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exaly
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Wessex Regional Genetics Laboratory
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Top Articles
Wessex Regional Genetics Laboratory
United Kingdom
()
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
Title
Journal
Year
Citations
Molecular and chromosomal mechanisms of resistance to imatinib (STI571) therapy
Leukemia
2002
769
Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders
Blood
2005
706
Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas
Nature Genetics
2013
686
Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function
Nature
1997
606
Mutations and prognosis in primary myelofibrosis
Leukemia
2013
520
Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy
Nature Genetics
1998
440
Aberrations of EZH2 in cancer
Clinical Cancer Research
2011
422
Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57
Nature Genetics
2008
417
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 LeukemiaNet
Blood
2011
395
Frequent CBL mutations associated with 11q acquired uniparental disomy in myeloproliferative neoplasms
Blood
2009
321
JAK2 haplotype is a major risk factor for the development of myeloproliferative neoplasms
Nature Genetics
2009
320
Minimal residual disease assessed by multiparameter flow cytometry in multiple myeloma: impact on outcome in the Medical Research Council Myeloma IX Study
Journal of Clinical Oncology
2013
313
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities
Genetics in Medicine
2011
306
Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles
American Journal of Human Genetics
2003
294
Standardized definitions of molecular response in chronic myeloid leukemia
Leukemia
2012
293
Extensive normal copy number variation of a beta-defensin antimicrobial-gene cluster
American Journal of Human Genetics
2003
285
Age- and tissue-specific variation of X chromosome inactivation ratios in normal women
Human Genetics
2000
281
Recurrent SETBP1 mutations in atypical chronic myeloid leukemia
Nature Genetics
2013
272
The role of maintenance thalidomide therapy in multiple myeloma: MRC Myeloma IX results and meta-analysis
Blood
2012
270
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 trial
Leukemia
2012
236
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome
Journal of Medical Genetics
2009
226
Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding
Journal of Medical Genetics
1992
219
EZH2 mutational status predicts poor survival in myelofibrosis
Blood
2011
204
Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathways
American Journal of Human Genetics
2008
198
Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study
Lancet Oncology, The
2011
197
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