Resultados da pesquisa - Nag, Abhishek
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Gene-SCOUT: identifying genes with similar continuous trait fingerprints from phenome-wide association analyses Por Middleton, Lawrence, Harper, Andrew R, Nag, Abhishek, Wang, Quanli, Reznichenko, Anna, Vitsios, Dimitrios, Petrovski, Slavé
Publicado em 2022Text -
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Covalency does not suppress O(2) formation in 4d and 5d Li-rich O-redox cathodes Por House, Robert A., Marie, John-Joseph, Park, Joohyuk, Rees, Gregory J., Agrestini, Stefano, Nag, Abhishek, Garcia-Fernandez, Mirian, Zhou, Ke-Jin, Bruce, Peter G.
Publicado em 2021Text -
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Paramagnons and high-temperature superconductivity in a model family of cuprates Por Wang, Lichen, He, Guanhong, Yang, Zichen, Garcia-Fernandez, Mirian, Nag, Abhishek, Zhou, Kejin, Minola, Matteo, Tacon, Matthieu Le, Keimer, Bernhard, Peng, Yingying, Li, Yuan
Publicado em 2022Text -
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Candidate gene study of macular response to supplemental lutein and zeaxanthin() Por Yonova-Doing, Ekaterina, Hysi, Pirro G., Venturini, Cristina, Williams, Katie M., Nag, Abhishek, Beatty, Stephen, Liew, S.H. Melissa, Gilbert, Clare E., Hammond, Christopher J.
Publicado em 2013Text -
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Multiorbital charge-density wave excitations and concomitant phonon anomalies in Bi(2)Sr(2)LaCuO(6+δ) Por Li, Jiemin, Nag, Abhishek, Pelliciari, Jonathan, Robarts, Hannah, Walters, Andrew, Garcia-Fernandez, Mirian, Eisaki, Hiroshi, Song, Dongjoon, Ding, Hong, Johnston, Steven, Comin, Riccardo, Zhou, Ke-Jin
Publicado em 2020Text -
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Charge order lock-in by electron-phonon coupling in La(1.675)Eu(0.2)Sr(0.125)CuO(4) Por Wang, Qisi, von Arx, Karin, Horio, Masafumi, Mukkattukavil, Deepak John, Küspert, Julia, Sassa, Yasmine, Schmitt, Thorsten, Nag, Abhishek, Pyon, Sunseng, Takayama, Tomohiro, Takagi, Hidenori, Garcia-Fernandez, Mirian, Zhou, Ke-Jin, Chang, Johan
Publicado em 2021Text -
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Copy Number Variation at Chromosome 5q21.2 Is Associated With Intraocular Pressure Por Nag, Abhishek, Venturini, Cristina, Hysi, Pirro G., Arno, Matthew, Aldecoa-Otalora Astarloa, Estibaliz, MacGregor, Stuart, Hewitt, Alex W., Young, Terri L., Mitchell, Paul, Viswanathan, Ananth C., Mackey, David A., Hammond, Christopher J.
