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[Not Available].

Progres en urologie : journal de l'Association francaise d'urologie et de la Societe francaise d'urologie

Bigot P, Jessop L, Machiela M, Colli L, Myers T, Azzouzi A, Cussenot O, Chanock S.
PMID: 26461637
Prog Urol. 2014 Nov;24(13):833-4. doi: 10.1016/j.purol.2014.08.111. Epub 2014 Oct 30.

No abstract available.

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Bigot P, Jessop L, Machiela M, et al. La caractérisation fonctionnelle du locus de susceptibilité au cancer du rein 12p11.23 implique le gène SHARP1. [Not Available]. Prog Urol. 2014;24(13):833-4doi: 10.1016/j.purol.2014.08.111.
Bigot, P., Jessop, L., Machiela, M., Colli, L., Myers, T., Azzouzi, A., Cussenot, O., & Chanock, S. (2014). La caractérisation fonctionnelle du locus de susceptibilité au cancer du rein 12p11.23 implique le gène SHARP1. [Not Available]. Progres en urologie : journal de l'Association francaise d'urologie et de la Societe francaise d'urologie, 24(13), 833-4. https://doi.org/10.1016/j.purol.2014.08.111
Bigot, P, et al. "La caractérisation fonctionnelle du locus de susceptibilité au cancer du rein 12p11.23 implique le gène SHARP1." [Not Available]. Progres en urologie : journal de l'Association francaise d'urologie et de la Societe francaise d'urologie vol. 24,13 (2014): 833-4. doi: https://doi.org/10.1016/j.purol.2014.08.111
Bigot P, Jessop L, Machiela M, Colli L, Myers T, Azzouzi A, Cussenot O, Chanock S. La caractérisation fonctionnelle du locus de susceptibilité au cancer du rein 12p11.23 implique le gène SHARP1. [Not Available]. Prog Urol. 2014 Nov;24(13):833-4. doi: 10.1016/j.purol.2014.08.111. Epub 2014 Oct 30. French. PMID: 26461637.
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Polymorphisms in Th1/Th2 cytokine genes, hormone replacement therapy, and risk of non-Hodgkin lymphoma.

Frontiers in oncology

Zhu G, Pan D, Zheng T, Lan Q, Chen X, Chen Y, Kim C, Bi X, Holford T, Boyle P, Leaderer B, Chanock SJ, Rothman N, Zhang Y.
PMID: 22180854
Front Oncol. 2011 Jul 28;1(21). doi: 10.3389/fonc.2011.00021.

We conducted a population-based case-control study in Connecticut women to test the hypothesis that genetic variations in Th1 and Th2 cytokine genes modify the relationship between hormone replacement therapy (HRT) and risk of non-Hodgkin lymphoma (NHL). Compared to women...

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Zhu G, Pan D, Zheng T, et al. Polymorphisms in Th1/Th2 cytokine genes, hormone replacement therapy, and risk of non-Hodgkin lymphoma. Front Oncol. 2011;1(21)doi: 10.3389/fonc.2011.00021.
Zhu, G., Pan, D., Zheng, T., Lan, Q., Chen, X., Chen, Y., Kim, C., Bi, X., Holford, T., Boyle, P., Leaderer, B., Chanock, S. J., Rothman, N., & Zhang, Y. (2011). Polymorphisms in Th1/Th2 cytokine genes, hormone replacement therapy, and risk of non-Hodgkin lymphoma. Frontiers in oncology, 1(21), . https://doi.org/10.3389/fonc.2011.00021
Zhu, Gongjian, et al. "Polymorphisms in Th1/Th2 cytokine genes, hormone replacement therapy, and risk of non-Hodgkin lymphoma." Frontiers in oncology vol. 1,21 (2011). doi: https://doi.org/10.3389/fonc.2011.00021
Zhu G, Pan D, Zheng T, Lan Q, Chen X, Chen Y, Kim C, Bi X, Holford T, Boyle P, Leaderer B, Chanock SJ, Rothman N, Zhang Y. Polymorphisms in Th1/Th2 cytokine genes, hormone replacement therapy, and risk of non-Hodgkin lymphoma. Front Oncol. 2011 Jul 28;1(21). doi: 10.3389/fonc.2011.00021. PMID: 22180854; PMCID: PMC3237699.
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The DARC side of GWAS.

Blood

Chanock SJ.
PMID: 20595521
Blood. 2010 Jul 01;115(26):5285-6. doi: 10.1182/blood-2010-02-263699.

No abstract available.

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Chanock SJ. The DARC side of GWAS. Blood. 2010;115(26):5285-6doi: 10.1182/blood-2010-02-263699.
Chanock, S. J. (2010). The DARC side of GWAS. Blood, 115(26), 5285-6. https://doi.org/10.1182/blood-2010-02-263699
Chanock, Stephen J. "The DARC side of GWAS." Blood vol. 115,26 (2010): 5285-6. doi: https://doi.org/10.1182/blood-2010-02-263699
Chanock SJ. The DARC side of GWAS. Blood. 2010 Jul 01;115(26):5285-6. doi: 10.1182/blood-2010-02-263699. PMID: 20595521.
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Genetic approaches to control of influenza.

