Metformin Use in Practice: Compliance With Guidelines for Patients With Diabetes and Preserved Renal Function by Salber, Gregory J, Wang, Yu-Bo, Lynch, John T, Pasquale, Karen M, Rajan, Thiruchandurai V, Stevens, Richard G, Grady, James J, Kenny, Anne M

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Prenatal stress assessment using heart rate variability and salivary cortisol: A machine learning-based approach by Cao, Rui, Rahmani, Amir M, Lindsay, Karen L

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Divergence of gut permeability and mucosal immune gene expression in two gluten-associated conditions: celiac disease and gluten sensitivity by Sapone, Anna, Lammers, Karen M, Casolaro, Vincenzo, Cammarota, Marcella, Giuliano, Maria Teresa, De Rosa, Mario, Stefanile, Rosita, Mazzarella, Giuseppe, Tolone, Carlo, Russo, Maria Itria, Esposito, Pasquale, Ferraraccio, Franca, Cartenì, Maria, Riegler, Gabriele, de Magistris, Laura, Fasano, Alessio

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Gene × physical activity interactions in obesity: combined analysis of 111,421 individuals of European ancestry by Ahmad, Shafqat, Rukh, Gull, Varga, Tibor V, Ali, Ashfaq, Kurbasic, Azra, Shungin, Dmitry, Ericson, Ulrika, Koivula, Robert W, Chu, Audrey Y, Rose, Lynda M, Ganna, Andrea, Qi, Qibin, Stančáková, Alena, Sandholt, Camilla H, Elks, Cathy E, Curhan, Gary, Jensen, Majken K, Tamimi, Rulla M, Allin, Kristine H, Jørgensen, Torben, Brage, Soren, Langenberg, Claudia, Aadahl, Mette, Grarup, Niels, Linneberg, Allan, Paré, Guillaume, Magnusson, Patrik K E, Pedersen, Nancy L, Boehnke, Michael, Hamsten, Anders, Mohlke, Karen L, Pasquale, Louis T, Pedersen, Oluf, Scott, Robert A, Ridker, Paul M, Ingelsson, Erik, Laakso, Markku, Hansen, Torben, Qi, Lu, Wareham, Nicholas J, Chasman, Daniel I, Hallmans, Göran, Hu, Frank B, Renström, Frida, Orho-Melander, Marju, Franks, Paul W

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Cerclage in twin pregnancy with dilated cervix between 16 to 24 weeks of gestation: retrospective cohort study by Roman, Amanda, MD, Rochelson, Burton, MD, Martinelli, Pasquale, MD, Saccone, Gabriele, MD, Harris, Kemoy, MD, Zork, Noelia, MD, Spiel, Melissa, MD, O’Brien, Karen, MD, Calluzzo, Ilia, MD, Palomares, Kristy, MD, PhD, Rosen, Todd, MD, Berghella, Vincenzo, MD, Fleischer, Adiel, MD

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Inhibition of RANK signaling in breast cancer induces an anti-tumor immune response orchestrated by CD8+ T cells by Gómez-Aleza, Clara, Nguyen, Bastien, Yoldi, Guillermo, Ciscar, Marina, Barranco, Alexandra, Hernández-Jiménez, Enrique, Maetens, Marion, Salgado, Roberto, Zafeiroglou, Maria, Pellegrini, Pasquale, Venet, David, Garaud, Soizic, Trinidad, Eva M., Benítez, Sandra, Vuylsteke, Peter, Polastro, Laura, Wildiers, Hans, Simon, Philippe, Lindeman, Geoffrey, Larsimont, Denis, Van den Eynden, Gert, Velghe, Chloé, Rothé, Françoise, Willard-Gallo, Karen, Michiels, Stefan, Muñoz, Purificación, Walzer, Thierry, Planelles, Lourdes, Penninger, Josef, Azim, Hatem A., Loi, Sherene, Piccart, Martine, Sotiriou, Christos, González-Suárez, Eva

