Computation of Resistance Distances in a Sub-divided Cyclic Silicate Network and Applications von Ayub, Humaira, Jamil, Muhammad Kamran, Azeem, Muhammad

Volltext

Prescribing Patterns of Antibiotics in Tertiary Care Hospital of Abbottabad, Khyber Pakhtunkhwa von Alam, Fiaz, Zahid, Palwasha, Ayub, Humaira, Atif, Muhammad, Aslam, Rabbia

Volltext

Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families von Shafique, Sobia, Siddiqi, Saima, Schraders, Margit, Oostrik, Jaap, Ayub, Humaira, Bilal, Ammad, Ajmal, Muhammad, Seco, Celia Zazo, Strom, Tim M, Mansoor, Atika, Mazhar, Kehkashan, Shah, Syed Tahir A, Hussain, Alamdar, Azam, Maleeha, Kremer, Hannie, Qamar, Raheel

Volltext

Exome sequencing identifies three novel candidate genes implicated in intellectual disability von Agha, Zehra, Iqbal, Zafar, Azam, Maleeha, Ayub, Humaira, Vissers, Lisenka E L M, Gilissen, Christian, Ali, Syeda Hafiza Benish, Riaz, Moeen, Veltman, Joris A, Pfundt, Rolph, van Bokhoven, Hans, Qamar, Raheel

Volltext

Variants in the ASB10 Gene Are Associated with Primary Open Angle Glaucoma von Micheal, Shazia, Ayub, Humaira, Islam, Farrah, Siddiqui, Sorath Noorani, Khan, Wajid Ali, Akhtar, Farah, Qamar, Raheel, Khan, Muhammad Imran, den Hollander, Anneke I

Volltext

Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistan von Maria, Maleeha, Ajmal, Muhammad, Azam, Maleeha, Waheed, Nadia Khalida, Siddiqui, Sorath Noorani, Mustafa, Bilal, Ayub, Humaira, Ali, Liaqat, Ahmad, Shakeel, Micheal, Shazia, Hussain, Alamdar, Shah, Syed Tahir Abbas, Ali, Syeda Hafiza Benish, Ahmed, Waqas, Khan, Yar Muhammad, den Hollander, Anneke I, Haer-Wigman, Lonneke, Collin, Rob W J, Khan, Muhammad Imran, Qamar, Raheel, Cremers, Frans P M

Volltext

The genetic spectrum of familial hypercholesterolemia in Pakistan von Ahmed, Waqas, Whittall, Ros, Riaz, Moeen, Ajmal, Muhammad, Sadeque, Ahmed, Ayub, Humaira, Qamar, Raheel, Humphries, Steve E.

Volltext

Association of a polymorphism in the BIRC6 gene with pseudoexfoliative glaucoma von Ayub, Humaira, Micheal, Shazia, Akhtar, Farah, Khan, Muhammad Imran, Bashir, Shaheena, Waheed, Nadia K, Ali, Mahmood, Schoenmaker-Koller, Frederieke E, Shafique, Sobia, Qamar, Raheel, Hollander, Anneke I den

Volltext

MicroRNA biogenesis, gene silencing mechanisms and role in breast, ovarian and prostate cancer von Khan, Sanna, Ayub, Humaira, Khan, Taous, Wahid, Fazli

Volltext

Prescribing Patterns of Antibiotics in Tertiary Care Hospital of Abbottabad, Khyber Pakhtunkhwa von Fiaz Alam, Palwasha Zahid, Humaira Ayub, Muhammad Atif, Rabbia Aslam

Volltext

Prescribing Patterns of Antibiotics in Tertiary Care Hospital of Abbottabad, Khyber Pakhtunkhwa von Fiaz Alam, Palwasha Zahid, Humaira Ayub, Muhammad Atif, Rabbia Aslam

Volltext

Association of IL-17A promoter region SNP-rs2275913 with urinary bladder cancer von Anwar, Maryam, Ejaz, Muhammad, Ijaz, Muhammad, Ahmad, Gulzar, Ayub, Humaira, Ali, Syeda Hafiza Benish

