Swift Monitoring of NGC 4151: Evidence for a Second X-Ray/UV Reprocessing

by Edelson, R., Gelbord, J., Cackett, E., Connolly, S., Done, C., Fausnaugh, M., Gardner, E., Gehrels, N., Goad, M., Horne, K., McHardy, I., Peterson, B. M., Vaughan, S., Vestergaard, M., Breeveld, A., Barth, A. J., Bentz, M., Bottorff, M., Brandt, W. N., Crawford, S. M., Bonta, E. Dalla, Emmanoulopoulos, D., Evans, P., Jaimes, R. Figuera, Filippenko, A. V., Ferland, G., Grupe, D., Joner, M., Kennea, J., Korista, K. T., Krimm, H. A., Kriss, G., Leonard, D. C., Mathur, S., Netzer, H., Nousek, J., Page, K., Romero-Colmenero, E., Siegel, M., Starkey, D. A., Treu, T., Vogler, H. A., Winkler, H., Zheng, W.
Published 2017

Biogeography of key mesozooplankton species in the North Atlantic and egg production of <i>Calanus finmarchicus</i>

by W. Melle, J. A. Runge, E. Head, S. Plourde, C. Castellani, P. Licandro, J. Pierson, S. H. Jónasdóttir, C. Johnson, C. Broms, H. Debes, T. Falkenhaug, E. Gaard, A. Gislason, M. R. Heath, B. Niehoff, T. G. Nielsen, P. Pepin, E. K. Stenevik, G. Chust
Published 2015-08-01

Neuronal intranuclear inclusion disease is genetically heterogeneous

by Zhongbo Chen, Wai Yan Yau, Zane Jaunmuktane, Arianna Tucci, Prasanth Sivakumar, Sarah A. Gagliano Taliun, Chris Turner, Stephanie Efthymiou, Kristina Ibáñez, Roisin Sullivan, Farah Bibi, Alkyoni Athanasiou‐Fragkouli, Thomas Bourinaris, David Zhang, Tamas Revesz, Tammaryn Lashley, Michael DeTure, Dennis W. Dickson, Keith A. Josephs, Ellen Gelpi, Gabor G. Kovacs, Glenda Halliday, Dominic B. Rowe, Ian Blair, Pentti J. Tienari, Anu Suomalainen, Nick C. Fox, Nicholas W. Wood, Andrew J. Lees, Matti J. Haltia, Genomics England Research Consortium, John Hardy, Mina Ryten, Jana Vandrovcova, Henry Houlden
Published 2020-09-01

Expanding Aquatic Observations through Recreation

by Robert J. W. Brewin, Robert J. W. Brewin, Kieran Hyder, Andreas J. Andersson, Oliver Billson, Oliver Billson, Philip J. Bresnahan, Thomas G. Brewin, Tyler Cyronak, Giorgio Dall'Olmo, Giorgio Dall'Olmo, Lee de Mora, George Graham, Thomas Jackson, Dionysios E. Raitsos, Dionysios E. Raitsos
Published 2017-11-01

MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load

by Yi Shiau Ng, Nichola Z. Lax, Paul Maddison, Charlotte L. Alston, Emma L. Blakely, Philippa D. Hepplewhite, Gillian Riordan, Surita Meldau, Patrick F. Chinnery, Germaine Pierre, Efstathia Chronopoulou, Ailian Du, Imelda Hughes, Andrew A. Morris, Smaragda Kamakari, Georgia Chrousos, Richard J. Rodenburg, Christiaan G.J. Saris, Catherine Feeney, Steven A. Hardy, Takafumi Sakakibara, Akira Sudo, Yasushi Okazaki, Kei Murayama, Helen Mundy, Michael G. Hanna, Akira Ohtake, Andrew M. Schaefer, Mike P. Champion, Doug M. Turnbull, Robert W. Taylor, Robert D.S. Pitceathly, Robert McFarland, Gráinne S. Gorman
Published 2018-04-01

ACE and UCP2 gene polymorphisms and their association with baseline and exercise-related changes in the functional performance of older adults

by Justin W.L. Keogh, Barry R. Palmer, Denise Taylor, Andrew E. Kilding
Published 2015-05-01

