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Garrison, Erik; Guarracino, Andrea; Heumos, Simon; Villani, Flavia; Bao, Zhigui; Tattini, Lorenzo; Hagmann, Joerg; Vorbrugg, Sebastian; Marco-Sola, Santiago; Kubica, Christian; Ashbrook, David G.; Thorell, Kaisa; Rusholme-Pilcher, Rachel L.; Liti, Gianni; Rudbeck, Emilio; Golicz, Agnieszka A.; Nahnsen, Sven; Yang, Zuyu; Mwaniki, Moses Njagi; Nobrega, Franklin L.; Wu, Yi; Chen, Hao; de Ligt, Joep; Sudmant, Peter H.; Huang, Sanwen; Weigel, Detlef; Soranzo, Nicole; Colonna, Vincenza; Williams, Robert W.; Prins, Pjotr Share Save Misexpression of inactive genes in whole blood is associated with nearby rare structural variantsVanderstichele, Thomas; Burnham, Katie L.; de Klein, Niek; Tardaguila, Manuel; Howell, Brittany; Walter, Klaudia; Kundu, Kousik; Koeppel, Jonas; Lee, Wanseon; Tokolyi, Alex; Persyn, Elodie; Nath, Artika P.; Marten, Jonathan; Petrovski, Slave; Roberts, David J.; Di Angelantonio, Emanuele; Danesh, John; Berton, Alix; Platt, Adam; Butterworth, Adam S.; Soranzo, Nicole; Parts, Leopold; Inouye, Michael; Paul, Dirk S.; Davenport, Emma E. Share Save Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk predictionSchormair, Barbara; Zhao, Chen; Bell, Steven; Didriksen, Maria; Nawaz, Muhammad S.; Schandra, Nathalie; Stefani, Ambra; Hoegl, Birgit; Dauvilliers, Yves; Bachmann, Cornelius G.; Kemlink, David; Sonka, Karel; Paulus, Walter; Trenkwalder, Claudia; Oertel, Wolfgang H.; Hornyak, Magdolna; Teder-Laving, Maris; Metspalu, Andres; Hadjigeorgiou, Georgios M.; Polo, Olli; Fietze, Ingo; Ross, Owen A.; Wszolek, Zbigniew K.; Ibrahim, Abubaker; Bergmann, Melanie; Kittke, Volker; Harrer, Philip; Dowsett, Joseph; Chenini, Sofiene; Ostrowski, Sisse Rye; Sorensen, Erik; Erikstrup, Christian; Pedersen, Ole B.; Bruun, Mie Topholm; Nielsen, Kaspar R.; Butterworth, Adam S.; Soranzo, Nicole; Ouwehand, Willem H.; Roberts, David J.; Danesh, John; Burchell, Brendan; Furlotte, Nicholas A.; Nandakumar, Priyanka; Earley, Christopher J.; Ondo, William G.; Xiong, Lan; Desautels, Alex; Perola, Markus; Vodicka, Pavel; Dina, Christian; Stoll, Monika; Franke, Andre; Lieb, Wolfgang; Stewart, Alexandre F. R.; Shah, Svati H.; Gieger, Christian; Peters, Annette; Rye, David B.; Rouleau, Guy A.; Berger, Klaus; Stefansson, Hreinn; Ullum, Henrik; Stefansson, Kari; Hinds, David A.; Di Angelantonio, Emanuele; Oexle, Konrad; Winkelmann, Juliane Share Save Share Save Rare and common genetic determinants of metabolic individuality and their effects on human healthSurendran, Praveen; Stewart, Isobel D.; Yeung, Victoria P. W. Au; Pietzner, Maik; Raffler, Johannes; Worheide, Maria A.; Li, Chen; Smith, Rebecca F.; Wittemans, Laura B. L.; Bomba, Lorenzo; Menni, Cristina; Zierer, Jonas; Rossi, Niccolo; Sheridan, Patricia A.; Watkins, Nicholas A.; Mangino, Massimo; Hysi, Pirro G.; Di Angelantonio, Emanuele; Falchi, Mario; Spector, Tim D.; Soranzo, Nicole; Michelotti, Gregory A.; Arlt, Wiebke; Lotta, Luca A.; Denaxas, Spiros; Hemingway, Harry; Gamazon, Eric R.; Howson, Joanna M. M.; Wood, Angela M.; Danesh, John; Wareham, Nicholas