THE THEORY AND CONSTRUCTION OF A LIQUID HELIUM CRYOGENIC PUMP von LaChance, George M

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THE THEORY AND CONSTRUCTION OF A LIQUID HELIUM CRYOGENIC PUMP von LaChance, George M

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Identification of Producibility Inhibitors in Standard NAVSEA Ship Design Practices von Wilkins, James R, Kraine, Gilbert L, LaChance, George M, Burnett, Victor R

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Variation in Demographics, Hospital, and Patient-Reported Outcomes Following Total Hip Arthroplasty According to Biological Sex von Call, Catherine M., Lachance, Andrew D., Zink, Thomas M., Stoddard, Henry, Babikian, George M., Rana, Adam J., McGrory, Brian J.

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A Founder Mutation in VPS11 Causes an Autosomal Recessive Leukoencephalopathy Linked to Autophagic Defects von Zhang, Jinglan, Lachance, Véronik, Schaffner, Adam, Li, Xianting, Fedick, Anastasia, Kaye, Lauren E, Liao, Jun, Rosenfeld, Jill, Yachelevich, Naomi, Chu, Mary-Lynn, Mitchell, Wendy G, Boles, Richard G, Moran, Ellen, Tokita, Mari, Gorman, Elizabeth, Bagley, Kaytee, Zhang, Wei, Xia, Fan, Leduc, Magalie, Yang, Yaping, Eng, Christine, Wong, Lee-Jun, Schiffmann, Raphael, Diaz, George A, Kornreich, Ruth, Thummel, Ryan, Wasserstein, Melissa, Yue, Zhenyu, Edelmann, Lisa

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The UK10K project identifies rare variants in health and disease von Walter, Klaudia, Min, Josine L, Huang, Jie, Crooks, Lucy, Memari, Yasin, McCarthy, Shane, Perry, John R B, Xu, ChangJiang, Futema, Marta, Lawson, Daniel, Iotchkova, Valentina, Schiffels, Stephan, Hendricks, Audrey E, Danecek, Petr, Li, Rui, Floyd, James, Wain, Louise V, Barroso, Inês, Humphries, Steve E, Hurles, Matthew E, Zeggini, Eleftheria, Barrett, Jeffrey C, Plagnol, Vincent, Richards, J Brent, Greenwood, Celia M T, Timpson, Nicholas J, Durbin, Richard, Soranzo, Nicole

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OA13.05 Strategies to Increase Acceptance of Referral to Smoking Cessation at an Ontario Regional Cancer Centre von Evans, B.K., Saunders, D., George, M., Schwartz, N., Reich, M., Lachance, T., Santi, S.

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Rural-Urban Differences in Hospital and Patient-Reported Outcomes Following Total Hip Arthroplasty von Lachance, Andrew D., Call, Catherine, Radford, Zachary, Stoddard, Henry, Sturgeon, Callahan, Babikian, George, Rana, Adam, McGrory, Brian J.

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A low-frequency variant at 8q24.21 is strongly associated with risk of oligodendroglial tumors and astrocytomas with IDH1 or IDH2 mutation von Jenkins, Robert B, Xiao, Yuanyuan, Sicotte, Hugues, Decker, Paul A, Kollmeyer, Thomas M, Hansen, Helen M, Kosel, Matthew L, Zheng, Shichun, Walsh, Kyle M, Rice, Terri, Bracci, Paige, McCoy, Lucie S, Smirnov, Ivan, Patoka, Joseph S, Hsuang, George, Wiemels, Joe L, Tihan, Tarik, Pico, Alexander R, Prados, Michael D, Chang, Susan M, Berger, Mitchel S, Caron, Alissa A, Fink, Stephanie R, Halder, Chandralekha, Rynearson, Amanda L, Fridley, Brooke L, Buckner, Jan C, O'Neill, Brian P, Giannini, Caterina, Lachance, Daniel H, Wiencke, John K, Eckel-Passow, Jeanette E, Wrensch, Margaret R

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The Association of Season of Surgery and Patient Reported Outcomes following Total Hip Arthroplasty von Lachance, Andrew D., Call, Catherine, Radford, Zachary, Stoddard, Henry, Sturgeon, Callahan, Babikian, George, Rana, Adam, McGrory, Brian J.