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Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study by Whelan, Christopher D, Altmann, Andre, Botía, Juan A, Jahanshad, Neda, Hibar, Derrek P, Absil, Julie, Alhusaini, Saud, Alvim, Marina K M, Auvinen, Pia, Bartolini, Emanuele, Bergo, Felipe P G, Bernardes, Tauana, Blackmon, Karen, Braga, Barbara, Caligiuri, Maria Eugenia, Calvo, Anna, Carr, Sarah J, Chen, Jian, Chen, Shuai, Cherubini, Andrea, David, Philippe, Domin, Martin, Foley, Sonya, França, Wendy, Haaker, Gerrit, Isaev, Dmitry, Keller, Simon S, Kotikalapudi, Raviteja, Kowalczyk, Magdalena A, Kuzniecky, Ruben, Langner, Soenke, Lenge, Matteo, Leyden, Kelly M, Liu, Min, Loi, Richard Q, Martin, Pascal, Mascalchi, Mario, Morita, Marcia E, Pariente, Jose C, Rodríguez-Cruces, Raul, Rummel, Christian, Saavalainen, Taavi, Semmelroch, Mira K, Severino, Mariasavina, Thomas, Rhys H, Tondelli, Manuela, Tortora, Domenico, Vaudano, Anna Elisabetta, Vivash, Lucy, von Podewils, Felix, Wagner, Jan, Weber, Bernd, Yao, Yi, Yasuda, Clarissa L, Zhang, Guohao, Bargalló, Nuria, Bender, Benjamin, Bernasconi, Neda, Bernasconi, Andrea, Bernhardt, Boris C, Blümcke, Ingmar, Carlson, Chad, Cavalleri, Gianpiero L, Cendes, Fernando, Concha, Luis, Delanty, Norman, Depondt, Chantal, Devinsky, Orrin, Doherty, Colin P, Focke, Niels K, Gambardella, Antonio, Guerrini, Renzo, Hamandi, Khalid, Jackson, Graeme D, Kälviäinen, Reetta, Kochunov, Peter, Kwan, Patrick, Labate, Angelo, McDonald, Carrie R, Meletti, Stefano, O'Brien, Terence J, Ourselin, Sebastien, Richardson, Mark P, Striano, Pasquale, Thesen, Thomas, Wiest, Roland, Zhang, Junsong, Vezzani, Annamaria, Ryten, Mina, Thompson, Paul M, Sisodiya, Sanjay M

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Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders by Wolff, Markus, Johannesen, Katrine M, Hedrich, Ulrike B S, Masnada, Silvia, Rubboli, Guido, Gardella, Elena, Lesca, Gaetan, Ville, Dorothée, Milh, Mathieu, Villard, Laurent, Afenjar, Alexandra, Chantot-Bastaraud, Sandra, Mignot, Cyril, Lardennois, Caroline, Nava, Caroline, Schwarz, Niklas, Gérard, Marion, Perrin, Laurence, Doummar, Diane, Auvin, Stéphane, Miranda, Maria J, Hempel, Maja, Brilstra, Eva, Knoers, Nine, Verbeek, Nienke, van Kempen, Marjan, Braun, Kees P, Mancini, Grazia, Biskup, Saskia, Hörtnagel, Konstanze, Döcker, Miriam, Bast, Thomas, Loddenkemper, Tobias, Wong-Kisiel, Lily, Baumeister, Friedrich M, Fazeli, Walid, Striano, Pasquale, Dilena, Robertino, Fontana, Elena, Zara, Federico, Kurlemann, Gerhard, Klepper, Joerg, Thoene, Jess G, Arndt, Daniel H, Deconinck, Nicolas, Schmitt-Mechelke, Thomas, Maier, Oliver, Muhle, Hiltrud, Wical, Beverly, Finetti, Claudio, Brückner, Reinhard, Pietz, Joachim, Golla, Günther, Jillella, Dinesh, Linnet, Karen M, Charles, Perrine, Moog, Ute, Õiglane-Shlik, Eve, Mantovani, John F, Park, Kristen, Deprez, Marie, Lederer, Damien, Mary, Sandrine, Scalais, Emmanuel, Selim, Laila, Van Coster, Rudy, Lagae, Lieven, Nikanorova, Marina, Hjalgrim, Helle, Korenke, G Christoph, Trivisano, Marina, Specchio, Nicola, Ceulemans, Berten, Dorn, Thomas, Helbig, Katherine L, Hardies, Katia, Stamberger, Hannah, de Jonghe, Peter, Weckhuysen, Sarah, Lemke, Johannes R, Krägeloh-Mann, Ingeborg, Helbig, Ingo, Kluger, Gerhard, Lerche, Holger, Møller, Rikke S