J.; Kastenmueller, Gabi; Fauman, Eric B.; Suhre, Karsten; Butterworth, Adam S.; Langenberg, Claudia Share Save Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics InitiativeButler-Laporte, Guillaume; Povysil, Gundula; Kosmicki, Jack A.; Cirulli, Elizabeth T.; Drivas, Theodore; Furini, Simone; Saad, Chadi; Schmidt, Axel; Olszewski, Pawel; Korotko, Urszula; Quinodoz, Mathieu; Celik, Elifnaz; Kundu, Kousik; Walter, Klaudia; Jung, Junghyun; Stockwell, Amy D.; Sloofman, Laura G.; Jordan, Daniel M.; Thompson, Ryan C.; Del Valle, Diane; Simons, Nicole; Cheng, Esther; Sebra, Robert; Schadt, Eric E.; Kim-Schulze, Seunghee; Gnjatic, Sacha; Merad, Miriam; Buxbaum, Joseph D.; Beckmann, Noam D.; Charney, Alexander W.; Przychodzen, Bartlomiej; Chang, Timothy; Pottinger, Tess D.; Shang, Ning; Brand, Fabian; Fava, Francesca; Mari, Francesca; Chwialkowska, Karolina; Niemira, Magdalena; Pula, Szymon; Baillie, J. Kenneth; Stuckey, Alex; Salas, Antonio; Bello, Xabier; Pardo-Seco, Jacobo; Gomez-Carballa, Alberto; Rivero-Calle, Irene; Martinon-Torres, Federico; Ganna, Andrea; Karczewski, Konrad J.; Veerapen, Kumar; Bourgey, Mathieu; Bourque, Guillaume; Eveleigh, Robert Jm; Forgetta, Vincenzo; Morrison, David; Langlais, David; Lathrop, Mark; Mooser, Vincent; Nakanishi, Tomoko; Frithiof, Robert; Hultstrom, Michael; Lipcsey, Miklos; Marincevic-Zuniga, Yanara; Nordlund, Jessica; Barrett, Kelly M. Schiabor; Lee, William; Bolze, Alexandre; White, Simon; Riffle, Stephen; Tanudjaja, Francisco; Sandoval, Efren; Neveux, Iva; Dabe, Shaun; Casadei, Nicolas; Motameny, Susanne; Alaamery, Manal; Massadeh, Salam; Aljawini, Nora; Almutairi, Mansour S.; Arabi, Yaseen M.; Alqahtani, Saleh A.; Al Harthi, Fawz S.; Almutairi, Amal; Alqubaishi, Fatima; Alotaibi, Sarah; Binowayn, Albandari; Alsolm, Ebtehal A.; El Bardisy, Hadeel; Fawzy, Mohammad; Cai, Fang; Soranzo, Nicole; Butterworth, Adam; Geschwind, Daniel H.; Arteaga, Stephanie; Stephens, Alexis; Butte, Manish J.; Boutros, Paul C.; Yamaguchi, Takafumi N.; Tao, Shu; Eng, Stefan; Sanders, Timothy; Tung, Paul J.; Broudy, Michael E.; Pan, Yu; Gonzalez, Alfredo; Chavan, Nikhil; Johnson, Ruth; Pasaniuc, Bogdan; Yaspan, Brian; Smieszek, Sandra; Rivolta, Carlo; Bibert, Stephanie; Bochud, Pierre-Yves; Dabrowski, Maciej; Zawadzki, Pawel; Sypniewski, Mateusz; Kaja, Elzbieta; Chariyavilaskul, Pajaree; Nilaratanakul, Voraphoj; Hirankarn, Nattiya; Shotelersuk, Vorasuk; Pongpanich, Monnat; Phokaew, Chureerat; Chetruengchai, Wanna; Tokunaga, Katsushi; Sugiyama, Masaya; Kawai, Yosuke; Hasegawa, Takanori; Naito, Tatsuhiko; Namkoong, Ho; Edahiro, Ryuya; Kimura, Akinori; Ogawa, Seishi; Kanai, Takanori; Fukunaga, Koichi; Okada, Yukinori; Imoto, Seiya; Miyano, Satoru; Mangul, Serghei; Abedalthagafi, Malak S.; Zeberg, Hugo; Grzymski, Joseph J.; Washington, Nicole L.; Ossowski, Stephan; Ludwig, Kerstin U.; Schulte, Eva C.; Riess, Olaf; Moniuszko, Marcin; Kwasniewski, Miroslaw; Mbarek, Hamdi; Ismail, Said I.; Verma, Anurag; Goldstein, David B.; Kiryluk, Krzysztof; Renieri, Alessandra; Ferreira, Manuel A. R.; Richards, J. Brent Share Save GWAS of genetic factors