Risultati della ricerca - Metcalf, Ginger A.

The Implementation Science for Genomic Health Translation (INSIGHT) Study in Epilepsy: Protocol for a Learning Health Care System di Feofanova, Elena Valeryevna, Zhang, Guo-Qiang, Lhatoo, Samden, Metcalf, Ginger A, Boerwinkle, Eric, Venner, Eric

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Loss-of-function variants influence the human serum metabolome di Yu, Bing, Li, Alexander H., Metcalf, Ginger A., Muzny, Donna M., Morrison, Alanna C., White, Simon, Mosley, Thomas H., Gibbs, Richard A., Boerwinkle, Eric

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Sequence-Based Analysis of Lipid-Related Metabolites in a Multiethnic Study di Feofanova, Elena V., Yu, Bing, Metcalf, Ginger A., Liu, Xiaoming, Muzny, Donna, Below, Jennifer E., Wagenknecht, Lynne E., Gibbs, Richard A., Morrison, Alanna C., Boerwinkle, Eric

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Whole genome sequence analysis of serum amino acid levels di Yu, Bing, de Vries, Paul S., Metcalf, Ginger A., Wang, Zhe, Feofanova, Elena V., Liu, Xiaoming, Muzny, Donna Marie, Wagenknecht, Lynne E., Gibbs, Richard A., Morrison, Alanna C., Boerwinkle, Eric

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Whole-genome sequencing study of serum peptide levels: the Atherosclerosis Risk in Communities study di de Vries, Paul S., Yu, Bing, Feofanova, Elena V., Metcalf, Ginger A., Brown, Michael R., Zeighami, Atefeh L., Liu, Xiaoming, Muzny, Donna M., Gibbs, Richard A., Boerwinkle, Eric, Morrison, Alanna C.

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The gut mycobiome of the Human Microbiome Project healthy cohort di Nash, Andrea K., Auchtung, Thomas A., Wong, Matthew C., Smith, Daniel P., Gesell, Jonathan R., Ross, Matthew C., Stewart, Christopher J., Metcalf, Ginger A., Muzny, Donna M., Gibbs, Richard A., Ajami, Nadim J., Petrosino, Joseph F.

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Structure and function of the healthy pre-adolescent pediatric gut microbiome di Hollister, Emily B., Riehle, Kevin, Luna, Ruth Ann, Weidler, Erica M., Rubio-Gonzales, Michelle, Mistretta, Toni-Ann, Raza, Sabeen, Doddapaneni, Harsha V., Metcalf, Ginger A., Muzny, Donna M., Gibbs, Richard A., Petrosino, Joseph F., Shulman, Robert J., Versalovic, James

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Whole exome sequencing in the Framingham Heart Study identifies rare variation in HYAL2 that influences platelet aggregation di Eicher, John D., Chen, Ming-Huei, Pitsillides, Achilleas N., Lin, Honghuang, Veeraraghavan, Narayanan, Brody, Jennifer A., Metcalf, Ginger A., Muzny, Donna M., Gibbs, Richard A., Becker, Diane M., Becker, Lewis C., Faraday, Nauder, Mathias, Rasika A., Yanek, Lisa R., Boerwinkle, Eric, Cupples, L. Adrienne, Johnson, Andrew D.

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Leveraging Human Microbiome Features to Diagnose and Stratify Children with Irritable Bowel Syndrome di Hollister, Emily B., Oezguen, Numan, Chumpitazi, Bruno P., Luna, Ruth Ann, Weidler, Erica M., Rubio-Gonzales, Michelle, Dahdouli, Mahmoud, Cope, Julia L., Mistretta, Toni-Ann, Raza, Sabeen, Metcalf, Ginger A., Muzny, Donna M., Gibbs, Richard A., Petrosino, Joseph F., Heitkemper, Margaret, Savidge, Tor C., Shulman, Robert J., Versalovic, James

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Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program di Venner, Eric, Muzny, Donna, Smith, Joshua D., Walker, Kimberly, Neben, Cynthia L., Lockwood, Christina M., Empey, Phillip E., Metcalf, Ginger A., Kachulis, Chris, Mian, Sana, Musick, Anjene, Rehm, Heidi L., Harrison, Steven, Gabriel, Stacey, Gibbs, Richard A., Nickerson, Deborah, Zhou, Alicia Y., Doheny, Kimberly, Ozenberger, Bradley, Topper, Scott E., Lennon, Niall J.

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Fully resolved assembly of Cryptosporidium parvum di Menon, Vipin K, Okhuysen, Pablo C, Chappell, Cynthia L, Mahmoud, Medhat, Mahmoud, Medhat, Meng, Qingchang, Doddapaneni, Harsha, Vee, Vanesa, Han, Yi, Salvi, Sejal, Bhamidipati, Sravya, Kottapalli, Kavya, Weissenberger, George, Shen, Hua, Ross, Matthew C, Hoffman, Kristi L, Cregeen, Sara Javornik, Muzny, Donna M, Metcalf, Ginger A, Gibbs, Richard A, Petrosino, Joseph F, Sedlazeck, Fritz J

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Temporal development of the gut microbiome in early childhood from the TEDDY study di Stewart, Christopher J., Ajami, Nadim J., O’Brien, Jacqueline L., Hutchinson, Diane S., Smith, Daniel P., Wong, Matthew C., Ross, Matthew C., Lloyd, Richard E., Doddapaneni, HarshaVardhan, Metcalf, Ginger A., Muzny, Donna, Gibbs, Richard A., Vatanen, Tommi, Huttenhower, Curtis, Xavier, Ramnik J., Rewers, Marian, Hagopian, William, Toppari, Jorma, Ziegler, Anette-G., She, Jin-Xiong, Akolkar, Beena, Lernmark, Ake, Hyoty, Heikki, Vehik, Kendra, Krischer, Jeffrey P., Petrosino, Joseph F.

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Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk di Yu, Bing, Pulit, Sara L., Hwang, Shih-Jen, Brody, Jennifer A., Amin, Najaf, Auer, Paul L., Bis, Joshua C., Boerwinkle, Eric, Burke, Gregory L., Chakravarti, Aravinda, Correa, Adolfo, Dreisbach, Albert W., Franco, Oscar H., Ehret, Georg B., Franceschini, Nora, Hofman, Albert, Lin, Dan-Yu, Metcalf, Ginger A., Musani, Solomon K., Muzny, Donna, Palmas, Walter, Raffel, Leslie, Reiner, Alex, Rice, Ken, Rotter, Jerome I., Veeraraghavan, Narayanan, Fox, Ervin, Guo, Xiuqing, North, Kari E., Gibbs, Richard A., van Duijn, Cornelia M., Psaty, Bruce M., Levy, Daniel, Newton-Cheh, Christopher, Morrison, Alanna C.

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Genetic testing in ambulatory cardiology clinics reveals high rate of findings with clinical management implications di Murdock, David R., Venner, Eric, Muzny, Donna M., Metcalf, Ginger A., Murugan, Mullai, Hadley, Trevor D., Chander, Varuna, De Vries, Paul, Jia, Xiaoming, Hussain, Aliza, Agha, Ali M., Sabo, Aniko, Li, Shoudong, Meng, Qingchang, Hu, Jianhong, Tian, Xia, Cohen, Michelle, Yi, Victoria, Kovar, Christie L., Gingras, Marie-Claude, Korchina, Viktoriya, Howard, Chad, Riconda, Daniel L., Pereira, Stacey, Smith, Hadley, Huda, Zohra A., Buentello, Alexandria, Marino, Patricia R., Leiber, Lee, Balasubramanyam, Ashok, Amos, Christopher I., Civitello, Andrew, Chelu, Mihail G., Maag, Ronald, McGuire, Amy L., Boerwinkle, Eric, Wehrens, Xander H.T., Ballantyne, Christie M., Gibbs, Richard A.

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Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts di Raffield, Laura M., Iyengar, Apoorva K., Wang, Biqi, Gaynor, Sheila M., Spracklen, Cassandra N., Zhong, Xue, Kowalski, Madeline H., Salimi, Shabnam, Polfus, Linda M., Benjamin, Emelia J., Bis, Joshua C., Bowler, Russell, Cade, Brian E., Choi, Won Jung, Comellas, Alejandro P., Correa, Adolfo, Cruz, Pedro, Doddapaneni, Harsha, Durda, Peter, Gogarten, Stephanie M., Jain, Deepti, Kim, Ryan W., Kral, Brian G., Lange, Leslie A., Larson, Martin G., Laurie, Cecelia, Lee, Jiwon, Lee, Seonwook, Lewis, Joshua P., Metcalf, Ginger A., Mitchell, Braxton D., Momin, Zeineen, Muzny, Donna M., Pankratz, Nathan, Park, Cheol Joo, Rich, Stephen S., Rotter, Jerome I., Ryan, Kathleen, Seo, Daekwan, Tracy, Russell P., Viaud-Martinez, Karine A., Yanek, Lisa R., Zhao, Lue Ping, Lin, Xihong, Li, Bingshan, Li, Yun, Dupuis, Josée, Reiner, Alexander P., Mohlke, Karen L., Auer, Paul L.

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Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program di Hu, Xiaowei, Qiao, Dandi, Kim, Wonji, Moll, Matthew, Balte, Pallavi P., Lange, Leslie A., Bartz, Traci M., Kumar, Rajesh, Li, Xingnan, Yu, Bing, Cade, Brian E., Laurie, Cecelia A., Sofer, Tamar, Ruczinski, Ingo, Nickerson, Deborah A., Muzny, Donna M., Metcalf, Ginger A., Doddapaneni, Harshavardhan, Gabriel, Stacy, Gupta, Namrata, Dugan-Perez, Shannon, Cupples, L. Adrienne, Loehr, Laura R., Jain, Deepti, Rotter, Jerome I., Wilson, James G., Psaty, Bruce M., Fornage, Myriam, Morrison, Alanna C., Vasan, Ramachandran S., Washko, George, Rich, Stephen S., O’Connor, George T., Bleecker, Eugene, Kaplan, Robert C., Kalhan, Ravi, Redline, Susan, Gharib, Sina A., Meyers, Deborah, Ortega, Victor, Dupuis, Josée, London, Stephanie J., Lappalainen, Tuuli, Oelsner, Elizabeth C., Silverman, Edwin K., Barr, R. Graham, Thornton, Timothy A., Wheeler, Heather E., Cho, Michael H., Im, Hae Kyung, Manichaikul, Ani

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Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants di Zhao, Xutong, Qiao, Dandi, Yang, Chaojie, Kasela, Silva, Kim, Wonji, Ma, Yanlin, Shrine, Nick, Batini, Chiara, Sofer, Tamar, Taliun, Sarah A. Gagliano, Sakornsakolpat, Phuwanat, Balte, Pallavi P., Prokopenko, Dmitry, Yu, Bing, Lange, Leslie A., Dupuis, Josée, Cade, Brian E., Lee, Jiwon, Gharib, Sina A., Daya, Michelle, Laurie, Cecelia A., Ruczinski, Ingo, Cupples, L. Adrienne, Loehr, Laura R., Bartz, Traci M., Morrison, Alanna C., Psaty, Bruce M., Vasan, Ramachandran S., Wilson, James G., Taylor, Kent D., Durda, Peter, Johnson, W. Craig, Cornell, Elaine, Guo, Xiuqing, Liu, Yongmei, Tracy, Russell P., Ardlie, Kristin G., Aguet, François, VanDenBerg, David J., Papanicolaou, George J., Rotter, Jerome I., Barnes, Kathleen C., Jain, Deepti, Nickerson, Deborah A., Muzny, Donna M., Metcalf, Ginger A., Doddapaneni, Harshavardhan, Dugan-Perez, Shannon, Gupta, Namrata, Gabriel, Stacey, Rich, Stephen S., O’Connor, George T., Redline, Susan, Reed, Robert M., Laurie, Cathy C., Daviglus, Martha L., Preudhomme, Liana K., Burkart, Kristin M., Kaplan, Robert C., Wain, Louise V., Tobin, Martin D., London, Stephanie J., Lappalainen, Tuuli, Oelsner, Elizabeth C., Abecasis, Goncalo R., Silverman, Edwin K., Barr, R. Graham, Cho, Michael H., Manichaikul, Ani

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Somatic mutations affect key pathways in lung adenocarcinoma di Ding, Li, Getz, Gad, Wheeler, David A., Mardis, Elaine R., McLellan, Michael D., Cibulskis, Kristian, Sougnez, Carrie, Greulich, Heidi, Muzny, Donna M., Morgan, Margaret B., Fulton, Lucinda, Fulton, Robert S., Zhang, Qunyuan, Wendl, Michael C., Lawrence, Michael S., Larson, David E., Chen, Ken, Dooling, David J., Sabo, Aniko, Hawes, Alicia C., Shen, Hua, Jhangiani, Shalini N., Lewis, Lora R., Hall, Otis, Zhu, Yiming, Mathew, Tittu, Ren, Yanru, Yao, Jiqiang, Scherer, Steven E., Clerc, Kerstin, Metcalf, Ginger A., Ng, Brian, Milosavljevic, Aleksandar, Gonzalez-Garay, Manuel L., Osborne, John R., Meyer, Rick, Shi, Xiaoqi, Tang, Yuzhu, Koboldt, Daniel C., Lin, Ling, Abbott, Rachel, Miner, Tracie L., Pohl, Craig, Fewell, Ginger, Haipek, Carrie, Schmidt, Heather, Dunford-Shore, Brian H., Kraja, Aldi, Crosby, Seth D., Sawyer, Christopher S., Vickery, Tammi, Sander, Sacha, Robinson, Jody, Winckler, Wendy, Baldwin, Jennifer, Chirieac, Lucian R., Dutt, Amit, Fennell, Tim, Hanna, Megan, Johnson, Bruce E., Onofrio, Robert C., Thomas, Roman K., Tonon, Giovanni, Weir, Barbara A., Zhao, Xiaojun, Ziaugra, Liuda, Zody, Michael C., Giordano, Thomas, Orringer, Mark B., Roth, Jack A., Spitz, Margaret R., Wistuba, Ignacio I., Ozenberger, Bradley, Good, Peter J., Chang, Andrew C., Beer, David G., Watson, Mark A., Ladanyi, Marc, Broderick, Stephen, Yoshizawa, Akihiko, Travis, William D., Pao, William, Province, Michael A., Weinstock, George M., Varmus, Harold E., Gabriel, Stacey B., Lander, Eric S., Gibbs, Richard A., Meyerson, Matthew, Wilson, Richard K.

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Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes di Hindy, George, Dornbos, Peter, Chaffin, Mark D., Liu, Dajiang J., Wang, Minxian, Selvaraj, Margaret Sunitha, Zhang, David, Park, Joseph, Aguilar-Salinas, Carlos A., Antonacci-Fulton, Lucinda, Ardissino, Diego, Arnett, Donna K., Aslibekyan, Stella, Atzmon, Gil, Ballantyne, Christie M., Barajas-Olmos, Francisco, Barzilai, Nir, Becker, Lewis C., Bielak, Lawrence F., Bis, Joshua C., Blangero, John, Boerwinkle, Eric, Bonnycastle, Lori L., Bottinger, Erwin, Bowden, Donald W., Bown, Matthew J., Brody, Jennifer A., Broome, Jai G., Burtt, Noël P., Cade, Brian E., Centeno-Cruz, Federico, Chan, Edmund, Chang, Yi-Cheng, Chen, Yii-Der I., Cheng, Ching-Yu, Choi, Won Jung, Chowdhury, Rajiv, Contreras-Cubas, Cecilia, Córdova, Emilio J., Correa, Adolfo, Cupples, L. Adrienne, Curran, Joanne E., Danesh, John, de Vries, Paul S., DeFronzo, Ralph A., Doddapaneni, Harsha, Duggirala, Ravindranath, Dutcher, Susan K., Ellinor, Patrick T., Emery, Leslie S., Florez, Jose C., Fornage, Myriam, Freedman, Barry I., Fuster, Valentin, Garay-Sevilla, Ma. Eugenia, García-Ortiz, Humberto, Germer, Soren, Gibbs, Richard A., Gieger, Christian, Glaser, Benjamin, Gonzalez, Clicerio, Gonzalez-Villalpando, Maria Elena, Graff, Mariaelisa, Graham, Sarah E., Grarup, Niels, Groop, Leif C., Guo, Xiuqing, Gupta, Namrata, Han, Sohee, Hanis, Craig L., Hansen, Torben, He, Jiang, Heard-Costa, Nancy L., Hung, Yi-Jen, Hwang, Mi Yeong, Irvin, Marguerite R., Islas-Andrade, Sergio, Jarvik, Gail P., Kang, Hyun Min, Kardia, Sharon L.R., Kelly, Tanika, Kenny, Eimear E., Khan, Alyna T., Kim, Bong-Jo, Kim, Ryan W., Kim, Young Jin, Koistinen, Heikki A., Kooperberg, Charles, Kuusisto, Johanna, Kwak, Soo Heon, Laakso, Markku, Lange, Leslie A., Lee, Jiwon, Lee, Juyoung, Lee, Seonwook, Lehman, Donna M., Lemaitre, Rozenn N., Linneberg, Allan, Liu, Jianjun, Loos, Ruth J.F., Lubitz, Steven A., Lyssenko, Valeriya, Ma, Ronald C.W., Martin, Lisa Warsinger, Martínez-Hernández, Angélica, Mathias, Rasika A., McGarvey, Stephen T., McPherson, Ruth, Meigs, James B., Meitinger, Thomas, Melander, Olle, Mendoza-Caamal, Elvia, Metcalf, Ginger A., Mi, Xuenan, Mohlke, Karen L., Montasser, May E., Moon, Jee-Young, Moreno-Macías, Hortensia, Morrison, Alanna C., Muzny, Donna M., Nelson, Sarah C., Nilsson, Peter M., O’Connell, Jeffrey R., Orho-Melander, Marju, Orozco, Lorena, Palmer, Colin N.A., Palmer, Nicholette D., Park, Cheol Joo, Park, Kyong Soo, Pedersen, Oluf, Peralta, Juan M., Peyser, Patricia A., Post, Wendy S., Preuss, Michael, Psaty, Bruce M., Qi, Qibin, Rao, D.C., Redline, Susan, Reiner, Alexander P., Revilla-Monsalve, Cristina, Rich, Stephen S., Samani, Nilesh, Schunkert, Heribert, Schurmann, Claudia, Seo, Daekwan, Seo, Jeong-Sun, Sim, Xueling, Sladek, Rob, Small, Kerrin S., So, Wing Yee, Stilp, Adrienne M., Tai, E. Shyong, Tam, Claudia H.T., Taylor, Kent D., Teo, Yik Ying, Thameem, Farook, Tomlinson, Brian, Tsai, Michael Y., Tuomi, Tiinamaija, Tuomilehto, Jaakko, Tusié-Luna, Teresa, Udler, Miriam S., van Dam, Rob M., Vasan, Ramachandran S., Viaud Martinez, Karine A., Wang, Fei Fei, Wang, Xuzhi, Watkins, Hugh, Weeks, Daniel E., Wilson, James G., Witte, Daniel R., Wong, Tien-Yin, Yanek, Lisa R., Kathiresan, Sekar, Rader, Daniel J., Rotter, Jerome I., Boehnke, Michael, McCarthy, Mark I., Willer, Cristen J., Natarajan, Pradeep, Flannick, Jason A., Khera, Amit V., Peloso, Gina M.

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Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility di Wessel, Jennifer, Chu, Audrey Y, Willems, Sara M, Wang, Shuai, Yaghootkar, Hanieh, Brody, Jennifer A, Dauriz, Marco, Hivert, Marie-France, Raghavan, Sridharan, Lipovich, Leonard, Hidalgo, Bertha, Fox, Keolu, Huffman, Jennifer E, An, Ping, Lu, Yingchang, Rasmussen-Torvik, Laura J, Grarup, Niels, Ehm, Margaret G, Li, Li, Baldridge, Abigail S, Stančáková, Alena, Abrol, Ravinder, Besse, Céline, Boland, Anne, Bork-Jensen, Jette, Fornage, Myriam, Freitag, Daniel F, Garcia, Melissa E, Guo, Xiuqing, Hara, Kazuo, Isaacs, Aaron, Jakobsdottir, Johanna, Lange, Leslie A, Layton, Jill C, Li, Man, Hua Zhao, Jing, Meidtner, Karina, Morrison, Alanna C, Nalls, Mike A, Peters, Marjolein J, Sabater-Lleal, Maria, Schurmann, Claudia, Silveira, Angela, Smith, Albert V, Southam, Lorraine, Stoiber, Marcus H, Strawbridge, Rona J, Taylor, Kent D, Varga, Tibor V, Allin, Kristine H, Amin, Najaf, Aponte, Jennifer L, Aung, Tin, Barbieri, Caterina, Bihlmeyer, Nathan A, Boehnke, Michael, Bombieri, Cristina, Bowden, Donald W, Burns, Sean M, Chen, Yuning, Chen, Yii-DerI, Cheng, Ching-Yu, Correa, Adolfo, Czajkowski, Jacek, Dehghan, Abbas, Ehret, Georg B, Eiriksdottir, Gudny, Escher, Stefan A, Farmaki, Aliki-Eleni, Frånberg, Mattias, Gambaro, Giovanni, Giulianini, Franco, Goddard, William A, Goel, Anuj, Gottesman, Omri, Grove, Megan L, Gustafsson, Stefan, Hai, Yang, Hallmans, Göran, Heo, Jiyoung, Hoffmann, Per, Ikram, Mohammad K, Jensen, Richard A, Jørgensen, Marit E, Jørgensen, Torben, Karaleftheri, Maria, Khor, Chiea C, Kirkpatrick, Andrea, Kraja, Aldi T, Kuusisto, Johanna, Lange, Ethan M, Lee, I T, Lee, Wen-Jane, Leong, Aaron, Liao, Jiemin, Liu, Chunyu, Liu, Yongmei, Lindgren, Cecilia M, Linneberg, Allan, Malerba, Giovanni, Mamakou, Vasiliki, Marouli, Eirini, Maruthur, Nisa M, Matchan, Angela, McKean-Cowdin, Roberta, McLeod, Olga, Metcalf, Ginger A, Mohlke, Karen L, Muzny, Donna M, Ntalla, Ioanna, Palmer, Nicholette D, Pasko, Dorota, Peter, Andreas, Rayner, Nigel W, Renström, Frida, Rice, Ken, Sala, Cinzia F, Sennblad, Bengt, Serafetinidis, Ioannis, Smith, Jennifer A, Soranzo, Nicole, Speliotes, Elizabeth K, Stahl, Eli A, Stirrups, Kathleen, Tentolouris, Nikos, Thanopoulou, Anastasia, Torres, Mina, Traglia, Michela, Tsafantakis, Emmanouil, Javad, Sundas, Yanek, Lisa R, Zengini, Eleni, Becker, Diane M, Bis, Joshua C, Brown, James B, Adrienne Cupples, L, Hansen, Torben, Ingelsson, Erik, Karter, Andrew J, Lorenzo, Carlos, Mathias, Rasika A, Norris, Jill M, Peloso, Gina M, Sheu, Wayne H.-H., Toniolo, Daniela, Vaidya, Dhananjay, Varma, Rohit, Wagenknecht, Lynne E, Boeing, Heiner, Bottinger, Erwin P, Dedoussis, George, Deloukas, Panos, Ferrannini, Ele, Franco, Oscar H, Franks, Paul W, Gibbs, Richard A, Gudnason, Vilmundur, Hamsten, Anders, Harris, Tamara B, Hattersley, Andrew T, Hayward, Caroline, Hofman, Albert, Jansson, Jan-Håkan, Langenberg, Claudia, Launer, Lenore J, Levy, Daniel, Oostra, Ben A, O'Donnell, Christopher J, O'Rahilly, Stephen, Padmanabhan, Sandosh, Pankow, James S, Polasek, Ozren, Province, Michael A, Rich, Stephen S, Ridker, Paul M, Rudan, Igor, Schulze, Matthias B, Smith, Blair H, Uitterlinden, André G, Walker, Mark, Watkins, Hugh, Wong, Tien Y, Zeggini, Eleftheria, Laakso, Markku, Borecki, Ingrid B, Chasman, Daniel I, Pedersen, Oluf, Psaty, Bruce M, Shyong Tai, E, van Duijn, Cornelia M, Wareham, Nicholas J, Waterworth, Dawn M, Boerwinkle, Eric, Linda Kao, W H, Florez, Jose C, Loos, Ruth J.F., Wilson, James G, Frayling, Timothy M, Siscovick, David S, Dupuis, Josée, Rotter, Jerome I, Meigs, James B, Scott, Robert A, Goodarzi, Mark O

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