日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Whole genome sequence analysis of pulmonary function and COPD in 44,287 multi-ancestry participants

对 44,287 名多族裔参与者进行肺功能和慢性阻塞性肺病的全基因组序列分析

Kim, Wonji; Hu, Xiaowei; Kim, Kangjin; Chun, Sung; Orchard, Peter; Qiao, Dandi; Ruczinski, Ingo; Saferali, Aabida; Aguet, Francois; Antonacci-Fulton, Lucinda; Balte, Pallavi P; Bartz, Traci M; Anamika, Wardatul Jannat; Zhou, Xiaobo; Duan, JunYi; Brody, Jennifer A; Cade, Brian E; Daviglus, Martha L; Doddapaneni, Harshavadran; Dugan-Perez, Shannon; Dutcher, Susan K; Frazar, Christian D; Gabriel, Stacey B; Gharib, Sina A; Gupta, Namrata; Hobbs, Brian D; Kasela, Silva; Loehr, Laura R; Metcalf, Ginger A; Muzny, Donna M; Oelsner, Elizabeth C; Rasmussen-Torvik, Laura J; Sitlani, Colleen M; Smith, Joshua; Sofer, Tamar; Xu, Hanfei; Yu, Bing; Zhang, David; Ziniti, John; Barr, R Graham; Carson, April P; Fornage, Myriam; Hou, Lifang; Kalhan, Ravi; Kaplan, Robert; Lappalainen, Tuuli; London, Stephanie J; Morrison, Alanna C; O'Connor, George T; Psaty, Bruce M; Raffield, Laura M; Redline, Susan; Rich, Stephen S; Rotter, Jerome I; Silverman, Edwin K; Manichaikul, Ani; Cho, Michael H

Geospatial and demographic patterns of SARS-CoV-2 spread in Massachusetts from over 130,000 genomes

基于超过13万个基因组的SARS-CoV-2在马萨诸塞州传播的地理空间和人口统计学模式

Moreno, Gage K; Brock-Fisher, Taylor; Krasilnikova, Lydia A; Schaffner, Steve F; Burns, Meagan; Casiello, Carolyn E; Messer, Katelyn S; Petros, Brittany; Specht, Ivan; DeRuff, Katherine C; Siddle, Katherine J; Loreth, Christine; Fitzgerald, Nicholas A; Rooke, Heather M; Gabriel, Stacey B; Smole, Sandra; Wohl, Shirlee; Park, Daniel J; Madoff, Lawrence C; Brown, Catherine M; MacInnis, Bronwyn L; Sabeti, Pardis C

Author Correction: Multiplexed CRISPR-based microfluidic platform for clinical testing of respiratory viruses and identification of SARS-CoV-2 variants

作者更正:用于呼吸道病毒临床检测和SARS-CoV-2变异株鉴定的多重CRISPR微流控平台

Welch, Nicole L; Zhu, Meilin; Hua, Catherine; Weller, Juliane; Mirhashemi, Marzieh Ezzaty; Nguyen, Tien G; Mantena, Sreekar; Bauer, Matthew R; Shaw, Bennett M; Ackerman, Cheri M; Thakku, Sri Gowtham; Tse, Megan W; Kehe, Jared; Uwera, Marie-Martine; Eversley, Jacqueline S; Bielwaski, Derek A; McGrath, Graham; Braidt, Joseph; Johnson, Jeremy; Cerrato, Felecia; Moreno, Gage K; Krasilnikova, Lydia A; Petros, Brittany A; Gionet, Gabrielle L; King, Ewa; Huard, Richard C; Jalbert, Samantha K; Cleary, Michael L; Fitzgerald, Nicholas A; Gabriel, Stacey B; Gallagher, Glen R; Smole, Sandra C; Madoff, Lawrence C; Brown, Catherine M; Keller, Matthew W; Wilson, Malania M; Kirby, Marie K; Barnes, John R; Park, Daniel J; Siddle, Katherine J; Happi, Christian T; Hung, Deborah T; Springer, Michael; MacInnis, Bronwyn L; Lemieux, Jacob E; Rosenberg, Eric; Branda, John A; Blainey, Paul C; Sabeti, Pardis C; Myhrvold, Cameron

Dysanapsis Genetic Risk Predicts Lung Function Across the Lifespan

先天性异常遗传风险可预测终生肺功能

Debban, Catherine L; Ambalavanan, Amirthagowri; Ghosh, Auyon; Li, Zhonglin; Buschur, Kristina L; Ma, Yanlin; George, Elizabeth; Pistenmaa, Carrie; Bertoni, Alain G; Oelsner, Elizabeth C; Michos, Erin D; Moraes, Theo J; Jacobs, David R Jr; Christenson, Stephanie; Bhatt, Surya P; Kaner, Robert J; Simons, Elinor; Turvey, Stuart E; Vameghestahbanati, Motahareh; Engert, James C; Kirby, Miranda; Bourbeau, Jean; Tan, Wan C; Gabriel, Stacey B; Gupta, Namrata; Woodruff, Prescott G; Subbarao, Padmaja; Ortega, Victor E; Bleecker, Eugene R; Meyers, Deborah A; Rich, Stephen S; Hoffman, Eric A; Barr, R Graham; Cho, Michael H; Bossé, Yohan; Duan, Qingling; Manichaikul, Ani; Smith, Benjamin M