Perspectives in biology and medicine

Chanock RM, Murphy BR.
PMID: 25578237
Perspect Biol Med. 1979;22(2):S37-48. doi: 10.1353/pbm.1979.0049.

No abstract available.

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Chanock RM, Murphy BR. Genetic approaches to control of influenza. Perspect Biol Med. 1979;22(2):S37-48doi: 10.1353/pbm.1979.0049.
Chanock, R. M., & Murphy, B. R. (1979). Genetic approaches to control of influenza. Perspectives in biology and medicine, 22(2), S37-48. https://doi.org/10.1353/pbm.1979.0049
Chanock, R M, and Murphy, B R. "Genetic approaches to control of influenza." Perspectives in biology and medicine vol. 22,2 (1979): S37-48. doi: https://doi.org/10.1353/pbm.1979.0049
Chanock RM, Murphy BR. Genetic approaches to control of influenza. Perspect Biol Med. 1979;22(2):S37-48. doi: 10.1353/pbm.1979.0049. PMID: 25578237.
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Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer.

Nature genetics

Bolton KL, Tyrer J, Song H, Ramus SJ, Notaridou M, Jones C, Sher T, Gentry-Maharaj A, Wozniak E, Tsai YY, Weidhaas J, Paik D, Van Den Berg DJ, Stram DO, Pearce CL, Wu AH, Brewster W, Anton-Culver H, Ziogas A, Narod SA, Levine DA, Kaye SB, Brown R, Paul J, Flanagan J, Sieh W, McGuire V, Whittemore AS, Campbell I, Gore ME, Lissowska J, Yang HP, Medrek K, Gronwald J, Lubinski J, Jakubowska A, Le ND, Cook LS, Kelemen LE, Brooks-Wilson A, Massuger LF, Kiemeney LA, Aben KK, van Altena AM, Houlston R, Tomlinson I, Palmieri RT, Moorman PG, Schildkraut J, Iversen ES, Phelan C, Vierkant RA, Cunningham JM, Goode EL, Fridley BL, Kruger-Kjaer S, Blaeker J, Hogdall E, Hogdall C, Gross J, Karlan BY, Ness RB, Edwards RP, Odunsi K, Moyisch KB, Baker JA, Modugno F, Heikkinenen T, Butzow R, Nevanlinna H, Leminen A, Bogdanova N, Antonenkova N, Doerk T, Hillemanns P, Dürst M, Runnebaum I, Thompson PJ, Carney ME, Goodman MT, Lurie G, Wang-Gohrke S, Hein R, Chang-Claude J, Rossing MA, Cushing-Haugen KL, Doherty J, Chen C, Rafnar T, Besenbacher S, Sulem P, Stefansson K, Birrer MJ, Terry KL, Hernandez D, Cramer DW, Vergote I, Amant F, Lambrechts D, Despierre E, Fasching PA, Beckmann MW, Thiel FC, Ekici AB, Chen X, Johnatty SE, Webb PM, Beesley J, Chanock S, Garcia-Closas M, Sellers T, Easton DF, Berchuck A, Chenevix-Trench G, Pharoah PD, Gayther SA.
PMID: 26711112
Nat Genet. 2016 Jan;48(1):101. doi: 10.1038/ng0116-101b.

No abstract available.

