Identification of 42 Genes Linked to Stage II Colorectal Cancer Metastatic Relapse von Al-Temaimi, Rabeah A, Tan, Tuan Zea, Marafie, Makia J, Thiery, Jean Paul, Quirke, Philip, Al-Mulla, Fahd

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Gender-associated genomic differences in colorectal cancer: clinical insight from feminization of male cancer cells von Ali, Rola H, Marafie, Makia J, Bitar, Milad S, Al-Dousari, Fahad, Ismael, Samar, Bin Haider, Hussain, Al-Ali, Waleed, Jacob, Sindhu P, Al-Mulla, Fahd

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Capturing all disease-causing mutations for clinical and research use: Toward an effortless system for the Human Variome Project von Cotton, Richard G H, Al Aqeel, Aida I, Al-Mulla, Fahd, Carrera, Paola, Claustres, Mireille, Ekong, Rosemary, Hyland, Valentine J, Macrae, Finlay A, Marafie, Makia J, Paalman, Mark H, Patrinos, George P, Qi, Ming, Ramesar, Rajkumar S, Scott, Rodney J, Sijmons, Rolf H, Sobrido, María-Jesús, Vihinen, Mauno

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The spectrum of BRCA1 and BRCA2 pathogenic sequence variants in Middle Eastern, North African, and South European countries von Laitman, Yael, Friebel, Tara M., Yannoukakos, Drakoulis, Fostira, Florentia, Konstantopoulou, Irene, Figlioli, Gisella, Bonanni, Bernardo, Manoukian, Siranoush, Zuradelli, Monica, Tondini, Carlo, Pasini, Barbara, Peterlongo, Paolo, Plaseska‐Karanfilska, Dijana, Jakimovska, Milena, Majidzadeh, Keivan, Zarinfam, Shiva, Loizidou, Maria A., Hadjisavvas, Andreas, Michailidou, Kyriaki, Kyriacou, Kyriacos, Behar, Doron M., Molho, Rinat Bernstein, Ganz, Patricia, James, Paul, Parsons, Michael T., Sallam, Aminah, Olopade, Olufunmilayo I., Seth, Arun, Chenevix ‐ Trench, Georgia, Leslie, Goska, McGuffog, Lesley, Marafie, Makia J, Megarbane, Andre, Al‐Mulla, Fahd, Rebbeck, Timothy R., Friedman, Eitan

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The characterization of metal complexes in typical Kuwait atmospheric residues using both GPC coupled with ICP–MS and HT GC–AED von Park, Joo-Il, Al-Mutairi, Adel, Marafie, Abdulazeem M.J., Yoon, Seong-Ho, Mochida, Isao, Ma, Xiaoliang

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Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection von Patrinos, George P., Al Aama, Jumana, Al Aqeel, Aida, Al-Mulla, Fahd, Borg, Joseph, Devereux, Andrew, Felice, Alex E., Macrae, Finlay, Marafie, Makia J., Petersen, Michael B., Qi, Ming, Ramesar, Rajkumar S., Zlotogora, Joel, Cotton, Richard G.H.

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Senior-Loken syndrome: A novel NPHP5 gene mutation in a family from Kuwait von Marafie, Makia J, Al-Mulla, Fahd

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Next-generation sequencing in familial breast cancer patients from Lebanon von Jalkh, Nadine, Chouery, Eliane, Haidar, Zahraa, Khater, Christina, Atallah, David, Ali, Hamad, Marafie, Makia J, Al-Mulla, Mohamed R, Al-Mulla, Fahd, Megarbane, Andre

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Identification of a rare germline NBN gene mutation by whole exome sequencing in a lung-cancer survivor from a large family with various types of cancer von Marafie, Makia J., Dashti, Mohammed, Al-Mulla, Fahd

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Identification and management of Lynch syndrome in the Middle East and North African countries: outcome of a survey in 12 countries von Sina, Mohammad, Ghorbanoghli, Zeinab, Abedrabbo, Amal, Al-Mulla, Fahd, Sghaier, Rihab Ben, Buisine, Marie-Pierre, Cortas, George, Goshayeshi, Ladan, Hadjisavvas, Andreas, Hammoudeh, Wail, Hamoudi, Waseem, Jabari, Carol, Loizidou, Maria A., Majidzadeh-A, Keivan, Marafie, Makia J., Muslumov, Gurbankhan, Rifai, Laila, Seir, Rania Abu, Talaat, Suzan M., Tunca, Berrin, Ziada-Bouchaar, Hadia, Velthuizen, Mary E., Sharara, Ala I., Ahadova, Aysel, Georgiou, Demetra, Vasen, Hans F. A.

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Primary ciliary dyskinesia: Kartagener syndrome in a family with a novel DNAH5 gene mutation and variable phenotypes von Marafie, Makia J., Al Suliman, Ibrahim S., Redha, Abdullah M., Alshati, Abdulrahman M.

