Breastfeeding after anaesthesia: a review of the pharmacological impact on children by Chu, T C, McCallum, J, Yii, M F

Get full text

Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels by Meyer, Tamra E, Verwoert, Germaine C, Hwang, Shih-Jen, Glazer, Nicole L, Smith, Albert V, van Rooij, Frank J A, Ehret, Georg B, Boerwinkle, Eric, Felix, Janine F, Leak, Tennille S, Harris, Tamara B, Yang, Qiong, Dehghan, Abbas, Aspelund, Thor, Katz, Ronit, Homuth, Georg, Kocher, Thomas, Rettig, Rainer, Ried, Janina S, Gieger, Christian, Prucha, Hanna, Pfeufer, Arne, Meitinger, Thomas, Coresh, Josef, Hofman, Albert, Sarnak, Mark J, Chen, Yii-Der Ida, Uitterlinden, André G, Chakravarti, Aravinda, Psaty, Bruce M, van Duijn, Cornelia M, Kao, W H Linda, Witteman, Jacqueline C M, Gudnason, Vilmundur, Siscovick, David S, Fox, Caroline S, Köttgen, Anna

Get full text

Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Gen... by Ng, Maggie C Y, Graff, Mariaelisa, Lu, Yingchang, Justice, Anne E, Mudgal, Poorva, Liu, Ching-Ti, Young, Kristin, Yanek, Lisa R, Feitosa, Mary F, Wojczynski, Mary K, Rand, Kristin, Brody, Jennifer A, Cade, Brian E, Dimitrov, Latchezar, Duan, Qing, Guo, Xiuqing, Lange, Leslie A, Nalls, Michael A, Okut, Hayrettin, Tajuddin, Salman M, Tayo, Bamidele O, Vedantam, Sailaja, Bradfield, Jonathan P, Chen, Guanjie, Chen, Wei-Min, Chesi, Alessandra, Irvin, Marguerite R, Padhukasahasram, Badri, Smith, Jennifer A, Zheng, Wei, Allison, Matthew A, Ambrosone, Christine B, Bandera, Elisa V, Bartz, Traci M, Berndt, Sonja I, Bernstein, Leslie, Blot, William J, Bottinger, Erwin P, Carpten, John, Chanock, Stephen J, Chen, Yii-Der Ida, Conti, David V, Cooper, Richard S, Fornage, Myriam, Freedman, Barry I, Garcia, Melissa, Goodman, Phyllis J, Hsu, Yu-Han H, Hu, Jennifer, Huff, Chad D, Ingles, Sue A, John, Esther M, Kittles, Rick, Klein, Eric, Li, Jin, McKnight, Barbara, Nayak, Uma, Nemesure, Barbara, Ogunniyi, Adesola, Olshan, Andrew, Press, Michael F, Rohde, Rebecca, Rybicki, Benjamin A, Salako, Babatunde, Sanderson, Maureen, Shao, Yaming, Siscovick, David S, Stanford, Janet L, Stevens, Victoria L, Stram, Alex, Strom, Sara S, Vaidya, Dhananjay, Witte, John S, Yao, Jie, Zhu, Xiaofeng, Ziegler, Regina G, Zonderman, Alan B, Adeyemo, Adebowale, Ambs, Stefan, Cushman, Mary, Faul, Jessica D, Hakonarson, Hakon, Levin, Albert M, Nathanson, Katherine L, Ware, Erin B, Weir, David R, Zhao, Wei, Zhi, Degui, Arnett, Donna K, Grant, Struan F A, Kardia, Sharon L R, Oloapde, Olufunmilayo I, Rao, D C, Rotimi, Charles N, Sale, Michele M, Williams, L Keoki, Zemel, Babette S, Becker, Diane M, Borecki, Ingrid B, Evans, Michele K

