검색결과 : 6건
| No. | Article |
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| 1 |
Inherited causes of clonal haematopoiesis in 97,691 whole genomes (vol 586 , pg 763, 2020) Bick AG, Weinstock JS, Nandakumar SK, Fulco CP, Bao EL, Zekavat SM, Szeto MD, Liao XT, Leventhal MJ, Nasser J, Chang K, Laurie C, Burugula BB, Gibson CJ, Niroula A, Lin AE, Taub MA, Aguet F, Ardlie K, Mitchell BD, Barnes KC, Moscati A, Fornage M, Redline S, Psaty BM, Silverman EK, Weiss ST, Palmer ND, Vasan RS, Burchard EG, Kardia SLR, He J, Kaplan RC, Smith NL, Arnett DK, Schwartz DA, Correa A, de Andrade M, Guo XQ, Konkle BA, Custer B, Peralta JM, Gui HS, Meyers DA, McGarvey ST, Chen IYD, Shoemaker MB, Peyser PA, Broome JG, Gogarten SM, Wang FF, Wong QN, Montasser ME, Daya M, Kenny EE, North KE, Launer LJ, Cade BE, Bis JC, Cho MH, Lasky-Su J, Bowden DW, Cupples LA, Mak ACY, Becker LC, Smith JA, Kelly TN, Aslibekyan S, Heckbert SR, Tiwari HK, Yang IV, Heit JA, Lubitz SA, Johnsen JM, Curran JE, Wenzel SE, Weeks DE, Rao DC, Darbar D, Moon JY, Tracy RP, Buth EJ, Rafaels N, Loos RJF, Durda P, Liu YM, Hou LF, Lee J, Kachroo P, Freedman BI, Levy D, Bielak LF, Hixson JE, Floyd JS, Whitsel EA, Ellinor PT, Irvin MR, Fingerlin TE, Raffield LM, Armasu SM, Wheeler MM, Sabino EC, Blangero J, Williams LK, Levy BD, Sheu WHH, Roden DM, Boerwinkle E, Manson JE, Mathias RA, Desai P, Taylor KD, Johnson AD, Auer PL, Kooperberg C, Laurie CC, Blackwell TW, Smith AV, Zhao HY, Lange E, Lange L, Rich SS, Rotter JI, Wilson JG, Scheet P, Kitzman JO, Lander ES, Engreitz JM, Ebert BL, Reiner AP, Jaiswal S, Abecasis G, Sankaran VG, Kathiresan S, Natarajan P Nature, 591(7851), E27, 2021 |
| 2 |
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program Taliun D, Harris DN, Kessler MD, Carlson J, Szpiech ZA, Torres R, Taliun SAG, Corvelo A, Gogarten SM, Kang HM, Pitsillides AN, LeFaive J, Lee SB, Tian XW, Browning BL, Das S, Emde AK, Clarke WE, Loesch DP, Shetty AC, Blackwell TW, Smith AV, Wong Q, Liu XM, Conomos MP, Bobo DM, Aguet F, Albert C, Alonso A, Ardlie KG, Arking DE, Aslibekyan S, Auer PL, Barnard J, Barr RG, Barwick L, Becker LC, Beer RL, Benjamin EJ, Bielak LF, Blangero J, Boehnke M, Bowden DW, Brody JA, Burchard EG, Cade BE, Casella JF, Chalazan B, Chasman DI, Chen YDI, Cho MH, Choi SH, Chung MK, Clish CB, Correa A, Curran JE, Custer B, Darbar D, Daya M, de Andrade M, DeMeo DL, Dutcher SK, Ellinor PT, Emery LS, Eng C, Fatkin D, Fingerlin T, Forer L, Fornage M, Franceschini N, Fuchsberger C, Fullerton SM, Germer S, Gladwin MT, Gottlieb DJ, Guo XQ, Hall ME, He J, Heard-Costa NL, Heckbert SR, Irvin MR, Johnsen JM, Johnson AD, Kaplan R, Kardia SLR, Kelly