Year |
Citation |
Score |
1998 |
Blancher C, Harris AL. The molecular basis of the hypoxia response pathway: Tumour hypoxia as a therapy target Cancer and Metastasis Reviews. 17: 187-194. PMID 9770115 DOI: 10.1023/A:1006002419244 |
0.417 |
|
Low-probability matches (unlikely to be authored by this person) |
2006 |
Hooi CF, Blancher C, Qiu W, Revet IM, Williams LH, Ciavarella ML, Anderson RL, Thompson EW, Connor A, Phillips WA, Campbell IG. ST7-mediated suppression of tumorigenicity of prostate cancer cells is characterized by remodeling of the extracellular matrix. Oncogene. 25: 3924-33. PMID 16474848 DOI: 10.1038/sj.onc.1209418 |
0.238 |
|
2001 |
Crisanti P, Raguenez G, Blancher C, Neron B, Mamoune A, Omri B. Cloning and characterization of a novel transcription factor involved in cellular proliferation arrest: PATF. Oncogene. 20: 5475-83. PMID 11571645 DOI: 10.1038/sj.onc.1204711 |
0.183 |
|
2009 |
Mole DR, Blancher C, Copley RR, Pollard PJ, Gleadle JM, Ragoussis J, Ratcliffe PJ. Genome-wide association of hypoxia-inducible factor (HIF)-1alpha and HIF-2alpha DNA binding with expression profiling of hypoxia-inducible transcripts. The Journal of Biological Chemistry. 284: 16767-75. PMID 19386601 DOI: 10.1074/Jbc.M901790200 |
0.152 |
|
2012 |
Orr N, Lemnrau A, Cooke R, Fletcher O, Tomczyk K, Jones M, Johnson N, Lord CJ, Mitsopoulos C, Zvelebil M, McDade SS, Buck G, Blancher C, Trainer AH, et al. Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk. Nature Genetics. 44: 1182-4. PMID 23001122 DOI: 10.1038/ng.2417 |
0.149 |
|
2021 |
Eyres M, Lanfredini S, Xu H, Burns A, Blake A, Willenbrock F, Goldin R, Hughes D, Hughes S, Thapa A, Vavoulis D, Hubert A, D'Costa Z, Sabbagh A, Abraham AG, ... Blancher C, et al. TET2 drives 5hmc marking of GATA6 and epigenetically defines pancreatic ductal adenocarcinoma transcriptional subtypes. Gastroenterology. PMID 33915173 DOI: 10.1053/j.gastro.2021.04.044 |
0.133 |
|
2017 |
Dumas ME, Rothwell AR, Hoyles L, Aranias T, Chilloux J, Calderari S, Noll EM, Péan N, Boulangé CL, Blancher C, Barton RH, Gu Q, Fearnside JF, Deshayes C, Hue C, et al. Microbial-Host Co-metabolites Are Prodromal Markers Predicting Phenotypic Heterogeneity in Behavior, Obesity, and Impaired Glucose Tolerance. Cell Reports. 20: 136-148. PMID 28683308 DOI: 10.1016/j.celrep.2017.06.039 |
0.105 |
|
2008 |
Fearnside JF, Dumas ME, Rothwell AR, Wilder SP, Cloarec O, Toye A, Blancher C, Holmes E, Tatoud R, Barton RH, Scott J, Nicholson JK, Gauguier D. Phylometabonomic patterns of adaptation to high fat diet feeding in inbred mice. Plos One. 3: e1668. PMID 18301746 DOI: 10.1371/journal.pone.0001668 |
0.101 |
|
1996 |
Blancher C, Omri B, Bidou L, Pessac B, Crisanti P. Nectinepsin: a new extracellular matrix protein of the pexin family. Characterization of a novel cDNA encoding a protein with an RGD cell binding motif. The Journal of Biological Chemistry. 271: 26220-6. PMID 8824271 DOI: 10.1074/JBC.271.42.26220 |
0.097 |
|
2012 |
Blancher C, Cormick RM. Sodium dodecyl sulphate-polyacrylamide denaturing gel electrophoresis and Western blotting techniques. Methods in Molecular Biology (Clifton, N.J.). 878: 89-110. PMID 22674128 DOI: 10.1007/978-1-61779-854-2_6 |
0.095 |
|
2006 |
Dumas ME, Barton RH, Toye A, Cloarec O, Blancher C, Rothwell A, Fearnside J, Tatoud R, Blanc V, Lindon JC, Mitchell SC, Holmes E, McCarthy MI, Scott J, Gauguier D, et al. Metabolic profiling reveals a contribution of gut microbiota to fatty liver phenotype in insulin-resistant mice. Proceedings of the National Academy of Sciences of the United States of America. 103: 12511-6. PMID 16895997 DOI: 10.1073/pnas.0601056103 |
