Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study

por Wang, Yuxuan, Selvaraj, Margaret Sunitha, Li, Xihao, Li, Zilin, Holdcraft, Jacob A., Arnett, Donna K., Bis, Joshua C., Blangero, John, Boerwinkle, Eric, Bowden, Donald W., Cade, Brian E., Carlson, Jenna C., Carson, April P., Chen, Yii-Der Ida, Curran, Joanne E., de Vries, Paul S., Dutcher, Susan K., Ellinor, Patrick T., Floyd, James S., Fornage, Myriam, Freedman, Barry I., Gabriel, Stacey, Germer, Soren, Gibbs, Richard A., Guo, Xiuqing, He, Jiang, Heard-Costa, Nancy, Hildalgo, Bertha, Hou, Lifang, Irvin, Marguerite R., Joehanes, Roby, Kaplan, Robert C., Kardia, Sharon LR., Kelly, Tanika N., Kim, Ryan, Kooperberg, Charles, Kral, Brian G., Levy, Daniel, Li, Changwei, Liu, Chunyu, Lloyd-Jone, Don, Loos, Ruth JF., Mahaney, Michael C., Martin, Lisa W., Mathias, Rasika A., Minster, Ryan L., Mitchell, Braxton D., Montasser, May E., Morrison, Alanna C., Murabito, Joanne M., Naseri, Take, O’Connell, Jeffrey R., Palmer, Nicholette D., Preuss, Michael H., Psaty, Bruce M., Raffield, Laura M., Rao, Dabeeru C., Redline, Susan, Reiner, Alexander P., Rich, Stephen S., Ruepena, Muagututi’a Sefuiva, Sheu, Wayne H-H., Smith, Jennifer A., Smith, Albert, Tiwari, Hemant K., Tsai, Michael Y., Viaud-Martinez, Karine A., Wang, Zhe, Yanek, Lisa R., Zhao, Wei, Rotter, Jerome I., Lin, Xihong, Natarajan, Pradeep, Peloso, Gina M.
Publicado 2023

A Loss-of-Function Splice Acceptor Variant in IGF2 Is Protective for Type 2 Diabetes

por Mercader, Josep M., Liao, Rachel G., Bell, Avery D., Dymek, Zachary, Estrada, Karol, Tukiainen, Taru, Huerta-Chagoya, Alicia, Moreno-Macías, Hortensia, Jablonski, Kathleen A., Hanson, Robert L., Walford, Geoffrey A., Moran, Ignasi, Chen, Ling, Agarwala, Vineeta, Ordoñez-Sánchez, María Luisa, Rodríguez-Guillen, Rosario, Rodríguez-Torres, Maribel, Segura-Kato, Yayoi, García-Ortiz, Humberto, Centeno-Cruz, Federico, Barajas-Olmos, Francisco, Caulkins, Lizz, Puppala, Sobha, Fontanillas, Pierre, Williams, Amy L., Bonàs-Guarch, Sílvia, Hartl, Chris, Ripke, Stephan, Tooley, Katherine, Lane, Jacqueline, Zerrweck, Carlos, Martínez-Hernández, Angélica, Córdova, Emilio J., Mendoza-Caamal, Elvia, Contreras-Cubas, Cecilia, González-Villalpando, María E., Cruz-Bautista, Ivette, Muñoz-Hernández, Liliana, Gómez-Velasco, Donaji, Alvirde, Ulises, Henderson, Brian E., Wilkens, Lynne R., Le Marchand, Loic, Arellano-Campos, Olimpia, Riba, Laura, Harden, Maegan, Gabriel, Stacey, Abboud, Hanna E., Cortes, Maria L., Revilla-Monsalve, Cristina, Islas-Andrade, Sergio, Soberon, Xavier, Curran, Joanne E., Jenkinson, Christopher P., DeFronzo, Ralph A., Lehman, Donna M., Hanis, Craig L., Bell, Graeme I., Boehnke, Michael, Blangero, John, Duggirala, Ravindranath, Saxena, Richa, MacArthur, Daniel, Ferrer, Jorge, McCarroll, Steven A., Torrents, David, Knowler, William C., Baier, Leslie J., Burtt, Noel, González-Villalpando, Clicerio, Haiman, Christopher A., Aguilar-Salinas, Carlos A., Tusié-Luna, Teresa, Flannick, Jason, Jacobs, Suzanne B.R., Orozco, Lorena, Altshuler, David, Florez, Jose C.
Publicado 2017

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixe...

por Kowalski, Madeline H., Qian, Huijun, Hou, Ziyi, Rosen, Jonathan D., Tapia, Amanda L., Shan, Yue, Jain, Deepti, Argos, Maria, Arnett, Donna K., Avery, Christy, Barnes, Kathleen C., Becker, Lewis C., Bien, Stephanie A., Bis, Joshua C., Blangero, John, Boerwinkle, Eric, Bowden, Donald W., Buyske, Steve, Cai, Jianwen, Cho, Michael H., Choi, Seung Hoan, Choquet, Hélène, Cupples, L. Adrienne, Cushman, Mary, Daya, Michelle, de Vries, Paul S., Ellinor, Patrick T., Faraday, Nauder, Fornage, Myriam, Gabriel, Stacey, Ganesh, Santhi K., Graff, Misa, Gupta, Namrata, He, Jiang, Heckbert, Susan R., Hidalgo, Bertha, Hodonsky, Chani J., Irvin, Marguerite R., Johnson, Andrew D., Jorgenson, Eric, Kaplan, Robert, Kardia, Sharon L. R., Kelly, Tanika N., Kooperberg, Charles, Lasky-Su, Jessica A., Loos, Ruth J. F., Lubitz, Steven A., Mathias, Rasika A., McHugh, Caitlin P., Montgomery, Courtney, Moon, Jee-Young, Morrison, Alanna C., Palmer, Nicholette D., Pankratz, Nathan, Papanicolaou, George J., Peralta, Juan M., Peyser, Patricia A., Rich, Stephen S., Rotter, Jerome I., Silverman, Edwin K., Smith, Jennifer A., Smith, Nicholas L., Taylor, Kent D., Thornton, Timothy A., Tiwari, Hemant K., Tracy, Russell P., Wang, Tao, Weiss, Scott T., Weng, Lu-Chen, Wiggins, Kerri L., Wilson, James G., Yanek, Lisa R., Zöllner, Sebastian, North, Kari E., Auer, Paul L., Raffield, Laura M., Reiner, Alexander P., Li, Yun
Publicado 2019

