Items where Author is "Ratnapriya, Rinki"

Article

Advani, Jayshree and Mehta, Puja A. and Hamel, Andrew R. and Mehrotra, Sudeep and Kiel, Christina and Strunz, Tobias and Corso-Diaz, Ximena and Kwicklis, Madeline and van Asten, Freekje and Ratnapriya, Rinki and Chew, Emily Y. and Hernandez, Dena G. and Montezuma, Sandra R. and Ferrington, Deborah A. and Weber, Bernhard H. F. and Segre, Ayellet V. and Swaroop, Anand (2024) QTL mapping of human retina DNA methylation identifies 87 gene-epigenome interactions in age-related macular degeneration. NATURE COMMUNICATIONS, 15 (1): 1972. ISSN 2041-1723

Strunz, Tobias and Kiel, Christina and Grassmann, Felix and Ratnapriya, Rinki and Kwicklis, Madeline and Karlstetter, Marcus and Fauser, Sascha and Arend, Nicole and Swaroop, Anand and Langmann, Thomas and Wolf, Armin and Weber, Bernhard H. F. (2020) A mega-analysis of expression quantitative trait loci in retinal tissue. PLOS GENETICS, 16 (9): e1008934. ISSN 1553-7404

Grassmann, Felix and Harsch, Sebastian and Brandl, Caroline and Kiel, Christina and Nuernberg, Peter and Toliat, Mohammad R. and Fleckenstein, Monika and Pfau, Maximilian and Schmitz-Valckenberg, Steffen and Holz, Frank G. and Chew, Emily Y. and Swaroop, Anand and Ratnapriya, Rinki and Klein, Michael L. and Mulyukov, Zufar and Zamiri, Parisa and Weber, Bernhard H. F. (2019) Assessment of Novel Genome-Wide Significant Gene Loci and Lesion Growth in Geographic Atrophy Secondary to Age-Related Macular Degeneration. JAMA OPHTHALMOLOGY, 137 (8). pp. 867-876. ISSN 2168-6165, 2168-6173

