Analysis of Risk Alleles and Complement Activation Levels in Familial and Non-Familial Age-Related Macular Degeneration von Saksens, Nicole T M, Lechanteur, Yara T E, Verbakel, Sanne K, Groenewoud, Joannes M M, Daha, Mohamed R, Schick, Tina, Fauser, Sascha, Boon, Camiel J F, Hoyng, Carel B, den Hollander, Anneke I

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Physical Activity and Age-related Macular Degeneration: A systematic literature review and meta-analysis von McGuinness, Myra B, Le, Jerome, Mitchell, Paul, Gopinath, Bamini, Cerin, Ester, Saksens, Nicole T.M, Schick, Tina, Hoyng, Carel B, Guymer, Robyn H, Finger, Robert P

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Whole Exome Sequencing in Patients with the Cuticular Drusen Subtype of Age-Related Macular Degeneration von Duvvari, Maheswara R, van de Ven, Johannes P H, Geerlings, Maartje J, Saksens, Nicole T M, Bakker, Bjorn, Henkes, Arjen, Neveling, Kornelia, del Rosario, Marisol, Westra, Dineke, van den Heuvel, Lambertus P W J, Schick, Tina, Fauser, Sascha, Boon, Camiel J F, Hoyng, Carel B, de Jong, Eiko K, den Hollander, Anneke I

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Identification of TP53BP2 as a Novel Candidate Gene for Primary Open Angle Glaucoma by Whole Exome Sequencing in a Large Multiplex Family von Micheal, Shazia, Saksens, Nicole T.M., Hogewind, Barend F., Khan, Muhammad Imran, Hoyng, Carel B., den Hollander, Anneke I.

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Analysis of rare variants in the CFH gene in patients with the cuticular drusen subtype of age-related macular degeneration von Duvvari, Maheswara R, Saksens, Nicole T M, van de Ven, Johannes P H, de Jong-Hesse, Yvonne, Schick, Tina, Nillesen, Willy M, Fauser, Sascha, Hoefsloot, Lies H, Hoyng, Carel B, de Jong, Eiko K, den Hollander, Anneke I

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Rare Genetic Variants Associated With Development of Age-Related Macular Degeneration von Saksens, Nicole T M, Geerlings, Maartje J, Bakker, Bjorn, Schick, Tina, Daha, Mohamed R, Fauser, Sascha, Boon, Camiel J F, de Jong, Eiko K, Hoyng, Carel B, den Hollander, Anneke I

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Macular dystrophies mimicking age-related macular degeneration von Saksens, Nicole T.M., Fleckenstein, Monika, Schmitz-Valckenberg, Steffen, Holz, Frank G., den Hollander, Anneke I., Keunen, Jan E.E., Boon, Camiel J.F., Hoyng, Carel B.

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Family-based exome sequencing identifies rare coding variants in age-related macular degeneration von Ratnapriya, Rinki, Acar, İlhan E, Geerlings, Maartje J, Branham, Kari, Kwong, Alan, Saksens, Nicole T M, Pauper, Marc, Corominas, Jordi, Kwicklis, Madeline, Zipprer, David, Starostik, Margaret R, Othman, Mohammad, Yashar, Beverly, Abecasis, Goncalo R, Chew, Emily Y, Ferrington, Deborah A, Hoyng, Carel B, Swaroop, Anand, den Hollander, Anneke I

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Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrity von Saksens, Nicole T M, Krebs, Mark P, Schoenmaker-Koller, Frederieke E, Hicks, Wanda, Yu, Minzhong, Shi, Lanying, Rowe, Lucy, Collin, Gayle B, Charette, Jeremy R, Letteboer, Stef J, Neveling, Kornelia, van Moorsel, Tamara W, Abu-Ltaif, Sleiman, De Baere, Elfride, Walraedt, Sophie, Banfi, Sandro, Simonelli, Francesca, Cremers, Frans P M, Boon, Camiel J F, Roepman, Ronald, Leroy, Bart P, Peachey, Neal S, Hoyng, Carel B, Nishina, Patsy M, den Hollander, Anneke I

