Zobrazeno 1 - 10
of 228
pro vyhledávání: '"Burdon, KP"'
Autor:
Landi MT, Bishop DT, MacGregor S, Machiela MJ, Stratigos AJ, Ghiorzo P, Brossard M, Calista D, Choi J, Fargnoli MC, Zhang T, Rodolfo M, Trower AJ, Menin C, Martinez J, Hadjisavvas A, Song L, Stefanaki I, Scolyer R, Yang R, Goldstein AM, Potrony M, Kypreou KP, Pastorino L, Queirolo P, Pellegrini C, Cattaneo L, Zawistowski M, Gimenez-Xavier P, Rodriguez A, Elefanti L, Manoukian S, Rivoltini L, Smith BH, Loizidou MA, Del Regno L, Massi D, Mandala M, Khosrotehrani K, Akslen LA, Amos CI, Andresen PA, Avril MF, Azizi E, Soyer HP, Bataille V, Dalmasso B, Bowdler LM, Burdon KP, Chen WV, Codd V, Craig JE, Debniak T, Falchi M, Fang S, Friedman E, Simi S, Galan P, Garcia-Casado Z, Gillanders EM, Gordon S, Green A, Gruis NA, Hansson J, Harland M, Harris J, Helsing P, Henders A, Hocevar M, Höiom V, Hunter D, Ingvar C, Kumar R, Lang J, Lathrop GM, Lee JE, Li X, Lubinski J, Mackie RM, Malt M, Malvehy J, McAloney K, Mohamdi H, Molven A, Moses EK, Neale RE, Novakovic S, Nyholt DR, Olsson H, Orr N, Fritsche LG, Puig-Butille JA, Qureshi AA, Radford-Smith GL, Randerson-Moor J, Requena C, Rowe C, Samani NJ, Sanna M, Schadendorf D, Schulze HJ, Simms LA, Smithers M, Song F, Swerdlow AJ, van der Stoep N, Kukutsch NA, Visconti A, Wallace L, Ward SV, Wheeler L, Sturm RA, Hutchinson A, Jones K, Malasky M, Vogt A, Zhou W, Pooley KA, Elder DE, Han J, Hicks B, Hayward NK, Kanetsky PA, Brummett C, Montgomery GW, Olsen CM, Hayward C, Dunning AM, Martin NG, Evangelou E, Mann GJ, Long G, Pharoah PDP, Easton DF, Barrett JH, Cust AE, Abecasis G, Duffy DL, Whiteman DC, Gogas H, De Nicolo A, Tucker MA, Newton-Bishop JA, GenoMEL Consortium, Q-MEGA and QTWIN Investigators, ATHENS Melanoma Study Group, 23andMe, SDH Study Group, IBD Investigators, Essen-Heidelberg Investigators, AMFS Investigators, MelaNostrum Consortium, Peris K, Chanock SJ, Demenais F, Brown KM, Puig S, Nagore E, Shi J, Iles MM, Law MH
Publikováno v:
NATURE GENETICS
r-FISABIO. Repositorio Institucional de Producción Científica
instname
r-FISABIO: Repositorio Institucional de Producción Científica
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)
r-FISABIO. Repositorio Institucional de Producción Científica
instname
r-FISABIO: Repositorio Institucional de Producción Científica
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)
Meta-analysis of 36,760 cases and 375,188 controls identifies 54 loci associated with susceptibility to cutaneous melanoma. Further analysis combining nevus count and hair color GWAS results provide insights into the genetic architecture of melanoma.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::49ffdffa88c2703a078a866f66e1098f
http://hdl.handle.net/11391/1480983
http://hdl.handle.net/11391/1480983
Autor:
Iglesias, AI, Mishra, A, Vitart, V, Bykhovskaya, Y, Hoehn, R, Springelkamp, H, Cuellar-Partida, G, Gharahkhani, P, Bailey, JNC, Willoughby, CE, Li, X, Yazar, S, Nag, A, Khawaja, AP, Polasek, O, Siscovick, D, Mitchell, P, Tham, YC, Haines, JL, Kearns, LS, Hayward, C, Shi, Y, van Leeuwen, EM, Taylor, KD, Bonnemaijer, P, Rotter, JI, Martin, NG, Zeller, T, Mills, RA, Souzeau, E, Staffieri, SE, Jonas, JB, Schmidtmann, I, Boutin, T, Kang, JH, Lucas, SEM, Wong, TY, Beutel, ME, Wilson, JF, Uitterlinden, AG, Vithana, EN, Foster, PJ, Hysi, PG, Hewitt, AW, Khor, CC, Pasquale, LR, Montgomery, GW, Klaver, CCW, Aung, T, Pfeiffer, N, Mackey, DA, Hammond, CJ, Cheng, C-Y, Craig, JE, Rabinowitz, YS, Wiggs, JL, Burdon, KP, van Duijn, CM, MacGregor, S, Wang, JJ, Rochtchina, E, Attia, J, Scott, R, Holliday, EG, Baird, PN, Xie, J, Inouye, M, Viswanathan, A, Sim, X, Allingham, RR, Brilliant, MH, Budenz, DL, Christen, WG, Fingert, J, Friedman, DS, Gaasterland, D, Gaasterland, T, Hauser, MA, Kraft, P, Lee, RK, Lichter, PR, Liu, Y, Loomis, SJ, Moroi, SE, Pericak-Vance, MA, Realini, A, Richards, JE, Schuman, JS, Scott, WK, Singh, K, Sit, AJ, Vollrath, D, Weinreb, RN, Wollstein, G, Zack, DJ, Zhang, K, Donnelly, P, Barroso, I, Blackwell, JM, Bramon, E, Brown, MA, Casas, JP, Corvin, A, Deloukas, P, Duncanson, A, Jankowski, J, Markus, HS, Mathew, CG, Palmer, CNA, Plomin, R, Rautanen, A, Sawcer, SJ, Trembath, RC, Wood, NW, Spencer, CCA, Band, G, Bellenguez, C, Freeman, C, Hellenthal, G, Giannoulatou, E, Pirinen, M, Pearson, R, Strange, A, Su, Z, Vukcevic, D, Langford, C, Hunt, SE, Edkins, S, Gwilliam, R, Blackburn, H, Bumpstead, SJ, Dronov, S, Gillman, M, Gray, E, Hammond, N, Jayakumar, A, McCann, OT, Liddle, J, Potter, SC, Ravindrarajah, R, Ricketts, M, Waller, M, Weston, P, Widaa, S, Whittaker, P, Grp, BMES-G, Consortium, N, Control, WTC
Publikováno v:
Nature Communications
2019, ' Author Correction : Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases ', Nature Communications, vol. 10, no. 1, pp. 155 . https://doi.org/10.1038/s41467-018-07819-1
Nature communications, vol 10, iss 1
Nature Communications, Vol 10, Iss 1, Pp 1-3 (2019)
2019, ' Author Correction : Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases ', Nature Communications, vol. 10, no. 1, pp. 155 . https://doi.org/10.1038/s41467-018-07819-1
Nature communications, vol 10, iss 1
Nature Communications, Vol 10, Iss 1, Pp 1-3 (2019)
Central corneal thickness (CCT) is a highly heritable trait associated with complex eye diseases such as keratoconus and glaucoma. We perform a genome-wide association meta-analysis of CCT and identify 19 novel regions. In addition to adding support
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1c74ca8820ef6681bb83631982eb0bd
http://ora.ox.ac.uk/objects/uuid:
http://ora.ox.ac.uk/objects/uuid:
Autor:
