COVID-19 mRNA vaccine induced antibody responses against three SARS-CoV-2 variants by Jalkanen, Pinja, Kolehmainen, Pekka, Häkkinen, Hanni K, Huttunen, Moona, Tähtinen, Paula A, Lundberg, Rickard, Maljanen, Sari, Reinholm, Arttu, Tauriainen, Sisko, Pakkanen, Sari H, Levonen, Iris, Nousiainen, Arttu, Miller, Taru, Välimaa, Hanna, Ivaska, Lauri, Pasternack, Arja, Naves, Rauno, Ritvos, Olli, Österlund, Pamela, Kuivanen, Suvi, Smura, Teemu, Hepojoki, Jussi, Vapalahti, Olli, Lempainen, Johanna, Kakkola, Laura, Kantele, Anu, Julkunen, Ilkka

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Thalamo-cortical network hyperconnectivity in preclinical progranulin mutation carriers by Lee, Suzee E, Sias, Ana C, Kosik, Eena L, Flagan, Taru M, Deng, Jersey, Chu, Stephanie A, Brown, Jesse A, Vidovszky, Anna A, Ramos, Eliana Marisa, Gorno-Tempini, Maria Luisa, Karydas, Anna M, Coppola, Giovanni, Geschwind, Daniel H, Rademakers, Rosa, Boeve, Bradley F, Boxer, Adam L, Rosen, Howard J, Miller, Bruce L, Seeley, William W

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Network Connectivity Alterations across the MAPT Mutation Clinical Spectrum by Zhang, Liwen, Flagan, Taru M, Häkkinen, Suvi, Chu, Stephanie A, Brown, Jesse A, Lee, Alex J, Pasquini, Lorenzo, Mandelli, Maria Luisa, Gorno-Tempini, Maria Luisa, Sturm, Virginia E, Yokoyama, Jennifer S, Appleby, Brian S, Cobigo, Yann, Dickerson, Bradford C, Domoto-Reilly, Kimiko, Geschwind, Daniel H, Ghoshal, Nupur, Graff-Radford, Neill R, Grossman, Murray, Hsiung, Ging-Yuek Robin, Huey, Edward D, Kantarci, Kejal, Lario Lago, Argentina, Litvan, Irene, Mackenzie, Ian R, Mendez, Mario F, Onyike, Chiadi U, Ramos, Eliana Marisa, Roberson, Erik D, Tartaglia, Maria Carmela, Toga, Arthur W, Weintraub, Sandra, Wszolek, Zbigniew K, Forsberg, Leah K, Heuer, Hilary W, Boeve, Bradley F, Boxer, Adam L, Rosen, Howard J, Miller, Bruce L, Seeley, William W, Lee, Suzee E

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Functional connectivity trajectories in genetic frontotemporal dementia by Zhang, Liwen, Flagan, Taru M., Staffaroni, Adam M., Häkkinen, Suvi, Brown, Jesse A., Mandelli, Maria Luisa, Rosen, Howard J., Kantarci, Kejal, Ramos, Eliana Marisa, Tempini, Maria Luisa Gorno, Miller, Bruce L, Seeley, William W., Lee, Suzee E.

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Gyrification abnormalities in young adult presymptomatic carriers of frontotemporal lobar degeneration mutations by Vargas, Andrea Gorham, Lombardi, Jolina, Zhang, Liwen, Flagan, Taru M., Mandelli, Maria Luisa, Brown, Jesse A., Rosen, Howard J., Kantarci, Kejal, Ramos, Eliana Marisa, Miller, Bruce L., Seeley, William W., Tempini, Maria Luisa Gorno, Lee, Suzee E.

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Structural and functional alterations in young adult presymptomatic frontotemporal lobar degeneration mutation carriers by Lombardi, Jolina, Zhang, Liwen, Flagan, Taru M., Vargas, Andrea Gorham, Mandelli, Maria Luisa, Brown, Jesse A., Häkkinen, Suvi, Rosen, Howard J., Kantarci, Kejal, Ramos, Eliana Marisa, Miller, Bruce L, Tempini, Maria Luisa Gorno, Seeley, William W., Lee, Suzee E.

