parazitCUB: An R package to streamline the process of investigating the adaptations of parasites' codon usage bias [version 1; peer review: awaiting peer review] by Anwar, Ali Mostafa, Bayoumi, Salma, Elzalabany, Sagy, Magdeldin, Sameh, Ahmed, Amr E.

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Gene Polymorphisms of IL-10 and MxA in Responders and Non-responders to Interferon Therapy in HCV Egyptian Patients Genotype 4 by Shaker, Olfat G., Abdel-Rahim, Mohamed T., Bayoumi, Salma T.

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Patient and public preferences for being recontacted with updated genomic results: a mixed methods study by Mighton, Chloe, Clausen, Marc, Sebastian, Agnes, Muir, Sarah M., Shickh, Salma, Baxter, Nancy N., Scheer, Adena, Glogowski, Emily, Schrader, Kasmintan A., Thorpe, Kevin E., Kim, Theresa H. M., Lerner-Ellis, Jordan, Kim, Raymond H., Regier, Dean A., Bayoumi, Ahmed M., Bombard, Yvonne

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Regenerative potential of immature permanent non-vital teeth following different dentin surface treatments by El Ashry, Salma H., Abu-Seida, Ashraf M., Bayoumi, Amr A., Hashem, Ahmed A.

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Synovial fluid analysis of MMP-2, MMP-9, and COX-2 as diagnostic markers for naturally occurring septic and aseptic arthritis in horses by Abdelhaleem, Salma W., Bashandy, Mostafa M., Salem, Shaymaa I., Torad, Faisal A., AbuBakr, Huda O., Bayoumi, Mahmoud M.

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Development of patient "profiles" to tailor counseling for incidental genomic sequencing results by Mighton, Chloe, Carlsson, Lindsay, Clausen, Marc, Casalino, Selina, Shickh, Salma, McCuaig, Laura, Joshi, Esha, Panchal, Seema, Graham, Tracy, Aronson, Melyssa, Piccinin, Carolyn, Winter-Paquette, Laura, Semotiuk, Kara, Lorentz, Justin, Mancuso, Talia, Ott, Karen, Silberman, Yael, Elser, Christine, Eisen, Andrea, Kim, Raymond H, Lerner-Ellis, Jordan, Carroll, June C, Glogowski, Emily, Schrader, Kasmintan, Bombard, Yvonne

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Mutations in DDHD2, Encoding an Intracellular Phospholipase A^sub 1^, Cause a Recessive Form of Complex Hereditary Spastic Paraplegia by Schuurs-Hoeijmakers, Janneke HM, Geraghty, Michael T, Kamsteeg, Erik-Jan, Ben-Salem, Salma, de Bot, Susanne T, Nijhof, Bonnie, van de Vondervoort, Ilse IGM, van der Graaf, Marinette, Nobau, Anna Castells, Otte-Höller, Irene, Vermeer, Sascha, Smith, Amanda C, Humphreys, Peter, Schwartzentruber, Jeremy, Ali, Bassam R, Al-Yahyaee, Saeed A, Tariq, Said, Pramathan, Thachillath, Bayoumi, Riad, Kremer, Hubertus PH, van de Warrenburg, Bart P, van den Akker, Willem MR, Gilissen, Christian, Veltman, Joris A, Janssen, Irene M, Vulto-van Silfhout, Anneke T, van der Velde-Visser, Saskia, Lefeber, Dirk J, Diekstra, Adinda, Erasmus, Corrie E, Willemsen, Michèl A, Vissers, Lisenka ELM, Lammens, Martin, van Bokhoven, Hans, Brunner, Han G, Wevers, Ron A, Schenck, Annette, Al-Gazali, Lihadh, de Vries, Bert BA, de Brouwer, Arjan PM

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Autonomous GUI Testing using Deep Reinforcement Learning by Saber, Salma, Elbadry, Fatma, Negm, Hagar, El-Ershad, Rana Abu, Magdy, Omar, Bahnassawi, Mohamed, El Adawi, Reem, Bayoumi, AbdElMoniem

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Mutations in DDHD2, encoding an intracellular phospholipase A(1), cause a recessive form of complex hereditary spastic paraplegia by Schuurs-Hoeijmakers, Janneke H M, Geraghty, Michael T, Kamsteeg, Erik-Jan, Ben-Salem, Salma, de Bot, Susanne T, Nijhof, Bonnie, van de Vondervoort, Ilse I G M, van der Graaf, Marinette, Nobau, Anna Castells, Otte-Höller, Irene, Vermeer, Sascha, Smith, Amanda C, Humphreys, Peter, Schwartzentruber, Jeremy, Ali, Bassam R, Al-Yahyaee, Saeed A, Tariq, Said, Pramathan, Thachillath, Bayoumi, Riad, Kremer, Hubertus P H, van de Warrenburg, Bart P, van den Akker, Willem M R, Gilissen, Christian, Veltman, Joris A, Janssen, Irene M, Vulto-van Silfhout, Anneke T, van der Velde-Visser, Saskia, Lefeber, Dirk J, Diekstra, Adinda, Erasmus, Corrie E, Willemsen, Michèl A, Vissers, Lisenka E L M, Lammens, Martin, van Bokhoven, Hans, Brunner, Han G, Wevers, Ron A, Schenck, Annette, Al-Gazali, Lihadh, de Vries, Bert B A, de Brouwer, Arjan P M

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