Waksmunski, Andrea R. and Grunin, Michelle and Kinzy, Tyler G. and Igo, Robert P. and Haines, Jonathan L. and Bailey, Jessica N. Cooke and Fritsche, Lars G. and Igl, Wilmar and Grassmann, Felix and Sengupta, Sebanti and Bragg-Gresham, Jennifer L. and Burdon, Kathryn P. and Hebbring, Scott J. and Wen, Cindy and Gorski, Mathias and Kim, Ivana K. and Cho, David and Zack, Donald and Souied, Eric and Scholl, Hendrik P. N. and Bala, Elisa and Lee, Kristine E. and Hunter, David J. and Sardell, Rebecca J. and Mitchell, Paul and Merriam, Joanna E. and Cipriani, Valentina and Hoffman, Joshua D. and Schick, Tina and Lechanteur, Yara T. E. and Guymer, Robyn H. and Johnson, Matthew P. and Jiang, Yingda and Stanton, Chloe M. and Buitendijk, Gabrielle H. S. and Zhan, Xiaowei and Kwong, Alan M. and Boleda, Alexis and Brooks, Matthew and Gieser, Linn and Ratnapriya, Rinki and Branham, Kari E. and Foerster, Johanna R. and Heckenlively, John R. and Othman, Mohammad and Vote, Brendan J. and Liang, Helena Hai and Souzeau, Emmanuelle and McAllister, Ian L. and Isaacs, Timothy and Hall, Janette and Lake, Stewart and Mackey, David A. and Constable, Ian J. and Craig, Jamie E. and Kitchner, Terrie E. and Yang, Zhenglin and Su, Zhiguang and Luo, Hongrong and Chen, Daniel and Ouyang, Hong and Flagg, Ken and Lin, Danni and Mao, Guanping and Ferreyra, Henry and Stark, Klaus and von Strachwitz, Claudia N. and Wolf, Armin and Brandl, Caroline and Rudolph, Guenther and Olden, Matthias and Morrison, Margaux A. and Morgan, Denise J. and Schu, Matthew and Ahn, Jeeyun and Silvestri, Giuliana and Tsironi, Evangelia E. and Park, Kyu Hyung and Farrer, Lindsay A. and Orlin, Anton and Brucker, Alexander and Li, Mingyao and Curcio, Christine A. and Mohand-Said, Saddek and Sahel, Jose-Alain and Audo, Isabelle and Benchaboune, Mustapha and Cree, Angela J. and Rennie, Christina A. and Goverdhan, Srinivas and Hagbi-Levi, Shira and Campochiaro, Peter and Katsanis, Nicholas and Holz, Frank G. and Blond, Frederic and Blanche, Helene and Deleuze, Jean-Francois and Truitt, Barbara and Peachey, Neal S. and Meuer, Stacy M. and Myers, Chelsea E. and Moore, Emily L. and Klein, Ronald and Hauser, Michael A. and Postel, Eric A. and Courtenay, Monique D. and Schwartz, Stephen G. and Kovach, Jaclyn L. and Scott, William K. and Liew, Gerald and Tan, Ava G. and Gopinath, Bamini and Merriam, John C. and Smith, R. Theodore and Khan, Jane C. and Shahid, Humma and Moore, Anthony T. and McGrath, J. Allie and Laux, Renee and Brantley, Milam A. and Agarwal, Anita and Ersoy, Lebriz and Caramoy, Albert and Langmann, Thomas and Saksens, Nicole T. M. and de Jong, Eiko K. and Hoyng, Carel B. and Cain, Melinda S. and Richardson, Andrea J. and Martin, Tammy M. and Blangero, John and Weeks, Daniel E. and Dhillon, Bal and van Duijn, Cornelia M. and Doheny, Kimberly F. and Romm, Jane and Klaver, Caroline C. W. and Hayward, Caroline and Gorin, Michael B. and Klein, Michael L. and Baird, Paul N. and den Hollander, Anneke and Fauser, Sascha and Yates, John R. W. and Allikmets, Rando and Wang, Jie Jin and Schaumberg, Debra A. and Klein, Barbara E. K. and Hagstrom, Stephanie A. and Chowers, Itay and Lotery, Andrew J. and Leveillard, Thierry and Zhang, Kang and Brilliant, Murray H. and Hewitt, Alex W. and Swaroop, Anand and Chew, Emily Y. and Pericak-Vance, Margaret A. and DeAngelis, Margaret and Stambolian, Dwight and Iyengar, Sudha K. and Weber, Bernhard H. F. and Abecasis, Goncalo R. and Heid, Iris M. (2019) Pathway Analysis Integrating Genome-Wide and Functional Data Identifies PLCG2 as a Candidate Gene for Age-Related Macular Degeneration. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 60 (12). pp. 4041-4051. ISSN 0146-0404, 1552-5783

