Genetic testing for hypertrophic cardiomyopathy: ongoing voyage from exploration to clinical exploitation

by Iacopo Olivotto, Heba Sh. Kassem, Francesca Girolami
Published 2011-07-01

Molecular genetics made simple

by Heba Sh. Kassem, Francesca Girolami, Despina Sanoudou
Published 2012-07-01

Expression of O6-Alkylguanine-DNA Alkyltransferase in Normal and Malignant Bladder Tissue of Egyptian Patients

by Abir A. Saad, Heba Sh. Kassem, Andrew C. Povey, Geoffrey P. Margison
Published 2010-01-01

Molecular modeling of disease causing mutations in domain C1 of cMyBP-C.

by Poornima Gajendrarao, Navaneethakrishnan Krishnamoorthy, Heba Sh Kassem, Sarah Moharem-Elgamal, Franco Cecchi, Iacopo Olivotto, Magdi H Yacoub
Published 2013-01-01

Angiotensin-converting enzyme insertion/deletion polymorphism in hypertrophic cardiomyopathy: An Egyptian case control study

by Heba Sh. Kassem, Sherif A. Algendy, Remon S. Azer, Sarah Moharem, Maha S. Ayad, Gehan Magdy, Ahmed Elguindy, Magdi H. Yacoub
Published 2014-03-01

A comparative study of mutation screening of sarcomeric genes (MYBPC3, MYH7, TNNT2) using single gene approach versus targeted gene panel next generation sequencing in a cohort of...

by Heba Sh. Kassem, Roddy Walsh, Paul J. Barton, Besra S. Abdelghany, Remon S. Azer, Rachel Buchan, Shibu John, Ahmed Elguindy, Sarah Moharem-ElGamal, Hala M. Badran, Hoda Shehata, Stuart A. Cook, Magdi H. Yacoub
Published 2017-10-01