화학공학소재연구정보센터
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No. Article
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
3 A brief history of human disease genetics
Claussnitzer M, Cho JH, Collins R, Cox NJ, Dermitzakis ET, Hurles ME, Kathiresan S, Kenny EE, Lindgren CM, MacArthur DG, North KN, Plon SE, Rehm HL, Risch N, Rotimi CN, Shendure J, Soranzo N, McCarthy MI
Nature, 577(7789), 179, 2020
4 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
5 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
6 A positively selected FBN1 missense variant reduces height in Peruvian individuals
Asgari S, Luo Y, Akbari A, Belbin GM, Li XY, Harris DN, Selig M, Bartell E, Calderon R, Slowikowski K, Contreras C, Yataco R, Galea JT, Jimenez J, Coit JM, Farronay C, Nazarian RM, O'Connor TD, Dietz HC, Hirschhorn JN, Guio H, Lecca L, Kenny EE, Freeman EE, Murray MB, Raychaudhuri S
Nature, 582(7811), 234, 2020
7 Genetic analyses of diverse populations improves discovery for complex traits
Wojcik GL, Graff M, Nishimura KK, Tao R, Haessler J, Gignoux CR, Highland HM, Patel YM, Sorokin EP, Avery CL, Belbin GM, Bien SA, Cheng I, Cullina S, Hodonsky CJ, Hu Y, Huckins LM, Jeff J, Justice AE, Kocarnik JM, Lim U, Lin BM, Lu YC, Nelson SC, Park SSL, Poisner H, Preuss MH, Richard MA, Schurmann C, Setiawan VW, Sockell A, Vahi K, Verbanck M, Vishnu A, Walker RW, Young KL, Zubair N, Acuna-Alonso V, Ambite JL, Barnes KC, Boerwinkle E, Bottinger EP, Bustamante CD, Caberto C, Canizales-Quinteros S, Conomos MP, Deelman E, Do R, Doheny K, Fernandez-Rhodes L, Fornage M, Hailu B, Heiss G, Henn BM, Hindorff LA, Jackson RD, Laurie CA, Laurie CC, Li YQ, Lin DY, Moreno-Estrada A, Nadkarni G, Norman PJ, Pooler LC, Reiner AP, Romm J, Sabatti C, Sandoval K, Sheng X, Stahl EA, Stram DO, Thornton TA, Wassel CL, Wilkens LR, Winkler CA, Yoneyama S, Buyske S, Haiman CA, Kooperberg C, Le Marchand L, Loos RJF, Matise TC, North KE, Peters U, Kenny EE, Carlson CS
Nature, 570(7762), 514, 2019
8 A global reference for human genetic variation
Altshuler DM, Durbin RM, Abecasis GR, Bentley DR, Chakravarti A, Clark AG, Donnelly P, Eichler EE, Flicek P, Gabriel SB, Gibbs RA, Green ED, Hurles ME, Knoppers BM, Korbel JO, Lander ES, Lee C, Lehrach H, Mardis ER, Marth GT, McVean GA, Nickerson DA, Schmidt JP, Sherry ST, Wang J, Wilson RK, Gibbs RA, Boerwinkle E, Doddapaneni H, Han Y, Korchina V, Kovar C, Lee S, Muzny D, Reid JG, Zhu YM, Wang J, Chang YQ, Feng Q, Fang XD, Guo XS, Jian M, Jiang H, Jin X, Lan TM, Li GQ, Li JX, Li YR, Liu SM, Liu X, Lu Y, Ma XD, Tang MF, Wang B, Wang GB, Wu HL, Wu RH, Xu X, Yin Y, Zhang DD, Zhang WW, Zhao J, Zhao MR, Zheng XL, Lander ES, Altshuler DM, Gabriel SB, Gupta N, Gharani N, Toji LH, Gerry NP, Resch AM, Flicek P, Barker J, Clarke L, Gil L, Hunt SE, Kelman G, Kulesha E, Leinonen R, McLaren WM, Radhakrishnan R, Roa A, Smirnov D, Smith RE, Streeter I, Thormann A, Toneva I, Vaughan B, Zheng-Bradley X, Bentley DR, Grocock R, Humphray S, James T, Kingsbury Z, Lehrach H, Sudbrak R, Albrecht MW, 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