Publicado em 2013Text -
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Genome-wide scan identifies novel genetic loci regulating salivary metabolite levels Por Nag, Abhishek, Kurushima, Yuko, Bowyer, Ruth C E, Wells, Philippa M, Weiss, Stefan, Pietzner, Maik, Kocher, Thomas, Raffler, Johannes, Völker, Uwe, Mangino, Massimo, Spector, Timothy D, Milburn, Michael V, Kastenmüller, Gabi, Mohney, Robert P, Suhre, Karsten, Menni, Cristina, Steves, Claire J
Publicado em 2020Text -
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Rare variant contribution to human disease in 281,104 UK Biobank exomes Por Wang, Quanli, Dhindsa, Ryan S., Carss, Keren, Harper, Andrew R., Nag, Abhishek, Tachmazidou, Ioanna, Vitsios, Dimitrios, Deevi, Sri V. V., Mackay, Alex, Muthas, Daniel, Hühn, Michael, Monkley, Susan, Olsson, Henric, Wasilewski, Sebastian, Smith, Katherine R., March, Ruth, Platt, Adam, Haefliger, Carolina, Petrovski, Slavé
Publicado em 2021Text -
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I21: an advanced high-resolution resonant inelastic X-ray scattering beamline at Diamond Light Source Por Zhou, Ke-Jin, Walters, Andrew, Garcia-Fernandez, Mirian, Rice, Thomas, Hand, Matthew, Nag, Abhishek, Li, Jiemin, Agrestini, Stefano, Garland, Peter, Wang, Hongchang, Alcock, Simon, Nistea, Ioana, Nutter, Brian, Rubies, Nicholas, Knap, Giles, Gaughran, Martin, Yuan, Fajin, Chang, Peter, Emmins, John, Howell, George
Publicado em 2022Text -
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Evolution of spin excitations from bulk to monolayer FeSe Por Pelliciari, Jonathan, Karakuzu, Seher, Song, Qi, Arpaia, Riccardo, Nag, Abhishek, Rossi, Matteo, Li, Jiemin, Yu, Tianlun, Chen, Xiaoyang, Peng, Rui, García-Fernández, Mirian, Walters, Andrew C., Wang, Qisi, Zhao, Jun, Ghiringhelli, Giacomo, Feng, Donglai, Maier, Thomas A., Zhou, Ke-Jin, Johnston, Steven, Comin, Riccardo
Publicado em 2021Text -
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Identification of a missense variant in SPDL1 associated with idiopathic pulmonary fibrosis Por Dhindsa, Ryan S., Mattsson, Johan, Nag, Abhishek, Wang, Quanli, Wain, Louise V., Allen, Richard, Wigmore, Eleanor M., Ibanez, Kristina, Vitsios, Dimitrios, Deevi, Sri V. V., Wasilewski, Sebastian, Karlsson, Maria, Lassi, Glenda, Olsson, Henric, Muthas, Daniel, Monkley, Susan, Mackay, Alex, Murray, Lynne, Young, Simon, Haefliger, Carolina, Maher, Toby M., Belvisi, Maria G., Jenkins, Gisli, Molyneaux, Philip L., Platt, Adam, Petrovski, Slavé
Publicado em 2021Text -
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CNV Analysis in Tourette Syndrome Implicates Large Genomic Rearrangements in COL8A1 and NRXN1 Por Nag, Abhishek, Bochukova, Elena G., Kremeyer, Barbara, Campbell, Desmond D., Muller, Heike, Valencia-Duarte, Ana V., Cardona, Julio, Rivas, Isabel C., Mesa, Sandra C., Cuartas, Mauricio, Garcia, Jharley, Bedoya, Gabriel, Cornejo, William, Herrera, Luis D., Romero, Roxana, Fournier, Eduardo, Reus, Victor I., Lowe, Thomas L., Farooqi, I. Sadaf, Mathews, Carol A., McGrath, Lauren M., Yu, Dongmei, Cook, Ed, Wang, Kai, Scharf, Jeremiah M., Pauls, David L., Freimer, Nelson B., Plagnol, Vincent, Ruiz-Linares, Andrés
Publicado em 2013Text -
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Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition Por Small, Kerrin S., Todorčević, Marijana, Civelek, Mete, El-Sayed Moustafa, Julia S., Wang, Xiao, Simon, Michelle M., Fernandez-Tajes, Juan, Mahajan, Anubha, Horikoshi, Momoko, Hugill, Alison, Glastonbury, Craig A., Quaye, Lydia, Neville, Matt J., Sethi, Siddharth, Yon, Marianne, Pan, Calvin, Che, Nam, Viñuela, Ana, Tsai, Pei-Chien, Nag, Abhishek, Buil, Alfonso, Thorleifsson, Gudmar, Raghavan, Avanthi, Ding, Qiurong, Morris, Andrew P., Bell, Jordana T., Thorsteinsdottir, Unnur, Stefansson, Kari, Laakso, Markku, Dahlman, Ingrid, Arner, Peter, Gloyn, Anna L., Musunuru, Kiran, Lusis, Aldons J., Cox, Roger, Karpe, Fredrik, McCarthy, Mark I.