Cite
Bolton KL, Tyrer J, Song H, et al. Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer. Nat Genet. 2016;48(1):101doi: 10.1038/ng0116-101b.
Bolton, K. L., Tyrer, J., Song, H., Ramus, S. J., Notaridou, M., Jones, C., Sher, T., Gentry-Maharaj, A., Wozniak, E., Tsai, Y. Y., Weidhaas, J., Paik, D., Van Den Berg, D. J., Stram, D. O., Pearce, C. L., Wu, A. H., Brewster, W., Anton-Culver, H., Ziogas, A., Narod, S. A., Levine, D. A., Kaye, S. B., Brown, R., Paul, J., Flanagan, J., Sieh, W., McGuire, V., Whittemore, A. S., Campbell, I., Gore, M. E., Lissowska, J., Yang, H. P., Medrek, K., Gronwald, J., Lubinski, J., Jakubowska, A., Le, N. D., Cook, L. S., Kelemen, L. E., Brooks-Wilson, A., Massuger, L. F., Kiemeney, L. A., Aben, K. K., van Altena, A. M., Houlston, R., Tomlinson, I., Palmieri, R. T., Moorman, P. G., Schildkraut, J., Iversen, E. S., Phelan, C., Vierkant, R. A., Cunningham, J. M., Goode, E. L., Fridley, B. L., Kruger-Kjaer, S., Blaeker, J., Hogdall, E., Hogdall, C., Gross, J., Karlan, B. Y., Ness, R. B., Edwards, R. P., Odunsi, K., Moyisch, K. B., Baker, J. A., Modugno, F., Heikkinenen, T., Butzow, R., Nevanlinna, H., Leminen, A., Bogdanova, N., Antonenkova, N., Doerk, T., Hillemanns, P., Dürst, M., Runnebaum, I., Thompson, P. J., Carney, M. E., Goodman, M. T., Lurie, G., Wang-Gohrke, S., Hein, R., Chang-Claude, J., Rossing, M. A., Cushing-Haugen, K. L., Doherty, J., Chen, C., Rafnar, T., Besenbacher, S., Sulem, P., Stefansson, K., Birrer, M. J., Terry, K. L., Hernandez, D., Cramer, D. W., Vergote, I., Amant, F., Lambrechts, D., Despierre, E., Fasching, P. A., Beckmann, M. W., Thiel, F. C., Ekici, A. B., Chen, X., Johnatty, S. E., Webb, P. M., Beesley, J., Chanock, S., Garcia-Closas, M., Sellers, T., Easton, D. F., Berchuck, A., Chenevix-Trench, G., Pharoah, P. D., & Gayther, S. A. (2016). Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer. Nature genetics, 48(1), 101. https://doi.org/10.1038/ng0116-101b
Bolton, Kelly L, et al. "Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer." Nature genetics vol. 48,1 (2016): 101. doi: https://doi.org/10.1038/ng0116-101b
Bolton KL, Tyrer J, Song H, Ramus SJ, Notaridou M, Jones C, Sher T, Gentry-Maharaj A, Wozniak E, Tsai YY, Weidhaas J, Paik D, Van Den Berg DJ, Stram DO, Pearce CL, Wu AH, Brewster W, Anton-Culver H, Ziogas A, Narod SA, Levine DA, Kaye SB, Brown R, Paul J, Flanagan J, Sieh W, McGuire V, Whittemore AS, Campbell I, Gore ME, Lissowska J, Yang HP, Medrek K, Gronwald J, Lubinski J, Jakubowska A, Le ND, Cook LS, Kelemen LE, Brooks-Wilson A, Massuger LF, Kiemeney LA, Aben KK, van Altena AM, Houlston R, Tomlinson I, Palmieri RT, Moorman PG, Schildkraut J, Iversen ES, Phelan C, Vierkant RA, Cunningham JM, Goode EL, Fridley BL, Kruger-Kjaer S, Blaeker J, Hogdall E, Hogdall C, Gross J, Karlan BY, Ness RB, Edwards RP, Odunsi K, Moyisch KB, Baker JA, Modugno F, Heikkinenen T, Butzow R, Nevanlinna H, Leminen A, Bogdanova N, Antonenkova N, Doerk T, Hillemanns P, Dürst M, Runnebaum I, Thompson PJ, Carney ME, Goodman MT, Lurie G, Wang-Gohrke S, Hein R, Chang-Claude J, Rossing MA, Cushing-Haugen KL, Doherty J, Chen C, Rafnar T, Besenbacher S, Sulem P, Stefansson K, Birrer MJ, Terry KL, Hernandez D, Cramer DW, Vergote I, Amant F, Lambrechts D, Despierre E, Fasching PA, Beckmann MW, Thiel FC, Ekici AB, Chen X, Johnatty SE, Webb PM, Beesley J, Chanock S, Garcia-Closas M, Sellers T, Easton DF, Berchuck A, Chenevix-Trench G, Pharoah PD, Gayther SA. Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer. Nat Genet. 2016 Jan;48(1):101. doi: 10.1038/ng0116-101b. PMID: 26711112.
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Corrigendum: genome-wide association study of colorectal cancer identifies six new susceptibility loci.

Nature communications

Schumacher FR, Schmit SL, Jiao S, Edlund CK, Wang H, Zhang B, Hsu L, Huang SC, Fischer CP, Harju JF, Idos GE, Lejbkowicz F, Manion FJ, McDonnell K, McNeil CE, Melas M, Rennert HS, Shi W, Thomas DC, Van Den Berg DJ, Hutter CM, Aragaki AK, Butterbach K, Caan BJ, Carlson CS, Chanock SJ, Curtis KR, Fuchs CS, Gala M, Giovannucci EL, Gogarten SM, Hayes RB, Henderson B, Hunter DJ, Jackson RD, Kolonel LN, Kooperberg C, Küry S, LaCroix A, Laurie CC, Laurie CA, Lemire M, Levine D, Ma J, Makar KW, Qu C, Taverna D, Ulrich CM, Wu K, Kono S, West DW, Berndt SI, Bezieau S, Brenner H, Campbell PT, Chan AT, Chang-Claude J, Coetzee GA, Conti DV, Duggan D, Figueiredo JC, Fortini BK, Gallinger SJ, Gauderman WJ, Giles G, Green R, Haile R, Harrison TA, Hoffmeister M, Hopper JL, Hudson TJ, Jacobs E, Iwasaki M, Jee SH, Jenkins M, Jia WH, Joshi A, Li L, Lindor NM, Matsuo K, Moreno V, Mukherjee B, Newcomb PA, Potter JD, Raskin L, Rennert G, Rosse S, Severi G, Schoen RE, Seminara D, Shu XO, Slattery ML, Tsugane S, White E, Xiang YB, Zanke BW, Zheng W, Le Marchand L, Casey G, Gruber SB, Peters U.
PMID: 26498495
Nat Commun. 2015 Oct 26;6:8739. doi: 10.1038/ncomms9739.

