S. Shahzad

发表

Optical screening of nasopharyngeal cancer using Raman spectroscopy and support vector machine

Asifullah Khan, Saranjam Khan, R. Ullah, 2018 .

A novel homozygous frameshift mutation in the DCC gene in a Pakistani family with autosomal recessive horizontal gaze palsy with progressive scoliosis‐2 with impaired intellectual development

S. Basit, Y. Hashim, S. Shahzad, 2020, American journal of medical genetics. Part A.

Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities

Imran Afzal, A. Gul, Madiha Rasheed, 2017, Archives of Dermatological Research.

Effect of oxidative stress and calcium deregulation on FAM26F (CALHM6) expression during hepatitis B virus infection

U. Malik, A. Javed, S. Shahzad, 2021, BMC Infectious Diseases.

Plant beneficial endophytic bacteria: Mechanisms, diversity, host range and genetic determinants.

Shomaila Sikandar, Imran Afzal, Z. Shinwari, 2019, Microbiological research.

On the modeling and analysis of the biological regulatory network of NF ‐ κ B activation in HIV ‐ 1 infection

Samar H. K. Tareen, Amjad Ali, J. Ahmad, 2016 .

Facile Synthesis as well as Structural, Raman, Dielectric and Antibacterial Characteristics of Cu Doped ZnO Nanoparticles

J. Iqbal, T. Jan, S. Shahzad, 2015 .

In silico Analysis of Candidate Genes Involved in Sanfilippo Syndrome

S. Shahzad, Shagufta Shafique, M. Zaka, 2015 .

Cost effective and efficient screening of tuberculosis disease with Raman spectroscopy and machine learning algorithms.

Saranjam Khan, R. Ullah, S. Shahzad, 2020, Photodiagnosis and photodynamic therapy.

A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family

S. Leal, W. Ahmad, Muhammad Umair, 2018, European Journal of Dermatology.

Polymerase Chain Reaction

Shomaila Sikandar, Imran Afzal, S. Shahzad, 2020, Genetic Engineering - A Glimpse of Techniques and Applications.

Diagnosis of thalassemia and iron deficiency anemia using confocal and atomic force microscopy

S. Firdous, S. Shahzad, M. Bilal, 2017 .

CDKN2A/P16INK4A variants association with breast cancer and their in-silico analysis

S. Tabassum, S. Shahzad, R. Khan, 2018, Breast Cancer.

Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2.

D. Nickerson, S. Leal, Joshua D. Smith, 2016, American journal of human genetics.

Fabry Disease: from Diagnosis to Therapy

S. Shahzad, Ifrah Shafqat, 2012 .

On the modeling and analysis of the biological regulatory network of NF-$${\kappa }$$κB activation in HIV-1 infection

Jamil Ahmad, Amjad Ali, Shah Khusro, 2016, Complex Adapt. Syst. Model..

Homozygous variants in the HEXB and MBOAT7 genes underlie neurological diseases in consanguineous families

E. Baple, A. Crosby, W. Ahmad, 2019, BMC Medical Genetics.

Pasting, thermal, textural and rheological properties of rice starch blended with 6 different hydrocolloid gums.

S. Shahzad, S. Hussain, M. Osman, 2019 .

Sequence variants in nine different genes underlying rare skin disorders in 10 consanguineous families

D. Nickerson, S. Leal, M. Bamshad, 2017, International journal of dermatology.

Analysis of tuberculosis disease through Raman spectroscopy and machine learning.

Asifullah Khan, Saranjam Khan, R. Ullah, 2018, Photodiagnosis and photodynamic therapy.

Raman Spectroscopy Combined with Principal Component Analysis for Screening Nasopharyngeal Cancer in Human Blood Sera

Muhammad Bilal, Mushtaq Ahmed, Saranjam Khan, 2017, Applied spectroscopy.

Demonstrating the application of Raman spectroscopy together with chemometric technique for screening of asthma disease.

C. Krafft, Saranjam Khan, R. Ullah, 2019, Biomedical optics express.

A homozygous missense mutation in SLC25A16 associated with autosomal recessive isolated fingernail dysplasia in a Pakistani family

D. Nickerson, S. Leal, M. Bamshad, 2018, The British journal of dermatology.

Restoration of IL-11 and IL-15 cytokine production post calcium modulators and ROS treatment can assist viral clearance both in vitro and in vivo

A. Javed, Asim Waris, S. Shahzad, 2023, Iranian journal of basic medical sciences.

Structural and functional insights into a novel homozygous missense pathogenic variant in CUL7 identified in consanguineous Pakistani family.

S. Siddiqi, S. Shahzad, J. Foo, 2023, Journal of biomolecular structure & dynamics.

An intrafamilial phenotypic variability in Ellis‐Van Creveld syndrome due to a novel 27 bps deletion mutation

S. Basit, A. Gul, S. Shahzad, 2021, American journal of medical genetics. Part A.

Antiviral Pills against SARS-CoV-2 Virus to Combat Future Epidemic Threats in Pakistan

S. Shahzad, Ayesha Khan, Hadia Batool, 2023, Proceedings of the Pakistan Academy of Sciences: B. Life and Environmental Sciences.

Exome sequencing revealed a novel nonsense variant in ALX3 gene underlying frontorhiny

S. Basit, W. Ahmad, Muhammad Umair, 2017, Journal of Human Genetics.

Characterization and applications of glutaminase free L-asparaginase from indigenous Bacillus halotolerans ASN9

Imran Afzal, A. Yasmin, S. Shahzad, 2023, PloS one.

Efficient Production, Purification and Characterization of Therapeutically Significant L-Asparaginase from Bacillus licheniformis ASN51

A. Yasmin, S. Shahzad, W. Al-Megrin, 2023, Polish Journal of Environmental Studies.

A homozygous missense mutation in SLC25A16 associated with autosomal recessive isolated fingernail dysplasia in a Pakistani family

D. Nickerson, R. Santos-Cortez, S. Shahzad, 2018, The British journal of dermatology.