1. A comprehensive review of federated learning for COVID‐19 detection. Issue 3 (6th December 2021) Authors: Naz, Sadaf; Phan, Khoa T.; Chen, Yi‐Ping Phoebe Journal: International journal of intelligent systems Issue: Volume 37:Issue 3(2022) Page Start: 2371 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A Frameshift Mutation in GRXCR2 Causes Recessively Inherited Hearing Loss. Issue 5 (7th April 2014) Authors: Imtiaz, Ayesha; Kohrman, David C.; Naz, Sadaf Journal: Human mutation Issue: Volume 35:Issue 5(2014:May) Page Start: 618 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss. Issue 8 (4th May 2015) Authors: Mujtaba, Ghulam; Schultz, Julie M; Imtiaz, Ayesha; Morell, Robert J; Friedman, Thomas B; Naz, Sadaf Journal: Journal of medical genetics Issue: Volume 52:Issue 8(2015) Page Start: 548 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A novel mutation in ALS2 associated with severe and progressive infantile onset of spastic paralysis. (3rd April 2017) Authors: Tariq, Huma; Mukhtar, Shahid; Naz, Sadaf Journal: Journal of neurogenetics Issue: Volume 31:Number 1/2(2017) Page Start: 26 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Are some C19orf12 variants monoallelic for neurological disorders?. (August 2019) Authors: Tariq, Huma; Butt, Jalil ur Rehman; Houlden, Henry; Naz, Sadaf Journal: Parkinsonism & related disorders Issue: Volume 65(2019) Page Start: 267 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Ataxia and dysarthria due to an ABCA2 variant: Extension of the phenotypic spectrum. (July 2019) Authors: Aslam, Faiza; Naz, Sadaf Journal: Parkinsonism & related disorders Issue: Volume 64(2019) Page Start: 328 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Autosomal recessive chondrodysplasia with severe short stature caused by a biallelic COL10A1 variant. Issue 6 (22nd August 2017) Authors: Ain, Noor ul; Makitie, Outi; Naz, Sadaf Journal: Journal of medical genetics Issue: Volume 55:Issue 6(2018) Page Start: 403 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Barriers and enablers of women's academic careers in Pakistan. Issue 2 (3rd April 2019) Authors: Fazal, Shawana; Naz, Sadaf; Khan, Muhammad Ilyas; Pedder, David Journal: Asian journal of women's studies Issue: Volume 25:Issue 2(2019) Page Start: 217 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Bi-allelic TTC5 variants cause delayed developmental milestones and intellectual disability. Issue 4 (21st May 2020) Authors: Rasheed, Arisha; Gumus, Evren; Zaki, Maha; Johnson, Katherine; Manzoor, Humera; LaForce, Geneva; Ross, Danica; McEvoy-Venneri, Jennifer; Stanley, Valentina; Lee, Sangmoon; Virani, Abbir; Ben-Omran, Tawfeg; Gleeson, Joseph G; Naz, Sadaf; Schaffer, Ashleigh Journal: Journal of medical genetics Issue: Volume 58:Issue 4(2021) Page Start: 237 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Biallelic KIF24 Variants Are Responsible for a Spectrum of Skeletal Disorders Ranging From Lethal Skeletal Ciliopathy to Severe Acromesomelic Dysplasia. (19th July 2022) Authors: Reilly, Madeline Louise; Ain, Noor ul; Muurinen, Mari; Tata, Alice; Huber, Céline; Simon, Marleen; Ishaq, Tayyaba; Shaw, Nick; Rusanen, Salla; Pekkinen, Minna; Högler, Wolfgang; Knapen, Maarten F. C. M.; van den Born, Myrthe; Saunier, Sophie; Naz, Sadaf; Cormier‐Daire, Valérie; Benmerah, Alexandr... Journal: Journal of bone and mineral research Issue: Volume 37:Number 9(2022) Page Start: 1642 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