Family-based association analysis: a fast and efficient method of multivariate association analysis with multiple variants

por Won, Sungho, Kim, Wonji, Lee, Sungyoung, Lee, Young, Sung, Joohon, Park, Taesung
Publicado 2015

Lack of Association between Oxytocin Receptor (OXTR) Gene Polymorphisms and Alexithymia: Evidence from Patients with Obsessive-Compulsive Disorder

por Koh, Min Jung, Kim, Wonji, Kang, Jee In, Namkoong, Kee, Kim, Se Joo
Publicado 2015

Heritability Analyses Uncover Shared Genetic Effects of Lung Function and Change over Time

por Li, Donghe, Kim, Woojin, An, Jahoon, Kim, Soriul, Lee, Seungku, Do, Ahra, Kim, Wonji, Lee, Sanghun, Yoon, Dankyu, Lee, Kwangbae, Ha, Seounguk, Silverman, Edwin K., Cho, Michael, Shin, Chol, Won, Sungho
Publicado 2022

Effect of 6p21 region on lung function is modified by smoking: a genome-wide interaction study

por Park, Boram, An, Jaehoon, Kim, Wonji, Kang, Hae Yeon, Koh, Sang Baek, Oh, Bermseok, Jung, Keum Ji, Jee, Sun Ha, Kim, Woo Jin, Cho, Michael H., Silverman, Edwin K., Park, Taesung, Won, Sungho
Publicado 2020

A robust and adaptive framework for interaction testing in quantitative traits between multiple genetic loci and exposure variables

por Hecker, Julian, Prokopenko, Dmitry, Moll, Matthew, Lee, Sanghun, Kim, Wonji, Qiao, Dandi, Voorhies, Kirsten, Kim, Woori, Vansteelandt, Stijn, Hobbs, Brian D., Cho, Michael H., Silverman, Edwin K., Lutz, Sharon M., DeMeo, Dawn L., Weiss, Scott T., Lange, Christoph
Publicado 2022

Family-based exome sequencing combined with linkage analyses identifies rare susceptibility variants of MUC4 for gastric cancer

por Choi, Yoon Jin, Ohn, Jung Hun, Kim, Nayoung, Kim, Wonji, Park, Kyungtaek, Won, Sungho, Sael, Lee, Shin, Cheol Min, Lee, Sun Min, Lee, Sejoon, An, Hyun Joo, Jang, Dong Man, Han, Byung Woo, Lee, Hye Seung, Kang, Seung Joo, Kim, Joo Sung, Lee, Dong Ho
Publicado 2020

Evidence for shared genetic risk factors between lymphangioleiomyomatosis and pulmonary function

por Farré, Xavier, Espín, Roderic, Baiges, Alexandra, Blommaert, Eline, Kim, Wonji, Giannikou, Krinio, Herranz, Carmen, Román, Antonio, Sáez, Berta, Casanova, Álvaro, Ancochea, Julio, Valenzuela, Claudia, Ussetti, Piedad, Laporta, Rosalía, Rodríguez-Portal, José A., van Moorsel, Coline H.M., van der Vis, Joanne J., Quanjel, Marian J.R., Tena-Garitaonaindia, Mireia, Sánchez de Medina, Fermín, Mateo, Francesca, Molina-Molina, María, Won, Sungho, Kwiatkowski, David J., de Cid, Rafael, Pujana, Miquel Angel
Publicado 2022