Duffy, David L, Zhu, Gu, Xin, Li, Sanna, Marianna, Iles, Mark M, Jacobs, Leonie C, Evans, David M, Yazar, Seyhan, Beesley, Jonathan, Law, Matthew H, Kraft, Peter, Visconti, Alessia, Taylor, John C, Lui, Fan, Wright, Margaret J, Henders, Anjali K, Bowdler, Lisa, Glass, Dan, Ikram, Arfan M, Uitterlinden, André G, Madden, Pamela A, Heath, Andrew C, Nelson, Elliot C, Green, Adele C, Chanock, Stephen, Barrett, Jennifer H, Brown, Matthew A, Hayward, Nicholas K, Macgregor, Stuart, Sturm, Richard A, Hewitt, Alex W, Kayser, Manfred, Hunter, David J, Newton Bishop, Julia A, Spector, Timothy D, Montgomery, Grant W, Mackey, David A, Smith, George Davey, Nijsten, Tamar E, Bishop, D Timothy, Bataille, Veronique, Falchi, Mario, Han, Jiali, Martin, Nicholas, G, Lee, Je, Brossard, M, Moses, Ek, Song, F, Kumar, R, Easton, Df, Pharoah, Pdp, Swerdlow, Aj, Kypreou, Kp, Harland, M, Randerson-Moor, J, Akslen, La, Andresen, Pa, Avril, Mf, Azizi, E, Scarrà, Gb, Brown, Km, Dębniak, T, Elder, De, Fang, S, Friedman, E, Galan, P, Ghiorzo, P, Gillanders, Em, Goldstein, Am, Gruis, Na, Hansson, J, Helsing, P, Hočevar, M, Höiom, V, Ingvar, C, Kanetsky, Pa, Chen, Wv, Landi, Mt, Lang, J, Lathrop, Gm, Lubiński, J, Mackie, Rm, Mann, Gj, Molven, A, Novaković, S, Olsson, H, Puig, S, Puig-Butille, Ja, Radford-Smith, Gl, van der Stoep, N, van Doorn, R, Whiteman, Dc, Craig, Je, Schadendorf, D, Simms, La, Burdon, Kp, Nyholt, Dr, Pooley, Ka, Orr, N, Stratigos, Aj, Cust, Ae, Ward, Sv, Schulze, Hj, Dunning, Am, Demenais, F, Amos, Ci.
Publikováno v:
Nature Communications, 9:4774. Nature Publishing Group
Nature Communications, Vol 9, Iss 1, Pp 1-10 (2018)
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, Lui, F, Henders, A K, Bowdler, L, Glass, D, Ikram, A M, Uitterlinden, A G, Wright, M J, 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 2018, ' Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways ', Nature Communications, vol. 9, no. 1, pp. 4774 . https://doi.org/10.1038/s41467-018-06649-5
Melanoma GWAS Consortium 2018, ' Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways ', Nature Communications, vol. 9, no. 1, 4774 . https://doi.org/10.1038/s41467-018-06649-5
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, Lui, F, Wright, M J, Henders, A K, Bowdler, L, Glass, D, Ikram, A M, 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, Lee, J E, Brossard, M, Moses, E K, Song, F, Kumar, R, Easton, D F, Pharoah, P D P, Swerdlow, A J, Kypreou, K P, Harland, M, Randerson-Moor, J, Akslen, L A, Andresen, P A, Avril, M F, Azizi, E, Scarrà, G B, Brown, K M & Dębniak, T & Smith, G D 2018, ' Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways ', Nature Communications, vol. 9, 4774 . https://doi.org/10.1038/s41467-018-06649-5
Nature Communications, Vol 9, Iss 1, Pp 1-10 (2018)
