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USD 50 /hr
Hire Noor Ul Ain ..
Pakistan
USD 50 /hr

Molecular Biology & Genetics Expert | Sanger, NGS, Rare Disease Research & Diagnostic Test Development

Profile Summary
Subject Matter Expertise
Services
Writing Medical Writing, Non-Medical Regulatory Writing, Technical Writing, Creative Writing, General Proofreading & Editing, Translation
Research Scientific and Technical Research, Systematic Literature Review
Consulting Scientific and Technical Consulting
Data & AI Predictive Modeling, Data Processing
Product Development Recipe Development
Work Experience

Scientist II / Senior Scientist

IBGE

March 2017 - Present

Education

PhD (School of Biological Sciences)

University of the Punjab

2014 - 2022

MPhil

University of the Punjab

October 2011 - August 2013

M.Sc Biochemistry

PMAS Arid Agriculture University

October 2008 - August 2010

BSc

University of the Punjab

October 2005 - September 2008

Certifications

  • Medical Laboratory Scientist

    University of the Punjab

    October 2008 - Present

Publications
JOURNAL ARTICLE
Shakeel M, Irfan M, Nisa ZU, Farooq S, Ain NU, Iqbal W, Kakar N, Jahan S, Shahzad M, Siddiqi S, et al. (2022). Genome sequencing and analysis of genomic diversity in the locally transmitted SARS-CoV-2 in Pakistan . Transboundary and emerging diseases.
Shakeel, M., Irfan, M., Nisa, Z.U., Farooq, S., Ain, N.U., Iqbal, W., Kakar, N., Jahan, S., Shahzad, M., Siddiqi, S., et al.(2022). Genome sequencing and analysis of genomic diversity in the locally transmitted SARS-CoV-2 in Pakistan . Transboundary and Emerging Diseases. 69. (5). p. e2418-e2430.
Reilly, M.L., Ain, N.U., Muurinen, M., Tata, A., Huber, C., Simon, M., Ishaq, T., Shaw, N., Rusanen, S., Pekkinen, M., et al.(2022). Biallelic KIF24 Variants Are Responsible for a Spectrum of Skeletal Disorders Ranging From Lethal Skeletal Ciliopathy to Severe Acromesomelic Dysplasia . Journal of Bone and Mineral Research.
Kausar, M., Ain, N.U., Hayat, F., Fatima, H., Azim, S., Ullah, H., Mushtaq, M., Khalid, S., Hussain, S., Naz, S., et al.(2022). Biallelic variants in CHST3 cause Spondyloepiphyseal dysplasia with joint dislocations in three Pakistani kindreds . BMC Musculoskeletal Disorders. 23. (1).
Ain, N.U., Muhammad, N., Dianatpour, M., Baroncelli, M., Iqbal, M., Fard, M.A.F., Bukhari, I., Ahmed, S., Hajipour, M., Tabatabaie, Z., et al.(2021). Biallelic TMEM251 variants in patients with severe skeletal dysplasia and extreme short stature . Human Mutation. 42. (1). p. 89-101.
Nian, L., Zhang, X., Yi, X., Liu, X., Ain, N., Yang, Y., Li, X., Haider, F.U., Zhu, X.(2021). Genome-wide identification of ABA receptor PYL/RCAR gene family and their response to cold stress in Medicago sativa L . Physiology and Molecular Biology of Plants. 27. (9). p. 1979-1995.
Ain, N.U., Baroncelli, M., Costantini, A., Ishaq, T., Taylan, F., Nilsson, O., Mäkitie, O., Naz, S.(2021). Novel form of rhizomelic skeletal dysplasia associated with a homozygous variant in GNPNAT1 . Journal of Medical Genetics. 58. (5). p. 351-356.
Ain, N., Fatima, Z., Naz, S., Makitie, O.(2021). RAB33B and PCNT variants in two Pakistani families with skeletal dysplasia and short stature . BMC Musculoskeletal Disorders. 22. (1).
Noor ul Ain, Niaz Muhammad, Samina Yasin, Zunaira Fatima, Muhammad Faizan, Sadaf Naz(2021). The c.1138G>A Variant of Fibroblast Growth Factor Receptor 3 is a Common Cause of Achondroplasia in Pakistan . Pakistan Journal of Zoology. 53. (6). {ResearchersLinks} Ltd
Noor ul Ain, Madeline Louise Reilly, Mari Muurinen, Alice Tata, Céline Huber, Marleen Simon, Tayyaba Ishaq, Nick Shaw, Salla Rusanen, Minna Pekkinen, et al. (2020). Biallelic KIF24 Variants Are Responsible for a Spectrum of Skeletal Disorders Ranging From Lethal Skeletal Ciliopathy to Severe Acromesomelic Dysplasia . Journal of Bone and Mineral Research.
Ain, N.U., Abrar, S., Sherwani, R.A.K., Hannan, A., Imran, N., Riaz, S.(2020). Systematic surveillance and meta-analysis on the prevalence of metallo-β-lactamase producers among carbapenem resistant clinical isolates in Pakistan . Journal of Global Antimicrobial Resistance. 23. p. 55-63.
Ain, N.U., Iqbal, M., Valta, H., Emerling, C.A., Ahmed, S., Makitie, O., Naz, S.(2019). Novel variants in natriuretic peptide receptor 2 in unrelated patients with acromesomelic dysplasia type Maroteaux . European Journal of Medical Genetics. 62. (9).
Costantini A, Tournis S, Kämpe A, Ul Ain N, Taylan F, Doulgeraki A, Mäkitie O (2018). Autosomal Recessive Osteogenesis Imperfecta Caused by a Novel Homozygous COL1A2 Mutation . Calcified tissue international.
Ain, N.U., Makitie, O., Naz, S.(2018). Autosomal recessive chondrodysplasia with severe short stature caused by a biallelic COL10A1 variant . Journal of medical genetics. 55. (6). p. 403-407.
John, P., Bhatti, A., Ain, N.U., Iqbal, T., Sadaf, T., Malik, J.M.(2017). Case‐control study of vitamin D receptor gene polymorphism in Pakistani rheumatoid arthritis patients,Estudo caso‐controle do polimorfismo do gene receptor da vitamina D em pacientes paquistaneses com artrite reumatoide . Revista Brasileira de Reumatologia. 57. (6). p. 633-636.
Ramzan, M., Ain, N.U., Ilyas, S., Umer, M., Bano, S., Sarwar, S., Shahzad, N., Shakoori, A.R.(2015). A cornucopia of screening and diagnostic techniques for human papillomavirus associated cervical carcinomas . Journal of Virological Methods. 222. p. 192-201.