An overview of the Prince Salman Center for Disability Research scientific outcomes

por Al-Odaib, Ali N., Al-Sedairy, Sultan T.
Publicado 2014

Assessment of the Knowledge and Attitudes of Saudi Mothers towards Newborn Screening

por Al-Sulaiman, Ayman, Kondkar, Altaf A., Saeedi, Mohammad Y., Saadallah, Amal, Al-Odaib, Ali, Abu-Amero, Khaled K.
Publicado 2015

The Gln27Glu Polymorphism in β2-Adrenergic receptor gene is linked to hypertriglyceridemia, hyperinsulinemia and hyperleptinemia in Saudis

por Daghestani, Maha H, Warsy, Arjumand, Daghestani, Mazin H, Al-odaib, Ali N, Eldali, Abdelmoneim, Al-Eisa, Nadia A, Al-zhrani, Sabah
Publicado 2010

Glutaric Aciduria Type 1: First Reported Cases in Three Saudi Patients

por Coates, Robert, Rashed, Mohammed, Rahbeeni, Zuhair, Al-Garawi, Sami, Al-Odaib, Ali N., Sakati, Nadia, Gascon, Generoso, Worthen, Howard, Ozand, Pinar T.
Publicado 1994

Arginine 16 Glycine Polymorphism in β2-Adrenergic Receptor Gene is Associated with Obesity, Hyperlipidemia, Hyperleptinemia, and Insulin Resistance in Saudis

por Daghestani, Maha H., Warsy, Arjumand, Daghestani, Mazin H., Al-odaib, Ali N., Eldali, Abdelmoneim, Al-Eisa, Nadia A., Omer, Sawsan A., Hassan, Zeinab K.
Publicado 2012

Chromosome 12q24.31-q24.33 deletion causes multiple dysmorphic features and developmental delay: First mosaic patient and overview of the phenotype related to 12q24qter defects

por Al-Zahrani, Jawaher, Al-Dosari, Naji, AbuDheim, Nada, Alshidi, Tarfa A, Colak, Dilek, Al-Habit, Ola, Al-Odaib, Ali, Sakati, Nadia, Meyer, Brian, Ozand, Pinar T, Kaya, Namik
Publicado 2011

The Prevalence of Phenylketonuria in Arab Countries, Turkey, and Iran: A Systematic Review

por El-Metwally, Ashraf, Yousef Al-Ahaidib, Lujane, Ayman Sunqurah, Alaa, Al-Surimi, Khaled, Househ, Mowafa, Alshehri, Ali, Da'ar, Omar B., Abdul Razzak, Hira, AlOdaib, Ali Nasser
Publicado 2018

First report of two successive deletions on chromosome 15q13 cytogenetic bands in a boy and girl: additional data to 15q13.3 syndrome with a report of high IQ patient

por Alsagob, Maysoon, Salih, Mustafa A., Hamad, Muddathir H. A., Al-Yafee, Yusra, Al-Zahrani, Jawaher, Al-Bakheet, Albandary, Nester, Michael, Sakati, Nadia, Wakil, Salma M., AlOdaib, Ali, Colak, Dilek, Kaya, Namik
Publicado 2019

Clinical, radiological, and genetic characterization of SLC13A5 variants in Saudi families: Genotype phenotype correlation and brief review of the literature

por AlQudairy, Hanan, AlDhalaan, Hesham, AlRuways, Sarah, AlMutairi, Nouf, AlNakiyah, Maha, AlGhofaili, Reema, AlBakheet, Albandary, Alomrani, Adeeb, Alharbi, Omar A., Tous, Ehab, AlSayed, Moeen, AlZaidan, Hamad, AlRasheed, Maha M., AlOdaib, Ali, Kaya, Namik
Publicado 2023

Targeted SLC19A3 gene sequencing of 3000 Saudi newborn: a pilot study toward newborn screening

por Alfadhel, Majid, Umair, Muhammad, Almuzzaini, Bader, Alsaif, Saif, AlMohaimeed, Sulaiman A., Almashary, Maher A., Alharbi, Wardah, Alayyar, Latifah, Alasiri, Abdulrahman, Ballow, Mariam, AlAbdulrahman, Abdulkareem, Alaujan, Monira, Nashabat, Marwan, Al‐Odaib, Ali, Altwaijri, Waleed, Al‐Rumayyan, Ahmed, Alrifai, Muhammad T., Alfares, Ahmed, AlBalwi, Mohammed, Tabarki, Brahim
Publicado 2019

