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Publications:  Mr Michael Mueller

Afzali B, Grönholm J, Vandrovcova J, O'Brien C, Sun HW, Vanderleyden I, Davis FP, Khoder A et al.(2017). BACH2 immunodeficiency illustrates an association between super-enhancers and haploinsufficiency. Nature Immunology vol. 18, (7) 813-823.
10.1038/ni.3753
https://qmro.qmul.ac.uk/xmlui/handle/123456789/32047
Alikian M, Ellery P, Forbes M, Gerrard G, Kasperaviciute D, Sosinsky A, Mueller M, Whale AS et al.(2016). Next-Generation Sequencing-Assisted DNA-Based Digital PCR for a Personalized Approach to the Detection and Quantification of Residual Disease in Chronic Myeloid Leukemia Patients. Journal of Molecular Diagnostics vol. 18, (2) 176-189.
10.1016/j.jmoldx.2015.09.005
Wilkins MR, Aldashev AA, Wharton J, Rhodes CJ, Vandrovcova J, Kasperaviciute D, Bhosle SG, Mueller M et al.(2014). α1-A680T variant in GUCY1A3 as a candidate conferring protection from pulmonary hypertension among kyrgyz highlanders. Circulation: Cardiovascular Genetics vol. 7, (6) 920-929.
10.1161/CIRCGENETICS.114.000763
Vandrovcova J, Thomas ERA, Atanur SS, Norsworthy PJ, Neuwirth C, Tan Y, Kasperaviciute D, Biggs J et al.(2013). The use of next-generation sequencing in clinical diagnosis of familial hypercholesterolemia. Genetics in Medicine vol. 15, (12) 948-957.
10.1038/gim.2013.55
Gerrard G, Valgañón M, Foong HE, Kasperaviciute D, Iskander D, Game L, Müller M, Aitman TJ et al.(2013). Target enrichment and high-throughput sequencing of 80 ribosomal protein genes to identify mutations associated with Diamond-Blackfan anaemia. British Journal of Haematology vol. 162, (4) 530-536.
10.1111/bjh.12397
Gerrard G, Valganon M, Foong HE, Kasperaviciute D, Mueller M, Game L, Iskander D, Roberts I et al. (2012). Target Enrichment and High-Throughput Sequencing of 80 Ribosomal Protein Genes to Identify Mutations Associated with Diamond-Blackfan Anaemia. BLOOD. vol. 120,
10.1182/blood.V120.21.2369.2369
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