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JAMA Network Open|May 26, 2021
Assessment of the Implementation of Pharmacogenomic Testing in a Pediatric Tertiary Care SettingIris Cohn, Roozbeh Manshaei, Eriskay Liston, et al.
Infection|March 30, 2013
Delay in the administration of appropriate antimicrobial therapy in Staphylococcus aureus bloodstream infection: a prospective multicenter hospital-based cohort studyA J Kaasch, S Rieg, J Kuetscher, et al.
Circulation. Genomic and Precision Medicine|July 30, 2021
Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of FallotMiriam S Reuter, Rajiv R Chaturvedi, Rebekah K Jobling, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|August 17, 2016
Prospective Analyses of Circulating B Cell Subsets in ABO-Compatible and ABO-Incompatible Kidney Transplant RecipientsH A Schlößer, M Thelen, G Dieplinger, et al.
European Journal of Human Genetics : EJHG|February 18, 2018
Periodic reanalysis of whole-genome sequencing data enhances the diagnostic advantage over standard clinical genetic testingGregory Costain, Rebekah Jobling, Susan Walker, et al.
Infection|April 13, 2016
Strategies to enhance rational use of antibiotics in hospital: a guideline by the German Society for Infectious DiseasesK de With, F Allerberger, S Amann, et al.
Human Genetics|March 12, 2014
Expanding the clinical and mutational spectrum of Kaufman oculocerebrofacial syndrome with biallelic UBE3B mutationsLina Basel-Vanagaite, Rüstem Yilmaz, Sha Tang, et al.
Human Genetics|November 15, 2022
SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencingQiliang Ding, Cherith Somerville, Roozbeh Manshaei, et al.
Leukemia|July 1, 2017
An atlas of bloodstream-accessible bone marrow proteins for site-directed therapy of acute myeloid leukemiaL Angenendt, S Reuter, D Kentrup, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 21, 2018
Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of FallotMiriam S Reuter, Rebekah Jobling, Rajiv R Chaturvedi, et al.
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