No abstract available.

Cite
Schumacher FR, Schmit SL, Jiao S, et al. Corrigendum: genome-wide association study of colorectal cancer identifies six new susceptibility loci. Nat Commun. 2015;6:8739doi: 10.1038/ncomms9739.
Schumacher, F. R., Schmit, S. L., Jiao, S., Edlund, C. K., Wang, H., Zhang, B., Hsu, L., Huang, S. C., Fischer, C. P., Harju, J. F., Idos, G. E., Lejbkowicz, F., Manion, F. J., McDonnell, K., McNeil, C. E., Melas, M., Rennert, H. S., Shi, W., Thomas, D. C., Van Den Berg, D. J., Hutter, C. M., Aragaki, A. K., Butterbach, K., Caan, B. J., Carlson, C. S., Chanock, S. J., Curtis, K. R., Fuchs, C. S., Gala, M., Giovannucci, E. L., Gogarten, S. M., Hayes, R. B., Henderson, B., Hunter, D. J., Jackson, R. D., Kolonel, L. N., Kooperberg, C., Küry, S., LaCroix, A., Laurie, C. C., Laurie, C. A., Lemire, M., Levine, D., Ma, J., Makar, K. W., Qu, C., Taverna, D., Ulrich, C. M., Wu, K., Kono, S., West, D. W., Berndt, S. I., Bezieau, S., Brenner, H., Campbell, P. T., Chan, A. T., Chang-Claude, J., Coetzee, G. A., Conti, D. V., Duggan, D., Figueiredo, J. C., Fortini, B. K., Gallinger, S. J., Gauderman, W. J., Giles, G., Green, R., Haile, R., Harrison, T. A., Hoffmeister, M., Hopper, J. L., Hudson, T. J., Jacobs, E., Iwasaki, M., Jee, S. H., Jenkins, M., Jia, W. H., Joshi, A., Li, L., Lindor, N. M., Matsuo, K., Moreno, V., Mukherjee, B., Newcomb, P. A., Potter, J. D., Raskin, L., Rennert, G., Rosse, S., Severi, G., Schoen, R. E., Seminara, D., Shu, X. O., Slattery, M. L., Tsugane, S., White, E., Xiang, Y. B., Zanke, B. W., Zheng, W., Le Marchand, L., Casey, G., Gruber, S. B., & Peters, U. (2015). Corrigendum: genome-wide association study of colorectal cancer identifies six new susceptibility loci. Nature communications, 68739. https://doi.org/10.1038/ncomms9739
Schumacher, Fredrick R, et al. "Corrigendum: genome-wide association study of colorectal cancer identifies six new susceptibility loci." Nature communications vol. 6 (2015): 8739. doi: https://doi.org/10.1038/ncomms9739
Schumacher FR, Schmit SL, Jiao S, Edlund CK, Wang H, Zhang B, Hsu L, Huang SC, Fischer CP, Harju JF, Idos GE, Lejbkowicz F, Manion FJ, McDonnell K, McNeil CE, Melas M, Rennert HS, Shi W, Thomas DC, Van Den Berg DJ, Hutter CM, Aragaki AK, Butterbach K, Caan BJ, Carlson CS, Chanock SJ, Curtis KR, Fuchs CS, Gala M, Giovannucci EL, Gogarten SM, Hayes RB, Henderson B, Hunter DJ, Jackson RD, Kolonel LN, Kooperberg C, Küry S, LaCroix A, Laurie CC, Laurie CA, Lemire M, Levine D, Ma J, Makar KW, Qu C, Taverna D, Ulrich CM, Wu K, Kono S, West DW, Berndt SI, Bezieau S, Brenner H, Campbell PT, Chan AT, Chang-Claude J, Coetzee GA, Conti DV, Duggan D, Figueiredo JC, Fortini BK, Gallinger SJ, Gauderman WJ, Giles G, Green R, Haile R, Harrison TA, Hoffmeister M, Hopper JL, Hudson TJ, Jacobs E, Iwasaki M, Jee SH, Jenkins M, Jia WH, Joshi A, Li L, Lindor NM, Matsuo K, Moreno V, Mukherjee B, Newcomb PA, Potter JD, Raskin L, Rennert G, Rosse S, Severi G, Schoen RE, Seminara D, Shu XO, Slattery ML, Tsugane S, White E, Xiang YB, Zanke BW, Zheng W, Le Marchand L, Casey G, Gruber SB, Peters U. Corrigendum: genome-wide association study of colorectal cancer identifies six new susceptibility loci. Nat Commun. 2015 Oct 26;6:8739. doi: 10.1038/ncomms9739. PMID: 26498495.
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Lack of transgenerational effects of ionizing radiation exposure from the Chernobyl accident.

