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Mutations in BRIP1 confer high risk of ovarian cancer
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Cites
Fast and accurate short read alignment with Burrows-Wheeler transform
Li, H., & Durbin, R. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp324 · Cited by 58,607
Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008
Ferlay, J., Shin, H., Bray, F., Forman, D., Mathers, C., & Parkin, D. M. (2010) · International Journal of Cancer · doi:10.1002/ijc.25516 · Cited by 21,293
A new multipoint method for genome-wide association studies by imputation of genotypes
Marchini, J., Howie, B., Myers, S., McVean, G., & Donnelly, P. (2007) · Nature Genetics · doi:10.1038/ng2088 · Cited by 2,609
A high-resolution recombination map of the human genome
Kong, A., Gudbjartsson, D. F., Sainz, J., Jonsdottir, G. M., Gudjonsson, S. A., Richardsson, B., Sigurdardottir, S., Barnard, J., Hallbeck, B., Masson, G., et al. (2002) · Nature Genetics · doi:10.1038/ng917 · Cited by 1,736
Self-citationThe BRCT Domain Is a Phospho-Protein Binding Domain
Yu, X., Chini, C. C. S., He, M., Mer, G., & Chen, J. (2003) · Science · doi:10.1126/science.1088753 · Cited by 862
The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds
Tavtigian, S. V., Simard, J., Rommens, J., Couch, F., Shattuck-Eidens, D., Neuhausen, S., Merajver, S., Thorlacius, S., Offit, K., Stoppa-Lyonnet, D., et al. (1996) · Nature Genetics · doi:10.1038/ng0396-333 · Cited by 839
The Breast Cancer Susceptibility Collaboration (UK), Seal, S., Thompson, D., Renwick, A., Elliott, A., Kelly, P., Barfoot, R., Chagtai, T., Jayatilake, H., Ahmed, M., et al. (2006) · Nature Genetics · doi:10.1038/ng1902 · Cited by 746
Cantor, S. B., Bell, D. W., Ganesan, S., Kass, E. M., Drapkin, R., Grossman, S., Wahrer, D. C. R., Sgroi, D. C., Lane, W. S., Haber, D. A., et al. (2001) · Cell · doi:10.1016/s0092-8674(01)00304-x · Cited by 674
Thorlacius, S., Olafsdottir, G., Tryggvadottir, L., Neuhausen, S., Jonasson, J. G., Tavtigian, S. V., Tulinius, H., Ögmundsdottir, H. M., & Eyfjörd, J. E. (1996) · Nature Genetics · doi:10.1038/ng0596-117 · Cited by 525
Self-citationDetection of sharing by descent, long-range phasing and haplotype imputation
Kong, A., Masson, G., Frigge, M. L., Gylfason, A., Zusmanovich, P., Thorleifsson, G., Olason, P. I., Ingason, A., Steinberg, S., Rafnar, T., et al. (2008) · Nature Genetics · doi:10.1038/ng.216 · Cited by 447 · cited 1×
“The SNPs identified through sequencing are then imputed to 41,675 Icelanders who were genotyped with chips of 300,000–1,000,000 SNPs by using long-range phasing informatio”
MethodSelf-citationThe DNA helicase BRIP1 is defective in Fanconi anemia complementation group J
Levitus, M., Waisfisz, Q., Godthelp, B. C., Vries, Y. D., Hussain, S., Wiegant, W. W., Elghalbzouri-Maghrani, E., Steltenpool, J., Rooimans, M. A., Pals, G., et al. (2005) · Nature Genetics · doi:10.1038/ng1625 · Cited by 432
Litman, R., Peng, M., Jin, Z., Zhang, F., Zhang, J., Powell, S., Andreassen, P. R., & Cantor, S. B. (2005) · Cancer Cell · doi:10.1016/j.ccr.2005.08.004 · Cited by 396
Wetzels, J. F. M., Kiemeney, L. A. L. M., Swinkels, D. W., Willems, H. L., & Heijer, M. D. (2007) · Kidney International · doi:10.1038/sj.ki.5002374 · Cited by 378