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HD 219134 Revisited: Planet d Transit Upper Limit and Planet f Transit Nondetection with ASTERIA and TESS by Seager, Sara, Knapp, Mary, Demory, Brice-Olivier, Krishnamurthy, Akshata, Huang, Chelsea X., Agusti, Mariona Badenas, Shporer, Avi, Weisserman, Drew, Becker, Juliette, Vanderburg, Andrew, Smith, Matthew, Pong, Christopher M., Bailey, Vanessa P., Donner, Amanda, Pasquale, Peter Di, Campuzano, Brian, Smith, Colin, Luu, Jason, Babuscia, Alessandra, Bocchino, Robert L., Loveland, Jessica, Colley, Cody, Gedenk, Tobias, Kulkarni, Tejas, Hughes, Kyle, White, Mary, Krajewski, Joel, Fesq, Lorraine, Ricker, George, Vanderspek, Roland, Latham, David W., Jenkins, Jon M., Winn, Joshua N., Caldwell, Douglas A., Collins, Karen A., Dragomir, Diana, Fausnaugh, Michael, Glidden, Ana, Schlieder, Joshua E., Twicken, Joseph D., Wohler, Bill

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FTO genetic variants, dietary intake and body mass index: insights from 177,330 individuals by Qi, Qibin, Kilpeläinen, Tuomas O, Downer, Mary K, Tanaka, Toshiko, Smith, Caren E, Sluijs, Ivonne, Sonestedt, Emily, Chu, Audrey Y, Renström, Frida, Lin, Xiaochen, Ängquist, Lars H, Huang, Jinyan, Liu, Zhonghua, Li, Yanping, Asif Ali, Muhammad, Xu, Min, Ahluwalia, Tarunveer Singh, Boer, Jolanda M A, Chen, Peng, Daimon, Makoto, Eriksson, Johan, Perola, Markus, Friedlander, Yechiel, Gao, Yu-Tang, Heppe, Denise H M, Holloway, John W, Houston, Denise K, Kanoni, Stavroula, Kim, Yu-Mi, Laaksonen, Maarit A, Jääskeläinen, Tiina, Lee, Nanette R, Lehtimäki, Terho, Lemaitre, Rozenn N, Lu, Wei, Luben, Robert N, Manichaikul, Ani, Männistö, Satu, Marques-Vidal, Pedro, Monda, Keri L, Ngwa, Julius S, Perusse, Louis, van Rooij, Frank J A, Xiang, Yong-Bing, Wen, Wanqing, Wojczynski, Mary K, Zhu, Jingwen, Borecki, Ingrid B, Bouchard, Claude, Cai, Qiuyin, Cooper, Cyrus, Dedoussis, George V, Deloukas, Panos, Ferrucci, Luigi, Forouhi, Nita G, Hansen, Torben, Christiansen, Lene, Hofman, Albert, Johansson, Ingegerd, Jørgensen, Torben, Karasawa, Shigeru, Khaw, Kay-Tee, Kim, Mi-Kyung, Kristiansson, Kati, Li, Huaixing, Lin, Xu, Liu, Yongmei, Lohman, Kurt K, Long, Jirong, Mikkilä, Vera, Mozaffarian, Dariush, North, Kari, Pedersen, Oluf, Raitakari, Olli, Rissanen, Harri, Tuomilehto, Jaakko, van der Schouw, Yvonne T, Uitterlinden, André G, Zillikens, M Carola, Franco, Oscar H, Shyong Tai, E, Ou Shu, Xiao, Siscovick, David S, Toft, Ulla, Verschuren, W M Monique, Vollenweider, Peter, Wareham, Nicholas J, Witteman, Jacqueline C M, Zheng, Wei, Ridker, Paul M, Kang, Jae H, Liang, Liming, Jensen, Majken K, Curhan, Gary C, Pasquale, Louis R, Hunter, David J, Mohlke, Karen L, Uusitupa, Matti, Cupples, L Adrienne, Rankinen, Tuomo

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Gene x physical activity interactions in obesity: combined analysis of 111,421 individuals of European ancestry by Ahmad, Shafqat, Rukh, Gull, Varga, Tibor V, Ali, Ashfaq, Kurbasic, Azra, Shungin, Dmitry, Ericson, Ulrika, Koivula, Robert W, Chu, Audrey Y, Rose, Lynda M, Ganna, Andrea, Qi, Qibin, Stancakova, Alena, Sandholt, Camilla H, Elks, Cathy E, Curhan, Gary, Jensen, Majken K, Tamimi, Rulla M, Allin, Kristine H, Jorgensen, Torben, Brage, Soren, Langenberg, Claudia, Aadahl, Mette, Grarup, Niels, Linneberg, Allan, Pare, Guillaume, Magnusson, Patrik KE, Pedersen, Nancy L, Boehnke, Michael, Hamsten, Anders, Mohlke, Karen L, Pasquale, Louis T, Pedersen, Oluf, Scott, Robert A, Ridker, Paul M, Ingelsson, Erik, Laakso, Markku, Hansen, Torben, Qi, Lu, Wareham, Nicholas J, Chasman, Daniel I, Hallmans, Göran, Hu, Frank B, Renström, Frida, Orho-Melander, Marju, Franks, Paul W.