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Functional connectivity trajectories in genetic frontotemporal dementia by Zhang, Liwen, Flagan, Taru M., Staffaroni, Adam M., Häkkinen, Suvi, Brown, Jesse A., Mandelli, Maria Luisa, Rosen, Howard J., Kantarci, Kejal, Ramos, Eliana Marisa, Tempini, Maria Luisa Gorno, Miller, Bruce L, Seeley, William W., Lee, Suzee E.

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Identification of novel genetic markers of breast cancer survival by Chen, Constance, Khan, Sofia, Tyrer, Jonathan, Bolla, Manjeet K, Wang, Qin, Kar, Siddhartha, Beesley, Jonathan, Czene, Kamila, Eriksson, Mikael, Lambrechts, Diether, Weltens, Caroline, Leunen, Karin, Bojesen, Stig E, Nordestgaard, Børge G, Nielsen, Sune F, Flyger, Henrik, Chang-Claude, Jenny, Seibold, Petra, Flesch-Janys, Dieter, Blomqvist, Carl, Aittomäki, Kristiina, Fagerholm, Rainer, Couch, Fergus J, Olson, Janet E, Vachon, Celine, Knight, Julia A, Glendon, Gord, Mulligan, Anna Marie, Broeks, Annegien, Hogervorst, Frans B, Haiman, Christopher A, Schumacher, Fredrick, Le Marchand, Loic, Hopper, John L, Tsimiklis, Helen, Apicella, Carmel, Southey, Melissa C, Cox, Angela, Reed, Malcolm W R, Milne, Roger L, McLean, Catriona, Pylkäs, Katri, Jukkola-Vuorinen, Arja, Grip, Mervi, Hooning, Maartje J, Hollestelle, Antoinette, van den Ouweland, Ans M W, Yang, Rongxi, Burwinkel, Barbara, Figueroa, Jonine, Chanock, Stephen J, Kerin, Michael J, Miller, Nicola, Dieffenbach, Aida Karina, Mannermaa, Arto, Kosma, Veli-Matti, Hartikainen, Jaana M, Li, Jingmei, Brand, Judith S, Humphreys, Keith, Devilee, Peter, Seynaeve, Caroline, Radice, Paolo, Bonanni, Bernardo, Beckmann, Matthias W, Hein, Alexander, Balleine, Rosemary, Phillips, Kelly-Anne, Benitez, Javier, Arias Perez, Jose Ignacio, Jakubowska, Anna, Lubinski, Jan, Jaworska-Bieniek, Katarzyna, Durda, Katarzyna, Hamann, Ute, Kabisch, Maria, Rüdiger, Thomas, Margolin, Sara, Nord, Silje, Evans, D Gareth, Abraham, Jean E, Hiller, Louise, Dunn, Janet A, Bowden, Sarah, Berg, Christine, Diver, W Ryan, Gapstur, Susan M, Hankinson, Susan E, Hoover, Robert N, Hüsing, Anika, Kaaks, Rudolf, Willett, Walter, Canzian, Federico, Chin, Suet-Feung, Caldas, Carlos, Hunter, David J, García-Closas, Montserrat, Hall, Per, Easton, Douglas F, Nevanlinna, Heli

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Presymptomatic and symptomatic MAPT mutation carriers feature functional connectivity alterations by Zhang, Liwen, Flagan, Taru M., Chu, Stephanie A., Häkkinen, Suvi, Brown, Jesse A., Lee, Alex Jihun, Pasquini, Lorenzo, Mandelli, Maria Luisa, Tempini, Maria Luisa Gorno, Appleby, Brian, Dickerson, Brad C., Domoto‐Reilly, Kimiko, Geschwind, Daniel H., Ghoshal, Nupur, Graff‐Radford, Neill R., Grossman, Murray, Hsiung, Ging‐Yuek Robin, Huey, Edward D., Kantarci, Kejal, Karydas, Anna M., Kaufer, Daniel, Knopman, David S., Litvan, Irene, Mackenzie, Ian R., Mendez, Mario, Onyike, Chiadi U., Ramos, Eliana Marisa, Roberson, Erik D., Trataglia, Maria Carmela, Toga, Arthur W., Weintraub, Sandra, Forsberg, Leah K., Heuer, Hilary W., Boeve, Bradley F., Boxer, Adam L., Rosen, Howard J., Miller, Bruce L., Seeley, William W., Lee, Suzee E.

