1.Identification of methylation haplotype blocks aids in deconvolution of heterogeneous tissue samples and tumor tissue-of-origin mapping from plasma DNA

Guo, SC, Diep, D, Pl     More...

Guo, SC, Diep, D, Plongthongkum, N, Fung, HL, Zhang, K, Zhang, K     Less

NATURE GENETICS[1061-4036], Published 2017, Volume 49, Issue 4, Pages 635-642

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WOS核心合集引用: 274  2022影響因子:  30.8  发表年影響因子:  27.125 

2.A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants

Fritsche, LG, Igl, W     More...

Fritsche, LG, Igl, W, Bailey, JNC, Grassmann, F, Sengupta, S, Bragg-Gresham, JL, Burdon, KP, Hebbring, SJ, Wen, C, Gorski, M, Kim, IK, Cho, D, Zack, D, Souied, E, Scholl, HPN, Bala, E, Lee, KE, Hunter, DJ, Sardell, RJ, Mitchell, P, Merriam, JE, Cipriani, V, Hoffman, JD, Schick, T, Lechanteur, YTE, Guymer, RH, Johnson, MP, Jiang, YD, Stanton, CM, Buitendijk, GHS, Zhan, XW, Kwong, AM, Boleda, A, Brooks, M, Gieser, L, Ratnapriya, R, Branham, KE, Foerster, JR, Heckenlively, JR, Othman, MI, Vote, BJ, Liang, HH, Souzeau, E, McAllister, IL, Isaacs, T, Hall, J, Lake, S, Mackey, DA, Constable, IJ, Craig, JE, Kitchner, TE, Yang, ZL, Su, ZG, Luo, HR, Chen, D, Hong, OY, Flagg, K, Lin, D, Mao, GP, Ferreyra, H, Starke, K, von Strachwitz, CN, Wolf, A, Brandl, C, Rudolph, G, Olden, M, Morrison, MA, Morgan, DJ, Schu, M, Ahn, J, Silvestri, G, Tsironi, EE, Park, KH, Farrer, LA, Orlin, A, Brucker, A, Li, MY, Curcio, CA, Mohand-Said, S, Sahel, JM, Audo, I, Benchaboune, M, Cree, AJ, Rennie, CA, Goverdhan, SV, Grunin, M, Hagbi-Levi, S, Campochiaro, P, Katsanis, N, Holz, FG, Blond, F, Blanche, H, Deleuze, JF, Igo, RP, Truitt, B, Peachey, NS, Meuer, SM, Myers, CE, Moore, EL, Klein, R, Hauser, MA, Postel, EA, Courtenay, MD, Schwartz, SG, Kovach, JL, Scott, WK, Liew, G, Tan, AG, Gopinath, B, Merriam, JC, Smith, RT, Khan, JC, Shahid, H, Moore, AT, McGrath, JA, Laux, R, Brantley, MA, Agarwal, A, Ersoy, L, Caramoy, A, Langmann, T, Saksens, NTM, de Jong, EK, Hoyng, CB, Cain, MS, Richardson, AJ, Martin, TM, Blangero, J, Weeks, DE, Dhillon, B, van Duijn, CM, Doheny, KF, Romm, J, Klaver, CCW, Hayward, C, Gorin, MB, Klein, ML, Baird, PN, den Hollander, AI, Fauser, S, Yates, JRW, Allikmets, R, Wang, JJ, Schaumberg, DA, Klein, BEK, Hagstrom, SA, Chowers, I, Lotery, AJ, Leveillard, T, Zhang, K, Brilliant, MH, Hewitt, AW, Swaroop, A, Chew, EY, Pericak-Vance, MA, DeAngelis, M, Stambolian, D, Haines, JL, Iyengar, SK, Weber, BHF, Abecasis, GR, Heid, IM     Less

NATURE GENETICS[1061-4036], Published 2016, Volume 48, Issue 2, Pages 134-143

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WOS核心合集引用: 886  2022影響因子:  30.8  发表年影響因子:  27.959 

3.Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma

Bailey, JNC, Loomis,     More...

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, QB, 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, YT, Vithana, EN, MacGregor, S, Craig, JE, Kraftl, P, Howell, G, Hauser, MA, Pasguale, LR, Haines, JL, Wiggs, JL     Less

NATURE GENETICS[1061-4036], Published 2016, Volume 48, Issue 2, Pages 189-194

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WOS核心合集引用: 162  2022影響因子:  30.8  发表年影響因子:  27.959 

4.Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma

Hysi, PG, Cheng, CY,     More...