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Genomic analyses inform on migration events during the peopling of Eurasia von Pagani, Luca, Lawson, Daniel John, Jagoda, Evelyn, Mörseburg, Alexander, Eriksson, Anders, Mitt, Mario, Clemente, Florian, Hudjashov, Georgi, DeGiorgio, Michael, Saag, Lauri, Wall, Jeffrey D., Cardona, Alexia, Mägi, Reedik, Sayres, Melissa A. Wilson, Kaewert, Sarah, Inchley, Charlotte, Scheib, Christiana L., Järve, Mari, Karmin, Monika, Jacobs, Guy S., Antao, Tiago, Iliescu, Florin Mircea, Kushniarevich, Alena, Ayub, Qasim, Tyler-Smith, Chris, Xue, Yali, Yunusbayev, Bayazit, Tambets, Kristiina, Mallick, Chandana Basu, Saag, Lehti, Pocheshkhova, Elvira, Andriadze, George, Muller, Craig, Westaway, Michael C., Lambert, David M., Zoraqi, Grigor, Turdikulova, Shahlo, Dalimova, Dilbar, Sabitov, Zhaxylyk, Sultana, Gazi Nurun Nahar, Lachance, Joseph, Tishkoff, Sarah, Momynaliev, Kuvat, Isakova, Jainagul, Damba, Larisa D., Gubina, Marina, Nymadawa, Pagbajabyn, Evseeva, Irina, Atramentova, Lubov, Utevska, Olga, Ricaut, François-Xavier, Brucato, Nicolas, Sudoyo, Herawati, Letellier, Thierry, Cox, Murray P., Barashkov, Nikolay A., Škaro, Vedrana, Mulahasanovic´, Lejla, Primorac, Dragan, Sahakyan, Hovhannes, Mormina, Maru, Eichstaedt, Christina A., Lichman, Daria V., Abdullah, Syafiq, Chaubey, Gyaneshwer, Wee, Joseph T. S., Mihailov, Evelin, Karunas, Alexandra, Litvinov, Sergei, Khusainova, Rita, Ekomasova, Natalya, Akhmetova, Vita, Khidiyatova, Irina, Marjanović, Damir, Yepiskoposyan, Levon, Behar, Doron M., Balanovska, Elena, Metspalu, Andres, Derenko, Miroslava, Malyarchuk, Boris, Voevoda, Mikhail, Fedorova, Sardana A., Osipova, Ludmila P., Lahr, Marta Mirazón, Gerbault, Pascale, Leavesley, Matthew, Migliano, Andrea Bamberg, Petraglia, Michael, Balanovsky, Oleg, Khusnutdinova, Elza K., Metspalu, Ene, Thomas, Mark G., Manica, Andrea, Nielsen, Rasmus, Villems, Richard, Willerslev, Eske, Kivisild, Toomas, Metspalu, Mait

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“Doubling Up” on Produce at Detroit Farmers Markets: Patterns and Correlates of Use of a Healthy Food Incentive von Cohen, Alicia J., Lachance, Laurie L., Richardson, Caroline R., Mahmoudi, Elham, Buxbaum, Jason D., Noonan, George K., Murphy, Ellen C., Roberson, Dana N., Hesterman, Oran B., Heisler, Michele, Zick, Suzanna M.