0.094 |
|
2016 |
Kanduri C, Kantojärvi K, Salo PM, Vanhala R, Buck G, Blancher C, Lähdesmäki H, Järvelä I. The landscape of copy number variations in Finnish families with autism spectrum disorders. Autism Research : Official Journal of the International Society For Autism Research. 9: 9-16. PMID 26052927 DOI: 10.1002/aur.1502 |
0.086 |
|
2016 |
Kanduri C, Kantojärvi K, Salo PM, Vanhala R, Buck G, Blancher C, Lähdesmäki H, Järvelä I. The landscape of copy number variations in Finnish families with autism spectrum disorders Autism Research. 9: 9-16. DOI: 10.1002/aur.1502 |
0.085 |
|
2013 |
Ukkola-Vuoti L, Kanduri C, Oikkonen J, Buck G, Blancher C, Raijas P, Karma K, Lähdesmäki H, Järvelä I. Genome-Wide Copy Number Variation Analysis in Extended Families and Unrelated Individuals Characterized for Musical Aptitude and Creativity in Music Plos One. 8. PMID 23460800 DOI: 10.1371/journal.pone.0056356 |
0.081 |
|
2012 |
Blancher C, Jones A. SDS -PAGE and Western Blotting Techniques. Methods in Molecular Medicine. 57: 145-62. PMID 21340897 DOI: 10.1385/1-59259-136-1:145 |
0.079 |
|
2007 |
Toye AA, Dumas ME, Blancher C, Rothwell AR, Fearnside JF, Wilder SP, Bihoreau MT, Cloarec O, Azzouzi I, Young S, Barton RH, Holmes E, McCarthy MI, Tatoud R, Nicholson JK, et al. Subtle metabolic and liver gene transcriptional changes underlie diet-induced fatty liver susceptibility in insulin-resistant mice. Diabetologia. 50: 1867-79. PMID 17618414 DOI: 10.1007/s00125-007-0738-5 |
0.075 |
|
1994 |
Bidou L, Crisanti P, Blancher C, Pessac B. A novel cDNA corresponding to transcripts expressed in retina post-mitotic neurons. Mechanisms of Development. 43: 159-73. PMID 8297788 DOI: 10.1016/0925-4773(93)90033-T |
0.074 |
|
2005 |
Cloarec O, Dumas ME, Craig A, Barton RH, Trygg J, Hudson J, Blancher C, Gauguier D, Lindon JC, Holmes E, Nicholson J. Statistical total correlation spectroscopy: an exploratory approach for latent biomarker identification from metabolic 1H NMR data sets. Analytical Chemistry. 77: 1282-9. PMID 15732908 DOI: 10.1021/ac048630x |
0.074 |
|
2016 |
Wahl S, Drong A, Lehne B, Loh M, Scott WR, Kunze S, Tsai PC, Ried JS, Zhang W, Yang Y, Tan S, Fiorito G, Franke L, Guarrera S, Kasela S, ... ... Blancher C, et al. Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity. Nature. PMID 28002404 DOI: 10.1038/Nature20784 |
0.071 |
|
2007 |
Dumas ME, Wilder SP, Bihoreau MT, Barton RH, Fearnside JF, Argoud K, D'Amato L, Wallis RH, Blancher C, Keun HC, Baunsgaard D, Scott J, Sidelmann UG, Nicholson JK, Gauguier D. Direct quantitative trait locus mapping of mammalian metabolic phenotypes in diabetic and normoglycemic rat models. Nature Genetics. 39: 666-72. PMID 17435758 DOI: 10.1038/ng2026 |
0.069 |
|
2015 |
Mahajan A, Sim X, Ng HJ, Manning A, Rivas MA, Highland HM, Locke AE, Grarup N, Im HK, Cingolani P, Flannick J, Fontanillas P, Fuchsberger C, Gaulton KJ, Teslovich TM, ... ... Blancher C, et al. Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus. Plos Genetics. 11: e1004876. PMID 25625282 DOI: 10.1371/Journal.Pgen.1004876 |
0.068 |
|
2010 |
Favaro E, Ramachandran A, McCormick R, Gee H, Blancher C, Crosby M, Devlin C, Blick C, Buffa F, Li JL, Vojnovic B, Pires das Neves R, Glazer P, Iborra F, Ivan M, et al. MicroRNA-210 regulates mitochondrial free radical response to hypoxia and krebs cycle in cancer cells by targeting iron sulfur cluster protein ISCU. Plos One. 5: e10345. PMID 20436681 DOI: 10.1371/Journal.Pone.0010345 |
