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Vincent P. Collins - Publications

Affiliations: 
University of Cambridge, Cambridge, England, United Kingdom 
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27 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2015 Gessi M, Engels AC, Lambert S, Rothämel T, von Hornstein S, Collins VP, Denkhaus D, Gnekow A, Pietsch T. Molecular characterization of disseminated pilocytic astrocytomas. Neuropathology and Applied Neurobiology. PMID 26084390 DOI: 10.1111/Nan.12256  0.362
2015 Piccirillo SG, Spiteri I, Sottoriva A, Touloumis A, Ber S, Price SJ, Heywood R, Francis NJ, Howarth KD, Collins VP, Venkitaraman AR, Curtis C, Marioni JC, Tavaré S, Watts C. Contributions to drug resistance in glioblastoma derived from malignant cells in the sub-ependymal zone. Cancer Research. 75: 194-202. PMID 25406193 DOI: 10.1158/0008-5472.Can-13-3131  0.302
2014 Collins VP, Ichimura K, Di Y, Pearson D, Chan R, Thompson LC, Gabe R, Brada M, Stenning SP. Prognostic and predictive markers in recurrent high grade glioma; results from the BR12 randomised trial. Acta Neuropathologica Communications. 2: 68. PMID 24952577 DOI: 10.1186/2051-5960-2-68  0.327
2013 Piccirillo SGM, Spiteri I, Sottoriva A, Touloumis A, Ber S, Price SJ, Heywood R, Francis N, Collins VP, Venkitaraman AR, Curtis C, Marioni JC, Tavare S, Watts C. Abstract 5016: The human sub-ependymal zone harbors glioblastoma precursors and represents a distinct therapeutic target. Cancer Research. 73: 5016-5016. DOI: 10.1158/1538-7445.Am2013-5016  0.333
2011 Cin H, Meyer C, Herr R, Janzarik W, Lambert S, Jones D, Jacob K, Benner A, Witt H, Remke M, Bender S, Falkenstein F, Anh TV, Olbrich H, Deimling Av, ... ... Collins V, et al. FAM131B-BRAF Fusion Gene Resulting From 7q34 Deletion Leads to MAPK Pathway Activation in Pilocytic Astrocytoma Klinische Padiatrie. 223. DOI: 10.1055/S-0031-1277077  0.336
2010 Kullar PJ, Pearson DM, Malley DS, Collins VP, Ichimura K. CpG island hypermethylation of the neurofibromatosis type 2 (NF2) gene is rare in sporadic vestibular schwannomas. Neuropathology and Applied Neurobiology. 36: 505-14. PMID 20831745 DOI: 10.1111/J.1365-2990.2010.01090.X  0.339
2010 Pohl U, Dean AF, Ichimura K, Liu L, Nicholson J, Cross J, Collins VP. Genomic analysis of chromosome 22 in synchronous and histologically distinct intracranial tumours in a child. Neuropathology and Applied Neurobiology. 36: 359-63. PMID 20345646 DOI: 10.1111/J.1365-2990.2010.01085.X  0.326
2009 Jones DT, Kocialkowski S, Liu L, Pearson DM, Ichimura K, Collins VP. Oncogenic RAF1 rearrangement and a novel BRAF mutation as alternatives to KIAA1549:BRAF fusion in activating the MAPK pathway in pilocytic astrocytoma. Oncogene. 28: 2119-23. PMID 19363522 DOI: 10.1038/Onc.2009.73  0.326
2009 Zeng N, Liu L, McCabe MG, Jones DT, Ichimura K, Collins VP. Real-time quantitative polymerase chain reaction (qPCR) analysis with fluorescence resonance energy transfer (FRET) probes reveals differential expression of the four ERBB4 juxtamembrane region variants between medulloblastoma and pilocytic astrocytoma. Neuropathology and Applied Neurobiology. 35: 353-66. PMID 19017278 DOI: 10.1111/J.1365-2990.2008.01001.X  0.307
2009 Chanudet E, Ye H, Ferry J, Bacon CM, Adam P, Müller-Hermelink HK, Radford J, Pileri SA, Ichimura K, Collins VP, Hamoudi RA, Nicholson AG, Wotherspoon AC, Isaacson PG, Du MQ. A20 deletion is associated with copy number gain at the TNFA/B/C locus and occurs preferentially in translocation-negative MALT lymphoma of the ocular adnexa and salivary glands. The Journal of Pathology. 217: 420-30. PMID 19006194 DOI: 10.1002/Path.2466  0.335
2009 Howarth K, Batty E, Beavis J, Blood K, Newman S, Ng B, Pole J, Chua Y, Ichimura K, Collins V, Chin S, Caldas C, Carter N, Edwards P. Chromosome translocations and fusion genes in breast cancer. Cancer Research. 69: 2021. DOI: 10.1158/0008-5472.Sabcs-2021  0.331
2008 Howarth KD, Blood KA, Ng BL, Beavis JC, Chua Y, Cooke SL, Raby S, Ichimura K, Collins VP, Carter NP, Edwards PA. Array painting reveals a high frequency of balanced translocations in breast cancer cell lines that break in cancer-relevant genes. Oncogene. 27: 3345-59. PMID 18084325 DOI: 10.1038/Sj.Onc.1210993  0.345
