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Molecular Genetics and Genomics : MGG|June 30, 2026
A CLN8 biallelic missense variant causes epilepsy with severe treatment-resistant psychosisRimsha Zulfiqar, Ambreen Kanwal, Maham Hameed, et al.
Scientific Reports|September 13, 2024
Genetic investigations on singleton school aged children reveal novel variants and new candidate genes for hearing lossHina Khan, Fariha Muzaffar, Midhat Salman, et al.
Food Chemistry|November 2, 2013
Studies on molecular interactions of some sweeteners in water by volumetric and ultrasonic velocity measurements at T=(20.0-45.0°C)Muhammad Asghar Jamal, Muhammad Kaleem Khosa, Muhammad Rashad, et al.
JPMA. the Journal of the Pakistan Medical Association|August 18, 2020
Antimicrobial susceptibility patterns among community and health care acquired carbapenem resistant Enterobacteriaceae, in a tertiary care hospital of LahoreQanita Fahim, Irfan Ali Mirza, Anum Imtiaz, et al.
JPMA. the Journal of the Pakistan Medical Association|August 16, 2018
Clinical variability of CYP1B1 gene variants in Pakistani primary congenital glaucoma familiesRasheeda Bashir, Khazeema Yousaf, Hafsa Tahir, et al.
Gene|July 1, 2023
Genomic analysis of multiplex consanguineous families reveals causes of neurodevelopmental disorders with epilepsyAnum Shafique, Tipu Sultan, Fatema Alzahrani, et al.
Cureus|February 7, 2020
Frequency of Hypogonadism in Type 2 Diabetes Mellitus Patients with and without Coronary Artery DiseaseMuhammad T Raza, Sabira Sharif, Zohaib Ahmad Khan, et al.
Psychiatric Genetics|June 17, 2026
A rare missense variant in Bruton's tyrosine kinase is associated with bipolar disorder accompanied by psychosisAmbreen Kanwal, Husnain Arshad Cheema, Nauman Jabbar, et al.
JPMA. the Journal of the Pakistan Medical Association|February 18, 2020
Association of hepatocyte growth factor gene polymorphisms with primary angle closure glaucoma from Lahore, PakistanRasheeda Bashir, Bushra Irfan, Mehak Khalid, et al.
BMC Musculoskeletal Disorders|September 14, 2023
Clinical, radiographic and molecular characterization of two unrelated families with multicentric osteolysis, nodulosis, and arthropathyTayyaba Ishaq, Petra Loid, Hafiza Abida Ishaq, et al.
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