The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations

por Wang, Zhe, Choi, Shing Wan, Chami, Nathalie, Boerwinkle, Eric, Fornage, Myriam, Redline, Susan, Bis, Joshua C., Brody, Jennifer A., Psaty, Bruce M., Kim, Wonji, McDonald, Merry-Lynn N., Regan, Elizabeth A., Silverman, Edwin K., Liu, Ching-Ti, Vasan, Ramachandran S., Kalyani, Rita R., Mathias, Rasika A., Yanek, Lisa R., Arnett, Donna K., Justice, Anne E., North, Kari E., Kaplan, Robert, Heckbert, Susan R., de Andrade, Mariza, Guo, Xiuqing, Lange, Leslie A., Rich, Stephen S., Rotter, Jerome I., Ellinor, Patrick T., Lubitz, Steven A., Blangero, John, Shoemaker, M. Benjamin, Darbar, Dawood, Gladwin, Mark T., Albert, Christine M., Chasman, Daniel I., Jackson, Rebecca D., Kooperberg, Charles, Reiner, Alexander P., O’Reilly, Paul F., Loos, Ruth J. F.
Publicado 2022

Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program

por Wheeler, Marsha M., Stilp, Adrienne M., Rao, Shuquan, Halldórsson, Bjarni V., Beyter, Doruk, Wen, Jia, Mihkaylova, Anna V., McHugh, Caitlin P., Lane, John, Jiang, Min-Zhi, Raffield, Laura M., Jun, Goo, Sedlazeck, Fritz J., Metcalf, Ginger, Yao, Yao, Bis, Joshua B., Chami, Nathalie, de Vries, Paul S., Desai, Pinkal, Floyd, James S., Gao, Yan, Kammers, Kai, Kim, Wonji, Moon, Jee-Young, Ratan, Aakrosh, Yanek, Lisa R., Almasy, Laura, Becker, Lewis C., Blangero, John, Cho, Michael H., Curran, Joanne E., Fornage, Myriam, Kaplan, Robert C., Lewis, Joshua P., Loos, Ruth J. F., Mitchell, Braxton D., Morrison, Alanna C., Preuss, Michael, Psaty, Bruce M., Rich, Stephen S., Rotter, Jerome I., Tang, Hua, Tracy, Russell P., Boerwinkle, Eric, Abecasis, Goncalo R., Blackwell, Thomas W., Smith, Albert V., Johnson, Andrew D., Mathias, Rasika A., Nickerson, Deborah A., Conomos, Matthew P., Li, Yun, Þorsteinsdóttir, Unnur, Magnússon, Magnús K., Stefansson, Kari, Pankratz, Nathan D., Bauer, Daniel E., Auer, Paul L., Reiner, Alex P.
Publicado 2022

Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants

por Young, Kristin L., Fisher, Virginia, Deng, Xuan, Brody, Jennifer A., Graff, Misa, Lim, Elise, Lin, Bridget M., Xu, Hanfei, Amin, Najaf, An, Ping, Aslibekyan, Stella, Fohner, Alison E., Hidalgo, Bertha, Lenzini, Petra, Kraaij, Robert, Medina-Gomez, Carolina, Prokić, Ivana, Rivadeneira, Fernando, Sitlani, Colleen, Tao, Ran, van Rooij, Jeroen, Zhang, Di, Broome, Jai G., Buth, Erin J., Heavner, Benjamin D., Jain, Deepti, Smith, Albert V., Barnes, Kathleen, Boorgula, Meher Preethi, Chavan, Sameer, Darbar, Dawood, De Andrade, Mariza, Guo, Xiuqing, Haessler, Jeffrey, Irvin, Marguerite R., Kalyani, Rita R., Kardia, Sharon L.R., Kooperberg, Charles, Kim, Wonji, Mathias, Rasika A., McDonald, Merry-Lynn, Mitchell, Braxton D., Peyser, Patricia A., Regan, Elizabeth A., Redline, Susan, Reiner, Alexander P., Rich, Stephen S., Rotter, Jerome I., Smith, Jennifer A., Weiss, Scott, Wiggins, Kerri L., Yanek, Lisa R., Arnett, Donna, Heard-Costa, Nancy L., Leal, Suzanne, Lin, Danyu, McKnight, Barbara, Province, Michael, van Duijn, Cornelia M., North, Kari E., Cupples, L. Adrienne, Liu, Ching-Ti
Publicado 2022

Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants

por 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
Publicado 2020

Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations

por Liang, Jingjing, Le, Thu H., Edwards, Digna R. Velez, Tayo, Bamidele O., Gaulton, Kyle J., Smith, Jennifer A., Lu, Yingchang, Jensen, Richard A., Chen, Guanjie, Yanek, Lisa R., Schwander, Karen, Tajuddin, Salman M., Sofer, Tamar, Kim, Wonji, Kayima, James, McKenzie, Colin A., Fox, Ervin, Nalls, Michael A., Young, J. Hunter, Sun, Yan V., Lane, Jacqueline M., Cechova, Sylvia, Zhou, Jie, Tang, Hua, Fornage, Myriam, Musani, Solomon K., Wang, Heming, Lee, Juyoung, Adeyemo, Adebowale, Dreisbach, Albert W., Forrester, Terrence, Chu, Pei-Lun, Cappola, Anne, Evans, Michele K., Morrison, Alanna C., Martin, Lisa W., Wiggins, Kerri L., Hui, Qin, Zhao, Wei, Jackson, Rebecca D., Ware, Erin B., Faul, Jessica D., Reiner, Alex P., Bray, Michael, Denny, Joshua C., Mosley, Thomas H., Palmas, Walter, Guo, Xiuqing, Papanicolaou, George J., Penman, Alan D., Polak, Joseph F., Rice, Kenneth, Taylor, Ken D., Boerwinkle, Eric, Bottinger, Erwin P., Liu, Kiang, Risch, Neil, Hunt, Steven C., Kooperberg, Charles, Zonderman, Alan B., Laurie, Cathy C., Becker, Diane M., Cai, Jianwen, Loos, Ruth J. F., Psaty, Bruce M., Weir, David R., Kardia, Sharon L. R., Arnett, Donna K., Won, Sungho, Edwards, Todd L., Redline, Susan, Cooper, Richard S., Rao, D. C., Rotter, Jerome I., Rotimi, Charles, Levy, Daniel, Chakravarti, Aravinda, Zhu, Xiaofeng, Franceschini, Nora
Publicado 2017

Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations

por Liang, Jingjing, Le, Thu H., Velez Edwards, Digna R., Tayo, Bamidele O., Gaulton, Kyle J., Smith, Jennifer A., Lu, Yingchang, Jensen, Richard A., Chen, Guanjie, Yanek, Lisa R., Schwander, Karen, Tajuddin, Salman M., Sofer, Tamar, Kim, Wonji, Kayima, James, McKenzie, Colin A., Fox, Ervin, Nalls, Michael A., Young, J. Hunter, Sun, Yan V., Lane, Jacqueline M., Cechova, Sylvia, Zhou, Jie, Tang, Hua, Fornage, Myriam, Musani, Solomon K., Wang, Heming, Lee, Juyoung, Adeyemo, Adebowale, Dreisbach, Albert W., Forrester, Terrence, Chu, Pei-Lun, Cappola, Anne, Evans, Michele K., Morrison, Alanna C., Martin, Lisa W., Wiggins, Kerri L., Hui, Qin, Zhao, Wei, Jackson, Rebecca D., Ware, Erin B., Faul, Jessica D., Reiner, Alex P., Bray, Michael, Denny, Joshua C., Mosley, Thomas H., Palmas, Walter, Guo, Xiuqing, Papanicolaou, George J., Penman, Alan D., Polak, Joseph F., Rice, Kenneth, Taylor, Ken D., Boerwinkle, Eric, Bottinger, Erwin P., Liu, Kiang, Risch, Neil, Hunt, Steven C., Kooperberg, Charles, Zonderman, Alan B., Laurie, Cathy C., Becker, Diane M., Cai, Jianwen, Loos, Ruth J. F., Psaty, Bruce M., Weir, David R., Kardia, Sharon L. R., Arnett, Donna K., Won, Sungho, Edwards, Todd L., Redline, Susan, Cooper, Richard S., Rao, D. C., Rotter, Jerome I., Rotimi, Charles, Levy, Daniel, Chakravarti, Aravinda, Zhu, Xiaofeng, Franceschini, Nora
Publicado 2018