T, Kelly S, Kenny EE, Kiel DP, Klemmer R, Konkle BA, Kooperberg C, Kottgen A, Lange LA, Lasky-Su J, Levy D, Lin XH, Lin KH, Liu CY, Loos RJF, Garman L, Gerszten R, Lubitz SA, Lunetta KL, Mak ACY, Manichaikul A, Manning AK, Mathias RA, McManus DD, McGarvey ST, Meigs JB, Meyers DA, Mikulla JL, Minear MA, Mitchell BD, Mohanty S, Montasser ME, Montgomery C, Morrison AC, Murabito JM, Natale A, Natarajan P, Nelson SC, North KE, O'Connell JR, Palmer ND, Pankratz N, Peloso GM, Peyser PA, Pleiness J, Post WS, Psaty BM, Rao DC, Redline S, Reiner AP, Roden D, Rotter JI, Ruczinski I, Sarnowski C, Schoenherr S, Schwartz DA, Seo JS, Seshadri S, Sheehan VA, Sheu WH, Shoemaker MB, Smith NL, Smith JA, Sotoodehnia N, Stilp AM, Tang WH, Taylor KD, Telen M, Thornton TA, Tracy RP, Van den Berg DJ, Vasan RS, Viaud-Martinez KA, Vrieze S, Weeks DE, Weir BS, Weiss ST, Weng LC, Willer CJ, Zhang YZ, Zhao XT, Arnett DK, Ashley-Koch AE, Barnes KC, Boerwinkle E, Gabriel S, Gibbs R, Rice KM, Rich SS, Silverman EK, Qasba P, Gan WN, Papanicolaou GJ, Nickerson DA, Browning SR, Zody MC, Zollner S, Wilson JG, Cupples LA, Laurie CC, Jaquish CE, Hernandez RD, O'Connor TD, Abecasis GR Nature, 590(7845), 2021 |
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Inherited causes of clonal haematopoiesis in 97,691 whole genomes Bick AG, Weinstock JS, Nandakumar SK, Fulco CP, Bao EL, Zekavat SM, Szeto MD, Liao XT, Leventhal MJ, Nasser J, Chang K, Laurie C, Burugula BB, Gibson CJ, Lin AE, Taub MA, Aguet F, Ardlie K, Mitchell BD, Barnes KC, Moscati A, Fornage M, Redline S, Psaty BM, Silverman EK, Weiss ST, Palmer ND, Vasan RS, Burchard EG, Kardia SLR, He J, Kaplan RC, Smith NL, Arnett DK, Schwartz DA, Correa A, de Andrade M, Guo XQ, Konkle BA, Custer B, Peralta JM, Gui HS, Meyers DA, McGarvey ST, Chen IYD, Shoemaker MB, Peyser PA, Broome JG, Gogarten SM, Wang FF, Wong QN, Montasser ME, Daya M, Kenny EE, North KE, Launer LJ, Cade BE, Bis JC, Cho MH, Lasky-Su J, Bowden DW, Cupples LA, Mak ACY, Becker LC, Smith JA, Kelly TN, Aslibekyan S, Heckbert SR, Tiwari HK, Yang IV, Heit JA, Lubitz SA, Johnsen JM, Curran JE, Wenzel SE, Weeks DE, Rao DC, Darbar D, Moon JY, Tracy RP, Buth EJ, Rafaels N, Loos RJF, Durda P, Liu YM, Hou LF, Lee J, Kachroo P, Freedman BI, Levy D, Bielak LF, Hixson JE, Floyd JS, Whitsel EA, Ellinor PT, Irvin MR, Fingerlin TE, Raffield LM, Armasu SM, Wheeler MM, Sabino EC, Blangero J, Williams LK, Levy BD, Sheu WHH, Roden DM, Boerwinkle E, Manson JE, Mathias RA, Desai P, Taylor KD, Johnson AD, Auer PL, Kooperberg C, Laurie CC, Blackwell TW, Smith AV, Zhao HY, Lange E, Lange L, Rich SS, Rotter JI, Wilson JG, Scheet P, Kitzman JO, Lander