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Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals by Howrigan, Daniel P., Abbott, Liam E., Tashman, Katherine, Singh, Tarjinder, Watts, Nick, Lal, Dennis, Hakonarson, Hakon, Weckhuysen, Sarah, Petrovski, Slavé, Cossette, Patrick, Cotsapas, Chris, De Jonghe, Peter, Guerrini, Renzo, Marson, Anthony G., Depondt, Chantal, Striano, Pasquale, Freyer, Catharine, Regan, Brigid M., Leu, Costin, Johns, Esther M.C., Macdonald, Alexandra, Bahlo, Melanie, Todaro, Marian, Stamberger, Hannah, Sadoway, Tara R., Kousiappa, Ioanna, Tanteles, George A., Štěrbová, Katalin, Kunz, Wolfram S., Zsurka, Gábor, Elger, Christian E., Rademacher, Michael, van Baalen, Andreas, von Spiczak, Sarah, Afawi, Zaid, Canavati, Christina, Kluger, Gerhard, Blatt, Ilan, Weber, Yvonne G., Wolking, Stefan, Rau, Sarah, Steinhoff, Bernhard J., Schulze-Bonhage, Andreas, Borggräfe, Ingo, Madeleyn, Rene, Kälviäinen, Reetta, Linnankivi, Tarja, Chung, Seo-Kyung, Balestrini, Simona, Braatz, Vera, Johnson, Michael R., Auce, Pauls, Sham, Pak C., Lui, Colin H.T., Doherty, Colin P., Shukralla, Arif, El-Naggar, Hany, Vari, Maria Stella, Salpietro, Vincenzo, Tinuper, Paolo, Gagliardi, Monica, Montomoli, Martino, Doccini, Viola, Inoue, Yushi, Yamakawa, Kazuhiro, Tumiene, Birute, Sadleir, Lynette G., Caglayan, S. Hande, Arslan, Mutluay, Yis, Uluc, Topaloglu, Pınar, Baykan, Betül, Salman, Barış, Haryanyan, Garen, Özkara, Çiğdem, Poduri, Annapurna, Shiedley, Beth R., Shain, Catherine, French, Jacqueline A., Kuzniecky, Ruben I., Hegde, Manu, Helbig, Katherine L., Piras, Federica, Reif, Andreas, McQuillin, Andrew, Johnstone, Mandy, Palotie, Aarno, Carvalho, Celia Barreto, Achtyes, Eric D., Azevedo, Maria Helena, Kotov, Roman, Lehrer, Douglas S., Marder, Stephen R., Medeiros, Helena, Morley, Christopher P., Rapaport, Mark H., Knowles, James A., McCarroll, Steven A., Lowenstein, Daniel H., Goldstein, David B.

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In vivo multiplex molecular imaging of vascular inflammation using surface-enhanced Raman spectroscopy by Noonan, Jonathan, Asiala, Steven M, Grassia, Gianluca, MacRitchie, Neil, Gracie, Kirsten, Carson, Jake, Moores, Matthew, Girolami, Mark, Bradshaw, Angela C, Guzik, Tomasz J, Meehan, Gavin R, Scales, Hannah E, Brewer, James M, McInnes, Iain B, Sattar, Naveed, Faulds, Karen, Garside, Paul, Graham, Duncan, Maffia, Pasquale