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Genetic variants in telomerase-related genes are associated with an older age at diagnosis in glioma patients: evidence for distinct pathways of gliomagenesis von Walsh, Kyle M, Rice, Terri, Decker, Paul A, Kosel, Matthew L, Kollmeyer, Thomas, Hansen, Helen M, Zheng, Shichun, McCoy, Lucie S, Bracci, Paige M, Anderson, Erik, Hsuang, George, Wiemels, Joe L, Pico, Alexander R, Smirnov, Ivan, Molinaro, Annette M, Tihan, Tarik, Berger, Mitchell S, Chang, Susan M, Prados, Michael D, Lachance, Daniel H, Sicotte, Hugues, Eckel-Passow, Jeanette E, Wiencke, John K, Jenkins, Robert B, Wrensch, Margaret R

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A recent bottleneck of Y chromosome diversity coincides with a global change in culture von Karmin, Monika, Saag, Lauri, Vicente, Mário, Wilson Sayres, Melissa A, Järve, Mari, Talas, Ulvi Gerst, Rootsi, Siiri, Ilumäe, Anne-Mai, Mägi, Reedik, Mitt, Mario, Pagani, Luca, Puurand, Tarmo, Faltyskova, Zuzana, Clemente, Florian, Cardona, Alexia, Metspalu, Ene, Sahakyan, Hovhannes, Yunusbayev, Bayazit, Hudjashov, Georgi, DeGiorgio, Michael, Loogväli, Eva-Liis, Eichstaedt, Christina, Eelmets, Mikk, Chaubey, Gyaneshwer, Tambets, Kristiina, Litvinov, Sergei, Mormina, Maru, Xue, Yali, Ayub, Qasim, Zoraqi, Grigor, Korneliussen, Thorfinn Sand, Akhatova, Farida, Lachance, Joseph, Tishkoff, Sarah, Momynaliev, Kuvat, Ricaut, François-Xavier, Kusuma, Pradiptajati, Razafindrazaka, Harilanto, Pierron, Denis, Cox, Murray P, Sultana, Gazi Nurun Nahar, Willerslev, Rane, Muller, Craig, Westaway, Michael, Lambert, David, Skaro, Vedrana, Kovačevic, Lejla, Turdikulova, Shahlo, Dalimova, Dilbar, Khusainova, Rita, Trofimova, Natalya, Akhmetova, Vita, Khidiyatova, Irina, Lichman, Daria V, Isakova, Jainagul, Pocheshkhova, Elvira, Sabitov, Zhaxylyk, Barashkov, Nikolay A, Nymadawa, Pagbajabyn, Mihailov, Evelin, Seng, Joseph Wee Tien, Evseeva, Irina, Migliano, Andrea Bamberg, Abdullah, Syafiq, Andriadze, George, Primorac, Dragan, Atramentova, Lubov, Utevska, Olga, Yepiskoposyan, Levon, Marjanovic, Damir, Kushniarevich, Alena, Behar, Doron M, Gilissen, Christian, Vissers, Lisenka, Veltman, Joris A, Balanovska, Elena, Derenko, Miroslava, Malyarchuk, Boris, Metspalu, Andres, Fedorova, Sardana, Eriksson, Anders, Manica, Andrea, Mendez, Fernando L, Karafet, Tatiana M, Veeramah, Krishna R, Bradman, Neil, Hammer, Michael F, Osipova, Ludmila P, Balanovsky, Oleg, Khusnutdinova, Elza K, Johnsen, Knut, Remm, Maido, Thomas, Mark G, Tyler-Smith, Chris, Underhill, Peter A, Willerslev, Eske, Nielsen, Rasmus, Metspalu, Mait, Villems, Richard, Kivisild, Toomas

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Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps (vol 48, pg 1303, 2016) von Iotchkova, V, Huang, J, Morris, JA, Jain, D, Barbieri, C, Walter, K, Min, JL, Chen, L, Astle, W, Cocca, M

