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	521.	Sugar-sweetened beverage intake associations with fasting glucose and insulin concentrations are not modified by selected genetic variants in a ChREBP-FGF21 pathway: a meta-analysis. [electronic resource] by McKeown, Nicola M Dashti, Hassan S Ma, Jiantao Haslam, Danielle E Kiefte-de Jong, Jessica C Smith, Caren E Tanaka, Toshiko Graff, Mariaelisa Lemaitre, Rozenn N Rybin, Denis Sonestedt, Emily Frazier-Wood, Alexis C Mook-Kanamori, Dennis O Li, Yanping Wang, Carol A Leermakers, Elisabeth T M Mikkilä, Vera Young, Kristin L Mukamal, Kenneth J Cupples, L Adrienne Schulz, Christina-Alexandra Chen, Tzu-An Li-Gao, Ruifang Huang, Tao Oddy, Wendy H Raitakari, Olli Rice, Kenneth Meigs, James B Ericson, Ulrika Steffen, Lyn M Rosendaal, Frits R Hofman, Albert Kähönen, Mika Psaty, Bruce M Brunkwall, Louise Uitterlinden, Andre G Viikari, Jorma Siscovick, David S Seppälä, Ilkka North, Kari E Mozaffarian, Dariush Dupuis, Josée Orho-Melander, Marju Rich, Stephen S de Mutsert, Renée Qi, Lu Pennell, Craig E Franco, Oscar H Lehtimäki, Terho Herman, Mark A Producer: 20181105 In: Diabetologia vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	522.	Common Coding Variants in [electronic resource] by Macri, Vincenzo Brody, Jennifer A Arking, Dan E Hucker, William J Yin, Xiaoyan Lin, Honghuang Mills, Robert W Sinner, Moritz F Lubitz, Steven A Liu, Ching-Ti Morrison, Alanna C Alonso, Alvaro Li, Ning Fedorov, Vadim V Janssen, Paul M Bis, Joshua C Heckbert, Susan R Dolmatova, Elena V Lumley, Thomas Sitlani, Colleen M Cupples, L Adrienne Pulit, Sara L Newton-Cheh, Christopher Barnard, John Smith, Jonathan D Van Wagoner, David R Chung, Mina K Vlahakes, Gus J O'Donnell, Christopher J Rotter, Jerome I Margulies, Kenneth B Morley, Michael P Cappola, Thomas P Benjamin, Emelia J Muzny, Donna Gibbs, Richard A Jackson, Rebecca D Magnani, Jared W Herndon, Caroline N Rich, Stephen S Psaty, Bruce M Milan, David J Boerwinkle, Eric Mohler, Peter J Sotoodehnia, Nona Ellinor, Patrick T Producer: 20190715 In: Circulation. Genomic and precision medicine vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	523.	Genetic diversity is a predictor of mortality in humans. [electronic resource] by Bihlmeyer, Nathan A Brody, Jennifer A Smith, Albert Vernon Lunetta, Kathryn L Nalls, Mike Smith, Jennifer A Tanaka, Toshiko Davies, Gail Yu, Lei Mirza, Saira Saeed Teumer, Alexander Coresh, Josef Pankow, James S Franceschini, Nora Scaria, Anish Oshima, Junko Psaty, Bruce M Gudnason, Vilmundur Eiriksdottir, Gudny Harris, Tamara B Li, Hanyue Karasik, David Kiel, Douglas P Garcia, Melissa Liu, Yongmei Faul, Jessica D Kardia, Sharon Lr Zhao, Wei Ferrucci, Luigi Allerhand, Michael Liewald, David C Redmond, Paul Starr, John M De Jager, Philip L Evans, Denis A Direk, Nese Ikram, Mohammed Arfan Uitterlinden, André Homuth, Georg Lorbeer, Roberto Grabe, Hans J Launer, Lenore Murabito, Joanne M Singleton, Andrew B Weir, David R Bandinelli, Stefania Deary, Ian J Bennett, David A Tiemeier, Henning Kocher, Thomas Lumley, Thomas Arking, Dan E Producer: 20151001 In: BMC genetics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	524.	