Scanning Micropipet Contact Method for High-Resolution Imaging of Electrode Surface Redox Activity von Williams, Cara G, Edwards, Martin A, Colley, Anna L, Macpherson, Julie V, Unwin, Patrick R

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Examination of the Spatially Heterogeneous Electroactivity of Boron-Doped Diamond Microarray Electrodes von Colley, Anna L, Williams, Cara G, D'Haenens Johansson, Ulrika, Newton, Mark E, Unwin, Patrick R, Wilson, Neil R, Macpherson, Julie V

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Effect of high rates of mass transport on oxygen reduction at copper electrodes: Implications for aluminium corrosion von Colley, Anna L., Macpherson, Julie V., Unwin, Patrick R.

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Endocannabinoid dysfunction in neurological disease: neuro-ocular DAGLA-related syndrome von Bainbridge, Matthew N, Mazumder, Aloran, Ogasawara, Daisuke, Abou Jamra, Rami, Bernard, Geneviève, Bertini, Enrico, Burglen, Lydie, Cope, Heidi, Crawford, Ali, Derksen, Alexa, Dure, Leon, Gantz, Emily, Koch-Hogrebe, Margarete, Hurst, Anna C E, Mahida, Sonal, Marshall, Paige, Micalizzi, Alessia, Novelli, Antonio, Peng, Hongfan, Rodriguez, Diana, Robbins, Shira L, Rutledge, S Lane, Scalise, Roberta, Schließke, Sophia, Shashi, Vandana, Srivastava, Siddharth, Thiffault, Isabella, Topol, Sarah, Qebibo, Leila, Wieczorek, Dagmar, Cravatt, Benjamin, Haricharan, Svasti, Torkamani, Ali, Friedman, Jennifer

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Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowth von Loveday, Chey, Tatton-Brown, Katrina, Clarke, Matthew, Westwood, Isaac, Renwick, Anthony, Ramsay, Emma, Nemeth, Andrea, Campbell, Jennifer, Joss, Shelagh, Gardner, McKinlay, Zachariou, Anna, Elliott, Anna, Ruark, Elise, van Montfort, Rob, Rahman, Nazneen

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Co-observation of germline pathogenic variants in breast cancer predisposition genes: Results from analysis of the BRIDGES sequencing dataset von Davidson, Aimee L., Parsons, Michael T., Bolla, Manjeet K., Wang, Qin, Dennis, Joe, Andrulis, Irene L., Antoniou, Antonis C., Behrens, Sabine, Bogdanova, Natalia V., Brüning, Thomas, Castelao, Jose E., Sahlberg, Kristine K., Børresen-Dale, Anne-Lise, Olsen, Karina Standahl, Engebråten, Olav, Grenaker Alnæs, Grethe I., Collée, J. Margriet, Eriksson, Mikael, Fasching, Peter A., Gago-Dominguez, Manuela, Glendon, Gord, Grassmann, Felix, Gronwald, Jacek, Guénel, Pascal, Hadjisavvas, Andreas, Haeberle, Lothar, Hamann, Ute, Ho, Peh Joo, Hoppe, Reiner, Antill, Yoland, Bogwitz, Michael, Brennan, Meagan, Caldon, Liz, Cao, Michelle, Chakrabarti, Anannya, Chauhan, Deepa, Colley, Alison, Crook, Ashley, Cui, James, Courtney, Eliza, Dawson, Sarah-Jane, deFazio, Anna, Delatycki, Martin, Dixon, Joanne, Edwards, Stacey, French, Juliet, Gattas, Mike, Greening, Sian, Hart, Stewart, Hayward, Nick, Hopper, John, Jenkins, Mark, Kirk, Judy, Koehler, Jessica, Lakhani, Sunil, Lawrence, Mitchell, Lippey, Jocelyn, Loi, Sherene, McLachlan, Sue Anne, O'Sullivan, Sarah, Pang, Jia-Min, Pathak, Gargi, Pearn, Amy, Phillips, Kelly, Pieper, Ellen, Ragunathan, Abi, Robinson, Bridget, Saleh, Mona, Salisbury, Elizabeth, Saunders, Christobel, Saunus, Jodi, Sexton, Adrienne, Shelling, Andrew, Visvader, Jane, Young, Mary Ann, Jakubowska, Anna, Khusnutdinova, Elza K., Kristensen, Vessela N., Lim, Joanna, Liu, Jenny, Lophatananon, Artitaya, Mannermaa, Arto, Mavroudis, Dimitrios A., Mensenkamp, Arjen R., Milne, Roger L., Newman, William G., Panayiotidis, Mihalis I., Park, Sue K., Park-Simon, Tjoung-Won, Rhenius, Valerie, Saloustros, Emmanouil, Sawyer, Elinor J., Schmidt, Marjanka K., Shah, Mitul, Teo, Soo Hwang, Torres, Diana, Truong, Thérèse, van de Beek, Irma, Wendt, Camilla C., Dunning, Alison M.

