Search Results - Mullin, Lee B.

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    MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis by Mak, Christopher C Y, Doherty, Dan, Lin, Angela E, Vegas, Nancy, Cho, Megan T, Viot, Géraldine, Dimartino, Clémantine, Weisfeld-Adams, James D, Lessel, Davor, Joss, Shelagh, Li, Chumei, Gonzaga-Jauregui, Claudia, Zarate, Yuri A, Ehmke, Nadja, Horn, Denise, Troyer, Caitlin, Kant, Sarina G, Lee, Youngha, Ishak, Gisele E, Leung, Gordon, Barone Pritchard, Amanda, Yang, Sandra, Bend, Eric G, Filippini, Francesca, Roadhouse, Chelsea, Lebrun, Nicolas, Mehaffey, Michele G, Martin, Pierre-Marie, Apple, Benjamin, Millan, Francisca, Puk, Oliver, Hoffer, Mariette J V, Henderson, Lindsay B, McGowan, Ruth, Wentzensen, Ingrid M, Pei, Steven, Zahir, Farah R, Yu, Mullin, Gibson, William T, Seman, Ann, Steeves, Marcie, Murrell, Jill R, Luettgen, Sabine, Francisco, Elizabeth, Strom, Tim M, Amlie-Wolf, Louise, Kaindl, Angela M, Wilson, William G, Halbach, Sara, Basel-Salmon, Lina, Lev-El, Noa, Denecke, Jonas, Vissers, Lisenka E L M, Radtke, Kelly, Chelly, Jamel, Zackai, Elaine, Friedman, Jan M, Bamshad, Michael J, Nickerson, Deborah A, Reid, Russell R, Devriendt, Koenraad, Chae, Jong-Hee, Stolerman, Elliot, McDougall, Carey, Powis, Zöe, Bienvenu, Thierry, Tan, Tiong Y, Orenstein, Naama, Dobyns, William B, Shieh, Joseph T, Choi, Murim, Waggoner, Darrel, Gripp, Karen W, Parker, Michael J, Stoler, Joan, Lyonnet, Stanislas, Cormier-Daire, Valérie, Viskochil, David, Hoffman, Trevor L, Amiel, Jeanne, Chung, Brian H Y, Gordon, Christopher T

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    Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk by Shrine, Nick, Izquierdo, Abril G, Guyatt, Anna L, Batini, Chiara, Pavuluri, Chandan, Malik, Vidhi, Hobbs, Brian D, Moll, Matthew, Kim, Wonji, Tal-Singer, Ruth, Bakke, Per S, John, Catherine, Coley, Kayesha, Piga, Noemi Nicole, Pozarickij, Alfred, Chen, Zhengming, Wijnant, Sara R A, Lahousse, Lies, Brusselle, Guy, Manichaikul, Ani, Oelsner, Elizabeth C, Rich, Stephen S, Barr, R Graham, Kerr, Shona M, Brown, Michael R, Gharib, Sina A, Flexeder, Claudia, Karrasch, Stefan, Gieger, Christian, Peters, Annette, Hu, Xiaowei, Meyers, Deborah A, Gabriel, Stacey B, Smith, Albert Vernon, Luan, Jian'an, Zhao, Jing-Hua, Hansen, Ailin Falkmo, Langhammer, Arnulf, Smith, Blair H, Campbell, Archie, Sofer, Tamar, Lee, Jiwon, Daviglus, Martha L, Lim, Elise, Xu, Hanfei, O'Connor, George T, Thareja, Gaurav, Suhre, Karsten, Granell, Raquel, Faquih, Tariq O, Hiemstra, Pieter S, 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, Pirastu, Nicola, Kentistou, Katherine A, Joshi, Peter K, Timmers, Paul R H J, 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, Lind, Lars, Palviainen, Teemu, Lehtimäki, Terho, Pietiläinen, Kirsi H, Pennell, Craig E, Gauderman, W James, Brightling, Chris, Wilson, James F, Salomaa, Veikko, Mook-Kanamori, Dennis O, Dupuis, Josée, Hayward, Caroline, Brumpton, Ben Michael, Weiss, Stefan, Schmidt, Carsten Oliver, Jarvelin, Marjo-Riitta, Lee, Joo-Hyeon, Dudbridge, Frank, Silverman, Edwin K, Strachan, David P, Walters, Robin G, Cho, Michael H, Wain, Louise V, Hall, Ian P

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    Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk by Shrine, Nick, Izquierdo, Abril G, Guyatt, Anna L, Batini, Chiara, Pavuluri, Chandan, Malik, Vidhi, Hobbs, Brian D, Moll, Matthew, Kim, Wonji, Tal-Singer, Ruth, Bakke, Per S, John, Catherine, Coley, Kayesha, Piga, Noemi Nicole, Pozarickij, Alfred, Chen, Zhengming, Wijnant, Sara R A, Lahousse, Lies, Brusselle, Guy, Manichaikul, Ani, Oelsner, Elizabeth C, Rich, Stephen S, Barr, R Graham, Kerr, Shona M, Brown, Michael R, Gharib, Sina A, Flexeder, Claudia, Karrasch, Stefan, Gieger, Christian, Peters, Annette, Hu, Xiaowei, Meyers, Deborah A, Gabriel, Stacey B, Smith, Albert Vernon, Luan, Jian'an, Zhao, Jing-Hua, Hansen, Ailin Falkmo, Langhammer, Arnulf, Smith, Blair H, Campbell, Archie, Sofer, Tamar, Lee, Jiwon, Daviglus, Martha L, Lim, Elise, Xu, Hanfei, O'Connor, George T, Thareja, Gaurav, Suhre, Karsten, Granell, Raquel, Faquih, Tariq O, Hiemstra, Pieter S, 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, Pirastu, Nicola, Kentistou, Katherine A, Joshi, Peter K, Timmers, Paul R H J, 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, Lind, Lars, Palviainen, Teemu, Lehtimäki, Terho, Pietiläinen, Kirsi H, Pennell, Craig E, Gauderman, W James, Brightling, Chris, Wilson, James F, Salomaa, Veikko, Mook-Kanamori, Dennis O, Dupuis, Josée, Hayward, Caroline, Brumpton, Ben Michael, Weiss, Stefan, Schmidt, Carsten Oliver, Jarvelin, Marjo-Riitta, Lee, Joo-Hyeon, Dudbridge, Frank, Silverman, Edwin K, Strachan, David P, Walters, Robin G, Cho, Michael H, Wain, Louise V, Hall, Ian P

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