Fritsche, Lars G. and Igl, Wilmar and Bailey, Jessica N. Cooke and Grassmann, Felix and Sengupta, Sebanti and Bragg-Gresham, Jennifer L. and Burdon, Kathryn P. and Hebbring, Scott J. and Wen, Cindy and Gorski, Mathias and Kim, Ivana K. and Cho, David and Zack, Donald and Souied, Eric and Scholl, Hendrik P. N. and Bala, Elisa and Lee, Kristine E. and Hunter, David J. and Sardell, Rebecca J. and Mitchell, Paul and Merriam, Joanna E. and Cipriani, Valentina and Hoffman, Joshua D. and Schick, Tina and Lechanteur, Yara T. E. and Guymer, Robyn H. and Johnson, Matthew P. and Jiang, Yingda and Stanton, Chloe M. and Buitendijk, Gabrielle H. S. and Zhan, Xiaowei and Kwong, Alan M. and Boleda, Alexis and Brooks, Matthew and Gieser, Linn and Ratnapriya, Rinki and Branham, Kari E. and Foerster, Johanna R. and Heckenlively, John R. and Othman, Mohammad I. and Vote, Brendan J. and Liang, Helena Hai and Souzeau, Emmanuelle and McAllister, Ian L. and Isaacs, Timothy and Hall, Janette and Lake, Stewart and Mackey, David A. and Constable, Ian J. and Craig, Jamie E. and Kitchner, Terrie E. and Yang, Zhenglin and Su, Zhiguang and Luo, Hongrong and Chen, Daniel and Hong Ouyang, and Flagg, Ken and Lin, Danni and Mao, Guanping and Ferreyra, Henry and Starke, Klaus and von Strachwitz, Claudia N. and Wolf, Armin and Brandl, Caroline and Rudolph, Guenther and Olden, Matthias and Morrison, Margaux A. and Morgan, Denise J. and Schu, Matthew and Ahn, Jeeyun and Silvestri, Giuliana and Tsironi, Evangelia E. and Park, Kyu Hyung and Farrer, Lindsay A. and Orlin, Anton and Brucker, Alexander and Li, Mingyao and Curcio, Christine A. and Mohand-Said, Saddek and Sahel, Jose-Main and Audo, Isabelle and Benchaboune, Mustapha and Cree, Angela J. and Rennie, Christina A. and Goverdhan, Srinivas V. and Grunin, Michelle and Hagbi-Levi, Shira and Campochiaro, Peter and Katsanis, Nicholas and Holz, Frank G. and Blond, Frederic and Blanche, Helene and Deleuze, Jean-Francois and Igo, Robert P. and Truitt, Barbara and Peachey, Neal S. and Meuer, Stacy M. and Myers, Chelsea E. and Moore, Emily L. and Klein, Ronald and Hauser, Michael A. and Postel, Eric A. and Courtenay, Monique D. and Schwartz, Stephen G. and Kovach, Jaclyn L. and Scott, William K. and Liew, Gerald and Tan, Ava G. and Gopinath, Bamini and Merriam, John C. and Smith, R. Theodore and Khan, Jane C. and Shahid, Humma and Moore, Anthony T. and McGrath, J. Allie and Laux, Renee and Brantley, Milam A. and Agarwal, Anita and Ersoy, Lebriz and Caramoy, Albert and Langmann, Thomas and Saksens, Nicole T. M. and de Jong, Eiko K. and Hoyng, Carel B. and Cain, Melinda S. and Richardson, Andrea J. and Martin, Tammy M. and Blangero, John and Weeks, Daniel E. and Dhillon, Bal and van Duijn, Cornelia M. and Doheny, Kimberly F. and Romm, Jane and Klaver, Caroline C. W. and Hayward, Caroline and Gorin, Michael B. and Klein, Michael L. and Baird, Paul N. and den Hollander, Anneke I. and Fauser, Sascha and Yates, John R. W. and Allikmets, Rando and Wang, Jie Jin and Schaumberg, Debra A. and Klein, Barbara E. K. and Hagstrom, Stephanie A. and Chowers, Itay and Lotery, Andrew J. and Leveillard, Thierry and Zhang, Kang and Brilliant, Murray H. and Hewitt, Alex W. and Swaroop, Anand and Chew, Emily Y. and Pericak-Vance, Margaret A. and DeAngelis, Margaret and Stambolian, Dwight and Haines, Jonathan L. and Iyengar, Sudha K. and Weber, Bernhard H. F. and Abecasis, Goncalo R. and Heid, Iris M. (2016) A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants. NATURE GENETICS, 48 (2). pp. 134-143. ISSN 1061-4036, 1546-1718

Grassmann, Felix and Fleckenstein, Monika and Chew, Emily Y. and Strunz, Tobias and Schmitz-Valckenberg, Steffen and Goebel, Arno P. and Klein, Michael L. and Ratnapriya, Rinki and Swaroop, Anand and Holz, Frank G. and Weber, Bernhard H. F. (2015) Clinical and Genetic Factors Associated with Progression of Geographic Atrophy Lesions in Age-Related Macular Degeneration. PLOS ONE, 10 (5): e0126636. ISSN 1932-6203

