroy Bondhus

BMC Med Genomics· November 2024

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DNA methylation signatures for chromatinopathies: current challenges and future applications.
Zain Awamleh, Sarah Goodman, Sanaa Choufani, Rosanna Weksberg

Hum Genet· April 2024

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A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells.
Zain Awamleh, Sanaa Choufani, Wendy Wu, Dmitrijs Rots, Alexander J M Dingemans

Eur J Hum Genet· March 2024

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Correction: A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells.
Zain Awamleh, Sanaa Choufani, Wendy Wu, Dmitrijs Rots, Alexander J M Dingemans

Eur J Hum Genet· March 2024

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Multiomics of Bohring-Opitz syndrome truncating ASXL1 mutations identify canonical and noncanonical Wnt signaling dysregulation.
Isabella Lin, Angela Wei, Zain Awamleh, Meghna Singh, Aileen Ning

JCI Insight· May 2023

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ANKRD11 pathogenic variants and 16q24.3 microdeletions share an altered DNA methylation signature in patients with KBG syndrome.
Zain Awamleh, Sanaa Choufani, Cheryl Cytrynbaum, Fowzan S Alkuraya, Stephen Scherer

Hum Mol Genet· April 2023

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Generation of DNA Methylation Signatures and Classification of Variants in Rare Neurodevelopmental Disorders Using EpigenCentral.
Zain Awamleh, Sarah Goodman, Prajkta Kallurkar, Wendy Wu, Kevin Lu

Curr Protoc· November 2022

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Suleiman-El-Hattab syndrome: a histone modification disorder caused by TASP1 deficiency.
Korbinian M Riedhammer, Anna L Burgemeister, Vincent Cantagrel, Jeanne Amiel, Karine Siquier-Pernet, Zain Awamleh

Hum Mol Genet· September 2022

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DNA methylation signature associated with Bohring-Opitz syndrome: a new tool for functional classification of variants in ASXL genes.
Zain Awamleh, Eric Chater-Diehl, Sanaa Choufani, Elizabeth Wei, Rebecca R Kianmahd

Eur J Hum Genet· June 2022

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The utility of DNA methylation signatures in directing genome sequencing workflow: Kabuki syndrome and CDK13-related disorder.
Ashish Marwaha, Gregory Costain, Cheryl Cytrynbaum, Roberto Mendoza-Londono, Lauren Chad, Zain Awamleh

Am J Med Genet A· May 2022

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Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature.
Dmitrijs Rots, Eric Chater-Diehl, Alexander J M Dingemans, Sarah J Goodman, Michelle T Siu, Zain Awamleh

Am J Hum Genet· June 2021

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Exposure to Gestational Diabetes Mellitus (GDM) alters DNA methylation in placenta and fetal cord blood.
Zain Awamleh, Darci T Butcher, Anthony Hanley, Ravi Retnakaran, Larissa Haertle

Diabetes Res Clin Pract· April 2021

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Potential pathophysiological role of microRNA 193b-5p in human placentae from pregnancies complicated by preeclampsia and intrauterine growth restriction.
Zain Awamleh, Victor K M Han

Mol Biol Rep· September 2020

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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, Victor K M Han

Pregnancy Hypertens· January 2020

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Placental microRNAs in pregnancies with early onset intrauterine growth restriction and preeclampsia: potential impact on gene expression and pathophysiology.
Zain Awamleh, Gregory B Gloor, Victor K M Han

BMC Med Genomics· June 2019

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Creation of matrix protein gene variants of two serotypes of vesicular stomatitis virus as prime-boost vaccine vectors.
Gyoung Nyoun Kim, Kunyu Wu, Jiho Patrick Hong, Zain Awamleh, C Yong Kang

J Virol· June 2015

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Copy number variation distribution in six monozygotic twin pairs discordant for schizophrenia.
Christina A Castellani, Zain Awamleh, Melkaye G Melka, Richard L O'Reilly, Shiva M Singh

Twin Res Hum Genet· April 2014

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Biological relevance of CNV calling methods using familial relatedness including monozygotic twins.
Christina A Castellani, Melkaye G Melka, Andrea E Wishart, M Elizabeth O Locke, Zain Awamleh

BMC Bioinformatics· April 2014

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