Published Research in 2018

Mufti, A.H., Ogiwara, K., Swystun, L.L., Eikenboom, J.C., Budde, U., Hopman, W.M., Halldén, C., Goudemand, J., Peake, I.R., Goodeve, A.C. and Lillicrap, D., 2018. The common VWF single nucleotide variants c. 2365A> G and c. 2385T> C modify VWF biosynthesis and clearance. Blood advances, 2(13), pp.1585-1594.

Morad, F.A., Rashidi, O.M., Sadath, S.S., Al-Allaf, F.A., Athar, M., Alama, M.N., Edris, S.E., Bondagji, N.S., Shaik, N.A., Banaganapalli, B. and Awan, Z., 2018. In Silico Approach to Investigate the Structural and Functional Attributes of Familial Hypercholesterolemia Variants Reported in the Saudi Population. Journal of Computational Biology, 25(2), pp.170-181.

Elhawary, N.A., Jiffri, E.H., Jambi, S., Mufti, A.H., Dannoun, A., Kordi, H., Khogeer, A., Jiffri, O.H., Elhawary, A.N. and Tayeb, M.T., 2018. Molecular characterization of exonic rearrangements and frame shifts in the dystrophin gene in Duchenne muscular dystrophy patients in a Saudi community. Human genomics, 12(1), p.18.

Alnouri, F., Athar, M., Al-Allaf, F.A., Abduljaleel, Z., Taher, M.M., Bouazzaoui, A., Al Ammari, D., Karrar, H. and Albabtain, M., 2018. Novel combined variants of LDLR and LDLRAP1 genes causing severe familial hypercholesterolemia. Atherosclerosis, 277, pp.425-433.

Khan, W., Abduljaleel, Z., Al-Allaf, F.A., Shahzad, N., El-Huneidi, W., Elrobh, M., Alanazi, M. and Faidah, H., 2018. Prediction of OGG1 structural and functional motifs with active binding sites from Camelus dromedaries. JAPS: Journal of Animal & Plant Sciences, 28(5).