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The impact of coding germline variants on contralateral breast cancer risk and survival von Morra, Anna, Mavaddat, Nasim, Muranen, Taru A., Allen, Jamie, Andrulis, Irene L., Auvinen, Päivi, Behrens, Sabine, Bolla, Manjeet K., Brauch, Hiltrud, Camp, Nicola J., Geisler, Jürgen, Grenaker Alnæs, Grethe I., Czene, Kamila, Decker, Brennan, Dorling, Leila, Ekici, Arif B., Fasching, Peter A., Gago-Dominguez, Manuela, García-Closas, Montserrat, Giles, Graham G., Guénel, Pascal, Gündert, Melanie, Hamann, Ute, Harrington, Patricia A., He, Wei, Hooning, Maartje J., Hoppe, Reiner, Howell, Anthony, Amor, David, Andrews, Lesley, Balleine, Rosemary, Bennett, Ian, Bogwitz, Michael, Botes, Leon, Caldon, Liz, Cao, Michelle, Chakrabarti, Anannya, Chauhan, Deepa, Cohen, Paul, Cui, James, DeFazio, Anna, Delatycki, Martin, Dixon, Joanne, Edkins, Ted, Farshid, Gelareh, Fellows, Andrew, Flanagan, James, Fox, Stephen, French, Juliet, Gaff, Clara, George, Peter, Hunt, Clare, Kidd, Alexa, Koehler, Jessica, Kollias, James, Li, Shuai, Lipton, Lara, Loi, Sherene, Mann, Graham, Marsh, Deborah, McLachlan, Sue Anne, Milne, Roger, Nightingale, Sophie, O'Sullivan, Sarah, Ortega, David Gallego, Pachter, Nick, Patterson, Briony, Phillips, Kelly, Ramus, Susan, Rickard, Edwina, Robinson, Bridget, Saleh, Mona, Skandarajah, Anita, Saunders, Christobel, Scott, Rodney, Sexton, Adrienne, Shelling, Andrew, Taylor, Jessica, Thorne, Heather, Visvader, Jane, Young, Mary Ann, Zaheed, Milita, Jakubowska, Anna, Keeman, Renske, Kristensen, Vessela N., Milne, Roger L., Mulligan, Anna Marie, Park-Simon, Tjoung-Won, Peterlongo, Paolo, Pharoah, Paul D.P., Rhenius, Valerie, Sawyer, Elinor J., Schmutzler, Rita K., Shah, Mitul, Tomlinson, Ian, Vreeswijk, Maaike P.G., Wendt, Camilla, Yang, Xiaohong R., Devilee, Peter, Easton, Douglas F.

