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A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population

A. Antoniou, X. Wang, Z. Fredericksen, L. McGuffog, R. Tarrell, O. Sinilnikova, S. Healey, J. Morrison, C. Kartsonaki, T. Lesnick, M. Ghoussaini, D. Barrowdale, S. Peock, M. Cook, C. Oliver, D. Frost, D. Eccles, D. Evans, R. Eeles, L. Izatt, C. Chu, F. Douglas, J. Paterson, D. Stoppa-Lyonnet, C. Houdayer, S. Mazoyer, S. Giraud, C. Lasset, A. Remenieras, O. Caron, A. Hardouin, P. Berthet, Hogervorst, Frans B L, M. Rookus, A. Jager, van den Ouweland, Ans, N. Hoogerbrugge, van der Luijt, Rob B, H. Meijers-Heijboer, Gómez García, Encarna B, P. Devilee, Vreeswijk, Maaike P G, J. Lubinski, A. Jakubowska, J. Gronwald, T. Huzarski, T. Byrski, B. Górski, C. Cybulski, A. Spurdle, H. Holland, D. Goldgar, E. John, J. Hopper, M. Southey, S. Buys, M. Daly, M. Terry, R. Schmutzler, B. Wappenschmidt, C. Engel, A. Meindl, S. Preisler-Adams, N. Arnold, D. Niederacher, C. Sutter, S. Domchek, K. Nathanson, T. Rebbeck, J. Blum, M. Piedmonte, G. Rodriguez, K. Wakeley, J. Boggess, J. Basil, S. Blank, E. Friedman, B. Kaufman, Y. Laitman, R. Milgrom, I. Andrulis, G. Glendon, H. Ozcelik, T. Kirchhoff, J. Vijai, M. Gaudet, D. Altshuler, C. Guiducci, N. Loman, K. Harbst, J. Rantala, H. Ehrencrona, A. Gerdes, M. Thomassen, L. Sunde, P. Peterlongo, S. Manoukian, B. Bonanni, A. Viel, P. Radice, T. Caldes, de la Hoya, Miguel, C. Singer, A. Fink-Retter, M. Greene, P. Mai, J. Loud, L. Guidugli, N. Lindor, Hansen, Thomas V O, F. Nielsen, I. Blanco, C. Lazaro, J. Garber, S. Ramus, S. Gayther, C. Phelan, S. Narod, C. Szabo, J. Benitez, A. Osorio, H. Nevanlinna, T. Heikkinen, M. Caligo, M. Beattie, U. Hamann, A. Godwin, M. Montagna, C. Casella, S. Neuhausen, B. Karlan, N. Tung, A. Toland, J. Weitzel, O. Olopade, J. Simard, P. Soucy, W. Rubinstein, A. Arason, G. Rennert, N. Martin, G. Montgomery, J. Chang-Claude, D. Flesch-Janys, H. Brauch, G. Severi, L. Baglietto, A. Cox, S. Cross, P. Miron, S. Gerty, W. Tapper, D. Yannoukakos, G. Fountzilas, P. Fasching, M. Beckmann, dos Santos Silva, Isabel, J. Peto, D. Lambrechts, R. Paridaens, T. Rüdiger, A. Försti, R. Winqvist, K. Pylkäs, R. Diasio, A. Lee, J. Eckel-Passow, C. Vachon, F. Blows, K. Driver, A. Dunning, Pharoah, Paul P D, K. Offit, V. Pankratz, H. Hakonarson, G. Chenevix-Trench, D. Easton, and F. Couch. Nature genetics, 42 (10): 885–892 (2010)

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Hakon Karlsson

Håkon Jacobsen

Hakon Karlsson

Hakon Gudbjartsson

Hakon Auerbach

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137 ancient human genomes from across the Eurasian steppesP. Damgaard, N. Marchi, S. Rasmussen, M. Peyrot, G. Renaud, T. Korneliussen, J. Moreno-Mayar, M. Pedersen, A. Goldberg, E. Usmanova and 65 other author(s). Nature, 557 (7705): 369--374 (2018)Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traitsS. Vogelezang, J. Bradfield, T. Ahluwalia, J. Curtin, T. Lakka, N. Grarup, M. Scholz, P. van der Most, C. Monnereau, E. Stergiakouli and 136 other author(s). PLOS Genetics, 16 (10): 1-26 (October 2020)Biofilter as a Functional Annotation Pipeline for Common and Rare Copy Number Burden.D. Kim, A. Lucas, J. Glessner, S. Verma, Y. Bradford, R. Li, A. Frase, H. Hakonarson, P. Peissig, M. Brilliant and 1 other author(s). PSB, page 357-368. (2016)High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applicationsT. Shaikh, X. Gai, J. Perin, J. Glessner, H. Xie, K. Murphy, R. O'Hara, T. Casalunovo, L. Conlin, M. D'Arcy and 27 other author(s). Genome Research, (2009)Neuroimaging of the Philadelphia Neurodevelopmental Cohort.T. Satterthwaite, M. Elliott, K. Ruparel, J. Loughead, K. Prabhakaran, M. Calkins, R. Hopson, C. Jackson, J. Keefe, M. Riley and 7 other author(s). NeuroImage, (2014)Heterogeneous impact of motion on fundamental patterns of developmental changes in functional connectivity during youth.T. Satterthwaite, D. Wolf, K. Ruparel, G. Erus, M. Elliott, S. Eickhoff, E. Gennatas, C. Jackson, K. Prabhakaran, A. Smith and 5 other author(s). NeuroImage, (2013)ATOM: a powerful gene-based association test by combining optimally weighted markers.M. Li, K. Wang, S. Grant, H. Hakonarson, and C. Li. Bioinform., 25 (4): 497-503 (2009)Mitochondrial Genome Sequence Analysis: A custom bioinformatics pipeline substantially improves Affymetrix MitoChip v2.0 call rate and accuracy.H. Xie, J. Perin, T. Schurr, M. Dulik, S. Zhadanov, J. Baur, M. King, E. Place, C. Clarke, M. Grauer and 8 other author(s). BMC Bioinform., (2011)Genomic considerations for FHIR®; eMERGE implementation lessons.M. Murugan, L. Babb, C. Taylor, L. Rasmussen, R. Freimuth, E. Venner, F. Yan, V. Yi, S. Granite, H. Zouk and 16 other author(s). J. Biomed. Informatics, (2021)Characterizing variability of electronic health record-driven phenotype definitions.P. Brandt, A. Kho, Y. Luo, J. Pacheco, T. Walunas, H. Hakonarson, G. Hripcsak, C. Liu, N. Shang, C. Weng and 15 other author(s). J. Am. Medical Informatics Assoc., 30 (3): 427-437 (February 2023)

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Please choose a person to relate this publication to

Hakon Karlsson

Håkon Jacobsen

Hakon Karlsson

Hakon Gudbjartsson

Hakon Auerbach

Other publications of authors with the same name

Disambiguation