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.
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.
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.
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.
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.
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,