2008 Ichimura K, Vogazianou AP, Liu L, Pearson DM, Bäcklund LM, Plant K, Baird K, Langford CF, Gregory SG, Collins VP. 1p36 is a preferential target of chromosome 1 deletions in astrocytic tumours and homozygously deleted in a subset of glioblastomas. Oncogene. 27: 2097-108. PMID 17934521 DOI: 10.1038/Sj.Onc.1210848  0.393
2006 McCabe MG, Ichimura K, Liu L, Plant K, Bäcklund LM, Pearson DM, Collins VP. High-resolution array-based comparative genomic hybridization of medulloblastomas and supratentorial primitive neuroectodermal tumors. Journal of Neuropathology and Experimental Neurology. 65: 549-61. PMID 16783165 DOI: 10.1097/00005072-200606000-00003  0.346
2005 Bäcklund LM, Nilsson BR, Liu L, Ichimura K, Collins VP. Mutations in Rb1 pathway-related genes are associated with poor prognosis in anaplastic astrocytomas. British Journal of Cancer. 93: 124-30. PMID 15970925 DOI: 10.1038/Sj.Bjc.6602661  0.311
2004 Reifenberger G, Collins VP. Pathology and molecular genetics of astrocytic gliomas. Journal of Molecular Medicine (Berlin, Germany). 82: 656-70. PMID 15316624 DOI: 10.1007/S00109-004-0564-X  0.348
2003 Mahler-Araujo MB, Sanoudou D, Tingby O, Liu L, Coleman N, Ichimura K, Collins VP. Structural genomic abnormalities of chromosomes 9 and 18 in myxopapillary ependymomas. Journal of Neuropathology and Experimental Neurology. 62: 927-35. PMID 14533782 DOI: 10.1093/Jnen/62.9.927  0.372
2002 Collins VP, Ichimura K, Liu L. The expression of the EGF receptor family and their ligands in human medulloblastomas Neuropathology and Applied Neurobiology. 28: 156-157. DOI: 10.1046/J.1365-2990.2002.39286_24.X  0.301
2001 Büschges R, Boström J, Wolter M, Blaschke B, Weber RG, Lichter P, Collins VP, Reifenberger G. Analysis of human meningiomas for aberrations of the MADH2, MADH4, APM-1 and DCC tumor suppressor genes on the long arm of chromosome 18. International Journal of Cancer. Journal International Du Cancer. 92: 551-4. PMID 11304690 DOI: 10.1002/Ijc.1219  0.336
2000 Miyakawa A, Ichimura K, Schmidt EE, Varmeh-Ziaie S, Collins VP. Multiple deleted regions on the long arm of chromosome 6 in astrocytic tumours. British Journal of Cancer. 82: 543-9. PMID 10682663 DOI: 10.1054/Bjoc.1999.0961  0.402
1999 Bruder CE, Ichimura K, Tingby O, Hirakawa K, Komatsuzaki A, Tamura A, Yuasa Y, Collins VP, Dumanski JP. A group of schwannomas with interstitial deletions on 22q located outside the NF2 locus shows no detectable mutations in the NF2 gene. Human Genetics. 104: 418-24. PMID 10394935 DOI: 10.1007/S004390050978  0.396
1998 Liu L, Ichimura K, Pettersson EH, Collins VP. Chromosome 7 rearrangements in glioblastomas; loci adjacent to EGFR are independently amplified. Journal of Neuropathology and Experimental Neurology. 57: 1138-45. PMID 9862636 DOI: 10.1097/00005072-199812000-00005  0.4
1998 Boström J, Cobbers JM, Wolter M, Tabatabai G, Weber RG, Lichter P, Collins VP, Reifenberger G. Mutation of the PTEN (MMAC1) tumor suppressor gene in a subset of glioblastomas but not in meningiomas with loss of chromosome arm 10q. Cancer Research. 58: 29-33. PMID 9426052  0.308
1997 Schmidt EE, Ichimura K, Messerle KR, Goike HM, Collins VP. Infrequent methylation of CDKN2A(MTS1/p16) and rare mutation of both CDKN2A and CDKN2B(MTS2/p15) in primary astrocytic tumours. British Journal of Cancer. 75: 2-8. PMID 9000591 DOI: 10.1038/Bjc.1997.2  0.376
1994 Reifenberger J, Reifenberger G, Liu L, James CD, Wechsler W, Collins VP. Molecular genetic analysis of oligodendroglial tumors shows preferential allelic deletions on 19q and 1p. The American Journal of Pathology. 145: 1175-90. PMID 7977648  0.308
1993 Karlbom AE, James CD, Boethius J, Cavenee WK, Collins VP, Nordenskjöld M, Larsson C. Loss of heterozygosity in malignant gliomas involves at least three distinct regions on chromosome 10. Human Genetics. 92: 169-74. PMID 8370584 DOI: 10.1007/BF00219686  0.302
1993 Collins VP, James CD. Gene and chromosomal alterations associated with the development of human gliomas. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 7: 926-30. PMID 8344489 DOI: 10.1096/fasebj.7.10.8344489  0.313
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