Concurrent Obsessive-Compulsive Symptoms in Patients With Schizophrenia: A Retrospective Study From a Tertiary Care Centre in Sindh, Pakistan

por Shoaib, Marium, Iqbal, Maria, Waqas, Uzma J, Ahmed, Sheikh M, Sangeet, Fnu, Raza, Fatima A, Shahab, Azka, Fatima, Kiran, Siddiqui, Maham, Nadeem, Ammar
Publicado 2023

Body Mass Index versus Other Adiposity Traits: Best Predictor of Cardiometabolic Risk

por SAQLAIN, Muhammad, AKHTAR, Zainab, KARAMAT, Raheela, MUNAWAR, Samra, IQBAL, Maria, FIAZ, Muhammad, ZAFAR, Muhammad Mubeen, SAEED, Sadia, NASIR, Muhammad Farooq, NAQVI, S.M. Saqlan, RAJA, Ghazala Kaukab
Publicado 2019

A Homozygous AKNA Frameshift Variant Is Associated with Microcephaly in a Pakistani Family

por Waseem, Syeda Seema, Moawia, Abubakar, Budde, Birgit, Tariq, Muhammad, Khan, Ayaz, Ali, Zafar, Khan, Sheraz, Iqbal, Maria, Malik, Naveed Altaf, Haque, Saif ul, Altmüller, Janine, Thiele, Holger, Hussain, Muhammad Sajid, Cirak, Sebahattin, Baig, Shahid Mahmood, Nürnberg, Peter
Publicado 2021

Deleterious Variants in WNT10A, EDAR, and EDA Causing Isolated and Syndromic Tooth Agenesis: A Structural Perspective from Molecular Dynamics Simulations

por Parveen, Asia, Khan, Sher Alam, Mirza, Muhammad Usman, Bashir, Hina, Arshad, Fatima, Iqbal, Maria, Ahmad, Waseem, Wahab, Ahsan, Fiaz, Amal, Naz, Sidra, Ashraf, Fareeha, Mobeen, Tayyaba, Aziz, Salman, Ahmed, Syed Shoaib, Muhammad, Noor, Hassib, Nehal F., Mostafa, Mostafa I., Gaboon, Nagwa E., Gul, Roquyya, Khan, Saadullah, Froeyen, Matheus, Shoaib, Muhammad, Wasif, Naveed
Publicado 2019

Modifier Genes in Microcephaly: A Report on WDR62, CEP63, RAD50 and PCNT Variants Exacerbating Disease Caused by Biallelic Mutations of ASPM and CENPJ

por Makhdoom, Ehtisham Ul Haq, Waseem, Syeda Seema, Iqbal, Maria, Abdullah, Uzma, Hussain, Ghulam, Asif, Maria, Budde, Birgit, Höhne, Wolfgang, Tinschert, Sigrid, Saadi, Saadia Maryam, Yousaf, Hammad, Ali, Zafar, Fatima, Ambrin, Kaygusuz, Emrah, Khan, Ayaz, Jameel, Muhammad, Khan, Sheraz, Tariq, Muhammad, Anjum, Iram, Altmüller, Janine, Thiele, Holger, Höning, Stefan, Baig, Shahid Mahmood, Nürnberg, Peter, Hussain, Muhammad Sajid
Publicado 2021

An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan

por Rasool, Sajida, Baig, Jamshaid Mahmood, Moawia, Abubakar, Ahmad, Ilyas, Iqbal, Maria, Waseem, Syeda Seema, Asif, Maria, Abdullah, Uzma, Makhdoom, Ehtisham Ul Haq, Kaygusuz, Emrah, Zakaria, Muhammad, Ramzan, Shafaq, Haque, Saif ul, Mir, Asif, Anjum, Iram, Fiaz, Mehak, Ali, Zafar, Tariq, Muhammad, Saba, Neelam, Hussain, Wajid, Budde, Birgit, Irshad, Saba, Noegel, Angelika Anna, Höning, Stefan, Baig, Shahid Mahmood, Nürnberg, Peter, Hussain, Muhammad Sajid
Publicado 2020

Biallelic variants in PCDHGC4 cause a novel neurodevelopmental syndrome with progressive microcephaly, seizures, and joint anomalies

por Iqbal, Maria, Maroofian, Reza, Çavdarlı, Büşranur, Riccardi, Florence, Field, Michael, Banka, Siddharth, Bubshait, Dalal K., Li, Yun, Hertecant, Jozef, Baig, Shahid Mahmood, Dyment, David, Efthymiou, Stephanie, Abdullah, Uzma, Makhdoom, Ehtisham Ul Haq, Ali, Zafar, Scherf de Almeida, Tobias, Molinari, Florence, Mignon-Ravix, Cécile, Chabrol, Brigitte, Antony, Jayne, Ades, Lesley, Pagnamenta, Alistair T., Jackson, Adam, Douzgou, Sofia, Beetz, Christian, Karageorgou, Vasiliki, Vona, Barbara, Rad, Aboulfazl, Baig, Jamshaid Mahmood, Sultan, Tipu, Alvi, Javeria Raza, Maqbool, Shazia, Rahman, Fatima, Toosi, Mehran Beiraghi, Ashrafzadeh, Farah, Imannezhad, Shima, Karimiani, Ehsan Ghayoor, Sarwar, Yasra, Khan, Sheraz, Jameel, Muhammad, Noegel, Angelika A., Budde, Birgit, Altmüller, Janine, Motameny, Susanne, Höhne, Wolfgang, Houlden, Henry, Nürnberg, Peter, Wollnik, Bernd, Villard, Laurent, Alkuraya, Fowzan Sami, Osmond, Matthew, Hussain, Muhammad Sajid, Yigit, Gökhan
Publicado 2021