LINKING PROTEOME AND GENOME FOR BIOMARKER DISCOVERY IN CLL-ESTABLISHMENT OF A CLL PROTEIN DATABASE

N Kitteringham , P Hillmen , A Pettitt , M Oates
Haematologica 101 420 -421

2016
Atypical congenital dyserythropoietic anaemia: a novel mutation in LPIN2 causes Majeed syndrome with incomplete penetrance

S McGowan , D Ferguson , G Hall , D Roberts
British Journal of Haematology 161 11 -11

2013
JUVENILE HAEMOCHROMATOSIS MUTATIONS ARE NOT THAT SIMPLE

K Robson , P Bignell , A Schuh
American Journal of Hematology 88

2013
COMPREHENSIVE GENETIC TESTING IS REQUIRED FOR PATIENTS WITH UNEXPLAINED IRON OVERLOAD

A Merryweather-Clarke , K Robson , P Bignell , A Schuh
American Journal of Hematology 88

2013
NOVEL GENE DELETIONS RESULT IN HAEMOCHROMATOSIS

S Knight , K Robson , P Bignell , A Schuh
American Journal of Hematology 88

2013
ESTIMATING DISEASE PENETRANCE IN P.C282Y HOMOZYGOTES IN THE UK

A Merryweather-Clarke , K Robson , P Bignell , A Schuh
American Journal of Hematology 88

2013
A NOVEL TMPRSS6 MUTATION IN 2 BULGARIAN SIBLINGS

K Robson , P Bignell , A Schuh , M Sheikh
American Journal of Hematology 88

2013
A GENOMEWIDE ASSOCIATION STUDY IDENTIFIES NOVEL LOCI THAT PREDISPOSE TO MYELOPROLIFERATIVE NEOPLASMS

P Guglielmelli , R Kralovics , K Zoi , D Oscier
Haematologica 98 221 -222

2013
Two unusual cases of type 2N von Willebrand disease

N Curry , J Beavis , S Henderson , A Schuh
Journal of Thrombosis and Haemostasis 13 738 -738

2015
The use of next-generation sequencing to screen for disorders of coagulation using a 24 gene panel

D Keeling , N Curry , P Giangrande , J Mason
Journal of Thrombosis and Haemostasis 13 499 -500

2015
Understanding the cellular function of SAMHD1: from HIV restriction to tumor suppression

Lin Y-L. , Judde J-G. , P Pasero , T Louis
FEBS Journal 281 768 -768

2014