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Complement and NfL associations with brain structure and functional connectivity alterations in presymptomatic and symptomatic GRN mutation carriers by Flagan, Taru M., Chu, Stephanie A., Häkkinen, Suvi, McFall, David, Heller, Carolin, Rohrer, Jonathan D, Brown, Jesse A., Lee, Alex Jihun, Pasquini, Lorenzo, Mandelli, Maria Luisa, Gorno‐Tempini, Marilu, Appleby, Brian, Dickerson, Brad C., Domoto‐Reilly, Kimiko, Foroud, Tatiana M., Geschwind, Daniel H., Ghoshal, Nupur, Graff‐Radford, Neill R., Grossman, Murray, Hsiung, Ging‐Yuek Robin, Huang, Eric J., Huey, Edward D., Kantarci, Kejal, Karydas, Anna M., Kaufer, Daniel, Knopman, David S., Litvan, Irene, Mackenzie, Ian R, Mendez, Mario F., Onyike, Chiadi U, Petrucelli, Leonard, Ramos, Eliana Marisa, Roberson, Erik D., Rojas, Julio C., Tartaglia, Maria Carmela, Toga, Arthur W., Weintraub, Sandra, Forsberg, Leah K., Heuer, Hilary W., Boeve, Bradley F., Boxer, Adam L., Rosen, Howard J., Miller, Bruce L., Moreno, Fermin, Seeley, William W., Lee, Suzee E.

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A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium by Milne, Roger L, Dennis, Joe, Tyrer, Jonathan P, Zamora, M Pilar, Arias-Perez, José Ignacio, González-Neira, Anna, Pita, Guillermo, Alonso, M Rosario, Bolla, Manjeet K, Czene, Kamila, Eriksson, Mikael, Darabi, Hatef, Li, Jingmei, Anton-Culver, Hoda, Neuhausen, Susan L, Ziogas, Argyrios, Hopper, John L, Dite, Gillian S, Apicella, Carmel, Chenevix-Trench, Georgia, Ashworth, Alan, Orr, Nicholas, Jakubowska, Anna, Lubinski, Jan, Jaworska-Bieniek, Katarzyna, Knight, Julia A, Glendon, Gord, Bojesen, Stig E, Nordestgaard, Børge G, Flyger, Henrik, Muranen, Taru A, Chang-Claude, Jenny, Rudolph, Anja, Seibold, Petra, Flesch-Janys, Dieter, Vachon, Celine, Purrington, Kristen, Pylkäs, Katri, Jukkola-Vuorinen, Arja, Grip, Mervi, Shah, Mitul, Guénel, Pascal, Sanchez, Marie, Dieffenbach, Aida Karina, Stegmaier, Christa, Margolin, Sara, Hooning, Maartje J, Hollestelle, Antoinette, Collée, J Margriet, Jager, Agnes, Cox, Angela, Brock, Ian W, Reed, Malcolm W R, Henderson, Brian E, Schumacher, Fredrick, Le Marchand, Loic, Dumont, Martine, Soucy, Penny, Hamann, Ute, Ulmer, Hans-Ulrich, Fasching, Peter A, Häberle, Lothar, Ekici, Arif B, Beckmann, Matthias W, Johnson, Nichola, dos Santos Silva, Isabel, Peto, Julian, Radice, Paolo, Peterlongo, Paolo, Mariani, Paolo, Giles, Graham G, Severi, Gianluca, Baglietto, Laura, Sawyer, Elinor, Kerin, Michael, Marme, Federik, Burwinkel, Barbara, Mannermaa, Arto, Kataja, Vesa, Lambrechts, Diether, Yesilyurt, Betul T, Floris, Giuseppe, Leunen, Karin, Alnæs, Grethe Grenaker, Børresen-Dale, Anne-Lise, García-Closas, Montserrat, Chanock, Stephen J, Figueroa, Jonine D, Schmidt, Marjanka K, Broeks, Annegien, Verhoef, Senno, Rutgers, Emiel J, Brüning, Thomas, Ko, Yon-Dschun, Couch, Fergus J, Pharoah, Paul D P, Hall, Per, Benítez, Javier, Malats, Núria, Easton, Douglas F

