Structural brain alterations in community dwelling individuals with chronic joint pain

by De Kruijf, M, Bos, D, Huygen, F.J.P.M, Niessen, W.J, Tiemeier, H, Hofman, A, Uitterlinden, A.G, Vernooij, M.W, Ikram, M.A, Van Meurs, J.B.J
Published 2020

Heritability of the shape of subcortical brain structures in the general population

by Roshchupkin, G.V, Gutman, B.A, Vernooij, M.W, Jahanshad, N, Martin, N.G, Hofman, A, McMahon, K.L, Van Der Lee, S.J, Van Duijn, C.M, De Zubicaray, G.I, Uitterlinden, A.G, Wright, M.J, Niessen, W.J, Thompson, P.M, Ikram, M.A, Adams, H.H.H
Published 2020

A genome-wide association study of optic disc parameters

by Ramdas W.D., van Koolwijk L.M.E., Ikram M.K., Jansonius N.M., de Jong P.T.V.M., Bergen A.A.B., Isaacs A., Amin N., Aulchenko Y.S., Wolfs R.C.W., Hofman A., Rivadeneira F., Oostra B.A., Uitterlinden A.G., Hysi P., Hammond C.J., Lemij H.G., Vingerling J.R., Klaver C.C.W., van Duijn C.M.
Published 2019

Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic discarea

by Khor, C.C., Ramdas, W.D., Vithana, E.N., Cornes, B.K., Sim, X., Tay, W.-T., Saw, S.-M., Lavanya, Y.Z., Wu, R., Wang, J.J., Mitchell, P., Uitterlinden, A.G., Rivadeneira, F., Teo, Y.-Y., Chia, K.-S., Seielstad, M., Hibberd, M., Vingerling, J.R., Klaver, C.C., Jansonius, N.M., Tai, E.-S., Wong, T.-Y., van Duijn, C.M., Aung, T.
Published 2014

Insights into the Genetic Architecture of Early Stage Age-Related Macular Degeneration: A Genome-Wide Association Study Meta-Analysis

by Holliday, E.G., Smith, A.V., Cornes, B.K., Buitendijk, G.H.S., Jensen, R.A., Sim, X., Aspelund, T., Aung, T., Baird, P.N., Boerwinkle, E., Cheng, C.Y., van Duijn, C.M., Eiriksdottir, G., Gudnason, V., Harris, T., Hewitt, A.W., Inouye, M., Jonasson, F., Klein, B.E.K., Launer, L., Li, X., Liew, G., Lumley, T., McElduff, P., McKnight, B., Mitchell, P., Psaty, B.M., Rochtchina, E., Rotter, J.I., Scott, R.J., Tay, W., Taylor, K., Teo, Y.Y., Uitterlinden, A.G., Viswanathan, A., Xie, S., Vingerling, J.R., Klaver, C.C.W., Tai, E.S., Siscovick, D., Klein, R., Cotch, M.F., Wong, T.Y., Attia, J., Wang, J.J.
Published 2014

Genome-Wide Association Study of Retinopathy in Individuals without Diabetes

by Jensen, R.A., Sim, X., Li, X., Cotch, M.F., Ikram, M.K., Holliday, E.G., Eiriksdottir, G., Harris, T.B., Jonasson, F., Klein, B.E.K., Launer, L.J., Smith, A.V., Boerwinkle, E., Cheung, N., Hewitt, A.W., Liew, G., Mitchell, P., Wang, J.J., Attia, J., Scott, R., Glazer, N.L., Lumley, T., McKnight, B., Psaty, B.M., Taylor, K., Hofman, A., de Jong, P.T.V.M., Rivadeneira, F., Uitterlinden, A.G., Tay, W.-T., Teo, Y.Y., Seielstad, M., Liu, J., Cheng, C.-Y., Saw, S.-M., Aung, T., Ganesh, S.K., O'Donnell, C.J., Nalls, M.A., Wiggins, K.L., Kuo, J.Z., van Duijn, C.M., Gudnason, V., Klein, R., Siscovick, D.S., Rotter, J.I., Tai, E.S., Vingerling, J., Wong, T.Y.
Published 2014

Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease

by Jakobsdottir J., van der Lee S.J., Bis J.C., Chouraki V., Li-Kroeger D., Yamamoto S., Grove M.L., Naj A., Vronskaya M., Salazar J.L., DeStefano A.L., Brody J.A., Smith A.V., Amin N., Sims R., Ibrahim-Verbaas C.A., Choi S.-H., Satizabal C.L., Lopez O.L., Beiser A., Ikram M.A., Garcia M.E., Hayward C., Varga T.V., Ripatti S., Franks P.W., Hallmans G., Rolandsson O., Jansson J.-H., Porteous D.J., Salomaa V., Eiriksdottir G., Rice K.M., Bellen H.J., Levy D., Uitterlinden A.G., Emilsson V., Rotter J.I., Aspelund T., O?Donnell C.J., Fitzpatrick A.L., Launer L.J., Hofman A., Wang L.-S., Williams J., Schellenberg G.D., Boerwinkle E., Psaty B.M., Seshadri S.
Published 2019

Evaluation of presumably disease causing SCN1A variants in a cohort of common epilepsy syndromes

by Lal D., Reinthaler E.M., Dejanovic B., May P., Thiele H., Lehesjoki A.-E., Schwarz G., Riesch E., Ikram M.A., Van Duijn C.M., Uitterlinden A.G., Hofman A., Steinböck H., Gruber-Sedlmayr U., Neophytou B., Zara F., Hahn A., Gormley P., Becker F., Weber Y.G., Cilio M.R., Kunz W.S., Krause R., Zimprich F., Lemke J.R., Nürnberg P., Sander T., Lerche H., Neubauer B.A., Palotie A., Ruppert A.-K., Suls A., Siren A., Koeleman B., Haberlandt E., Ronen G.M., Caglayan H., Hjalgrim H., Muhle H., Schulz H., Helbig I., Altmüller J., Geldner J., Schubert J., Jabbari K., Everett K., Feucht M., Balestri M., Nothnagel M., Striano P., Møller R.S., Nabbout R., Balling R., Baulac S., Bianchi A., La Neve A., Minetti C., Giuseppe C.
Published 2019

Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci

by Simpson C.L., Wojciechowski R., Oexle K., Murgia F., Portas L., Li X., Virginie J.M.V., Vitart V., Schache M., Mohsen Hosseini S., Hysi P.G., Raffel L.J., Cotch M.F., Chew E., Klein B.E.K., Klein R., Wong T.Y., Van Duijn C.M., Mitchell P., Saw S.M., Fossarello M., Wang J.J., Polašek O., Campbell H., Rudan I., Oostra B.A., Uitterlinden A.G., Hofman A., Rivadeneira F., Amin N., Karssen L.C., Vingerling J.R., Döring A., Bettecken T., Bencic G., Gieger C., Wichmann H.-E., Wilson J.F., Venturini C., Fleck B., Cumberland P.M., Rahi J.S., Hammond C.J., Hayward C., Wright A.F., Paterson A.D., Baird P.N., Klaver C.C.W., Rotter J.I., Pirastu M., Meitinger T., Bailey-Wilson J.E., Stambolian D.
Published 2018

Cell Specific eQTL Analysis without Sorting Cells

by Westra H.-J., Arends D., Esko T., Peters M.J., Schurmann C., Schramm K., Kettunen J., Yaghootkar H., Fairfax B.P., Andiappan A.K., Li Y., Fu J., Karjalainen J., Platteel M., Visschedijk M., Weersma R.K., Kasela S., Milani L., Tserel L., Peterson P., Reinmaa E., Hofman A., Uitterlinden A.G., Rivadeneira F., Homuth G., Petersmann A., Lorbeer R., Prokisch H., Meitinger T., Herder C., Roden M., Grallert H., Ripatti S., Perola M., Wood A.R., Melzer D., Ferrucci L., Singleton A.B., Hernandez D.G., Knight J.C., Melchiotti R., Lee B., Poidinger M., Zolezzi F., Larbi A., Wang D.Y., van den Berg L.H., Veldink J.H., Rotzschke O., Makino S., Salomaa V., Strauch K., Völker U., van Meurs J.B.J., Metspalu A., Wijmenga C., Jansen R.C., Franke L.
Published 2020