Science (New York, N.Y.)

Yeager M, Machiela MJ, Kothiyal P, Dean M, Bodelon C, Suman S, Wang M, Mirabello L, Nelson CW, Zhou W, Palmer C, Ballew B, Colli LM, Freedman ND, Dagnall C, Hutchinson A, Vij V, Maruvka Y, Hatch M, Illienko I, Belayev Y, Nakamura N, Chumak V, Bakhanova E, Belyi D, Kryuchkov V, Golovanov I, Gudzenko N, Cahoon EK, Albert P, Drozdovitch V, Little MP, Mabuchi K, Stewart C, Getz G, Bazyka D, Berrington de Gonzalez A, Chanock SJ.
PMID: 33888597
Science. 2021 May 14;372(6543):725-729. doi: 10.1126/science.abg2365. Epub 2021 Apr 22.

Effects of radiation exposure from the Chernobyl nuclear accident remain a topic of interest. We investigated germline de novo mutations (DNMs) in children born to parents employed as cleanup workers or exposed to occupational and environmental ionizing radiation after...

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Yeager M, Machiela MJ, Kothiyal P, et al. Lack of transgenerational effects of ionizing radiation exposure from the Chernobyl accident. Science. 2021;372(6543):725-729doi: 10.1126/science.abg2365.
Yeager, M., Machiela, M. J., Kothiyal, P., Dean, M., Bodelon, C., Suman, S., Wang, M., Mirabello, L., Nelson, C. W., Zhou, W., Palmer, C., Ballew, B., Colli, L. M., Freedman, N. D., Dagnall, C., Hutchinson, A., Vij, V., Maruvka, Y., Hatch, M., Illienko, I., Belayev, Y., Nakamura, N., Chumak, V., Bakhanova, E., Belyi, D., Kryuchkov, V., Golovanov, I., Gudzenko, N., Cahoon, E. K., Albert, P., Drozdovitch, V., Little, M. P., Mabuchi, K., Stewart, C., Getz, G., Bazyka, D., Berrington de Gonzalez, A., & Chanock, S. J. (2021). Lack of transgenerational effects of ionizing radiation exposure from the Chernobyl accident. Science (New York, N.Y.), 372(6543), 725-729. https://doi.org/10.1126/science.abg2365
Yeager, Meredith, et al. "Lack of transgenerational effects of ionizing radiation exposure from the Chernobyl accident." Science (New York, N.Y.) vol. 372,6543 (2021): 725-729. doi: https://doi.org/10.1126/science.abg2365
Yeager M, Machiela MJ, Kothiyal P, Dean M, Bodelon C, Suman S, Wang M, Mirabello L, Nelson CW, Zhou W, Palmer C, Ballew B, Colli LM, Freedman ND, Dagnall C, Hutchinson A, Vij V, Maruvka Y, Hatch M, Illienko I, Belayev Y, Nakamura N, Chumak V, Bakhanova E, Belyi D, Kryuchkov V, Golovanov I, Gudzenko N, Cahoon EK, Albert P, Drozdovitch V, Little MP, Mabuchi K, Stewart C, Getz G, Bazyka D, Berrington de Gonzalez A, Chanock SJ. Lack of transgenerational effects of ionizing radiation exposure from the Chernobyl accident. Science. 2021 May 14;372(6543):725-729. doi: 10.1126/science.abg2365. Epub 2021 Apr 22. PMID: 33888597.
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Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry.

Nature communications

Matejcic M, Saunders EJ, Dadaev T, Brook MN, Wang K, Sheng X, Olama AAA, Schumacher FR, Ingles SA, Govindasami K, Benlloch S, Berndt SI, Albanes D, Koutros S, Muir K, Stevens VL, Gapstur SM, Tangen CM, Batra J, Clements J, Gronberg H, Pashayan N, Schleutker J, Wolk A, West C, Mucci L, Kraft P, Cancel-Tassin G, Sorensen KD, Maehle L, Grindedal EM, Strom SS, Neal DE, Hamdy FC, Donovan JL, Travis RC, Hamilton RJ, Rosenstein B, Lu YJ, Giles GG, Kibel AS, Vega A, Bensen JT, Kogevinas M, Penney KL, Park JY, Stanford JL, Cybulski C, Nordestgaard BG, Brenner H, Maier C, Kim J, Teixeira MR, Neuhausen SL, De Ruyck K, Razack A, Newcomb LF, Lessel D, Kaneva R, Usmani N, Claessens F, Townsend PA, Gago-Dominguez M, Roobol MJ, Menegaux F, Khaw KT, Cannon-Albright LA, Pandha H, Thibodeau SN, Schaid DJ, Wiklund F, Chanock SJ, Easton DF, Eeles RA, Kote-Jarai Z, Conti DV, Haiman CA.
PMID: 30655571
Nat Commun. 2019 Jan 17;10(1):382. doi: 10.1038/s41467-019-08293-z.