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Correction: Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation by Edwards, Stacey L., Michailidou, Kyriaki, Desai, Kinjal, Hillman, Kristine M., Kaufmann, Susanne, Glubb, Dylan M., Dennis, Joe, Bolla, Manjeet K., Wang, Qin, Shah, Mitul, Luben, Robert, Eriksson, Mikael, Klevebring, Daniel, Bojesen, Stig E., Lambrechts, Diether, Wildiers, Hans, Broeks, Annegien, Van’t Veer, Laura J., Chang-Claude, Jenny, Flesch-Janys, Dieter, Peto, Julian, dos-Santos-Silva, Isabel, Gibson, Lorna, Muranen, Taru A., Blomqvist, Carl, Choi, Ji-Yeob, Ito, Hidemi, Iwata, Hiroji, Yatabe, Yasushi, Guénel, Pascal, Truong, Thérèse, Menegaux, Florence, Sanchez, Marie, Schneeweiss, Andreas, Sohn, Christof, Wu, Anna H., Tseng, Chiu-chen, Benitez, Javier, Pilar Zamora, M, Gao, Yu-Tang, Cox, Angela, Cross, Simon S., Andrulis, Irene L., Knight, Julia A., Sawyer, Elinor J., Tomlinson, Ian, Miller, Nicola, Le Marchand, Loic, Yip, Cheng Har, Lee, Daphne S. C., Hooning, Maartje J., Martens, John W. M., Collée, J. Margriet, van Deurzen, Carolien H. M., Tsimiklis, Helen, Shen, Chen-Yang, Wu, Pei-Ei, Yu, Jyh-Cherng, Alnæs, Grethe Grenaker, Borresen-Dale, Anne-Lise, Milne, Roger L., Muir, Kenneth, Lophatananon, Artitaya, Siriwanarangsan, Pornthep, Hartman, Mikael, Miao, Hui, Fasching, Peter A., Ekici, Arif B., Brenner, Hermann, Dieffenbach, Aida Karina, Arndt, Volker, Swerdlow, Anthony, Ashworth, Alan, Orr, Nick, Schoemaker, Minouk J., Chanock, Stephen J., Simard, Jacques, Winqvist, Robert, Pylkäs, Katri, Brauch, Hiltrud, Koto, Yon-Dschun, Bonanni, Bernardo, Volorio, Sara, Kataja, Vesa, Devilee, Peter, Tollenaar, Robert A. E. M., Jakubowska, Anna, Durda, Katarzyna, Sangrajrang, Suleeporn, Brennan, Paul, Torres, Diana, Healey, Catherine S., Pita, Guillermo, Tessier, Daniel C., Carroll, Jason, Caldas, Carlos, Lupien, Mathieu, Kristensen, Vessela N., Pharoah, Paul D. P., Dunning, Alison M.

