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Science Advances|October 13, 2021
Copy-scAT: Deconvoluting single-cell chromatin accessibility of genetic subclones in cancerAna Nikolic, Divya Singhal, Katrina Ellestad, et al.Cell Reports|July 3, 2026
Glioblastoma stem cell growth requires DOT1L-MED23 control of enhancer accessibilitySamir Assaf, Danielle A Bozek, Kyle Heemskerk, et al.Journal of the Peripheral Nervous System : JPNS|January 24, 2018
Neuromuscular disease-specific questionnaire to assess quality of life in patients with chronic inflammatory demyelinating polyradiculoneuropathyAleksandra Kacar, Bogdan Bjelica, Ivo Bozovic, et al.Neuromuscular Disorders : NMD|November 6, 2017
Early onset facioscapulohumeral dystrophy - a systematic review using individual patient dataRianne J M Goselink, Nicol C Voermans, Kees Okkersen, et al.Biorxiv : the Preprint Server for Biology|June 4, 2025
Spatial epigenomic niches underlie glioblastoma cell state plasticitySam Kint, Subhi Talal Younes, Shuozhen Bao, et al.Journal of Neurology|April 30, 2016
A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypesGiulia Ricci, Lucia Ruggiero, Liliana Vercelli, et al.Genome Research|June 29, 2019
High-resolution structural genomics reveals new therapeutic vulnerabilities in glioblastomaMichael J Johnston, Ana Nikolic, Nicoletta Ninkovic, et al.BMJ Open|January 7, 2016
Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1-3 D4Z4 reduced alleles: experience of the FSHD Italian National RegistryAna Nikolic, Giulia Ricci, Francesco Sera, et al.Brain : a Journal of Neurology|September 14, 2013
Large scale genotype-phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophyGiulia Ricci, Isabella Scionti, Francesco Sera, et al.Elife|January 11, 2021
Single-cell chromatin accessibility profiling of glioblastoma identifies an invasive cancer stem cell population associated with lower survivalPaul Guilhamon, Charles Chesnelong, Michelle M Kushida, et al.Pageof 5