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Synthesis of a Luminescent Arsolo[2,3-d:5,4-d']bis(thiazole) Building Block and Comparison to Its Phosphole Analogue von Green, JP, Cryer, SJ, Marafie, J, White, AJP, Heeney, M

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Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database von Thompson, Bryony A, Spurdle, Amanda B, Plazzer, John-Paul, Greenblatt, Marc S, Akagi, Kiwamu, Al-Mulla, Fahd, Bapat, Bharati, Bernstein, Inge, Capellá, Gabriel, den Dunnen, Johan T, du Sart, Desiree, Fabre, Aurelie, Farrell, Michael P, Farrington, Susan M, Frayling, Ian M, Frebourg, Thierry, Goldgar, David E, Heinen, Christopher D, Holinski-Feder, Elke, Kohonen-Corish, Maija, Robinson, Kristina Lagerstedt, Leung, Suet Yi, Martins, Alexandra, Moller, Pal, Morak, Monika, Nystrom, Minna, Peltomaki, Paivi, Pineda, Marta, Qi, Ming, Ramesar, Rajkumar, Rasmussen, Lene Juel, Royer-Pokora, Brigitte, Scott, Rodney J, Sijmons, Rolf, Tavtigian, Sean V, Tops, Carli M, Weber, Thomas, Wijnen, Juul, Woods, Michael O, Macrae, Finlay, Genuardi, Maurizio

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Impact of 226C>T MSH2 gene mutation on cancer phenotypes in two HNPCC-associated highly-consanguineous families from Kuwait: emphasis on premarital genetic testing von Marafie, Makia J., Al-Awadi, Sadiqa, Al-Mosawi, Fatemah, Elshafey, Alaa, Al-Ali, Waleed, Al-Mulla, Fahd

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Wolcott-Rallison syndrome in a Bedouin boy von Marafie, Makia J, Redha, Mary A, Al-Naggar, Rezk L

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Germline mutations in early-onset or hereditary breast cancer from the Middle East von Marafie, Makia J, Al-Temaimi, Rabea, Megarbane, Andre, Al-Mulla, Fahd

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Ruthenium-catalyzed meta sulfonation of 2-phenylpyridines von Saidi, Ourida, Marafie, J, Ledger, Araminta E W, Liu, Po Man, Mahon, Mary F, Kociok-Kohn, Gabriele, Whittlesey, Michael K, Frost, Christopher G

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Baraitser–Winter syndrome: An additional Arab patient von Abou Henedy, Maha M., Marafie, Makia J., Abulhasan, Sawsan J.

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The newly recognised limb/pelvis-hypoplasia/aplasia syndrome: report of a Bedouin patient and review von Farag, T I, al-Awadi, S A, Marafie, M J, Bastaki, L, al-Othman, S A, Mohammed, F M, AlSuliman, I S, Murthy, D S

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Planning the Human Variome Project: The Spain report von Kaput, Jim, Cotton, Richard G.H, Hardman, Lauren, Watson, Michael, Al Aqeel, Aida I, Al-Aama, Jumana Y, Al-Mulla, Fahd, Alonso, Santos, Aretz, Stefan, Auerbach, Arleen D, Bapat, Bharati, Bernstein, Inge T, Bhak, Jong, Bleoo, Stacey L, Blöcker, Helmut, Brenner, Steven E, Burn, John, Bustamante, Mariona, Calzone, Rita, Cambon-Thomsen, Anne, Cargill, Michele, Carrera, Paola, Cavedon, Lawrence, Cho, Yoon Shin, Chung, Yeun-Jun, Claustres, Mireille, Cutting, Garry, Dalgleish, Raymond, den Dunnen, Johan T, Díaz, Carlos, Dobrowolski, Steven, dos Santos, M. Rosário N, Ekong, Rosemary, Flanagan, Simon B, Flicek, Paul, Furukawa, Yoichi, Genuardi, Maurizio, Ghang, Ho, Golubenko, Maria V, Greenblatt, Marc S, Hamosh, Ada, Hancock, John M, Hardison, Ross, Harrison, Terence M, Hoffmann, Robert, Horaitis, Rania, Howard, Heather J, Barash, Carol Isaacson, Izagirre, Neskuts, Jung, Jongsun, Kojima, Toshio, Laradi, Sandrine, Lee, Yeon-Su, Lee, Jong-Young, Gil-da-Silva-Lopes, Vera L, Macrae, Finlay A, Maglott, Donna, Marafie, Makia J, Marsh, Steven G.E, Matsubara, Yoichi, Messiaen, Ludwine M, Möslein, Gabriela, Netea, Mihai G, Norton, Melissa L, Oefner, Peter J, Oetting, William S, O'Leary, James C, de Ramirez, Ana Maria Oller, Paalman, Mark H, Parboosingh, Jillian, Patrinos, George P, Perozzi, Giuditta, Phillips, Ian R, Povey, Sue, Qi, Ming, Quin, David J, Ramesar, Rajkumar S, Richards, C. Sue, Savige, Judith, Scheible, Dagmar G, Scott, Rodney J, Seminara, Daniela, Shephard, Elizabeth A, Sijmons, Rolf H, Smith, Timothy D, Tanaka, Toshihiro, Tavtigian, Sean V, Taylor, Graham R, Teague, Jon, Töpel, Thoralf, Ullman-Cullere, Mollie, Utsunomiya, Joji, van Kranen, Henk J, Vihinen, Mauno, Webb, Elizabeth, Weber, Thomas K, Yeager, Meredith, Yeom, Young I, Yim, Seon-Hee, Yoo, Hyang-Sook

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