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Functional Pace-Mapping Responses for Identification of Targets for Catheter Ablation of Scar-Mediated Ventricular Tachycardia
Tung, Roderick, Mathuria, Nilesh, Michowitz, Yoav, Yu, Ricky, Buch, Eric, Bradfield, Jason, Mandapati, Ravi, Wiener, Isaac, Boyle, Noel, Shivkumar, Kalyanam
Published in Circulation. Arrhythmia and electrophysiology (01.04.2012)
Published in Circulation. Arrhythmia and electrophysiology (01.04.2012)
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Genome-wide Association Study of Smoking Initiation and Current Smoking
Vink, Jacqueline M., Smit, August B., de Geus, Eco J.C., Sullivan, Patrick, Willemsen, Gonneke, Hottenga, Jouke-Jan, Smit, Johannes H., Hoogendijk, Witte J., Zitman, Frans G., Peltonen, Leena, Kaprio, Jaakko, Pedersen, Nancy L., Magnusson, Patrik K., Spector, Tim D., Kyvik, Kirsten Ohm, Morley, Katherine I., Heath, Andrew C., Martin, Nicholas G., Westendorp, Rudi G.J., Slagboom, P. Eline, Tiemeier, Henning, Hofman, Albert, Uitterlinden, Andre G., Aulchenko, Yurii S., Amin, Najaf, van Duijn, Cornelia, Penninx, Brenda W., Boomsma, Dorret I.
Published in American journal of human genetics (13.03.2009)
Published in American journal of human genetics (13.03.2009)
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Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium
Figueroa, Jonine D., Garcia-Closas, Montserrat, Humphreys, Manjeet, Platte, Radka, Apicella, Carmel, Hammet, Fleur, Schmidt, Marjanka K., Broeks, Annegien, Van't Veer, Laura J., Fasching, Peter A., Beckmann, Matthias W., Ekici, Arif B., Strick, Reiner, Peto, Julian, dos Santos Silva, Isabel, Fletcher, Olivia, Marme, Federik, Sohn, Christof, Flyger, Henrik, Nordestgaard, Børge G., Milne, Roger L., Ignacio Arias, Jose, Müller, Heiko, Arndt, Volker, Turnbull, Clare, Brauch, Hiltrud, Brüning, Thomas, Chang-Claude, Jenny, Wang-Gohrke, Shan, Dörk, Thilo, Schürmann, Peter, Bremer, Michael, Heikkinen, Tuomas, Aittomäki, Kristiina, Blomqvist, Carl, Bogdanova, Natalia, Antonenkova, Natalia, Rogov, Yuri I., Karstens, Johann Hinrich, Bermisheva, Marina, Prokofieva, Darya, Hanafievich Gantcev, Shamil, Khusnutdinova, Elza, Lindblom, Annika, Margolin, Sara, Chenevix-Trench, Georgia, Beesley, Jonathan, Chen, Xiaoqing, Mannermaa, Arto, Kosma, Veli-Matti, Soini, Ylermi, Yesilyurt, Betül T., Peeters, Stephanie, Radice, Paolo, Manoukian, Siranoush, Barile, Monica, Lee, Adam M., Diasio, Robert, Wang, Xianshu, Giles, Graham G., Severi, Gianluca, Baglietto, Laura, Offit, Ken, Robson, Mark, Joseph, Vijai, Pylkäs, Katri, Jukkola-Vuorinen, Arja, Grip, Mervi, Andrulis, Irene, Knight, Julia A., O'Malley, Frances P., Brinton, Louise A., Sherman, Mark E., Lissowska, Jolanta, Chanock, Stephen J., van den Ouweland, Ans M.W., Collée, J. Margriet, Hall, Per, Cross, Simon S., Pharoah, Paul, Dunning, Alison M., Yoo, Keun-Young, Ahn, Sei-Hyun, Jakubowska, Anna, Jaworska, Katarzyna, Durda, Katarzyna, Gaborieau, Valerie, Brennan, Paul, McKay, James, Shen, Chen-Yang, Ding, Shian-ling, Hsu, Huan-Ming, Yu, Jyh-Cherng, Anton-Culver, Hoda, Ziogas, Argyrios, Swerdlow, Anthony, Jones, Michael, Trentham-Dietz, Amy, Egan, Kathleen, Titus-Ernstoff, Linda
Published in Human molecular genetics (01.12.2011)
Published in Human molecular genetics (01.12.2011)
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Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction
Ræder, Helge, Johansson, Stefan, Holm, Pål I, Haldorsen, Ingfrid S, Mas, Eric, Sbarra, Véronique, Nermoen, Ingrid, Eide, Stig Å, Grevle, Louise, Bjørkhaug, Lise, Sagen, Jørn V, Aksnes, Lage, Søvik, Oddmund, Lombardo, Dominique, Molven, Anders, Njølstad, Pål Rasmus
Published in Nature genetics (01.01.2006)
Published in Nature genetics (01.01.2006)
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Population stratification confounds genetic association studies among Latinos
Choudhry, Shweta, Coyle, Natasha E., Tang, Hua, Salari, Keyan, Lind, Denise, Clark, Suzanne L., Tsai, Hui-Ju, Naqvi, Mariam, Phong, Angie, Ung, Ngim, Matallana, Henry, Avila, Pedro C., Casal, Jesus, Torres, Alfonso, Nazario, Sylvette, Castro, Richard, Battle, Natalie C., Perez-Stable, Eliseo J., Kwok, Pui-Yan, Sheppard, Dean, Shriver, Mark D., Rodriguez-Cintron, William, Risch, Neil, Ziv, Elad, Burchard, Esteban Gonzàlez