Common genetic determinants of intraocular pressure and primary open-angle Glaucoma

by van Koolwijk, L.M.E., Ramdas, W.D., Ikram, M.K., Jansonius, N.M., Pasutto, F., Hysi, P.G., Macgregor, S., Janssen, S.F., Hewitt, A.W., Viswanathan, A.C., ten Brink, J.B., Hosseini, S.M., Amin, N., Despriet, D.D.G., Willemse-Assink, J.J.M., Kramer, R., Rivadeneira, F., Struchalin, M., Aulchenko, Y.S., Weisschuh, N., Zenkel, M., Mardin, C.Y., Gramer, E., Welge-Lüssen, U., Montgomery, G.W., Carbonaro, F., Young, T.L., Bellenguez, C., McGuffin, P., Foster, P.J., Topouzis, F., Mitchell, P., Wang, J.J., Wong, T.Y., Czudowska, M.A., Hofman, A., Uitterlinden, A.G., Wolfs, R.C.W., de Jong, P.T.V.M., Oostra, B.A., Paterson, A.D., Mackey, D.A., Bergen, A.A.B., Reis, A., Hammond, C.J., Vingerling, J.R., Lemij, H.G., Klaver, C.C.W., van Duijn, C.M.
Published 2014

Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error

by Stambolian, D., Wojciechowski, R., Oexle, K., Pirastu, M., Li, X., Raffe, L.J., Cotch, M.F., Chew, E.Y., Klein, B., Klein, R., Wong, T.Y., Simpson, C.L., Klaver, C.C.W., van Duijn, C.M., Verhoeven, V.J.M., Baird, P.N., Vitart, V., Paterson, A.D., Mitchell, P., Saw, S.M., Fossarello, M., Kazmierkiewicz, K., Murgia, F., Portas, L., Schache, M., Richardson, A., Xie, J., Wang, J.J., Rochtchina, E., Viswanathan, A.C., Hayward, C., Wright, A.F., Polašek, O., Campbell, H., Rudan, I., Oostra, B.A., Uitterlinden, A.G., Hofman, A., Rivadeneira, F., Amin, N., Karssen, L.C., Vingerling, J.R., Hosseini, S.M., Döring, A., Bettecken, T., Vatavuk, Z., Gieger, C., Wichmann, H.-E., Wilson, J.F., Fleck, B., Foster, P.J., Topouzis, F., McGuffin, P., Sim, X., Inouye, M., Holliday, E.G., Attia, J., Scott, R.J., Rotter, J.I., Meitinger, T., Bailey-Wilson, J.E.
Published 2014

Genetic Loci for Retinal Arteriolar Microcirculation

by Sim, X., Jensen, R.A., Ikram, M.K., Cotch, M.F., Li, X., MacGregor, S., Xie, J., Smith, A.V., Boerwinkle, E., Mitchell, P., Klein, R., Klein, B.E.K., Glazer, N.L., Lumley, T., McKnight, B., Psaty, B.M., de Jong, P.T.V.M., Hofman, A., Rivadeneira, F., Uitterlinden, A.G., van Duijn, C.M., Aspelund, T., Eiriksdottir, G., Harris, T.B., Jonasson, F., Launer, L.J., Attia, J., Baird, P.N., Harrap, S., Holliday, E.G., Inouye, M., Rochtchina, E., Scott, R.J., Viswanathan, A., Li, G., Smith, N.L., Wiggins, K.L., Kuo, J.Z., Taylor, K.D., Hewitt, A.W., Martin, N.G., Montgomery, G.W., Sun, C., Young, T.L., Mackey, D.A., van Zuydam, N.R., Doney, A.S.F., Palmer, C.N.A., Morris, A.D., Rotter, J.I., Tai, E.S., Gudnason, V., Vingerling, J.R., Siscovick, D.S., Wang, J.J., Wong, T.Y.
Published 2014