affecting white blood cell morphological parameters in Sardinians uncovers influence of chromosome 11 innate immunity gene cluster on eosinophil morphologyMarongiu, Michele; Perez-Mejias, Gonzalo; Orru, Valeria; Steri, Maristella; Sidore, Carlo; Diaz-Quintana, Antonio; Mulas, Antonella; Busonero, Fabio; Maschio, Andrea; Walter, Klaudia; Tardaguila, Manuel; Akbari, Parsa; Soranzo, Nicole; Fiorillo, Edoardo; Gorospe, Myriam; Schlessinger, David; Diaz-Moreno, Irene; Cucca, Francesco; Zoledziewska, Magdalena Share Save Whole-exome sequencing identifies rare genetic variants associated with human plasma metabolitesBomba, Lorenzo; Walter, Klaudia; Guo, Qi; Surendran, Praveen; Kundu, Kousik; Nongmaithem, Suraj; Karim, Mohd Anisul; Stewart, Isobel D.; Langenberg, Claudia; Danesh, John; Di Angelantonio, Emanuele; Roberts, David J.; Ouwehand, Willem H.; Dunham, Ian; Butterworth, Adam S.; Soranzo, Nicole Share Save Immune disease variants modulate gene expression in regulatory CD4+ T cellsBossini-Castillo, Lara; Glinos, Dafni A.; Kunowska, Natalia; Golda, Gosia; Lamikanra, Abigail A.; Spitzer, Michaela; Soskic, Blagoje; Cano-Gamez, Eddie; Smyth, Deborah J.; Cattermole, Claire; Alasoo, Kaur; Mann, Alice; Kundu, Kousik; Lorenc, Anna; Soranzo, Nicole; Dunham, Ian; Roberts, David J.; Trynka, Gosia Share Save Transcriptome-wide association study in UK Biobank Europeans identifies associations with blood cell traitsRowland, Bryce; Venkatesh, Sanan; Tardaguila, Manuel; Wen, Jia; Rosen, Jonathan D.; Tapia, Amanda L.; Sun, Quan; Graff, Mariaelisa; Vuckovic, Dragana; Lettre, Guillaume; Sankaran, Vijay G.; Voloudakis, Georgios; Roussos, Panos; Huffman, Jennifer E.; Reiner, Alexander P.; Soranzo, Nicole; Raffield, Laura M.; Li, Yun Share Save Machine learning optimized polygenic scores for blood cell traits identify sex-specific trajectories and genetic correlations with diseaseXu, Yu; Vuckovic, Dragana; Ritchie, Scott C.; Akbari, Parsa; Jiang, Tao; Grealey, Jason; Butterworth, Adam S.; Ouwehand, Willem H.; Roberts, David J.; Di Angelantonio, Emanuele; Danesh, John; Soranzo, Nicole; Inouye, Michael Share Save Share Save Integrative analysis of the plasma proteome and polygenic risk of cardiometabolic diseasesRitchie, Scott C.; Lambert, Samuel A.; Arnold, Matthew; Teo, Shu Mei; Lim, Sol; Scepanovic, Petar; Marten, Jonathan; Zahid, Sohail; Chaffin, Mark; Liu, Yingying; Abraham, Gad; Ouwehand, Willem H.; Roberts, David J.; Watkins, Nicholas A.; Drew, Brian G.; Calkin, Anna C.; Di Angelantonio, Emanuele; Soranzo, Nicole; Burgess, Stephen; Chapman, Michael; Kathiresan, Sekar; Khera, Amit, V; Danesh, John; Butterworth, Adam S.; Inouye, Michael Share Save Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed programMikhaylova, Anna, V; McHugh, Caitlin P.; Polfus, Linda M.; Raffield, Laura M.; Boorgula, Meher Preethi; Blackwell, Thomas W.; Brody, Jennifer A.; Broome, Jai; Chami, Nathalie; Chen, Ming-Huei; Conomos, Matthew P.; Cox, Corey; Curran, Joanne E.; Daya, Michelle; Ekunwe, Lynette; Glahn, David C.; Heard-Costa, Nancy; Highland, Heather M.; Hobbs, Brian