PUBLICATIONS 

A. Research Articles  

1. Aman Ullah, Ranjha Khan, Muhammad Naeem. 2025. Ullah, A., Khan, R. & Naeem, M. A Homozygous IGHMBP2 Missense Variant Segregating in a Large Consanguineous Pakistani Family Affected with Autosomal Recessive Charcot–Marie–Tooth Disease Type 2S. Curr Genet Med Rep 13, 17 (2025). https://doi.org/10.1007/s40142-025-00229-y 

 2. Aman Ullah, Ranjha Khan, Muhammad Naeem. 2025. Whole Exome Sequencing in a Pakistani Family Affected with Demyelinating Hereditary Sensorimotor Polyneuropathy with Spinocerebellar Degeneration. Curr Genet Med Rep 13, 11 (2025). https://doi.org/10.1007/s40142-025-00219-0 

3. Aman Ullah, Sadaf Iftikhar. 2025. Whole Exome Sequencing Reveals Novel Genetic Mutations in the ADAM10 Underlying Familial Alzheimer’s Disease. Curr Genet Med Rep 13, 10 (2025). https://doi.org/10.1007/s40142-025-00220-7 

4. Aman Ullah, Bibi Zubaida, Huma Arshad Cheema and Muhammad Naeem. 2020. Identification of two novel variants in GAA underlying infantile-onset Pompe disease in two Pakistani families. Journal of Pediatric Endocrinology and Metabolism. Apr 28 33(4):553-556. DOI: https://doi.org/10.1515/jpem-2019-0477 

5. Aman Ullah, Ranjha Khan, Muhammad Naeem. 2019. Whole exome sequencing identified a heterozygous KCNJ2 missense variant underlying autosomal dominant familial hypokalemic periodic paralysis in a Pakistani family. Journal of Pediatric Endocrinology and Metabolism, 2019 Dec 18 32(12):1385-1389. DOI: https://doi.org/10.1515/jpem-2019-0276 

6. Noreen Karim, Aman Ullah, Ghulam Murtaza, and Muhammad Naeem. 2019. Molecular genetic study of a large inbred Pakistani family affected with autosomal recessive congenital ichthyosis through whole exome sequencing. Genetic Testing and Molecular Biomarkers. 23(6): 428-432. DOI: https://doi.org/10.1089/gtmb.2018.0310 

7. Muhammad Aman Khan, Aman Ullah, Muhammad Naeem. 2018. Whole exome sequencing identified two novel homozygous missense variants in the same codon of CLCN7 underlying autosomal recessive infantile malignant osteopetrosis in a Pakistani family. Molecular Biology Reports. 45: 565-570, 2018 DOI: https://doi.org/10.1007/s11033-018-4194-8 

8. Aman Ullah, Bushra Mirza, Zarrin Fatima, Muhammad Zia. 2016. Production of artemisinin and its derivatives in hairy roots of Artemisia dubia induced by rolA gene transformation. Pakistan Journal of Botany. 48(2): 699-706, ISSN: 0556-3321. URL: https://www.pakbs.org/pjbot/PDFs/48(2)/37.pdf 

B. Book(s) 

 1. Muhammad Nauman Aftab, Aman Ullah. Motifs of untranslated regions in C. elegans and C. briggsae: Identification of repeated nucleotide motifs in untranslated regions of C. elegans and C. briggsae. ISBN-10: 9783846500385, ISBN-13: 978-3846500385, ASIN: 3846500380. LAP LAMBERT Academic Publishing (September 16, 2011) 

C. Book Chapter(s) 

1. Ullah A. Perspective Chapter: Technological Advances in Population Genetics [Internet]. Advances and Trends in Population Genetics Studies [Working Title]. IntechOpen 2025. Available from: http://dx.doi.org/10.5772/intechopen.1009271