Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Hakeem Almabrazi"'
Autor:
Basma Haris, Ikhlak Ahmed, Najeeb Syed, Hakeem Almabrazi, Saras Saraswathi, Sara Al-Khawaga, Amira Saeed, Shihab Mundekkadan, Idris Mohammed, Sanaa Sharari, Iman Hawari, Noor Hamed, Houda Afyouni, Tasneem Abdel-Karim, Shayma Mohammed, Amel Khalifa, Maryam Al-Maadheed, Mahmoud Zyoud, Ahmed Shamekh, Ahmed Elawwa, Mohammed Y. Karim, Fawziya Al-Khalaf, Zohreh Tatari-Calderone, Goran Petrovski, Khalid Hussain
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Abstract To describe the clinical features, epidemiology, autoantibody status, HLA haplotypes and genetic mechanisms of type 1 diabetes mellitus (T1DM). Patients (0–18 years) with diabetes were recruited. Clinical data was collected, autoantibodies
Externí odkaz:
https://doaj.org/article/9405a71b574d47d8b7c24add1de0fccd
Autor:
Ann M. Mc Cartney, Medhat Mahmoud, Michael Jochum, Daniel Paiva Agustinho, Barry Zorman, Ahmad Al Khleifat, Fawaz Dabbaghie, Rupesh K Kesharwani, Moritz Smolka, Moez Dawood, Dreycey Albin, Elbay Aliyev, Hakeem Almabrazi, Ahmed Arslan, Advait Balaji, Sairam Behera, Kimberley Billingsley, Daniel L Cameron, Joyjit Daw, Eric T. Dawson, Wouter De Coster, Haowei Du, Christopher Dunn, Rocio Esteban, Angad Jolly, Divya Kalra, Chunxiao Liao, Yunxi Liu, Tsung-Yu Lu, James M Havrilla, Michael M Khayat, Maximillian Marin, Jean Monlong, Stephen Price, Alejandro Rafael Gener, Jingwen Ren, Sagayamary Sagayaradj, Nicolae Sapoval, Claude Sinner, Daniela C. Soto, Arda Soylev, Arun Subramaniyan, Najeeb Syed, Neha Tadimeti, Pamella Tater, Pankaj Vats, Justin Vaughn, Kimberly Walker, Gaojianyong Wang, Qiandong Zeng, Shangzhe Zhang, Tingting Zhao, Bryce Kille, Evan Biederstedt, Mark Chaisson, Adam English, Zev Kronenberg, Todd J. Treangen, Timothy Hefferon, Chen-Shan Chin, Ben Busby, Fritz J Sedlazeck
Publikováno v:
F1000Research, Vol 10 (2021)
In October 2020, 62 scientists from nine nations worked together remotely in the Second Baylor College of Medicine & DNAnexus hackathon, focusing on different related topics on Structural Variation, Pan-genomes, and SARS-CoV-2 related research. The o
Externí odkaz:
https://doaj.org/article/52994138986c4640b0eb0fcc835acd81
Autor:
Lee Silcock, Hakeem Almabrazi, Younes Mokrab, Puthen Jithesh, Muna Al-Hashmi, Nicola James, Rebecca Mathew, Valentina Mattei, Davide Bedognetti, Francesca Lessi, Ramzi Temanni, Barbara Seliger, Rashid Al-Ali, Francesco M. Marincola, Ena Wang, Sara Tomei
Publikováno v:
Journal of Translational Medicine, Vol 17, Iss 1, Pp 1-7 (2019)
Abstract Background Monoallelic expression (MAE) is a frequent genomic phenomenon in normal tissues, however its role in cancer is yet to be fully understood. MAE is defined as the expression of a gene that is restricted to one allele in the presence
Externí odkaz:
https://doaj.org/article/fd11d94296a64e7f83edce668d7c986b
Publikováno v:
Journal of Personalized Medicine, Vol 12, Iss 5, p 722 (2022)
Essential hypertension (EH) is a leading risk condition for cardiovascular and renal complications. While multiple genes are associated with EH, little is known about its genetic etiology. Therefore, this study aimed to screen for variants that are a
Externí odkaz:
https://doaj.org/article/70e1352d59ec458a88e98343991c497b
The clinical and genetic characteristics of permanent neonatal diabetes (PNDM) in the state of Qatar
Autor:
Sara Al‐Khawaga, Idris Mohammed, Saras Saraswathi, Basma Haris, Reem Hasnah, Amira Saeed, Hakeem Almabrazi, Najeeb Syed, Puthen Jithesh, Ahmed El Awwa, Amal Khalifa, Fawziya AlKhalaf, Goran Petrovski, Essam M. Abdelalim, Khalid Hussain
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 10, Pp n/a-n/a (2019)
Abstract Background Neonatal diabetes mellitus (NDM) is a rare condition that occurs within the first six months of life. Permanent NDM (PNDM) is caused by mutations in specific genes that are known for their expression at early and/or late stages of
Externí odkaz:
https://doaj.org/article/13c76bfb87ac45c783f1de1f50fc2ba4
Autor:
Mohamad Saad, Younes Mokrab, Najeeb Halabi, Jingxuan Shan, Rozaimi Razali, Khalid Kunji, Najeeb Syed, Ramzi Temanni, Murugan Subramanian, Michele Ceccarelli, Arash Rafii Tabrizi, Davide Bedognetti, Lotfi Chouchane, Said I Ismail, Wadha Al-Muftah, Radja Badji, Hamdi Mbarek, Dima Darwish, Tasnim Fadl, Heba Yasin, Maryem Ennaifar, Rania Abdellatif, Fatima Alkuwari, Muhammad Alvi, Yasser Al-Sarraj, Chadi Saad, Eleni Fethnou, Fatima Qafoud, Eiman Alkhayat, Nahla Afifi, Sara Tomei, Wei Liu, Stephan Lorenz, Hakeem Almabrazi, Fazulur R Vempalli, Tariq Abu Saqri, Mohammedhusen Khatib, Mehshad Hamza, Tariq Abu Zaid, Ahmed El Khouly, Tushar Pathare, Shafeeq Poolat, Rashid Al-Ali, Omar Albagha, Souhaila Al-Khodor, Mashael Alshafai, Ramin Badii, Xavier Estivill, Khalid Fakhro, Jithesh V Puthen, Karsten Suhre, Zohreh Tatari
Publikováno v:
The Lancet. Oncology. 23(3)
Background: Disparities in the genetic risk of cancer among various ancestry groups and populations remain poorly defined. This challenge is even more acute for Middle Eastern populations, where the paucity of genomic data could affect the clinical p
Autor:
Jean Monlong, Claude Sinner, Dreycey Albin, Ann M Mc Cartney, Justin N. Vaughn, Arun Subramaniyan, Advait Balaji, Medhat Mahmoud, Moez Dawood, Qiandong Zeng, Eric T. Dawson, Najeeb Syed, Zev N. Kronenberg, Todd J. Treangen, Daniel L Cameron, Timothy Hefferon, Mark Chaisson, Ahmad Al Khleifat, Michael M. Khayat, Hakeem Almabrazi, Moritz Smolka, Fritz J. Sedlazeck, Evan Biederstedt, Alejandro Rafael Gener, Rupesh K. Kesharwani, Ahmed Arslan, James M Havrilla, Arda Soylev, Sagayamary Sagayaradj, Pamella Tater, Christopher Dunn, Fawaz Dabbaghie, Daniela C. Soto, Pankaj Vats, Barry Zorman, Wouter De Coster, Neha Tadimeti, Yunxi Liu, Ben Busby, Tsung-Yu Lu, Gaojianyong Wang, Kimberley Billingsley, Stephen J. Price, Kimberly Walker, Elbay Aliyev, Haowei Du, Daniel Paiva Agustinho, Divya Kalra, Tingting Zhao, Maximillian Marin, Adam C. English, Jingwen Ren, Bryce Kille, Shangzhe Zhang, Sairam Behera, Michael Jochum, Rocio Esteban, Angad Jolly, Nicolae Sapoval, Chunxiao Liao, Joyjit Daw, Chen-Shan Chin
Publikováno v:
F1000Research
In October 2020, 62 scientists from nine nations worked together remotely in the Second Baylor College of Medicine & DNAnexus hackathon, focusing on different related topics on Structural Variation, Pan-genomes, and SARS-CoV-2 related research. The o
Autor:
Khalid Hussain, Fawziya Al-Khalaf, Idris Mohammed, Ikhlak Ahmed, Maryam Al-Maadheed, Goran Petrovski, Sara Al-Khawaga, Shayma Mohammed, Ahmed Shamekh, Najeeb Syed, Hakeem Almabrazi, Zohreh Tatari-Calderone, Saras Saraswathi, Iman Hawari, Amira Saeed, Noor Hamed, Shihab Mundekkadan, Houda Afyouni, Mohammed Yousuf Karim, Amel Khalifa, Basma Haris, Ahmed Elawwa, Sanaa Sharari, Mahmoud Zyoud, Tasneem Abdel-Karim
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
To describe the clinical features, epidemiology, autoantibody status, HLA haplotypes and genetic mechanisms of type 1 diabetes mellitus (T1DM). Patients (0–18 years) with diabetes were recruited. Clinical data was collected, autoantibodies and c-pe
The clinical and genetic characteristics of permanent neonatal diabetes (PNDM) in the State of Qatar
Autor:
Amel Khalifa, Hakeem Almabrazi, Reem Hasnah, Saras Saraswathi, Essam M. Abdelalim, Basma Haris, Puthen V. Jithesh, Goran Petrovski, Idris Mohammed, Najeeb Syed, Fawziya Al-Khalaf, El Awwa A, Amira Saeed, Khalid Hussain, Sara Al-Khawaga
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 10, Pp n/a-n/a (2019)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Background Neonatal diabetes mellitus (NDM) is a rare condition that occurs within the first six months of life. Permanent NDM (PNDM) is caused by mutations in specific genes that are known for their expression at early and/or late stages of pancreat
Autor:
Valentina Mattei, Ramzi Temanni, Rebecca Mathew, Davide Bedognetti, Lee Silcock, Barbara Seliger, Rashid Al-Ali, Ena Wang, Francesca Lessi, Sara Tomei, Puthen V. Jithesh, Hakeem Almabrazi, Francesco M. Marincola, Muna Al-Hashmi, Nicola James, Younes Mokrab
Publikováno v:
Journal of Translational Medicine
Journal of Translational Medicine, Vol 17, Iss 1, Pp 1-7 (2019)
Journal of Translational Medicine, Vol 17, Iss 1, Pp 1-7 (2019)
Background Monoallelic expression (MAE) is a frequent genomic phenomenon in normal tissues, however its role in cancer is yet to be fully understood. MAE is defined as the expression of a gene that is restricted to one allele in the presence of a dip