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

Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

por Shrine, Nick, Izquierdo, Abril G., Chen, Jing, Packer, Richard, Hall, Robert J., Guyatt, Anna L., Batini, Chiara, Thompson, Rebecca J., Pavuluri, Chandan, Malik, Vidhi, Hobbs, Brian D., Moll, Matthew, Kim, Wonji, Tal-Singer, Ruth, Bakke, Per, Fawcett, Katherine A., John, Catherine, Coley, Kayesha, Piga, Noemi Nicole, Pozarickij, Alfred, Lin, Kuang, Millwood, Iona Y., Chen, Zhengming, Li, Liming, Wijnant, Sara R. A., Lahousse, Lies, Brusselle, Guy, Uitterlinden, Andre G., Manichaikul, Ani, Oelsner, Elizabeth C., Rich, Stephen S., Barr, R. Graham, Kerr, Shona M., Vitart, Veronique, Brown, Michael R., Wielscher, Matthias, Imboden, Medea, Jeong, Ayoung, Bartz, Traci M., Gharib, Sina A., Flexeder, Claudia, Karrasch, Stefan, Gieger, Christian, Peters, Annette, Stubbe, Beate, Hu, Xiaowei, Ortega, Victor E., Meyers, Deborah A., Bleecker, Eugene R., Gabriel, Stacey B., Gupta, Namrata, Smith, Albert Vernon, Luan, Jian’an, Zhao, Jing-Hua, Hansen, Ailin F., Langhammer, Arnulf, Willer, Cristen, Bhatta, Laxmi, Porteous, David, Smith, Blair H., Campbell, Archie, Sofer, Tamar, Lee, Jiwon, Daviglus, Martha L., Yu, Bing, Lim, Elise, Xu, Hanfei, O’Connor, George T., Thareja, Gaurav, Albagha, Omar M. E., Suhre, Karsten, Granell, Raquel, Faquih, Tariq O., Hiemstra, Pieter S., Slats, Annelies M., Mullin, Benjamin H., Hui, Jennie, James, Alan, Beilby, John, Patasova, Karina, Hysi, Pirro, Koskela, Jukka T., Wyss, Annah B., Jin, Jianping, Sikdar, Sinjini, Lee, Mikyeong, May-Wilson, Sebastian, Pirastu, Nicola, Kentistou, Katherine A., Joshi, Peter K., Timmers, Paul R. H. J., Williams, Alexander T., Free, Robert C., Wang, Xueyang, Morrison, John L., Gilliland, Frank D., Chen, Zhanghua, Wang, Carol A., Foong, Rachel E., Harris, Sarah E., Taylor, Adele, Redmond, Paul, Cook, James P., Mahajan, Anubha, Lind, Lars, Palviainen, Teemu, Lehtimäki, Terho, Raitakari, Olli T., Kaprio, Jaakko, Rantanen, Taina, Pietiläinen, Kirsi H., Cox, Simon R., Pennell, Craig E., Hall, Graham L., Gauderman, W. James, Brightling, Chris, Wilson, James F., Vasankari, Tuula, Laitinen, Tarja, Salomaa, Veikko, Mook-Kanamori, Dennis O., Timpson, Nicholas J., Zeggini, Eleftheria, Dupuis, Josée, Hayward, Caroline, Brumpton, Ben, Langenberg, Claudia, Weiss, Stefan, Homuth, Georg, Schmidt, Carsten Oliver, Probst-Hensch, Nicole, Jarvelin, Marjo-Riitta, Morrison, Alanna C., Polasek, Ozren, Rudan, Igor, Lee, Joo-Hyeon, Sayers, Ian, Rawlins, Emma L., Dudbridge, Frank, Silverman, Edwin K., Strachan, David P., Walters, Robin G., Morris, Andrew P., London, Stephanie J., Cho, Michael H., Wain, Louise V., Hall, Ian P., Tobin, Martin D.
Publicado 2023

Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

por Shrine, Nick, Izquierdo, Abril G., Chen, Jing, Packer, Richard, Hall, Robert J., Guyatt, Anna L., Batini, Chiara, Thompson, Rebecca J., Pavuluri, Chandan, Malik, Vidhi, Hobbs, Brian D., Moll, Matthew, Kim, Wonji, Tal-Singer, Ruth, Bakke, Per, Fawcett, Katherine A., John, Catherine, Coley, Kayesha, Piga, Noemi Nicole, Pozarickij, Alfred, Lin, Kuang, Millwood, Iona Y., Chen, Zhengming, Li, Liming, Wijnant, Sara R. A., Lahousse, Lies, Brusselle, Guy, Uitterlinden, Andre G., Manichaikul, Ani, Oelsner, Elizabeth C., Rich, Stephen S., Barr, R. Graham, Kerr, Shona M., Vitart, Veronique, Brown, Michael R., Wielscher, Matthias, Imboden, Medea, Jeong, Ayoung, Bartz, Traci M., Gharib, Sina A., Flexeder, Claudia, Karrasch, Stefan, Gieger, Christian, Peters, Annette, Stubbe, Beate, Hu, Xiaowei, Ortega, Victor E., Meyers, Deborah A., Bleecker, Eugene R., Gabriel, Stacey B., Gupta, Namrata, Smith, Albert Vernon, Luan, Jian’an, Zhao, Jing-Hua, Hansen, Ailin F., Langhammer, Arnulf, Willer, Cristen, Bhatta, Laxmi, Porteous, David, Smith, Blair H., Campbell, Archie, Sofer, Tamar, Lee, Jiwon, Daviglus, Martha L., Yu, Bing, Lim, Elise, Xu, Hanfei, O’Connor, George T., Thareja, Gaurav, Albagha, Omar M. E., Suhre, Karsten, Granell, Raquel, Faquih, Tariq O., Hiemstra, Pieter S., Slats, Annelies M., Mullin, Benjamin H., Hui, Jennie, James, Alan, Beilby, John, Patasova, Karina, Hysi, Pirro, Koskela, Jukka T., Wyss, Annah B., Jin, Jianping, Sikdar, Sinjini, Lee, Mikyeong, May-Wilson, Sebastian, Pirastu, Nicola, Kentistou, Katherine A., Joshi, Peter K., Timmers, Paul R. H. J., Williams, Alexander T., Free, Robert C., Wang, Xueyang, Morrison, John L., Gilliland, Frank D., Chen, Zhanghua, Wang, Carol A., Foong, Rachel E., Harris, Sarah E., Taylor, Adele, Redmond, Paul, Cook, James P., Mahajan, Anubha, Lind, Lars, Palviainen, Teemu, Lehtimäki, Terho, Raitakari, Olli T., Kaprio, Jaakko, Rantanen, Taina, Pietiläinen, Kirsi H., Cox, Simon R., Pennell, Craig E., Hall, Graham L., Gauderman, W. James, Brightling, Chris, Wilson, James F., Vasankari, Tuula, Laitinen, Tarja, Salomaa, Veikko, Mook-Kanamori, Dennis O., Timpson, Nicholas J., Zeggini, Eleftheria, Dupuis, Josée, Hayward, Caroline, Brumpton, Ben, Langenberg, Claudia, Weiss, Stefan, Homuth, Georg, Schmidt, Carsten Oliver, Probst-Hensch, Nicole, Jarvelin, Marjo-Riitta, Morrison, Alanna C., Polasek, Ozren, Rudan, Igor, Lee, Joo-Hyeon, Sayers, Ian, Rawlins, Emma L., Dudbridge, Frank, Silverman, Edwin K., Strachan, David P., Walters, Robin G., Morris, Andrew P., London, Stephanie J., Cho, Michael H., Wain, Louise V., Hall, Ian P., Tobin, Martin D.
Publicado 2023