Author details

Full Name

Dejan Lazarevic

Affiliation

ORCID

Career Start Year

1996

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36792589	Harnessing the reverse cholesterol transport pathway to favor differentiation of monocyte-derived APCs and antitumor responses.		2023
36260368	Mutations in MYO9B are associated with Charcot-Marie-Tooth disease type 2 neuropathies and isolated optic atrophy.	Eur J Neurol	2023
37823593	PML modulates epigenetic composition of chromatin to regulate expression of pro-metastatic genes in triple-negative breast cancer.		2023
37399271	Revealing and harnessing CD39 for the treatment of colorectal cancer and liver metastases by engineered T cells.		2023
37077538	Enhancing clinical potential of liquid biopsy through a multi-omic approach: A systematic review.		2023
37000619	Analyzing genomic and epigenetic profiles in single cells by hybrid transposase (scGET-seq).		2023
34635836	Chromatin Velocity reveals epigenetic dynamics by single-cell profiling of heterochromatin and euchromatin.	Nat Biotechnol	2022
35439174	Longitudinal analysis of T cell receptor repertoires reveals shared patterns of antigen-specific response to SARS-CoV-2 infection.	JCI Insight	2022
36138183	Cellular and transcriptional dynamics of human neutrophils at steady state and upon stress.	Nat Immunol	2022
36699457	The frequency of somatic mutations in cancer predicts the phenotypic relevance of germline mutations.		2022
36553660	A Whole-Genome Sequencing Study Implicates GRAMD1B in Multiple Sclerosis Susceptibility.	Genes (Basel)	2022
35280651	Radiomic and gEnomic approaches for the enhanced DIagnosis of clear cell REnal Cancer (REDIRECt): a translational pilot methodological study.	Transl Androl Urol	2022
34976437	Time-controlled and muscle-specific CRISPR/Cas9-mediated deletion of CTG-repeat expansion in the gene.	Molecular Therapy - Nucleic Acids	2022
35267633	High-Throughput Monoclonal Antibody Discovery from Phage Libraries: Challenging the Current Preclinical Pipeline to Keep the Pace with the Increasing mAb Demand.	Cancers	2022
35215992	Rapid SARS-CoV-2 Intra-Host and Within-Household Emergence of Novel Haplotypes.	Viruses	2022
34577784	Gene Expression Analysis in Patients with Cocaine-Induced Midline Destructive Lesions.	Medicina (Lithuania)	2021
34129840	A PGE-MEF2A axis enables context-dependent control of inflammatory gene expression.	Immunity	2021
33991750	Identification of differential DNA methylation associated with multiple sclerosis: A family-based study.	J Neuroimmunol	2021
34323407	Plasmatic and myocardial microRNA profiles in patients with Hypertrophic Cardiomyopathy.	Clinical and Translational Medicine	2021
33246884	Transcriptional dynamics of induced pluripotent stem cell differentiation into Î² cells reveals full endodermal commitment and homology with human islets.	Cytotherapy	2021
32583022	Identification of novel genetic variants associated with short stature in a Baka Pygmies population.	Human Genetics	2020
31851094	MSH6 gene pathogenic variant identified in familial pancreatic cancer in the absence of colon cancer.	European Journal of Gastroenterology and Hepatology	2020
32601433	Efficient gene editing of human long-term hematopoietic stem cells validated by clonal tracking.	Nat Biotechnol	2020
31214169	Corrigendum: Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies.	Frontiers in Immunology	2019
30629636	A novel truncating variant of GLI2 associated with Culler-Jones syndrome impairs Hedgehog signalling.	PLoS One	2019
30925779	Integrated Somatic and Germline Whole-Exome Sequencing Analysis in Women with Lung Cancer after a Previous Breast Cancer.	Cancers	2019
31031743	Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies.	Frontiers in Immunology	2019
31167812	Expanding the spectrum of genes responsible for hereditary motor neuropathies.	Journal of Neurology, Neurosurgery and Psychiatry	2019
30911134	Immune signature drives leukemia escape and relapse after hematopoietic cell transplantation.	Nat Med	2019
31406136	Autosomal Dominant Tubulointerstitial Kidney Disease with Adult Onset due to a Novel Renin Mutation Mapping in the Mature Protein.	Scientific Reports	2019
29725010	A retinoic acid-dependent stroma-leukemia crosstalk promotes chronic lymphocytic leukemia progression.	Nat Commun	2018
29396481	Conserved DNA Methylation Signatures in Early Maternal Separation and in Twins Discordant for CO Sensitivity.	Scientific Reports	2018
29499100	A CD8Î±- Subset of CD4+SLAMF7+ Cytotoxic T Cells Is Expanded in Patients With IgG4-Related Disease and Decreases Following Glucocorticoid Treatment.	Arthritis and Rheumatology	2018
27770395	Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection.	J Clin Immunol	2017
28667090	Lentiviral vectors escape innate sensing but trigger p53 in human hematopoietic stem and progenitor cells.	EMBO Mol Med	2017
28437467	Mutant uromodulin expression leads to altered homeostasis of the endoplasmic reticulum and activates the unfolded protein response.	PLoS ONE	2017
26732860	The case of an APDS patient: Defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment.	Clin Immunol	2017
27902597	Whole exome sequencing of independent lung adenocarcinoma, lung squamous cell carcinoma, and malignant peritoneal mesothelioma: A case report.	Medicine (United States)	2016
25652421	Broadening of cohesinopathies: exome sequencing identifies mutations in ANKRD11 in two patients with Cornelia de Lange-overlapping phenotype.	Clin Genet	2016
27113846	A novel genomic inversion in Wiskott-Aldrich-associated autoinflammation.	Journal of Allergy and Clinical Immunology	2016
26844700	MicroRNA-222 regulates muscle alternative splicing through Rbm24 during differentiation of skeletal muscle cells.	Cell Death and Disease	2016
27019695	Chromas from chromatin: sonification of the epigenome.	F1000Research	2016
26876171	Targeting Macrophages Sensitizes Chronic Lymphocytic Leukemia to Apoptosis and Inhibits Disease Progression.	Cell Reports	2016
27578032	Performance comparison of two commercial human whole-exome capture systems on formalin-fixed paraffin-embedded lung adenocarcinoma samples.	BMC Cancer	2016
27801678	Histone demethylase JARID1C inactivation triggers genomic instability in sporadic renal cancer.	J Clin Invest	2016
27717396	Viable phenotype of ILNEB syndrome without nephrotic impairment in siblings heterozygous for unreported integrin alpha3 mutations.	Orphanet Journal of Rare Diseases	2016
26617488	REST-Governed Gene Expression Profiling in a Neuronal Cell Model Reveals Novel Direct and Indirect Processes of Repression and Up-Regulation.	Front Cell Neurosci	2015
25925570	The ribonuclease DIS3 promotes let-7 miRNA maturation by degrading the pluripotency factor LIN28B mRNA.	Nucleic Acids Research	2015
25578394	Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns: A pilot study.	Clin Chim Acta	2015
25389151	Mycobacterium celeriflavum sp. nov., a rapidly growing scotochromogenic bacterium isolated from clinical specimens.	International Journal of Systematic and Evolutionary Microbiology	2015