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, Lui, F, Henders, A K, Bowdler, L, Glass, D, Ikram, A M, Uitterlinden, A G, Wright, M J, 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 2018, ' Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways ', Nature Communications, vol. 9, no. 1, pp. 4774 . https://doi.org/10.1038/s41467-018-06649-5
Melanoma GWAS Consortium 2018, ' Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways ', Nature Communications, vol. 9, no. 1, 4774 . https://doi.org/10.1038/s41467-018-06649-5
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, Lui, F, Wright, M J, Henders, A K, Bowdler, L, Glass, D, Ikram, A M, 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, Lee, J E, Brossard, M, Moses, E K, Song, F, Kumar, R, Easton, D F, Pharoah, P D P, Swerdlow, A J, Kypreou, K P, Harland, M, Randerson-Moor, J, Akslen, L A, Andresen, P A, Avril, M F, Azizi, E, Scarrà, G B, Brown, K M & Dębniak, T & Smith, G D 2018, ' Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways ', Nature Communications, vol. 9, 4774 . https://doi.org/10.1038/s41467-018-06649-5
The total number of acquired melanocytic nevi on the skin is strongly correlated with melanoma risk. Here we report a meta-analysis of 11 nevus GWAS from Australia, Netherlands, United Kingdom, and United States, comprising a total of 52,506 phenotyp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fdc17d2ba531806731975db2a684a16
https://www.repository.cam.ac.uk/handle/1810/288608
https://www.repository.cam.ac.uk/handle/1810/288608
Autor:
Zhang, Tongwu, Choi, Jiyeon, Kovacs, Michael A., Shi, Jianxin, Mai, Xu, Goldstein, Alisa M., Trower, Adam J., Bishop, D. Timothy, Iles, Mark M., Duffy, David L., Macgregor, Stuart, Amundadottir, Laufey T., Law, Matthew H., Loftus, Stacie K., Pavan, William J., Brown, Kevin M., Lee, Je, Brossard, M, Martin, Ng, Moses, Ek, Song, F, Barrett, Jh, Kumar, R, Easton, Df, Pharoah, Pdp, Swerdlow, Aj, Kypreou, Kp, Taylor, Jc, Harland, M, Randerson-Moor, J, Akslen, La, Andresen, Pa, Avril, Mf, Azizi, E, Bianchi Scarrà, G, Dȩbniak, T, Duffy, Dl, Elder, De, Fang, S, Friedman, E, Galan, P, Ghiorzo, P, Gillanders, Em, Goldstein, Am, Gruis, Na, Hansson, J, Helsing, P, Hočevar, M, Höiom, V, Ingvar, C, Kanetsky, Pa, Chen, Wv, Landi, Mt, Lang, J, Lathrop, Gm, Lubiński, J, Mackie, Rm, Mann, Gj, Molven, A, Montgomery, Gw, Novaković, S, Olsson, H, Puig, S, Puig-Butille, Ja, Wu, W, Qureshi, Aa, Radford-Smith, Gl, van der Stoep, N, van Doorn, R, Whiteman, Dc, Craig, Je, Schadendorf, D, Simms, La, Burdon, Kp, Nyholt, Dr, Pooley, Ka, Orr, N, Stratigos, Aj, Cust, Ae, Ward, Sv, Hayward, Nk, Han, J, Schulze, Hj, Dunning, Am, Bishop, Jan, Demenais, F, Amos, Ci, Macgregor, S, Iles, Mm, Barnabas, Bb, Bouffard, Gg, Brooks, Sy, Coleman, H, Dekhtyar, L, Guan, X, Ho, Sl, Legaspi, R, Maduro, Ql, Masiello, Ca, Mcdowell, Jc, Montemayor, C, Mullikin, Jc, Park, M, Riebow, Nl, Schandler, K, Schmidt, B, Sison, C, Smith, R, Stantripop, S, Thomas, Jw, Thomas, Pj, Vemulapalli, M, Young, Ac.