Bi-allelic variants in HOPS complex subunit VPS41 cause cerebellar ataxia and abnormal membrane trafficking

por Sanderson, Leslie E, Lanko, Kristina, Alsagob, Maysoon, Almass, Rawan, Al-Ahmadi, Nada, Najafi, Maryam, Al-Muhaizea, Mohammad A, Alzaidan, Hamad, AlDhalaan, Hesham, Perenthaler, Elena, van der Linde, Herma C, Nikoncuk, Anita, Kühn, Nikolas A, Antony, Dinu, Owaidah, Tarek Mustafa, Raskin, Salmo, Vieira, Luana Gabriela Dalla Rosa, Mombach, Romulo, Ahangari, Najmeh, Silveira, Tainá Regina Damaceno, Ameziane, Najim, Rolfs, Arndt, Alharbi, Aljohara, Sabbagh, Raghda M, AlAhmadi, Khalid, Alawam, Bashayer, Ghebeh, Hazem, AlHargan, Aljouhra, Albader, Anoud A, Binhumaid, Faisal S, Goljan, Ewa, Monies, Dorota, Mustafa, Osama M, Aldosary, Mazhor, AlBakheet, Albandary, Alyounes, Banan, Almutairi, Faten, Al-Odaib, Ali, Aksoy, Durdane Bekar, Basak, A Nazli, Palvadeau, Robin, Trabzuni, Daniah, Rosenfeld, Jill A, Karimiani, Ehsan Ghayoor, Meyer, Brian F, Karakas, Bedri, Al-Mohanna, Futwan, Arold, Stefan T, Colak, Dilek, Maroofian, Reza, Houlden, Henry, Bertoli-Avella, Aida M, Schmidts, Miriam, Barakat, Tahsin Stefan, van Ham, Tjakko J, Kaya, Namik
Publicado 2021

New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism

por Horikoshi, Momoko, Yaghootkar, Hanieh, Mook-Kanamori, Dennis O., Sovio, Ulla, Taal, H. Rob, Hennig, Branwen J., Bradfield, Jonathan P., St. Pourcain, Beate, Evans, David M., Charoen, Pimphen, Kaakinen, Marika, Cousminer, Diana L., Lehtimäki, Terho, Kreiner-Møller, Eskil, Warrington, Nicole M., Bustamante, Mariona, Feenstra, Bjarke, Berry, Diane J., Thiering, Elisabeth, Pfab, Thiemo, Barton, Sheila J., Shields, Beverley M., Kerkhof, Marjan, van Leeuwen, Elisabeth M., Fulford, Anthony J., Kutalik, Zoltán, Zhao, Jing Hua, den Hoed, Marcel, Mahajan, Anubha, Lindi, Virpi, Goh, Liang-Kee, Hottenga, Jouke-Jan, Wu, Ying, Raitakari, Olli T., Harder, Marie N., Meirhaeghe, Aline, Ntalla, Ioanna, Salem, Rany M., Jameson, Karen A., Zhou, Kaixin, Monies, Dorota M., Lagou, Vasiliki, Kirin, Mirna, Heikkinen, Jani, Adair, Linda S., Alkuraya, Fowzan S., Al-Odaib, Ali, Amouyel, Philippe, Andersson, Ehm Astrid, Bennett, Amanda J., Blakemore, Alexandra I.F., Buxton, Jessica L., Dallongeville, Jean, Das, Shikta, de Geus, Eco J. C., Estivill, Xavier, Flexeder, Claudia, Froguel, Philippe, Geller, Frank, Godfrey, Keith M., Gottrand, Frédéric, Groves, Christopher J., Hansen, Torben, Hirschhorn, Joel N., Hofman, Albert, Hollegaard, Mads V., Hougaard, David M., Hyppönen, Elina, Inskip, Hazel M., Isaacs, Aaron, Jørgensen, Torben, Kanaka-Gantenbein, Christina, Kemp, John P., Kiess, Wieland, Kilpeläinen, Tuomas O., Klopp, Norman, Knight, Bridget A., Kuzawa, Christopher W., McMahon, George, Newnham, John P., Niinikoski, Harri, Oostra, Ben A., Pedersen, Louise, Postma, Dirkje S., Ring, Susan M., Rivadeneira, Fernando, Robertson, Neil R., Sebert, Sylvain, Simell, Olli, Slowinski, Torsten, Tiesler, Carla M.T., Tönjes, Anke, Vaag, Allan, Viikari, Jorma S., Vink, Jacqueline M., Vissing, Nadja Hawwa, Wareham, Nicholas J., Willemsen, Gonneke, Witte, Daniel R., Zhang, Haitao, Zhao, Jianhua, Wilson, James F., Stumvoll, Michael, Prentice, Andrew M., Meyer, Brian F., Pearson, Ewan R., Boreham, Colin A.G., Cooper, Cyrus, Gillman, Matthew W., Dedoussis, George V., Moreno, Luis A, Pedersen, Oluf, Saarinen, Maiju, Mohlke, Karen L., Boomsma, Dorret I., Saw, Seang-Mei, Lakka, Timo A., Körner, Antje, Loos, Ruth J.F., Ong, Ken K., Vollenweider, Peter, van Duijn, Cornelia M., Koppelman, Gerard H., Hattersley, Andrew T., Holloway, John W., Hocher, Berthold, Heinrich, Joachim, Power, Chris, Melbye, Mads, Guxens, Mònica, Pennell, Craig E., Bønnelykke, Klaus, Bisgaard, Hans, Eriksson, Johan G., Widén, Elisabeth, Hakonarson, Hakon, Uitterlinden, André G., Pouta, Anneli, Lawlor, Debbie A., Smith, George Davey, Frayling, Timothy M., McCarthy, Mark I., Grant, Struan F.A., Jaddoe, Vincent W.V., Jarvelin, Marjo-Riitta, Timpson, Nicholas J., Prokopenko, Inga, Freathy, Rachel M.
Publicado 2012