NaNog: A pluripotency homeobox (master) molecule

od Allouba, Mona H., ElGuindy, Ahmed M., Krishnamoorthy, Navaneethakrishnan, Yacoub, Magdi H., Aguib, Yasmine E.
Wydane w Glob Cardiol Sci Pract (2015)

Reprogramming for cardiac regeneration

od Raynaud, Christophe Michel, Ahmad, Faizzan Syed, Allouba, Mona, Abou-Saleh, Haissam, Lui, Kathy O., Yacoub, Magdi
Wydane w Glob Cardiol Sci Pract (2014)

An Investigation of Fibulin-2 in Hypertrophic Cardiomyopathy

od Ibrahim, Ayman M., Roshdy, Mohamed, Elshorbagy, Sara, Hosny, Mohammed, Halawa, Sarah, Yehia, Dina, Elfawy, Hasnaa A., Eldessouki, Ahmed, Mohamed, Faisal, Ellithy, Amany, Abdelfattah, Mohamed, Elsawy, Amr, Elkhatib, Mohamed, Allouba, Mona, Elguindy, Ahmed, Aguib, Yasmine, Yacoub, Magdi
Wydane w Int J Mol Sci (2020)

Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy

od Walsh, Roddy, Mazzarotto, Francesco, Whiffin, Nicola, Buchan, Rachel, Midwinter, William, Wilk, Alicja, Li, Nicholas, Felkin, Leanne, Ingold, Nathan, Govind, Risha, Ahmad, Mian, Mazaika, Erica, Allouba, Mona, Zhang, Xiaolei, de Marvao, Antonio, Day, Sharlene M., Ashley, Euan, Colan, Steven D., Michels, Michelle, Pereira, Alexandre C., Jacoby, Daniel, Ho, Carolyn Y., Thomson, Kate L., Watkins, Hugh, Barton, Paul J. R., Olivotto, Iacopo, Cook, Stuart A., Ware, James S.
Wydane w Genome Med (2019)

The Egyptian Collaborative Cardiac Genomics (ECCO-GEN) Project: defining a healthy volunteer cohort

od Aguib, Yasmine, Allouba, Mona, Afify, Alaa, Halawa, Sarah, El-Khatib, Mohamed, Sous, Marina, Galal, Aya, Abdelrahman, Eslam, Shehata, Nairouz, El Sawy, Amr, Elmaghawry, Mohamed, Anwer, Shehab, Kamel, Omnia, El Mozy, Wesam, Khedr, Hadir, Kharabish, Ahmed, Thabet, Nagwa, Theotokis, Pantazis I., Buchan, Rachel, Govind, Risha, Whiffin, Nicola, Walsh, Roddy, Aguib, Heba, Elguindy, Ahmed, O’Regan, Declan P., Cook, Stuart A., Barton, Paul J., Ware, James S., Yacoub, Magdi
Wydane w NPJ Genom Med (2020)

Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies

od Mazzarotto, Francesco, Hawley, Megan H., Beltrami, Matteo, Beekman, Leander, de Marvao, Antonio, McGurk, Kathryn A., Statton, Ben, Boschi, Beatrice, Girolami, Francesca, Roberts, Angharad M., Lodder, Elisabeth M., Allouba, Mona, Romeih, Soha, Aguib, Yasmine, Baksi, A. John, Pantazis, Antonis, Prasad, Sanjay K., Cerbai, Elisabetta, Yacoub, Magdi H., O’Regan, Declan P., Cook, Stuart A., Ware, James S., Funke, Birgit, Olivotto, Iacopo, Bezzina, Connie R., Barton, Paul J. R., Walsh, Roddy
Wydane w Genet Med (2021)

Disease-specific variant pathogenicity prediction significantly improves variant interpretation in inherited cardiac conditions

od Zhang, Xiaolei, Walsh, Roddy, Whiffin, Nicola, Buchan, Rachel, Midwinter, William, Wilk, Alicja, Govind, Risha, Li, Nicholas, Ahmad, Mian, Mazzarotto, Francesco, Roberts, Angharad, Theotokis, Pantazis I., Mazaika, Erica, Allouba, Mona, de Marvao, Antonio, Pua, Chee Jian, Day, Sharlene M., Ashley, Euan, Colan, Steven D., Michels, Michelle, Pereira, Alexandre C., Jacoby, Daniel, Ho, Carolyn Y., Olivotto, Iacopo, Gunnarsson, Gunnar T., Jefferies, John L., Semsarian, Chris, Ingles, Jodie, O’Regan, Declan P., Aguib, Yasmine, Yacoub, Magdi H., Cook, Stuart A., Barton, Paul J. R., Bottolo, Leonardo, Ware, James S.
Wydane w Genet Med (2020)