Get full text

A genome‐wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes by Meng, Weihua, Shah, Kaanan P., Pollack, Samuela, Toppila, Iiro, Hebert, Harry L., McCarthy, Mark I., Groop, Leif, Ahlqvist, Emma, Lyssenko, Valeriya, Agardh, Elisabet, Daniell, Mark, Kaidonis, Georgia, Craig, Jamie E., Mitchell, Paul, Liew, Gerald, Kifley, Annette, Wang, Jie Jin, Christiansen, Mark W., Jensen, Richard A., Penman, Alan, Hancock, Heather A., Chen, Ching J., Correa, Adolfo, Kuo, Jane Z., Li, Xiaohui, Chen, Yii‐der I., Rotter, Jerome I., Klein, Ronald, Klein, Barbara, Wong, Tien Y., Morris, Andrew D., Doney, Alexander S.F., Colhoun, Helen M., Price, Alkes L., Burdon, Kathryn P., Groop, Per‐Henrik, Sandholm, Niina, Grassi, Michael A., Sobrin, Lucia, Palmer, Colin N.A.

Get full text

DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation by Richard, Melissa A., Huan, Tianxiao, Ligthart, Symen, Gondalia, Rahul, Jhun, Min A., Brody, Jennifer A., Irvin, Marguerite R., Montasser, May E., Jia, Yucheng, Syme, Catriona, Salfati, Elias L., Boerwinkle, Eric, Guan, Weihua, Mosley, Thomas H., Bressler, Jan, Morrison, Alanna C., Liu, Chunyu, Mendelson, Michael M., Uitterlinden, André G., van Meurs, Joyce B., ’t Hoen, Peter A.C., van Meurs, Joyce, Isaacs, Aaron, Franke, Lude, Boomsma, Dorret I., Pool, René, Hottenga, Jouke J., van Greevenbroek, Marleen M.J., Stehouwer, Coen D.A., Wijmenga, Cisca, Zhernakova, Alexandra, Slagboom, P. Eline, Beekman, Marian, Deelen, Joris, van Heemst, Diana, Veldink, Jan H., van den Berg, Leonard H., van Duijn, Cornelia M., Hofman, Albert, Uitterlinden, André G., Jhamai, P. Mila, Verbiest, Michael, Suchiman, H. Eka D., Verkerk, Marijn, van der Breggen, Ruud, van Rooij, Jeroen, Lakenberg, Nico, Mei, Hailiang, van Iterson, Maarten, van Galen, Michiel, Bot, Jan, Nooren, Irene, Moed, Matthijs, Vermaat, Martijn, Zhernakova, Dasha V., Luijk, René, Bonder, Marc Jan, van Dijk, Freerk, Arindrarto, Wibowo, Kielbasa, Szymon M., Swertz, Morris A., van Zwet, Erik W., Franco, Oscar H., Zhang, Guosheng, Li, Yun, Stewart, James D., Bis, Joshua C., Psaty, Bruce M., Chen, Yii-Der Ida, Kardia, Sharon L.R., Zhao, Wei, Absher, Devin, Aslibekyan, Stella, Starr, John M., McRae, Allan F., Schwartz, Joel D., Vokonas, Pantel S., Menni, Cristina, Spector, Tim D., Shuldiner, Alan, Damcott, Coleen M., Rotter, Jerome I., Palmas, Walter, Liu, Yongmei, Paus, Tomáš, Horvath, Steve, O’Connell, Jeffrey R., Guo, Xiuqing, Pausova, Zdenka, Assimes, Themistocles L., Sotoodehnia, Nona, Smith, Jennifer A., Arnett, Donna K., Deary, Ian J., Baccarelli, Andrea A., Bell, Jordana T., Whitsel, Eric, Dehghan, Abbas, Levy, Daniel, Fornage, Myriam

Get full text

The genetic underpinnings of variation in ages at menarche and natural menopause among women from the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) St... by Fernández-Rhodes, Lindsay, Malinowski, Jennifer R, Wang, Yujie, Tao, Ran, Pankratz, Nathan, Jeff, Janina M, Yoneyama, Sachiko, Carty, Cara L, Setiawan, V Wendy, Le Marchand, Loic, Haiman, Christopher, Corbett, Steven, Demerath, Ellen, Heiss, Gerardo, Gross, Myron, Buzkova, Petra, Crawford, Dana C, Hunt, Steven C, Rao, D C, Schwander, Karen, Chakravarti, Aravinda, Gottesman, Omri, Abul-Husn, Noura S, Bottinger, Erwin P, Loos, Ruth J F, Raffel, Leslie J, Yao, Jie, Guo, Xiuqing, Bielinski, Suzette J, Rotter, Jerome I, Vaidya, Dhananjay, Chen, Yii-Der Ida, Castañeda, Sheila F, Daviglus, Martha, Kaplan, Robert, Talavera, Gregory A, Ryckman, Kelli K, Peters, Ulrike, Ambite, Jose Luis, Buyske, Steven, Hindorff, Lucia, Kooperberg, Charles, Matise, Tara, Franceschini, Nora, North, Kari E

