Author of the publication

copy delete add this publication to your clipboard
community post
history of this post
URL
DOI
BibTeX
EndNote
APA
Chicago
DIN 1505
Harvard
MSOffice XML

Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers

J. French, M. Ghoussaini, S. Edwards, K. Meyer, K. Michailidou, S. Ahmed, S. Khan, M. Maranian, M. O'Reilly, K. Hillman, J. Betts, T. Carroll, P. Bailey, E. Dicks, J. Beesley, J. Tyrer, A. Maia, A. Beck, N. Knoblauch, C. Chen, P. Kraft, D. Barnes, A. González-Neira, M. Alonso, D. Herrero, D. Tessier, D. Vincent, F. Bacot, C. Luccarini, C. Baynes, D. Conroy, J. Dennis, M. Bolla, Q. Wang, J. Hopper, M. Southey, M. Schmidt, A. Broeks, S. Verhoef, S. Cornelissen, K. Muir, A. Lophatananon, S. Stewart-Brown, P. Siriwanarangsan, P. Fasching, C. Loehberg, A. Ekici, M. Beckmann, J. Peto, dos Santos Silva, Isabel, N. Johnson, Z. Aitken, E. Sawyer, I. Tomlinson, M. Kerin, N. Miller, F. Marme, A. Schneeweiss, C. Sohn, B. Burwinkel, P. Guénel, T. Truong, P. Laurent-Puig, F. Menegaux, S. Bojesen, B. Nordestgaard, S. Nielsen, H. Flyger, R. Milne, M. Zamora, Arias Perez, Jose Ignacio, J. Benitez, H. Anton-Culver, H. Brenner, H. Müller, V. Arndt, C. Stegmaier, A. Meindl, P. Lichtner, R. Schmutzler, C. Engel, H. Brauch, U. Hamann, C. Justenhoven, K. Aaltonen, P. Heikkilä, K. Aittomäki, C. Blomqvist, K. Matsuo, H. Ito, H. Iwata, A. Sueta, N. Bogdanova, N. Antonenkova, T. Dörk, A. Lindblom, S. Margolin, A. Mannermaa, V. Kataja, V. Kosma, J. Hartikainen, A. Wu, C. Tseng, van den Berg, David, D. Stram, D. Lambrechts, S. Peeters, A. Smeets, G. Floris, J. Chang-Claude, A. Rudolph, S. Nickels, D. Flesch-Janys, P. Radice, P. Peterlongo, B. Bonanni, D. Sardella, F. Couch, X. Wang, V. Pankratz, A. Lee, G. Giles, G. Severi, L. Baglietto, C. Haiman, B. Henderson, F. Schumacher, L. Le Marchand, J. Simard, M. Goldberg, F. Labrèche, M. Dumont, S. Teo, C. Yip, C. Ng, E. Vithana, V. Kristensen, W. Zheng, S. Deming-Halverson, M. Shrubsole, J. Long, R. Winqvist, K. Pylkäs, A. Jukkola-Vuorinen, M. Grip, I. Andrulis, J. Knight, G. Glendon, A. Mulligan, P. Devilee, C. Seynaeve, M. García-Closas, J. Figueroa, S. Chanock, J. Lissowska, K. Czene, D. Klevebring, N. Schoof, M. Hooning, Martens, John W M, J. Collée, M. Tilanus-Linthorst, P. Hall, J. Li, J. Liu, K. Humphreys, X. Shu, W. Lu, Y. Gao, H. Cai, A. Cox, S. Balasubramanian, W. Blot, L. Signorello, Q. Cai, Pharoah, Paul D P, C. Healey, M. Shah, K. Pooley, D. Kang, K. Yoo, D. Noh, M. Hartman, H. Miao, J. Sng, X. Sim, A. Jakubowska, J. Lubinski, K. Jaworska-Bieniek, K. Durda, S. Sangrajrang, V. Gaborieau, J. McKay, A. Toland, C. Ambrosone, D. Yannoukakos, A. Godwin, C. Shen, C. Hsiung, P. Wu, S. Chen, A. Swerdlow, A. Ashworth, N. Orr, M. Schoemaker, Ponder, Bruce A J, H. Nevanlinna, M. Brown, G. Chenevix-Trench, D. Easton, and A. Dunning. American journal of human genetics, 92 (4): 489–503 (2013)

Please choose a person to relate this publication to

To differ between persons with the same name, the academic degree and the title of an important publication will be displayed. You can also use the button next to the name to display some publications already assigned to the person.

