연구자에게
내 논문이 여기 있나요?
논문 2,663편이 이 사이트를 떠받치고 있습니다. 모든 변이·질환 페이지가
자기가 어떤 연구로부터 쓰였는지 밝히며, 이것이 그 목록을 페이지들에서 모은 것입니다.
성함이나 학술지명, PMID로 찾아보십시오.
Reynolds R에 대해
12건.
Genome-wide associations for birth weight and correlations with adult disease
Horikoshi M,
Beaumont RN,
Day FR,
Warrington NM,
Kooijman MN,
Fernandez-Tajes J,
Feenstra B,
van Zuydam NR,
Gaulton KJ,
Grarup N,
Bradfield JP,
Strachan DP
외 157명 — 모두 보기
Li-Gao R,
Ahluwalia TS,
Kreiner E,
Rueedi R,
Lyytikäinen LP,
Cousminer DL,
Wu Y,
Thiering E,
Wang CA,
Have CT,
Hottenga JJ,
Vilor-Tejedor N,
Joshi PK,
Boh ETH,
Ntalla I,
Pitkänen N,
Mahajan A,
van Leeuwen EM,
Joro R,
Lagou V,
Nodzenski M,
Diver LA,
Zondervan KT,
Bustamante M,
Marques-Vidal P,
Mercader JM,
Bennett AJ,
Rahmioglu N,
Nyholt DR,
Ma RCW,
Tam CHT,
Tam WH,
Ganesh SK,
van Rooij FJ,
Jones SE,
Loh PR,
Ruth KS,
Tuke MA,
Tyrrell J,
Wood AR,
Yaghootkar H,
Scholtens DM,
Paternoster L,
Prokopenko I,
Kovacs P,
Atalay M,
Willems SM,
Panoutsopoulou K,
Wang X,
Carstensen L,
Geller F,
Schraut KE,
Murcia M,
van Beijsterveldt CE,
Willemsen G,
Appel EVR,
Fonvig CE,
Trier C,
Tiesler CM,
Standl M,
Kutalik Z,
Bonas-Guarch S,
Hougaard DM,
Sánchez F,
Torrents D,
Waage J,
Hollegaard MV,
de Haan HG,
Rosendaal FR,
Medina-Gomez C,
Ring SM,
Hemani G,
McMahon G,
Robertson NR,
Groves CJ,
Langenberg C,
Luan J,
Scott RA,
Zhao JH,
Mentch FD,
MacKenzie SM,
Reynolds RM,
Lowe WL Jr,
Tönjes A,
Stumvoll M,
Lindi V,
Lakka TA,
van Duijn CM,
Kiess W,
Körner A,
Sørensen TI,
Niinikoski H,
Pahkala K,
Raitakari OT,
Zeggini E,
Dedoussis GV,
Teo YY,
Saw SM,
Melbye M,
Campbell H,
Wilson JF,
Vrijheid M,
de Geus EJ,
Boomsma DI,
Kadarmideen HN,
Holm JC,
Holm JC,
Hansen T,
Sebert S,
Hattersley AT,
Beilin LJ,
Newnham JP,
Newnham JP,
Pennell CE,
Heinrich J,
Adair LS,
Borja JB,
Mohlke KL,
Eriksson JG,
Widén EE,
Kähönen M,
Viikari JS,
Lehtimäki T,
Vollenweider P,
Vollenweider P,
Bønnelykke K,
Bisgaard H,
Mook-Kanamori DO,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
Pisinger C,
Pisinger C,
Pedersen O,
Power C,
Hyppönen E,
Wareham NJ,
Hakonarson H,
Davies E,
Walker BR,
Jaddoe VW,
Jarvelin MR,
Grant SF,
Vaag AA,
Lawlor DA,
Frayling TM,
Frayling TM,
Davey Smith G,
Morris AP,
Ong KK,
Felix JF,
Timpson NJ,
Perry JR,
Evans DM,
McCarthy MI,
McCarthy MI,
Freathy RM
CHARGE Consortium Hematology Working Group · Early Growth Genetics (EGG) Consortium
Nature · 2016 · PMID 27680694
페이지 12개+
A genome-wide association analysis reveals new pathogenic pathways in gout
Major TJ,
Takei R,
Matsuo H,
Leask MP,
Sumpter NA,
Topless RK,
Shirai Y,
Wang W,
Cadzow MJ,
Phipps-Green AJ,
Li Z,
Ji A
외 86명 — 모두 보기
Merriman ME,
Morice E,
Kelley EE,
Wei WH,
McCormick SPA,
Bixley MJ,
Reynolds RJ,
Saag KG,
Fadason T,
Golovina E,
O'Sullivan JM,
Stamp LK,
Dalbeth N,
Abhishek A,
Doherty M,
Roddy E,
Jacobsson LTH,
Kapetanovic MC,
Melander O,
Andrés M,
Pérez-Ruiz F,
Torres RJ,
Radstake T,
Jansen TL,
Janssen M,
Joosten LAB,
Liu R,
Gaal OI,
Crişan TO,
Rednic S,
Kurreeman F,
Huizinga TWJ,
Toes R,
Lioté F,
Richette P,
Bardin T,
Ea HK,
Pascart T,
McCarthy GM,
Helbert L,
Stibůrková B,
Tausche AK,
Uhlig T,
Vitart V,
Boutin TS,
Hayward C,
Riches PL,
Ralston SH,
Campbell A,
MacDonald TM,
Nakayama A,
Takada T,
Nakatochi M,
Shimizu S,
Kawamura Y,
Toyoda Y,
Nakaoka H,
Yamamoto K,
Matsuo K,
Shinomiya N,
Ichida K,
Lee C,
Bradbury LA,
Brown MA,
Robinson PC,
Buchanan RRC,
Hill CL,
Lester S,
Smith MD,
Rischmueller M,
Choi HK,
Stahl EA,
Miner JN,
Solomon DH,
Cui J,
Giacomini KM,
Brackman DJ,
Jorgenson EM,
Liu H,
Susztak K,
Shringarpure S,
So A,
Okada Y,
Li C,
Shi Y,
Merriman TR
FAST Study Group · Japan Gout Genomics Consortium 외 컨소시엄 3곳
Nature genetics · 2024 · PMID 39406924
페이지 12개+
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Sawcer S,
Hellenthal G,
Pirinen M,
Spencer CC,
Patsopoulos NA,
Moutsianas L,
Dilthey A,
Su Z,
Freeman C,
Hunt SE,
Edkins S,
Gray E
외 230명 — 모두 보기
Booth DR,
Potter SC,
Goris A,
Band G,
Oturai AB,
Strange A,
Saarela J,
Bellenguez C,
Fontaine B,
Gillman M,
Hemmer B,
Gwilliam R,
Zipp F,
Jayakumar A,
Martin R,
Leslie S,
Hawkins S,
Giannoulatou E,
D'alfonso S,
Blackburn H,
Martinelli Boneschi F,
Liddle J,
Harbo HF,
Perez ML,
Spurkland A,
Waller MJ,
Mycko MP,
Ricketts M,
Comabella M,
Hammond N,
Kockum I,
McCann OT,
Ban M,
Whittaker P,
Kemppinen A,
Weston P,
Hawkins C,
Widaa S,
Zajicek J,
Dronov S,
Robertson N,
Bumpstead SJ,
Barcellos LF,
Ravindrarajah R,
Abraham R,
Alfredsson L,
Ardlie K,
Aubin C,
Baker A,
Baker K,
Baranzini SE,
Bergamaschi L,
Bergamaschi R,
Bernstein A,
Berthele A,
Boggild M,
Bradfield JP,
Brassat D,
Broadley SA,
Buck D,
Butzkueven H,
Capra R,
Carroll WM,
Cavalla P,
Celius EG,
Cepok S,
Chiavacci R,
Clerget-Darpoux F,
Clysters K,
Comi G,
Cossburn M,
Cournu-Rebeix I,
Cox MB,
Cozen W,
Cree BA,
Cross AH,
Cusi D,
Daly MJ,
Davis E,
de Bakker PI,
Debouverie M,
D'hooghe MB,
Dixon K,
Dobosi R,
Dubois B,
Ellinghaus D,
Elovaara I,
Esposito F,
Fontenille C,
Foote S,
Franke A,
Galimberti D,