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Common germline polymorphisms associated with breast cancer-specific survival by Pirie, Ailith, Guo, Qi, Kraft, Peter, Canisius, Sander, Rahman, Nazneen, Nevanlinna, Heli, Khan, Sofia, Tyrer, Jonathan, Bolla, Manjeet K, Wang, Qin, Dennis, Joe, Michailidou, Kyriaki, Lush, Michael, Dunning, Alison M, Czene, Kamila, Eriksson, Mikael, Leunen, Karin, van Ongeval, Chantal, Nielsen, Sune F, Flyger, Henrik, Seibold, Petra, Flesch-Janys, Dieter, Aittomäki, Kristiina, Fagerholm, Rainer, Muranen, Taru A, Olsen, Janet E, Knight, Julia A, Mulligan, Anna Marie, Broeks, Annegien, Cornelissen, Sten, Haiman, Christopher A, Henderson, Brian E, Schumacher, Frederick, Le Marchand, Loic, Apicella, Carmel, Southey, Melissa C, Cross, Simon S, Winqvist, Robert, Jukkola-Vuorinen, Arja, Grip, Mervi, Hooning, Maartje J, Hollestelle, Antoinette, Schneeweiss, Andreas, Yang, Rongxi, Burwinkel, Barbara, Figueroa, Jonine, Lissowska, Jolanta, Sawyer, Elinor J, Tomlinson, Ian, Kerin, Michael J, Brenner, Hermann, Butterbach, Katja, Holleczek, Bernd, Kataja, Vesa, Hartikainen, Jaana M, Humphreys, Keith, Devilee, Peter, Seynaeve, Caroline, Radice, Paolo, Peterlongo, Paolo, Manoukian, Siranoush, Ficarazzi, Filomena, Beckmann, Matthias W, Ekici, Arif B, Phillips, Kelly-Anne, Benitez, Javier, Zamora, M Pilar, Menéndez, Primitiva, Jakubowska, Anna, Lubinski, Jan, Gronwald, Jacek, Kabisch, Maria, Ulmer, Hans Ulrich, Rüdiger, Thomas, Margolin, Sara, Kristensen, Vessela, Nord, Siljie, Dunn, Janet A, Bowden, Sarah, Yang, Rose, Campa, Daniele, Gaudet, Mia M, Hoover, Robert N, Kaaks, Rudolf, Machiela, Mitchell J, Willett, Walter, Canzian, Federico, Chin, Suet-Feung, Caldas, Carlos, Lindstrom, Sara, Garcia-Closas, Montserrat, Couch, Fergus J, Chenevix-Trench, Georgia, Andrulis, Irene L, Hall, Per, Chang-Claude, Jenny, Easton, Douglas F, Cox, Angela, Pharoah, Paul Dp, Schmidt, Marjanka K

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Brain volumetric deficits in MAPT mutation carriers: a multisite study by Chu, Stephanie A., Flagan, Taru M., Staffaroni, Adam M., Jiskoot, Lize C., Deng, Jersey, Spina, Salvatore, Zhang, Liwen, Sturm, Virginia E., Yokoyama, Jennifer S., Seeley, William W., Papma, Janne M., Geschwind, Dan H., Rosen, Howard J., Boeve, Bradley F., Boxer, Adam L., Heuer, Hilary W., Forsberg, Leah K., Brushaber, Danielle E., Grossman, Murray, Coppola, Giovanni, Dickerson, Bradford C., Bordelon, Yvette M., Faber, Kelley, Feldman, Howard H., Fields, Julie A., Fong, Jamie C., Foroud, Tatiana, Gavrilova, Ralitza H., Ghoshal, Nupur, Graff‐Radford, Neill R., Hsiung, Ging‐Yuek Robin, Huey, Edward D., Irwin, David J., Kantarci, Kejal, Kaufer, Daniel I., Karydas, Anna M., Knopman, David S., Kornak, John, Kramer, Joel H., Kukull, Walter A., Lapid, Maria I., Litvan, Irene, Mackenzie, Ian R.A., Mendez, Mario F., Miller, Bruce L., Onyike, Chiadi U., Pantelyat, Alexander Y., Rademakers, Rosa, Marisa Ramos, Eliana, Roberson, Erik D., Carmela Tartaglia, Maria, Tatton, Nadine A., Toga, Arthur W., Vetor, Ashley, Weintraub, Sandra, Wong, Bonnie, Wszolek, Zbigniew K., Van Swieten, John C., Lee, Suzee E.