Get full text

Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies by Morris, Andrew P., Le, Thu H., Wu, Haojia, Akbarov, Artur, van der Most, Peter J., Hemani, Gibran, Smith, George Davey, Mahajan, Anubha, Gaulton, Kyle J., Nadkarni, Girish N., Valladares-Salgado, Adan, Wacher-Rodarte, Niels, Mychaleckyj, Josyf C., Dueker, Nicole D., Guo, Xiuqing, Hai, Yang, Haessler, Jeffrey, Kamatani, Yoichiro, Stilp, Adrienne M., Zhu, Gu, Cook, James P., Ärnlöv, Johan, Blanton, Susan H., de Borst, Martin H., Bottinger, Erwin P., Buchanan, Thomas A., Cechova, Sylvia, Charchar, Fadi J., Chu, Pei-Lun, Damman, Jeffrey, Eales, James, Gharavi, Ali G., Giedraitis, Vilmantas, Heath, Andrew C., Ipp, Eli, Kiryluk, Krzysztof, Kramer, Holly J., Kubo, Michiaki, Larsson, Anders, Lindgren, Cecilia M., Lu, Yingchang, Madden, Pamela A. F., Montgomery, Grant W., Papanicolaou, George J., Raffel, Leslie J., Sacco, Ralph L., Sanchez, Elena, Stark, Holger, Sundstrom, Johan, Taylor, Kent D., Xiang, Anny H., Zivkovic, Aleksandra, Lind, Lars, Ingelsson, Erik, Martin, Nicholas G., Whitfield, John B., Cai, Jianwen, Laurie, Cathy C., Okada, Yukinori, Matsuda, Koichi, Kooperberg, Charles, Chen, Yii-Der Ida, Rundek, Tatjana, Rich, Stephen S., Loos, Ruth J. F., Parra, Esteban J., Cruz, Miguel, Rotter, Jerome I., Snieder, Harold, Tomaszewski, Maciej, Humphreys, Benjamin D., Franceschini, Nora

Get full text

Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND) by Iyengar, Sudha K, Sedor, John R, Freedman, Barry I, Kao, W H Linda, Kretzler, Matthias, Keller, Benjamin J, Abboud, Hanna E, Adler, Sharon G, Best, Lyle G, Bowden, Donald W, Burlock, Allison, Chen, Yii-Der Ida, Cole, Shelley A, Comeau, Mary E, Curtis, Jeffrey M, Divers, Jasmin, Drechsler, Christiane, Duggirala, Ravi, Elston, Robert C, Guo, Xiuqing, Huang, Huateng, Hoffmann, Michael Marcus, Howard, Barbara V, Ipp, Eli, Kimmel, Paul L, Klag, Michael J, Knowler, William C, Kohn, Orly F, Leak, Tennille S, Leehey, David J, Li, Man, Malhotra, Alka, März, Winfried, Nair, Viji, Nelson, Robert G, Nicholas, Susanne B, O'Brien, Stephen J, Pahl, Madeleine V, Parekh, Rulan S, Pezzolesi, Marcus G, Rasooly, Rebekah S, Rotimi, Charles N, Rotter, Jerome I, Schelling, Jeffrey R, Seldin, Michael F, Shah, Vallabh O, Smiles, Adam M, Smith, Michael W, Taylor, Kent D, Thameem, Farook, Thornley-Brown, Denyse P, Truitt, Barbara J, Wanner, Christoph, Weil, E Jennifer, Winkler, Cheryl A, Zager, Philip G, Igo, Jr, Robert P, Hanson, Robert L, Langefeld, Carl D

Get full text

A structural variation reference for medical and population genetics by Collins, Ryan L., Brand, Harrison, Karczewski, Konrad J., Zhao, Xuefang, Alföldi, Jessica, Francioli, Laurent C., Khera, Amit V., Lowther, Chelsea, Gauthier, Laura D., Wang, Harold, Watts, Nicholas A., Solomonson, Matthew, O’Donnell-Luria, Anne, Baumann, Alexander, Munshi, Ruchi, Walker, Mark, Whelan, Christopher W., Huang, Yongqing, Brookings, Ted, Sharpe, Ted, Stone, Matthew R., Valkanas, Elise, Fu, Jack, Tiao, Grace, Laricchia, Kristen M., Ruano-Rubio, Valentin, Stevens, Christine, Gupta, Namrata, Cusick, Caroline, Margolin, Lauren, Taylor, Kent D., Lin, Henry J., Rich, Stephen S., Post, Wendy S., Chen, Yii-Der Ida, Rotter, Jerome I., Nusbaum, Chad, Philippakis, Anthony, Lander, Eric, Gabriel, Stacey, Neale, Benjamin M., Kathiresan, Sekar, Daly, Mark J., Banks, Eric, MacArthur, Daniel G., Talkowski, Michael E.

Get full text

rs641738C>T near MBOAT7 is associated with liver fat, ALT and fibrosis in NAFLD: A meta-analysis by Teo, Kevin, Abeysekera, Kushala W.M., Adams, Leon, Aigner, Elmar, Anstee, Quentin M., Banales, Jesus M., Banerjee, Rajarshi, Basu, Priyadarshi, Berg, Thomas, Bhatnagar, Pallav, Buch, Stephan, Canbay, Ali, Caprio, Sonia, Chatterjee, Ankita, Ida Chen, Yii-Der, Chowdhury, Abhijit, Daly, Ann K., Datz, Christian, de Gracia Hahn, Dana, DiStefano, Johanna K., Dong, Jiawen, Duret, Amedine, Vreugdenhil, Anita, Alisi, Anna, Jańczyk, Wojciech, Baumann, Ulrich, van Mourik, Indra, Lacaille, Florence, Dabbas, Myriam, Kelly, Deirdre A., Nobili, Valerio, Fairey, Madison, Gerhard, Glenn S., Eiriksdottir, Gudny, Garcia, Melissa E., Harris, Tamara B., Kim, Lauren J., Launer, Lenore J., Nalls, Michael A., Smith, Albert V., Clark, Jeanne M., Hernaez, Ruben, Kao, W.H. Linda, Mitchell, Braxton D., Shuldiner, Alan R., Yerges-Armstrong, Laura M., Borecki, Ingrid B., Carr, J. Jeffrey, Feitosa, Mary F., Butler, Johannah L., Fox, Caroline S., Hirschhorn, Joel N., Hoffmann, Udo, Massaro, Joseph M., O'Donnell, Christopher J., Palmer, Cameron D., Sahani, Dushyant V., Speliotes, Elizabeth K., Guo, Xiuqing, Hampe, Jochen, Hickman, Matthew, Heintz, Lena, Hudert, Christian, Kelly, Matt, Krawczyk, Marcin, Langenberg, Claudia, Lavine, Joel, Li, Lin, Lim, Hong Kai, Loomba, Rohit, Luukkonen, Panu K., Melton, Phillip E., Mori, Trevor A., Palmer, Nicholette D., Parisinos, Constantinos A., Pillai, Sreekumar G., Qayyum, Faiza, Reichert, Matthias C., Romeo, Stefano, Rotter, Jerome I., Im, Yu Ri, Santoro, Nicola, Schafmayer, Clemens, Speliotes, Elizabeth K., Stender, Stefan, Stickel, Felix, Still, Christopher D., Strnad, Pavel, Taylor, Kent D., Tybjærg-Hansen, Anne, Umano, Giuseppina Rosaria, Utukuri, Mrudula, Valenti, Luca, Wagenknecht, Lynne E., Wareham, Nicholas J., Watanabe, Richard M., Wattacheril, Julia, Yki-Järvinen, Hannele, Young, Kendra A., Mann, Jake P.

Get full text

Identification of candidate genes and pathways in retinopathy of prematurity by whole exome sequencing of preterm infants enriched in phenotypic extremes by Kim, Sang Jin, Sonmez, Kemal, Swan, Ryan, Campbell, J. Peter, Ostmo, Susan, Chan, R. V. Paul, Nagiel, Aaron, Drenser, Kimberly A., Berrocal, Audina M., Horowitz, Jason D., Li, Xiaohui, Chen, Yii-Der Ida, Taylor, Kent D., Simmons, Charles, Rotter, Jerome I., Chiang, Michael F.

Get full text

DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases by Ligthart, Symen, Marzi, Carola, Aslibekyan, Stella, Mendelson, Michael M, Conneely, Karen N, Tanaka, Toshiko, Colicino, Elena, Waite, Lindsay L, Joehanes, Roby, Guan, Weihua, Brody, Jennifer A, Elks, Cathy, Marioni, Riccardo, Jhun, Min A, Agha, Golareh, Bressler, Jan, Ward-Caviness, Cavin K, Chen, Brian H, Huan, Tianxiao, Bakulski, Kelly, Salfati, Elias L, Fiorito, Giovanni, Wahl, Simone, Schramm, Katharina, Sha, Jin, Hernandez, Dena G, Just, Allan C, Smith, Jennifer A, Sotoodehnia, Nona, Pilling, Luke C, Pankow, James S, Tsao, Phil S, Liu, Chunyu, Zhao, Wei, Guarrera, Simonetta, Michopoulos, Vasiliki J, Smith, Alicia K, Peters, Marjolein J, Melzer, David, Vokonas, Pantel, Fornage, Myriam, Prokisch, Holger, Bis, Joshua C, Chu, Audrey Y, Herder, Christian, Grallert, Harald, Yao, Chen, Shah, Sonia, McRae, Allan F, Lin, Honghuang, Horvath, Steve, Fallin, Daniele, Hofman, Albert, Wareham, Nicholas J, Wiggins, Kerri L, Feinberg, Andrew P, Starr, John M, Visscher, Peter M, Murabito, Joanne M, Kardia, Sharon L R, Absher, Devin M, Binder, Elisabeth B, Singleton, Andrew B, Bandinelli, Stefania, Peters, Annette, Waldenberger, Melanie, Matullo, Giuseppe, Schwartz, Joel D, Demerath, Ellen W, Uitterlinden, André G, van Meurs, Joyce B J, Franco, Oscar H, Chen, Yii-Der Ida, Levy, Daniel, Turner, Stephen T, Deary, Ian J, Ressler, Kerry J, Dupuis, Josée, Ferrucci, Luigi, Ong, Ken K, Assimes, Themistocles L, Boerwinkle, Eric, Koenig, Wolfgang, Arnett, Donna K, Baccarelli, Andrea A, Benjamin, Emelia J, Dehghan, Abbas

Get full text

Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Co... by Hahn, Julie, Fu, Yi-Ping, Brown, Michael R, Bis, Joshua C, de Vries, Paul S, Feitosa, Mary F, Yanek, Lisa R, Weiss, Stefan, Giulianini, Franco, Smith, Albert Vernon, Guo, Xiuqing, Bartz, Traci M, Becker, Diane M, Becker, Lewis C, Boerwinkle, Eric, Brody, Jennifer A, Chen, Yii-Der Ida, Franco, Oscar H, Grove, Megan, Harris, Tamara B, Hofman, Albert, Hwang, Shih-Jen, Kral, Brian G, Launer, Lenore J, Markus, Marcello R P, Rice, Kenneth M, Rich, Stephen S, Ridker, Paul M, Rivadeneira, Fernando, Rotter, Jerome I, Sotoodehnia, Nona, Taylor, Kent D, Uitterlinden, André G, Völker, Uwe, Völzke, Henry, Yao, Jie, Chasman, Daniel I, Dörr, Marcus, Gudnason, Vilmundur, Mathias, Rasika A, Post, Wendy, Psaty, Bruce M, Dehghan, Abbas, O'Donnell, Christopher J, Morrison, Alanna C

Get full text

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program by Taliun, Daniel, Kessler, Michael D., Carlson, Jedidiah, Taliun, Sarah A. Gagliano, Kang, Hyun Min, Pitsillides, Achilleas N., Emde, Anne-Katrin, Clarke, Wayne E., Shetty, Amol C., Wong, Quenna, Bobo, Dean M., Aguet, François, Albert, Christine, Aslibekyan, Stella, Barnard, John, Barr, R. Graham, Barwick, Lucas, Becker, Lewis C., Bielak, Lawrence F., Blangero, John, Bowden, Donald W., Burchard, Esteban G., Chalazan, Brandon, Chasman, Daniel I., Chen, Yii-Der Ida, Choi, Seung Hoan, Chung, Mina K., Curran, Joanne E., Daya, Michelle, Ellinor, Patrick T., Fatkin, Diane, Fingerlin, Tasha, Forer, Lukas, Franceschini, Nora, Germer, Soren, Gladwin, Mark T., Hall, Michael E., He, Jiang, Johnsen, Jill M., Johnson, Andrew D., Kardia, Sharon L. R., Klemmer, Robert, Kooperberg, Charles, Köttgen, Anna, Lange, Leslie A., Lin, Xihong, Lin, Keng-Han, Liu, Chunyu, Loos, Ruth J. F., Gerszten, Robert, Lunetta, Kathryn L., Mak, Angel C. Y., Manichaikul, Ani, Manning, Alisa K., Mathias, Rasika A., McManus, David D., McGarvey, Stephen T., Meigs, James B., Minear, Mollie A., Mitchell, Braxton D., Mohanty, Sanghamitra, Montasser, May E., Montgomery, Courtney, Morrison, Alanna C., Murabito, Joanne M., Natale, Andrea, Nelson, Sarah C., Palmer, Nicholette D., Pankratz, Nathan, Peyser, Patricia A., Post, Wendy S., Psaty, Bruce M., Rao, D. C., Reiner, Alexander P., Roden, Dan, Rotter, Jerome I., Schoenherr, Sebastian, Seo, Jeong-Sun, Sheu, Wayne H., Smith, Nicholas L., Smith, Jennifer A., Stilp, Adrienne M., Telen, Marilyn, Thornton, Timothy A., Tracy, Russell P., Van Den Berg, David J., Vasan, Ramachandran S., Vrieze, Scott, Weng, Lu-Chen, Zhao, Xutong, Boerwinkle, Eric, Gibbs, Richard, Rich, Stephen S., Silverman, Edwin K., Qasba, Pankaj, Gan, Weiniu, Zöllner, Sebastian, Wilson, James G., Laurie, Cathy C., Jaquish, Cashell E.

Get full text

A metabolically healthy obese phenotype in hispanic participants in the IRAS family study by Samaropoulos, Xanthia F., Hairston, Kristen G., Anderson, Andrea, Haffner, Steven M., Lorenzo, Carlos, Montez, Maria, Norris, Jill M., Scherzinger, Ann L., Chen, Yii‐Der Ida, Wagenknecht, Lynne E.