ES, Engreitz JM, Ebert BL, Reiner AP, Jaiswal S, Abecasis G, Sankaran VG, Kathiresan S, Natarajan P, Abe N, Albert C, Almasy L, Alonso A, Ament S, Anderson P, Anugu P, Applebaum-Bowden D, Arking D, Ashley-Koch A, Aslibekyan S, Assimes T, Avramopoulos D, Barnard J, Barr RG, Barron-Casella E, Barwick L, Beaty T, Beck G, Becker D, Beer R, Beitelshees A, Benjamin E, Benos P, Bezerra M, Bielak L, Bowler R, Brody J, Broeckel U, Bunting K, Bustamante C, Cardwell J, Carey V, Carty C, Casaburi R, Casella J, Castaldi P, Chaffin M, Chang C, Chang YC, Chasman D, Chavan S, Chen BJ, Chen WM, Choi SH, Chuang LM, Chung M, Chung RH, Clish C, Comhair S, Cornell E, Crandall C, Crapo J, Curtis J, Damcott C, Das S, David S, Davis C, De Baun M, Deka R, Demeo D, Devine S, Duan Q, Duggirala R, Dutcher S, Eaton C, Ekunwe L, El Boueiz A, Emery L, Erzurum S, Farber C, Flickinger M, Franceschini N, Frazar C, Fu M, Fullerton SM, Fulton L, Gabriel S, Gan WN, Gao SS, Gao Y, Gass M, Gelb B, Geng XQ, Geraci M, Germer S, Gerszten R, Ghosh A, Gibbs R, Gignoux C, Gladwin M, Glahn D, Gong DW, Goring H, Graw S, Grine D, Gu CC, Guan Y, Gupta N, Haessler J, Hall M, Harris D, Hawley NL, Heavner B, Hernandez R, Herrington D, Hersh C, Hidalgo B, Hobbs B, Hokanson J, Hong E, Hoth K, Hsiung CA, Hung YJ, Huston H, Hwu CM, Jackson R, Jain D, Jaquish C, Jhun MA, Johnson C, Johnston R, Jones K, Kang HM, Kelly S, Kessler M, Khan A, Kim W, Kinney G, Kramer H, Lange C, LeBoff M, Lee SS, Lee WJ, LeFaive J, Levine D, Lewis J, Li XH, Li Y, Lin H, Lin HH, Lin KH, Lin XH, Liu SM, Liu Y, Lunetta K, Luo J, Mahaney M, Make B, Manichaikul A, Margolin L, Martin L, Mathai S, May S, McArdle P, McDonald ML, McFarland S, McGoldrick D, McHugh C, Mei H, Mestroni L, Mikulla J, Min N, Minear M, Minster RL, Moll M, Montgomery C, Musani S, Mwasongwe S, Mychaleckyj JC, Nadkarni G, Naik R, Naseri T, Nekhai S, Nelson SC, Neltner B, Nickerson D, O'Connell J, O'Connor T, Ochs-Balcom H, Paik D, Pankow J, Papanicolaou G, Parsa A, Perez M, Perry J, Peters U, Peyser P, Phillips LS, Pollin T, Post W, Becker JP, Boorgula MP, Preuss M, Qasba P, Qiao DD, Qin ZH, Rasmussen-Torvik L, Ratan A, Reed R, Regan E, Reupena MS, Rice K, Roselli C, Ruczinski I, Russell P, Ruuska S, Ryan K, Saleheen D, Salimi S, Salzberg S, Sandow K, Scheller C, Schmidt E, Schwander K, Sciurba F, Seidman C, Seidman J, Sheehan V, Sherman SL, Shetty A, Shetty A, Silver B, Smith J, Smith T, Smoller S, Snively B, Snyder M, Sofer T, Sotoodehnia N, Stilp AM, Storm G, Streeten E, Su JL, Sung YJ, Sylvia J, Szpiro A, Sztalryd C, Taliun D, Tang H, Taylor M, Taylor S, Telen M, Thornton TA, Threlkeld M, Tinker L, Tirschwell D, Tishkoff S, Tiwari H, Tong C, Tsai M, Vaidya D, Van den Berg D, VandeHaar P, Vrieze S, Walker T, Wallace R, Walts A, Wang HM, Watson K, Weir B, Weng LC, Wessel J, Willer C, Williams K, Wilson C, Wu J, Xu HC, Yanek L, Yang RZ, Zaghloul N, Zhang YZ, Zhao SX, Zhao W, Zhi DG, Zhou X, Zhu XF, Zody M, Zoellner S Nature, 586(7831), 763, 2020 |