Stephen J Maxfield

Stephen J Hannahs

Stephen Wagner

Stephen Novak

Stephen Robinson

Other publications of authors with the same name

Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancerS. Bojesen, K. Pooley, S. Johnatty, J. Beesley, K. Michailidou, J. Tyrer, S. Edwards, H. Pickett, H. Shen, C. Smart and 427 other author(s). Nature genetics, 45 (4): 371-84, 384e1-2 (2013)LDassoc: an online tool for interactively exploring genome-wide association study results and prioritizing variants for functional investigation.M. Machiela, and S. Chanock. Bioinform., 34 (5): 887-889 (2018)SNP500Cancer: a public resource for sequence validation, assay development, and frequency analysis for genetic variation in candidate genes.B. Packer, M. Yeager, L. Burdett, R. Welch, M. Beerman, L. Qi, H. Sicotte, B. Staats, M. Acharya, A. Crenshaw and 4 other author(s). Nucleic Acids Res., 34 (Database-Issue): 617-621 (2006)LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants.M. Machiela, and S. Chanock. Bioinform., 31 (21): 3555-3557 (2015)The landscape of recombination in African AmericansA. Hinch, A. Tandon, N. Patterson, Y. Song, N. Rohland, C. Palmer, G. Chen, K. Wang, S. Buxbaum, E. Akylbekova and 71 other author(s). Nature, (July 2011)Tumor necrosis factor (TNF) and lymphotoxin-alpha (LTA) polymorphisms and risk of non-Hodgkin lymphoma in the InterLymph Consortium.C. Skibola, P. Bracci, A. Nieters, A. Brooks-Wilson, S. de Sanjosé, A. Hughes, J. Cerhan, D. Skibola, M. Purdue, E. Kane and 32 other author(s). American journal of epidemiology, 171 (3): 267--276 (Feb 1, 2010)PRRC2A and BCL2L11 gene variants influence risk of non-Hodgkin lymphoma: results from the InterLymph consortium.A. Nieters, L. Conde, S. Slager, A. Brooks-Wilson, L. Morton, D. Skibola, A. Novak, J. Riby, S. Ansell, E. Halperin and 33 other author(s). Blood, 120 (23): 4645--4648 (Nov 29, 2012)PLCOjs, a FAIR GWAS web SDK for the NCI Prostate, Lung, Colorectal and Ovarian Cancer Genetic Atlas project.E. Ruan, E. Nemeth, R. Moffitt, L. Sandoval, M. Machiela, N. Freedman, W. Huang, W. Wong, K. Chen, B. Park and 9 other author(s). Bioinform., 38 (18): 4434-4436 (2022)Variation in DNA repair genes XRCC3, XRCC4, XRCC5 and susceptibility to myeloma.P. Hayden, P. Tewari, D. Morris, A. Staines, D. Crowley, A. Nieters, N. Becker, S. de Sanjosé, L. Foretova, M. Maynadié and 6 other author(s). Human molecular genetics, 16 (24): 3117--3127 (Dec 15, 2007)Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriersX. Wang, V. Pankratz, Z. Fredericksen, R. Tarrell, M. Karaus, L. McGuffog, Pharaoh, Paul D P, Ponder, Bruce A J, A. Dunning, S. Peock and 34 other author(s). Human molecular genetics, 19 (14): 2886–2897 (2010)

BibSonomy

Disambiguation of "Chanock, Stephen J."

copy delete add this publication to your clipboard
community post
history of this post
URL
DOI
BibTeX
EndNote
APA
Chicago
DIN 1505
Harvard
MSOffice XML

Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers

Please choose a person to relate this publication to

Stephen J Maxfield

Stephen J Hannahs

Stephen Wagner

Stephen Novak

Stephen Robinson

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Chanock, Stephen J."

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers

Please choose a person to relate this publication to

Stephen J Maxfield

Stephen J Hannahs

Stephen Wagner

Stephen Novak

Stephen Robinson

Other publications of authors with the same name

Disambiguation

copy delete add this publication to your clipboard
community post
history of this post
URL
DOI
BibTeX
EndNote
APA
Chicago
DIN 1505
Harvard
MSOffice XML

Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers