Výsledky vyhledávání - Ayellet V. Segrè
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Photoreceptor Layer Thinning Is an Early Biomarker for Age-Related Macular Degeneration Autor Seyedeh M. Zekavat, Sayuri Sekimitsu, Yixuan Ye, Vineet K. Raghu, Hongyu Zhao, Tobias Elze, Ayellet V. Segrè, Janey L. Wiggs, Pradeep Natarajan, Lucian Del Priore, Nazlee Zebardast, Jay Wang
Vydáno 2022Artigo -
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The Lin28/let-7 Axis Regulates Glucose Metabolism Autor Hao Zhu, Ng Shyh‐Chang, Ayellet V. Segrè, Gen Shinoda, Samar P. Shah, William S. Einhorn, Ayumu Takeuchi, J Engreitz, John P. Hagan, Michael G. Kharas, Achia Urbach, James E. Thornton, Robinson Triboulet, Richard I. Gregory, David Altshuler, George Q. Daley
Vydáno 2011Artigo -
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Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease Autor Derek Klarin, Qiuyu Zhu, Connor A. Emdin, Mark Chaffin, Steven Horner, Brian J. McMillan, Alison Leed, Michael E. Weale, Chris C. A. Spencer, François Aguet, Ayellet V. Segrè, Kristin Ardlie, Amit V. Khera, Virendar K. Kaushik, Pradeep Natarajan, Sekar Kathiresan
Vydáno 2017Artigo -
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RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues Autor Keren Yizhak, François Aguet, Jaegil Kim, Julian M. Hess, Kirsten Kübler, Jonna Grimsby, Ruslana Frazer, Hailei Zhang, Nicholas J. Haradhvala, Daniel Rosebrock, Dimitri Livitz, Xiao Li, Eila Arich-Landkof, Noam Shoresh, Chip Stewart, Ayellet V. Segrè, Philip A. Branton, Paz Polak, Kristin Ardlie, Gad Getz
Vydáno 2019Artigo -
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QTL mapping of human retina DNA methylation identifies 87 gene-epigenome interactions in age-related macular degeneration Autor Jayshree Advani, Puja A. Mehta, Andrew R. Hamel, Sudeep Mehrotra, Christina Kiel, Tobias Strunz, Ximena Corso‐Díaz, Madeline Kwicklis, Freekje van Asten, Rinki Ratnapriya, Emily Y. Chew, Dena Hernández, Sandra R. Montezuma, Deborah A. Ferrington, Bernhard H. F. Weber, Ayellet V. Segrè, Anand Swaroop
Vydáno 2024Artigo -
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Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation Autor Eric R. Gamazon, Ayellet V. Segrè, Martijn van de Bunt, Xiaoquan Wen, Hualin Simon Xi, Farhad Hormozdiari, Halit Ongen, Anuar Konkashbaev, Eske M. Derks, François Aguet, Jie Quan, Dan L. Nicolae, Eleazar Eskin, Manolis Kellis, Gad Getz, Mark I. McCarthy, Emmanouil T. Dermitzakis, Nancy J. Cox, Kristin Ardlie
Vydáno 2018Revisão -
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The Clinical Usefulness of a Glaucoma Polygenic Risk Score in 4 Population-Based European Ancestry Cohorts Autor Victor A. de Vries, Akiko Hanyuda, Joëlle Vergroesen, Ron Do, David Friedman, Peter Kraft, Constance Turman, Yuyang Luo, Jessica Tran, Bart Liefers, Sze H. Wong, Rachel H. Lee, Nazlee Zebardast, Caroline C. W. Klaver, Ayellet V. Segrè, Louis R. Pasquale, Janey L. Wiggs, Jae H. Kang, Wishal D. Ramdas
Vydáno 2024Artigo -
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Author response: Pyruvate and related energetic metabolites modulate resilience against high genetic risk for glaucoma Autor Keva Li, Nicholas Tolman, Ayellet V. Segrè, Kelsey V. Stuart, Oana A. Zeleznik, Neeru A. Vallabh, Kuang Hu, Nazlee Zebardast, Akiko Hanyuda, Yoshihiko Raita, Christa Montgomery, Chi Zhang, Pirro G. Hysi, Ron Do, Anthony P. Khawaja, Janey L. Wiggs, Jae H. Kang, Simon W. M. John, Louis R. Pasquale
Vydáno 2025Revisão por Pares -
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The human transcriptome across tissues and individuals Autor Marta Melé, Pedro G. Ferreira, Ferrán Reverter, David S. DeLuca, Jean Monlong, Michael Sammeth, Taylor Young, Jakob M. Goldmann, Dmitri D. Pervouchine, Timothy J. Sullivan, Rory Johnson, Ayellet V. Segrè, Sarah Djebali, Anastasia Niarchou, The GTEx Consortium, Fred A. Wright, Tuuli Lappalainen, Miquel Calvo, Gad Getz, Emmanouil T. Dermitzakis, Kristin Ardlie, Roderic Guigó
Vydáno 2015Artigo -
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Characteristics of p.Gln368Ter Myocilin Variant and Influence of Polygenic Risk on Glaucoma Penetrance in the UK Biobank Autor Nazlee Zebardast, Sayuri Sekimitsu, Jiali Wang, Tobias Elze, Puya Gharahkhani, Brian Cole, Michael M. Lin, Ayellet V. Segrè, Janey L. Wiggs, Tin Aung, Jamie E. Craig, Ching‐Yu Cheng, Jessica N. Cooke Bailey, Angela J. Cree, Paul J. Foster, Puya Gharahkhani, Christopher J. Hammond, Alex W. Hewitt, René Höhn, Pirro G. Hysi, Adriana I. Iglesias, Jost B. Jonas, Caroline C. W. Klaver, Anthony P. Khawaja, Chiea Chuen Khor, Andrew Lotery, Stuart MacGregor, David A. Mackey, Jue‐Sheng Ong, Paul Mitchell, Louis R. Pasquale, Chi‐Pui Pang, Francesca Pasutto, Norbert Pfeiffer, Ayellet V. Segrè, Cornelia M. van Duijn, Ananth C. Viswanathan, Véronique Vitart, Eranga N. Vithana, Janey L. Wiggs, Robert Wojciechowski, Terri L. Young, Tien Yin Wong, Seyhan Yazar
Vydáno 2021Artigo -
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Genetic and environmental risk factors in congenital heart disease functionally converge in protein networks driving heart development Autor Kasper Lage, Steven C. Greenway, Jill A. Rosenfeld, Hiroko Wakimoto, Joshua M. Gorham, Ayellet V. Segrè, Amy E. Roberts, Leslie Smoot, William T. Pu, Alexandre C. Pereira, Sonia M Mesquita, Niels Tommerup, Søren Brunak, Blake C. Ballif, Lisa G. Shaffer, Patricia K. Donahoe, Mark J. Daly, Jonathan G. Seidman, Christine E. Seidman, Lars Allan Larsen
Vydáno 2012Artigo -
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Deep Learning of the Retina Enables Phenome- and Genome-Wide Analyses of the Microvasculature Autor Seyedeh M. Zekavat, Vineet K. Raghu, Mark Trinder, Yixuan Ye, Satoshi Koyama, Michael C. Honigberg, Zhi Yu, Akhil Pampana, Sarah Urbut, Sara Haidermota, Declan P. O’Regan, Hongyu Zhao, Patrick T. Ellinor, Ayellet V. Segrè, Tobias Elze, Janey L. Wiggs, James F. Martone, Ron A. Adelman, Nazlee Zebardast, Lucian Del Priore, Jay Wang, Pradeep Natarajan
Vydáno 2021Artigo -
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Single-nucleus cross-tissue molecular reference maps toward understanding disease gene function Autor Gökçen Eraslan, Eugene Drokhlyansky, Shankara Anand, Evgenij Fiškin, Ayshwarya Subramanian, Michal Slyper, Jiali Wang, Nicholas Van Wittenberghe, John M. Rouhana, Julia Waldman, Orr Ashenberg, Monkol Lek, Danielle Dionne, Thet Su Win, Michael S. Cuoco, Olena Kuksenko, Alexander M. Tsankov, Philip A. Branton, Jamie L. Marshall, Anna Greka, Gad Getz, Ayellet V. Segrè, François Aguet, Orit Rozenblatt–Rosen, Kristin Ardlie, Aviv Regev
Vydáno 2022Artigo -
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Systems Genetics Analysis of Genome-Wide Association Study Reveals Novel Associations Between Key Biological Processes and Coronary Artery Disease Autor Sujoy Ghosh, Juan C. Vivar, Christopher P. Nelson, Christina Willenborg, Ayellet V. Segrè, Ville‐Petteri Mäkinen, Majid Nikpay, Jeanette Erdmann, Stefan Blankenberg, Christopher J. O’Donnell, Winfried März, Reijo Laaksonen, Alexandre F.R. Stewart, Stephen E. Epstein, Svati H. Shah, Christopher B. Granger, Stanley L. Hazen, Sekar Kathiresan, Muredach P. Reilly, Xia Yang, Thomas Quertermous, Nilesh J. Samani, Heribert Schunkert, Themistocles L. Assimes, Ruth McPherson
Vydáno 2015Revisão -
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Exploiting the GTEx resources to decipher the mechanisms at GWAS loci Autor Alvaro Barbeira, Rodrigo Bonazzola, Eric R. Gamazon, Yanyu Liang, YoSon Park, Sarah Kim-Hellmuth, Gao Wang, Zhuoxun Jiang, Dan Zhou, Farhad Hormozdiari, Boxiang Liu, Abhiram Rao, Andrew R. Hamel, Milton Pividori, François Aguet, Lisa Bastarache, Daniel M. Jordan, Marie Verbanck, Ron Do, Matthew Stephens, Kristin Ardlie, Mark McCarthy, Stephen B. Montgomery, Ayellet V. Segrè, Christopher D. Brown, Tuuli Lappalainen, Xiaoquan Wen, Hae Kyung Im
Vydáno 2019Pré-impressão
Vyhledávací nástroje:
Související témata
Biology
Genetics
Gene
Genotype
Computational biology
Single-nucleotide polymorphism
Gene expression
Genome-wide association study
Medicine
Genetic association
Bioinformatics
Phenotype
Quantitative trait locus
Transcriptome
Computer science
Endocrinology
Evolutionary biology
Expression quantitative trait loci
Genome
Internal medicine
Neuroscience
Regulation of gene expression
Disease
Genetic variation
Ophthalmology
RNA
Diabetes mellitus
Glaucoma
Allele
Genomics