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

多种族全基因组关联分析提高了影响肺功能和慢性阻塞性肺疾病风险的基因和通路的分辨率。

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

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

作者更正:多祖先全基因组关联分析提高了影响肺功能和慢性阻塞性肺疾病风险的基因和通路的分辨率。

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

Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program

静脉血栓栓塞的全基因组分析:精准医学跨组学计划

Seyerle, Amanda A; Laurie, Cecelia A; Coombes, Brandon J; Jain, Deepti; Conomos, Matthew P; Brody, Jennifer; Chen, Ming-Huei; Gogarten, Stephanie M; Beutel, Kathleen M; Gupta, Namrata; Heckbert, Susan R; Jackson, Rebecca D; Johnson, Andrew D; Ko, Darae; Manson, JoAnn E; McKnight, Barbara; Metcalf, Ginger A; Morrison, Alanna C; Reiner, Alexander P; Sofer, Tamar; Tang, Weihong; Wiggins, Kerri L; Boerwinkle, Eric; de Andrade, Mariza; Gabriel, Stacey B; Gibbs, Richard A; Laurie, Cathy C; Psaty, Bruce M; Vasan, Ramachandran S; Rice, Ken; Kooperberg, Charles; Pankow, James S; Smith, Nicholas L; Pankratz, Nathan

Multiplexed CRISPR-based microfluidic platform for clinical testing of respiratory viruses and identification of SARS-CoV-2 variants

用于呼吸道病毒临床检测和SARS-CoV-2变异株鉴定的多重CRISPR微流控平台

Welch, Nicole L; Zhu, Meilin; Hua, Catherine; Weller, Juliane; Mirhashemi, Marzieh Ezzaty; Nguyen, Tien G; Mantena, Sreekar; Bauer, Matthew R; Shaw, Bennett M; Ackerman, Cheri M; Thakku, Sri Gowtham; Tse, Megan W; Kehe, Jared; Uwera, Marie-Martine; Eversley, Jacqueline S; Bielwaski, Derek A; McGrath, Graham; Braidt, Joseph; Johnson, Jeremy; Cerrato, Felecia; Moreno, Gage K; Krasilnikova, Lydia A; Petros, Brittany A; Gionet, Gabrielle L; King, Ewa; Huard, Richard C; Jalbert, Samantha K; Cleary, Michael L; Fitzgerald, Nicholas A; Gabriel, Stacey B; Gallagher, Glen R; Smole, Sandra C; Madoff, Lawrence C; Brown, Catherine M; Keller, Matthew W; Wilson, Malania M; Kirby, Marie K; Barnes, John R; Park, Daniel J; Siddle, Katherine J; Happi, Christian T; Hung, Deborah T; Springer, Michael; MacInnis, Bronwyn L; Lemieux, Jacob E; Rosenberg, Eric; Branda, John A; Blainey, Paul C; Sabeti, Pardis C; Myhrvold, Cameron