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Inherited causes of clonal haematopoiesis in 97,691 whole genomes Bick AG, Weinstock JS, Nandakumar SK, Fulco CP, Bao EL, Zekavat SM, Szeto MD, Liao XT, Leventhal MJ, Nasser J, Chang K, Laurie C, Burugula BB, Gibson CJ, Lin AE, Taub MA, Aguet F, Ardlie K, Mitchell BD, Barnes KC, Moscati A, Fornage M, Redline S, Psaty BM, Silverman EK, Weiss ST, Palmer ND, Vasan RS, Burchard EG, Kardia SLR, He J, Kaplan RC, Smith NL, Arnett DK, Schwartz DA, Correa A, de Andrade M, Guo XQ, Konkle BA, Custer B, Peralta JM, Gui HS, Meyers DA, McGarvey ST, Chen IYD, Shoemaker MB, Peyser PA, Broome JG, Gogarten SM, Wang FF, Wong QN, Montasser ME, Daya M, Kenny EE, North KE, Launer LJ, Cade BE, Bis JC, Cho MH, Lasky-Su J, Bowden DW, Cupples LA, Mak ACY, Becker LC, Smith JA, Kelly TN, Aslibekyan S, Heckbert SR, Tiwari HK, Yang IV, Heit JA, Lubitz SA, Johnsen JM, Curran JE, Wenzel SE, Weeks DE, Rao DC, Darbar D, Moon JY, Tracy RP, Buth EJ, Rafaels N, Loos RJF, Durda P, Liu YM, Hou LF, Lee J, Kachroo P, Freedman BI, Levy D, Bielak LF, Hixson JE, Floyd JS, Whitsel EA, Ellinor PT, Irvin MR, Fingerlin TE, Raffield LM, Armasu SM, Wheeler MM, Sabino EC, Blangero J, Williams LK, Levy BD, Sheu WHH, Roden DM, Boerwinkle E, Manson JE, Mathias RA, Desai P, Taylor KD, Johnson AD, Auer PL, Kooperberg C, Laurie CC, Blackwell TW, Smith AV, Zhao HY, Lange E, Lange L, Rich SS, Rotter JI, Wilson JG, Scheet P, Kitzman JO, Lander ES, Engreitz JM, Ebert BL, Reiner AP, Jaiswal S, Abecasis G, Sankaran VG, Kathiresan S, Natarajan P, Abe N, Albert C, Almasy L, Alonso A, Ament S, Anderson P, Anugu P, Applebaum-Bowden D, Arking D, Ashley-Koch A, Aslibekyan S, Assimes T, Avramopoulos D, Barnard J, Barr RG, Barron-Casella E, Barwick L, Beaty T, Beck G, Becker D, Beer R, Beitelshees A, Benjamin E, Benos P, Bezerra M, Bielak L, Bowler R, Brody J, Broeckel U, Bunting K, Bustamante C, Cardwell J, Carey V, Carty C, Casaburi R, Casella J, Castaldi P, Chaffin M, Chang C, Chang YC, Chasman D, Chavan S, Chen BJ, Chen WM, Choi SH, Chuang LM, Chung M, Chung RH, Clish C, Comhair S, Cornell E, Crandall C, Crapo J, Curtis J, Damcott C, Das S, David S, Davis C, De Baun M, Deka R, Demeo D, Devine S, Duan Q, Duggirala R, Dutcher S, Eaton C, Ekunwe L, El Boueiz A, Emery L, Erzurum S, Farber C, Flickinger