Effect of polymorphism in the porcine cytochrome b5 (CYB5A) gene on androstenone and skatole concentrations and sexual development in Swedish pig populations

by G. Zamaratskaia, Y. Lou, J. Peacock, L. Rydhmer, H.K. Andersson, R.K. Juneja, G. Chen, K. Lundström, E.J. Squires
Published 2008-01-01

The safety of double- and triple-drug community mass drug administration for lymphatic filariasis: A multicenter, open-label, cluster-randomized study.

by Gary J Weil, Joshua Bogus, Michael Christian, Christine Dubray, Yenny Djuardi, Peter U Fischer, Charles W Goss, Myra Hardy, Purushothaman Jambulingam, Christopher L King, Vijesh Sridhar Kuttiat, Kaliannagounder Krishnamoorthy, Moses Laman, Jean Frantz Lemoine, Katiuscia K O'Brian, Leanne J Robinson, Josaia Samuela, Kenneth B Schechtman, Anita Sircar, Adinarayanan Srividya, Andrew C Steer, Taniawati Supali, Swaminathan Subramanian, DOLF IDA Safety Study Group
Published 2019-06-01

CD8+ T cell-mediated endotheliopathy is a targetable mechanism of neuro-inflammation in Susac syndrome

by Catharina C. Gross, Céline Meyer, Urvashi Bhatia, Lidia Yshii, Ilka Kleffner, Jan Bauer, Anna R. Tröscher, Andreas Schulte-Mecklenbeck, Sebastian Herich, Tilman Schneider-Hohendorf, Henrike Plate, Tanja Kuhlmann, Markus Schwaninger, Wolfgang Brück, Marc Pawlitzki, David-Axel Laplaud, Delphine Loussouarn, John Parratt, Michael Barnett, Michael E. Buckland, Todd A. Hardy, Stephen W. Reddel, Marius Ringelstein, Jan Dörr, Brigitte Wildemann, Markus Kraemer, Hans Lassmann, Romana Höftberger, Eduardo Beltrán, Klaus Dornmair, Nicholas Schwab, Luisa Klotz, Sven G. Meuth, Guillaume Martin-Blondel, Heinz Wiendl, Roland Liblau
Published 2019-12-01

Mutational signatures of ionizing radiation in second malignancies

by Sam Behjati, Gunes Gundem, David C. Wedge, Nicola D. Roberts, Patrick S. Tarpey, Susanna L. Cooke, Peter Van Loo, Ludmil B. Alexandrov, Manasa Ramakrishna, Helen Davies, Serena Nik-Zainal, Claire Hardy, Calli Latimer, Keiran M. Raine, Lucy Stebbings, Andy Menzies, David Jones, Rebecca Shepherd, Adam P. Butler, Jon W. Teague, Mette Jorgensen, Bhavisha Khatri, Nischalan Pillay, Adam Shlien, P. Andrew Futreal, Christophe Badie, ICGC Prostate Group, Ultan McDermott, G. Steven Bova, Andrea L. Richardson, Adrienne M. Flanagan, Michael R. Stratton, Peter J. Campbell
Published 2016-09-01

Exceptionally low likelihood of Alzheimer’s dementia in APOE2 homozygotes from a 5,000-person neuropathological study

by Eric M. Reiman, Joseph F. Arboleda-Velasquez, Yakeel T. Quiroz, Matthew J. Huentelman, Thomas G. Beach, Richard J. Caselli, Yinghua Chen, Yi Su, Amanda J. Myers, John Hardy, Jean Paul Vonsattel, Steven G. Younkin, David A. Bennett, Philip L. De Jager, Eric B. Larson, Paul K. Crane, C. Dirk Keene, M. Ilyas Kamboh, Julia K. Kofler, Linda Duque, John R. Gilbert, Harry E. Gwirtsman, Joseph D. Buxbaum, Dennis W. Dickson, Matthew P. Frosch, Bernardino F. Ghetti, Kathryn L. Lunetta, Li-San Wang, Bradley T. Hyman, Walter A. Kukull, Tatiana Foroud, Jonathan L. Haines, Richard P. Mayeux, Margaret A. Pericak-Vance, Julie A. Schneider, John Q. Trojanowski, Lindsay A. Farrer, Gerard D. Schellenberg, Gary W. Beecham, Thomas J. Montine, Gyungah R. Jun, The Alzheimer’s Disease Genetics Consortium
Published 2020-02-01

