The Management of Osteoporosis in Chronic Kidney Disease: A Review of Diagnostic and Therapeutic Approaches von Tariq, Fatima, Ahmad, Mehjabeen, Subhan, Muhammad, Zaid Alvi, Syed Muhammad, Tariq, Muhammad Umar, Ullah, Sami, Khalid, Asma, Bibi, Ruqiya, Shafique Ur Rehman, Muaz, Abbas, Ayesha

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Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk von Shrine, Nick, Chen, Jing, Packer, Richard, Hall, Robert J., Guyatt, Anna L., Batini, Chiara, Thompson, Rebecca J., Malik, Vidhi, Moll, Matthew, Tal-Singer, Ruth, Bakke, Per, Fawcett, Katherine A., John, Catherine, Piga, Noemi Nicole, Pozarickij, Alfred, Lin, Kuang, Chen, Zhengming, Li, Liming, Lahousse, Lies, Uitterlinden, Andre G., Oelsner, Elizabeth C., Rich, Stephen S., Kerr, Shona M., Vitart, Veronique, Brown, Michael R., Wielscher, Matthias, Imboden, Medea, Bartz, Traci M., Gharib, Sina A., Flexeder, Claudia, Karrasch, Stefan, Peters, Annette, Hu, Xiaowei, Ortega, Victor E., Meyers, Deborah A., Bleecker, Eugene R., Gupta, Namrata, Smith, Albert Vernon, Luan, Jian’an, Zhao, Jing-Hua, Hansen, Ailin F., Langhammer, Arnulf, Willer, Cristen, Bhatta, Laxmi, Porteous, David, Smith, Blair H., Lee, Jiwon, Daviglus, Martha L., Yu, Bing, Lim, Elise, Xu, Hanfei, O’Connor, George T., Thareja, Gaurav, Suhre, Karsten, Granell, Raquel, Faquih, Tariq O., Hiemstra, Pieter S., Hui, Jennie, James, Alan, Beilby, John, Hysi, Pirro, Koskela, Jukka T., Jin, Jianping, Sikdar, Sinjini, May-Wilson, Sebastian, Kentistou, Katherine A., Free, Robert C., Wang, Xueyang, Gilliland, Frank D., Chen, Zhanghua, Foong, Rachel E., Harris, Sarah E., Taylor, Adele, Redmond, Paul, Cook, James P., Lind, Lars, Lehtimäki, Terho, Pietiläinen, Kirsi H., Pennell, Craig E., Hall, Graham L., Gauderman, W. James, Wilson, James F., Laitinen, Tarja, Salomaa, Veikko, Timpson, Nicholas J., Zeggini, Eleftheria, Dupuis, Josée, Hayward, Caroline, Brumpton, Ben, Weiss, Stefan, Homuth, Georg, Probst-Hensch, Nicole, Jarvelin, Marjo-Riitta, Morrison, Alanna C., Sayers, Ian, Rawlins, Emma L., Strachan, David P., Walters, Robin G., Morris, Andrew P., Tobin, Martin D.

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Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits von Thareja, Gaurav, Al-Sarraj, Yasser, Belkadi, Aziz, Almotawa, Maryam, Suhre, Karsten, Albagha, Omar M. E.

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Comparative Safety and Efficacy of Low/Moderate-Intensity Statin plus Ezetimibe Combination Therapy vs. High-Intensity Statin Monotherapy in Patients with Atherosclerotic Cardiovas... von Hameed, Ishaque, Shah, Syeda Ayesha, Aijaz, Ashnah, Mushahid, Hasan, Farhan, Syed Husain, Dada, Muhammad, Khan, Adam Bilal, Amjad, Reeha, Alvi, Fawad, Murtaza, Mustafa, Zuberi, Zaid, Hamza, Mohammad

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Qatar genome: Insights on genomics from the Middle East von Mbarek, Hamdi, Devadoss Gandhi, Geethanjali, Selvaraj, Senthil, Al‐Muftah, Wadha, Badji, Radja, Al‐Sarraj, Yasser, Saad, Chadi, Darwish, Dima, Alvi, Muhammad, Fadl, Tasnim, Yasin, Heba, Alkuwari, Fatima, Razali, Rozaimi, Aamer, Waleed, Abbaszadeh, Fatemeh, Ahmed, Ikhlak, Mokrab, Younes, Suhre, Karsten, Albagha, Omar, Fakhro, Khalid, Badii, Ramin, Ismail, Said I., Althani, Asma