Ghezzi A,
Glessner J,
Gomez R,
Gout O,
Graham C,
Grant SF,
Guerini FR,
Hakonarson H,
Hall P,
Hamsten A,
Hartung HP,
Heard RN,
Heath S,
Hobart J,
Hoshi M,
Infante-Duarte C,
Ingram G,
Ingram W,
Islam T,
Jagodic M,
Kabesch M,
Kermode AG,
Kilpatrick TJ,
Kim C,
Klopp N,
Koivisto K,
Larsson M,
Lathrop M,
Lechner-Scott JS,
Leone MA,
Leppä V,
Liljedahl U,
Bomfim IL,
Lincoln RR,
Link J,
Liu J,
Lorentzen AR,
Lupoli S,
Macciardi F,
Mack T,
Marriott M,
Martinelli V,
Mason D,
McCauley JL,
Mentch F,
Mero IL,
Mihalova T,
Montalban X,
Mottershead J,
Myhr KM,
Naldi P,
Ollier W,
Page A,
Palotie A,
Pelletier J,
Piccio L,
Pickersgill T,
Piehl F,
Pobywajlo S,
Quach HL,
Ramsay PP,
Reunanen M,
Reynolds R,
Rioux JD,
Rodegher M,
Roesner S,
Rubio JP,
Rückert IM,
Salvetti M,
Salvi E,
Santaniello A,
Schaefer CA,
Schreiber S,
Schulze C,
Scott RJ,
Sellebjerg F,
Selmaj KW,
Sexton D,
Shen L,
Simms-Acuna B,
Skidmore S,
Sleiman PM,
Smestad C,
Sørensen PS,
Søndergaard HB,
Stankovich J,
Strange RC,
Sulonen AM,
Sundqvist E,
Syvänen AC,
Taddeo F,
Taylor B,
Blackwell JM,
Tienari P,
Bramon E,
Tourbah A,
Brown MA,
Tronczynska E,
Casas JP,
Tubridy N,
Corvin A,
Vickery J,
Jankowski J,
Villoslada P,
Markus HS,
Wang K,
Mathew CG,
Wason J,
Palmer CN,
Wichmann HE,
Plomin R,
Willoughby E,
Rautanen A,
Winkelmann J,
Wittig M,
Trembath RC,
Yaouanq J,
Viswanathan AC,
Zhang H,
Wood NW,
Zuvich R,
Deloukas P,
Langford C,
Duncanson A,
Oksenberg JR,
Pericak-Vance MA,
Haines JL,
Olsson T,
Hillert J,
Ivinson AJ,
De Jager PL,
Peltonen L,
Stewart GJ,
Hafler DA,
Hauser SL,
McVean G,
Donnelly P,
Compston A
International Multiple Sclerosis Genetics Consortium · Wellcome Trust Case Control Consortium 2
Nature · 2011 · PMID 21833088 · open access
페이지 11개
Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth
Beaumont RN,
Flatley C,
Vaudel M,
Wu X,
Chen J,
Moen GH,
Skotte L,
Helgeland Ø,
Solé-Navais P,
Banasik K,
Albiñana C,
Ronkainen J
외 76명 — 모두 보기
Fadista J,
Stinson SE,
Trajanoska K,
Wang CA,
Westergaard D,
Srinivasan S,
Sánchez-Soriano C,
Bilbao JR,
Allard C,
Groleau M,
Kuulasmaa T,
Leirer DJ,
White F,
Jacques PÉ,
Cheng H,
Hao K,
Andreassen OA,
Åsvold BO,
Atalay M,
Bhatta L,
Bouchard L,
Brumpton BM,
Brunak S,
Bybjerg-Grauholm J,
Ebbing C,
Elliott P,
Engelbrechtsen L,
Erikstrup C,
Estarlich M,
Franks S,
Gaillard R,
Geller F,
Grove J,
Hougaard DM,
Kajantie E,
Morgen CS,
Nohr EA,
Nyegaard M,
Palmer CNA,
Pedersen OB,
Rivadeneira F,
Sebert S,
Shields BM,
Stoltenberg C,
Surakka I,
