| Role of capping agents in the application of nanoparticles in biomedicine and environmental remediation: recent trends and future prospects R Javed, M Zia, S Naz, SO Aisida, N Ain, Q Ao Journal of Nanobiotechnology 18, 1-15, 2020 | 550 | 2020 |
| CDC14A phosphatase is essential for hearing and male fertility in mouse and human A Imtiaz, IA Belyantseva, AJ Beirl, C Fenollar-Ferrer, R Bashir, I Bukhari, ... Human molecular genetics 27 (5), 780-798, 2018 | 60 | 2018 |
| High frequency and molecular epidemiology of metallo-β-lactamase-producing gram-negative bacilli in a tertiary care hospital in Lahore, Pakistan NU Ain, A Iftikhar, SS Bukhari, S Abrar, S Hussain, MH Haider, F Rasheed, ... Antimicrobial Resistance & Infection Control 7, 1-9, 2018 | 34 | 2018 |
| Influence of PVP/PEG impregnated CuO NPs on physiological and biochemical characteristics of Trigonella foenum‐graecum L N Ain, I Haq, BH Abbasi, R Javed, M Zia IET Nanobiotechnology 12 (3), 349-356, 2018 | 30 | 2018 |
| Autosomal recessive chondrodysplasia with severe short stature caused by a biallelic COL10A1 variant N ul Ain, O Makitie, S Naz Journal of Medical Genetics 55 (6), 403-407, 2018 | 19 | 2018 |
| Biallelic TMEM251 variants in patients with severe skeletal dysplasia and extreme short stature NU Ain, N Muhammad, M Dianatpour, M Baroncelli, M Iqbal, MAF Fard, ... Human mutation 42 (1), 89-101, 2021 | 16 | 2021 |
| Autosomal Recessive Osteogenesis Imperfecta Caused by a Novel Homozygous COL1A2 Mutation A Costantini, S Tournis, A Kämpe, N Ul Ain, F Taylan, A Doulgeraki, ... Calcified tissue international 103, 353-358, 2018 | 16 | 2018 |
| Novel variants in natriuretic peptide receptor 2 in unrelated patients with acromesomelic dysplasia type Maroteaux N ul Ain, M Iqbal, H Valta, CA Emerling, S Ahmed, O Makitie, S Naz European Journal of Medical Genetics 62 (9), 103554, 2019 | 13 | 2019 |
| A cornucopia of screening and diagnostic techniques for human papillomavirus associated cervical carcinomas M Ramzan, N ul Ain, S Ilyas, M Umer, S Bano, S Sarwar, N Shahzad, ... Journal of virological methods 222, 192-201, 2015 | 10 | 2015 |
| Novel form of rhizomelic skeletal dysplasia associated with a homozygous variant in GNPNAT1 NU Ain, M Baroncelli, A Costantini, T Ishaq, F Taylan, O Nilsson, O Mäkitie, ... Journal of Medical Genetics 58 (5), 351-356, 2021 | 8 | 2021 |
| Biallelic KIF24 Variants Are Responsible for a Spectrum of Skeletal Disorders Ranging From Lethal Skeletal Ciliopathy to Severe Acromesomelic Dysplasia ML Reilly, N Ain, M Muurinen, A Tata, C Huber, M Simon, T Ishaq, N Shaw, ... Journal of Bone and Mineral Research 37 (9), 1642-1652, 2022 | 7 | 2022 |
| Biallelic variants in CHST3 cause Spondyloepiphyseal dysplasia with joint dislocations in three Pakistani kindreds M Kausar, NU Ain, F Hayat, H Fatima, S Azim, H Ullah, M Mushtaq, ... BMC Musculoskeletal Disorders 23 (1), 818, 2022 | 7 | 2022 |
| Noonan syndrome: a case report F Khan, S Waqar, NUA Jamal, A Saleem Annals of Health Research (The Journal of the Medical and Dental Consultants …, 2018 | 4 | 2018 |
| Horizontal gene transfer and antibacterial effect of Allium sativum (garlic) on methicillin-resistant Staphylococcus aureus NU Ain, S Riaz, S Abrar, M Ahmad, Z Khan, S Hafiz, S Hussain, ... Annals of PIMS ISSN 1815, 2287, 2017 | 4 | 2017 |
| Genome sequencing and analysis of genomic diversity in the locally transmitted SARS‐CoV‐2 in Pakistan M Shakeel, M Irfan, ZU Nisa, S Farooq, N Ain, W Iqbal, N Kakar, S Jahan, ... Transboundary and Emerging Diseases 69 (5), e2418-e2430, 2022 | 3 | 2022 |
| RAB33B and PCNT variants in two Pakistani families with skeletal dysplasia and short stature N Ain, Z Fatima, S Naz, O Makitie BMC Musculoskeletal Disorders 22, 1-6, 2021 | 3 | 2021 |
| The c. 1138G> a variant of fibroblast growth factor receptor 3 is a common cause of achondroplasia in Pakistan. N Muhammad, S Yasin, Z Fatima, NU Ain, M Faizan, S Naz | 1 | 2021 |
| Metabolic changes and their characterization N Ain, H Gull 'Essentials of Cancer Genomic, Computational Approaches and Precision …, 2020 | 1 | 2020 |
| Variants in FREM1 and trisomy 18 identified in a neonatal progeria patient S Siddiqi, N Ain, M Kauser, Z Mukhtar, M Ansar, M Umair Molecular Biology Reports 50 (9), 7935-7939, 2023 | | 2023 |
| EXPRESSION OF EUKARYOTIC PROTEINS WITHIN IN-VIVO AND IN-VITRO EXPRESSION SYSTEMS: A COMPARATIVE ANALYSIS N ul Ain, M Ramzan Online Journal of BioSciences and Informatics 4 (2), 2013 | | 2013 |
Sadaf NazSchool of Biological Sciences, University of the Punjab在 pu.edu.pk 的电子邮件经过验证