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Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps von Iotchkova, Valentina, Huang, Jie, Morris, John A, Jain, Deepti, Barbieri, Caterina, Walter, Klaudia, Min, Josine L, Chen, Lu, Astle, William, Cocca, Massimilian, Deelen, Patrick, Elding, Heather, Farmaki, Aliki-Eleni, Franklin, Christopher S, Franberg, Mattias, Gaunt, Tom R, Hofman, Albert, Jiang, Tao, Kleber, Marcus E, Lachance, Genevieve, Luan, Jian’an, Malerba, Giovanni, Matchan, Angela, Mead, Daniel, Memari, Yasin, Ntalla, Ioanna, Panoutsopoulou, Kalliope, Pazoki, Raha, Perry, John R B, Rivadeneira, Fernando, Sabater-Lleal, Maria, Sennblad, Bengt, Shin, So-Youn, Southam, Lorraine, Traglia, Michela, van Dijk, Freerk, van Leeuwen, Elisabeth M, Zaza, Gianluigi, Zhang, Weihua, Amin, Najaf, Butterworth, Adam, Chambers, John C, Dedoussis, George, Dehghan, Abbas, Franco, Oscar H, Franke, Lude, Frontini, Mattia, Gambaro, Giovanni, Gasparini, Paolo, Hamsten, Anders, Isaacs, Aaron, Kooner, Jaspal S, Kooperberg, Charles, Langenberg, Claudia, Marz, Winfried, Scott, Robert A, Swertz, Morris A, Toniolo, Daniela, Uitterlinden, Andre G, van Duijn, Cornelia M, Watkins, Hugh, Zeggini, Eleftheria, Maurano, Mathew T, Timpson, Nicholas J, Reiner, Alexander P, Auer, Paul L, Soranzo, Nicole

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Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk von Day, Felix R, Thompson, Deborah J, Helgason, Hannes, Chasman, Daniel I, Finucane, Hilary, Sulem, Patrick, Ruth, Katherine S, Whalen, Sean, Sarkar, Abhishek K, Albrecht, Eva, Altmaier, Elisabeth, Franceschini, Nora, Gieger, Christian, Gudnason, Vilmundur, Hayward, Caroline, Kraft, Peter, Lawlor, Debbie A, Magnusson, Patrik K.E, Martin, Nicholas G, Mook-Kanamori, Dennis O, Karlsson, Robert, Kutalik, Zoltan, Nohr, Ellen A, Polasek, Ozren, Porteous, David, Price, Alkes L, Ridker, Paul M, Snieder, Harold, Spector, Tim D, Stöckl, Doris, Toniolo, Daniela, Ulivi, Sheila, LaChance, Genevieve, Kolcic, Ivana, Visser, Jenny A, Völzke, Henry, Wareham, Nicholas J, Wilson, James F, Spurdle, Amanda B, Thorsteindottir, Unnur, Pollard, Katherine S, Easton, Douglas F, Tung, Joyce Y, Lambrechts, Diether, Chang-Claude, Jenny, Loh, Po-Ru, Hinds, David, Murray, Anna, Murabito, Joanne M, Stefansson, Kari, Ong, Ken K, Perry, John R.B, Lunetta, Kathryn L, Mangino, Massimo, Langenberg, Claudia, Marco, Brumat, McMahon, George, Medland, Sarah E, Nolte, Ilja M, Noordam, Raymond, Nutile, Teresa, Paternoster, Lavinia, Perjakova, Natalia, Porcu, Eleonora, Rose, Lynda M, Launer, Lenore J, Schraut, Katharina E, Segrè, Ayellet V, Smith, Albert V, Stolk, Lisette, Teumer, Alexander, Andrulis, Irene L, Bandinelli, Stefania, Beckmann, Matthias W, Benitez, Javier, Bergmann, Sven, Laven, Joop S.E, Bochud, Murielle, Boerwinkle, Eric, Bojesen, Stig E, Bolla, Manjeet K, Brand, Judith S, Brauch, Hiltrud, Brenner, Hermann, Broer, Linda, Brüning, Thomas, Buring, Julie E, Lenarduzzi, Stefania, Campbell, Harry, Catamo, Eulalia, Chanock, Stephen, Chenevix-Trench, Georgia, Corre, Tanguy, Couch, Fergus J, Cousminer, Diana L, Cox, Angela, Crisponi, Laura, Czene, Kamila, Li, Jingmei, Davey Smith, George

