Distribution of the Lactase Persistence-Associated Variant Alleles -13910*T and -13915*G among the People of Oman and Yemen

Authors: Al-Abri, Abdul Rahim, Al-Rawas, Omar, Al-Yahyaee, Saeed, Al-Habori, Molham, Al-Zubairi, Adel Sharaf, Bayoumi, Riad

Source: Human Biology. 84(3):271-286

Availability: https://muse.jhu.edu/article/486778

Erratum: Distribution of the Lactase Persistence-Associated Variant Alleles - 13910*T and - 13915*G among the People of Oman and Yemen

Authors: AL-ABRI, ABDUL RAHIM, AL-RAWAS, OMAR, AL-YAHYAEE, SAEED, AL-HABORI, MOLHAM, AL-ZUBAIRI, ADEL SHARAF, BAYOUMI, RIAD

Source: Human Biology, 2012 Aug 01. 84(4), 449-465.

Access URL: https://www.jstor.org/stable/41851001

The genetic basis of inherited primary nocturnal enuresis: a UAE study

Authors: Bayoumi, Riad A., Eapen, Valsamma, Al-Yahyaee, Saeed, Al Barwani, Hameeda S., Hill, Robert S., Al Gazali, Lihadh

Source: In Journal of Psychosomatic Research 2006 61(3):317-320

Mutations in DDHD2, Encoding an Intracellular Phospholipase A1, Cause a Recessive Form of Complex Hereditary Spastic Paraplegia

Authors: 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.

Source: In The American Journal of Human Genetics 7 December 2012 91(6):1073-1081

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Mutations in DDHD2, Encoding an Intracellular Phospholipase A1, Cause a Recessive Form of Complex Hereditary Spastic Paraplegia

Authors: Schuurs-Hoeijmakers, Janneke H.M.^1,2,3, Geraghty, Michael T.⁴, Kamsteeg, Erik-Jan¹, Ben-Salem, Salma⁵, de Bot, Susanne T.^6,7, Nijhof, Bonnie^1,3,7, van de Vondervoort, Ilse I.G.M.¹, van der Graaf, Marinette⁸, Nobau, Anna Castells^1,3,7, Otte-Höller, Irene⁹, Vermeer, Sascha¹, Smith, Amanda C.¹⁰, Humphreys, Peter⁴, Schwartzentruber, Jeremy¹¹, Ali, Bassam R.⁵, Al-Yahyaee, Saeed A.¹², Tariq, Said¹³, Pramathan, Thachillath⁵, Bayoumi, Riad¹⁴, Kremer, Hubertus P.H.¹⁵

Source: American Journal of Human Genetics; Dec2012, Vol. 91 Issue 6, p1073-1081, 9p

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Abstract 440.

Authors: Hassan, Mohammed O, Jaju, Deepali S, Bayoumi, Riad A, Al-Yahyaee, Saeed, Comuzzie, Anthony G, Voruganti, Saroja V, Albarwani, Sulayma A

Source: Hypertension (0194911X); 2014 Supplement, Vol. 64, pA440-A440, 1p

Do We Have to Increase Sensibility of Metabolic Syndrome Components? The Oman Family Study.

Authors: Lopez-Alvarenga, Juan C., Solis-Herrera, Carolina, Kent Jr., Jack W., Jaju, Deepali, Albarwani, Sulayma, Al-Yahyaee, Saeed, Hassan, M. Osman, Bayoumi, Riad, Comuzzie, Anthony G.

Source: Diabetes; Jun2007 Supplement 1, Vol. 56, pA266-A266, 1/4p

Subject Terms: METABOLIC syndrome, DISEASE risk factors, FAMILIAL diseases, TRIGLYCERIDES, BLOOD pressure, BLOOD sugar

Geographic Terms: OMAN