750(top 15%)
articles
35K(top 9%)
citations
281(top 10%)
★★ articles
13(top 8%)
★★★ articles
3.6(top 8%)
Avg IF
100(top 7%)
H-Index
153(top 8%)
G-Index
151
journals

Most Cited Articles of Wessex Regional Genetics Laboratory

TitleJournalYearCitations
Molecular and chromosomal mechanisms of resistance to imatinib (STI571) therapyLeukemia2002769
Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disordersBlood2005706
Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomasNature Genetics2013686
Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive functionNature1997606
Mutations and prognosis in primary myelofibrosisLeukemia2013520
Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsyNature Genetics1998440
Aberrations of EZH2 in cancerClinical Cancer Research2011422
Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57Nature Genetics2008417
BCR-ABL kinase domain mutation analysis in chronic myeloid leukemia patients treated with tyrosine kinase inhibitors: recommendations from an expert panel on behalf of European LeukemiaNetBlood2011395
Frequent CBL mutations associated with 11q acquired uniparental disomy in myeloproliferative neoplasmsBlood2009321
JAK2 haplotype is a major risk factor for the development of myeloproliferative neoplasmsNature Genetics2009320
Minimal residual disease assessed by multiparameter flow cytometry in multiple myeloma: impact on outcome in the Medical Research Council Myeloma IX StudyJournal of Clinical Oncology2013313
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilitiesGenetics in Medicine2011306
Expansion of the fragile X CGG repeat in females with premutation or intermediate allelesAmerican Journal of Human Genetics2003294
Standardized definitions of molecular response in chronic myeloid leukemiaLeukemia2012293
Extensive normal copy number variation of a beta-defensin antimicrobial-gene clusterAmerican Journal of Human Genetics2003285
Age- and tissue-specific variation of X chromosome inactivation ratios in normal womenHuman Genetics2000281
Recurrent SETBP1 mutations in atypical chronic myeloid leukemiaNature Genetics2013272
The role of maintenance thalidomide therapy in multiple myeloma: MRC Myeloma IX results and meta-analysisBlood2012270
A novel prognostic model in myeloma based on co-segregating adverse FISH lesions and the ISS: analysis of patients treated in the MRC Myeloma IX trialLeukemia2012236
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcomeJournal of Medical Genetics2009226
Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of bandingJournal of Medical Genetics1992219
EZH2 mutational status predicts poor survival in myelofibrosisBlood2011204
Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathwaysAmerican Journal of Human Genetics2008198
Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort studyLancet Oncology, The2011197