NaNog: A pluripotency homeobox (master) molecule

Por Allouba, Mona H., ElGuindy, Ahmed M., Krishnamoorthy, Navaneethakrishnan, Yacoub, Magdi H., Aguib, Yasmine E.
Publicado no 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 no 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 no 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 no 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 no NPJ Genom Med (2020)

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 no Genet Med (2020)