Publications by authors named "Mona O Ruby"

Claim this Profile
N
New drug-like small molecule antagonizes phosphatidylinositol (3,4,5)-trisphosphate (PIP3) in patients with conotruncal heart defects.
Alaaeldin G Fayez, Nora N Esmaiel, Engy A Ashaat, Miral M Refeat, Randa S Lotfy, Mona O El Ruby

J Taibah Univ Med Sci· December 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
miR-454-3p and miR-194-5p targeting cardiac sarcolemma ion exchange transcripts are potential noninvasive diagnostic biomarkers for childhood dilated cardiomyopathy in Egyptian patients.
Alaaeldin G Fayez, Nora N Esmaiel, Sohair M Salem, Engy A Ashaat, Sonia A El-Saiedi, Mona O El Ruby

Egypt Heart J· September 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Correction: Correlating SFTPC gene variants to interstitial lung disease in Egyptian children.
Azza K Abdel Megeid, Miral M Refeat, Engy A Ashaat, Ghada El-Kamah, Sonia A El-Saiedi, Mona O El Ruby

J Genet Eng Biotechnol· September 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Correlating SFTPC gene variants to interstitial lung disease in Egyptian children.
Azza K Abdel Megeid, Miral M Refeat, Engy A Ashaat, Ghada El-Kamah, Sonia A El-Saiedi, Mona O El Ruby

J Genet Eng Biotechnol· August 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
First Report of Two Egyptian Patients with Desbuquois Dysplasia due to Homozygous Mutations.
Manal M Thomas, Engy A Ashaat, Ghada A Otaify, Samira Ismail, Mona L Essawi, Mona O El Ruby

Mol Syndromol· August 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical and genetic characterization of ten Egyptian patients with Wolf-Hirschhorn syndrome and review of literature.
Mona K Mekkawy, Alaa K Kamel, Manal M Thomas, Engy A Ashaat, Maha S Zaki, Mona O El Ruby

Mol Genet Genomic Med· February 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
Blepharophimosis-ptosis-intellectual disability syndrome: A report of nine Egyptian patients with further expansion of phenotypic and mutational spectrum.
Maha S Zaki, Ghada A Otaify, Samira Ismail, Mahmoud Y Issa, Mona O El-Ruby

Am J Med Genet A· December 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Rubinstein-Taybi syndrome in diverse populations.
Cedrik Tekendo-Ngongang, Babajide Owosela, Nicole Fleischer, Yonit A Addissie, Bryan Malonga, Mona O El Ruby

Am J Med Genet A· December 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Phenotypic and Molecular Cytogenetic Analysis of a Case of Monosomy 1p36 Syndrome due to Unbalanced Translocation.
Dalia F Hussen, Alaa K Kamel, Mona K Mekkawy, Engy A Ashaat, Mona O El Ruby

Mol Syndromol· December 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Turner syndrome in diverse populations.
Paul Kruszka, Yonit A Addissie, Cedrik Tekendo-Ngongang, Kelly L Jones, Sarah K Savage, Mona O El Ruby

Am J Med Genet A· February 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
W
Williams-Beuren syndrome in diverse populations.
Paul Kruszka, Antonio R Porras, Deise Helena de Souza, Angélica Moresco, Victoria Huckstadt, Mona O El Ruby

Am J Med Genet A· May 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Methylenetetrahydrofolate reductase gene polymorphisms in Egyptian Turner Syndrome patients.
Manal F Ismail, Waheba A Zarouk, Mona O Ruby, Wael M Mahmoud, Randa S Gad

Acta Biochim Pol· July 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Human Variome Project country nodes: documenting genetic information within a country.
George P Patrinos, Timothy D Smith, Heather Howard, Fahd Al-Mulla, Lotfi Chouchane, Mona O El-Ruby

Hum Mutat· November 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Phenotypic characterization of rare interstitial deletion of chromosome 4.
Samira Ismail, Nivine A Helmy, Wael M Mahmoud, Mona O El-Ruby

J Pediatr Genet· September 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Muenke syndrome with pigmentary disorder and probable hemimegalencephaly: An expansion of the phenotype.
Ghada M H Abdel-Salam, Laura Flores-Sarnat, Mona O El-Ruby, Jillian Parboosingh, Peter Bridge

Am J Med Genet A· January 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Assessment of pubertal development in Egyptian girls.
Laila A Hosny, Mona O El-Ruby, Moushira E Zaki, Mona S Aglan, Maha S Zaki

J Pediatr Endocrinol Metab· June 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis