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Frontiers in Endocrinology|February 21, 2022
Case Report: Phenotype-Gene Correlation in a Case of Novel Tandem 4q Microduplication With Short Stature, Speech Delay and MicrocephalyUmm-Kulthum Ismail Umlai, Basma Haris, Khalid Hussain, et al.Briefings in Bioinformatics|September 9, 2021
Genome sequencing data analysis for rare disease gene discoveryUmm-Kulthum Ismail Umlai, Dhinoth Kumar Bangarusamy, Xavier Estivill, et al.Journal of Clinical Research in Pediatric Endocrinology|February 2, 2023
Severe Growth Hormone Deficiency in an Indian Boy Caused by a Novel 6 kb Homozygous Deletion Spanning the <i>GH1</i> GeneBasma Haris, Idris Mohammed, Umm-Kulthum Ismail Umlai, et al.Frontiers in Nutrition|October 16, 2023
Genetic determinants of Vitamin D deficiency in the Middle Eastern Qatari population: a genome-wide association studyNagham Nafiz Hendi, Yasser Al-Sarraj, Umm-Kulthum Ismail Umlai, et al.Diabetes, Obesity & Metabolism|June 5, 2025
Genetic risk and polygenic risk score assessment of prediabetes and progression to type 2 diabetesUsama Aliyu, Umm-Kulthum Ismail Umlai, Nayra M Al-Thani, et al.BMC Medical Genomics|April 29, 2024
Genome-wide association study and trans-ethnic meta-analysis identify novel susceptibility loci for type 2 diabetes mellitusAsma A Elashi, Salman M Toor, Umm-Kulthum Ismail Umlai, et al.Frontiers in Endocrinology|June 28, 2024
Genome-wide association study and polygenic score assessment of insulin resistanceUsama Aliyu, Umm-Kulthum Ismail Umlai, Salman M Toor, et al.Journal of Lipid Research|February 5, 2025
A multi-ancestry genome-wide association study and evaluation of polygenic scores of LDL-C levelsUmm-Kulthum Ismail Umlai, Salman M Toor, Yasser A Al-Sarraj, et al.Pageof 1