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Genetic predisposition to cancer across people of different ancestries in Qatar: a population-based, cohort study von Saad, Mohamad, Mokrab, Younes, Halabi, Najeeb, Shan, Jingxuan, Razali, Rozaimi, Kunji, Khalid, Syed, Najeeb, Temanni, Ramzi, Subramanian, Murugan, Ceccarelli, Michele, Rafii Tabrizi, Arash, Bedognetti, Davide, Chouchane, Lotfi

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Analysis of 14,392 whole genomes reveals 3.5% of Qataris carry medically actionable variants von Elfatih, Amal, Saad, Chadi, Mifsud, Borbala, Mbarek, Hamdi

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Mapping the genetic landscape of treatable inherited metabolic disorders in a large Middle Eastern biobank von Devadoss Gandhi, Geethanjali, Aliyev, Elbay, Syed, Najeeb, Vempalli, Fazulur Rehaman, Saad, Chadi, Mbarek, Hamdi, Al-Saei, Omayma, Al-Maraghi, Aljazi, Abdi, Mona, Krishnamoorthy, Navaneethakrishnan, Badii, Ramin, Ismail, Said I., Al-Muftah, Wadha, Badji, Radja, Mbarek, Hamdi, Darwish, Dima, Fadl, Tasnim, Yasin, Heba, Ennaifar, Maryem, Abdellatif, Rania, Alkuwari, Fatima, Alvi, Muhammad, Al-Sarraj, Yasser, Saad, Chadi, Althani, Asmaa, Fethnou, Eleni, Qafoud, Fatima, Alkhayat, Eiman, Afifi, Nahla, Tomei, Sara, Liu, Wei, Lorenz, Stephan, Syed, Najeeb, Almabrazi, Hakeem, Vempalli, Fazulur Rehaman, Temanni, Ramzi, Saqri, Tariq Abu, Khatib, Mohammedhusen, Hamza, Mehshad, Zaid, Tariq Abu, El Khouly, Ahmed, Pathare, Tushar, Poolat, Shafeeq, Al-Ali, Rashid, Albagha, Omar, Al-Khodor, Souhaila, Alshafai, Mashael, Badii, Ramin, Chouchane, Lotfi, Estivill, Xavier, Fakhro, Khalid A., Mokrab, Younes, Puthen, Jithesh V., Suhre, Karsten, Tatari, Zohreh, Akil, Ammira A., Ben-Omran, Tawfeg, Fakhro, Khalid A.

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Actionable genomic variants in 6045 participants from the Qatar Genome Program von Elfatih, Amal, Mifsud, Borbala, Syed, Najeeb, Badii, Ramin, Mbarek, Hamdi, Abbaszadeh, Fatemeh, Estivill, Xavier, Ismail, Said, Al‐Muftah, Wadha, Badji, Radja, Mbarek, Hamdi, Darwish, Dima, Fadl, Tasnim, Yasin, Heba, Ennaifar, Maryem, Abdel‐latif, Rania, Alkuwari, Fatima, Alvi, Muhammad, Sarraj, Yasser Al, Saad, Chadi, Althani, Asmaa, Fethnou, Eleni, Qafoud, Fatima, Alkhayat, Eiman, Afifi, Nahla, Tomei, Sara, Liu, Wei, Lorenz, Stephan, Syed, Najeeb, Almabrazi, Hakeem, Vempalli, Fazulur Rehaman, Temanni, Ramzi, Saqri, Tariq Abu, Khatib, Mohammedhusen, Hamza, Mehshad, Zaid, Tariq Abu, El Khouly, Ahmed, Pathare, Tushar, Poolat, Shafeeq, Al‐Ali, Rashid, Albagha, Omar M. E., Al‐Khodor, Souhaila, Alshafai, Mashael, Badii, Ramin, Chouchane, Lotfi, Estivill, Xavier, Fakhro, Khalid, Mbarek, Hamdi, Mokrab, Younes, Puthen, Jithesh V., Suhre, Karsten, Tatari, Zohreh