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ALK-positive histiocytosis: a new clinicopathologic spectrum highlighting neurologic involvement and responses to ALK inhibition by Kemps, Paul G., Picarsic, Jennifer, Durham, Benjamin H., Hélias-Rodzewicz, Zofia, Hiemcke-Jiwa, Laura, van den Bos, Cor, van de Wetering, Marianne D., van Noesel, Carel J.M., van Laar, Jan A.M., Verdijk, Robert M., Flucke, Uta E., Hogendoorn, Pancras C.W., Woei-A-Jin, F. J. Sherida H., Sciot, Raf, Beilken, Andreas, Feuerhake, Friedrich, Ebinger, Martin, Möhle, Robert, Fend, Falko, Bornemann, Antje, Wiegering, Verena, Ernestus, Karen, Méry, Tina, Gryniewicz-Kwiatkowska, Olga, Dembowska-Baginska, Bozenna, Evseev, Dmitry A., Potapenko, Vsevolod, Baykov, Vadim V., Gaspari, Stefania, Rossi, Sabrina, Gessi, Marco, Tamburrini, Gianpiero, Héritier, Sébastien, Donadieu, Jean, Bonneau-Lagacherie, Jacinthe, Lamaison, Claire, Farnault, Laure, Fraitag, Sylvie, Jullié, Marie-Laure, Haroche, Julien, Collin, Matthew, Allotey, Jackie, Madni, Majid, Turner, Kerry, Picton, Susan, Barbaro, Pasquale M., Poulin, Alysa, Tam, Ingrid S., El Demellawy, Dina, Empringham, Brianna, Whitlock, James A., Raghunathan, Aditya, Swanson, Amy A., Suchi, Mariko, Brandt, Jon M., Yaseen, Nabeel R., Weinstein, Joanna L., Eldem, Irem, Sisk, Bryan A., Sridhar, Vaishnavi, Atkinson, Mandy, Massoth, Lucas R., Hornick, Jason L., Alexandrescu, Sanda, Yeo, Kee Kiat, Petrova-Drus, Kseniya, Peeke, Stephen Z., Muñoz-Arcos, Laura S., Leino, Daniel G., Grier, David D., Lorsbach, Robert, Roy, Somak, Kumar, Ashish R., Garg, Shipra, Tiwari, Nishant, Schafernak, Kristian T., Henry, Michael M., van Halteren, Astrid G.S., Abla, Oussama, Diamond, Eli L., Emile, Jean-François

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Progressive myoclonus epilepsies—Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genes by Courage, Carolina, Oliver, Karen L., Park, Eon Joo, Cameron, Jillian M., Grabińska, Kariona A., Muona, Mikko, Canafoglia, Laura, Gambardella, Antonio, Said, Edith, Afawi, Zaid, Baykan, Betul, Brandt, Christian, di Bonaventura, Carlo, Chew, Hui Bein, Criscuolo, Chiara, Dibbens, Leanne M., Castellotti, Barbara, Riguzzi, Patrizia, Labate, Angelo, Filla, Alessandro, Giallonardo, Anna T., Berecki, Geza, Jackson, Christopher B., Joensuu, Tarja, Damiano, John A., Kivity, Sara, Korczyn, Amos, Palotie, Aarno, Striano, Pasquale, Uccellini, Davide, Giuliano, Loretta, Andermann, Eva, Scheffer, Ingrid E., Michelucci, Roberto, Bahlo, Melanie, Franceschetti, Silvana, Sessa, William C., Berkovic, Samuel F., Lehesjoki, Anna-Elina

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Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies by Anon

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Biobanking for better healthcare by Riegman, Peter H.J., Morente, Manuel M., Betsou, Fay, de Blasio, Pasquale, Geary, Peter

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Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects by Niestroj, Lisa-Marie, Perez-Palma, Eduardo, Howrigan, Daniel P, Zhou, Yadi, Cheng, Feixiong, Saarentaus, Elmo, Nürnberg, Peter, Stevelink, Remi, Daly, Mark J, Palotie, Aarno, Lal, Dennis

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Age and sex differences in the association between neighborhood socioeconomic environment and incident diabetes: Results from the diabetes location, environmental attributes and di... by Uddin, Jalal, Zhu, Sha, Adhikari, Samrachana, Nordberg, Cara M., Howell, Carrie R., Malla, Gargya, Judd, Suzanne E., Cherrington, Andrea L., Rummo, Pasquale E., Lopez, Priscilla, Kanchi, Rania, Siegel, Karen, De Silva, Shanika A., Algur, Yasemin, Lovasi, Gina S., Lee, Nora L., Carson, April P., Hirsch, Annemarie G., Thorpe, Lorna E., Long, D. Leann

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Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals by Montanucci, Ludovica, Lewis-Smith, David, Collins, Ryan L., Niestroj, Lisa-Marie, Parthasarathy, Shridhar, Xian, Julie, Ganesan, Shiva, Macnee, Marie, Brünger, Tobias, Thomas, Rhys H., Talkowski, Michael, Helbig, Ingo, Leu, Costin, Lal, Dennis

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