Volltext

Prevalence and Factors Associated with Personal and Work-related Burnout among Primary Health Care Physicians in Tabuk, Saudi Arabia von Ishaq, Hajira Saba, Ayub, Humaira, Albelawi, Shaima Hamid, Altawili, Mohammed Ahmad, Alenazi, Saada Shayeh, Omer, Hamza Mohamed Ibrahim, Al Mamun, Mohammad

Volltext

The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome von Berner, Daniel, Hoja, Ursula, Zenkel, Matthias, Ross, James Julian, Uebe, Steffen, Paoli, Daniela, Frezzotti, Paolo, Rautenbach, Robyn M, Ziskind, Ari, Williams, Susan E, Carmichael, Trevor R, Ramsay, Michele, Topouzis, Fotis, Chatzikyriakidou, Anthi, Lambropoulos, Alexandros, Sundaresan, Periasamy, Ayub, Humaira, Akhtar, Farah, Qamar, Raheel, Zenteno, Juan C, Cruz-Aguilar, Marisa, Astakhov, Yury S, Dubina, Michael, Wiggs, Janey, Ozaki, Mineo, Kruse, Friedrich E, Aung, Tin, Reis, André, Khor, Chiea Chuen, Pasutto, Francesca, Schlötzer-Schrehardt, Ursula

Volltext

Association of rs10490924 in ARMS2/HTRA1 with age‐related macular degeneration in the Pakistani population von Ayub, Humaira, Shafique, Sobia, Azam, Aisha, Muslim, Irfan, Qazi, Nauman A, Akhtar, Farah, Khan, Muhammad Asim, Ayub, Adil, Bashir, Shaheena, Bakker, Bjorn, Ahmed, Shakil, Azam, Maleeha, Hollander, Anneke I., Qamar, Raheel

Volltext

Association of known common genetic variants with primary open angle, primary angle closure, and pseudoexfoliation glaucoma in Pakistani cohorts von Micheal, Shazia, Ayub, Humaira, Khan, Muhammad Imran, Bakker, Bjorn, Schoenmaker-Koller, Frederieke E, Ali, Mahmood, Akhtar, Farah, Khan, Wajid Ali, Qamar, Raheel, den Hollander, Anneke I

Volltext

Identification of novel CYP1B1 gene mutations in patients with primary congenital and primary open-angle glaucoma von Micheal, Shazia, Ayub, Humaira, Zafar, Saemah N, Bakker, Bjorn, Ali, Mahmood, Akhtar, Farah, Islam, Farrah, Khan, Muhammad I, Qamar, Raheel, den Hollander, Anneke I

Volltext

Association of eNOS and HSP70 gene polymorphisms with glaucoma in Pakistani cohorts von Ayub, Humaira, Khan, Muhammad Imran, Micheal, Shazia, Akhtar, Farah, Ajmal, Muhammad, Shafique, Sobia, Ali, Syeda Hafiza Benish, den Hollander, Anneke I, Ahmed, Asifa, Qamar, Raheel

Volltext

Exome sequencing identifies a novel and a recurrent BBS1 mutation in Pakistani families with Bardet-Biedl syndrome von Ajmal, Muhammad, Khan, Muhammad Imran, Neveling, Kornelia, Tayyab, Ali, Jaffar, Sulman, Sadeque, Ahmed, Ayub, Humaira, Abbasi, Nasir Mahmood, Riaz, Moeen, Micheal, Shazia, Gilissen, Christian, Ali, Syeda Hafiza Benish, Azam, Maleeha, Collin, Rob W J, Cremers, Frans P M, Qamar, Raheel

Volltext

Identification of novel CYP1B 1 gene mutations in patients with primary congenital and primary open‐angle glaucoma von Micheal, Shazia, Ayub, Humaira, Zafar, Saemah N, Bakker, Bjorn, Ali, Mahmood, Akhtar, Farah, Islam, Farrah, Khan, Muhammad I, Qamar, Raheel, den Hollander, Anneke I

Volltext