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Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer by Kabisch, Maria, Lorenzo Bermejo, Justo, Dünnebier, Thomas, Ying, Shibo, Bolla, Manjeet K, Wang, Qin, Dennis, Joe, Shah, Mitul, Eriksson, Mikael, Bojesen, Stig E, Nordestgaard, Børge G, Nielsen, Sune F, Neven, Patrick, Weltens, Caroline, Olson, Janet E, Wang, Xianshu, Rudolph, Anja, Seibold, Petra, Flesch-Janys, Dieter, Peto, Julian, Nevanlinna, Heli, Muranen, Taru A, Aittomäki, Kristiina, Blomqvist, Carl, Schmidt, Marjanka K, Broeks, Annegien, Hogervorst, Frans B L, Li, Jingmei, Humphreys, Keith, Guénel, Pascal, Truong, Thérèse, Menegaux, Florence, Burwinkel, Barbara, Marmé, Frederik, Yang, Rongxi, González-Neira, Anna, Benitez, Javier, Pilar Zamora, M, Arias Perez, Jose I, Cox, Angela, Cross, Simon S, Reed, Malcolm W R, Andrulis, Irene L, Glendon, Gord, Sawyer, Elinor J, Tomlinson, Ian, Miller, Nicola, Haiman, Christopher A, Schumacher, Fredrick, Henderson, Brian E, Le Marchand, Loic, Margolin, Sara, Hooning, Maartje J, Hollestelle, Antoinette, Koppert, Linetta B, Hopper, John L, Southey, Melissa C, Apicella, Carmel, Slettedahl, Seth, Vachon, Celine, Yannoukakos, Drakoulis, Milne, Roger L, McLean, Catriona, Ekici, Arif B, Beckmann, Matthias W, Arndt, Volker, Stegmaier, Christa, Ashworth, Alan, Swerdlow, Anthony, García-Closas, Montserrat, Chanock, Stephen J, Goldberg, Mark S, Labrèche, France, Dumont, Martine, Winqvist, Robert, Brauch, Hiltrud, Ko, Yon-Dschun, Radice, Paolo, Bogdanova, Natalia, Dörk, Thilo, Kataja, Vesa, Kosma, Veli-Matti, Hartikainen, Jaana M, Devilee, Peter, Tollenaar, Robert A E M, Seynaeve, Caroline, Van Asperen, Christi J, Jakubowska, Anna, Lubinski, Jan, Shrubsole, Martha J, Cai, Qiuyin, Kristensen, Vessela, Bacot, François, Tessier, Daniel C, Vincent, Daniel, Baynes, Caroline, Ahmed, Shahana, Chenevix-Trench, Georgia, Pharoah, Paul D P, Easton, Douglas F

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P1‐433: GRAY MATTER DEFICITS IN SYMPTOMATIC AND PRESYMPTOMATIC MAPT MUTATION CARRIERS by Chu, Stephanie A., Flagan, Taru M., Jiskoot, Lize C., Seeley, William W., Papma, Janne M., Deng, Jersey, Rosen, Howard J., Boeve, Bradley F., Boxer, Adam L., Heuer, Hilary W., Brushaber, Danielle, Grossman, Murray, Coppola, Giovanni, Dickerson, Brad C., Bordelon, Yvette M., Dheel, Christina, Faber, Kelley, Feldman, Howard H., Fields, Julie A., Fong, Jamie, Foroud, Tatiana M., Forsberg, Leah K., Gavrilova, Ralitza H., Ghoshal, Nupur, Graff-Radford, Neill R., Robin Hsiung, Ging-Yuek, Huey, Edward D., Irwin, David, Kantarci, Kejal, Kaufer, Daniel, Karydas, Anna M., Klein, Alex, Knopman, David S., Kornak, John, Kramer, Joel H., Kukull, Walter A., Lapid, Maria I., Laxineta, Samara, Litvan, Irene, Mackenzie, Ian R., Mendez, Mario F., Miller, Bruce L., Onyike, Chiadi U., Pantelyat, Alex, Potter, Madeline, Rademakers, Rosa, Roberson, Erik D., Tartaglia, Maria Carmela, Tatton, Nadine, Toga, Arthur W., Vetor, Ashley, Weintraub, Sandra, Wong, Bonnie, Wszolek, Zbigniew, Swieten, John C., Lee, Suzee E.

