Publications Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. Nature genetics 44 (5), 491. GWAS ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology. Acta neuropathologica 127 (6), 825-843. Large common deletions associate with mortality at old age. Human molecular genetics 20 (21), 4290-4296. A genome-wide copy number association study of osteoporotic fractures points to the 6p25. 1 locus. Journal of medical genetics, jmedgenet-2013-102064. Targeted sequencing of genome wide significant loci associated with bone mineral density (BMD) reveals significant novel and rare variants: the Cohorts for Heart and Aging. Human molecular genetics 25 (23), 5234-5243. On family-based genome-wide association studies with large pedigrees: observations and recommendations. BMC proceedings 8 (1), S26. Mihajlovic, A., Machine Learning-Based Imputation of Missing SNP Genotypes in SNP Genotype Arrays, ISBN 9781461487852, 2013, Computational Medicine in Data Mining and Modeling, Springer New York Prevalence of pathogenic mutations in cancer predisposition genes among pancreatic cancer patients. Cancer Epidemiology and Prevention Biomarkers. R&D NGS The association of glioma germline risk SNPs with mutation-based molecular subgroups. Cancer Research 74 (19 Supplement), 4714-4714. Clarke, D, et. al., Playbook Workflow Builder: Interactive Construction of Bioinformatics Workflows from a Network of Microservices, 2024, Cold Spring Harbor Laboratory. Constellation: A secure self-optimizing framework for genomic processing. e-Health Networking, Applications and Services (Healthcom), 2016 IEEE 18th ... Clinical NGS Lau, J.W., Lehnert E., et. al., The Cancer Genomics Cloud: Collaborative, Reproducible, and Democratized—A New Paradigm in Large-Scale Computational Research, ISSN 1538-7445, DOI 10.1158/0008-5472.can-17-0387, 2017, Cancer Research, American Association for Cancer Research (AACR) Mihajlovic A., AI and its Involvement in the Future of Neoantigen Discovery, 2020, Innovations in Pharmaceutical Technology Bioinformatics Strategies for Identifying Regions of Epigenetic Deregulation Associated with Aberrant Transcript Splicing and RNA-editing. Bioinformatics, 163-170. Bulk RNA-seq Leong P, Mihajlović A, Xi L, et. Al., Reconstructing and counting genomic fragments through tagmentation-based haploid phasing, volume 11, ISSN=2045-2322, September 2021, Nature Scientific Reports, Springer Science and Business Media LLC scRNA-seq Long P, Mihajlovic A., Xi L, Preparing Single-cell DNA Library Using Nextera for Detection of CNV, ISSN 2331-8325, DOI 10.21769/bioprotoc.3175, 2019, BIO-PROTOCOL