Publicado em 2018Text -
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A genome-wide association study of intra-ocular pressure suggests a novel association in the gene FAM125B in the TwinsUK cohort Por Nag, Abhishek, Venturini, Cristina, Small, Kerrin S., Young, Terri L., Viswanathan, Ananth C., Mackey, David A., Hysi, Pirro G., Hammond, Christopher, Aung, Tin, Cheng, Ching-Yu, Fleck, Brian W, Gibson, Jane, Hewitt, Alex W, Hofman, Albert, Höhn, René, Jonas, Jost B, Khor, Chiea-Cheun, Klaver, Caroline CW, Lemij, Hans G, Liao, Jiemin, Lotery, Andrew J, Lu, Yi, Macgregor, Stuart, Mitchell, Paul, Ramdas, Wishal D, Springelkamp, Henriët, Tai, E-Shyong, Teo, Yik-Ying, Uitterlinden, André G, van Duijn, Cornelia M, van Koolwijk, Leonieke ME, Vingerling, Johannes R, Vitart, Veronique, Vithana, Eranga, Wang, Jie Jin, Williams, Katie M, Wojciechowski, Robert, Wong, Tien-Yin, Xu, Liang, Yonova-Doing, Ekaterina, Tanja, Zeller
Publicado em 2014Text -
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Genome-wide association study of primary open-angle glaucoma in continental and admixed African populations Por Bonnemaijer, Pieter W. M., Iglesias, Adriana I., Nadkarni, Girish N., Sanyiwa, Anna J., Hassan, Hassan G., Cook, Colin, Simcoe, Mark, Taylor, Kent D., Schurmann, Claudia, Belbin, Gillian M., Kenny, Eimear E., Bottinger, Erwin P., van de Laar, Suzanne, Wiliams, Susan E. I., Akafo, Stephen K., Ashaye, Adeyinka O., Zangwill, Linda M., Girkin, Christopher A., Ng, Maggie C. Y., Rotter, Jerome I., Weinreb, Robert N., Li, Zheng, Allingham, R. Rand, Nag, Abhishek, Hysi, Pirro G., Meester-Smoor, Magda A., Wiggs, Janey L, Hauser, Michael A., Hammond, Christopher J., Lemij, Hans G., Loos, Ruth J. F., van Duijn, Cornelia M., Thiadens, Alberta A. H. J., Klaver, Caroline C. W.
Publicado em 2018Text -
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Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology Por Springelkamp, Henriët, Mishra, Aniket, Hysi, Pirro G., Gharahkhani, Puya, Höhn, René, Khor, Chiea-Chuen, Cooke Bailey, Jessica N., Luo, Xiaoyan, Ramdas, Wishal D., Vithana, Eranga, Koh, Victor, Yazar, Seyhan, Xu, Liang, Forward, Hannah, Kearns, Lisa S., Amin, Najaf, Iglesias, Adriana I., Sim, Kar-Seng, van Leeuwen, Elisabeth M., Demirkan, Ayse, van der Lee, Sven, Loon, Seng-Chee, Rivadeneira, Fernando, Nag, Abhishek, Sanfilippo, Paul G., Schillert, Arne, de Jong, Paulus T. V. M., Oostra, Ben A., Uitterlinden, André G., Hofman, Albert, Zhou, Tiger, Burdon, Kathryn P., Spector, Timothy D., Lackner, Karl J., Saw, Seang-Mei, Vingerling, Johannes R., Teo, Yik-Ying, Pasquale, Louis R., Wolfs, Roger C. W., Lemij, Hans G., Tai, E-Shyong, Jonas, Jost B., Cheng, Ching-Yu, Aung, Tin, Jansonius, Nomdo M., Klaver, Caroline C. W., Craig, Jamie E., Young, Terri L., Haines, Jonathan L., MacGregor, Stuart, Mackey, David A., Pfeiffer, Norbert, Wong, Tien-Yin, Wiggs, Janey L., Hewitt, Alex W., van Duijn, Cornelia M., Hammond, Christopher J.