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Genomics Research with Undiagnosed Children: Ethical Challenges at the Boundaries of Research and Clinical Care von Maghiro, AudreyStephannie, Tabor, Holly K., Acosta, Maria T., Amendola, Laura, Andrews, Ashley, Balasubramanyam, Ashok, Baldridge, Dustin, Bennett, Jimmy, Berg-Rood, Beverly, Berry, Gerard T., Bican, Anna, Bohnsack, John, Boyd, Brenna, Burke, Elizabeth A., Byers, Peter, Peter Chang, Ta Chen, Chanprasert, Sirisak, Clark, Gary D., Cobban, Laurel A., Cogan, Joy D., Sessions Cole, F., Colley, Heather A., Cope, Heidi, D'Souza, Precilla, Dasari, Surendra, Dipple, Katrina, Doherty, Daniel, Dorrani, Naghmeh, Earl, Dawn, Falk, Marni, Fieg, Elizabeth L., Fisher, Paul G., Gahl, William A., Goddard, Page C., Golden-Grant, Katie, Grajewski, Alana, Hahn, Sihoun, Hamid, Rizwan, Hassey, Kelly, Holm, Ingrid A., Hom, Jason, Introne, Wendy, Izumi, Kosuke, Jayadev, Suman, Kiley, Dana, Kobren, Shilpa N., Korrick, Susan, Krasnewich, Donna M., Lam, Christina, Lanza, Ian R., Lee, Brendan H., Loo, Sandra K., Maas, Richard L., Macnamara, Ellen F., MacRae, Calum A., Manolio, Teri A., Marth, Gabor, McConkie-Rosell, Allyn, Mefford, Heather, Nickerson, Deborah, Nieves-Rodriguez, Shirley, Novacic, Donna, Oglesbee, Devin, Pace, Laura, Posey, Jennifer E., Potocki, Lorraine, Rao, Deepak A., Raskind, Wendy, Renteria, Genecee, Robertson, Amy K., Rossignol, Francis, Ruzhnikov, Maura, Scott, Daryl A., Shashi, Vandana, Shin, Jimann, Sisco, Kathy, Smith, Edward C., Solomon, Ben, Sullivan, Jennifer A., Sybert, Virginia, Tan, Amelia L.M., Tekin, Mustafa, Telischi, Fred, Toro, Camilo, Ungar, Rachel A., Vanderver, Adeline, Walker, Melissa, Walley, Nicole M., Wambach, Jennifer, Wan, Jijun, Wang, Lee-kai, Ward, Patricia A., Wegner, Daniel, Hubshman, Monika Weisz, Wener, Mark, Wenger, Tara, Westerfield, Monte, Worley, Kim, Xiao, Changrui, Yang, John

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Macrocephaly and developmental delay caused by missense variants in RAB5C von Koop, Klaas, Yuan, Weimin, Tessadori, Federico, Rodriguez-Polanco, Wilmer R, Grubbs, Jeremy, Zhang, Bo, Osmond, Matt, Graham, Gail, Sawyer, Sarah, Conboy, Erin, Vetrini, Francesco, Treat, Kayla, Płoski, Rafal, Pienkowski, Victor Murcia, Kłosowska, Anna, Fieg, Elizabeth, Krier, Joel, Mallebranche, Coralie, Alban, Ziegler, Aldinger, Kimberly A, Ritter, Deborah, Macnamara, Ellen, Sullivan, Bonnie, Herriges, John, Alaimo, Joseph T, Helbig, Catherine, Ellis, Colin A, van Eyk, Clare, Gecz, Jozef, Farrugia, Daniel, Osei-Owusu, Ikeoluwa, Adès, Lesley, van den Boogaard, Marie-Jose, Fuchs, Sabine, Bakker, Jeroen, Duran, Karen, Dawson, Zachary D, Lindsey, Anika, Huang, Huiyan, Baldridge, Dustin, Silverman, Gary A, Grant, Barth D, Raizen, David, van Haaften, Gijs, Pak, Stephen C, Rehmann, Holger, Schedl, Tim, van Hasselt, Peter

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Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis von Briere, Lauren C., Acosta, Maria T., Andrews, Ashley, Ashley, Euan A., Bacino, Carlos A., Bale, Jim, Barbouth, Deborah, Bennett, Jimmy, Bivona, Stephanie, Blue, Elizabeth, Burke, Elizabeth A., Byers, Peter, Peter Chang, Ta Chen, Chanprasert, Sirisak, Coakley, Terra R., Cogan, Joy D., Colley, Heather A., Cope, Heidi, Craigen, William J., Cunningham, Michael, Dasari, Surendra, Dell'Angelica, Esteban C., Dipple, Katrina, Doherty, Daniel, Dorrani, Naghmeh, Doss, Argenia L., Douine, Emilie D., Earl, Dawn, Eng, Christine M., Fisher, Paul G., Gahl, William A., Glass, Ian, Gochuico, Bernadette, Hamid, Rizwan, Hayes, Nichole, Horike-Pyne, Martha, Isasi, Rosario, Jarvik, Gail P., Jarvik, Jeffrey, Jayadev, Suman, Jobanputra, Vaidehi, Kiley, Dana, Kohler, Jennefer N., Korrick, Susan, Lalani, Seema R., Lam, Byron, Lanpher, Brendan C., LeBlanc, Kimberly, Levitt, Roy, Lewis, Richard A., Liu, Pengfei, Liu, Xue Zhong, Longo, Nicola, Maas, Richard L., Macnamara, Ellen F., Mao, Rong, Marom, Ronit, Martin, Beth A., Martin, Martin G., Martínez-Agosto, Julian A., Marwaha, Shruti, Miller, Danny, Morava, Eva, Moretti, Paolo, Novacic, Donna, Orengo, James P., Pallais, J. Carl, Phillips, John A., Posey, Jennifer E., Potocki, Lorraine, Raskind, Wendy, Robertson, Amy K., Rosenfeld, Jill A., Rossignol, Francis, Ruzhnikov, Maura, Schaechter, Judy, Sisco, Kathy, Solnica-Krezel, Lilianna, Solomon, Ben, Spillmann, Rebecca C., Stergachis, Andrew, Sullivan, Kathleen, Sweetser, David A., Sybert, Virginia, Tabor, Holly K., Tarakad, Arjun, Thorson, Willa, Vanderver, Adeline, Velinder, Matt, Walley, Nicole M., Wambach, Jennifer, Wan, Jijun, Ward, Patricia A., Wegner, Daniel, Hubshman, Monika Weisz, Wenger, Tara, Wheeler, Matthew T., Yang, John, Zhang, Zhe, Zuchner, Stephan