Genome-wide association studies of MRI-defined brain infarcts: meta-analysis from the CHARGE Consortium. [electronic resource] by Debette, Stéphanie Bis, Joshua C Fornage, Myriam Schmidt, Helena Ikram, M Arfan Sigurdsson, Sigurdur Heiss, Gerardo Struchalin, Maksim Smith, Albert V van der Lugt, Aad DeCarli, Charles Lumley, Thomas Knopman, David S Enzinger, Christian Eiriksdottir, Gudny Koudstaal, Peter J DeStefano, Anita L Psaty, Bruce M Dufouil, Carole Catellier, Diane J Fazekas, Franz Aspelund, Thor Aulchenko, Yurii S Beiser, Alexa Rotter, Jerome I Tzourio, Christophe Shibata, Dean K Tscherner, Maria Harris, Tamara B Rivadeneira, Fernando Atwood, Larry D Rice, Kenneth Gottesman, Rebecca F van Buchem, Mark A Uitterlinden, Andre G Kelly-Hayes, Margaret Cushman, Mary Zhu, Yicheng Boerwinkle, Eric Gudnason, Vilmundur Hofman, Albert Romero, Jose R Lopez, Oscar van Duijn, Cornelia M Au, Rhoda Heckbert, Susan R Wolf, Philip A Mosley, Thomas H Seshadri, Sudha Breteler, Monique M B Schmidt, Reinhold Launer, Lenore J Longstreth, W T Producer: 20100223 In: Stroke vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	525.	Impact of ancestry and common genetic variants on QT interval in African Americans. [electronic resource] by Smith, J Gustav Avery, Christy L Evans, Daniel S Nalls, Michael A Meng, Yan A Smith, Erin N Palmer, Cameron Tanaka, Toshiko Mehra, Reena Butler, Anne M Young, Taylor Buxbaum, Sarah G Kerr, Kathleen F Berenson, Gerald S Schnabel, Renate B Li, Guo Ellinor, Patrick T Magnani, Jared W Chen, Wei Bis, Joshua C Curb, J David Hsueh, Wen-Chi Rotter, Jerome I Liu, Yongmei Newman, Anne B Limacher, Marian C North, Kari E Reiner, Alexander P Quibrera, P Miguel Schork, Nicholas J Singleton, Andrew B Psaty, Bruce M Soliman, Elsayed Z Solomon, Allen J Srinivasan, Sathanur R Alonso, Alvaro Wallace, Robert Redline, Susan Zhang, Zhu-Ming Post, Wendy S Zonderman, Alan B Taylor, Herman A Murray, Sarah S Ferrucci, Luigi Arking, Dan E Evans, Michele K Fox, Ervin R Sotoodehnia, Nona Heckbert, Susan R Whitsel, Eric A Newton-Cheh, Christopher Producer: 20130801 In: Circulation. Cardiovascular genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	526.	Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts. [electronic resource] by Butler, Anne M Yin, Xiaoyan Evans, Daniel S Nalls, Michael A Smith, Erin N Tanaka, Toshiko Li, Guo Buxbaum, Sarah G Whitsel, Eric A Alonso, Alvaro Arking, Dan E Benjamin, Emelia J Berenson, Gerald S Bis, Josh C Chen, Wei Deo, Rajat Ellinor, Patrick T Heckbert, Susan R Heiss, Gerardo Hsueh, Wen-Chi Keating, Brendan J Kerr, Kathleen F Li, Yun Limacher, Marian C Liu, Yongmei Lubitz, Steven A Marciante, Kristin D Mehra, Reena Meng, Yan A Newman, Anne B Newton-Cheh, Christopher North, Kari E Palmer, Cameron D Psaty, Bruce M Quibrera, P Miguel Redline, Susan Reiner, Alex P Rotter, Jerome I Schnabel, Renate B Schork, Nicholas J Singleton, Andrew B Smith, J Gustav Soliman, Elsayed Z Srinivasan, Sathanur R Zhang, Zhu-ming Zonderman, Alan B Ferrucci, Luigi Murray, Sarah S Evans, Michele K Sotoodehnia, Nona Magnani, Jared W Avery, Christy L Producer: 20130801 In: Circulation. Cardiovascular genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	527.	