The original version of this Article contained an error in the spelling of the author Manuela Gago-Dominguez, which was incorrectly given as Manuela G. Dominguez. This has now been corrected in both the PDF and HTML versions of the...

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Matejcic M, Saunders EJ, Dadaev T, et al. Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry. Nat Commun. 2019;10(1):382doi: 10.1038/s41467-019-08293-z.
Matejcic, M., Saunders, E. J., Dadaev, T., Brook, M. N., Wang, K., Sheng, X., Olama, A. A. A., Schumacher, F. R., Ingles, S. A., Govindasami, K., Benlloch, S., Berndt, S. I., Albanes, D., Koutros, S., Muir, K., Stevens, V. L., Gapstur, S. M., Tangen, C. M., Batra, J., Clements, J., Gronberg, H., Pashayan, N., Schleutker, J., Wolk, A., West, C., Mucci, L., Kraft, P., Cancel-Tassin, G., Sorensen, K. D., Maehle, L., Grindedal, E. M., Strom, S. S., Neal, D. E., Hamdy, F. C., Donovan, J. L., Travis, R. C., Hamilton, R. J., Rosenstein, B., Lu, Y. J., Giles, G. G., Kibel, A. S., Vega, A., Bensen, J. T., Kogevinas, M., Penney, K. L., Park, J. Y., Stanford, J. L., Cybulski, C., Nordestgaard, B. G., Brenner, H., Maier, C., Kim, J., Teixeira, M. R., Neuhausen, S. L., De Ruyck, K., Razack, A., Newcomb, L. F., Lessel, D., Kaneva, R., Usmani, N., Claessens, F., Townsend, P. A., Gago-Dominguez, M., Roobol, M. J., Menegaux, F., Khaw, K. T., Cannon-Albright, L. A., Pandha, H., Thibodeau, S. N., Schaid, D. J., Wiklund, F., Chanock, S. J., Easton, D. F., Eeles, R. A., Kote-Jarai, Z., Conti, D. V., & Haiman, C. A. (2019). Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry. Nature communications, 10(1), 382. https://doi.org/10.1038/s41467-019-08293-z
Matejcic, Marco, et al. "Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry." Nature communications vol. 10,1 (2019): 382. doi: https://doi.org/10.1038/s41467-019-08293-z
Matejcic M, Saunders EJ, Dadaev T, Brook MN, Wang K, Sheng X, Olama AAA, Schumacher FR, Ingles SA, Govindasami K, Benlloch S, Berndt SI, Albanes D, Koutros S, Muir K, Stevens VL, Gapstur SM, Tangen CM, Batra J, Clements J, Gronberg H, Pashayan N, Schleutker J, Wolk A, West C, Mucci L, Kraft P, Cancel-Tassin G, Sorensen KD, Maehle L, Grindedal EM, Strom SS, Neal DE, Hamdy FC, Donovan JL, Travis RC, Hamilton RJ, Rosenstein B, Lu YJ, Giles GG, Kibel AS, Vega A, Bensen JT, Kogevinas M, Penney KL, Park JY, Stanford JL, Cybulski C, Nordestgaard BG, Brenner H, Maier C, Kim J, Teixeira MR, Neuhausen SL, De Ruyck K, Razack A, Newcomb LF, Lessel D, Kaneva R, Usmani N, Claessens F, Townsend PA, Gago-Dominguez M, Roobol MJ, Menegaux F, Khaw KT, Cannon-Albright LA, Pandha H, Thibodeau SN, Schaid DJ, Wiklund F, Chanock SJ, Easton DF, Eeles RA, Kote-Jarai Z, Conti DV, Haiman CA. Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry. Nat Commun. 2019 Jan 17;10(1):382. doi: 10.1038/s41467-019-08293-z. PMID: 30655571; PMCID: PMC6336778.
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Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways.

Nature communications

Duffy DL, Zhu G, Li X, Sanna M, Iles MM, Jacobs LC, Evans DM, Yazar S, Beesley J, Law MH, Kraft P, Visconti A, Taylor JC, Liu F, Wright MJ, Henders AK, Bowdler L, Glass D, Ikram MA, Uitterlinden AG, Madden PA, Heath AC, Nelson EC, Green AC, Chanock S, Barrett JH, Brown MA, Hayward NK, MacGregor S, Sturm RA, Hewitt AW, Kayser M, Hunter DJ, Newton Bishop JA, Spector TD, Montgomery GW, Mackey DA, Smith GD, Nijsten TE, Bishop DT, Bataille V, Falchi M, Han J, Martin NG.
PMID: 30643134
Nat Commun. 2019 Jan 14;10(1):299. doi: 10.1038/s41467-018-08078-w.