Hysi, PG, Cheng, CY, Springelkamp, H, Macgregor, S, Bailey, JNC, Wojciechowski, R, Vitart, V, Nag, A, Hewitt, AW, Hohn, R, Venturini, C, Mirshahi, A, Ramdas, WD, Thorleifsson, G, Vithana, E, Khor, CC, Stefansson, AB, Liao, JM, Haines, JL, Amin, N, Wang, YX, Wild, PS, Ozel, AB, Li, JZ, Fleck, BW, Zeller, T, Staffieri, SE, Teo, YY, Cuellar-Partida, G, Luo, XY, Allingham, RR, Richards, JE, Senft, A, Karssen, LC, Zheng, YF, Bellenguez, C, Xu, L, Iglesias, AI, Wilson, JF, Kang, JH, van Leeuwen, EM, Jonsson, V, Thorsteinsdottir, U, Despriet, DDG, Ennis, S, Moroi, SE, Martin, NG, Jansonius, NM, Yazar, S, Tai, ES, Amouyel, P, Kirwan, J, van Koolwijk, LME, Hauser, MA, Jonasson, F, Leo, P, Loomis, SJ, Fogarty, R, Rivadeneira, F, Kearns, L, Lackner, KJ, de Jong, PTVM, Simpson, CL, Pennell, CE, Oostra, BA, Uitterlinden, AG, Saw, SM, Lotery, AJ, Bailey-Wilson, JE, Hofman, A, Vingerling, JR, Maubaret, C, Pfeiffer, N, Wolfs, RCW, Lemij, HG, Young, TL, Pasquale, LR, Delcourt, C, Spector, TD, Klaver, CCW, Small, KS, Burdon, KP, Stefansson, K, Wong, TY, Viswanathan, A, Mackey, DA, Craig, JE, Wiggs, JL, van Duijn, CM, Hammond, CJ, Aung, T     Less

NATURE GENETICS[1061-4036], Published 2014, Volume 46, Issue 10, Pages 1126-1130

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WOS核心合集引用: 176  2022影響因子:  30.8  发表年影響因子:  29.352 

5.Seven new loci associated with age-related macular degeneration

Fritsche, LG, Chen,     More...

Fritsche, LG, Chen, W, Schu, M, Yaspan, BL, Yu, Y, Thorleifsson, G, Zack, DJ, Arakawa, S, Cipriani, V, Ripke, S, Igo, RP, Buitendijk, GHS, Sim, XL, Weeks, DE, Guymer, RH, Merriam, JE, Francis, PJ, Hannum, G, Agarwal, A, Armbrecht, AM, Audo, I, Aung, T, Barile, GR, Benchaboune, M, Bird, AC, Bishop, PN, Branham, KE, Brooks, M, Brucker, AJ, Cade, WH, Cain, MS, Campochiaroll, PA, Chan, CC, Cheng, CY, Chew, EY, Chin, KA, Chowers, I, Clayton, DG, Cojocaru, R, Conley, YP, Cornes, BK, Daly, MJ, Dhillon, B, Edwards, A, Evangelou, E, Fagemess, J, Ferreyra, HA, Friedman, JS, Geirsdottir, A, George, RJ, Gieger, C, Gupta, N, Hagstrom, SA, Harding, SP, Haritoglou, C, Heckenlively, JR, Hoz, FG, Hughes, G, Ioannidis, JPA, Ishibashi, T, Joseph, P, Jun, G, Kamatani, Y, Katsanis, N, Keilhauer, CN, Khan, JC, Kim, IK, Kiyohara, Y, Klein, BEK, Klein, R, Kovach, JL, Kozak, I, Lee, CJ, Lee, KE, Lichtner, P, Lotery, AJ, Meitinger, T, Mitchell, P, Mohand-Said, S, Moore, AT, Morgan, DJ, Margaux, AM, Myers, CE, Naj, AC, Nakamura, Y, Okada, Y, Orlin, A, Ortube, MC, Othman, MI, Pappas, C, Park, KH, Pauer, GJT, Peachey, NS, Poch, O, Priya, RR, Reynolds, R, Richardson, AJ, Ripp, R, Rudolph, G, Ryu, E, Sahel, JA, Schaumberg, DA, Scholl, HPN, Schwartz, SG, Scott, WK, Shahid, H, Sigurdsson, H, Silvestri, G, Sivakumaran, TA, Smith, RT, Sobrin, L, Souied, EH, Stambolian, DE, Stefansson, H, Sturgill-Short, GM, Takahashi, A, Tosakulwong, N, Truitt, BJ, Tsironi, EE, Uitterlinden, AG, van Duijn, CM, Vijaya, L, Vingerling, JR, Vithana, EN, Webster, AR, Wichmann, HE, Winkler, TW, Wong, TY, Wright, AF, Zelenika, D, Zhang, M, Zhao, L, Zhang, K, Klein, ML, Hageman, GS, Lathrop, GM, Stefansson, K, Allikmets, R, Baird, PN, Gorin, MB, Wang, JJ, Klaver, CCW, Seddon, JM, Pericak-Vance, MA, Iyengar, SK, Yates, JRW, Swaroop, A, Weber, BHF, Kubo, M, DeAngelis, MM, Leveillard, T, Thorsteinsdottir, U, Haines, JL, Farrer, LA, Heid, IM, Abecasis, GR     Less