Self-citationThe BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia
Levran, O., Attwooll, C., Henry, R. T., Milton, K. L., Neveling, K., Rio, P., Batish, S. D., Kalb, R., Velleuer, E., Barral, S., et al. (2005) · Nature Genetics · doi:10.1038/ng1624 · Cited by 370
A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24
The Wellcome Trust Case-Control Consortium, Goode, E. L., Cancer), T. A. C. S. (., The Australian Ovarian Cancer Study Group, the Ovarian Cancer Association Consortium (OCAC), Chenevix-Trench, G., Song, H., Ramus, S. J., Notaridou, M., Lawrenson, K., et al. (2010) · Nature Genetics · doi:10.1038/ng.668 · Cited by 344
Self-citationA genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2
Study, A. C. (., Song, H., The Australian Ovarian Cancer Study Group, The Ovarian Cancer Association Consortium, Ramus, S. J., Tyrer, J., Bolton, K. L., Gentry-Maharaj, A., Wozniak, E., Anton-Culver, H., et al. (2009) · Nature Genetics · doi:10.1038/ng.424 · Cited by 313
A rare variant in MYH6 is associated with high risk of sick sinus syndrome
Holm, H., Gudbjartsson, D. F., Sulem, P., Masson, G., Helgadottir, H. T., Zanon, C., Magnusson, O. T., Helgason, A., Saemundsdottir, J., Gylfason, A., et al. (2011) · Nature Genetics · doi:10.1038/ng.781 · Cited by 299
Self-citationCommon variants at 19p13 are associated with susceptibility to ovarian cancer
the Australian Ovarian Cancer Study Group, Bolton, K. L., Cancer), T. A. C. S. (., on behalf of the Ovarian Cancer Association Consortium, Tyrer, J., Song, H., Ramus, S. J., Notaridou, M., Jones, C., Sher, T., et al. (2010) · Nature Genetics · doi:10.1038/ng.666 · Cited by 246
Self-citationThe Contribution of BRCA1 and BRCA2 to Ovarian Cancer
Ramus, S. J., & Gayther, S. A. (2009) · Molecular Oncology · doi:10.1016/j.molonc.2009.02.001 · Cited by 244
A systematic review and meta‐analysis of family history and risk of ovarian cancer
Stratton, J. F., Pharoah, P., Smith, S. K., Easton, D., & Ponder, B. A. J. (1998) · BJOG: An International Journal of Obstetrics & Gynaecology · doi:10.1111/j.1471-0528.1998.tb10148.x · Cited by 239
Bridge, W. L., Vandenberg, C. J., Franklin, R. J., & Hiom, K. (2005) · Nature Genetics · doi:10.1038/ng1627 · Cited by 211
Rubin, S. C., Blackwood, M. A., Bandera, C., Behbakht, K., Benjamin, I., Rebbeck, T. R., & Boyd, J. (1998) · American Journal of Obstetrics and Gynecology · doi:10.1016/s0002-9378(98)70476-4 · Cited by 179
Identification of low-frequency variants associated with gout and serum uric acid levels
Sulem, P., Gudbjartsson, D. F., Walters, G. B., Helgadottir, H. T., Helgason, A., Gudjonsson, S. A., Zanon, C., Besenbacher, S., Björnsdóttir, G., Magnússon, Ó. Þ., et al. (2011) · Nature Genetics · doi:10.1038/ng.972 · Cited by 159
Self-citationMalander, S., Rambech, E., Kristoffersson, U., Halvarsson, B., Ridderheim, M., Borg, Å., & Nilbert, M. C. (2005) · Gynecologic Oncology · doi:10.1016/j.ygyno.2005.10.029 · Cited by 126
Kumaraswamy, E., & Shiekhattar, R. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.00961-07 · Cited by 110
Hereditary Breast Cancer and the BRCA1-Associated FANCJ/BACH1/BRIP1