Get full text

Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry by Hauser, Michael A, Allingham, R. Rand, Aung, Tin, Van Der Heide, Carly J, Taylor, Kent D, Rotter, Jerome I, Wang, Shih-Hsiu J, Bonnemaijer, Pieter W. M, Williams, Susan E, Abdullahi, Sadiq M, Abu-Amero, Khaled K, Anderson, Michael G, Akafo, Stephen, Alhassan, Mahmoud B, Asimadu, Ifeoma, Ayyagari, Radha, Bakayoko, Saydou, Nyamsi, Prisca Biangoup, Bowden, Donald W, Bromley, William C, Budenz, Donald L, Carmichael, Trevor R, Challa, Pratap, Chen, Yii-Der Ida, Chuka-Okosa, Chimdi M, Cooke Bailey, Jessica N, Costa, Vital Paulino, Cruz, Dianne A, DuBiner, Harvey, Ervin, John F, Feldman, Robert M, Flamme-Wiese, Miles, Gaasterland, Douglas E, Garnai, Sarah J, Girkin, Christopher A, Guirou, Nouhoum, Guo, Xiuqing, Haines, Jonathan L, Hammond, Christopher J, Herndon, Leon, Hoffmann, Thomas J, Hulette, Christine M, Hydara, Abba, Igo, Robert P, Jorgenson, Eric, Kabwe, Joyce, Kilangalanga, Ngoy Janvier, Kizor-Akaraiwe, Nkiru, Kuchtey, Rachel W, Lamari, Hasnaa, Li, Zheng, Liebmann, Jeffrey M, Liu, Yutao, Loos, Ruth J.F, Melo, Monica B, Moroi, Sayoko E, Msosa, Joseph M, Mullins, Robert F, Nadkarni, Girish, Napo, Abdoulaye, Ng, Maggie C. Y, Nunes, Hugo Freire, Obeng-Nyarkoh, Ebenezer, Okeke, Anthony, Okeke, Suhanya, Olaniyi, Olusegun, Olawoye, Olusola, Oliveira, Mariana Borges, Pasquale, Louise R, Perez-Grossmann, Rodolfo A, Pericak-Vance, Margaret A, Qin, Xue, Ramsay, Michele, Resnikoff, Serge, Richards, Julia E, Schimiti, Rui Barroso, Sim, Kar Seng, Sponsel, William E, Svidnicki, Paulo Vinicius, Thiadens, Alberta A. H. J, Uche, Nkechinyere J, van Duijn, Cornelia M, de Vasconcellos, José Paulo Cabral, Wiggs, Janey L, Zangwill, Linda M, Risch, Neil, Milea, Dan, Ashaye, Adeyinka, Klaver, Caroline C. W, Weinreb, Robert N, Ashley Koch, Allison E, Fingert, John H, Khor, Chiea Chuen

Get full text

Genome-wide association of body fat distribution in African ancestry populations suggests new loci by Liu, Ching-Ti, Monda, Keri L, Taylor, Kira C, Lange, Leslie, Demerath, Ellen W, Palmas, Walter, Wojczynski, Mary K, Ellis, Jaclyn C, Vitolins, Mara Z, Liu, Simin, Papanicolaou, George J, Irvin, Marguerite R, Xue, Luting, Griffin, Paula J, Nalls, Michael A, Adeyemo, Adebowale, Liu, Jiankang, Li, Guo, Ruiz-Narvaez, Edward A, Chen, Wei-Min, Chen, Fang, Henderson, Brian E, Millikan, Robert C, Ambrosone, Christine B, Strom, Sara S, Guo, Xiuqing, Andrews, Jeanette S, Sun, Yan V, Mosley, Thomas H, Yanek, Lisa R, Shriner, Daniel, Haritunians, Talin, Rotter, Jerome I, Speliotes, Elizabeth K, Smith, Megan, Rosenberg, Lynn, Mychaleckyj, Josyf, Nayak, Uma, Spruill, Ida, Garvey, W Timothy, Pettaway, Curtis, Nyante, Sarah, Bandera, Elisa V, Britton, Angela F, Zonderman, Alan B, Rasmussen-Torvik, Laura J, Chen, Yii-Der Ida, Ding, Jingzhong, Lohman, Kurt, Kritchevsky, Stephen B, Zhao, Wei, Peyser, Patricia A, Kardia, Sharon L R, Kabagambe, Edmond, Broeckel, Ulrich, Chen, Guanjie, Zhou, Jie, Wassertheil-Smoller, Sylvia, Neuhouser, Marian L, Rampersaud, Evadnie, Psaty, Bruce, Kooperberg, Charles, Manson, Joann E, Kuller, Lewis H, Ochs-Balcom, Heather M, Johnson, Karen C, Sucheston, Lara, Ordovas, Jose M, Palmer, Julie R, Haiman, Christopher A, McKnight, Barbara, Howard, Barbara V, Becker, Diane M, Bielak, Lawrence F, Liu, Yongmei, Allison, Matthew A, Grant, Struan F A, Burke, Gregory L, Patel, Sanjay R, Schreiner, Pamela J, Borecki, Ingrid B, Evans, Michele K, Taylor, Herman, Sale, Michele M, Howard, Virginia, Carlson, Christopher S, Rotimi, Charles N, Cushman, Mary, Harris, Tamara B, Reiner, Alexander P, Cupples, L Adrienne, North, Kari E, Fox, Caroline S