The original version of this Article contained errors in the spelling of the authors Fan Liu and M. Arfan Ikram, which were incorrectly given as Fan Lui and Arfan M. Ikram. In addition, the original version of this Article...

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Duffy DL, Zhu G, Li X, et al. Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. Nat Commun. 2019;10(1):299doi: 10.1038/s41467-018-08078-w.
Duffy, D. L., Zhu, G., Li, X., Sanna, M., Iles, M. M., Jacobs, L. C., Evans, D. M., Yazar, S., Beesley, J., Law, M. H., Kraft, P., Visconti, A., Taylor, J. C., Liu, F., Wright, M. J., Henders, A. K., Bowdler, L., Glass, D., Ikram, M. A., Uitterlinden, A. G., Madden, P. A., Heath, A. C., Nelson, E. C., Green, A. C., Chanock, S., Barrett, J. H., Brown, M. A., Hayward, N. K., MacGregor, S., Sturm, R. A., Hewitt, A. W., Kayser, M., Hunter, D. J., Newton Bishop, J. A., Spector, T. D., Montgomery, G. W., Mackey, D. A., Smith, G. D., Nijsten, T. E., Bishop, D. T., Bataille, V., Falchi, M., Han, J., & Martin, N. G. (2019). Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. Nature communications, 10(1), 299. https://doi.org/10.1038/s41467-018-08078-w
Duffy, David L, et al. "Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways." Nature communications vol. 10,1 (2019): 299. doi: https://doi.org/10.1038/s41467-018-08078-w
Duffy DL, Zhu G, Li X, Sanna M, Iles MM, Jacobs LC, Evans DM, Yazar S, Beesley J, Law MH, Kraft P, Visconti A, Taylor JC, Liu F, Wright MJ, Henders AK, Bowdler L, Glass D, Ikram MA, Uitterlinden AG, Madden PA, Heath AC, Nelson EC, Green AC, Chanock S, Barrett JH, Brown MA, Hayward NK, MacGregor S, Sturm RA, Hewitt AW, Kayser M, Hunter DJ, Newton Bishop JA, Spector TD, Montgomery GW, Mackey DA, Smith GD, Nijsten TE, Bishop DT, Bataille V, Falchi M, Han J, Martin NG. Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. Nat Commun. 2019 Jan 14;10(1):299. doi: 10.1038/s41467-018-08078-w. PMID: 30643134; PMCID: PMC6331636.
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Differential Afa/Dr Fimbriae Expression in the Multidrug-Resistant Escherichia coli ST131 Clone.

mBio

Alvarez-Fraga L, Phan MD, Goh KGK, Nhu NTK, Hancock SJ, Allsopp LP, Peters KM, Forde BM, Roberts LW, Sullivan MJ, Totsika M, Beatson SA, Ulett GC, Schembri MA.
PMID: 35038925
mBio. 2022 Jan 18;e0351921. doi: 10.1128/mbio.03519-21. Epub 2022 Jan 18.

Many antibiotic resistant uropathogenic Escherichia coli (UPEC) strains belong to clones defined by their multilocus sequence type (ST), with ST131 being the most dominant. Although we have a good understanding of resistance development to fluoroquinolones and third-generation cephalosporins by...

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Alvarez-Fraga L, Phan MD, Goh KGK, et al. Differential Afa/Dr Fimbriae Expression in the Multidrug-Resistant Escherichia coli ST131 Clone. mBio. 2022;e0351921doi: 10.1128/mbio.03519-21.
Alvarez-Fraga, L., Phan, M. D., Goh, K. G. K., Nhu, N. T. K., Hancock, S. J., Allsopp, L. P., Peters, K. M., Forde, B. M., Roberts, L. W., Sullivan, M. J., Totsika, M., Beatson, S. A., Ulett, G. C., & Schembri, M. A. (2022). Differential Afa/Dr Fimbriae Expression in the Multidrug-Resistant Escherichia coli ST131 Clone. mBio, e0351921. https://doi.org/10.1128/mbio.03519-21
Alvarez-Fraga, Laura, et al. "Differential Afa/Dr Fimbriae Expression in the Multidrug-Resistant Escherichia coli ST131 Clone." mBio vol. (2022): e0351921. doi: https://doi.org/10.1128/mbio.03519-21
Alvarez-Fraga L, Phan MD, Goh KGK, Nhu NTK, Hancock SJ, Allsopp LP, Peters KM, Forde BM, Roberts LW, Sullivan MJ, Totsika M, Beatson SA, Ulett GC, Schembri MA. Differential Afa/Dr Fimbriae Expression in the Multidrug-Resistant Escherichia coli ST131 Clone. mBio. 2022 Jan 18;e0351921. doi: 10.1128/mbio.03519-21. Epub 2022 Jan 18. PMID: 35038925.
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Stomaching Multigene Panel Testing: What to Do About CDH1?.