Four novel loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation In vivo

by Kamran Ikram, M., Xueling, S., Jensen, R.A., Cotch, M.F., Hewitt, A.W., Ikram, M.A., Wang, J.J., Klein, R., Klein, B.E.K., Breteler, M.M.B., Cheung, N., Liew, G., Mitchell, P., Uitterlinden, A.G., Rivadeneira, F., Hofman, A., de Jong, P.T.V.M., van Duijn, C.M., Kao, L., Cheng, C.-Y., Smith, A.V., Glazer, N.L., Lumley, T., McKnight, B., Psaty, B.M., Jonasson, F., Eiriksdottir, G., Aspelund, T., Harris, T.B., Launer, L.J., Taylor, K.D., Li, X., Iyengar, S.K., Xi, Q., Sivakumaran, T.A., MacKey, D.A., MacGregor, S., Martin, N.G., Young, T.L., Bis, J.C., Wiggins, K.L., Heckbert, S.R., Hammond, C.J., Andrew, T., Fahy, S., Attia, J., Holliday, E.G., Scott, R.J., Islam, F.M.A., Rotter, J.I., McAuley, A.K., Boerwinkle, E., Tai, E.S., Gudnason, V., Siscovick, D.S., Vingerling, J.R., Wong, T.Y.
Published 2014

A genome-wide association study of early menopause and the combined impact of identified variants

by Perry, J.R.B., Corre, T., Esko, T., Chasman, D.I., Fischer, K., Franceschini, N., He, C., Kutalik, Z., Mangino, M., Rose, L.M., Vernon smith, A., Stolk, L., Sulem, P., Weedon, M.N., Zhuang, W.V., Arnold, A., Ashworth, A., Bergmann, S., Buring, J.E., Burri, A., Chen, C., Cornelis, M.C., Couper, D.J., Goodarzi, M.O., Gudnason, V., Harris, T., Hofman, A., Jones, M., Kraft, P., Launer, L., Laven, J.S.E., Li, G., Mcknight, B., Masciullo, C., Milani, L., Orr, N., Psaty, B.M., Ridker, P.M., Rivadeneira, F., Sala, C., Salumets, A., Schoemaker, M., Traglia, M., Waeber, G., Chanock, S.J., Demerath, E.W., Garcia, M., Hankinson, S.E., Hu, F.B., Hunter, D.J., Lunetta, K.L., Metspalu, A., Montgomery, G.W., Murabito, J.M., Newman, A.B., Ong, K.K., Spector, T.D., Stefansson, K., Swerdlow, A.J., Thorsteinsdottir, U., Van dam, R.M., Uitterlinden, A.G., Visser, J.A., Vollenweider, P., Toniolo, D., Murray, A.
Published 2014

Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology

by Springelkamp, Henriet, Mishra, Aniket, Hysi, Pirro G., Gharahkhani, Puyo, Hohn, Rene, Khor, Chiea Chuen, Cooke, Bailey Jessica N., Luo Xiaoyan, Ramdas, Wishal D., Vithana, Eranga Nishanthie, Koh, Victor, Yazar, Seyhan, Xu, Liang, Forward, H., Kearns, L.S., Amin, N., Iglesias, A.I., Sim, K.-S., van Leeuwen, E.M., Demirkan, A., van der Lee, S., Loon, Seng-Chee, Rivadeneira, F., Nag, A., Sanfilippo, P.G., Schillert, A., de Jong, P.T.V.M., Oostra, B.A., Uitterlinden, A.G., Hofman, A., Zhou, T., Burdon, K.P., Spector, T.D., Lackner, K.J., Saw, Seang-Mei, Vingerling, J.R., Teo,Yik-Ying, Pasquale L.R., Wolfs, R.C.W., Lemij, H.G., Tai, E.-Shyong, Jonas, J.B., Cheng, Ching-Yu, Aung, Tin, Jansonius, N.M., Klaver, C.C.W., Craig, J.E., Young, T.L., Haines, J.L., Macgregor, S., Mackey, D.A., Pfeiffer, N., Wong, Tien Yin, Wiggs, J.L., Hewitt, A.W., van Duijn, C.M., Hammond, C.J., Allingham, R.R., Brilliant, M.H., Budenz, D.L., Bailey, J.N.C., Christen, W.G., Fingert, J., Gaasterland, D., Gaasterland, T., Hauser, M.A., Kang, J.H., Kraft, P., Lee, R.K., Lichter, P.A., Liu, Y., Loomis, S.J., Moroi, S.E., Pericak-Vance, M.A., Realini, A., Richards, J.E., Schuman, J.S., Scott, W.K., Singh, K., Sit, A.J., Vollrath, D., Weinreb, R.N., Wollstein, G., Zack, D.J., Zhang, K.
Published 2016