Publikováno v:
Genome Research, 28(11), 1621-1635
Most expression quantitative trait locus (eQTL) studies to date have been performed in heterogeneous tissues as opposed to specific cell types. To better understand the cell-type–specific regulatory landscape of human melanocytes, which give rise t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15f62743de9139d3fa5865ac39a0f335
https://europepmc.org/articles/PMC6211648/
https://europepmc.org/articles/PMC6211648/
Autor:
Gorin, Michael, Moore, Anthony, Fritsche, LG, Igl, W, Bailey, JNC, Grassmann, F, Sengupta, S, Bragg-Gresham, JL, Burdon, KP, Hebbring, SJ, Wen, C, Gorski, M
Publikováno v:
Gorin, Michael; Moore, Anthony; Fritsche, LG; Igl, W; Bailey, JNC; Grassmann, F; et al.(2016). A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/0d36b4wt
© 2016 Nature America, Inc.Advanced age-related macular degeneration (AMD) is the leading cause of blindness in the elderly, with limited therapeutic options. Here we report on a study of >12 million variants, including 163,714 directly genotyped, m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::4e81445caba4f6ca9eae8e743002fea8
http://www.escholarship.org/uc/item/0d36b4wt
http://www.escholarship.org/uc/item/0d36b4wt
Autor:
Bailey, JNC, Loomis, SJ, Kang, JH, Allingham, RR, Gharahkhani, P, Khor, CC, Burdon, KP, Aschard, H, Chasman, DI, Igo, RP, Hysi, PG, Glastonbury, CA, Ashley-Koch, A, Brilliant, M, Brown, AA, Budenz, DL, Buil, A, Cheng, CY, Choi, H, Christen, WG, Curhan, G, De Vivo, I, Fingert, JH, Foster, PJ, Fuchs, C, Gaasterland, D, Gaasterland, T, Hewitt, AW, Hu, F, Hunter, DJ, Khawaja, AP, Lee, RK, Li, Z, Lichter, PR, Mackey, DA, McGuffin, P, Mitchell, P, Moroi, SE, Perera, SA, Pepper, KW, Qi, Q, Realini, T, Richards, JE, Ridker, PM, Rimm, E, Ritch, R, Ritchie, M, Schuman, JS, Scott, WK, Singh, K, Sit, AJ, Song, YE, Tamimi, RM, Topouzis, F, Viswanathan, AC, Verma, SS, Vollrath, D, Wang, JJ, Weisschuh, N, Wissinger, B, Wollstein, G, Wong, TY, Yaspan, BL, Zack, DJ, Zhang, K, Weinreb, RN, Pericak-Vance, MA, Small, K, Hammond, CJ, Aung, T, Liu, Y, Vithana, EN, MacGregor, S, Craig, JE, Kraft, P, Howell, G, Hauser, MA, Pasquale, LR
Publikováno v:
Bailey, JNC; Loomis, SJ; Kang, JH; Allingham, RR; Gharahkhani, P; Khor, CC; et al.(2016). Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma. Nature Genetics, 48(2), 189-194. doi: 10.1038/ng.3482. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/1sh4p2w9
© 2016 Nature America, Inc. Primary open-angle glaucoma (POAG) is a leading cause of blindness worldwide. To identify new susceptibility loci, we performed meta-analysis on genome-wide association study (GWAS) results from eight independent studies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::0dcfbd0062b24171ab7afeacfac4f9d0
http://www.escholarship.org/uc/item/1sh4p2w9
http://www.escholarship.org/uc/item/1sh4p2w9
Autor:
Law, M, Bishop, DT, Lee, JE, Brossard, M, Martin, NG, Moses, EK, Song, F, Barrett, JH, Kumar, R, Easton, DF, Pharoah, PDP, Swerdlow, AJ, Kypreou, KP, Taylor, JC, Harland, M, Randerson-Moor, J, Akslen, LA, Andresen, PA, Avril, MF, Azizi, E, Scarra, GB, Brown, KM, Debniak, T, Duffy, DL, Elder, DE, Fang, S, Friedman, E, Galan, P, Ghiorzo, P, Gillanders, EM, Goldstein, AM, Gruis, NE, Hansson, J, Helsing, P, Hocevar, M, Hoiom, V, Ingvar, C, Kanetsky, PA, Chen, WV, GenoMEL Consortium, Essen-Heidelberg Investigators, The SDH Study Group, Q-MEGA and QTWIN Investigators, AMFS Investigators, ATHENS Melanoma Study Group, Landi, MT, Lang, J, Lathrop, M, Lubinski, J, Mackie, RM, Mann, GJ, Molvern, A, Montgomery, GW, Novakovic, S, Olsson, H, Puig, S, Puig-Butille, JA, Qureshi, AA, Radford-Smith, GL, van der Stoep, N, van Doorn, R, Whiteman, DC, Craig, JE, Schadendorf, D, Simms, LA, Burdon, KP, Nyholt, DR, Pooley, KA, Orr, N, Stratigos, AJ, Cust, AE, Ward, SV, Hayward, NK, Han, J, Schulze, HJ, Dunning, AM, Newton-Bishop, JA, Demenais, F, Amos, CI, MacGregor, S, Iles, MM
Publikováno v:
Nature genetics
Nature Genetics, 47(9), 987
Nature Genetics, 47(9), 987
© 2015 Nature America, Inc. All rights reserved.Thirteen common susceptibility loci have been reproducibly associated with cutaneous malignant melanoma (CMM). We report the results of an international 2-stage meta-analysis of CMM genome-wide associa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6e5f9ff31a6c8a038f83a3f0a16ecbf
https://hdl.handle.net/1887/107531
https://hdl.handle.net/1887/107531
Autor:
Springelkamp, H, Mishra, A, Hysi, PG, Gharahkhani, P, Höhn, R, Khor, CC, Cooke Bailey, JN, Luo, X, Ramdas, WD, Vithana, E, Koh, V, Yazar, S, Xu, L, Forward, H, Kearns, LS, Amin, N, Iglesias, AI, Sim, KS, van Leeuwen, EM, Demirkan, A, van der Lee, S, Loon, SC, Rivadeneira, F, Nag, A, Sanfilippo, PG, Schillert, A, de Jong, PTVM, Oostra, BA, Uitterlinden, AG, Hofman, A, Zhou, T, Burdon, KP, Spector, TD, Lackner, KJ, Saw, SM, Vingerling, JR, Teo, YY, Pasquale, LR, Wolfs, RCW, Lemij, HG, Tai, ES, Jonas, JB, Cheng, CY, Aung, T, Jansonius, NM, Klaver, CCW, Craig, JE, Young, TL, Haines, JL, Macgregor, S, Mackey, DA, Pfeiffer, N, Wong, TY, Wiggs, JL, Hewitt, AW, van Duijn, CM, Hammond, CJ, Allingham, RR, Brilliant, MH, Budenz, DL, Bailey, JNC, Christen, WG, Fingert, J
Publikováno v:
Springelkamp, H; Mishra, A; Hysi, PG; Gharahkhani, P; Höhn, R; Khor, CC; et al.(2015). Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology. Genetic Epidemiology, 39(3), 207-216. doi: 10.1002/gepi.21886. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/4kg6w8wk
© 2015 Wiley Periodicals, Inc. Primary open-angle glaucoma is the most common optic neuropathy and an important cause of irreversible blindness worldwide. The optic nerve head or optic disc is divided in two parts: a central cup (without nerve fiber
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::b9f992d7ae4f268c1f4d2c601900a09f
http://www.escholarship.org/uc/item/4kg6w8wk
http://www.escholarship.org/uc/item/4kg6w8wk
Autor:
Springelkamp, H, Höhn, R, Mishra, A, Hysi, PG, Khor, CC, Loomis, SJ, Bailey, JNC, Gibson, J, Thorleifsson, G, Janssen, SF, Luo, X, Ramdas, WD, Vithana, E, Nongpiur, ME, Montgomery, GW, Xu, L, Mountain, JE, Gharahkhani, P, Lu, Y, Amin, N, Karssen, LC, Sim, KS, Van Leeuwen, EM, Iglesias, AI, Verhoeven, VJM, Hauser, MA, Loon, SC, Despriet, DDG, Nag, A, Venturini, C, Sanfilippo, PG, Schillert, A, Kang, JH, Landers, J, Jonasson, F, Cree, AJ, Van Koolwijk, LME, Rivadeneira, F, Souzeau, E, Jonsson, V, Menon, G, Mitchell, P, Wang, JJ, Rochtchina, E, Attia, J, Scott, R, Holliday, EG, Baird, PN, Xie, J, Inouye, M, Viswanathan, A, Sim, X, Weinreb, RN, De Jong, PTVM, Oostra, BA, Uitterlinden, AG, Hofman, A, Ennis, S, Thorsteinsdottir, U, Burdon, KP, Allingham, RR, Brilliant, MH, Budenz, DL, Christen, WG, Fingert, J, Friedman, DS, Gaasterland, D, Gaasterland, T, Haines, JL, Kraft, P, Lee, RK, Lichter, PR, Liu, Y
Publikováno v:
Springelkamp, H; Höhn, R; Mishra, A; Hysi, PG; Khor, CC; Loomis, SJ; et al.(2014). Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process. Nature Communications, 5. doi: 10.1038/ncomms5883. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/8tq3b2r0
© 2014 Macmillan Publishers Limited. All rights reserved. Glaucoma is characterized by irreversible optic nerve degeneration and is the most frequent cause of irreversible blindness worldwide. Here, the International Glaucoma Genetics Consortium con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::432a7734471df3879f32c6d2d291d0b9
http://www.escholarship.org/uc/item/8tq3b2r0
http://www.escholarship.org/uc/item/8tq3b2r0
Autor:
Verhoeven, Virginie, Hysi, PG, Wojciechowski, R, Fan, Q, Guggenheim, JA, Hohn, R, Macgregor, S, Hewitt, AW, Nag, A, Cheng, CY (Ching-Yu), Yonova-Doing, E, Zhou, X, Ikram, Kamran, Buitendijk, Gabriëlle, McMahon, G, Kemp, JP, St Pourcain, B, Simpson, CL, Makela, KM, Lehtimaki, T, Kahonen, M, Paterson, AD, Hosseini, SM, Wong, HS, Xu, L, Jonas, JB, Parssinen, O, Wedenoja, J, Yip, SP, Ho, DWH, Pang, CP, Chen, LJ, Burdon, KP, Craig, JE, Klein, BEK, Klein, R, Haller, T, Metspalu, A, Khor, CC, Tai, ES, Aung, T, Vithana, E, Tay, WT, Barathi, VA, Chen, Peng, Li, RY, Liao, JM, Zheng, YF, Ong, RT, Doring, A, Evans, DM, Timpson, NJ, Verkerk, AJMH, Meitinger, T, Raitakari, O, Hawthorne, F, Spector, TD, Karssen, Lennart, Pirastu, M, Murgia, F, Ang, W, Mishra, A, Montgomery, GW, Pennell, CE, Cumberland, PM, Cotlarciuc, I, Mitchell, P, Wang, JJ, Schache, M, Janmahasathian, S, Igo, RP, Lass, JH, Chew, E, KIyengar, S, Gorgels, TGMF (Theo), Rudan, I, Hayward, C, Wright, AF, Polasek, O, Vatavuk, Z, Wilson, JF, Fleck, B, Zeller, T, Mirshahi, A, Müller, Caspar, Uitterlinden, André, Rivadeneira, Fernando, Vingerling, Hans, Hofman, Bert, Oostra, Ben, Amin, Najaf, Bergen, Arthur, Teo, YY, Rahi, JS, Vitart, V, Williams, C, Baird, PN, Wong, TY (Tien Yin), Oexle, K, Pfeiffer, N, Mackey, DA, Young, TL, Duijn, Cornelia, Saw, SM, Bailey-Wilson, JE, Stambolian, D, Klaver, Caroline, Hammond, CJ
Publikováno v:
Nature Genetics, 45(6), 712-712. Nature Publishing Group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::3e92fe2e5bd8b0cb5d78bc38a66b640d
https://pure.eur.nl/en/publications/929fed19-1960-493d-9153-0fd39eddeabb
https://pure.eur.nl/en/publications/929fed19-1960-493d-9153-0fd39eddeabb