Thørner LW,
Ullum H,
Vaarasmaki M,
Vilhjalmsson BJ,
Willer CJ,
Lakka TA,
Gybel-Brask D,
Bustamante M,
Hansen T,
Pearson ER,
Reynolds RM,
Ostrowski SR,
Pennell CE,
Jaddoe VWV,
Felix JF,
Hattersley AT,
Melbye M,
Lawlor DA,
Hveem K,
Werge T,
Nielsen HS,
Magnus P,
Evans DM,
Jacobsson B,
Järvelin MR,
Zhang G,
Hivert MF,
Johansson S,
Freathy RM,
Feenstra B,
Njølstad PR
Early Growth Genetics (EGG) Consortium
Nature genetics · 2023 · PMID 37798380 · open access
페이지 10개
Seven new loci associated with age-related macular degeneration
Fritsche LG,
Chen W,
Schu M,
Yaspan BL,
Yu Y,
Thorleifsson G,
Zack DJ,
Arakawa S,
Cipriani V,
Ripke S,
Igo RP Jr,
Buitendijk GH
외 144명 — 모두 보기
Sim X,
Weeks DE,
Guymer RH,
Merriam JE,
Francis PJ,
Hannum G,
Agarwal A,
Armbrecht AM,
Audo I,
Aung T,
Barile GR,
Benchaboune M,
Bird AC,
Bishop PN,
Branham KE,
Brooks M,
Brucker AJ,
Cade WH,
Cain MS,
Campochiaro PA,
Chan CC,
Cheng CY,
Chew EY,
Chin KA,
Chowers I,
Clayton DG,
Cojocaru R,
Conley YP,
Cornes BK,
Daly MJ,
Dhillon B,
Edwards AO,
Evangelou E,
Fagerness J,
Ferreyra HA,
Friedman JS,
Geirsdottir A,
George RJ,
Gieger C,
Gupta N,
Hagstrom SA,
Harding SP,
Haritoglou C,
Heckenlively JR,
Holz FG,
Hughes G,
Ioannidis JP,
Ishibashi T,
Joseph P,
Jun G,
Kamatani Y,
Katsanis N,
N Keilhauer C,
Khan JC,
Kim IK,
Kiyohara Y,
Klein BE,
Klein R,
Kovach JL,
Kozak I,
Lee CJ,
Lee KE,
Lichtner P,
Lotery AJ,
Meitinger T,
Mitchell P,
Mohand-Saïd S,
Moore AT,
Morgan DJ,
Morrison MA,
Myers CE,
Naj AC,
Nakamura Y,
Okada Y,
Orlin A,
Ortube MC,
Othman MI,
Pappas C,
Park KH,
Pauer GJ,
Peachey NS,
Poch O,
Priya RR,
Reynolds R,
Richardson AJ,
Ripp R,
Rudolph G,
Ryu E,
Sahel JA,
Schaumberg DA,
Scholl HP,
Schwartz SG,
Scott WK,
Shahid H,
Sigurdsson H,
Silvestri G,
Sivakumaran TA,
Smith RT,
Sobrin L,
Souied EH,
Stambolian DE,
Stefansson H,
Sturgill-Short GM,
Takahashi A,
Tosakulwong N,
Truitt BJ,
Tsironi EE,
Uitterlinden AG,
van Duijn CM,
Vijaya L,
Vingerling JR,
Vithana EN,
Webster AR,
Wichmann HE,
Winkler TW,
Wong TY,
Wright AF,
Zelenika D,
Zhang M,
Zhao L,
Zhang K,
Klein ML,
Hageman GS,
Lathrop GM,
Stefansson K,
Allikmets R,
Baird PN,
Gorin MB,
Wang JJ,
Klaver CC,
Seddon JM,
Pericak-Vance MA,
Iyengar SK,
Yates JR,
Swaroop A,
Weber BH,
Kubo M,
Deangelis MM,
Léveillard T,
Thorsteinsdottir U,
Haines JL,
Farrer LA,
Heid IM,
Abecasis GR
AMD Gene Consortium
Nature genetics · 2013 · PMID 23455636 · open access
페이지 7개
Genetic influences on susceptibility to rheumatoid arthritis in African-Americans