Habitual sleep duration is associated with BMI and macronutrient intake and may be modified by CLOCK genetic variants. [electronic resource] by Dashti, Hassan S Follis, Jack L Smith, Caren E Tanaka, Toshiko Cade, Brian E Gottlieb, Daniel J Hruby, Adela Jacques, Paul F Lamon-Fava, Stefania Richardson, Kris Saxena, Richa Scheer, Frank A J L Kovanen, Leena Bartz, Traci M Perälä, Mia-Maria Jonsson, Anna Frazier-Wood, Alexis C Kalafati, Ioanna-Panagiota Mikkilä, Vera Partonen, Timo Lemaitre, Rozenn N Lahti, Jari Hernandez, Dena G Toft, Ulla Johnson, W Craig Kanoni, Stavroula Raitakari, Olli T Perola, Markus Psaty, Bruce M Ferrucci, Luigi Grarup, Niels Highland, Heather M Rallidis, Loukianos Kähönen, Mika Havulinna, Aki S Siscovick, David S Räikkönen, Katri Jørgensen, Torben Rotter, Jerome I Deloukas, Panos Viikari, Jorma S A Mozaffarian, Dariush Linneberg, Allan Seppälä, Ilkka Hansen, Torben Salomaa, Veikko Gharib, Sina A Eriksson, Johan G Bandinelli, Stefania Pedersen, Oluf Rich, Stephen S Dedoussis, George Lehtimäki, Terho Ordovás, José M Producer: 20150218 In: The American journal of clinical nutrition vol. 101 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	528.	Lipid-related markers and cardiovascular disease prediction. [electronic resource] by Di Angelantonio, Emanuele Gao, Pei Pennells, Lisa Kaptoge, Stephen Caslake, Muriel Thompson, Alexander Butterworth, Adam S Sarwar, Nadeem Wormser, David Saleheen, Danish Ballantyne, Christie M Psaty, Bruce M Sundström, Johan Ridker, Paul M Nagel, Dorothea Gillum, Richard F Ford, Ian Ducimetiere, Pierre Kiechl, Stefan Koenig, Wolfgang Dullaart, Robin P F Assmann, Gerd D'Agostino, Ralph B Dagenais, Gilles R Cooper, Jackie A Kromhout, Daan Onat, Altan Tipping, Robert W Gómez-de-la-Cámara, Agustín Rosengren, Annika Sutherland, Susan E Gallacher, John Fowkes, F Gerry R Casiglia, Edoardo Hofman, Albert Salomaa, Veikko Barrett-Connor, Elizabeth Clarke, Robert Brunner, Eric Jukema, J Wouter Simons, Leon A Sandhu, Manjinder Wareham, Nicholas J Khaw, Kay-Tee Kauhanen, Jussi Salonen, Jukka T Howard, William J Nordestgaard, Børge G Wood, Angela M Thompson, Simon G Boekholdt, S Matthijs Sattar, Naveed Packard, Chris Gudnason, Vilmundur Danesh, John Producer: 20120719 In: JAMA vol. 307 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	529.	Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations. [electronic resource] by Ganesh, Santhi K Chasman, Daniel I Larson, Martin G Guo, Xiuqing Verwoert, Germain Bis, Joshua C Gu, Xiangjun Smith, Albert V Yang, Min-Lee Zhang, Yan Ehret, Georg Rose, Lynda M Hwang, Shih-Jen Papanicolau, George J Sijbrands, Eric J Rice, Kenneth Eiriksdottir, Gudny Pihur, Vasyl Ridker, Paul M Vasan, Ramachandran S Newton-Cheh, Christopher Raffel, Leslie J Amin, Najaf Rotter, Jerome I Liu, Kiang Launer, Lenore J Xu, Ming Caulfield, Mark Morrison, Alanna C Johnson, Andrew D Vaidya, Dhananjay Dehghan, Abbas Li, Guo Bouchard, Claude Harris, Tamara B Zhang, He Boerwinkle, Eric Siscovick, David S Gao, Wei Uitterlinden, Andre G Rivadeneira, Fernando Hofman, Albert Willer, Cristen J Franco, Oscar H Huo, Yong Witteman, Jacqueline C M Munroe, Patricia B Gudnason, Vilmundur Palmas, Walter van Duijn, Cornelia Fornage, Myriam Levy, Daniel Psaty, Bruce M Chakravarti, Aravinda Producer: 20140827 In: American journal of human genetics vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	530.	Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation. [electronic resource] by Sinner, Moritz F Tucker, Nathan R Lunetta, Kathryn L Ozaki, Kouichi Smith, J Gustav Trompet, Stella Bis, Joshua C Lin, Honghuang Chung, Mina K Nielsen, Jonas B Lubitz, Steven A Krijthe, Bouwe P Magnani, Jared W Ye, Jiangchuan Gollob, Michael H Tsunoda, Tatsuhiko Müller-Nurasyid, Martina Lichtner, Peter Peters, Annette Dolmatova, Elena Kubo, Michiaki Smith, Jonathan D Psaty, Bruce M Smith, Nicholas L Jukema, J Wouter Chasman, Daniel I Albert, Christine M Ebana, Yusuke Furukawa, Tetsushi Macfarlane, Peter W Harris, Tamara B Darbar, Dawood Dörr, Marcus Holst, Anders G Svendsen, Jesper H Hofman, Albert Uitterlinden, Andre G Gudnason, Vilmundur Isobe, Mitsuaki Malik, Rainer Dichgans, Martin Rosand, Jonathan Van Wagoner, David R Benjamin, Emelia J Milan, David J Melander, Olle Heckbert, Susan R Ford, Ian Liu, Yongmei Barnard, John Olesen, Morten S Stricker, Bruno H C Tanaka, Toshihiro Kääb, Stefan Ellinor, Patrick T Producer: 20150413 In: Circulation vol. 130 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	531.	Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease. [electronic resource] by Jakobsdottir, Johanna van der Lee, Sven J Bis, Joshua C Chouraki, Vincent Li-Kroeger, David Yamamoto, Shinya Grove, Megan L Naj, Adam Vronskaya, Maria Salazar, Jose L DeStefano, Anita L Brody, Jennifer A Smith, Albert V Amin, Najaf Sims, Rebecca Ibrahim-Verbaas, Carla A Choi, Seung-Hoan Satizabal, Claudia L Lopez, Oscar L Beiser, Alexa Ikram, M Arfan Garcia, Melissa E Hayward, Caroline Varga, Tibor V Ripatti, Samuli Franks, Paul W Hallmans, Göran Rolandsson, Olov Jansson, Jan-Håkon Porteous, David J Salomaa, Veikko Eiriksdottir, Gudny Rice, Kenneth M Bellen, Hugo J Levy, Daniel Uitterlinden, Andre G Emilsson, Valur Rotter, Jerome I Aspelund, Thor O'Donnell, Christopher J Fitzpatrick, Annette L Launer, Lenore J Hofman, Albert Wang, Li-San Williams, Julie Schellenberg, Gerard D Boerwinkle, Eric Psaty, Bruce M Seshadri, Sudha Shulman, Joshua M Gudnason, Vilmundur van Duijn, Cornelia M Producer: 20170509 In: PLoS genetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	532.	Fifteen Genetic Loci Associated With the Electrocardiographic P Wave. [electronic resource] by Christophersen, Ingrid E Magnani, Jared W Yin, Xiaoyan Barnard, John Weng, Lu-Chen Arking, Dan E Niemeijer, Maartje N Lubitz, Steven A Avery, Christy L Duan, Qing Felix, Stephan B Bis, Joshua C Kerr, Kathleen F Isaacs, Aaron Müller-Nurasyid, Martina Müller, Christian North, Kari E Reiner, Alex P Tinker, Lesley F Kors, Jan A Teumer, Alexander Petersmann, Astrid Sinner, Moritz F Buzkova, Petra Smith, Jonathan D Van Wagoner, David R Völker, Uwe Waldenberger, Melanie Peters, Annette Meitinger, Thomas Limacher, Marian C Wilhelmsen, Kirk C Psaty, Bruce M Hofman, Albert Uitterlinden, Andre Krijthe, Bouwe P Zhang, Zhu-Ming Schnabel, Renate B Kääb, Stefan van Duijn, Cornelia Rotter, Jerome I Sotoodehnia, Nona Dörr, Marcus Li, Yun Chung, Mina K Soliman, Elsayed Z Alonso, Alvaro Whitsel, Eric A Stricker, Bruno H Benjamin, Emelia J Heckbert, Susan R Ellinor, Patrick T Producer: 20180112 In: Circulation. Cardiovascular genetics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	533.	Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure. [electronic resource] by Smith, J Gustav Felix, Janine F Morrison, Alanna C Kalogeropoulos, Andreas Trompet, Stella Wilk, Jemma B Gidlöf, Olof Wang, Xinchen Morley, Michael Mendelson, Michael Joehanes, Roby Ligthart, Symen Shan, Xiaoyin Bis, Joshua C Wang, Ying A Sjögren, Marketa Ngwa, Julius Brandimarto, Jeffrey Stott, David J Aguilar, David Rice, Kenneth M Sesso, Howard D Demissie, Serkalem Buckley, Brendan M Taylor, Kent D Ford, Ian Yao, Chen Liu, Chunyu Sotoodehnia, Nona van der Harst, Pim Stricker, Bruno H Ch Kritchevsky, Stephen B Liu, Yongmei Gaziano, J Michael Hofman, Albert Moravec, Christine S Uitterlinden, André G Kellis, Manolis van Meurs, Joyce B Margulies, Kenneth B Dehghan, Abbas Levy, Daniel Olde, Björn Psaty, Bruce M Cupples, L Adrienne Jukema, J Wouter Djousse, Luc Franco, Oscar H Boerwinkle, Eric Boyer, Laurie A Newton-Cheh, Christopher Butler, Javed Vasan, Ramachandran S Cappola, Thomas P Smith, Nicholas L Producer: 20170512 In: PLoS genetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	534.	Blood Leukocyte DNA Methylation Predicts Risk of Future Myocardial Infarction and Coronary Heart Disease. [electronic resource] by Agha, Golareh Mendelson, Michael M Ward-Caviness, Cavin K Joehanes, Roby Huan, TianXiao Gondalia, Rahul Salfati, Elias Brody, Jennifer A Fiorito, Giovanni Bressler, Jan Chen, Brian H Ligthart, Symen Guarrera, Simonetta Colicino, Elena Just, Allan C Wahl, Simone Gieger, Christian Vandiver, Amy R Tanaka, Toshiko Hernandez, Dena G Pilling, Luke C Singleton, Andrew B Sacerdote, Carlotta Krogh, Vittorio Panico, Salvatore Tumino, Rosario Li, Yun Zhang, Guosheng Stewart, James D Floyd, James S Wiggins, Kerri L Rotter, Jerome I Multhaup, Michael Bakulski, Kelly Horvath, Steven Tsao, Philip S Absher, Devin M Vokonas, Pantel Hirschhorn, Joel Fallin, M Daniele Liu, Chunyu Bandinelli, Stefania Boerwinkle, Eric Dehghan, Abbas Schwartz, Joel D Psaty, Bruce M Feinberg, Andrew P Hou, Lifang Ferrucci, Luigi Sotoodehnia, Nona Matullo, Giuseppe Peters, Annette Fornage, Myriam Assimes, Themistocles L Whitsel, Eric A Levy, Daniel Baccarelli, Andrea A Producer: 20200527 In: Circulation vol. 140 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	535.	Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease. [electronic resource] by Rannikmäe, Kristiina Davies, Gail Thomson, Pippa A Bevan, Steve Devan, William J Falcone, Guido J Traylor, Matthew Anderson, Christopher D Battey, Thomas W K Radmanesh, Farid Deka, Ranjan Woo, Jessica G Martin, Lisa J Jimenez-Conde, Jordi Selim, Magdy Brown, Devin L Silliman, Scott L Kidwell, Chelsea S Montaner, Joan Langefeld, Carl D Slowik, Agnieszka Hansen, Björn M Lindgren, Arne G Meschia, James F Fornage, Myriam Bis, Joshua C Debette, Stéphanie Ikram, Mohammad A Longstreth, Will T Schmidt, Reinhold Zhang, Cathy R Yang, Qiong Sharma, Pankaj Kittner, Steven J Mitchell, Braxton D Holliday, Elizabeth G Levi, Christopher R Attia, John Rothwell, Peter M Poole, Deborah L Boncoraglio, Giorgio B Psaty, Bruce M Malik, Rainer Rost, Natalia Worrall, Bradford B Dichgans, Martin Van Agtmael, Tom Woo, Daniel Markus, Hugh S Seshadri, Sudha Rosand, Jonathan Sudlow, Cathie L M Producer: 20150615 In: Neurology vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	536.	Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. [electronic resource] by Benjamin, Emelia J Rice, Kenneth M Arking, Dan E Pfeufer, Arne van Noord, Charlotte Smith, Albert V Schnabel, Renate B Bis, Joshua C Boerwinkle, Eric Sinner, Moritz F Dehghan, Abbas Lubitz, Steven A D'Agostino, Ralph B Lumley, Thomas Ehret, Georg B Heeringa, Jan Aspelund, Thor Newton-Cheh, Christopher Larson, Martin G Marciante, Kristin D Soliman, Elsayed Z Rivadeneira, Fernando Wang, Thomas J Eiríksdottir, Gudny Levy, Daniel Psaty, Bruce M Li, Man Chamberlain, Alanna M Hofman, Albert Vasan, Ramachandran S Harris, Tamara B Rotter, Jerome I Kao, W H Linda Agarwal, Sunil K Stricker, Bruno H Ch Wang, Ke Launer, Lenore J Smith, Nicholas L Chakravarti, Aravinda Uitterlinden, André G Wolf, Philip A Sotoodehnia, Nona Köttgen, Anna van Duijn, Cornelia M Meitinger, Thomas Mueller, Martina Perz, Siegfried Steinbeck, Gerhard Wichmann, H-Erich Lunetta, Kathryn L Heckbert, Susan R Gudnason, Vilmundur Alonso, Alvaro Kääb, Stefan Ellinor, Patrick T Witteman, Jacqueline C M Producer: 20090909 In: Nature genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	537.	Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium. [electronic resource] by Bis, Joshua C Sitlani, Colleen Irvin, Ryan Avery, Christy L Smith, Albert Vernon Sun, Fangui Evans, Daniel S Musani, Solomon K Li, Xiaohui Trompet, Stella Krijthe, Bouwe P Harris, Tamara B Quibrera, P Miguel Brody, Jennifer A Demissie, Serkalem Davis, Barry R Wiggins, Kerri L Tranah, Gregory J Lange, Leslie A Sotoodehnia, Nona Stott, David J Franco, Oscar H Launer, Lenore J Stürmer, Til Taylor, Kent D Cupples, L Adrienne Eckfeldt, John H Smith, Nicholas L Liu, Yongmei Wilson, James G Heckbert, Susan R Buckley, Brendan M Ikram, M Arfan Boerwinkle, Eric Chen, Yii-Der Ida de Craen, Anton J M Uitterlinden, Andre G Rotter, Jerome I Ford, Ian Hofman, Albert Sattar, Naveed Slagboom, P Eline Westendorp, Rudi G J Gudnason, Vilmundur Vasan, Ramachandran S Lumley, Thomas Cummings, Steven R Taylor, Herman A Post, Wendy Jukema, J Wouter Stricker, Bruno H Whitsel, Eric A Psaty, Bruce M Arnett, Donna Producer: 20160616 In: PloS one vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	538.	Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data. [electronic resource] by He, Karen Y Li, Xiaoyin Kelly, Tanika N Liang, Jingjing Cade, Brian E Assimes, Themistocles L Becker, Lewis C Beitelshees, Amber L Bress, Adam P Chang, Yen-Pei Christy Chen, Yii-Der Ida de Vries, Paul S Fox, Ervin R Franceschini, Nora Furniss, Anna Gao, Yan Guo, Xiuqing Haessler, Jeffrey Hwang, Shih-Jen Irvin, Marguerite Ryan Kalyani, Rita R Liu, Ching-Ti Liu, Chunyu Martin, Lisa Warsinger Montasser, May E Muntner, Paul M Mwasongwe, Stanford Palmas, Walter Reiner, Alex P Shimbo, Daichi Smith, Jennifer A Snively, Beverly M Yanek, Lisa R Boerwinkle, Eric Correa, Adolfo Cupples, L Adrienne He, Jiang Kardia, Sharon L R Kooperberg, Charles Mathias, Rasika A Mitchell, Braxton D Psaty, Bruce M Vasan, Ramachandran S Rao, D C Rich, Stephen S Rotter, Jerome I Wilson, James G Chakravarti, Aravinda Morrison, Alanna C Levy, Daniel Arnett, Donna K Redline, Susan Zhu, Xiaofeng Producer: 20190219 In: Human genetics vol. 138 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	539.	Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis. [electronic resource] by Polfus, Linda M Khajuria, Rajiv K Schick, Ursula M Pankratz, Nathan Pazoki, Raha Brody, Jennifer A Chen, Ming-Huei Auer, Paul L Floyd, James S Huang, Jie Lange, Leslie van Rooij, Frank J A Gibbs, Richard A Metcalf, Ginger Muzny, Donna Veeraraghavan, Narayanan Walter, Klaudia Chen, Lu Yanek, Lisa Becker, Lewis C Peloso, Gina M Wakabayashi, Aoi Kals, Mart Metspalu, Andres Esko, Tõnu Fox, Keolu Wallace, Robert Franceschini, Nora Matijevic, Nena Rice, Kenneth M Bartz, Traci M Lyytikäinen, Leo-Pekka Kähönen, Mika Lehtimäki, Terho Raitakari, Olli T Li-Gao, Ruifang Mook-Kanamori, Dennis O Lettre, Guillaume van Duijn, Cornelia M Franco, Oscar H Rich, Stephen S Rivadeneira, Fernando Hofman, Albert Uitterlinden, André G Wilson, James G Psaty, Bruce M Soranzo, Nicole Dehghan, Abbas Boerwinkle, Eric Zhang, Xiaoling Johnson, Andrew D O'Donnell, Christopher J Johnsen, Jill M Reiner, Alexander P Ganesh, Santhi K Sankaran, Vijay G Producer: 20170509 In: American journal of human genetics vol. 99 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	540.	Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis. [electronic resource] by Manousaki, Despoina Dudding, Tom Haworth, Simon Hsu, Yi-Hsiang Liu, Ching-Ti Medina-Gómez, Carolina Voortman, Trudy van der Velde, Nathalie Melhus, Håkan Robinson-Cohen, Cassianne Cousminer, Diana L Nethander, Maria Vandenput, Liesbeth Noordam, Raymond Forgetta, Vincenzo Greenwood, Celia M T Biggs, Mary L Psaty, Bruce M Rotter, Jerome I Zemel, Babette S Mitchell, Jonathan A Taylor, Bruce Lorentzon, Mattias Karlsson, Magnus Jaddoe, Vincent V W Tiemeier, Henning Campos-Obando, Natalia Franco, Oscar H Utterlinden, Andre G Broer, Linda van Schoor, Natasja M Ham, Annelies C Ikram, M Arfan Karasik, David de Mutsert, Renée Rosendaal, Frits R den Heijer, Martin Wang, Thomas J Lind, Lars Orwoll, Eric S Mook-Kanamori, Dennis O Michaëlsson, Karl Kestenbaum, Bryan Ohlsson, Claes Mellström, Dan de Groot, Lisette C P G M Grant, Struan F A Kiel, Douglas P Zillikens, M Carola Rivadeneira, Fernando Sawcer, Stephen Timpson, Nicholas J Richards, J Brent Publication details: American journal of human genetics 12 2018 In: American journal of human genetics vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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