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

由 Al-Odaib, Ali N., Al-Sedairy, Sultan T.
發表在 Saudi Med J (2014)

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

由 Al-Sulaiman, Ayman, Kondkar, Altaf A., Saeedi, Mohammad Y., Saadallah, Amal, Al-Odaib, Ali, Abu-Amero, Khaled K.
發表在 Biomed Res Int (2015)

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

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

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

由 Coates, Robert, Rashed, Mohammed, Rahbeeni, Zuhair, Al-Garawi, Sami, Al-Odaib, Ali N., Sakati, Nadia, Gascon, Generoso, Worthen, Howard, Ozand, Pinar T.
發表在 Ann Saudi Med (1994)

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

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

由 Sakati Nadia, Al-Odaib Ali, Al-Habit Ola, Colak Dilek, Alshidi Tarfa A, AbuDheim Nada, Al-Dosari Naji, Al-Zahrani Jawaher, Meyer Brian, Ozand Pinar T, Kaya Namik
出版 2011-04-01

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

由 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
出版 2011

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

由 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
發表在 Biomed Res Int (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

由 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
發表在 Mol Cytogenet (2019)

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

由 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
發表在 Ann Clin Transl Neurol (2019)

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

由 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
發表在 Brain (2021)

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

由 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.
出版 2012