NaNog: A pluripotency homeobox (master) molecule

di Allouba, Mona H., ElGuindy, Ahmed M., Krishnamoorthy, Navaneethakrishnan, Yacoub, Magdi H., Aguib, Yasmine E.
Pubblicato in Glob Cardiol Sci Pract (2015)

Reprogramming for cardiac regeneration

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

An Investigation of Fibulin-2 in Hypertrophic Cardiomyopathy

di 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
Pubblicato in 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

di 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.
Pubblicato in Genome Med (2019)

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

di 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
Pubblicato in NPJ Genom Med (2020)

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

di 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
Pubblicato in Genet Med (2021)

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

di 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.
Pubblicato in Genet Med (2020)