Increasing Incidence of Liposarcoma: A Population-Based Study of National Surveillance Databases, 2001-2016 von Bock, Suzanne, Hoffmann, Douglas G., Jiang, Yi, Chen, Hao, Il'yasova, Dora

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Limited flow cytometry panels on bone marrow specimens reduce costs and predict negative cytogenetics von Hoffmann, Douglas G, Kim, Burton H

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CD8-positive mantle cell lymphoma : A report of two cases von HOFFMANN, D. G, TUCKER, S. J, EMMANOULIDES, C, ROSEN, P. A, NAEIM, F

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Minimal hepatic encephalopathy is associated with motor vehicle crashes: The reality beyond the driving test von Bajaj, Jasmohan S., Saeian, Kia, Schubert, Christine M., Hafeezullah, Muhammad, Franco, Jose, Varma, Rajiv R., Gibson, Douglas P., Hoffmann, Raymond G., Stravitz, R. Todd, Heuman, Douglas M., Sterling, Richard K., Shiffman, Mitchell, Topaz, Allyne, Boyett, Sherry, Bell, Debulon, Sanyal, Arun J.

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Cross-cancer evaluation of polygenic risk scores for 16 cancer types in two large cohorts von Graff, Rebecca E., Cavazos, Taylor B., Thai, Khanh K., Kachuri, Linda, Rashkin, Sara R., Hoffman, Joshua D., Alexeeff, Stacey E., Blatchins, Maruta, Meyers, Travis J., Leong, Lancelote, Tai, Caroline G., Emami, Nima C., Corley, Douglas A., Kushi, Lawrence H., Ziv, Elad, Van Den Eeden, Stephen K., Jorgenson, Eric, Hoffmann, Thomas J., Habel, Laurel A., Witte, John S., Sakoda, Lori C.

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Enhancing the usability of systematic reviews by improving the consideration and description of interventions von Hoffmann, Tammy C, Oxman, Andrew D, Ioannidis, John PA, Moher, David, Lasserson, Toby J, Tovey, David I, Stein, Ken, Sutcliffe, Katy, Ravaud, Philippe, Altman, Douglas G, Perera, Rafael, Glasziou, Paul

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Genetic predisposition to mosaic Y chromosome loss in blood von Thompson, Deborah J., Genovese, Giulio, Halvardson, Jonatan, Ulirsch, Jacob C., Wright, Daniel J., Terao, Chikashi, Davidsson, Olafur B., Day, Felix R., Sulem, Patrick, Jiang, Yunxuan, Danielsson, Marcus, Davies, Hanna, Dennis, Joe, Dunlop, Malcolm G., Easton, Douglas F., Fisher, Victoria A., Zink, Florian, Houlston, Richard S., Ingelsson, Martin, Kar, Siddhartha, Kerrison, Nicola D., Kinnersley, Ben, Kristjansson, Ragnar P., Law, Philip J., Li, Rong, Loveday, Chey, Mattisson, Jonas, McCarroll, Steven A., Murakami, Yoshinori, Murray, Anna, Olszewski, Pawel, Rychlicka-Buniowska, Edyta, Scott, Robert A., Thorsteinsdottir, Unnur, Tomlinson, Ian, Moghadam, Behrooz Torabi, Turnbull, Clare, Wareham, Nicholas J., Gudbjartsson, Daniel F., Kamatani, Yoichiro, Hoffmann, Eva R., Jackson, Steve P., Stefansson, Kari, Auton, Adam, Ong, Ken K., Machiela, Mitchell J., Loh, Po-Ru, Dumanski, Jan P., Chanock, Stephen J., Forsberg, Lars A., Perry, John R. B.

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Identification of common genetic risk variants for autism spectrum disorder von Grove, Jakob, Ripke, Stephan, Als, Thomas D., Mattheisen, Manuel, Walters, Raymond K., Won, Hyejung, Pallesen, Jonatan, Agerbo, Esben, Andreassen, Ole A., Anney, Richard, Awashti, Swapnil, Belliveau, Rich, Bettella, Francesco, Buxbaum, Joseph D., Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Christensen, Jane H., Churchhouse, Claire, Dellenvall, Karin, Demontis, Ditte, De Rubeis, Silvia, Devlin, Bernie, Djurovic, Srdjan, Dumont, Ashley L., Goldstein, Jacqueline I., Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Hope, Sigrun, Howrigan, Daniel P., Huang, Hailiang, Hultman, Christina M., Klei, Lambertus, Maller, Julian, Martin, Joanna, Martin, Alicia R., Moran, Jennifer L., Nyegaard, Mette, Nærland, Terje, Palmer, Duncan S., Palotie, Aarno, Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, dPoterba, Timothy, Poulsen, Jesper Buchhave, Pourcain, Beate St, Qvist, Per, Rehnström, Karola, Reichenberg, Abraham, Reichert, Jennifer, Robinson, Elise B., Roeder, Kathryn, Roussos, Panos, Saemundsen, Evald, Sandin, Sven, Satterstrom, F. Kyle, Davey Smith, George, Stefansson, Hreinn, Steinberg, Stacy, Stevens, Christine R., Sullivan, Patrick F., Turley, Patrick, Walters, G. Bragi, Xu, Xinyi, Stefansson, Kari, Geschwind, Daniel H., Nordentoft, Merete, Hougaard, David M., Werge, Thomas, Mors, Ole, Mortensen, Preben Bo, Neale, Benjamin M., Daly, Mark J., Børglum, Anders D.

