Search Results - Morgan, Denise J.

Differential Gene Expression in Age-Related Macular Degeneration by Morgan, Denise J., DeAngelis, Margaret M.

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Progressive optic nerve changes in cavitary optic disc anomaly: integration of copy number alteration and cis-expression quantitative trait loci to assess disease etiology by Hwang, Eileen S., Morgan, Denise J., Pennington, Katie L., Owen, Leah A., Fingert, John H., Bernstein, Paul S., DeAngelis, Margaret M.

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Genetics of age-related macular degeneration (AMD) by DeAngelis, Margaret M., Owen, Leah A., Morrison, Margaux A., Morgan, Denise J., Li, Mingyao, Shakoor, Akbar, Vitale, Albert, Iyengar, Sudha, Stambolian, Dwight, Kim, Ivana K., Farrer, Lindsay A.

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Genetics of age-related macular degeneration (AMD) by DeAngelis, Margaret M., Owen, Leah A., Morrison, Margaux A., Morgan, Denise J., Li, Mingyao, Shakoor, Akbar, Vitale, Albert, Iyengar, Sudha, Stambolian, Dwight, Kim, Ivana K., Farrer, Lindsay A.

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The Utah Protocol for Postmortem Eye Phenotyping and Molecular Biochemical Analysis by Owen, Leah A., Shakoor, Akbar, Morgan, Denise J., Hejazi, Andre A., McEntire, M. Wade, Brown, Jared J., Farrer, Lindsay A., Kim, Ivana, Vitale, Albert, DeAngelis, Margaret M.

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Genetic Epidemiologic Analysis of Hypertensive Retinopathy in an Underrepresented and Rare Federally Recognized Native American Population of the Intermountain West by Hicks, Patrice M, Melendez, Samuel A Collazo, Vitale, Albert, Self, William, Hartnett, Mary Elizabeth, Bernstein, Paul, Morgan, Denise J, Feehan, Michael, Shakoor, Akbar, Kim, Ivana, Owen, Leah A, DeAngelis, Margaret M

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Generation, transcriptome profiling, and functional validation of cone-rich human retinal organoids by Kim, Sangbae, Lowe, Albert, Dharmat, Rachayata, Lee, Seunghoon, Owen, Leah A., Wang, Jun, Shakoor, Akbar, Li, Yumei, Morgan, Denise J., Hejazi, Andre A., Cvekl, Ales, DeAngelis, Margaret M., Zhou, Z. Jimmy, Chen, Rui, Liu, Wei

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Influence of ROBO1 and RORA on Risk of Age-Related Macular Degeneration Reveals Genetically Distinct Phenotypes in Disease Pathophysiology by Jun, Gyungah, Nicolaou, Michael, Morrison, Margaux A., Buros, Jacqueline, Morgan, Denise J., Radeke, Monte J., Yonekawa, Yoshihiro, Tsironi, Evangelia E., Kotoula, Maria G., Zacharaki, Fani, Mollema, Nissa, Yuan, Yang, Miller, Joan W., Haider, Neena B., Hageman, Gregory S., Kim, Ivana K., Schaumberg, Debra A., Farrer, Lindsay A., DeAngelis, Margaret M.

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FLT1 Genetic Variation Predisposes to Neovascular AMD in Ethnically Diverse Populations and Alters Systemic FLT1 Expression by Owen, Leah A., Morrison, Margaux A., Ahn, Jeeyun, Woo, Se Joon, Sato, Hajime, Robinson, Rosann, Morgan, Denise J., Zacharaki, Fani, Simeonova, Marina, Uehara, Hironori, Chakravarthy, Usha, Hogg, Ruth E., Ambati, Balamurali K., Kotoula, Maria, Baehr, Wolfgang, Haider, Neena B., Silvestri, Giuliana, Miller, Joan W., Tsironi, Evangelia E., Farrer, Lindsay A., Kim, Ivana K., Park, Kyu Hyung, DeAngelis, Margaret M.

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Ancestry of the Timorese: age-related macular degeneration associated genotype and allele sharing among human populations from throughout the world by Morrison, Margaux A., Magalhaes, Tiago R., Ramke, Jacqueline, Smith, Silvia E., Ennis, Sean, Simpson, Claire L., Portas, Laura, Murgia, Federico, Ahn, Jeeyun, Dardenne, Caitlin, Mayne, Katie, Robinson, Rosann, Morgan, Denise J., Brian, Garry, Lee, Lucy, Woo, Se J., Zacharaki, Fani, Tsironi, Evangelia E., Miller, Joan W., Kim, Ivana K., Park, Kyu H., Bailey-Wilson, Joan E., Farrer, Lindsay A., Stambolian, Dwight, DeAngelis, Margaret M.

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ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder by Williams, Lloyd B., Javed, Asif, Sabri, Amin, Morgan, Denise J., Huff, Chad D., Grigg, John R., Heng, Xiu Ting, Khng, Alexis J., Hollink, Iris H. I. M., Morrison, Margaux A., Owen, Leah A., Anderson, Katherine, Kinard, Krista, Greenlees, Rebecca, Novacic, Danica, Nida Sen, H., Zein, Wadih M., Rodgers, George M., Vitale, Albert T., Haider, Neena B., Hillmer, Axel M., Ng, Pauline C., Shankaracharya, Cheng, Anson, Zheng, Linda, Gillies, Mark C., van Slegtenhorst, Marjon, van Hagen, P. Martin, Missotten, Tom O. A. R., Farley, Gary L., Polo, Michael, Malatack, James, Curtin, Julie, Martin, Frank, Arbuckle, Susan, Alexander, Stephen I., Chircop, Megan, Davila, Sonia, Digre, Kathleen B., Jamieson, Robyn V., DeAngelis, Margaret M.

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

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

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