NATURE GENETICS[1061-4036], Published 2013, Volume 45, Issue 4, Pages 433-439

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WOS核心合集引用: 594  2022影響因子:  30.8  发表年影響因子:  29.648 

6.Identification of a rare coding variant in complement 3 associated with age-related macular degeneration

Zhan, XW, Larson, DE     More...

Zhan, XW, Larson, DE, Wang, CL, Koboldt, DC, Sergeev, YV, Fulton, RS, Fulton, LL, Fronick, CC, Branham, KE, Bragg-Gresham, J, Jun, G, Hu, YN, Kang, HM, Liu, DJ, Othman, M, Brooks, M, Ratnapriya, R, Boleda, A, Grassmann, F, von Strachwitz, C, Olson, LM, Buitendijk, GHS, Hofman, A, van Duijn, CM, Cipriani, V, Moore, AT, Shahid, H, Jiang, YD, Conley, YP, Morgan, DJ, Kim, IK, Johnson, MP, Cantsilieris, S, Richardson, AJ, Guymer, RH, Luo, HR, Ouyang, H, Licht, C, Pluthero, FG, Zhang, MM, Zhang, K, Baird, PN, Blangero, J, Klein, ML, Farrer, LA, DeAngelis, MM, Weeks, DE, Gorin, MB, Yates, JRW, Klaver, CCW, Pericak-Vance, MA, Haines, JL, Weber, BHF, Wilson, RK, Heckenlively, JR, Chew, EY, Stambolian, D, Mardis, ER, Swaroop, A, Abecasis, GR     Less

NATURE GENETICS[1061-4036], Published 2013, Volume 45, Issue 11, Pages 1375-1381

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WOS核心合集引用: 133  2022影響因子:  30.8  发表年影響因子:  29.648 

7.A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration

Helgason, H, Sulem,     More...

Helgason, H, Sulem, P, Duvvari, MR, Luo, HR, Thorleifsson, G, Stefansson, H, Jonsdottir, I, Masson, G, Gudbjartsson, DF, Walters, GB, Magnusson, OT, Kong, A, Rafnar, T, Kiemeney, LA, Schoenmaker-Koller, FE, Zhao, L, Boon, CJF, Song, YJ, Fauser, S, Pei, M, Ristau, T, Patel, S, Liakopoulos, S, van de Ven, JPH, Hoyng, CB, Ferreyra, H, Duan, Y, Bernstein, PS, Geirsdottir, A, Helgadottir, G, Stefansson, E, den Hollander, AI, Zhang, K, Jonasson, F, Sigurdsson, H, Thorsteinsdottir, U, Stefansson, K     Less

NATURE GENETICS[1061-4036], Published 2013, Volume 45, Issue 11, Pages 1371-1376

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WOS核心合集引用: 102  2022影響因子:  30.8  发表年影響因子:  29.648 

8.A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy

Zhang, K, Kniazeva,     More...

Zhang, K, Kniazeva, M, Han, M, Li, W, Yu, ZY, Yang, ZL, Li, Y, Metzker, ML, Allikmets, R, Zack, DJ, Kakuk, LE, Lagali, PS, Wong, PW, MacDonald, IM, Sieving, PA, Figueroa, DJ, Austin, CP, Gould, RJ, Ayyagari, R, Petrukhin, K     Less

NATURE GENETICS[1061-4036], Published 2001, Volume 27, Issue 1, Pages 89-93

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WOS核心合集引用: 340  2022影響因子:  30.8  发表年影響因子:  29.600