D.; Ilboudo, Yann; Jain, Deepti; Lange, Leslie A.; Miller-Fleming, Tyne W.; Min, Nancy; Moon, Jee-Young; Preuss, Michael H.; Rosen, Jonathon; Ryan, Kathleen; Smith, Albert, V; Sun, Quan; Surendran, Praveen; de Vries, Paul S.; Walter, Klaudia; Wang, Zhe; Wheeler, Marsha; Yanek, Lisa R.; Zhong, Xue; Abecasis, Goncalo R.; Almasy, Laura; Barnes, Kathleen C.; Beaty, Terri H.; Becker, Lewis C.; Blangero, John; Boerwinkle, Eric; Butterworth, Adam S.; Chavan, Sameer; Cho, Michael H.; Choquet, Helene; Correa, Adolfo; Cox, Nancy; DeMeo, Dawn L.; Faraday, Nauder; Fornage, Myriam; Gerszten, Robert E.; Hou, Lifang; Johnson, Andrew D.; Jorgenson, Eric; Kaplan, Robert; Kooperberg, Charles; Kundu, Kousik; Laurie, Cecelia A.; Lettre, Guillaume; Lewis, Joshua P.; Li, Bingshan; Li, Yun; Lloyd-Jones, Donald M.; Loos, Ruth J. F.; Manichaikul, Ani; Meyers, Deborah A.; Mitchell, Braxton D.; Morrison, Alanna C.; Ngo, Debby; Nickerson, Deborah A.; Nongmaithem, Suraj; North, Kari E.; O'Connell, Jeffrey R.; Ortega, Victor E.; Pankratz, Nathan; Perry, James A.; Psaty, Bruce M.; Rich, Stephen S.; Soranzo, Nicole; Rotter, Jerome, I; Silverman, Edwin K.; Smith, Nicholas L.; Tang, Hua; Tracy, Russell P.; Thornton, Timothy A.; Vasan, Ramachandran S.; Zein, Joe; Mathias, Rasika A.; Reiner, Alexander P.; Auer, Paul L. Share Save Mitochondrial DNA variants modulate N-formylmethionine, proteostasis and risk of late-onset human diseasesCai, Na; Gomez-Duran, Aurora; Yonova-Doing, Ekaterina; Kundu, Kousik; Burgess, Annette, I; Golder, Zoe J.; Calabrese, Claudia; Bonder, Marc J.; Camacho, Marta; Lawson, Rachael A.; Li, Lixin; Williams-Gray, Caroline H.; Di Angelantonio, Emanuele; Roberts, David J.; Watkins, Nick A.; Ouwehand, Willem H.; Butterworth, Adam S.; Stewart, Isobel D.; Pietzner, Maik; Wareham, Nick J.; Langenberg, Claudia; Danesh, John; Walter, Klaudia; Rothwell, Peter M.; Howson, Joanna M. M.; Stegle, Oliver; Chinnery, Patrick F.; Soranzo, Nicole Share Save FUT6 deficiency compromises basophil function by selectively abrogating their sialyl-Lewis x expressionPuan, Kia Joo; Luis, Boris San; Yusof, Nurhashikin; Kumar, Dilip; Andiappan, Anand Kumar; Lee, Wendy; Cajic, Samanta; Vuckovic, Dragana; Chan, Jing De; Dollner, Tobias; Hou, Han Wei; Jiang, Yunxuan; Tian, Chao; Rapp, Erdmann; Poidinger, Michael; Wang, De Yun; Soranzo, Nicole; Lee, Bernett; Rotzschke, Olaf Share Save A map of transcriptional heterogeneity and regulatory variation in human microgliaYoung, Adam M. H.; Kumasaka, Natsuhiko; Calvert, Fiona; Hammond, Timothy R.; Knights, Andrew; Panousis, Nikolaos; Park, Jun Sung; Schwartzentruber, Jeremy; Liu, Jimmy; Kundu, Kousik; Segel, Michael; Murphy, Natalia A.; McMurran, Christopher E.; Bulstrode, Harry; Correia, Jason; Budohoski, Karol P.; Joannides, Alexis; Guilfoyle, Mathew R.; Trivedi, Rikin; Kirollos, Ramez; Morris, Robert; Garnett, Matthew R.; Timofeev, Ivan; Jalloh, Ibrahim; Holland, Katherine; Mannion, Richard; Mair, Richard; Watts, Colin; Price, Stephen J.; Kirkpatrick, Peter J.; Santarius, Thomas; Mountjoy, Edward; Ghoussaini, Maya; Soranzo, Nicole; Bayraktar, Omer