Comparison of HapMap and 1000 genomes reference panels in a large-scale genome-wide association study

by De Vries P.S., Sabater-Lleal M., Chasman D.I., Trompet S., Ahluwalia T.S., Teumer A., Kleber M.E., Chen M.-H., Wang J.J., Attia J.R., Marioni R.E., Steri M., Weng L.-C., Pool R., Grossmann V., Brody J.A., Venturini C., Tanaka T., Rose L.M., Oldmeadow C., Mazur J., Basu S., Frånberg M., Yang Q., Ligthart S., Hottenga J.J., Rumley A., Mulas A., De Craen A.J.M., Grotevendt A., Taylor K.D., Delgado G.E., Kifley A., Lopez L.M., Berentzen T.L., Mangino M., Bandinelli S., Morrison A.C., Hamsten A., Tofler G., De Maat M.P.M., Draisma H.H.M., Lowe G.D., Zoledziewska M., Sattar N., Lackner K.J., Völker U., McKnight B., Huang J., Holliday E.G., McEvoy M.A., Starr J.M., Hysi P.G., Hernandez D.G., Guan W., Rivadeneira F., McArdle W.L., Slagboom P.E., Zeller T., Psaty B.M., Uitterlinden A.G., De Geus E.J.C., Stott D.J., Binder H., Hofman A., Franco O.H., Rotter J.I., Ferrucci L., Spector T.D., Deary I.J., März W., Greinacher A., Wild P.S., Cucca F., Boomsma D.I., Watkins H., Tang W., Ridker P.M., Jukema J.W., Scott R.J., Mitchell P., Hansen T., O'Donnell C.J., Smith N.L., Strachan D.P., Dehghan A.
Published 2019

Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium

by Verhoeven, V.J.M., Hysi, P.G., Saw, S.-M., Vitart, V., Mirshahi, A., Guggenheim, J.A., Cotch, M.F., Yamashiro, K., Baird, P.N., Mackey, D.A., Wojciechowski, R., Kamran Ikram, M., Hewitt, A.W., Duggal, P., Janmahasatian, S., Khor, C.-C., Fan, Q., Zhou, X., Young, T.L., Tai, E.-S., Goh, L.-K., Li, Y.-J., Aung, T., Vithana, E., Teo, Y.-Y., Tay, W., Sim, X., Rudan, I., Hayward, C., Wright, A.F., Polasek, O., Campbell, H., Wilson, J.F., Fleck, B.W., Nakata, I., Yoshimura, N., Yamada, R., Matsuda, F., Ohno-Matsui, K., Nag, A., McMahon, G., St. Pourcain, B., Lu, Y., Rahi, J.S., Cumberland, P.M., Bhattacharya, S., Simpson, C.L., Atwood, L.D., Li, X., Raffel, L.J., Murgia, F., Portas, L., Despriet, D.D.G., Van Koolwijk, L.M.E., Wolfram, C., Lackner, K.J., Tönjes, A., Mägi, R., Lehtimäki, T., Kähönen, M., Esko, T., Metspalu, A., Rantanen, T., Pärssinen, O., Klein, B.E., Meitinger, T., Spector, T.D., Oostra, B.A., Smith, A.V., De Jong, P.T.V.M., Hofman, A., Amin, N., Karssen, L.C., Rivadeneira, F., Vingerling, J.R., Eiríksdóttir, G., Gudnason, V., Döring, A., Bettecken, T., Uitterlinden, A.G., Williams, C., Zeller, T., Castagné, R., Oexle, K., Van Duijn, C.M., Iyengar, S.K., Mitchell, P., Wang, J.J., Höhn, R., Pfeiffer, N., Bailey-Wilson, J.E., Stambolian, D., Wong, T.-Y., Hammond, C.J., Klaver, C.C.W.
Published 2014