Laufer VA,
Tiwari HK,
Reynolds RJ,
Danila MI,
Wang J,
Edberg JC,
Kimberly RP,
Kottyan LC,
Harley JB,
Mikuls TR,
Gregersen PK,
Absher DM
외 3명 — 모두 보기
Human molecular genetics · 2019 · PMID 30423114
페이지 4개
Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration
Chen W,
Stambolian D,
Edwards AO,
Branham KE,
Othman M,
Jakobsdottir J,
Tosakulwong N,
Pericak-Vance MA,
Campochiaro PA,
Klein ML,
Tan PL,
Conley YP
외 54명 — 모두 보기
Kanda A,
Kopplin L,
Li Y,
Augustaitis KJ,
Karoukis AJ,
Scott WK,
Agarwal A,
Kovach JL,
Schwartz SG,
Postel EA,
Brooks M,
Baratz KH,
Brown WL,
Brucker AJ,
Orlin A,
Brown G,
Ho A,
Regillo C,
Donoso L,
Tian L,
Kaderli B,
Hadley D,
Hagstrom SA,
Peachey NS,
Klein R,
Klein BE,
Gotoh N,
Yamashiro K,
Ferris Iii F,
Fagerness JA,
Reynolds R,
Farrer LA,
Kim IK,
Miller JW,
Cortón M,
Carracedo A,
Sanchez-Salorio M,
Pugh EW,
Doheny KF,
Brion M,
Deangelis MM,
Weeks DE,
Zack DJ,
Chew EY,
Heckenlively JR,
Yoshimura N,
Iyengar SK,
Francis PJ,
Katsanis N,
Seddon JM,
Haines JL,
Gorin MB,
Abecasis GR,
Swaroop A
Complications of Age-Related Macular Degeneration Prevention Trial Research Group
Proceedings of the National Academy of Sciences of the United States of America · 2010 · PMID 20385819
페이지 3개
Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC)
Neale BM,
Fagerness J,
Reynolds R,
Sobrin L,
Parker M,
Raychaudhuri S,
Tan PL,
Oh EC,
Merriam JE,
Souied E,
Bernstein PS,
Li B
외 14명 — 모두 보기
Frederick JM,
Zhang K,
Brantley MA Jr,
Lee AY,
Zack DJ,
Campochiaro B,
Campochiaro P,
Ripke S,
Smith RT,
Barile GR,
Katsanis N,
Allikmets R,
Daly MJ,
Seddon JM
Proceedings of the National Academy of Sciences of the United States of America · 2010 · PMID 20385826
페이지 2개
Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes
Sobrin L,
Ripke S,
Yu Y,
Fagerness J,
Bhangale TR,
Tan PL,
Souied EH,
Buitendijk GH,
Merriam JE,
Richardson AJ,
Raychaudhuri S,
Reynolds R
외 22명 — 모두 보기
Chin KA,
Lee AY,
Leveziel N,
Zack DJ,
Campochiaro P,
Smith RT,
Barile GR,
Hogg RE,
Chakravarthy U,
Behrens TW,
Uitterlinden AG,
van Duijn CM,
Vingerling JR,
Brantley MA Jr,
Baird PN,
Klaver CC,
Allikmets R,
Katsanis N,
Graham RR,
Ioannidis JP,
Daly MJ,
Seddon JM
Ophthalmology · 2012 · PMID 22705344
페이지 2개
Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects
Krohn L,
Heilbron K,
Blauwendraat C,
Reynolds RH,
Yu E,
Senkevich K,
Rudakou U,
Estiar MA,
Gustavsson EK,
Brolin K,
Ruskey JA,
Freeman K
외 46명 — 모두 보기
Asayesh F,
Chia R,
Arnulf I,
Hu MTM,
Montplaisir JY,
Gagnon JF,
Desautels A,
Dauvilliers Y,
Gigli GL,
Valente M,
Janes F,
Bernardini A,
Högl B,
Stefani A,
Ibrahim A,
Šonka K,
Kemlink D,
Oertel W,
Janzen A,
Plazzi G,
Biscarini F,
Antelmi E,
Figorilli M,
Puligheddu M,
Mollenhauer B,
Trenkwalder C,
Sixel-Döring F,
Cochen De Cock V,
Monaca CC,
Heidbreder A,
Ferini-Strambi L,
Dijkstra F,
Viaene M,
Abril B,
Boeve BF,
Scholz SW,
Ryten M,
Bandres-Ciga S,
Noyce A,
Cannon P,
Pihlstrøm L,
Nalls MA,
Singleton AB,
Rouleau GA,
Postuma RB,
Gan-Or Z
23andMe Research Team
Nature communications · 2022 · PMID 36470867 · open access
페이지 2개
Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study
Jabbari E,
Koga S,
Valentino RR,
Reynolds RH,
Ferrari R,
Tan MMX,
Rowe JB,
Dalgard CL,
Scholz SW,
Dickson DW,
Warner TT,
Revesz T
외 6명 — 모두 보기
PSP Genetics Group
The Lancet. Neurology · 2021 · PMID 33341150
페이지 1개
Association of Gout Polygenic Risk Score With Age at Disease Onset and Tophaceous Disease in European and Polynesian Men With Gout
Sumpter NA,
Takei R,
Cadzow M,
Topless RKG,
Phipps-Green AJ,
Murphy R,
de Zoysa J,
Watson H,
Qasim M,
Lupi AS,
Abhishek A,
Andrés M
외 27명 — 모두 보기
Crișan TO,
Doherty M,
Jacobsson L,
Janssen M,
Jansen TL,
Joosten LAB,
Kapetanovic M,
Lioté F,
Matsuo H,
McCarthy GM,
Perez-Ruiz F,
Riches P,
Richette P,
Roddy E,
Stiburkova B,
So A,
Tausche AK,
Torres RJ,
Uhlig T,
Major TJ,
Stamp LK,
Dalbeth N,
Choi HK,
Vazquez AI,
Leask MP,
Reynolds RJ,
Merriman TR
Arthritis & rheumatology (Hoboken, N.J.) · 2023 · PMID 36281732
페이지 1개
이 목록에 대한 질문
제 논문이 왜 여기 있습니까? 허락한 적이 없습니다.
논문의 내용은 여기에 전혀 옮겨져 있지 않습니다. 이 페이지가 기록하는 것은 MyGeneLog™의
어떤 페이지가 귀하의 연구를 인용하고 있다는 사실과 PubMed의 원문 링크뿐이며, 그것이 곧
인용입니다. 제목과 저자 목록은 도서관 목록이 쓰는 것과 같은 공개 기록인 Europe PMC에서
가져옵니다.
왜 "외 몇 명"이 아니라 저자를 다 적습니까?
622명이 필요했던 연구는 4명이 한 연구와 다른 종류의 연구인데, "et al."은 그것을 지우기
때문입니다. 12명을 먼저 보여 주고 나머지는 한 번 눌러 펼칩니다. 검색은 전원을 대상으로
합니다. 컨소시엄 논문의 187번째 이름도 실재하는 사람이고, 그 사람이 자기 이름을 찾고 있을
수 있습니다.
제 이름이 틀렸거나 논문 정보가 잘못되었습니다.
알려 주시면 고칩니다. 이름은 공개 기록에서 가져오는데 데이터베이스마다 이니셜 표기가
다르고, 같은 형태의 이름을 쓰는 두 사람을 저희가 구분할 수 없는 경우도 있습니다. 추측하기
보다 지적을 받는 편이 낫습니다.
제 논문이 없습니다. 탈락시킨 것입니까?
아닙니다. 이 카탈로그는 작은 팀이 읽을 수 있었던 것으로 모은 것이고, 유럽계 조상 코호트
바깥이 가장 얇습니다. 논문이 없는 것은 아직 아무도 거기까지 가지 못했기 때문이지 검토해서
제외한 것이 아닙니다.
어떤 페이지가 그 논문 위에 서 있는지 볼 수 있습니까?
각 줄에 최대 여섯 개까지 표시되며 각각 링크되어 있습니다. 줄 옆의 숫자는 그 논문을
인용하는 페이지가 모두 몇 개인지입니다.
얼마나 자주 갱신됩니까?
페이지들에서 매시간 다시 만들어집니다. 어떤 페이지가 그 논문 위에 서기 시작하면 그
순간 나타나고 그만두면 사라집니다. 따로 관리하는 목록이 없기 때문인데, 인용은 그 주장을
하는 페이지에 붙어 있어야 하기 때문입니다.