M, Franceschini N, Frazar C, Fu M, Fullerton SM, Fulton L, Gabriel S, Gan WN, Gao SS, Gao Y, Gass M, Gelb B, Geng XQ, Geraci M, Germer S, Gerszten R, Ghosh A, Gibbs R, Gignoux C, Gladwin M, Glahn D, Gong DW, Goring H, Graw S, Grine D, Gu CC, Guan Y, Gupta N, Haessler J, Hall M, Harris D, Hawley NL, Heavner B, Hernandez R, Herrington D, Hersh C, Hidalgo B, Hobbs B, Hokanson J, Hong E, Hoth K, Hsiung CA, Hung YJ, Huston H, Hwu CM, Jackson R, Jain D, Jaquish C, Jhun MA, Johnson C, Johnston R, Jones K, Kang HM, Kelly S, Kessler M, Khan A, Kim W, Kinney G, Kramer H, Lange C, LeBoff M, Lee SS, Lee WJ, LeFaive J, Levine D, Lewis J, Li XH, Li Y, Lin H, Lin HH, Lin KH, Lin XH, Liu SM, Liu Y, Lunetta K, Luo J, Mahaney M, Make B, Manichaikul A, Margolin L, Martin L, Mathai S, May S, McArdle P, McDonald ML, McFarland S, McGoldrick D, McHugh C, Mei H, Mestroni L, Mikulla J, Min N, Minear M, Minster RL, Moll M, Montgomery C, Musani S, Mwasongwe S, Mychaleckyj JC, Nadkarni G, Naik R, Naseri T, Nekhai S, Nelson SC, Neltner B, Nickerson D, O'Connell J, O'Connor T, Ochs-Balcom H, Paik D, Pankow J, Papanicolaou G, Parsa A, Perez M, Perry J, Peters U, Peyser P, Phillips LS, Pollin T, Post W, Becker JP, Boorgula MP, Preuss M, Qasba P, Qiao DD, Qin ZH, Rasmussen-Torvik L, Ratan A, Reed R, Regan E, Reupena MS, Rice K, Roselli C, Ruczinski I, Russell P, Ruuska S, Ryan K, Saleheen D, Salimi S, Salzberg S, Sandow K, Scheller C, Schmidt E, Schwander K, Sciurba F, Seidman C, Seidman J, Sheehan V, Sherman SL, Shetty A, Shetty A, Silver B, Smith J, Smith T, Smoller S, Snively B, Snyder M, Sofer T, Sotoodehnia N, Stilp AM, Storm G, Streeten E, Su JL, Sung YJ, Sylvia J, Szpiro A, Sztalryd C, Taliun D, Tang H, Taylor M, Taylor S, Telen M, Thornton TA, Threlkeld M, Tinker L, Tirschwell D, Tishkoff S, Tiwari H, Tong C, Tsai M, Vaidya D, Van den Berg D, VandeHaar P, Vrieze S, Walker T, Wallace R, Walts A, Wang HM, Watson K, Weir B, Weng LC, Wessel J, Willer C, Williams K, Wilson C, Wu J, Xu HC, Yanek L, Yang RZ, Zaghloul N, Zhang YZ, Zhao SX, Zhao W, Zhi DG, Zhou X, Zhu XF, Zody M, Zoellner S Nature, 586(7831), 763, 2020 |
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Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls Flannick J, Mercader JM, Fuchsberger C, Udler MS, Mahajan A, Wessel J, Teslovich TM, Caulkins L, Koesterer R, Barajas-Olmos F, Blackwell TW, Boerwinkle E, Brody JA, Centeno-Cruz F, Chen L, Chen SY, Contreras-Cubas C, Cordova E, Correa A, Cortes M, DeFronzo RA, Dolan L, Drews KL, Elliott A, Floyd JS, Gabriel S, Garay-Sevilla ME, Garcia-Ortiz H, Gross M, Han S, Heard-Costa NL, Jackson AU, Jorgensen ME, Kang HM, Kelsey