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Human Molecular Genetics|November 29, 2015
Fine mapping of meiotic NAHR-associated crossovers causing large NF1 deletionsMorten Hillmer, David Wagner, Anna Summerer, et al.Personalized Medicine|May 13, 2018
Critical appraisal of the views of healthcare professionals with respect to pharmacogenomics and personalized medicine in GreeceYuan Mai, Christina Mitropoulou, Xanthi E Papadopoulou, et al.Journal of Experimental Zoology. Part B, Molecular and Developmental Evolution|July 31, 2020
Linking gene expression and phenotypic changes in the developmental and evolutionary origins of osteosclerosis in the ribs of bowhead whales (Balaena mysticetus)Lisa N Cooper, Hope C Ball, Christopher J Vinyard, et al.Molecular Cancer Research : MCR|July 16, 2003
Telomerase can extend the proliferative capacity of human myoblasts, but does not lead to their immortalizationSilvia Di Donna, Kamel Mamchaoui, Racquel N Cooper, et al.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 1, 1993
A Gla domain mutation (Arg 15-->Trp) in the protein C (PROC) gene causing type 2 protein C deficiency and recurrent venous thrombosisD S Millar, C B Grundy, P Bignell, et al.British Journal of Haematology|November 1, 1993
A novel dysfunctional protein C (protein C Padua 2) associated with a thrombotic tendency: substitution of Cys for Arg-1 results in a strongly reduced affinity for binding of Ca++A Girolami, P Simioni, B Girolami, et al.Journal of Biopharmaceutical Statistics|October 19, 2012
Bayesian continual reassessment method for dose-finding trials infusing T cells with limited sample sizeYuan Ji, Lei Feng, Ping Liu, et al.BMC Pediatrics|July 1, 2023
Health service utilisation for acute respiratory infections in infants graduating from the neonatal intensive care unit: a population-based cohort studyPaul G Stevenson, Matthew N Cooper, Wesley Billingham, et al.Human Molecular Genetics|December 3, 2003
An association between variants in the IGF2 gene and Beckwith-Wiedemann syndrome: interaction between genotype and epigenotypeAdele Murrell, Sarah Heeson, Wendy N Cooper, et al.Genome Research|September 6, 2005
Independent intrachromosomal recombination events underlie the pericentric inversions of chimpanzee and gorilla chromosomes homologous to human chromosome 16Violaine Goidts, Justyna M Szamalek, Pieter J de Jong, et al.Pageof 125