Publications by authors named "Emad Muhammad"

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Efficacy and safety of direct oral anticoagulants in patients with venous thrombosis and inherited thrombophilia.
Amir Warwar, Iren Zargari, Nili Stein, Ibrahim Zoubi, Emad Muhammad

Int J Med Sci· August 2025

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Interpretable machine learning approaches to assess the compressive strength of metakaolin blended sustainable cement mortar.
Naseer Muhammad Khan, Liqiang Ma, Waleed Bin Inqiad, Muhammad Saud Khan, Imtiaz Iqbal, Muhammad Zaka Emad

Sci Rep· June 2025

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Bronchiectasis with Chronic Rhinosinusitis Is Associated with Eosinophilic Airway Inflammation and Is Distinct from Asthma.
Michal Shteinberg, James D Chalmers, Jayanth K Narayana, Alison J Dicker, Michal A Rahat, Emad Muhammad

Ann Am Thorac Soc· May 2024

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TCF3 haploinsufficiency defined by immune, clinical, gene-dosage, and murine studies.
Brigette Boast, Shubham Goel, Luis I González-Granado, Julie Niemela, Jennifer Stoddard, Emad Muhammad

J Allergy Clin Immunol· September 2023

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Specific antibody response of 14 patients with common variable immunodeficiency to 3 BNT162b2 messenger RNA coronavirus disease 2019 vaccinations.
Nizar Abo-Helo, Emad Muhammad, Sondus Ghaben-Amara, Shai Cohen

Ann Allergy Asthma Immunol· July 2022

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Specific antibody response of patients with common variable immunodeficiency to BNT162b2 coronavirus disease 2019 vaccination.
Nizar Abo-Helo, Emad Muhammad, Sondus Ghaben-Amara, Josef Panasoff, Shai Cohen

Ann Allergy Asthma Immunol· October 2021

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Exploring fear of childbirth in Kenya through evaluation of the readability of Wijma Delivery Expectancy/Experience Questionnaire Version A (W-DEQ-A).
David Onchonga, Sahar Hammoud, Stephen Kuriakose, Emad Ahmad Khan Muhammad

Sex Reprod Healthc· June 2021

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Novel mutation in coagulation factor VII (Carmel mutation): Identification and characterization.
Aliza Cassel, Nurit Rosenberg, Emad Muhammad, Tami Livnat, Rima Dardik

Res Pract Thromb Haemost· May 2021

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A Novel Recessive Mutation in SPEG Causes Early Onset Dilated Cardiomyopathy.
Aviva Levitas, Emad Muhammad, Yuan Zhang, Isaac Perea Gil, Ricardo Serrano

PLoS Genet· September 2020

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D117N in Cypher/ZASP may not be a causative mutation for dilated cardiomyopathy and ventricular arrhythmias.
Aviva Levitas, Yuval Konstantino, Emad Muhammad, Zaid Afawi, Jean Marc Weinstein

Eur J Hum Genet· May 2016

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PLEKHM2 mutation leads to abnormal localization of lysosomes, impaired autophagy flux and associates with recessive dilated cardiomyopathy and left ventricular noncompaction.
Emad Muhammad, Aviva Levitas, Sonia R Singh, Alex Braiman, Rivka Ofir

Hum Mol Genet· December 2015

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Essential role of carbonic anhydrase XII in secretory gland fluid and HCO3 (-) secretion revealed by disease causing human mutation.
Jeong Hee Hong, Emad Muhammad, Changyu Zheng, Eli Hershkovitz, Soliman Alkrinawi

J Physiol· December 2015

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Congenital myopathy is caused by mutation of HACD1.
Emad Muhammad, Orit Reish, Yusuke Ohno, Todd Scheetz, Adam Deluca

Hum Mol Genet· December 2013

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Autosomal recessive hyponatremia due to isolated salt wasting in sweat associated with a mutation in the active site of Carbonic Anhydrase 12.
Emad Muhammad, Neta Leventhal, Galit Parvari, Aaron Hanukoglu, Israel Hanukoglu

Hum Genet· April 2011

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Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenase.
Aviva Levitas, Emad Muhammad, Gali Harel, Ann Saada, Vered Chalifa Caspi

Eur J Hum Genet· October 2010

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