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by 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, Gabriëlle 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 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-Saïd, Saddek and Sahel, José-Alain 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, Frédéric and Blanché, Hélène and Deleuze, Jean-François 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 ...
Nature genetics, ISSN 1546-1718, 12/2015, Volume 48, Issue 2, pp. 134 - 143
Advanced age-related macular degeneration (AMD) is the leading cause of blindness in the elderly, with limited therapeutic options. Here we report on a study... 
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Macular degeneration | Genetic variation | Development and progression | Genetic aspects | Gene expression | Identification and classification | Health aspects | Proteins | Studies | Confidence intervals | Datasets | Angiogenesis | Data analysis | Genealogy | Disease | Genomics | Quality control | Genomes | Index Medicus
Journal Article
by Schmidt, Amand F and Swerdlow, Daniel I and Holmes, Michael V and Patel, Riyaz S and Fairhurst-Hunter, Zammy and Lyall, Donald M and Hartwig, Fernando Pires and Horta, Bernardo Lessa and Hyppönen, Elina and Power, Christine and Moldovan, Max and van Iperen, Erik and Hovingh, G Kees and Demuth, Ilja and Norman, Kristina and Steinhagen-Thiessen, Elisabeth and Demuth, Juri and Bertram, Lars and Liu, Tian and Coassin, Stefan and Willeit, Johann and Kiechl, Stefan and Willeit, Karin and Mason, Dan and Wright, John and Morris, Richard and Wanamethee, Goya and Whincup, Peter and Ben-Shlomo, Yoav and McLachlan, Stela and Price, Jackie F and Kivimaki, Mika and Welch, Catherine and Sanchez-Galvez, Adelaida and Marques-Vidal, Pedro and Nicolaides, Andrew and Panayiotou, Andrie G and Onland-Moret, N Charlotte and van der Schouw, Yvonne T and Matullo, Giuseppe and Fiorito, Giovanni and Guarrera, Simonetta and Sacerdote, Carlotta and Wareham, Nicholas J and Langenberg, Claudia and Scott, Robert and Luan, Jian'an and Bobak, Martin and Malyutina, Sofia and Pająk, Andrzej and Kubinova, Ruzena and Tamosiunas, Abdonas and Pikhart, Hynek and Husemoen, Lise Lotte Nystrup and Grarup, Niels and Pedersen, Oluf and Hansen, Torben and Linneberg, Allan and Simonsen, Kenneth Starup and Cooper, Jackie and Humphries, Steve E and Brilliant, Murray and Kitchner, Terrie and Hakonarson, Hakon and Carrell, David S and McCarty, Catherine A and Kirchner, H Lester and Larson, Eric B and Crosslin, David R and de Andrade, Mariza and Roden, Dan M and Denny, Joshua C and Carty, Cara and Hancock, Stephen and Attia, John and Holliday, Elizabeth and O'Donnell, Martin and Yusuf, Salim and Chong, Michael and Pare, Guillaume and van der Harst, Pim and Said, M Abdullah and Eppinga, Ruben N and Verweij, Niek and Snieder, Harold and Christen, Tim and Mook-Kanamori, Dennis O and Gustafsson, Stefan and Lind, Lars and Ingelsson, Erik and Pazoki, Raha and Franco, Oscar and Hofman, Albert and Uitterlinden, Andre and Dehghan, Abbas and Teumer, Alexander and Baumeister, Sebastian and Dörr, Marcus and Lerch, Markus M and Völker, Uwe and ... and UCLEB consortium and LifeLines Cohort study group and UCLEB Consortium and LifeLines Cohort Study Grp
The lancet. Diabetes & endocrinology, ISSN 2213-8587, 02/2017, Volume 5, Issue 2, pp. 97 - 105
Journal Article
JAMA : the journal of the American Medical Association, ISSN 0098-7484, 01/2016, Volume 315, Issue 1, pp. 47 - 57
Journal Article
Nature communications, ISSN 2041-1723, 08/2018, Volume 9, Issue 1, pp. 3522 - 11
Journal Article
Nature communications, ISSN 2041-1723, 05/2018, Volume 9, Issue 1, pp. 1864 - 11
Central corneal thickness (CCT) is a highly heritable trait associated with complex eye diseases such as keratoconus and glaucoma. We perform a genome-wide... 
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Lumican - metabolism | Glaucoma, Open-Angle - genetics | Humans | Corneal Diseases - metabolism | Corneal Dystrophies, Hereditary - ethnology | Corneal Diseases - genetics | Ehlers-Danlos Syndrome - genetics | Corneal Dystrophies, Hereditary - pathology | Loeys-Dietz Syndrome - metabolism | Mendelian Randomization Analysis | Fibrillin-1 - metabolism | Cornea - pathology | Keratoconus - pathology | Corneal Diseases - pathology | Decorin - genetics | Gene Expression | Eye Diseases, Hereditary - pathology | Lumican - genetics | ADAMTS Proteins - metabolism | Proteoglycans - metabolism | Ehlers-Danlos Syndrome - ethnology | European Continental Ancestry Group | Myopia - pathology | Cornea - metabolism | Myopia - ethnology | Loeys-Dietz Syndrome - pathology | Corneal Diseases - ethnology | Marfan Syndrome - metabolism | Marfan Syndrome - pathology | Cornea - abnormalities | Quantitative Trait Loci | Proteoglycans - genetics | ADAMTS Proteins - genetics | Transforming Growth Factor beta2 - metabolism | Corneal Dystrophies, Hereditary - genetics | Glaucoma, Open-Angle - pathology | Keratoconus - metabolism | Loeys-Dietz Syndrome - ethnology | Glaucoma, Open-Angle - ethnology | Myopia - metabolism | Ehlers-Danlos Syndrome - pathology | Marfan Syndrome - ethnology | Keratoconus - genetics | Glaucoma, Open-Angle - metabolism | Fibrillin-1 - genetics | Eye Diseases, Hereditary - ethnology | Genome-Wide Association Study | Quantitative Trait, Heritable | Corneal Dystrophies, Hereditary - metabolism | Marfan Syndrome - genetics | Eye Diseases, Hereditary - genetics | Myopia - genetics | Asian Continental Ancestry Group | Keratoconus - ethnology | Ehlers-Danlos Syndrome - metabolism | Loeys-Dietz Syndrome - genetics | Polymorphism, Single Nucleotide | Transforming Growth Factor beta2 - genetics | Genome, Human | Decorin - metabolism | Eye Diseases, Hereditary - metabolism | Glaucoma | Cornea | Genes | Myopia | Association analysis | Genomes | Gene expression | Tissues | Connective tissues | Keratoconus | Collagen | Eye diseases | Extracellular matrix | Index Medicus
Journal Article
Journal Article
Genetics in medicine, ISSN 1530-0366, 01/2013, Volume 15, Issue 4, pp. 258 - 267
Although the potential for genomics to contribute to clinical care has long been anticipated, the pace of defining the risks and benefits of incorporating... 
medical genomics | practice standards | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetics, Medical - trends | Research | Genomics | Humans | Index Medicus | Review
Journal Article