Rare coding variants in ten genes confer substantial risk for schizophrenia

十个基因中的罕见编码变异会显著增加患精神分裂症的风险。

Singh, Tarjinder; Poterba, Timothy; Curtis, David; Akil, Huda; Al Eissa, Mariam; Barchas, Jack D; Bass, Nicholas; Bigdeli, Tim B; Breen, Gerome; Bromet, Evelyn J; Buckley, Peter F; Bunney, William E; Bybjerg-Grauholm, Jonas; Byerley, William F; Chapman, Sinéad B; Chen, Wei J; Churchhouse, Claire; Craddock, Nicholas; Cusick, Caroline M; DeLisi, Lynn; Dodge, Sheila; Escamilla, Michael A; Eskelinen, Saana; Fanous, Ayman H; Faraone, Stephen V; Fiorentino, Alessia; Francioli, Laurent; Gabriel, Stacey B; Gage, Diane; Gagliano Taliun, Sarah A; Ganna, Andrea; Genovese, Giulio; Glahn, David C; Grove, Jakob; Hall, Mei-Hua; Hämäläinen, Eija; Heyne, Henrike O; Holi, Matti; Hougaard, David M; Howrigan, Daniel P; Huang, Hailiang; Hwu, Hai-Gwo; Kahn, René S; Kang, Hyun Min; Karczewski, Konrad J; Kirov, George; Knowles, James A; Lee, Francis S; Lehrer, Douglas S; Lescai, Francesco; Malaspina, Dolores; Marder, Stephen R; McCarroll, Steven A; McIntosh, Andrew M; Medeiros, Helena; Milani, Lili; Morley, Christopher P; Morris, Derek W; Mortensen, Preben Bo; Myers, Richard M; Nordentoft, Merete; O'Brien, Niamh L; Olivares, Ana Maria; Ongur, Dost; Ouwehand, Willem H; Palmer, Duncan S; Paunio, Tiina; Quested, Digby; Rapaport, Mark H; Rees, Elliott; Rollins, Brandi; Satterstrom, F Kyle; Schatzberg, Alan; Scolnick, Edward; Scott, Laura J; Sharp, Sally I; Sklar, Pamela; Smoller, Jordan W; Sobell, Janet L; Solomonson, Matthew; Stahl, Eli A; Stevens, Christine R; Suvisaari, Jaana; Tiao, Grace; Watson, Stanley J; Watts, Nicholas A; Blackwood, Douglas H; Børglum, Anders D; Cohen, Bruce M; Corvin, Aiden P; Esko, Tõnu; Freimer, Nelson B; Glatt, Stephen J; Hultman, Christina M; McQuillin, Andrew; Palotie, Aarno; Pato, Carlos N; Pato, Michele T; Pulver, Ann E; St Clair, David; Tsuang, Ming T; Vawter, Marquis P; Walters, James T; Werge, Thomas M; Ophoff, Roel A; Sullivan, Patrick F; Owen, Michael J; Boehnke, Michael; O'Donovan, Michael C; Neale, Benjamin M; Daly, Mark J

Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibility

大规模测序鉴定出多个与克罗恩病易感性相关的基因和罕见变异

Sazonovs, Aleksejs; Stevens, Christine R; Venkataraman, Guhan R; Yuan, Kai; Avila, Brandon; Abreu, Maria T; Ahmad, Tariq; Allez, Matthieu; Ananthakrishnan, Ashwin N; Atzmon, Gil; Baras, Aris; Barrett, Jeffrey C; Barzilai, Nir; Beaugerie, Laurent; Beecham, Ashley; Bernstein, Charles N; Bitton, Alain; Bokemeyer, Bernd; Chan, Andrew; Chung, Daniel; Cleynen, Isabelle; Cosnes, Jacques; Cutler, David J; Daly, Allan; Damas, Oriana M; Datta, Lisa W; Dawany, Noor; Devoto, Marcella; Dodge, Sheila; Ellinghaus, Eva; Fachal, Laura; Farkkila, Martti; Faubion, William; Ferreira, Manuel; Franchimont, Denis; Gabriel, Stacey B; Ge, Tian; Georges, Michel; Gettler, Kyle; Giri, Mamta; Glaser, Benjamin; Goerg, Siegfried; Goyette, Philippe; Graham, Daniel; Hämäläinen, Eija; Haritunians, Talin; Heap, Graham A; Hiltunen, Mikko; Hoeppner, Marc; Horowitz, Julie E; Irving, Peter; Iyer, Vivek; Jalas, Chaim; Kelsen, Judith; Khalili, Hamed; Kirschner, Barbara S; Kontula, Kimmo; Koskela, Jukka T; Kugathasan, Subra; Kupcinskas, Juozas; Lamb, Christopher A; Laudes, Matthias; Lévesque, Chloé; Levine, Adam P; Lewis, James D; Liefferinckx, Claire; Loescher, Britt-Sabina; Louis, Edouard; Mansfield, John; May, Sandra; McCauley, Jacob L; Mengesha, Emebet; Mni, Myriam; Moayyedi, Paul; Moran, Christopher J; Newberry, Rodney D; O'Charoen, Sirimon; Okou, David T; Oldenburg, Bas; Ostrer, Harry; Palotie, Aarno; Paquette, Jean; Pekow, Joel; Peter, Inga; Pierik, Marieke J; Ponsioen, Cyriel Y; Pontikos, Nikolas; Prescott, Natalie; Pulver, Ann E; Rahmouni, Souad; Rice, Daniel L; Saavalainen, Päivi; Sands, Bruce; Sartor, R Balfour; Schiff, Elena R; Schreiber, Stefan; Schumm, L Philip; Segal, Anthony W; Seksik, Philippe; Shawky, Rasha; Sheikh, Shehzad Z; Silverberg, Mark S; Simmons, Alison; Skeiceviciene, Jurgita; Sokol, Harry; Solomonson, Matthew; Somineni, Hari; Sun, Dylan; Targan, Stephan; Turner, Dan; Uhlig, Holm H; van der Meulen, Andrea E; Vermeire, Séverine; Verstockt, Sare; Voskuil, Michiel D; Winter, Harland S; Young, Justine; Duerr, Richard H; Franke, Andre; Brant, Steven R; Cho, Judy; Weersma, Rinse K; Parkes, Miles; Xavier, Ramnik J; Rivas, Manuel A; Rioux, John D; McGovern, Dermot P B; Huang, Hailiang; Anderson, Carl A; Daly, Mark J