排序方式:
1.A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy
Zhang, K, Kniazeva,
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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
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NATURE GENETICS[1061-4036],
Published 2001,
Volume 27,
Issue 1,
Pages 89-93
收錄情况:
WOS
SCOPUS
WOS核心合集引用: 351
2023影響因子:
31.8
发表年影響因子:
29.600
2.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
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NATURE GENETICS[1061-4036],
Published 2013,
Volume 45,
Issue 4,
Pages 433-439
收錄情况:
WOS
SCOPUS
WOS核心合集引用: 629
2023影響因子:
31.8
发表年影響因子:
29.648
3.Identification of a rare coding variant in complement 3 associated with age-related macular degeneration
Zhan, XW, Larson, DE
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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
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NATURE GENETICS[1061-4036],
Published 2013,
Volume 45,
Issue 11,
Pages 1375-1381
收錄情况:
WOS
SCOPUS
WOS核心合集引用: 140
2023影響因子:
31.8
发表年影響因子:
29.648
4.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
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NATURE GENETICS[1061-4036],
Published 2016,
Volume 48,
Issue 2,
Pages 134-143
收錄情况:
WOS
SCOPUS
WOS核心合集引用: 1049
2023影響因子:
31.8
发表年影響因子:
27.959
5.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
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NATURE GENETICS[1061-4036],
Published 2016,
Volume 48,
Issue 2,
Pages 189-194
收錄情况:
WOS
SCOPUS
WOS核心合集引用: 185
2023影響因子:
31.8
发表年影響因子:
27.959
6.A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration
Helgason, H, Sulem,
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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
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NATURE GENETICS[1061-4036],
Published 2013,
Volume 45,
Issue 11,
Pages 1371-1376
收錄情况:
WOS
SCOPUS
WOS核心合集引用: 107
2023影響因子:
31.8
发表年影響因子:
29.648
7.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
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Guo, SC, Diep, D, Plongthongkum, N, Fung, HL, Zhang, K, Zhang, K
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NATURE GENETICS[1061-4036],
Published 2017,
Volume 49,
Issue 4,
Pages 635-642
收錄情况:
WOS
SCOPUS
WOS核心合集引用: 329
2023影響因子:
31.8
发表年影響因子:
27.125
8.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
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NATURE GENETICS[1061-4036],
Published 2014,
Volume 46,
Issue 10,
Pages 1126-1130
收錄情况:
WOS
SCOPUS
WOS核心合集引用: 193
2023影響因子:
31.8
发表年影響因子:
29.352