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Analysis of rare variants in the C3 gene in patients with age-related macular degeneration von Duvvari, Maheswara R, Paun, Codrut C, Buitendijk, Gabriëlle H S, Saksens, Nicole T M, Volokhina, Elena B, Ristau, Tina, Schoenmaker-Koller, Frederieke E, van de Ven, Johannes P H, Groenewoud, Joannes M M, van den Heuvel, Lambertus P W J, Hofman, Albert, Fauser, Sascha, Uitterlinden, André G, Klaver, Caroline C W, Hoyng, Carel B, de Jong, Eiko K, den Hollander, Anneke I

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Dominant Cystoid Macular Dystrophy von Saksens, Nicole T.M., MD, van Huet, Ramon A.C., MD, van Lith-Verhoeven, Janneke J.C., MD, PhD, den Hollander, Anneke I., PhD, Hoyng, Carel B., MD, Boon, Camiel J.F., MD, PhD

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Clinical characteristics of familial and sporadic age-related macular degeneration: differences and similarities von Saksens, Nicole T M, Kersten, Eveline, Groenewoud, Joannes M M, van Grinsven, Mark J J P, van de Ven, Johannes P H, Sánchez, Clara I, Schick, Tina, Fauser, Sascha, den Hollander, Anneke I, Hoyng, Carel B, Boon, Camiel J F

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Smoking behaviour and attitudes in patients undergoing cardiac surgery. The Radboud experience von Saksens, Nicole T.M, Noyez, Luc

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A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants von Igl, Wilmar, Cooke Bailey, Jessica N, Grassmann, Felix, Sengupta, Sebanti, Bragg-Gresham, Jennifer L, Burdon, Kathryn P, Hebbring, Scott J, Wen, Cindy, Gorski, Mathias, Kim, Ivana K, Souied, Eric, Scholl, Hendrik P. N, Lee, Kristine E, Hunter, David J, Sardell, Rebecca J, Merriam, Joanna E, Hoffman, Joshua D, Schick, Tina, Lechanteur, Yara T. E, Guymer, Robyn H, Johnson, Matthew P, Buitendijk, Gabriëlle H. S, Kwong, Alan M, Boleda, Alexis, Brooks, Matthew, Branham, Kari E, Othman, Mohammad I, Souzeau, Emmanuelle, McAllister, Ian L, Hall, Janette, Lake, Stewart, Mackey, David A, Kitchner, Terrie E, Luo, Hongrong, Chen, Daniel, Ouyang, Hong, Flagg, Ken, von Strachwitz, Claudia N, Olden, Matthias, Morrison, Margaux A, Morgan, Denise J, Schu, Matthew, Silvestri, Giuliana, Tsironi, Evangelia E, Park, Kyu Hyung, Li, Mingyao, Audo, Isabelle, Benchaboune, Mustapha, Cree, Angela J, Rennie, Christina A, Grunin, Michelle, Hagbi-Levi, Shira, Campochiaro, Peter, Katsanis, Nicholas, Holz, Frank G, Blond, Frédéric, Blanché, Hélène, Deleuze, Jean-François, Truitt, Barbara, Klein, Ronald, Hauser, Michael A, Postel, Eric A, Kovach, Jaclyn L, Liew, Gerald, Smith, R. Theodore, Khan, Jane C, Shahid, Humma, Moore, Anthony T, Laux, Reneé, Brantley, Milam A, Ersoy, Lebriz, Caramoy, Albert, Langmann, Thomas, Saksens, Nicole T. M, Hoyng, Carel B, Cain, Melinda S, Richardson, Andrea J, Martin, Tammy M, Blangero, John, Dhillon, Bal, van Duijn, Cornelia M, Romm, Jane, Hayward, Caroline, Gorin, Michael B, den Hollander, Anneke I, Fauser, Sascha, Yates, John R. W, Hagstrom, Stephanie A, Chowers, Itay, Lotery, Andrew J, Zhang, Kang, Brilliant, Murray H, Hewitt, Alex W, Swaroop, Anand, Chew, Emily Y, DeAngelis, Margaret, Stambolian, Dwight, Iyengar, Sudha K, Weber, Bernhard H. F, Abecasis, Gonçalo R