A.; Stevens, Beth; Hutchinson, Peter J.; Franklin, Robin J. M.; Gaffney, Daniel J. Share Save Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program (vol 108, pg 874, 2021)Hu, Yao; Stilp, Adrienne M.; McHugh, Caitlin P.; Rao, Shuquan; Jain, Deepti; Zheng, Xiuwen; Lane, John; de Bellefon, Sebastian Meric; Raffield, Laura M.; Chen, Ming-Huei; Yanek, Lisa R.; Wheeler, Marsha; Yao, Yao; Ren, Chunyan; Broome, Jai; Moon, Jee-Young; de Vries, Paul S.; Hobbs, Brian D.; Sun, Quan; Surendran, Praveen; Brody, Jennifer A.; Blackwell, Thomas W.; Choquet, Helene; Ryan, Kathleen; Duggirala, Ravindranath; Heard-Costa, Nancy; Wang, Zhe; Chami, Nathalie; Preuss, Michael H.; Min, Nancy; Ekunwe, Lynette; Lange, Leslie A.; Cushman, Mary; Faraday, Nauder; Curran, Joanne E.; Almasy, Laura; Kundu, Kousik; Smith, Albert V.; Gabriel, Stacey; Rotter, Jerome I.; Fornage, Myriam; Lloyd-Jones, Donald M.; Vasan, Ramachandran S.; Smith, Nicholas L.; North, Kari E.; Boerwinkle, Eric; Becker, Lewis C.; Lewis, Joshua P.; Abecasis, Goncalo R.; Hou, Lifang; O'Connell, Jeffrey R.; Morrison, Alanna C.; Beaty, Terri H.; Kaplan, Robert; Correa, Adolfo; Blangero, John; Jorgenson, Eric; Psaty, Bruce M.; Kooperberg, Charles; Walton, Russell T.; Kleinstiver, Benjamin P.; Tang, Hua; Loos, Ruth J. F.; Soranzo, Nicole; Butterworth, Adam S.; Nickerson, Debbie; Rich, Stephen S.; Mitchell, Braxton D.; Johnson, Andrew D.; Auer, Paul L.; Li, Yun; Mathias, Rasika A.; Lettre, Guillaume; Pankratz, Nathan; Laurie, Cathy C.; Laurie, Cecelia A.; Bauer, Daniel E.; Conomos, Matthew P.; Reiner, Alexander P. Share Save Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed programHu, Yao; Stilp, Adrienne M.; McHugh, Caitlin P.; Rao, Shuquan; Jain, Deepti; Zheng, Xiuwen; Lane, John; de Bellefon, Sebastian Meric; Raffield, Laura M.; Chen, Ming-Huei; Yanek, Lisa R.; Wheeler, Marsha; Yao, Yao; Ren, Chunyan; Broome, Jai; Moon, Jee-Young; de Vries, Paul S.; Hobbs, Brian D.; Sun, Quan; Surendran, Praveen; Brody, Jennifer A.; Blackwell, Thomas W.; Choquet, Helene; Ryan, Kathleen; Duggirala, Ravindranath; Heard-Costa, Nancy; Wang, Zhe; Chami, Nathalie; Preuss, Michael H.; Min, Nancy; Ekunwe, Lynette; Lange, Leslie A.; Cushman, Mary; Faraday, Nauder; Curran, Joanne E.; Almasy, Laura; Kundu, Kousik; Smith, Albert, V; Gabriel, Stacey; Rotter, Jerome, I; Fornage, Myriam; Lloyd-Jones, Donald M.; Vasan, Ramachandran S.; Smith, Nicholas L.; North, Kari E.; Boerwinkle, Eric; Becker, Lewis C.; Lewis, Joshua P.; Abecasis, Goncalo R.; Hou, Lifang; O'Connell, Jeffrey R.; Morrison, Alanna C.; Beaty, Terri H.; Kaplan, Robert; Correa, Adolfo; Blangero, John; Jorgenson, Eric; Psaty, Bruce M.; Kooperberg, Charles; Walton, Russell T.; Kleinstiver, Benjamin P.; Tang, Hua; Loos, Ruth J. F.; Soranzo, Nicole; Butterworth, Adam S.; Nickerson, Debbie; Rich, Stephen S.; Mitchell, Braxton D.; Johnson, Andrew D.; Auer, Paul L.; Li, Yun; Mathias, Rasika A.; Lettre, Guillaume; Pankratz, Nathan; Laurie, Cathy C.; Laurie, Cecelia A.; Bauer, Daniel E.; Conomos, Matthew P.; Reiner, Alexander P. Share Save 
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