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Better reporting of interventions: template for intervention description and replication (TIDieR) checklist and guide von Hoffmann, Tammy C, Glasziou, Paul P, Boutron, Isabelle, Milne, Ruairidh, Perera, Rafael, Moher, David, Altman, Douglas G, Barbour, Virginia, Macdonald, Helen, Johnston, Marie, Lamb, Sarah E, Dixon-Woods, Mary, McCulloch, Peter, Wyatt, Jeremy C, Chan, An-Wen, Michie, Susan

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Coronary CT Angiography versus Standard Evaluation in Acute Chest Pain von Hoffmann, Udo, Truong, Quynh A, Schoenfeld, David A, Chou, Eric T, Woodard, Pamela K, Nagurney, John T, Pope, J. Hector, Hauser, Thomas H, White, Charles S, Weiner, Scott G, Kalanjian, Shant, Mullins, Michael E, Mikati, Issam, Peacock, W. Frank, Zakroysky, Pearl, Hayden, Douglas, Goehler, Alexander, Lee, Hang, Gazelle, G. Scott, Wiviott, Stephen D, Fleg, Jerome L, Udelson, James E

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OPTICAL IDENTIFICATION OF CEPHEIDS IN 19 HOST GALAXIES OF TYPE Ia SUPERNOVAE AND NGC 4258 WITH THE HUBBLE SPACE TELESCOPE von Hoffmann, Samantha L., Macri, Lucas M., Riess, Adam G., Yuan, Wenlong, Casertano, Stefano, Foley, Ryan J., Filippenko, Alexei V., Tucker, Brad E., Chornock, Ryan, Silverman, Jeffrey M., Welch, Douglas L., Goobar, Ariel, Amanullah, Rahman

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Estimating the real-world performance of the PROMISE minimal-risk tool von Nanna, MG, Wang, TY, Chiswell, K, Sun, JL, Vemulapalli, S, Hoffmann, U, Patel, MR, Udelson, JE, Fordyce, CB, Douglas, PS

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Association of Hepatic Steatosis With Major Adverse Cardiovascular Events, Independent of Coronary Artery Disease von Meyersohn, Nandini M., Mayrhofer, Thomas, Corey, Kathleen E., Bittner, Daniel O., Staziaki, Pedro V., Szilveszter, Balint, Hallett, Travis, Lu, Michael T., Puchner, Stefan B., Simon, Tracey G., Foldyna, Borek, Voora, Deepak, Ginsburg, Geoffrey S., Douglas, Pamela S., Hoffmann, Udo, Ferencik, Maros

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Reduction of brain kynurenic acid improves cognitive function von Kozak, Rouba, Campbell, Brian M, Strick, Christine A, Horner, Weldon, Hoffmann, William E, Kiss, Tamas, Chapin, Douglas S, McGinnis, Dina, Abbott, Amanda L, Roberts, Brooke M, Fonseca, Kari, Guanowsky, Victor, Young, Damon A, Seymour, Patricia A, Dounay, Amy, Hajos, Mihaly, Williams, Graham V, Castner, Stacy A

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Inflammatory markers and incident heart failure risk in older adults: the Health ABC (Health, Aging, and Body Composition) study von Kalogeropoulos, Andreas, Georgiopoulou, Vasiliki, Psaty, Bruce M, Rodondi, Nicolas, Smith, Andrew L, Harrison, David G, Liu, Yongmei, Hoffmann, Udo, Bauer, Douglas C, Newman, Anne B, Kritchevsky, Stephen B, Harris, Tamara B, Butler, Javed

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Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns von Czamara, Darina, Eraslan, Gökçen, Page, Christian M., Lahti, Jari, Lahti-Pulkkinen, Marius, Hämäläinen, Esa, Kajantie, Eero, Laivuori, Hannele, Villa, Pia M., Reynolds, Rebecca M., Nystad, Wenche, Håberg, Siri E., London, Stephanie J., O’Donnell, Kieran J., Garg, Elika, Meaney, Michael J., Entringer, Sonja, Wadhwa, Pathik D., Buss, Claudia, Jones, Meaghan J., Lin, David T. S., MacIsaac, Julie L., Kobor, Michael S., Koen, Nastassja, Zar, Heather J., Koenen, Karestan C., Dalvie, Shareefa, Stein, Dan J., Kondofersky, Ivan, Müller, Nikola S., Theis, Fabian J., Räikkönen, Katri, Binder, Elisabeth B.