Ratnapriya, Rinki and Zhan, Xiaowei and Fariss, Robert N. and Branham, Kari E. and Zipprer, David and Chakarova, Christina F. and Sergeev, Yuri V. and Campos, Maria M. and Othman, Mohammad and Friedman, James S. and Maminishkis, Arvydas and Waseem, Naushin H. and Brooks, Matthew and Rajasimha, Harsha K. and Edwards, Albert O. and Lotery, Andrew and Klein, Barbara E. and Truitt, Barbara J. and Li, Bingshan and Schaumberg, Debra A. and Morgan, Denise J. and Morrison, Margaux A. and Souied, Eric and Tsironi, Evangelia E. and Grassmann, Felix and Fishman, Gerald A. and Silvestri, Giuliana and Scholl, Hendrik P. N. and Kim, Ivana K. and Ramke, Jacqueline and Tuo, Jingsheng and Merriam, Joanna E. and Merriam, John C. and Park, Kyu Hyung and Olson, Lana M. and Farrer, Lindsay A. and Johnson, Matthew P. and Peachey, Neal S. and Lathrop, Mark and Baron, Robert V. and Igo, Robert P. and Klein, Ronald and Hagstrom, Stephanie A. and Kamatani, Yoichiro and Martin, Tammy M. and Jiang, Yingda and Conley, Yvette and Sahel, Jose-Alan and Zack, Donald J. and Chan, Chi-Chao and Pericak-Vance, Margaret A. and Jacobson, Samuel G. and Gorin, Michael B. and Klein, Michael L. and Allikmets, Rando and Iyengar, Sudha K. and Weber, Bernhard H. and Haines, Jonathan L. and Leveillard, Thierry and Deangelis, Margaret M. and Stambolian, Dwight and Weeks, Daniel E. and Bhattacharya, Shomi S. and Chew, Emily Y. and Heckenlively, John R. and Abecasis, Goncalo R. and Swaroop, Anand (2014) Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration. HUMAN MOLECULAR GENETICS, 23 (21). pp. 5827-5837. ISSN 0964-6906, 1460-2083

Zhan, Xiaowei and Larson, David E. and Wang, Chaolong and Koboldt, Daniel C. and Sergeev, Yuri V. and Fulton, Robert S. and Fulton, Lucinda L. and Fronick, Catrina C. and Branham, Kari E. and Bragg-Gresham, Jennifer and Jun, Goo and Hu, Youna and Kang, Hyun Min and Liu, Dajiang and Othman, Mohammad and Brooks, Matthew and Ratnapriya, Rinki and Boleda, Alexis and Grassmann, Felix and von Strachwitz, Claudia and Olson, Lana M. and Buitendijk, Gabrielle H. S. and Hofman, Albert and van Duijn, Cornelia M. and Cipriani, Valentina and Moore, Anthony T. and Shahid, Humma and Jiang, Yingda and Conley, Yvette P. and Morgan, Denise J. and Kim, Ivana K. and Johnson, Matthew P. and Cantsilieris, Stuart and Richardson, Andrea J. and Guymer, Robyn H. and Luo, Hongrong and Ouyang, Hong and Licht, Christoph and Pluthero, Fred G. and Zhang, Mindy M. and Zhang, Kang and Baird, Paul N. and Blangero, John and Klein, Michael L. and Farrer, Lindsay A. and DeAngelis, Margaret M. and Weeks, Daniel E. and Gorin, Michael B. and Yates, John R. W. and Klaver, Caroline C. W. and Pericak-Vance, Margaret A. and Haines, Jonathan L. and Weber, Bernhard H. F. and Wilson, Richard K. and Heckenlively, John R. and Chew, Emily Y. and Stambolian, Dwight and Mardis, Elaine R. and Swaroop, Anand and Abecasis, Goncalo R. (2013) Identification of a rare coding variant in complement 3 associated with age-related macular degeneration. NATURE GENETICS, 45 (11). 1375-+. ISSN 1061-4036, 1546-1718

Other

Weber, Bernhard H. F. and Fleckenstein, Monika and Chew, Emily Y. and Schmitz-Valckenberg, Steffen and Goebel, Arno P. and Klein, Michael L. and Ratnapriya, Rinki and Swaroop, Anand and Holz, Frank G. and Grassmann, Felix (2015) Genetic and clinical factors associated with progression of geographic atrophy in age-related macular degeneration. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, ROCKVILLE.