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GRAY MATTER DEFICITS IN SYMPTOMATIC AND PRESYMPTOMATIC MAPT MUTATION CARRIERS by Chu, Stephanie A., Flagan, Taru M., Jiskoot, Lize C., Seeley, William W., Papma, Janne M., Deng, Jersey, Rosen, Howard J., Boeve, Bradley F., Boxer, Adam L., Heuer, Hilary W., Brushaber, Danielle, Grossman, Murray, Coppola, Giovanni, Dickerson, Brad C., Bordelon, Yvette M., Dheel, Christina, Faber, Kelley, Feldman, Howard H., Fields, Julie A., Fong, Jamie, Foroud, Tatiana M., Forsberg, Leah K., Gavrilova, Ralitza H., Ghoshal, Nupur, Graff-Radford, Neill R., Robin Hsiung, Ging-Yuek, Huey, Edward D., Irwin, David, Kantarci, Kejal, Kaufer, Daniel, Karydas, Anna M., Klein, Alex, Knopman, David S., Kornak, John, Kramer, Joel H., Kukull, Walter A., Lapid, Maria I., Laxineta, Samara, Litvan, Irene, Mackenzie, Ian R., Mendez, Mario F., Miller, Bruce L., Onyike, Chiadi U., Pantelyat, Alex, Potter, Madeline, Rademakers, Rosa, Roberson, Erik D., Tartaglia, Maria Carmela, Tatton, Nadine, Toga, Arthur W., Vetor, Ashley, Weintraub, Sandra, Wong, Bonnie, Wszolek, Zbigniew, van Swieten, John C., Lee, Suzee E.

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Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation by Michailidou, Kyriaki, Cowper-Sal Lari, Richard, Desai, Kinjal, Hillman, Kristine M, Kaufmann, Susanne, Dennis, Joe, Wang, Qin, Shah, Mitul, Luben, Robert, Eriksson, Mikael, Klevebring, Daniel, Lambrechts, Diether, Wildiers, Hans, Broeks, Annegien, Van't Veer, Laura J, Rutgers, Emiel J Th, Olson, Janet E, Chang-Claude, Jenny, Flesch-Janys, Dieter, Peto, Julian, Dos-Santos-Silva, Isabel, Gibson, Lorna, Blomqvist, Carl, Choi, Ji-Yeob, Park, Sue K, Ito, Hidemi, Iwata, Hiroji, Yatabe, Yasushi, Guénel, Pascal, Truong, Thérèse, Menegaux, Florence, Sanchez, Marie, Schneeweiss, Andreas, Sohn, Christof, Benitez, Javier, Pilar Zamora, M, Gao, Yu-Tang, Cai, Qiuyin, Cox, Angela, Cross, Simon S, Knight, Julia A, Sawyer, Elinor J, Tomlinson, Ian, Miller, Nicola, Henderson, Brian E, Le Marchand, Loic, Yip, Cheng Har, Wong, Tien Y, Hooning, Maartje J, Hopper, John L, Southey, Melissa C, Tsimiklis, Helen, Kapuscinski, Miroslav K, Shen, Chen-Yang, Wu, Pei-Ei, Yu, Jyh-Cherng, Alnæs, Grethe Grenaker, Borresen-Dale, Anne-Lise, Giles, Graham G, Muir, Kenneth, Lophatananon, Artitaya, Siriwanarangsan, Pornthep, Hartman, Mikael, Miao, Hui, Ekici, Arif B, Brenner, Hermann, Dieffenbach, Aida Karina, Arndt, Volker, Swerdlow, Anthony, Ashworth, Alan, Orr, Nick, Schoemaker, Minouk J, Simard, Jacques, Winqvist, Robert, Pylkäs, Katri, Brauch, Hiltrud, Koto, Yon-Dschun, Bonanni, Bernardo, Volorio, Sara, Bogdanova, Natalia V, Kataja, Vesa, Devilee, Peter, Tollenaar, Robert A E M, Jakubowska, Anna, Durda, Katarzyna, Toland, Amanda E, Sangrajrang, Suleeporn, Brennan, Paul, Torres, Diana, Healey, Catherine S, Pita, Guillermo, Tessier, Daniel C, Carroll, Jason, Caldas, Carlos, Brown, Melissa A, Lupien, Mathieu, Kristensen, Vessela N, Pharoah, Paul D P, Easton, Douglas F, Dunning, Alison M

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