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_data/research-publications.csv

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 title,first_author,publication_name,publication_year,doi,pmid,publication_link,open_access,full_text_available,preprint_available,preprint_link
+scSNV-seq: high-throughput phenotyping of single nucleotide variants by coupled single-cell genotyping and transcriptomics,"Cooper, SE., Coelho, MA., Strauss, ME., et al.",Genome Biology,2024,10.1186/s13059-024-03169-y,38225637,https://genomebiology.biomedcentral.com/articles/10.1186/s13059-024-03169-y,TRUE,TRUE,,
+A comprehensive clinically informed map of dependencies in cancer cells and framework for target prioritization,"Pacini, C et al.",Cancer Cell,2024,10.1016/j.ccell.2023.12.016,38215750,https://www.cell.com/cancer-cell/fulltext/S1535-6108(23)00444-0,TRUE,TRUE,,
 An Alzheimer's disease-associated common regulatory variant in PTK2B has causal effects on microglial function,"Bello, E. et al.",bioRxiv,2023,10.1101/2023.11.04.565613,,https://www.biorxiv.org/content/10.1101/2023.11.04.565613v1,,TRUE,TRUE,https://www.biorxiv.org/content/10.1101/2023.11.04.565613v1
 Integrative GWAS and co-localisation analysis suggests novel genes associated with age-related multimorbidity,"West, C. et al. ",Scientific Data,2023,10.1038/s41597-023-02513-4,37749083,https://www.nature.com/articles/s41597-023-02513-4,TRUE,TRUE,,
 "eQTL Catalogue 2023: New datasets, X chromosome QTLs, and improved detection and visualisation of transcript-level QTLs","Kerimov, N et al.",PLOS Genetics,2023,10.1371/journal.pgen.1010932,37721944,https://journals.plos.org/plosgenetics/article?id=10.1371/journal.pgen.1010932,TRUE,TRUE,,