SPACE TELESCOPE AND OPTICAL REVERBERATION MAPPING PROJECT. IV. ANOMALOUS BEHAVIOR OF THE BROAD ULTRAVIOLET EMISSION LINES IN NGC 5548

by Goad, M. R., Korista, K. T., Rosa, G. De, Kriss, G. A., Edelson, R., Barth, A. J., Ferland, G. J., Kochanek, C. S., Netzer, H., Peterson, B. M., Bentz, M. C., Bisogni, S., Crenshaw, D. M., Denney, K. D., Ely, J., Fausnaugh, M. M., Grier, C. J., Gupta, A., Horne, K. D., Kaastra, J., Pancoast, A., Pei, L., Pogge, R. W., Skielboe, A., Starkey, D., Vestergaard, M., Zu, Y., Anderson, M. D., Arévalo, P., Bazhaw, C., Borman, G. A., Boroson, T. A., Bottorff, M. C., Brandt, W. N., Breeveld, A. A., Brewer, B. J., Cackett, E. M., Carini, M. T., Croxall, K. V., Bontà, E. Dalla, Lorenzo-Cáceres, A. De, Dietrich, M., Efimova, N. V., Evans, P. A., Filippenko, A. V., Flatland, K., Gehrels, N., Geier, S., Gelbord, J. M., Gonzalez, L., Gorjian, V., Grupe, D., Hall, P. B., Hicks, S., Horenstein, D., Hutchison, T., Im, M., Jensen, J. J., Joner, M. D., Jones, J., Kaspi, S., Kelly, B. C., Kennea, J. A., Kim, M., Kim, S. C., Klimanov, S. A., Lee, J. C., Leonard, D. C., Lira, P., MacInnis, F., Manne-Nicholas, E. R., Mathur, S., McHardy, I. M., Montouri, C., Musso, R., Nazarov, S. V., Norris, R. P., Nousek, J. A., Okhmat, D. N., Papadakis, I., Parks, J. R., Pott, J.-U., Rafter, S. E., Rix, H.-W., Saylor, D. A., Schimoia, J. S., Schnülle, K., Sergeev, S. G., Siegel, M., Spencer, M., Sung, H.-I., Teems, K. G., Treu, T., Turner, C. S., Uttley, P., Villforth, C., Weiss, Y., Woo, J.-H., Yan, H., Young, S., Zheng, W.-K.
Published 2016

Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias.

by Gary W Beecham, Kara Hamilton, Adam C Naj, Eden R Martin, Matt Huentelman, Amanda J Myers, Jason J Corneveaux, John Hardy, Jean-Paul Vonsattel, Steven G Younkin, David A Bennett, Philip L De Jager, Eric B Larson, Paul K Crane, M Ilyas Kamboh, Julia K Kofler, Deborah C Mash, Linda Duque, John R Gilbert, Harry Gwirtsman, Joseph D Buxbaum, Patricia Kramer, Dennis W Dickson, Lindsay A Farrer, Matthew P Frosch, Bernardino Ghetti, Jonathan L Haines, Bradley T Hyman, Walter A Kukull, Richard P Mayeux, Margaret A Pericak-Vance, Julie A Schneider, John Q Trojanowski, Eric M Reiman, Alzheimer's Disease Genetics Consortium (ADGC), Gerard D Schellenberg, Thomas J Montine
Published 2014-09-01

OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect

by Kyle Thompson, Nicole Mai, Monika Oláhová, Filippo Scialó, Luke E Formosa, David A Stroud, Madeleine Garrett, Nichola Z Lax, Fiona M Robertson, Cristina Jou, Andres Nascimento, Carlos Ortez, Cecilia Jimenez‐Mallebrera, Steven A Hardy, Langping He, Garry K Brown, Paula Marttinen, Robert McFarland, Alberto Sanz, Brendan J Battersby, Penelope E Bonnen, Michael T Ryan, Zofia MA Chrzanowska‐Lightowlers, Robert N Lightowlers, Robert W Taylor
Published 2018-11-01