Published in Human genetics (01.01.2006)
Published in Human genetics (01.01.2006)
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Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio
Godler, David Eugeny, Tassone, Flora, Loesch, Danuta Zuzanna, Taylor, Annette Kimball, Gehling, Freya, Hagerman, Randi Jenssen, Burgess, Trent, Ganesamoorthy, Devika, Hennerich, Debbie, Gordon, Lavinia, Evans, Andrew, Choo, K.H., Slater, Howard Robert
Published in Human molecular genetics (15.04.2010)
Published in Human molecular genetics (15.04.2010)
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A unique library of myogenic cells from facioscapulohumeral muscular dystrophy subjects and unaffected relatives: family, disease and cell function
Homma, Sachiko, Chen, Jennifer CJ, Rahimov, Fedik, Beermann, Mary Lou, Hanger, Kendal, Bibat, Genila M, Wagner, Kathryn R, Kunkel, Louis M, Emerson, Charles P, Miller, Jeffrey Boone
Published in European journal of human genetics : EJHG (01.04.2012)
Published in European journal of human genetics : EJHG (01.04.2012)
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Genome-wide Comparison of African-Ancestry Populations from CARe and Other Cohorts Reveals Signals of Natural Selection
Bhatia, Gaurav, Patterson, Nick, Pasaniuc, Bogdan, Zaitlen, Noah, Genovese, Giulio, Pollack, Samuela, Mallick, Swapan, Myers, Simon, Tandon, Arti, Spencer, Chris, Palmer, Cameron D., Adeyemo, Adebowale A., Akylbekova, Ermeg L., Cupples, L. Adrienne, Divers, Jasmin, Fornage, Myriam, Kao, W.H. Linda, Lange, Leslie, Li, Mingyao, Musani, Solomon, Mychaleckyj, Josyf C., Ogunniyi, Adesola, Papanicolaou, George, Rotimi, Charles N., Rotter, Jerome I., Ruczinski, Ingo, Salako, Babatunde, Siscovick, David S., Tayo, Bamidele O., Yang, Qiong, McCarroll, Steve, Sabeti, Pardis, Lettre, Guillaume, De Jager, Phil, Hirschhorn, Joel, Zhu, Xiaofeng, Cooper, Richard, Reich, David, Wilson, James G., Price, Alkes L.
Published in American journal of human genetics (09.09.2011)
Published in American journal of human genetics (09.09.2011)
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A mechanism for immediate reduction in mitral regurgitation after Cardiac resynchronization therapy: Insights from mechanical activation strain mapping
KANZAKI, Hideaki, BAZAZ, Raveen, SCHWARTZMAN, David, DOHI, Kaoru, SADE, L. Elif, GORCSAN, John III
Published in Journal of the American College of Cardiology (19.10.2004)
Published in Journal of the American College of Cardiology (19.10.2004)
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Reduced NODAL Signaling Strength via Mutation of Several Pathway Members Including FOXH1 Is Linked to Human Heart Defects and Holoprosencephaly
Roessler, Erich, Ouspenskaia, Maia V., Karkera, Jayaprakash D., Vélez, Jorge I., Kantipong, Amy, Lacbawan, Felicitas, Bowers, Peter, Belmont, John W., Towbin, Jeffrey A., Goldmuntz, Elizabeth, Feldman, Benjamin, Muenke, Maximilian
Published in American journal of human genetics (01.07.2008)
Published in American journal of human genetics (01.07.2008)
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A Genome-wide Association Study Identifies Three Loci Associated with Mean Platelet Volume
Meisinger, Christa, Prokisch, Holger, Gieger, Christian, Soranzo, Nicole, Mehta, Divya, Rosskopf, Dieter, Lichtner, Peter, Klopp, Norman, Stephens, Jonathan, Watkins, Nicholas A., Deloukas, Panos, Greinacher, Andreas, Koenig, Wolfgang, Nauck, Matthias, Rimmbach, Christian, Völzke, Henry, Peters, Annette, Illig, Thomas, Ouwehand, Willem H., Meitinger, Thomas, Wichmann, H.-Erich, Döring, Angela
Published in American journal of human genetics (09.01.2009)
Published in American journal of human genetics (09.01.2009)
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Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes
Meyre, David, Bouatia-Naji, Nabila, Tounian, Agnès, Samson, Chantal, Lecoeur, Cécile, Vatin, Vincent, Ghoussaini, Maya, Wachter, Christophe, Hercberg, Serge, Charpentier, Guillaume, Patsch, Wolfgang, Pattou, François, Charles, Marie-Aline, Tounian, Patrick, Clément, Karine, Jouret, Béatrice, Weill, Jacques, Maddux, Betty A, Goldfine, Ira D, Walley, Andrew, Boutin, Philippe, Dina, Christian, Froguel, Philippe
Published in Nature genetics (01.08.2005)
Published in Nature genetics (01.08.2005)
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Distinct Variants at LIN28B Influence Growth in Height from Birth to Adulthood
Widén, Elisabeth, Ripatti, Samuli, Cousminer, Diana L., Surakka, Ida, Lappalainen, Tuuli, Järvelin, Marjo-Riitta, Eriksson, Johan G., Raitakari, Olli, Salomaa, Veikko, Sovio, Ulla, Hartikainen, Anna-Liisa, Pouta, Anneli, McCarthy, Mark I., Osmond, Clive, Kajantie, Eero, Lehtimäki, Terho, Viikari, Jorma, Kähönen, Mika, Tyler-Smith, Chris, Freimer, Nelson, Hirschhorn, Joel N., Peltonen, Leena, Palotie, Aarno
Published in American journal of human genetics (14.05.2010)
Published in American journal of human genetics (14.05.2010)
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Replication of the five novel loci for uric acid concentrations and potential mediating mechanisms
van der Harst, Pim, Bakker, Stephan J.L., de Boer, Rudolf A., Wolffenbuttel, Bruce H.R., Johnson, Toby, Caulfield, Mark J., Navis, Gerjan
Published in Human molecular genetics (15.01.2010)
Published in Human molecular genetics (15.01.2010)
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Pathway-driven gene stability selection of two rheumatoid arthritis GWAS identifies and validates new susceptibility genes in receptor mediated signalling pathways
Eleftherohorinou, Hariklia, Hoggart, Clive J., Wright, Victoria J., Levin, Michael, Coin, Lachlan J.M.
Published in Human molecular genetics (01.09.2011)
Published in Human molecular genetics (01.09.2011)
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Mutation and polymorphism spectrum in osteogenesis imperfecta type II: implications for genotype–phenotype relationships
Bodian, Dale L., Chan, Ting-Fung, Poon, Annie, Schwarze, Ulrike, Yang, Kathleen, Byers, Peter H., Kwok, Pui-Yan, Klein, Teri E.
Published in Human molecular genetics (01.02.2009)
Published in Human molecular genetics (01.02.2009)
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A Genome-Wide Association Study Identifies LIPA as a Susceptibility Gene for Coronary Artery Disease
Wild, Philipp S., Zeller, Tanja, Schillert, Arne, Szymczak, Silke, Sinning, Christoph R., Deiseroth, Arne, Schnabel, Renate B., Lubos, Edith, Keller, Till, Eleftheriadis, Medea S., Bickel, Christoph, Rupprecht, Hans J., Wilde, Sandra, Rossmann, Heidi, Diemert, Patrick, Cupples, L. Adrienne, Perret, Claire, Erdmann, Jeanette, Stark, Klaus, Kleber, Marcus E., Epstein, Stephen E., Voight, Benjamin F., Kuulasmaa, Kari, Li, Mingyao, Schäfer, Arne S., Klopp, Norman, Braund, Peter S., Sager, Hendrik B., Demissie, Serkalem, Proust, Carole, König, Inke R., Wichmann, Heinz-Erich, Reinhard, Wibke, Hoffmann, Michael M., Virtamo, Jarmo, Burnett, Mary Susan, Siscovick, David, Wiklund, Per Gunnar, Qu, Liming, El Mokthari, Nour Eddine, Thompson, John R., Peters, Annette, Smith, Albert V., Yon, Emmanuelle, Baumert, Jens, Hengstenberg, Christian, März, Winfried, Amouyel, Philippe, Devaney, Joseph, Schwartz, Stephen M., Saarela, Olli, Mehta, Nehal N., Rubin, Diana, Silander, Kaisa, Hall, Alistair S., Ferrieres, Jean, Harris, Tamara B., Melander, Olle, Kee, Frank, Hakonarson, Hakon, Schrezenmeir, Juergen, Gudnason, Vilmundur, Elosua, Roberto, Arveiler, Dominique, Evans, Alun, Rader, Daniel J., Illig, Thomas, Schreiber, Stefan, Bis, Joshua C., Altshuler, David, Kavousi, Maryam, Witteman, Jaqueline C.M., Uitterlinden, Andre G., Hofman, Albert, Folsom, Aaron R., Barbalic, Maja, Boerwinkle, Eric, Kathiresan, Sekar, Reilly, Muredach P., OʼDonnell, Christopher J., Samani, Nilesh J., Schunkert, Heribert, Cambien, Francois, Lackner, Karl J., Tiret, Laurence, Salomaa, Veikko, Munzel, Thomas, Ziegler, Andreas, Blankenberg, Stefan
Published in Circulation. Cardiovascular genetics (01.08.2011)
Published in Circulation. Cardiovascular genetics (01.08.2011)
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