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Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk von Thompson, Deborah J, Whalen, Sean, Sarkar, Abhishek K, Boutin, Thibaud, Demerath, Ellen, Giri, Ayush, Loh, Po-Ru, Nolte, Ilja M, Noordam, Raymond, Nutile, Teresa, Paternoster, Lavinia, Porcu, Eleonora, Smith, Albert V, Stolk, Lisette, Andrulis, Irene L, Bandinelli, Stefania, Beckmann, Matthias W, Benitez, Javier, Bergmann, Sven, Bojesen, Stig E, Brand, Judith S, Brauch, Hiltrud, Broer, Linda, Buring, Julie E, Catamo, Eulalia, Chanock, Stephen, Chenevix-Trench, Georgia, Cousminer, Diana L, Crisponi, Laura, Czene, Kamila, De Vivo, Immaculata, Devilee, Peter, Fernández-Rhodes, Lindsay, Franke, Lude, Giles, Graham G, Grallert, Harald, Gudbjartsson, Daniel F, Hamann, Ute, Hartman, Catharina A, Ikram, M Arfan, Karasik, David, Kutalik, Zoltan, LaChance, Genevieve, Lambrechts, Diether, Langenberg, Claudia, Launer, Lenore J, Laven, Joop SE, Lenarduzzi, Stefania, Li, Jingmei, Lindstrom, Sara, Luan, Jian'an, Mägi, Reedik, Mannermaa, Arto, Meisinger, Christa, Menni, Cristina, Metspalu, Andres, Montgomery, Grant W, Nevanlinna, Heli, Nyholt, Dale R, O'Mara, Tracy A, Padmanabhan, Sandosh, Peters, Annette, Peto, Julian, Pharoah, Paul DP, Rahman, Iffat, Ring, Susan M, Rosendaal, Frits R, Ruggiero, Daniela, Sala, Cinzia F, Schmidt, Marjanka K, Sorice, Rossella, Southey, Melissa C, Sovio, Ulla, Steri, Maristella, Tanaka, Toshiko, Timpson, Nicholas J, Edwards, Digna R Velez, Vollenweider, Peter, Wang, Qin, van Dijk, Ko Willems, Winqvist, Robert, Zhao, Jing Hua, Zygmunt, Marek, Alizadeh, Behrooz Z, Cucca, Francesco, Gudnason, Vilmundur, Magnusson, Patrik KE, Martin, Nicholas G, Mook-Kanamori, Dennis O, Stöckl, Doris, Ulivi, Sheila, Visser, Jenny A, LifeLines Cohort Study, kConFab/AOCS Investigators, Endometrial Cancer Association Consortium, Ovarian Cancer Association Consortium, Pollard, Katherine S, Easton, Douglas F, Hinds, David, Murabito, Joanne M

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A low frequency variant at 8q24.21 is strongly associated with risk of oligodendroglial tumors and IDH1 or IDH2 mutated astrocytomas von Jenkins, Robert B., Xiao, Yuanyuan, Sicotte, Hugues, Decker, Paul A., Kollmeyer, Thomas M., Hansen, Helen M., Kosel, Matthew L., Zheng, Shichun, Walsh, Kyle M., Rice, Terri, Bracci, Paige, McCoy, Lucie S., Smirnov, Ivan, Patoka, Joseph S., Hsuang, George, Wiemels, Joe L., Tihan, Tarik, Pico, Alexander R., Prados, Michael D., Chang, Susan M., Berger, Mitchel S., Caron, Alissa A., Fink, Stephanie R., Halder, Chandralekha, Rynearson, Amanda L., Fridley, Brooke L., Buckner, Jan C., O’Neill, Brian P., Giannini, Caterina, Lachance, Daniel H., Wiencke, John K., Eckel-Passow, Jeanette E., Wrensch, Margaret R.

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The relationship between asthma and overweight in urban minority children von HASAN, Rashed A, ZUREIKAT, George Y, NOLAN, Brian M, LACHANCE, Jenny L, CAMPE, Julie L, AMIN, Raouf

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