Journal of the National Cancer Institute

Stewart DR, Frone MN, Chanock SJ.
PMID: 31841165
J Natl Cancer Inst. 2020 Apr 01;112(4):325-326. doi: 10.1093/jnci/djz230.

No abstract available.

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Stewart DR, Frone MN, Chanock SJ. Stomaching Multigene Panel Testing: What to Do About CDH1?. J Natl Cancer Inst. 2020;112(4):325-326doi: 10.1093/jnci/djz230.
Stewart, D. R., Frone, M. N., & Chanock, S. J. (2020). Stomaching Multigene Panel Testing: What to Do About CDH1?. Journal of the National Cancer Institute, 112(4), 325-326. https://doi.org/10.1093/jnci/djz230
Stewart, Douglas R, et al. "Stomaching Multigene Panel Testing: What to Do About CDH1?." Journal of the National Cancer Institute vol. 112,4 (2020): 325-326. doi: https://doi.org/10.1093/jnci/djz230
Stewart DR, Frone MN, Chanock SJ. Stomaching Multigene Panel Testing: What to Do About CDH1?. J Natl Cancer Inst. 2020 Apr 01;112(4):325-326. doi: 10.1093/jnci/djz230. PMID: 31841165; PMCID: PMC7156934.
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Author Correction to: Endemic Burkitt lymphoma in second-degree relatives in Northern Uganda: in-depth genome-wide analysis suggests clues about genetic susceptibility.

Leukemia

Gouveia MH, Otim I, Ogwang MD, Wang M, Zhu B, Cole N, Luo W, Hicks B, Jones K, Oehl-Huber K, Ayers LW, Pittaluga S, Legason ID, Nabalende H, Kerchan P, Kinyera T, Kawira E, Brubaker G, Levin AG, Guertler L, Kim J, Stewart DR, Adde M, Magrath I, Bergen AW, Reynolds SJ, Yeager M, Bhatia K, Adeyemo AA, Prokunina-Olsson L, Dean M, Shriner D, Rotimi CN, Chanock S, Siebert R, Mbulaiteye SM.
PMID: 33526862
Leukemia. 2021 Apr;35(4):1224. doi: 10.1038/s41375-021-01140-5.

No abstract available.

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Gouveia MH, Otim I, Ogwang MD, et al. Author Correction to: Endemic Burkitt lymphoma in second-degree relatives in Northern Uganda: in-depth genome-wide analysis suggests clues about genetic susceptibility. Leukemia. 2021;35(4):1224doi: 10.1038/s41375-021-01140-5.
Gouveia, M. H., Otim, I., Ogwang, M. D., Wang, M., Zhu, B., Cole, N., Luo, W., Hicks, B., Jones, K., Oehl-Huber, K., Ayers, L. W., Pittaluga, S., Legason, I. D., Nabalende, H., Kerchan, P., Kinyera, T., Kawira, E., Brubaker, G., Levin, A. G., Guertler, L., Kim, J., Stewart, D. R., Adde, M., Magrath, I., Bergen, A. W., Reynolds, S. J., Yeager, M., Bhatia, K., Adeyemo, A. A., Prokunina-Olsson, L., Dean, M., Shriner, D., Rotimi, C. N., Chanock, S., Siebert, R., & Mbulaiteye, S. M. (2021). Author Correction to: Endemic Burkitt lymphoma in second-degree relatives in Northern Uganda: in-depth genome-wide analysis suggests clues about genetic susceptibility. Leukemia, 35(4), 1224. https://doi.org/10.1038/s41375-021-01140-5
Gouveia, Mateus H, et al. "Author Correction to: Endemic Burkitt lymphoma in second-degree relatives in Northern Uganda: in-depth genome-wide analysis suggests clues about genetic susceptibility." Leukemia vol. 35,4 (2021): 1224. doi: https://doi.org/10.1038/s41375-021-01140-5
Gouveia MH, Otim I, Ogwang MD, Wang M, Zhu B, Cole N, Luo W, Hicks B, Jones K, Oehl-Huber K, Ayers LW, Pittaluga S, Legason ID, Nabalende H, Kerchan P, Kinyera T, Kawira E, Brubaker G, Levin AG, Guertler L, Kim J, Stewart DR, Adde M, Magrath I, Bergen AW, Reynolds SJ, Yeager M, Bhatia K, Adeyemo AA, Prokunina-Olsson L, Dean M, Shriner D, Rotimi CN, Chanock S, Siebert R, Mbulaiteye SM. Author Correction to: Endemic Burkitt lymphoma in second-degree relatives in Northern Uganda: in-depth genome-wide analysis suggests clues about genetic susceptibility. Leukemia. 2021 Apr;35(4):1224. doi: 10.1038/s41375-021-01140-5. PMID: 33526862; PMCID: PMC8182765.
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