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Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities von Atala, Kristhen, Dutta, Debdeep, Khanshour, Anas, Balasubramanyam, Ashok, Burrage, Lindsay C., Clark, Gary D., Ketkar, Shamika, Posey, Jennifer E., Rosenfeld, Jill A., Seto, Elaine, Scott, Daryl A., Tran, Alyssa A., Hubshman, Monika Weisz, Kanca, Oguz, Eng, Christine M., Falk, Marni, Hassey, Kelly, Zhang, Zhe, Mikati, Mohamad, Beggs, Alan H., Berry, Gerard T., Coggins, Matthew, Fieg, Elizabeth L., High, Frances, Holm, Ingrid A., Maas, Richard L., MacRae, Calum A., Pallais, J. Carl, Rao, Deepak A., Silverman, Edwin K., Sweetser, David A., Glanton, Emily, Maghiro, Audrey Stephannie C., McCray, Alexa T., Tan, Amelia L.M., Dasari, Surendra, Bademci, Guney, Barbouth, Deborah, Bivona, Stephanie, Borja, Nicholas, Gonzalez, Joanna M., Latchman, Kumarie, Tekin, Mustafa, Zuchner, Stephan, Gropman, Andrea, Macnamara, Ellen F., Maduro, Valerie V., Novacic, Donna, Toro, Camilo, Wahl, Colleen E., Adams, David R., Afzali, Ben, Burke, Elizabeth A., Fu, Jiayu, Wood, Heidi, Allworth, Aimee, Blue, Elizabeth, Chanprasert, Sirisak, Glass, Ian, Lam, Christina, Mirzaa, Ghayda, Raskind, Wendy, Alvarez, Raquel L., Bejerano, Gill, Bonner, Devon, Fisher, Paul G., Kohler, Jennefer N., Kravets, Elijah, Marwaha, Shruti, Ruzhnikov, Maura, Sutton, Shirley, Ungar, Rachel A., Crouse, Andrew B., Whitlock, Jordan, Butte, Manish J., Corona, Rosario, Dell'Angelica, Esteban C., Dorrani, Naghmeh, Fogel, Brent L., McGee, Elisabeth, Nieves-Rodriguez, Shirley, Alvey, Justin, Bohnsack, John, Moretti, Paolo, Quinlan, Aaron, Marth, Gabor, Bican, Anna, Cassini, Thomas, Corner, Brian, Hamid, Rizwan, Rives, Lynette, Robertson, Amy K., Ezell, Kimberly, Cogan, Joy D., Hayes, Nichole, Wegner, Daniel, Cole, F. Sessions, Schedl, Timothy, Wangler, Michael F., Bellen, Hugo J.

