Phenotypic Spectrum in Osteogenesis Imperfecta Due to Mutations in TMEM38B: Unraveling a Complex Cellular Defect von Webb, Emma A., Balasubramanian, Meena, Fratzl-Zelman, Nadja, Cabral, Wayne A., Titheradge, Hannah, Alsaedi, Atif, Saraff, Vrinda, Vogt, Julie, Cole, Trevor, Stewart, Susan, Crabtree, Nicola J., Sargent, Brandi M., Gamsjaeger, Sonja, Paschalis, Eleftherios P., Roschger, Paul, Klaushofer, Klaus, Shaw, Nick J., Marini, Joan C., Högler, Wolfgang

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Population insight of the relationship between lifestyle and cancer: A population-based survey von Alshammari, Fawaz Dabea, Ahmed, Hussain Gadelkarim, Alshammari, Dena, Alharbi, Ahmed Mulfy, Alsaedi, Atif Saud, Elasbaly, Abdulbaset

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Exome sequencing analysis of rare autosomal recessive disorders von Alsaedi, Atif Saud

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Germline mutations in RYR1 are associated with foetal akinesia deformation sequence/lethal multiple pterygium syndrome von McKie, Arthur B, Alsaedi, Atif, Vogt, Julie, Stuurman, Kyra E, Weiss, Marjan M, Shakeel, Hassan, Tee, Louise, Morgan, Neil V, Nikkels, Peter G J, van Haaften, Gijs, Park, Soo-Mi, van der Smagt, Jasper J, Bugiani, Marianna, Maher, Eamonn R

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Saudi-KAU Coupled Global Climate Model: Description and Performance von Almazroui, Mansour, Tayeb, Osama, Mashat, Abdulfattah S., Yousef, Ahmed, Al-Turki, Yusuf A., Abid, M. Adnan, Bafail, Abdullah O., Ehsan, M. Azhar, Zahed, Adnan, Rahman, M. Ashfaqur, Mohorji, Abduallah M., Kang, In-Sik, Noaman, Amin, Omar, Mohamed, Al-roqi, Abdullah M., Ammar, K., Al-Ghamdi, Abdullah S., Hussein, M. A. A., Katib, Iyad, O’Brien, Enda, Aljohani, Naif R., Islam, M. Nazrul, Alsaedi, Ahmed, Yang, Young-Min, Alkhalaf, Abdulrahman K., Ismail, Muhammad, Mashat, Abdulwahab, Kucharski, Fred, Assiri, Mazen, Ibrahim, Salem, Tippett, Michael, Rashid, Irfan Ur, Kamil, Shahzad, Alahmadi, Adel, Atif, Rana M., Bajunaid, Mohammed A., Hantoush, Ahmed S.

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