NaNog: A pluripotency homeobox (master) molecule

por Allouba, Mona H., ElGuindy, Ahmed M., Krishnamoorthy, Navaneethakrishnan, Yacoub, Magdi H., Aguib, Yasmine E.
Publicado en Glob Cardiol Sci Pract (2015)

Reprogramming for cardiac regeneration

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

An Investigation of Fibulin-2 in Hypertrophic Cardiomyopathy

por 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
Publicado en 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

por 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.
Publicado en Genome Med (2019)

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

por 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
Publicado en NPJ Genom Med (2020)

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

por 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
Publicado en Genet Med (2021)

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

por 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.
Publicado en Genet Med (2020)