0.053 |
|
2006 |
Parry S, Hadaschik D, Blancher C, Kumaran MK, Bochkina N, Morris HR, Richardson S, Aitman TJ, Gauguier D, Siddle K, Scott J, Dell A. Glycomics investigation into insulin action. Biochimica Et Biophysica Acta. 1760: 652-68. PMID 16473469 DOI: 10.1016/j.bbagen.2005.12.013 |
0.045 |
|
2017 |
Manning A, Highland HM, Gasser J, Sim X, Tukiainen T, Fontanillas P, Grarup N, Rivas MA, Mahajan A, Locke AE, Cingolani P, Pers TH, Viñuela A, Brown AA, Wu Y, ... ... Blancher C, et al. A Low-Frequency Inactivating Akt2 Variant Enriched in the Finnish Population is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk. Diabetes. PMID 28341696 DOI: 10.2337/Db16-1329 |
0.044 |
|
2013 |
Kanduri C, Ukkola-Vuoti L, Oikkonen J, Buck G, Blancher C, Raijas P, Karma K, Lähdesmäki H, Järvelä I. The genome-wide landscape of copy number variations in the MUSGEN study provides evidence for a founder effect in the isolated Finnish population European Journal of Human Genetics. 21: 1411-1416. PMID 23591402 DOI: 10.1038/ejhg.2013.60 |
0.038 |
|
1998 |
Omri B, Blancher C, Neron B, Marty MC, Rutin J, Molina TJ, Pessac B, Crisanti P. Retinal dysplasia in mice lacking p56(lck) Oncogene. 16: 2351-2356. PMID 9620552 DOI: 10.1038/sj.onc.1201761 |
0.037 |
|
2009 |
Hu Y, Kaisaki PJ, Argoud K, Wilder SP, Wallace KJ, Woon PY, Blancher C, Tarnow L, Groop PH, Hadjadj S, Marre M, Parving HH, Farrall M, Cox RD, Lathrop M, et al. Functional annotations of diabetes nephropathy susceptibility loci through analysis of genome-wide renal gene expression in rat models of diabetes mellitus. Bmc Medical Genomics. 2: 41. PMID 19586551 DOI: 10.1186/1755-8794-2-41 |
0.036 |
|
2016 |
Fuchsberger C, Flannick J, Teslovich TM, Mahajan A, Agarwala V, Gaulton KJ, Ma C, Fontanillas P, Moutsianas L, McCarthy DJ, Rivas MA, Perry JR, Sim X, Blackwell TW, Robertson NR, ... ... Blancher C, et al. The genetic architecture of type 2 diabetes. Nature. PMID 27398621 DOI: 10.1038/Nature18642 |
0.026 |
|
1997 |
Viengchareun S, Thenet-Gauci S, Steimberg N, Blancher C, Crisanti P, Adolphe M. The transfection of rabbit articular chondrocytes is independent of their differentiation state. In Vitro Cellular & Developmental Biology. Animal. 33: 15-7. PMID 9028829 DOI: 10.1007/s11626-997-0016-3 |
0.025 |
|
2017 |
Jason F, Fuchsberger C, Mahajan A, Teslovich TM, Agarwala V, Gaulton KJ, Caulkins L, Koesterer R, Ma C, Moutsianas L, McCarthy DJ, Rivas MA, Perry JRB, Sim X, Blackwell TW, ... ... Blancher C, et al. Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Scientific Data. 4: 170179. PMID 29257133 DOI: 10.1038/Sdata.2017.179 |
0.021 |
|
2018 |
Flannick J, Fuchsberger C, Mahajan A, Teslovich TM, Agarwala V, Gaulton KJ, Caulkins L, Koesterer R, Ma C, Moutsianas L, McCarthy DJ, Rivas MA, Perry JRB, Sim X, Blackwell TW, ... ... Blancher C, et al. Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Scientific Data. 5: 180002. PMID 29360107 DOI: 10.1038/sdata.2018.2 |
0.015 |
|
2015 |
Chambers JC, Loh M, Lehne B, Drong A, Kriebel J, Motta V, Wahl S, Elliott HR, Rota F, Scott WR, Zhang W, Tan ST, Campanella G, Chadeau-Hyam M, Yengo L, ... ... Blancher C, et al. Epigenome-wide association of DNA methylation markers in peripheral blood from Indian Asians and Europeans with incident type 2 diabetes: a nested case-control study. The Lancet. Diabetes & Endocrinology. PMID 26095709 DOI: 10.1016/S2213-8587(15)00127-8 |
0.013 |
|
Hide low-probability matches. |