Cantor, S. B., & Guillemette, S. (2011) · Future Oncology · doi:10.2217/fon.10.191 · Cited by 106
Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland
Sarantaus, L., Huusko, P., Eerola, H., Launonen, V., Vehmanen, P., Rapakko, K., Gillanders, E. M., Syrjäkoski, K., Kainu, T., Vahteristo, P., et al. (2000) · European Journal of Human Genetics · doi:10.1038/sj.ejhg.5200529 · Cited by 97
Godwin, A. K., Vanderveer, L., Schultz, D., Lynch, H. T., Altomare, D. A., Buetow, K. H., Daly, M., Getts, L. A., Masny, A., & Rosenblum, N. (1994) · PubMed Central · Cited by 81
Rafnar, Þ., Benediktsdóttir, K. R., Eldon, B., Gestsson, T., Saemundsson, H., Olafsson, K., Salvarsdottir, A., Steingrı́msson, E., & Thorlacius, S. (2004) · European Journal of Cancer · doi:10.1016/j.ejca.2004.09.008 · Cited by 62
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Jonsson, T., Stefansson, H., Steinberg, S., Jonsdottir, I., Jonsson, P. V., Snaedal, J., Bjornsson, S., Huttenlocher, J., Levey, A. I., Lah, J. J., et al. (2013) · New England Journal of Medicine · doi:10.1056/nejmoa1211103 · Cited by 2,558
Self-citationRate of de novo mutations and the importance of father’s age to disease risk
Kong, A., Frigge, M. L., Masson, G., Besenbacher, S., Sulem, P., Magnusson, G., Gudjonsson, S. A., Sigurdsson, A., Jonasdottir, A., Jonasdottir, A., et al. (2012) · Nature · doi:10.1038/nature11396 · Cited by 2,134
Self-citationRethinking ovarian cancer II: reducing mortality from high-grade serous ovarian cancer
Bowtell, D. D., Böhm, S., Ahmed, A. A., Aspuria, P.-J., Bast, R. C., Beral, V., Berek, J. S., Birrer, M. J., Blagden, S., Bookman, M. A., et al. (2015) · Nature Reviews Cancer · doi:10.1038/nrc4019 · Cited by 1,367
Pennington, K. P., Walsh, T., Harrell, M. I., Lee, M. K., Pennil, C. C., Rendi, M. H., Thornton, A., Norquist, B. M., Casadei, S., Nord, A. S., et al. (2014) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-13-2287 · Cited by 1,051
Homologous Recombination and Human Health: The Roles of BRCA1, BRCA2, and Associated Proteins
Prakash, R., Zhang, Y., Feng, W., & Jasin, M. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a016600 · Cited by 869
Metadata
- Authors
- Rafnar, T., Gudbjartsson, D. F., Sulem, P., Jonasdottir, A., Sigurdsson, A., Jonasdottir, A., Besenbacher, S., Lundin, P., Stacey, S. N., Gudmundsson, J., Magnusson, O. T., le Roux, L., Orlygsdottir, G., Helgadottir, H. T., Johannsdottir, H., Gylfason, A., Tryggvadottir, L., Jonasson, J. G., de Juan, A., Ortega, E., Ramon-Cajal, J. M., García-Prats, M. D., Mayordomo, C., Panadero, A., Rivera, F., Aben, K. K. H., van Altena, A. M., Massuger, L. F. A. G., Aavikko, M., Kujala, P. M., Staff, S., Aaltonen, L. A., Olafsdottir, K., Bjornsson, J., Kong, A., Salvarsdottir, A., Saemundsson, H., Olafsson, K., Benediktsdottir, K. R., Gulcher, J., Masson, G., Kiemeney, L. A., Mayordomo, J. I., Thorsteinsdottir, U., & Stefansson, K.
- Venue
- Nature Genetics
- Published
- 2011-10-02
- Volume
- 43
- Issue
- 11
- Pages
- 1104-1107
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2054367725
- Cited by
- 406
- References
- 29
- FWCI
- 13.15
- Type
- journal article
- Language
- en
- Open access
- closed
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