Get full text

Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease by Ward-Caviness, Cavin K, de Vries, Paul S, Wiggins, Kerri L, Huffman, Jennifer E, Yanek, Lisa R, Bielak, Lawrence F, Giulianini, Franco, Guo, Xiuqing, Kleber, Marcus E, Kacprowski, Tim, Groß, Stefan, Petersman, Astrid, Davey Smith, George, Hartwig, Fernando P, Bowden, Jack, Hemani, Gibran, Müller-Nuraysid, Martina, Strauch, Konstantin, Koenig, Wolfgang, Waldenberger, Melanie, Meitinger, Thomas, Pankratz, Nathan, Boerwinkle, Eric, Tang, Weihong, Fu, Yi-Ping, Johnson, Andrew D, Song, Ci, de Maat, Moniek P M, Uitterlinden, André G, Franco, Oscar H, Brody, Jennifer A, McKnight, Barbara, Chen, Yii-Der Ida, Psaty, Bruce M, Mathias, Rasika A, Becker, Diane M, Peyser, Patricia A, Smith, Jennifer A, Bielinski, Suzette J, Ridker, Paul M, Taylor, Kent D, Yao, Jie, Tracy, Russell, Delgado, Graciela, Trompet, Stella, Sattar, Naveed, Jukema, J Wouter, Becker, Lewis C, Kardia, Sharon L R, Rotter, Jerome I, März, Winfried, Dörr, Marcus, Chasman, Daniel I, Dehghan, Abbas, O'Donnell, Christopher J, Smith, Nicholas L, Peters, Annette, Morrison, Alanna C

Get full text

Common Genetic Variants Associate with Serum Phosphorus Concentration by KESTENBAUM, Bryan, GLAZER, Nicole L, GIEGER, Christian, RIED, Janina S, MEITINGER, Thomas, STROM, Tim M, WICHMANN, H. Erich, CAMPBELL, Harry, HAYWARD, Caroline, RUDAN, Igor, DE BOER, Ian H, PSATY, Bruce M, KÖTTGEN, Anna, RICE, Kenneth M, IDA CHEN, Yii-Der, MAN LI, ARKING, Dan E, BOERWINKLE, Eric, CORESH, Josef, QIONG YANG, LEVY, Daniel, VAN ROOIJ, Frank J. A, DEHGHAN, Abbas, FELIX, Janine F, RIVADENEIRA, Fernando, UITTERLINDEN, André G, HOFMAN, Albert, VAN DUIJN, Cornelia M, SHLIPAK, Michael G, LINDA KAO, W. H, WITTEMAN, Jacqueline C. M, SISCOVICK, David S, FOX, Caroline S, HWANG, Shih-Jen, YONGMEI LIU, LOHMAN, Kurt, KRITCHEVSKY, Stephen B, HAUSMAN, Dorothy B, PETERSEN, Ann-Kristin

Get full text

Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height by Hawkes, Gareth, Beaumont, Robin N., Li, Zilin, Mandla, Ravi, Li, Xihao, Albert, Christine M., Arnett, Donna K., Ashley-Koch, Allison E., Ashrani, Aneel A., Barnes, Kathleen C., Boerwinkle, Eric, Brody, Jennifer A., Carson, April P., Chami, Nathalie, Chen, Yii-Der Ida, Chung, Mina K., Curran, Joanne E., Darbar, Dawood, Ellinor, Patrick T., Fornage, Myrian, Gordeuk, Victor R., Guo, Xiuqing, He, Jiang, Hwu, Chii-Min, Kalyani, Rita R., Kaplan, Robert, Kardia, Sharon L. R., Kooperberg, Charles, Loos, Ruth J. F., Lubitz, Steven A., Minster, Ryan L., Naseri, Take, Viali, Satupa’itea, Mitchell, Braxton D., Murabito, Joanne M., Palmer, Nicholette D., Psaty, Bruce M., Redline, Susan, Shoemaker, M. Benjamin, Silverman, Edwin K., Telen, Marilyn J., Weiss, Scott T., Yanek, Lisa R., Zhou, Hufeng, Liu, Ching-Ti, North, Kari E., Justice, Anne E., Locke, Jonathan M., Owens, Nick, Murray, Anna, Patel, Kashyap, Frayling, Timothy M., Wright, Caroline F., Wood, Andrew R., Lin, Xihong, Manning, Alisa, Weedon, Michael N.

Get full text