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

by Verhoeven, V.J.M., Hysi, P.G., Wojciechowski, R., Fan, Q., Guggenheim, J.A., Höhn, R., Macgregor, S., Hewitt, A.W., Nag, A., Cheng, C.-Y., Yonova-Doing, E., Zhou, X., Ikram, M.K., Buitendijk, G.H.S., Mcmahon, G., Kemp, J.P., Pourcain, B.S., Simpson, C.L., Mäkelä, K.-M., Lehtimäki, T., Kähönen, M., Paterson, A.D., Hosseini, S.M., Wong, H.S., Xu, L., Jonas, J.B., Pärssinen, O., Wedenoja, J., Yip, S.P., Ho, D.W.H., Pang, C.P., Chen, L.J., Burdon, K.P., Craig, J.E., Klein, B.E.K., Klein, R., Haller, T., Metspalu, A., Khor, C.-C., Tai, E.-S., Aung, T., Vithana, E., Tay, W.-T., Barathi, V.A., Chen, P., Li, R., Liao, J., Zheng, Y., Ong, R.T., Döring, A., Evans, D.M., Timpson, N.J., Verkerk, A.J.M.H., Meitinger, T., Raitakari, O., Hawthorne, F., Spector, T.D., Karssen, L.C., Pirastu, M., Murgia, F., Ang, W., Mishra, A., Montgomery, G.W., Pennell, C.E., Cumberland, P.M., Cotlarciuc, I., Mitchell, P., Wang, J.J., Schache, M., Janmahasathian, S., Igo Jr., R.P., Lass, J.H., Chew, E., Iyengar, S.K., Gorgels, T.G.M.F., Rudan, I., Hayward, C., Wright, A.F., Polasek, O., Vatavuk, Z., Wilson, J.F., Fleck, B., Zeller, T., Mirshahi, A., Müller, C., Uitterlinden, A.G., Rivadeneira, F., Vingerling, J.R., Hofman, A., Oostra, B.A., Amin, N., Bergen, A.A.B., Teo, Y.-Y., Rahi, J.S., Vitart, V., Williams, C., Baird, P.N., Wong, T.-Y., Oexle, K., Pfeiffer, N., Mackey, D.A., Young, T.L., Van Duijn, C.M., Saw, S.-M., Bailey-Wilson, J.E., Stambolian, D., Klaver, C.C., Hammond, C.J.
Published 2014

Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics

by Garcia-Closas M., Hall P., Nevanlinna H., Pooley K., Morrison J., Richesson D.A., Bojesen S.E., Nordestgaard B.G., Axelsson C.K., Arias J.I., Milne R.L., Ribas G., González-Neira A., Benítez J., Zamora P., Brauch H., Justenhoven C., Hamann U., Ko Y.-D., Bruening T., Haas S., Dörk T., Schürmann P., Hillemanns P., Bogdanova N., Bremer M., Karstens J.H., Fagerholm R., Aaltonen K., Aittomäki K., Von Smitten K., Blomqvist C., Mannermaa A., Uusitupa M., Eskelinen M., Tengström M., Kosma V.-M., Kataja V., Chenevix-Trench G., Spurdle A.B., Beesley J., Chen X., Devilee P., Van Asperen C.J., Jacobi C.E., Tollenaar R.A.E.M., Huijts P.E.A., Klijn J.G.M., Chang-Claude J., Kropp S., Slanger T., Flesch-Janys D., Mutschelknauss E., Salazar R., Wang-Gohrke S., Couch F., Goode E.L., Olson J.E., Vachon C., Fredericksen Z.S., Giles G.G., Baglietto L., Severi G., Hopper J.L., English D.R., Southey M.C., Haiman C.A., Henderson B.E., Kolonel L.N., Le Marchand L., Stram D.O., Hunter D.J., Hankinson S.E., Cox D.G., Tamimi R., Kraft P., Sherman M.E., Chanock S.J., Lissowska J., Brinton L.A., Peplonska B., Hooning M.J., Meijers-Heijboer H., Collee J.M., Van Den Ouweland A., Uitterlinden A.G., Liu J., Low Y.L., Yuqing L., Humphreys K., Czene K., Cox A., Balasubramanian S.P., Cross S.S., Reed M.W.R., Blows F., Driver K., Dunning A., Tyrer J., Ponder B.A.J., Sangrajrang S., Brennan P., McKay J., Odefrey F., Gabrieau V., Sigurdson A., Doody M., Struewing J.P., Alexander B., Easton D.F., Pharoah P.D.
Published 2019