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Reply: To PMID 25267528 von Saksens, Nicole T M, van Huet, Ramon A C, van Lith-Verhoeven, Janneke J C, den Hollander, Anneke I, Hoyng, Carel B, Boon, Camiel J F

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Rare Genetic Variants Associated With Development of Age-Related Macular Degeneration von Saksens, Nicole T M, Geerlings, Maartje J, Bakker, Bjorn, Schick, Tina, Daha, Mohamed R, Fauser, Sascha, Boon, Camiel J F, de Jong, Eiko K, Hoyng, Carel B, den Hollander, Anneke I

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A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants von Igl, Wilmar, Bailey, Jessica N Cooke, Grassmann, Felix, Sengupta, Sebanti, Bragg-Gresham, Jennifer L, Burdon, Kathryn P, Hebbring, Scott J, Wen, Cindy, Gorski, Mathias, Kim, Ivana K, Zack, Donald, Souied, Eric, Lee, Kristine E, Hunter, David J, Sardell, Rebecca J, Merriam, Joanna E, Hoffman, Joshua D, Schick, Tina, Lechanteur, Yara TE, Guymer, Robyn H, Johnson, Matthew P, Kwong, Alan M, Boleda, Alexis, Brooks, Matthew, Branham, Kari E, Othman, Mohammad I, Souzeau, Emmanuelle, McAllister, Ian L, Hall, Janette, Lake, Stewart, Mackey, David A, Kitchner, Terrie E, Luo, Hongrong, Chen, Daniel, Ouyang, Hong, Flagg, Ken, Lin, Danni, Stark, Klaus, von Strachwitz, Claudia N, Wolf, Armin, Olden, Matthias, Morrison, Margaux A, Morgan, Denise J, Schu, Matthew, Silvestri, Giuliana, Tsironi, Evangelia E, Park, Kyu Hyung, Li, Mingyao, Audo, Isabelle, Benchaboune, Mustapha, Cree, Angela J, Rennie, Christina A, Grunin, Michelle, Hagbi-Levi, Shira, Campochiaro, Peter, Katsanis, Nicholas, Holz, Frank G, Blond, Frédéric, Blanché, Hélène, Deleuze, Jean-François, Truitt, Barbara, Klein, Ronald, Hauser, Michael A, Postel, Eric A, Kovach, Jaclyn L, Liew, Gerald, Tan, Ava G, Khan, Jane C, Shahid, Humma, Moore, Anthony T, Laux, Reneé, Brantley, Milam A, Ersoy, Lebriz, Caramoy, Albert, Langmann, Thomas, Hoyng, Carel B, Cain, Melinda S, Richardson, Andrea J, Martin, Tammy M, Blangero, John, Dhillon, Bal, van Duijn, Cornelia M, Romm, Jane, Klaver, Caroline CW, Hayward, Caroline, Gorin, Michael B, den Hollander, Anneke I, Fauser, Sascha, Hagstrom, Stephanie A, Chowers, Itay, Lotery, Andrew J, Zhang, Kang, Brilliant, Murray H, Hewitt, Alex W, Swaroop, Anand, Chew, Emily Y, DeAngelis, Margaret, Stambolian, Dwight, Iyengar, Sudha K, Abecasis, Gonçalo R

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The Functional Effect of Rare Variants in Complement Genes on C3b Degradation in Patients With Age-Related Macular Degeneration von Geerlings, Maartje J, Kremlitzka, Mariann, Bakker, Bjorn, Nilsson, Sara C, Saksens, Nicole T, Lechanteur, Yara T, Pauper, Marc, Corominas, Jordi, Fauser, Sascha, Hoyng, Carel B, Blom, Anna M, de Jong, Eiko K, den Hollander, Anneke I

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Reply von Saksens, Nicole T.M., MD, van Huet, Ramon A.C., MD, van Lith-Verhoeven, Janneke J.C., MD, PhD, den Hollander, Anneke I., PhD, Hoyng, Carel B., MD, PhD, Boon, Camiel J.F., MD, PhD

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