Publicado em 2015Text -
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Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases Por Iglesias, Adriana I., Mishra, Aniket, Vitart, Veronique, Bykhovskaya, Yelena, Höhn, René, Springelkamp, Henriët, Cuellar-Partida, Gabriel, Gharahkhani, Puya, Bailey, Jessica N. Cooke, Willoughby, Colin E., Li, Xiaohui, Yazar, Seyhan, Nag, Abhishek, Khawaja, Anthony P., Polašek, Ozren, Siscovick, David, Mitchell, Paul, Tham, Yih Chung, Haines, Jonathan L., Kearns, Lisa S., Hayward, Caroline, Shi, Yuan, van Leeuwen, Elisabeth M., Taylor, Kent D., Bonnemaijer, Pieter, Rotter, Jerome I., Martin, Nicholas G., Zeller, Tanja, Mills, Richard A., Souzeau, Emmanuelle, Staffieri, Sandra E., Jonas, Jost B., Schmidtmann, Irene, Boutin, Thibaud, Kang, Jae H., Lucas, Sionne E. M., Wong, Tien Yin, Beutel, Manfred E., Wilson, James F., Uitterlinden, André G., Vithana, Eranga N., Foster, Paul J., Hysi, Pirro G., Hewitt, Alex W., Khor, Chiea Chuen, Pasquale, Louis R., Montgomery, Grant W., Klaver, Caroline C. W., Aung, Tin, Pfeiffer, Norbert, Mackey, David A., Hammond, Christopher J., Cheng, Ching-Yu, Craig, Jamie E., Rabinowitz, Yaron S., Wiggs, Janey L., Burdon, Kathryn P., van Duijn, Cornelia M., MacGregor, Stuart
Publicado em 2018Text -
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Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases Por Iglesias, Adriana I., Mishra, Aniket, Vitart, Veronique, Bykhovskaya, Yelena, Höhn, René, Springelkamp, Henriët, Cuellar-Partida, Gabriel, Gharahkhani, Puya, Bailey, Jessica N. Cooke, Willoughby, Colin E., Li, Xiaohui, Yazar, Seyhan, Nag, Abhishek, Khawaja, Anthony P., Polašek, Ozren, Siscovick, David, Mitchell, Paul, Tham, Yih Chung, Haines, Jonathan L., Kearns, Lisa S., Hayward, Caroline, Shi, Yuan, van Leeuwen, Elisabeth M., Taylor, Kent D., Bonnemaijer, Pieter, Rotter, Jerome I., Martin, Nicholas G., Zeller, Tanja, Mills, Richard A., Souzeau, Emmanuelle, Staffieri, Sandra E., Jonas, Jost B., Schmidtmann, Irene, Boutin, Thibaud, Kang, Jae H., Lucas, Sionne E. M., Wong, Tien Yin, Beutel, Manfred E., Wilson, James F., Uitterlinden, André G., Vithana, Eranga N., Foster, Paul J., Hysi, Pirro G., Hewitt, Alex W., Khor, Chiea Chuen, Pasquale, Louis R., Montgomery, Grant W., Klaver, Caroline C. W., Aung, Tin, Pfeiffer, Norbert, Mackey, David A., Hammond, Christopher J., Cheng, Ching-Yu, Craig, Jamie E., Rabinowitz, Yaron S., Wiggs, Janey L., Burdon, Kathryn P., van Duijn, Cornelia M., MacGregor, Stuart
Publicado em 2019Text