Rare coding variants in RCN3 are associated with blood pressure

por He, Karen Y., Kelly, Tanika N., Wang, Heming, Liang, Jingjing, Zhu, Luke, Cade, Brian E., Assimes, Themistocles L., Becker, Lewis C., Beitelshees, Amber L., Bielak, Lawrence F., Bress, Adam P., Brody, Jennifer A., Chang, Yen-Pei Christy, Chang, Yi-Cheng, de Vries, Paul S., Duggirala, Ravindranath, Fox, Ervin R., Franceschini, Nora, Furniss, Anna L., Gao, Yan, Guo, Xiuqing, Haessler, Jeffrey, Hung, Yi-Jen, 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, Naseri, Take, Palmas, Walter, Reupena, Muagututi’a Sefuiva, Rice, Kenneth M., Sheu, Wayne H.-H., Shimbo, Daichi, Smith, Jennifer A., Snively, Beverly M., Yanek, Lisa R., Zhao, Wei, Blangero, John, Boerwinkle, Eric, Chen, Yii-Der Ida, Correa, Adolfo, Cupples, L. Adrienne, Curran, Joanne E., Fornage, Myriam, He, Jiang, Hou, Lifang, Kaplan, Robert C., Kardia, Sharon L. R., Kenny, Eimear E., Kooperberg, Charles, Lloyd-Jones, Donald, Loos, Ruth J. F., Mathias, Rasika A., McGarvey, Stephen T., Mitchell, Braxton D., North, Kari E., Peyser, Patricia A., Psaty, Bruce M., Raffield, Laura M., Rao, D. C., Redline, Susan, Reiner, Alex P., Rich, Stephen S., Rotter, Jerome I., Taylor, Kent D., Tracy, Russell, Vasan, Ramachandran S., Morrison, Alanna C., Levy, Daniel, Chakravarti, Aravinda, Arnett, Donna K., Zhu, Xiaofeng
Publicado 2022

The genetic determinants of recurrent somatic mutations in 43,693 blood genomes

por Weinstock, Joshua S., Laurie, Cecelia A., Broome, Jai G., Taylor, Kent D., Guo, Xiuqing, Shuldiner, Alan R., O’Connell, Jeffrey R., Lewis, Joshua P., Boerwinkle, Eric, Barnes, Kathleen C., Chami, Nathalie, Kenny, Eimear E., Loos, Ruth J. F., Fornage, Myriam, Redline, Susan, Cade, Brian E., Gilliland, Frank D., Chen, Zhanghua, Gauderman, W. James, Kumar, Rajesh, Grammer, Leslie, Schleimer, Robert P., Psaty, Bruce M., Bis, Joshua C., Brody, Jennifer A., Silverman, Edwin K., Yun, Jeong H., Qiao, Dandi, Weiss, Scott T., Lasky-Su, Jessica, DeMeo, Dawn L., Palmer, Nicholette D., Freedman, Barry I., Bowden, Donald W., Cho, Michael H., Vasan, Ramachandran S., Johnson, Andrew D., Yanek, Lisa R., Becker, Lewis C., Kardia, Sharon, He, Jiang, Kaplan, Robert, Heckbert, Susan R., Smith, Nicholas L., Wiggins, Kerri L., Arnett, Donna K., Irvin, Marguerite R., Tiwari, Hemant, Correa, Adolfo, Raffield, Laura M., Gao, Yan, de Andrade, Mariza, Rotter, Jerome I., Rich, Stephen S., Manichaikul, Ani W., Konkle, Barbara A., Johnsen, Jill M., Wheeler, Marsha M., Custer, Brian S., Duggirala, Ravindranath, Curran, Joanne E., Blangero, John, Gui, Hongsheng, Xiao, Shujie, Williams, L. Keoki, Meyers, Deborah A., Li, Xingnan, Ortega, Victor, McGarvey, Stephen, Gu, C. Charles, Chen, Yii-Der Ida, Lee, Wen-Jane, Shoemaker, M. Benjamin, Darbar, Dawood, Roden, Dan, Albert, Christine, Kooperberg, Charles, Desai, Pinkal, Blackwell, Thomas W., Abecasis, Goncalo R., Smith, Albert V., Kang, Hyun M., Mathias, Rasika, Natarajan, Pradeep, Jaiswal, Siddhartha, Reiner, Alexander P., Bick, Alexander G.
Publicado 2023

Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 Locus

por Mahajan, Anubha, Sim, Xueling, Ng, Hui Jin, Manning, Alisa, Rivas, Manuel A., Highland, Heather M., Locke, Adam E., Grarup, Niels, Im, Hae Kyung, Cingolani, Pablo, Flannick, Jason, Fontanillas, Pierre, Fuchsberger, Christian, Gaulton, Kyle J., Teslovich, Tanya M., Rayner, N. William, Robertson, Neil R., Beer, Nicola L., Rundle, Jana K., Bork-Jensen, Jette, Ladenvall, Claes, Blancher, Christine, Buck, David, Buck, Gemma, Burtt, Noël P., Gabriel, Stacey, Gjesing, Anette P., Groves, Christopher J., Hollensted, Mette, Huyghe, Jeroen R., Jackson, Anne U., Jun, Goo, Justesen, Johanne Marie, Mangino, Massimo, Murphy, Jacquelyn, Neville, Matt, Onofrio, Robert, Small, Kerrin S., Stringham, Heather M., Syvänen, Ann-Christine, Trakalo, Joseph, Abecasis, Goncalo, Bell, Graeme I., Blangero, John, Cox, Nancy J., Duggirala, Ravindranath, Hanis, Craig L., Seielstad, Mark, Wilson, James G., Christensen, Cramer, Brandslund, Ivan, Rauramaa, Rainer, Surdulescu, Gabriela L., Doney, Alex S. F., Lannfelt, Lars, Linneberg, Allan, Isomaa, Bo, Tuomi, Tiinamaija, Jørgensen, Marit E., Jørgensen, Torben, Kuusisto, Johanna, Uusitupa, Matti, Salomaa, Veikko, Spector, Timothy D., Morris, Andrew D., Palmer, Colin N. A., Collins, Francis S., Mohlke, Karen L., Bergman, Richard N., Ingelsson, Erik, Lind, Lars, Tuomilehto, Jaakko, Hansen, Torben, Watanabe, Richard M., Prokopenko, Inga, Dupuis, Josee, Karpe, Fredrik, Groop, Leif, Laakso, Markku, Pedersen, Oluf, Florez, Jose C., Morris, Andrew P., Altshuler, David, Meigs, James B., Boehnke, Michael, McCarthy, Mark I., Lindgren, Cecilia M., Gloyn, Anna L.
Publicado 2015

Chronic neuropsychiatric sequelae of SARS‐CoV‐2: Protocol and methods from the Alzheimer's Association Global Consortium

por de Erausquin, Gabriel A., Snyder, Heather, Brugha, Traolach S., Seshadri, Sudha, Carrillo, Maria, Sagar, Rajesh, Huang, Yueqin, Newton, Charles, Tartaglia, Carmela, Teunissen, Charlotte, Håkanson, Krister, Akinyemi, Rufus, Prasad, Kameshwar, D'Avossa, Giovanni, Gonzalez‐Aleman, Gabriela, Hosseini, Akram, Vavougios, George D., Sachdev, Perminder, Bankart, John, Mors, Niels Peter Ole, Lipton, Richard, Katz, Mindy, Fox, Peter T., Katshu, Mohammad Zia, Iyengar, M. Sriram, Weinstein, Galit, Sohrabi, Hamid R., Jenkins, Rachel, Stein, Dan J., Hugon, Jacques, Mavreas, Venetsanos, Blangero, John, Cruchaga, Carlos, Krishna, Murali, Wadoo, Ovais, Becerra, Rodrigo, Zwir, Igor, Longstreth, William T., Kroenenberg, Golo, Edison, Paul, Mukaetova‐Ladinska, Elizabeta, Staufenberg, Ekkehart, Figueredo‐Aguiar, Mariana, Yécora, Agustín, Vaca, Fabiana, Zamponi, Hernan P., Re, Vincenzina Lo, Majid, Abdul, Sundarakumar, Jonas, Gonzalez, Hector M., Geerlings, Mirjam I., Skoog, Ingmar, Salmoiraghi, Alberto, Boneschi, Filippo Martinelli, Patel, Vibuthi N., Santos, Juan M., Arroyo, Guillermo Rivera, Moreno, Antonio Caballero, Felix, Pascal, Gallo, Carla, Arai, Hidenori, Yamada, Masahito, Iwatsubo, Takeshi, Sharma, Malveeka, Chakraborty, Nandini, Ferreccio, Catterina, Akena, Dickens, Brayne, Carol, Maestre, Gladys, Blangero, Sarah Williams, Brusco, Luis I., Siddarth, Prabha, Hughes, Timothy M., Zuñiga, Alfredo Ramírez, Kambeitz, Joseph, Laza, Agustin Ruiz, Allen, Norrina, Panos, Stella, Merrill, David, Ibáñez, Agustín, Tsuang, Debby, Valishvili, Nino, Shrestha, Srishti, Wang, Sophia, Padma, Vasantha, Anstey, Kaarin J., Ravindrdanath, Vijayalakshmi, Blennow, Kaj, Mullins, Paul, Łojek, Emilia, Pria, Anand, Mosley, Thomas H., Gowland, Penny, Girard, Timothy D., Bowtell, Richard, Vahidy, Farhaan S.
Publicado 2022

Whole genome sequence analysis of blood lipid levels in >66,000 individuals

por Selvaraj, Margaret Sunitha, Li, Xihao, Li, Zilin, Pampana, Akhil, Zhang, David Y., Park, Joseph, Aslibekyan, Stella, Bis, Joshua C., Brody, Jennifer A., Cade, Brian E., Chuang, Lee-Ming, Chung, Ren-Hua, Curran, Joanne E., de las Fuentes, Lisa, de Vries, Paul S., Duggirala, Ravindranath, Freedman, Barry I., Graff, Mariaelisa, Guo, Xiuqing, Heard-Costa, Nancy, Hidalgo, Bertha, Hwu, Chii-Min, Irvin, Marguerite R., Kelly, Tanika N., Kral, Brian G., Lange, Leslie, Li, Xiaohui, Lisa, Martin, Lubitz, Steven A., Manichaikul, Ani W., Michael, Preuss, Montasser, May E., Morrison, Alanna C., Naseri, Take, O’Connell, Jeffrey R., Palmer, Nicholette D., Peyser, Patricia A., Reupena, Muagututia S., Smith, Jennifer A., Sun, Xiao, Taylor, Kent D., Tracy, Russell P., Tsai, Michael Y., Wang, Zhe, Wang, Yuxuan, Bao, Wei, Wilkins, John T., Yanek, Lisa R., Zhao, Wei, Arnett, Donna K., Blangero, John, Boerwinkle, Eric, Bowden, Donald W., Chen, Yii-Der Ida, Correa, Adolfo, Cupples, L. Adrienne, Dutcher, Susan K., Ellinor, Patrick T., Fornage, Myriam, Gabriel, Stacey, Germer, Soren, Gibbs, Richard, He, Jiang, Kaplan, Robert C., Kardia, Sharon L. R., Kim, Ryan, Kooperberg, Charles, Loos, Ruth J. F., Viaud-Martinez, Karine A, Mathias, Rasika A., McGarvey, Stephen T., Mitchell, Braxton D., Nickerson, Deborah, North, Kari E., Psaty, Bruce M., Redline, Susan, Reiner, Alexander P., Vasan, Ramachandran S., Rich, Stephen S., Willer, Cristen, Rotter, Jerome I., Rader, Daniel J., Lin, Xihong, Peloso, Gina M., Natarajan, Pradeep
Publicado 2022

Structural variation across 138,134 samples in the TOPMed consortium

por Jun, Goo, English, Adam C, Metcalf, Ginger A, Yang, Jianzhi, Chaisson, Mark JP, Pankratz, Nathan, Menon, Vipin K, Salerno, William J, Krasheninina, Olga, Smith, Albert V, Lane, John A, Blackwell, Tom, Kang, Hyun Min, Salvi, Sejal, Meng, Qingchang, Shen, Hua, Pasham, Divya, Bhamidipati, Sravya, Kottapalli, Kavya, Arnett, Donna K., Ashley-Koch, Allison, Auer, Paul L., Beutel, Kathleen M, Bis, Joshua C., Blangero, John, Bowden, Donald W., Brody, Jennifer A., Cade, Brian E., Chen, Yii-Der Ida, Cho, Michael H., Curran, Joanne E., Fornage, Myriam, Freedman, Barry I., Fingerlin, Tasha, Gelb, Bruce D., Hou, Lifang, Hung, Yi-Jen, Kane, John P, Kaplan, Robert, Kim, Wonji, Loos, Ruth J.F., Marcus, Gregory M, Mathias, Rasika A., McGarvey, Stephen T., Montgomery, Courtney, Naseri, Take, Nouraie, S. Mehdi, Preuss, Michael H., Palmer, Nicholette D., Peyser, Patricia A., Raffield, Laura M., Ratan, Aakrosh, Redline, Susan, Reupena, Sefuiva, Rotter, Jerome I., Rich, Stephen S., Rienstra, Michiel, Ruczinski, Ingo, Sankaran, Vijay G., Schwartz, David A., Seidman, Christine E., Seidman, Jonathan G., Silverman, Edwin K., Smith, Jennifer A., Stilp, Adrienne, Taylor, Kent D., Telen, Marilyn J., Weiss, Scott T., Williams, L. Keoki, Wu, Baojun, Yanek, Lisa R., Zhang, Yingze, Lasky-Su, Jessica, Gingras, Marie Claude, Dutcher, Susan K., Eichler, Evan E., Gabriel, Stacey, Germer, Soren, Kim, Ryan, Viaud-Martinez, Karine A., Nickerson, Deborah A., Luo, James, Reiner, Alex, Gibbs, Richard A, Boerwinkle, Eric, Abecasis, Goncalo, Sedlazeck, Fritz J
Publicado 2023

Structural variation across 138,134 samples in the TOPMed consortium

por Jun, Goo, English, Adam C, Metcalf, Ginger A, Yang, Jianzhi, Chaisson, Mark JP, Pankratz, Nathan, Menon, Vipin K, Salerno, William J, Krasheninina, Olga, Smith, Albert V, Lane, John A, Blackwell, Tom, Kang, Hyun Min, Salvi, Sejal, Meng, Qingchang, Shen, Hua, Pasham, Divya, Bhamidipati, Sravya, Kottapalli, Kavya, Arnett, Donna K., Ashley-Koch, Allison, Auer, Paul L., Beutel, Kathleen M, Bis, Joshua C., Blangero, John, Bowden, Donald W., Brody, Jennifer A., Cade, Brian E., Chen, Yii-Der Ida, Cho, Michael H., Curran, Joanne E., Fornage, Myriam, Freedman, Barry I., Fingerlin, Tasha, Gelb, Bruce D., Hou, Lifang, Hung, Yi-Jen, Kane, John P, Kaplan, Robert, Kim, Wonji, Loos, Ruth J.F., Marcus, Gregory M, Mathias, Rasika A., McGarvey, Stephen T., Montgomery, Courtney, Naseri, Take, Nouraie, S. Mehdi, Preuss, Michael H., Palmer, Nicholette D., Peyser, Patricia A., Raffield, Laura M., Ratan, Aakrosh, Redline, Susan, Reupena, Sefuiva, Rotter, Jerome I., Rich, Stephen S., Rienstra, Michiel, Ruczinski, Ingo, Sankaran, Vijay G., Schwartz, David A., Seidman, Christine E., Seidman, Jonathan G., Silverman, Edwin K., Smith, Jennifer A., Stilp, Adrienne, Taylor, Kent D., Telen, Marilyn J., Weiss, Scott T., Williams, L. Keoki, Wu, Baojun, Yanek, Lisa R., Zhang, Yingze, Lasky-Su, Jessica, Gingras, Marie Claude, Dutcher, Susan K., Eichler, Evan E., Gabriel, Stacey, Germer, Soren, Kim, Ryan, Viaud-Martinez, Karine A., Nickerson, Deborah A., Luo, James, Reiner, Alex, Gibbs, Richard A, Boerwinkle, Eric, Abecasis, Goncalo, Sedlazeck, Fritz J
Publicado 2023

Two neurostructural subtypes: results of machine learning on brain images from 4,291 individuals with schizophrenia

por Jiang, Yuchao, Luo, Cheng, Wang, Jijun, Palaniyappan, Lena, Chang, Xiao, Xiang, Shitong, Zhang, Jie, Duan, Mingjun, Huang, Huan, Gaser, Christian, Nemoto, Kiyotaka, Miura, Kenichiro, Hashimoto, Ryota, Westlye, Lars T., Richard, Genevieve, Fernandez-Cabello, Sara, Parker, Nadine, Andreassen, Ole A., Kircher, Tilo, Nenadić, Igor, Stein, Frederike, Thomas-Odenthal, Florian, Teutenberg, Lea, Usemann, Paula, Dannlowski, Udo, Hahn, Tim, Grotegerd, Dominik, Meinert, Susanne, Lencer, Rebekka, Tang, Yingying, Zhang, Tianhong, Li, Chunbo, Yue, Weihua, Zhang, Yuyanan, Yu, Xin, Zhou, Enpeng, Lin, Ching-Po, Tsai, Shih-Jen, Rodrigue, Amanda L., Glahn, David, Pearlson, Godfrey, Blangero, John, Karuk, Andriana, Pomarol-Clotet, Edith, Salvador, Raymond, Fuentes-Claramonte, Paola, Garcia-León, María Ángeles, Spalletta, Gianfranco, Piras, Fabrizio, Vecchio, Daniela, Banaj, Nerisa, Cheng, Jingliang, Liu, Zhening, Yang, Jie, Gonul, Ali Saffet, Uslu, Ozgul, Burhanoglu, Birce Begum, Demir, Aslihan Uyar, Rootes-Murdy, Kelly, Calhoun, Vince D., Sim, Kang, Green, Melissa, Quidé, Yann, Chung, Young Chul, Kim, Woo-Sung, Sponheim, Scott R., Demro, Caroline, Ramsay, Ian S., Iasevoli, Felice, de Bartolomeis, Andrea, Barone, Annarita, Ciccarelli, Mariateresa, Brunetti, Arturo, Cocozza, Sirio, Pontillo, Giuseppe, Tranfa, Mario, Park, Min Tae M., Kirschner, Matthias, Georgiadis, Foivos, Kaiser, Stefan, Rheenen, Tamsyn E Van, Rossell, Susan L, Hughes, Matthew, Woods, William, Carruthers, Sean P, Sumner, Philip, Ringin, Elysha, Spaniel, Filip, Skoch, Antonin, Tomecek, David, Homan, Philipp, Homan, Stephanie, Omlor, Wolfgang, Cecere, Giacomo, Nguyen, Dana D, Preda, Adrian, Thomopoulos, Sophia, Jahanshad, Neda, Cui, Long-Biao, Yao, Dezhong, Thompson, Paul M., Turner, Jessica A., van Erp, Theo G.M., Cheng, Wei, Feng, Jianfeng
Publicado 2023

Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program

por DiCorpo, Daniel, Gaynor, Sheila M., Russell, Emily M., Westerman, Kenneth E., Raffield, Laura M., Majarian, Timothy D., Wu, Peitao, Sarnowski, Chloé, Highland, Heather M., Jackson, Anne, Hasbani, Natalie R., de Vries, Paul S., Brody, Jennifer A., Hidalgo, Bertha, Guo, Xiuqing, Perry, James A., O’Connell, Jeffrey R., Lent, Samantha, Montasser, May E., Cade, Brian E., Jain, Deepti, Wang, Heming, D’Oliveira Albanus, Ricardo, Varshney, Arushi, Yanek, Lisa R., Lange, Leslie, Palmer, Nicholette D., Almeida, Marcio, Peralta, Juan M., Aslibekyan, Stella, Baldridge, Abigail S., Bertoni, Alain G., Bielak, Lawrence F., Chen, Chung-Shiuan, Chen, Yii-Der Ida, Choi, Won Jung, Goodarzi, Mark O., Floyd, James S., Irvin, Marguerite R., Kalyani, Rita R., Kelly, Tanika N., Lee, Seonwook, Liu, Ching-Ti, Loesch, Douglas, Manson, JoAnn E., Minster, Ryan L., Naseri, Take, Pankow, James S., Rasmussen-Torvik, Laura J., Reiner, Alexander P., Reupena, Muagututi’a Sefuiva, Selvin, Elizabeth, Smith, Jennifer A., Weeks, Daniel E., Xu, Huichun, Yao, Jie, Zhao, Wei, Parker, Stephen, Alonso, Alvaro, Arnett, Donna K., Blangero, John, Boerwinkle, Eric, Correa, Adolfo, Cupples, L. Adrienne, Curran, Joanne E., Duggirala, Ravindranath, He, Jiang, Heckbert, Susan R., Kardia, Sharon L. R., Kim, Ryan W., Kooperberg, Charles, Liu, Simin, Mathias, Rasika A., McGarvey, Stephen T., Mitchell, Braxton D., Morrison, Alanna C., Peyser, Patricia A., Psaty, Bruce M., Redline, Susan, Shuldiner, Alan R., Taylor, Kent D., Vasan, Ramachandran S., Viaud-Martinez, Karine A., Florez, Jose C., Wilson, James G., Sladek, Robert, Rich, Stephen S., Rotter, Jerome I., Lin, Xihong, Dupuis, Josée, Meigs, James B., Wessel, Jennifer, Manning, Alisa K.
Publicado 2022

Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing

por Chen, Fang, Wang, Xingyan, Jang, Seon-Kyeong, Quach, Bryan C., Weissenkampen, J. Dylan, Khunsriraksakul, Chachrit, Yang, Lina, Sauteraud, Renan, Albert, Christine M., Allred, Nicholette D. D., Arnett, Donna K., Ashley-Koch, Allison E., Barnes, Kathleen C., Barr, R. Graham, Becker, Diane M., Bielak, Lawrence F., Bis, Joshua C., Blangero, John, Boorgula, Meher Preethi, Chasman, Daniel I., Chavan, Sameer, Chen, Yii-Der I., Chuang, Lee-Ming, Correa, Adolfo, Curran, Joanne E., David, Sean P., Fuentes, Lisa de las, Deka, Ranjan, Duggirala, Ravindranath, Faul, Jessica D., Garrett, Melanie E., Gharib, Sina A., Guo, Xiuqing, Hall, Michael E., Hawley, Nicola L., He, Jiang, Hobbs, Brian D., Hokanson, John E., Hsiung, Chao A., Hwang, Shih-Jen, Hyde, Thomas M., Irvin, Marguerite R., Jaffe, Andrew E., Johnson, Eric O., Kaplan, Robert, Kardia, Sharon L. R., Kaufman, Joel D., Kelly, Tanika N., Kleinman, Joel E., Kooperberg, Charles, Lee, I-Te, Levy, Daniel, Lutz, Sharon M., Manichaikul, Ani W., Martin, Lisa W., Marx, Olivia, McGarvey, Stephen T., Minster, Ryan L., Moll, Matthew, Moussa, Karine A., Naseri, Take, North, Kari E., Oelsner, Elizabeth C., Peralta, Juan M., Peyser, Patricia A., Psaty, Bruce M., Rafaels, Nicholas, Raffield, Laura M., Reupena, Muagututi’a Sefuiva, Rich, Stephen S., Rotter, Jerome I., Schwartz, David A., Shadyab, Aladdin H., Sheu, Wayne H-H., Sims, Mario, Smith, Jennifer A., Sun, Xiao, Taylor, Kent D., Telen, Marilyn J., Watson, Harold, Weeks, Daniel E., Weir, David R., Yanek, Lisa R., Young, Kendra A., Young, Kristin L., Zhao, Wei, Hancock, Dana B., Jiang, Bibo, Vrieze, Scott, Liu, Dajiang J.
Publicado 2023

Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease

por Nielsen, Jonas B., Rom, Oren, Surakka, Ida, Graham, Sarah E., Zhou, Wei, Roychowdhury, Tanmoy, Fritsche, Lars G., Gagliano Taliun, Sarah A., Sidore, Carlo, Liu, Yuhao, Gabrielsen, Maiken E., Skogholt, Anne Heidi, Wolford, Brooke, Overton, William, Zhao, Ying, Chen, Jin, Zhang, He, Hornsby, Whitney E., Acheampong, Akua, Grooms, Austen, Schaefer, Amanda, Zajac, Gregory J. M., Villacorta, Luis, Zhang, Jifeng, Brumpton, Ben, Løset, Mari, Rai, Vivek, Lundegaard, Pia R., Olesen, Morten S., Taylor, Kent D., Palmer, Nicholette D., Chen, Yii-Der, Choi, Seung H., Lubitz, Steven A., Ellinor, Patrick T., Barnes, Kathleen C., Daya, Michelle, Rafaels, Nicholas, Weiss, Scott T., Lasky-Su, Jessica, Tracy, Russell P., Vasan, Ramachandran S., Cupples, L. Adrienne, Mathias, Rasika A., Yanek, Lisa R., Becker, Lewis C., Peyser, Patricia A., Bielak, Lawrence F., Smith, Jennifer A., Aslibekyan, Stella, Hidalgo, Bertha A., Arnett, Donna K., Irvin, Marguerite R., Wilson, James G., Musani, Solomon K., Correa, Adolfo, Rich, Stephen S., Guo, Xiuqing, Rotter, Jerome I., Konkle, Barbara A., Johnsen, Jill M., Ashley-Koch, Allison E., Telen, Marilyn J., Sheehan, Vivien A., Blangero, John, Curran, Joanne E., Peralta, Juan M., Montgomery, Courtney, Sheu, Wayne H-H, Chung, Ren-Hua, Schwander, Karen, Nouraie, Seyed M., Gordeuk, Victor R., Zhang, Yingze, Kooperberg, Charles, Reiner, Alexander P., Jackson, Rebecca D., Bleecker, Eugene R., Meyers, Deborah A., Li, Xingnan, Das, Sayantan, Yu, Ketian, LeFaive, Jonathon, Smith, Albert, Blackwell, Tom, Taliun, Daniel, Zollner, Sebastian, Forer, Lukas, Schoenherr, Sebastian, Fuchsberger, Christian, Pandit, Anita, Zawistowski, Matthew, Kheterpal, Sachin, Brummett, Chad M., Natarajan, Pradeep, Schlessinger, David, Lee, Seunggeun, Kang, Hyun Min, Cucca, Francesco, Holmen, Oddgeir L., Åsvold, Bjørn O., Boehnke, Michael, Kathiresan, Sekar, Abecasis, Goncalo R., Chen, Y. Eugene, Willer, Cristen J., Hveem, Kristian
Publicado 2020

Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices

por Natarajan, Pradeep, Pampana, Akhil, Graham, Sarah E., Ruotsalainen, Sanni E., Perry, James A., de Vries, Paul S., Broome, Jai G., Pirruccello, James P., Honigberg, Michael C., Aragam, Krishna, Wolford, Brooke, Brody, Jennifer A., Antonacci-Fulton, Lucinda, Arden, Moscati, Aslibekyan, Stella, Assimes, Themistocles L., Ballantyne, Christie M., Bielak, Lawrence F., Bis, Joshua C., Cade, Brian E., Do, Ron, Doddapaneni, Harsha, Emery, Leslie S., Hung, Yi-Jen, Irvin, Marguerite R., Khan, Alyna T., Lange, Leslie, Lee, Jiwon, Lemaitre, Rozenn N., Martin, Lisa W., Metcalf, Ginger, Montasser, May E., Moon, Jee-Young, Muzny, Donna, O’Connell, Jeffrey R., Palmer, Nicholette D., Peralta, Juan M., Peyser, Patricia A., Stilp, Adrienne M., Tsai, Michael, Wang, Fei Fei, Weeks, Daniel E., Yanek, Lisa R., Wilson, James G., Abecasis, Goncalo, Arnett, Donna K., Becker, Lewis C., Blangero, John, Boerwinkle, Eric, Bowden, Donald W., Chang, Yi-Cheng, Chen, Yii-Der I., Choi, Won Jung, Correa, Adolfo, Curran, Joanne E., Daly, Mark J., Dutcher, Susan K., Ellinor, Patrick T., Fornage, Myriam, Freedman, Barry I., Gabriel, Stacey, Germer, Soren, Gibbs, Richard A., He, Jiang, Hveem, Kristian, Jarvik, Gail P., Kaplan, Robert C., Kardia, Sharon L. R., Kenny, Eimear, Kim, Ryan W., Kooperberg, Charles, Laurie, Cathy C., Lee, Seonwook, Lloyd-Jones, Don M., Loos, Ruth J. F., Lubitz, Steven A., Mathias, Rasika A., Martinez, Karine A. Viaud, McGarvey, Stephen T., Mitchell, Braxton D., Nickerson, Deborah A., North, Kari E., Palotie, Aarno, Park, Cheol Joo, Psaty, Bruce M., Rao, D. C., Redline, Susan, Reiner, Alexander P., Seo, Daekwan, Seo, Jeong-Sun, Smith, Albert V., Tracy, Russell P., Vasan, Ramachandran S., Kathiresan, Sekar, Cupples, L. Adrienne, Rotter, Jerome I., Morrison, Alanna C., Rich, Stephen S., Ripatti, Samuli, Willer, Cristen, Peloso, Gina M.
Publicado 2021

The transcriptional landscape of age in human peripheral blood

por Peters, Marjolein J., Joehanes, Roby, Pilling, Luke C., Schurmann, Claudia, Conneely, Karen N., Powell, Joseph, Reinmaa, Eva, Sutphin, George L., Zhernakova, Alexandra, Schramm, Katharina, Wilson, Yana A., Kobes, Sayuko, Tukiainen, Taru, Ramos, Yolande F., Göring, Harald H. H., Fornage, Myriam, Liu, Yongmei, Gharib, Sina A., Stranger, Barbara E., De Jager, Philip L., Aviv, Abraham, Levy, Daniel, Murabito, Joanne M., Munson, Peter J., Huan, Tianxiao, Hofman, Albert, Uitterlinden, André G., Rivadeneira, Fernando, van Rooij, Jeroen, Stolk, Lisette, Broer, Linda, Verbiest, Michael M. P. J., Jhamai, Mila, Arp, Pascal, Metspalu, Andres, Tserel, Liina, Milani, Lili, Samani, Nilesh J., Peterson, Pärt, Kasela, Silva, Codd, Veryan, Peters, Annette, Ward-Caviness, Cavin K., Herder, Christian, Waldenberger, Melanie, Roden, Michael, Singmann, Paula, Zeilinger, Sonja, Illig, Thomas, Homuth, Georg, Grabe, Hans-Jörgen, Völzke, Henry, Steil, Leif, Kocher, Thomas, Murray, Anna, Melzer, David, Yaghootkar, Hanieh, Bandinelli, Stefania, Moses, Eric K., Kent, Jack W., Curran, Joanne E., Johnson, Matthew P., Williams-Blangero, Sarah, Westra, Harm-Jan, McRae, Allan F., Smith, Jennifer A., Kardia, Sharon L. R., Hovatta, Iiris, Perola, Markus, Ripatti, Samuli, Salomaa, Veikko, Henders, Anjali K., Martin, Nicholas G., Smith, Alicia K., Mehta, Divya, Binder, Elisabeth B., Nylocks, K Maria, Kennedy, Elizabeth M., Klengel, Torsten, Ding, Jingzhong, Suchy-Dicey, Astrid M., Enquobahrie, Daniel A., Brody, Jennifer, Rotter, Jerome I., Chen, Yii-Der I., Houwing-Duistermaat, Jeanine, Kloppenburg, Margreet, Slagboom, P. Eline, Helmer, Quinta, den Hollander, Wouter, Bean, Shannon, Raj, Towfique, Bakhshi, Noman, Wang, Qiao Ping, Oyston, Lisa J., Psaty, Bruce M., Tracy, Russell P., Montgomery, Grant W., Turner, Stephen T., Blangero, John, Meulenbelt, Ingrid, Ressler, Kerry J., Yang, Jian, Franke, Lude, Kettunen, Johannes, Visscher, Peter M., Neely, G. Gregory, Korstanje, Ron, Hanson, Robert L., Prokisch, Holger, Ferrucci, Luigi, Esko, Tonu, Teumer, Alexander, van Meurs, Joyce B. J., Johnson, Andrew D.
Publicado 2015

Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits—The Hispanic/Latino Anthropometry Consortium

por Fernández-Rhodes, Lindsay, Graff, Mariaelisa, Buchanan, Victoria L., Justice, Anne E., Highland, Heather M., Guo, Xiuqing, Zhu, Wanying, Chen, Hung-Hsin, Young, Kristin L., Adhikari, Kaustubh, Palmer, Nicholette D., Below, Jennifer E., Bradfield, Jonathan, Pereira, Alexandre C., Glover, LáShauntá, Kim, Daeeun, Lilly, Adam G., Shrestha, Poojan, Thomas, Alvin G., Zhang, Xinruo, Chen, Minhui, Chiang, Charleston W.K., Pulit, Sara, Horimoto, Andrea, Krieger, Jose E., Guindo-Martínez, Marta, Preuss, Michael, Schumann, Claudia, Smit, Roelof A.J., Torres-Mejía, Gabriela, Acuña-Alonzo, Victor, Bedoya, Gabriel, Bortolini, Maria-Cátira, Canizales-Quinteros, Samuel, Gallo, Carla, González-José, Rolando, Poletti, Giovanni, Rothhammer, Francisco, Hakonarson, Hakon, Igo, Robert, Adler, Sharon G., Iyengar, Sudha K., Nicholas, Susanne B., Gogarten, Stephanie M., Isasi, Carmen R., Papnicolaou, George, Stilp, Adrienne M., Qi, Qibin, Kho, Minjung, Smith, Jennifer A., Langefeld, Carl D., Wagenknecht, Lynne, Mckean-Cowdin, Roberta, Gao, Xiaoyi Raymond, Nousome, Darryl, Conti, David V., Feng, Ye, Allison, Matthew A., Arzumanyan, Zorayr, Buchanan, Thomas A., Ida Chen, Yii-Der, Genter, Pauline M., Goodarzi, Mark O., Hai, Yang, Hsueh, Willa, Ipp, Eli, Kandeel, Fouad R., Lam, Kelvin, Li, Xiaohui, Nadler, Jerry L., Raffel, Leslie J., Roll, Kathryn, Sandow, Kevin, Tan, Jingyi, Taylor, Kent D., Xiang, Anny H., Yao, Jie, Audirac-Chalifour, Astride, de Jesus Peralta Romero, Jose, Hartwig, Fernando, Horta, Bernando, Blangero, John, Curran, Joanne E., Duggirala, Ravindranath, Lehman, Donna E., Puppala, Sobha, Fejerman, Laura, John, Esther M., Aguilar-Salinas, Carlos, Burtt, Noël P., Florez, Jose C., García-Ortíz, Humberto, González-Villalpando, Clicerio, Mercader, Josep, Orozco, Lorena, Tusié-Luna, Teresa, Blanco, Estela, Gahagan, Sheila, Cox, Nancy J., Hanis, Craig, Butte, Nancy F., Cole, Shelley A., Comuzzie, Anthony G., Voruganti, V. Saroja, Rohde, Rebecca, Wang, Yujie, Sofer, Tamar, Ziv, Elad, Grant, Struan F.A., Ruiz-Linares, Andres, Rotter, Jerome I., Haiman, Christopher A., Parra, Esteban J., Cruz, Miguel, Loos, Ruth J.F., North, Kari E.
Publicado 2022

WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE

por Zhang, Xinruo, Brody, Jennifer A., Graff, Mariaelisa, Highland, Heather M., Chami, Nathalie, Xu, Hanfei, Wang, Zhe, Ferrier, Kendra, Chittoor, Geetha, Josyula, Navya S., Li, Xihao, Li, Zilin, Allison, Matthew A., Becker, Diane M., Bielak, Lawrence F., Bis, Joshua C., Boorgula, Meher Preethi, Bowden, Donald W., Broome, Jai G., Buth, Erin J., Carlson, Christopher S., Chang, Kyong-Mi, Chavan, Sameer, Chiu, Yen-Feng, Chuang, Lee-Ming, Conomos, Matthew P., DeMeo, Dawn L., Du, Margaret, Duggirala, Ravindranath, Eng, Celeste, Fohner, Alison E., Freedman, Barry I., Garrett, Melanie E., Guo, Xiuqing, Haiman, Chris, Heavner, Benjamin D., Hidalgo, Bertha, Hixson, James E., Ho, Yuk-Lam, Hobbs, Brian D., Hu, Donglei, Hui, Qin, Hwu, Chii-Min, Jackson, Rebecca D., Jain, Deepti, Kalyani, Rita R., Kardia, Sharon L.R., Kelly, Tanika N., Lange, Ethan M., LeNoir, Michael, Li, Changwei, Marchand, Loic Le., McDonald, Merry-Lynn N., McHugh, Caitlin P., Morrison, Alanna C., Naseri, Take, O’Connell, Jeffrey, O’Donnell, Christopher J., Palmer, Nicholette D., Pankow, James S., Perry, James A., Peters, Ulrike, Preuss, Michael H., Rao, D.C., Regan, Elizabeth A., Reupena, Sefuiva M., Roden, Dan M., Rodriguez-Santana, Jose, Sitlani, Colleen M., Smith, Jennifer A., Tiwari, Hemant K., Vasan, Ramachandran S., Wang, Zeyuan, Weeks, Daniel E., Wessel, Jennifer, Wiggins, Kerri L., Wilkens, Lynne R., Wilson, Peter W.F., Yanek, Lisa R., Yoneda, Zachary T., Zhao, Wei, Zöllner, Sebastian, Arnett, Donna K., Ashley-Koch, Allison E., Barnes, Kathleen C., Blangero, John, Boerwinkle, Eric, Burchard, Esteban G., Carson, April P., Chasman, Daniel I., Chen, Yii-Der Ida, Curran, Joanne E., Fornage, Myriam, Gordeuk, Victor R., He, Jiang, Heckbert, Susan R., Hou, Lifang, Irvin, Marguerite R., Kooperberg, Charles, Minster, Ryan L., Mitchell, Braxton D., Nouraie, Mehdi, Psaty, Bruce M., Raffield, Laura M., Reiner, Alexander P., Rich, Stephen S., Rotter, Jerome I., Shoemaker, M. Benjamin, Smith, Nicholas L., Taylor, Kent D., Telen, Marilyn J., Weiss, Scott T., Zhang, Yingze, Heard-Costa, Nancy, Sun, Yan V., Lin, Xihong, Adrienne Cupples, L., Lange, Leslie A., Liu, Ching-Ti, Loos, Ruth J.F., North, Kari E., Justice, Anne E.
Publicado 2023

Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

por Goodrich, Julia K., Singer-Berk, Moriel, Son, Rachel, Sveden, Abigail, Wood, Jordan, England, Eleina, Cole, Joanne B., Weisburd, Ben, Watts, Nick, Caulkins, Lizz, Dornbos, Peter, Koesterer, Ryan, Zappala, Zachary, Zhang, Haichen, Maloney, Kristin A., Dahl, Andy, Aguilar-Salinas, Carlos A., Atzmon, Gil, Barajas-Olmos, Francisco, Barzilai, Nir, Blangero, John, Boerwinkle, Eric, Bonnycastle, Lori L., Bottinger, Erwin, Bowden, Donald W., Centeno-Cruz, Federico, Chambers, John C., Chami, Nathalie, Chan, Edmund, Chan, Juliana, Cheng, Ching-Yu, Cho, Yoon Shin, Contreras-Cubas, Cecilia, Córdova, Emilio, Correa, Adolfo, DeFronzo, Ralph A., Duggirala, Ravindranath, Dupuis, Josée, Garay-Sevilla, Ma Eugenia, García-Ortiz, Humberto, Gieger, Christian, Glaser, Benjamin, González-Villalpando, Clicerio, Gonzalez, Ma Elena, Grarup, Niels, Groop, Leif, Gross, Myron, Haiman, Christopher, Han, Sohee, Hanis, Craig L., Hansen, Torben, Heard-Costa, Nancy L., Henderson, Brian E., Hernandez, Juan Manuel Malacara, Hwang, Mi Yeong, Islas-Andrade, Sergio, Jørgensen, Marit E., Kang, Hyun Min, Kim, Bong-Jo, Kim, Young Jin, Koistinen, Heikki A., Kooner, Jaspal Singh, Kuusisto, Johanna, Kwak, Soo-Heon, Laakso, Markku, Lange, Leslie, Lee, Jong-Young, Lee, Juyoung, Lehman, Donna M., Linneberg, Allan, Liu, Jianjun, Loos, Ruth J. F., Lyssenko, Valeriya, Ma, Ronald C. W., Martínez-Hernández, Angélica, Meigs, James B., Meitinger, Thomas, Mendoza-Caamal, Elvia, Mohlke, Karen L., Morris, Andrew D., Morrison, Alanna C., Ng, Maggie C. Y., Nilsson, Peter M., O’Donnell, Christopher J., Orozco, Lorena, Palmer, Colin N. A., Park, Kyong Soo, Post, Wendy S., Pedersen, Oluf, Preuss, Michael, Psaty, Bruce M., Reiner, Alexander P., Revilla-Monsalve, Cristina, Rich, Stephen S., Rotter, Jerome I., Saleheen, Danish, Schurmann, Claudia, Sim, Xueling, Sladek, Rob, Small, Kerrin S., So, Wing Yee, Spector, Timothy D., Strauch, Konstantin, Strom, Tim M., Tai, E. Shyong, Tam, Claudia H. T., Teo, Yik Ying, Thameem, Farook, Tomlinson, Brian, Tracy, Russell P., Tuomi, Tiinamaija, Tuomilehto, Jaakko, Tusié-Luna, Teresa, van Dam, Rob M., Vasan, Ramachandran S., Wilson, James G., Witte, Daniel R., Wong, Tien-Yin, Burtt, Noël P., Zaitlen, Noah, McCarthy, Mark I., Boehnke, Michael, Pollin, Toni I., Flannick, Jason, Mercader, Josep M., O’Donnell-Luria, Anne, Baxter, Samantha, Florez, Jose C., MacArthur, Daniel G., Udler, Miriam S.
Publicado 2021

Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential

por Nakao, Tetsushi, Bick, Alexander G., Taub, Margaret A., Zekavat, Seyedeh M., Uddin, Md M., Niroula, Abhishek, Carty, Cara L., Lane, John, Honigberg, Michael C., Weinstock, Joshua S., Pampana, Akhil, Gibson, Christopher J., Griffin, Gabriel K., Clarke, Shoa L., Bhattacharya, Romit, Assimes, Themistocles L., Emery, Leslie S., Stilp, Adrienne M., Wong, Quenna, Broome, Jai, Laurie, Cecelia A., Khan, Alyna T., Smith, Albert V., Blackwell, Thomas W., Codd, Veryan, Nelson, Christopher P., Yoneda, Zachary T., Peralta, Juan M., Bowden, Donald W., Irvin, Marguerite R., Boorgula, Meher, Zhao, Wei, Yanek, Lisa R., Wiggins, Kerri L., Hixson, James E., Gu, C. Charles, Peloso, Gina M., Roden, Dan M., Reupena, Muagututi’a S., Hwu, Chii-Min, DeMeo, Dawn L., North, Kari E., Kelly, Shannon, Musani, Solomon K., Bis, Joshua C., Lloyd-Jones, Donald M., Johnsen, Jill M., Preuss, Michael, Tracy, Russell P., Peyser, Patricia A., Qiao, Dandi, Desai, Pinkal, Curran, Joanne E., Freedman, Barry I., Tiwari, Hemant K., Chavan, Sameer, Smith, Jennifer A., Smith, Nicholas L., Kelly, Tanika N., Hidalgo, Bertha, Cupples, L. Adrienne, Weeks, Daniel E., Hawley, Nicola L., Minster, Ryan L., Deka, Ranjan, Naseri, Take T., de las Fuentes, Lisa, Raffield, Laura M., Morrison, Alanna C., Vries, Paul S., Ballantyne, Christie M., Kenny, Eimear E., Rich, Stephen S., Whitsel, Eric A., Cho, Michael H., Shoemaker, M. Benjamin, Pace, Betty S., Blangero, John, Palmer, Nicholette D., Mitchell, Braxton D., Shuldiner, Alan R., Barnes, Kathleen C., Redline, Susan, Kardia, Sharon L.R., Abecasis, Gonçalo R., Becker, Lewis C., Heckbert, Susan R., He, Jiang, Post, Wendy, Arnett, Donna K., Vasan, Ramachandran S., Darbar, Dawood, Weiss, Scott T., McGarvey, Stephen T., de Andrade, Mariza, Chen, Yii-Der Ida, Kaplan, Robert C., Meyers, Deborah A., Custer, Brian S., Correa, Adolfo, Psaty, Bruce M., Fornage, Myriam, Manson, JoAnn E., Boerwinkle, Eric, Konkle, Barbara A., Loos, Ruth J.F., Rotter, Jerome I., Silverman, Edwin K., Kooperberg, Charles, Danesh, John, Samani, Nilesh J., Jaiswal, Siddhartha, Libby, Peter, Ellinor, Patrick T., Pankratz, Nathan, Ebert, Benjamin L., Reiner, Alexander P., Mathias, Rasika A., Do, Ron, Natarajan, Pradeep
Publicado 2022