High precision measurement of Compton scattering in the 5 GeV region

by P. Ambrozewicz, L. Ye, Y. Prok, I. Larin, A. Ahmidouch, K. Baker, V. Baturin, L. Benton, A. Bernstein, V. Burkert, E. Clinton, P.L. Cole, P. Collins, D. Dale, S. Danagoulian, G. Davidenko, R. Demirchyan, A. Deur, A. Dolgolenko, D. Dutta, G. Dzyubenko, A. Evdokimov, G. Fedotov, J. Feng, M. Gabrielyan, L. Gan, H. Gao, A. Gasparian, N. Gevorkyan, S. Gevorkyan, A. Glamazdin, V. Goryachev, L. Guo, V. Gyurjyan, K. Hardy, J. He, E. Isupov, M.M. Ito, L. Jiang, H. Kang, D. Kashy, M. Khandaker, P. Kingsberry, F. Klein, A. Kolarkar, M. Konchatnyi, O. Korchin, W. Korsch, O. Kosinov, S. Kowalski, M. Kubantsev, A. Kubarovsky, V. Kubarovsky, D. Lawrence, X. Li, M. Levillain, H. Lu, L. Ma, P. Martel, V. Matveev, D. McNulty, B. Mecking, A. Micherdzinska, B. Milbrath, R. Minehart, R. Miskimen, V. Mochalov, B. Morrison, S. Mtingwa, I. Nakagawa, S. Overby, E. Pasyuk, M. Payen, K. Park, R. Pedroni, W. Phelps, D. Protopopescu, D. Rimal, B.G. Ritchie, D. Romanov, C. Salgado, A. Shahinyan, A. Sitnikov, D. Sober, S. Stepanyan, W. Stephens, V. Tarasov, S. Taylor, A. Teymurazyan, J. Underwood, A. Vasiliev, V. Vishnyakov, D.P. Weygand, M. Wood, Y. Zhang, S. Zhou, B. Zihlmann
Published 2019-10-01

Toll-like receptor polymorphisms in malaria-endemic populations

by Zimmerman Peter A, Bockarie Moses J, Vulule John, Moormann Ann M, Greene Jennifer A, Kazura James W
Published 2009-03-01

Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locus.

by Daniah Trabzuni, Mina Ryten, Warren Emmett, Adaikalavan Ramasamy, Karl J Lackner, Tanja Zeller, Robert Walker, Colin Smith, Patrick A Lewis, Adamantios Mamais, Rohan de Silva, Jana Vandrovcova, International Parkinson Disease Genomics Consortium (IPDGC), Dena Hernandez, Michael A Nalls, Manu Sharma, Sophie Garnier, Suzanne Lesage, Javier Simon-Sanchez, Thomas Gasser, Peter Heutink, Alexis Brice, Andrew Singleton, Huaibin Cai, Eric Schadt, Nicholas W Wood, Rina Bandopadhyay, Michael E Weale, John Hardy, Vincent Plagnol
Published 2013-01-01

Genetic etiology of renal agenesis: fine mapping of Renag1 and identification of Kit as the candidate functional gene.

by Nyssa Becker Samanas, Tessa W Commers, Kirsten L Dennison, Quincy Eckert Harenda, Scott G Kurz, Cynthia M Lachel, Kristen Leland Wavrin, Michael Bowler, Isaac J Nijman, Victor Guryev, Edwin Cuppen, Norbert Hubner, Ruth Sullivan, Chad M Vezina, James D Shull
Published 2015-01-01

SLCO1B1 and ABCG2 Gene Polymorphisms in a Thai Population

by Rattanacheeworn P, Chamnanphon M, Thongthip S, Kittanamongkolchai W, Townamchai N, Avihingsanon Y, Udomnilobol U, Prueksaritanont T, Jianmongkol S, Chariyavilaskul P
Published 2020-10-01