M, Kim BJ, Koistinen HA, Kuusisto J, Leader JB, Linneberg A, Liu CT, Liu JJ, Lyssenko V, Manning AK, Marcketta A, Malacara-Hernandez JM, Martinez-Hernandez A, Matsuo K, Mayer-Davis E, Mendoza-Caamal E, Mohlke KL, Morrison AC, Ndungu A, Ng MCY, O'Dushlaine C, Payne AJ, Pihoker C, Post WS, Preuss M, Psaty BM, Vasan RS, Rayner NW, Reiner AP, Revilla-Monsalve C, Robertson NR, Santoro N, Schurmann C, So WY, Soberon X, Stringham HM, Strom TM, Tam CHT, Thameem F, Tomlinson B, Torres JM, Tracy RP, van Dam RM, Vujkovic M, Wang S, Welch RP, Witte DR, Wong TY, Atzmon G, Barzilai N, Blangero J, Bonnycastle LL, Bowden DW, Chambers JC, Chan E, Cheng CY, Cho YS, Collins FS, De Vries PS, Duggirala R, Glaser B, Gonzalez C, Gonzalez ME, Groop L, Kooner JS, Kwak SH, Laakso M, Lehman DM, Nilsson P, Spector TD, Tai ES, Tuomi T, Tuomilehto J, Wilson JG, Aguilar-Salinas CA, Bottinger E, Burke B, Carey DJ, Chan JCN, Dupuis J, Frossard P, Heckbert SR, Hwang MY, Kim YJ, Kirchner HL, Lee JY, Lee J, Loos RJF, Ma RCW, Morris AD, O'Donnell CJ, Palmer CNA, Pankow J, Park KS, Rasheed A, Saleheen D, Sim X, Small KS, Teo YY, Haiman C, Hanis CL, Henderson BE, Orozco L, Tusie-Luna T, Dewey FE, Baras A, Gieger C, Meitinger T, Strauch K, Lange L, Grarup N, Hansen T, Pedersen O, Zeitler P, Dabelea D, Abecasis G, Bell GI, Cox NJ, Seielstad M, Sladek R, Meigs JB, Rich SS, Rotter JI, Altshuler D, Burtt NP, Scott LJ, Morris AP, Florez JC, McCarthy MI, Boehnke M Nature, 570(7759), 71, 2019 |
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Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction Do R, Stitziel NO, Won HH, Jorgensen AB, Duga S, Merlini PA, Kiezun A, Farrall M, Goel A, Zuk O, Guella I, Asselta R, Lange LA, Peloso GM, Auer PL, Girelli D, Martinelli N, Farlow DN, DePristo MA, Roberts R, Stewart AFR, Saleheen D, Danesh J, Epstein SE, Sivapalaratnam S, Hovingh GK, Kastelein JJ, Samani NJ, Schunkert H, Erdmann J, Shah SH, Kraus WE, Davies R, Nikpay M, Johansen CT, Wang J, Hegele RA, Hechter E, Marz W, Kleber ME, Huang J, Johnson AD, Li MY, Burke GL, Gross M, Liu YM, Assimes TL, Heiss G, Lange EM, Folsom AR, Taylor HA, Olivieri O, Hamsten A, Clarke R, Reilly DF, Yin W, Rivas MA, Donnelly P, Rossouw JE, Psaty BM, Herrington DM, Wilson JG, Rich SS, Bamshad MJ, Tracy RP, Cupples LA, Rader DJ, Reilly MP, Spertus JA, Cresci S, Hartiala J, Tang WHW, Hazen SL, Allayee H, Reiner AP, Carlson CS, Kooperberg C, Jackson RD, Boerwinkle E, Lander ES, Schwartz SM, Siscovick DS, McPherson R, Tybjaerg-Hansen A, Abecasis GR, Watkins H, Nickerson DA, Ardissino D, Sunyaev SR, O'Donnell CJ, Altshuler D, Gabriel S, Kathiresan S Nature, 518(7537), 102, 2015 |