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Clinical Characteristics and Genetic Variants of a Large Cohort of Patients with Retinitis Pigmentosa Using Multimodal Imaging and Next Generation Sequencing
Sather, Richard, Ihinger, Jacie, Simmons, Michael, Khundkar, Tahsin, Lobo, Glenn P., Montezuma, Sandra R.
Published in International journal of molecular sciences (30.06.2023)
Published in International journal of molecular sciences (30.06.2023)
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Disease Expression and Familial Transmission of Fuchs Endothelial Corneal Dystrophy With and Without CTG18.1 Expansion
Xu, Timothy T., Li, Yi-Ju, Afshari, Natalie A., Aleff, Ross A., Rinkoski, Tommy A., Patel, Sanjay V., Maguire, Leo J., Edwards, Albert O., Brown, William L., Fautsch, Michael P., Wieben, Eric D., Baratz, Keith H.
Published in Investigative ophthalmology & visual science (14.01.2021)
Published in Investigative ophthalmology & visual science (14.01.2021)
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Comparison of host susceptibilities to native and exotic pathogens provides evidence for pathogen-imposed selection in forest trees
Freeman, Jules S., Hamilton, Matthew G., Lee, David J., Pegg, Geoff S., Brawner, Jeremy T., Tilyard, Paul A., Potts, Brad M.
Published in The New phytologist (01.03.2019)
Published in The New phytologist (01.03.2019)
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Mitochondria, Cybrids, Aging, and Alzheimer's Disease
Swerdlow, R H, Koppel, S, Weidling, I, Hayley, C, Ji, Y, Wilkins, H M
Published in Progress in molecular biology and translational science (2017)
Published in Progress in molecular biology and translational science (2017)
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Mother–offspring and nest-mate resemblance but no heritability in early-life telomere length in white-throated dippers
Becker, Philipp J. J., Reichert, Sophie, Zahn, Sandrine, Hegelbach, Johann, Massemin, Sylvie, Keller, Lukas F., Postma, Erik, Criscuolo, François
Published in Proceedings of the Royal Society. B, Biological sciences (22.05.2015)
Published in Proceedings of the Royal Society. B, Biological sciences (22.05.2015)
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Role of TRAV locus in low caries experience
Briseño-Ruiz, Jessica, Shimizu, Takehiko, Deeley, Kathleen, Dizak, Piper M., Ruff, Timothy D., Faraco, Italo M., Poletta, Fernando A., Brancher, João A., Pecharki, Giovana D., Küchler, Erika C., Tannure, Patricia N., Lips, Andrea, Vieira, Thays C. S., Patir, Asli, Koruyucu, Mine, Mereb, Juan C., Resick, Judith M., Brandon, Carla A., Letra, Ariadne, Silva, Renato M., Cooper, Margaret E., Seymen, Figen, Costa, Marcelo C., Granjeiro, José M., Trevilatto, Paula C., Orioli, Iêda M., Castilla, Eduardo E., Marazita, Mary L., Vieira, Alexandre R.
Published in Human genetics (01.09.2013)
Published in Human genetics (01.09.2013)
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Inheritance pattern of molar-incisor hypomineralization
JEREMIAS, Fabiano, BUSSANELI, Diego Girotto, RESTREPO, Manuel, PIERRI, Ricardo Augusto Gonçalves, SOUZA, Juliana Feltrin de, FRAGELLI, Camila Maria Bullio, SECOLIN, Rodrigo, MAURER-MORELLI, Claudia Vianna, CORDEIRO, Rita de Cassia Loiola, SCAREL-CAMINAGA, Raquel Mantuaneli, SANTOS-PINTO, Lourdes
Published in Brazilian oral research (2021)
Published in Brazilian oral research (2021)
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Patterns and Mechanisms of Ancestral Histone Protein Inheritance in Budding Yeast
Radman-Livaja, Marta, Verzijlbergen, Kitty F., Weiner, Assaf, van Welsem, Tibor, Friedman, Nir, Rando, Oliver J., van Leeuwen, Fred
Published in PLoS biology (01.06.2011)
Published in PLoS biology (01.06.2011)
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The potential role of stress and sex steroids in heritable effects of sevoflurane
Martynyuk, Anatoly E., Ju, Ling-Sha, Morey, Timothy E.
Published in Biology of reproduction (01.09.2021)
Published in Biology of reproduction (01.09.2021)
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Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness
Bigdeli, Tim B., Ripke, Stephan, Bacanu, Silviu-Alin, Lee, Sang Hong, Wray, Naomi R., Gejman, Pablo V., Rietschel, Marcella, Cichon, Sven, St Clair, David, Corvin, Aiden, Kirov, George, McQuillin, Andrew, Gurling, Hugh, Rujescu, Dan, Andreassen, Ole A., Werge, Thomas, Blackwood, Douglas H. R., Pato, Carlos N., Pato, Michele T., Malhotra, Anil K., O'Donovan, Michael C., Kendler, Kenneth S., Fanous, Ayman H.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.03.2016)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.03.2016)
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Complex mode of inheritance in holoprosencephaly revealed by whole exome sequencing
Mouden, C., Dubourg, C., Carré, W., Rose, S., Quelin, C., Akloul, L., Hamdi-Rozé, H., Viot, G., Salhi, H., Darnault, P., Odent, S., Dupé, V., David, V.
Published in Clinical genetics (01.06.2016)
Published in Clinical genetics (01.06.2016)
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The Complex Genetic Architecture of the Metabolome
Chan, Eva K. F., Rowe, Heather C., Hansen, Bjarne G., Kliebenstein, Daniel J.
Published in PLoS genetics (01.11.2010)
Published in PLoS genetics (01.11.2010)
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A practical model for the identification of congenital cataracts using machine learning
Lin, Duoru, Chen, Jingjing, Lin, Zhuoling, Li, Xiaoyan, Zhang, Kai, Wu, Xiaohang, Liu, Zhenzhen, Huang, Jialing, Li, Jing, Zhu, Yi, Chen, Chuan, Zhao, Lanqin, Xiang, Yifan, Guo, Chong, Wang, Liming, Liu, Yizhi, Chen, Weirong, Lin, Haotian
Published in EBioMedicine (01.01.2020)
Published in EBioMedicine (01.01.2020)
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Complex segregation analysis of facial melasma in Brazil: evidence for a genetic susceptibility with a dominant pattern of segregation
Holmo, Nicole França, Ramos, Geovana Brotto, Salomão, Heloisa, Werneck, Renata Iani, Mira, Marcelo Távora, Miot, Luciane Donida Bartoli, Miot, Hélio Amante
Published in Archives of Dermatological Research (01.12.2018)
Published in Archives of Dermatological Research (01.12.2018)
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