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Sadaf Naz

Showing results (21-30 of 89) with videos related to

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BMC Musculoskeletal Disorders|July 21, 2021
RAB33B and PCNT variants in two Pakistani families with skeletal dysplasia and short statureNoor Ul Ain, Zunaira Fatima, Sadaf Naz, et al.
International Journal of Intelligent Systems|July 31, 2023
A comprehensive review of federated learning for COVID-19 detectionSadaf Naz, Khoa T Phan, Yi-Ping Phoebe Chen
Gene|July 13, 2015
Homozygous p.G61E mutation in a consanguineous Pakistani family with co-existence of juvenile-onset open angle glaucoma and primary congenital glaucomaRasheeda Bashir, Hafsa Tahir, Khazeema Yousaf, et al.
Biochemical Genetics|January 24, 2013
The c.42_52del11 mutation in TPRN and progressive hearing loss in a family from PakistanRasheeda Bashir, Ayesha Imtiaz, Amara Fatima, et al.
Molecular Biology Reports|November 1, 2025
Insights on inflammatory pathways and their cross-talk: a comprehensive review on asthmaSadaf Naz, Aimen Wajid, Marya Nawaz Malik, et al.
Gene|December 17, 2020
Some pathogenic SETX variants are partially conserved during evolutionHuma Tariq, Iqra Tariq, Thomas Bourinaris, et al.
BMC Psychiatry|November 17, 2022
Preliminary studies on apparent mendelian psychotic disorders in consanguineous familiesAmbreen Kanwal, Sohail A Sheikh, Amina Iftikhar, et al.
Pakistan Journal of Medical Sciences|February 13, 2015
Contribution of GLC3A locus to Primary Congenital Glaucoma in Pakistani populationRasheeda Bashir, Mahrukh Sanai, Adnan Azeem, et al.
Gene|April 28, 2019
Bi-allelic Pro291Leu variant in KCNQ4 leads to early onset non-syndromic hearing lossMemoona Ramzan, Hafiza Idrees, Ghulam Mujtaba, et al.
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.
Pageof 9

Showing results (21-30 of 89) with videos related to

Sort By:
Pageof 9
BMC Musculoskeletal Disorders|July 21, 2021
RAB33B and PCNT variants in two Pakistani families with skeletal dysplasia and short statureNoor Ul Ain, Zunaira Fatima, Sadaf Naz, et al.
International Journal of Intelligent Systems|July 31, 2023
A comprehensive review of federated learning for COVID-19 detectionSadaf Naz, Khoa T Phan, Yi-Ping Phoebe Chen
Gene|July 13, 2015
Homozygous p.G61E mutation in a consanguineous Pakistani family with co-existence of juvenile-onset open angle glaucoma and primary congenital glaucomaRasheeda Bashir, Hafsa Tahir, Khazeema Yousaf, et al.
Biochemical Genetics|January 24, 2013
The c.42_52del11 mutation in TPRN and progressive hearing loss in a family from PakistanRasheeda Bashir, Ayesha Imtiaz, Amara Fatima, et al.
Molecular Biology Reports|November 1, 2025
Insights on inflammatory pathways and their cross-talk: a comprehensive review on asthmaSadaf Naz, Aimen Wajid, Marya Nawaz Malik, et al.
Gene|December 17, 2020
Some pathogenic SETX variants are partially conserved during evolutionHuma Tariq, Iqra Tariq, Thomas Bourinaris, et al.
BMC Psychiatry|November 17, 2022
Preliminary studies on apparent mendelian psychotic disorders in consanguineous familiesAmbreen Kanwal, Sohail A Sheikh, Amina Iftikhar, et al.
Pakistan Journal of Medical Sciences|February 13, 2015
Contribution of GLC3A locus to Primary Congenital Glaucoma in Pakistani populationRasheeda Bashir, Mahrukh Sanai, Adnan Azeem, et al.
Gene|April 28, 2019
Bi-allelic Pro291Leu variant in KCNQ4 leads to early onset non-syndromic hearing lossMemoona Ramzan, Hafiza Idrees, Ghulam Mujtaba, et al.
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.
Pageof 9