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Burden of Mendelian disorders in a large Middle Eastern biobank von Aamer, Waleed, Al-Maraghi, Aljazi, Syed, Najeeb, Gandhi, Geethanjali Devadoss, Aliyev, Elbay, Al-Kurbi, Alya A, Al-Saei, Omayma, Kohailan, Muhammad, Krishnamoorthy, Navaneethakrishnan, Palaniswamy, Sasirekha, Al-Malki, Khulod, Abbasi, Saleha, Agrebi, Nourhen, Abbaszadeh, Fatemeh, Akil, Ammira S Al-Shabeeb, Badii, Ramin, Ben-Omran, Tawfeg, Lo, Bernice, Mokrab, Younes, Fakhro, Khalid A

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Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk von Shrine, Nick, Chen, Jing, Packer, Richard, Hall, Robert J., Guyatt, Anna L., Batini, Chiara, Thompson, Rebecca J., Malik, Vidhi, Moll, Matthew, Tal-Singer, Ruth, Bakke, Per, Fawcett, Katherine A., John, Catherine, Piga, Noemi Nicole, Pozarickij, Alfred, Lin, Kuang, Chen, Zhengming, Li, Liming, Lahousse, Lies, Uitterlinden, Andre G., Oelsner, Elizabeth C., Rich, Stephen S., Kerr, Shona M., Vitart, Veronique, Brown, Michael R., Wielscher, Matthias, Imboden, Medea, Bartz, Traci M., Gharib, Sina A., Flexeder, Claudia, Karrasch, Stefan, Peters, Annette, Hu, Xiaowei, Ortega, Victor E., Meyers, Deborah A., Bleecker, Eugene R., Gupta, Namrata, Smith, Albert Vernon, Luan, Jian’an, Zhao, Jing-Hua, Hansen, Ailin F., Langhammer, Arnulf, Willer, Cristen, Bhatta, Laxmi, Porteous, David, Smith, Blair H., Lee, Jiwon, Daviglus, Martha L., Yu, Bing, Lim, Elise, Xu, Hanfei, O’Connor, George T., Thareja, Gaurav, Suhre, Karsten, Granell, Raquel, Faquih, Tariq O., Hiemstra, Pieter S., Hui, Jennie, James, Alan, Beilby, John, Hysi, Pirro, Koskela, Jukka T., Jin, Jianping, Sikdar, Sinjini, May-Wilson, Sebastian, Kentistou, Katherine A., Free, Robert C., Wang, Xueyang, Gilliland, Frank D., Chen, Zhanghua, Foong, Rachel E., Harris, Sarah E., Taylor, Adele, Redmond, Paul, Cook, James P., Lind, Lars, Lehtimäki, Terho, Pietiläinen, Kirsi H., Pennell, Craig E., Hall, Graham L., Gauderman, W. James, Wilson, James F., Laitinen, Tarja, Salomaa, Veikko, Timpson, Nicholas J., Zeggini, Eleftheria, Dupuis, Josée, Hayward, Caroline, Brumpton, Ben, Weiss, Stefan, Homuth, Georg, Probst-Hensch, Nicole, Jarvelin, Marjo-Riitta, Morrison, Alanna C., Sayers, Ian, Rawlins, Emma L., Strachan, David P., Walters, Robin G., Morris, Andrew P., Tobin, Martin D.

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Analysis of incidental findings in Qatar genome participants reveals novel functional variants in LMNA and DSP von Elfatih, Amal, Da’as, Sahar I, Abdelrahman, Doua, Mbarek, Hamdi, Mohammed, Idris, Hasan, Waseem, Fakhro, Khalid A, Estivill, Xavier, Mifsud, Borbala

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A population study of clinically actionable genetic variation affecting drug response from the Middle East von Jithesh, Puthen Veettil, Abuhaliqa, Mohammed, Syed, Najeeb, Ahmed, Ikhlak, El Anbari, Mohammed, Bastaki, Kholoud, Sherif, Shimaa, Umlai, Umm-Kulthum, Jan, Zainab, Gandhi, Geethanjali, Manickam, Chidambaram, Selvaraj, Senthil, George, Chinnu, Bangarusamy, Dhinoth, Abdel-latif, Rania, Al-Shafai, Mashael, Tatari-Calderone, Zohreh, Estivill, Xavier, Pirmohamed, Munir

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