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Articles
exaly
›
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Wessex Regional Genetics Laboratory
›
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 in 2013
Title
Journal
Year
Citations
Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas
Nature Genetics
2013
686
Mutations and prognosis in primary myelofibrosis
Leukemia
2013
520
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
Recurrent SETBP1 mutations in atypical chronic myeloid leukemia
Nature Genetics
2013
272
Comprehensive mutational profiling in advanced systemic mastocytosis
Blood
2013
183
The clinical significance of NOTCH1 and SF3B1 mutations in the UK LRF CLL4 trial
Blood
2013
167
Long-term follow-up of MRC Myeloma IX trial: Survival outcomes with bisphosphonate and thalidomide treatment
Clinical Cancer Research
2013
116
The clinical utility of microarray technologies applied to prenatal cytogenetics in the presence of a normal conventional karyotype: a review of the literature
Prenatal Diagnosis
2013
109
The clinical implementation of non-invasive prenatal diagnosis for single-gene disorders: challenges and progress made
Prenatal Diagnosis
2013
101
Characterization of IGH locus breakpoints in multiple myeloma indicates a subset of translocations appear to occur in pregerminal center B cells
Blood
2013
101
Establishing optimal quantitative-polymerase chain reaction assays for routine diagnosis and tracking of minimal residual disease in JAK2-V617F-associated myeloproliferative neoplasms: a joint European LeukemiaNet/MPN&MPNr-EuroNet (COST action BM0902) study
Leukemia
2013
78
Ponatinib as targeted therapy for FGFR1 fusions associated with the 8p11 myeloproliferative syndrome
Haematologica
2013
60
Transient neonatal diabetes, ZFP57, and hypomethylation of multiple imprinted loci: a detailed follow-up
Diabetes Care
2013
48
Long-term follow-up of treatment with imatinib in eosinophilia-associated myeloid/lymphoid neoplasms with PDGFR rearrangements in blast phase
Leukemia
2013
46
Inherited predisposition to myeloproliferative neoplasms
Therapeutic Advances in Hematology
2013
40
Aberrant DNA methylation profile of chronic and transformed classic Philadelphia-negative myeloproliferative neoplasms
Haematologica
2013
37
8p23.1 duplication syndrome; common, confirmed, and novel features in six further patients
American Journal of Medical Genetics, Part A
2013
32
A TC classification-based predictor for multiple myeloma using multiplexed real-time quantitative PCR
Leukemia
2013
31
Next generation diagnostics in inherited arrhythmia syndromes : a comparison of two approaches
Journal of Cardiovascular Translational Research
2013
28
16p11.2-p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2
European Journal of Human Genetics
2013
28
Detailed clinical and molecular study of 20 females with Xq deletions with special reference to menstruation and fertility
European Journal of Medical Genetics
2013
26
Ruxolitinib as potential targeted therapy for patients with JAK2 rearrangements
Haematologica
2013
26
Diagnostic screening identifies a wide range of mutations involving the SHOX gene, including a common 47.5 kb deletion 160 kb downstream with a variable phenotypic effect
American Journal of Medical Genetics, Part A
2013
25
A comparison of methods for EGFR mutation testing in non-small cell lung cancer
Diagnostic Molecular Pathology
2013
22
JAK2V617F allele burden, JAK2 46/1 haplotype and clinical features of Chinese with myeloproliferative neoplasms
Leukemia
2013
20
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