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Urban-Rural Differences In Youth Emergency Department Visits For Suicidal Ideation And Self-Harm von Hoffmann, Jennifer A., Hall, Matt, Lorenz, Douglas, Berry, Jay G.

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Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression von Ripke, Stephan, Trzaskowski, Maciej, Byrne, Enda M., Adams, Mark J., Andlauer, Till M. F., Bacanu, Silviu-Alin, Beekman, Aartjan F. T., Bigdeli, Tim B., Binder, Elisabeth B., Blackwood, Douglas R. H., Bybjerg-Grauholm, Jonas, Castelao, Enrique, Couvy-Duchesne, Baptiste, Craddock, Nick, Deary, Ian J., Finucane, Hilary K., Forstner, Andreas J., Frank, Josef, Gill, Michael, Goes, Fernando S., Grove, Jakob, Hall, Lynsey S., Hannon, Eilis, Hansen, Thomas F., Hickie, Ian B., Hoffmann, Per, Horn, Carsten, Hougaard, David M., Hyde, Craig L., Jorgenson, Eric, Knowles, James A., Kraft, Julia, Krogh, Jesper, Kutalik, Zoltán, Lane, Jacqueline M., Li, Yihan, Li, Yun, Liu, Xiaoxiao, Lu, Leina, MacIntyre, Donald J., MacKinnon, Dean F., Maier, Robert M., Marchini, Jonathan, Mbarek, Hamdi, McGrath, Patrick, Mehta, Divya, Montgomery, Grant W., Nauck, Matthias, Nivard, Michel G., Pedersen, Carsten Bøcker, Posthuma, Danielle, Purcell, Shaun M., Quiroz, Jorge A., Saeed Mirza, Saira, Schoevers, Robert, Schulte, Eva C., Shi, Jianxin, Shyn, Stanley I., Smit, Johannes H., Smith, Daniel J., Stockmeier, Craig A., Teumer, Alexander, Thompson, Wesley, Thomson, Pippa A., Thorgeirsson, Thorgeir E., Tian, Chao, Treutlein, Jens, van Hemert, Albert M., Viktorin, Alexander, Visscher, Peter M., Wang, Yunpeng, Weinsheimer, Shantel Marie, Wellmann, Jürgen, Witt, Stephanie H., Wu, Yang, Xi, Hualin S., Yang, Jian, Zhang, Futao, Baune, Bernhard T., Berger, Klaus, de Geus, E. C. J., Domschke, Katharina, Esko, Tõnu, Hinds, David A., Li, Qingqin S., McIntosh, Andrew M., Metspalu, Andres, Mors, Ole, Müller-Myhsok, Bertram, O’Donovan, Michael C., Paciga, Sara A., Pedersen, Nancy L., Perlis, Roy H., Potash, James B., Schaefer, Catherine, Schulze, Thomas G., Uher, Rudolf, Völzke, Henry, Winslow, Ashley R., Børglum, Anders D.

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Identification of loci associated with schizophrenia by genome-wide association and follow-up von Georgieva, Lyudmila, Shifman, Sagiv, Quinn, Emma M, Peirce, Timothy, Giegling, Ina, He, Lin, Leung, Hin-Tak, Duan, Jubao, Moskvina, Valentina, Shi, YongYong, Schumacher, Johannes, Schulze, Thomas G, Craddock, Nicholas, Levinson, Douglas F, Kirov, George, Gill, Michael, O'Donovan, Michael C, Rujescu, Dan, Corvin, Aiden, Marchini, Jonathan L, Owen, Michael J, Zammit, Stanley, Williams, Hywel, Möller, Hans-Jürgen, Vasilescu, Catalina, Spencer, Chris C A, Nöthen, Markus M, Howie, Bryan, Rietschel, Marcella, Norton, Nadine, Nikolov, Ivan, Williams, Nigel M, Gejman, Pablo V, Iwata, Nakao, Hartmann, Annette M, Carroll, Liam, Hoffmann, Per, Darvasi, Ariel, Cichon, Sven, Morris, Derek W, Sanders, Alan R, Feng, GuoYin, Propping, Peter, Ikeda, Masashi, Dwyer, Sarah, Holmans, Peter, Hamshere, Marian, Maier, Wolfgang

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LD Score regression distinguishes confounding from polygenicity in genome-wide association studies von Bulik-Sullivan, Brendan K, Loh, Po-Ru, Finucane, Hilary K, Ripke, Stephan, Yang, Jian, Patterson, Nick, Daly, Mark J, Price, Alkes L, Neale, Benjamin M

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