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Mendelian randomisation study of smoking exposure in relation to breast cancer risk von Park, Hanla A., Neumeyer, Sonja, Michailidou, Kyriaki, Bolla, Manjeet K., Wang, Qin, Ahearn, Thomas U., Andrulis, Irene L., Anton-Culver, Hoda, Antonenkova, Natalia N., Arndt, Volker, Aronson, Kristan J., Beane Freeman, Laura E., Beckmann, Matthias W., Behrens, Sabine, Benitez, Javier, Bogdanova, Natalia V., Bojesen, Stig E., Brauch, Hiltrud, Campa, Daniele, Castelao, Jose E., Chanock, Stephen J., Chenevix-Trench, Georgia, Clarke, Christine L., Couch, Fergus J., Cross, Simon S., Czene, Kamila, Daly, Mary B., Devilee, Peter, Dwek, Miriam, Eliassen, A. Heather, Evans, D. Gareth, Fasching, Peter A., Flyger, Henrik, Giles, Graham G., Goldgar, David E., Grip, Mervi, Hahnen, Eric, Haiman, Christopher A., Håkansson, Niclas, Hall, Per, Hamann, Ute, Han, Sileny, Hart, Steven N., He, Wei, Heemskerk-Gerritsen, Bernadette A. M., Hopper, John L., Jakubowska, Anna, John, Esther M., Jung, Audrey, Kapoor, Pooja Middha, Keeman, Renske, Kitahara, Cari M., Koppert, Linetta B., Kristensen, Vessela N., Kurian, Allison W., Lambrechts, Diether, Le Marchand, Loic, Lo, Wing-Yee, Lubiński, Jan, Manoochehri, Mehdi, Margolin, Sara, Mavroudis, Dimitrios, Meindl, Alfons, Menon, Usha, Milne, Roger L., Nevanlinna, Heli, Nordestgaard, Børge G., Offit, Kenneth, Olshan, Andrew F., Olsson, Håkan, Park-Simon, Tjoung-Won, Peterlongo, Paolo, Peto, Julian, Plaseska-Karanfilska, Dijana, Presneau, Nadege, Radice, Paolo, Rennert, Gad, Rennert, Hedy S., Romero, Atocha, Saloustros, Emmanouil, Sawyer, Elinor J., Schmutzler, Rita K., Shu, Xiao-Ou, Simard, Jacques, Smeets, Ann, Southey, Melissa C., Spinelli, John J., Tamimi, Rulla M., Tapper, William J., Terry, Mary Beth, Troester, Melissa A., Truong, Thérèse, van Veen, Elke M., Vijai, Joseph, Wang, Sophia, Wendt, Camilla, Wolk, Alicja, Dunning, Alison M., Pharoah, Paul D. P., Chang-Claude, Jenny

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De novo variants in MRTFB have gain-of-function activity in Drosophila and are associated with a novel neurodevelopmental phenotype with dysmorphic features von Kanca, Oguz, Jangam, Sharayu, Tifft, Cynthia, Russell, Bianca E., Amendola, Laura, Andrews, Ashley, Ashley, Euan A., Bacino, Carlos A., Bademci, Guney, Baldridge, Dustin, Bale, Jim, Beck, Anita, Bennett, Jimmy, Bivona, Stephanie, Blue, Elizabeth, Boyd, Brenna, Briere, Lauren C., Burke, Elizabeth A., Burrage, Lindsay C., Byers, Peter, Carey, John, Cassini, Thomas, Coakley, Terra R., Cobban, Laurel A., Cogan, Joy D., Coggins, Matthew, Colley, Heather A., Cooper, Cynthia M., Corona, Rosario, Crouse, Andrew B., Dai, Hongzheng, Davis, Joie, Dell'Angelica, Esteban C., Eckstein, David J., Emrick, Lisa T., Hadley, Don, Hamid, Rizwan, Hassey, Kelly, Hayes, Nichole, Horike-Pyne, Martha, Huang, Alden, Isasi, Rosario, Izumi, Kosuke, Jarvik, Gail P., Jarvik, Jeffrey, Jayadev, Suman, Jobanputra, Vaidehi, Karaviti, Lefkothea, Kennedy, Jennifer, Kohler, Jennefer N., Korrick, Susan, Krakow, Deborah, Krasnewich, Donna M., Lanza, Ian R., Lee, Brendan H., Loo, Sandra K., MacRae, Calum A., Maghiro, AudreyStephannie, Marth, Gabor, McCauley, Jacob, McConkie-Rosell, Allyn, McCray, Alexa T., McGee, Elisabeth, Might, Matthew, Mirzaa, Ghayda, Mulvihill, John, Nicholas, Sarah K., Orengo, James P., Pak, Stephen, Pallais, J. Carl, Palmer, Christina G.S., Parker, Neil H., Pusey Swerdzewski, Barbara N., Quinlan, Aaron, Reuter, Chloe M., Rives, Lynette, Rossignol, Francis, Sacco, Ralph, Sampson, Jacinda B., Saporta, Mario, Schedl, Timothy, Shashi, Vandana, Shin, Jimann, Silverman, Edwin K., Solem, Emily, Solnica-Krezel, Lilianna, Solomon, Ben, Spillmann, Rebecca C., Sullivan, Kathleen, Sybert, Virginia, Tabor, Holly K., Vanderver, Adeline, Velinder, Matt, Walley, Nicole M., Wambach, Jennifer, Ward, Patricia A., Hubshman, Monika Weisz, Yamamoto, Shinya, Zhang, Zhe, Zuchner, Stephan

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Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height von Tatton-Brown, Katrina, Hanks, Sandra, Ruark, Elise, Zachariou, Anna, Duarte, Silvana Del Vecchio, Ramsay, Emma, Snape, Katie, Murray, Anne, Perdeaux, Elizabeth R, Seal, Sheila, Loveday, Chey, Banka, Siddharth, Clericuzio, Carol, Flinter, Frances, Magee, Alex, McConnell, Vivienne, Patton, Michael, Raith, Wolfgang, Rankin, Julia, Splitt, Miranda, Strenger, Volker, Taylor, Clare, Wheeler, Patricia, Temple, Karen I, Cole, Trevor, Douglas, Jenny, Rahman, Nazneen

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FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women von Figlioli, Gisella, Billaud, Amandine, Ahearn, Thomas U, Antonenkova, Natalia N, Becher, Heiko, Beckmann, Matthias W, Behrens, Sabine, Benitez, Javier, Bermisheva, Marina, Blok, Marinus J, Bogdanova, Natalia V, Bonanni, Bernardo, Burwinkel, Barbara, Camp, Nicola J, Campbell, Archie, Castelao, Jose E, Cessna, Melissa H, Chanock, Stephen J, Czene, Kamila, Devilee, Peter, Dörk, Thilo, Engel, Christoph, Eriksson, Mikael, Fasching, Peter A, Figueroa, Jonine D, Gabrielson, Marike, Gago-Dominguez, Manuela, García-Closas, Montserrat, González-Neira, Anna, Grassmann, Felix, Guénel, Pascal, Gündert, Melanie, Hadjisavvas, Andreas, Hahnen, Eric, Hall, Per, Hamann, Ute, Harrington, Patricia A, He, Wei, Hillemanns, Peter, Hollestelle, Antoinette, Hooning, Maartje J, Hoppe, Reiner, Howell, Anthony, Humphreys, Keith, Jager, Agnes, Jakubowska, Anna, Khusnutdinova, Elza K, Ko, Yon-Dschun, Kristensen, Vessela N, Lindblom, Annika, Lissowska, Jolanta, Lubiński, Jan, Mannermaa, Arto, Manoukian, Siranoush, Margolin, Sara, Mavroudis, Dimitrios, Newman, William G, Obi, Nadia, Panayiotidis, Mihalis I, Rashid, Muhammad U, Rhenius, Valerie, Rookus, Matti A, Saloustros, Emmanouil, Sawyer, Elinor J, Schmutzler, Rita K, Shah, Mitul, Sironen, Reijo, Southey, Melissa C, Suvanto, Maija, Tollenaar, Rob A E M, Tomlinson, Ian, Truong, Thérèse, van der Kolk, Lizet E, van Veen, Elke M, Wappenschmidt, Barbara, Yang, Xiaohong R, Bolla, Manjeet K, Dennis, Joe, Dunning, Alison M, Easton, Douglas F, Lush, Michael, Michailidou, Kyriaki, Pharoah, Paul D P, Wang, Qin, Adank, Muriel A, Schmidt, Marjanka K, Andrulis, Irene L, Chang-Claude, Jenny, Nevanlinna, Heli, Chenevix-Trench, Georgia, Evans, D Gareth, Milne, Roger L, Radice, Paolo, Peterlongo, Paolo

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Rare disease patient matchmaking: development and outcomes of an internet case-finding strategy in the Undiagnosed Diseases Network von LeBlanc, Kimberly, Kelley, Emily G., Nagy, Anna, Bater, Jorick, Berro, Tala, McGuinness, Molly A., Studwell, Courtney, Might, Matthew

