1.
Development of the EUCAST disk diffusion antimicrobial susceptibility testing method and its implementation in routine microbiology laboratories
by Matuschek, E
Clinical microbiology and infection, 2014, Vol.20 (4), p.O255-O266

2.
EUCAST expert rules in antimicrobial susceptibility testing
by Leclercq, R
Clinical microbiology and infection, 2013, Vol.19 (2), p.141-160

3.
Precise detection of chromosomal translocation or inversion breakpoints by whole-genome sequencing
by Suzuki, Toshifumi
Journal of human genetics, 2014, Vol.59 (12), p.649-654

4.
Breakpoint mapping by next generation sequencing reveals causative gene disruption in patients carrying apparently balanced chromosome rearrangements with intellectual deficiency a...
by Schluth-Bolard, Caroline
Journal of medical genetics, 2013, Vol.50 (3), p.144-150

5.
EUCAST technical note on isavuconazole breakpoints for Aspergillus, itraconazole breakpoints for Candida and updates for the antifungal susceptibility testing method documents
by Arendrup, M.C
Clinical microbiology and infection, 2016, Vol.22 (6), p.571.e1-571.e4

6.
Near-full length genetic characterization of a novel HIV-1 unique recombinant with similarities to A1, CRF01_AE and CRFO2_AG viruses in Yaoundé, Cameroon
by Acharya, Arpan
AIDS research and human retroviruses, 2019, Vol.35 (ja), p.762-768

7.
Antimicrobial susceptibility of Bacteroides fragilis group isolates in Europe: 20years of experience
by Nagy, E
Clinical microbiology and infection, 2011, Vol.17 (3), p.371-379

8.
Breakpoint beware: reliance on historical breakpoints for Enterobacteriaceae leads to discrepancies in interpretation of susceptibility testing for carbapenems and cephalosporins a...
by Yarbrough, Melanie L
European journal of clinical microbiology & infectious diseases, 2019, Vol.39 (1), p.187-195

9.
Next-Generation Sequencing of Duplication CNVs Reveals that Most Are Tandem and Some Create Fusion Genes at Breakpoints
by Newman, Scott
American journal of human genetics, 2015, Vol.96 (2), p.208-220

10.
Precise mapping of 17 deletion breakpoints within the central hotspot deletion region (introns 50 and 51) of the DMD gene
by Esposito, Gabriella
Journal of human genetics, 2017, Vol.62 (12), p.1057-1063

11.
The role of pharmacokinetics/pharmacodynamics in setting clinical MIC breakpoints: the EUCAST approach
by Mouton, J.W
Clinical microbiology and infection, 2012, Vol.18 (3), p.E37-E45

12.
Reassessment of the evolution of wheat chromosomes 4A, 5A, and 7B
by Dvorak, Jan
Theoretical and applied genetics, 2018, Vol.131 (11), p.2451-2462

13.
Translocation breakpoint disrupting the host SNHG14 gene but not coding genes or snoRNAs in typical Prader-Willi syndrome
by Lei, Ming
Journal of human genetics, 2019, Vol.64 (7), p.647-652

14.
Antimicrobial susceptibility testing of Kingella kingae with broth microdilution and disk diffusion using EUCAST recommended media
by Matuschek, E
Clinical microbiology and infection, 2018, Vol.24 (4), p.396-401

15.
Copy-Number Variation Contributes to the Mutational Load of Bardet-Biedl Syndrome
by Lindstrand, Anna
American journal of human genetics, 2016, Vol.99 (2), p.318-336

16.
Identification of a novel HIV-1 unique CRF01_AE/C recombinant in Yan`an city, Shaanxi province
by Cheng, Si-Wei
AIDS research and human retroviruses, 2020, Vol.36 (ja), p.952-956

17.
Molecular characterization of HDAC8 deletions in individuals with atypical Cornelia de Lange syndrome
by Helgeson, Maria
Journal of human genetics, 2018, Vol.63 (3), p.349-356

18.
Assessment of 2q23.1 Microdeletion Syndrome Implicates MBD5 as a Single Causal Locus of Intellectual Disability, Epilepsy, and Autism Spectrum Disorder
by Talkowski, Michael E
American journal of human genetics, 2011, Vol.89 (4), p.551-563

19.
Carbapenemase-producing Klebsiella pneumoniae: (when) might we still consider treating with carbapenems?
by Daikos, G.L
Clinical microbiology and infection, 2011, Vol.17 (8), p.1135-1141

20.
Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature
by Lowther, Chelsea Chelsea
Genetics in medicine, 2014, Vol.17 (2), p.149-157