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Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer‐specific survival von Morra, Anna, Schreurs, Maartje A. C., Anton‐Culver, Hoda, Augustinsson, Annelie, Bojesen, Stig E., Brauch, Hiltrud, Buys, Saundra S., Castelao, Jose E., Cessna, Melissa H., Chung, Wendy K., Gram, Inger Torhild, Naume, Bjørn, Geisler, Jürgen, Cross, Simon S., Easton, Douglas F., Eccles, Diana M., Eriksson, Mikael, Evans, D. Gareth, Fehm, Tanja N., Flyger, Henrik, Gabrielson, Marike, García‐Sáenz, José A., Gündert, Melanie, Hahnen, Eric, Hartikainen, Jaana M., Hoppe, Reiner, Clarke, Christine, Marsh, Deborah, Carpenter, Jane, Pathmanathan, Nirmala, Graham, J. Dinny, Sachchithananthan, Mythily, Amor, David, Balleine, Rosemary, Beesley, Jonathan, Bennett, Ian, Burke, Jo, Butow, Phyllis, Campbell, Ian, Chenevix‐Trench, Georgia, Cohen, Paul, Crook, Ashley, Cui, James, Dawson, Sarah‐Jane, Dixon, Joanne, Edwards, Stacey, Fong, Peter, Gattas, Mike, George, Peter, Kollias, James, Lakhani, Sunil, Lee, Jason, Lindeman, Geoff, Lipton, Lara, Lobb, Liz, Marsh, Deborah, O’Connell, Shona, Pachter, Nick, Phillips, Kelly, Pieper, Ellen, Ramus, Susan, Rickard, Edwina, Saunus, Jodi, Scott, Rodney, Scott, Clare, Shelling, Andrew, Taylor, Jessica, Taylor, Renea, Thorne, Heather, Trainer, Alison, Tucker, Kathy, Walker, Logan, Winship, Ingrid, Zaheed, Milita, Jakubowska, Anna, Jernström, Helena, John, Esther M., Kristensen, Vessela N., Lambrechts, Diether, Lindblom, Annika, Lubiński, Jan, Lux, Michael P., Mulligan, Anna Marie, Muranen, Taru A., Newman, William G., Obi, Nadia, Patel, Alpa V., Phillips, Kelly‐Anne, Plaseska‐Karanfilska, Dijana, Presneau, Nadege, Pylkäs, Katri, Rashid, Muhammad U., Sawyer, Elinor J., Schuetze, Sabine, Tapper, William J., Troester, Melissa A., Veen, Elke M., Wang, Qin, Winqvist, Robert, Ziogas, Argyrios

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Low-dose paclitaxel elution by novel bioerodible sol-gel coating on stents inhibits neointima with low toxicity in porcine coronary arteries von Shinke, Toshiro, Geva, Sarah, Pendyala, Lakshmana, Jabara, Refat, Li, Jinsheng, Chen, Jack P, Venegoni, Anna, Colley, Kenneth, Klein, Richard, Chronos, Nicolas, Robinson, Keith, Hou, Dongming

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Evaluation of a workshop to improve community involvement in community-based participatory research efforts von Stewart, M K, Colley, Dianne, Felix, Holly, Huff, Anna, Shelby, Beatrice, Strickland, Earline, McCabe-Sellers, Beverly, Redmond, Patricia, Evans, Margaret, Baker, Bessie, Stephens, Glenda, Bogle, Margaret L

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Around-the-Clock Observations of the Q0957+561A,B Gravitationally Lensed Quasar. II. Results for the Second Observing Season von Colley, Wesley N, Schild, Rudolph E, Abajas, Cristina, Alcalde, David, Aslan, Zeki, Bikmaev, Ilfan, Chavushyan, Vahram, Chinarro, Luis, Cournoyer, Jean-Philippe, Crowe, Richard, Dudinov, Vladimir, Evans, Anna Kathinka Dalland, Jeon, Young-Beom, Goicoechea, Luis J, Golbasi, Orhan, Khamitov, Irek, Kjernsmo, Kjetil, Lee, Hyun Ju, Lee, Jonghwan, Lee, Ki Won, Lee, Myung Gyoon, Lopez-Cruz, Omar, Mediavilla, Evencio, Moffat, Anthony F. J, Mujica, Raul, Ullan, Aurora, Muñoz, José, Oscoz, Alexander, Park, Myeong-Gu, Purves, Norman, Saanum, Oyvind, Sakhibullin, Nail, Serra-Ricart, Miquel, Sinelnikov, Igor, Stabell, Rolf, Stockton, Alan, Teuber, Jan, Thompson, Roy, Woo, Hwa-Sung, Zheleznyak, Alexander

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