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.
Li D에 대해
47건, 그중 20건 표시.
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
Michailidou K,
Beesley J,
Lindstrom S,
Canisius S,
Dennis J,
Lush MJ,
Maranian MJ,
Bolla MK,
Wang Q,
Shah M,
Perkins BJ,
Czene K
외 232명 — 모두 보기
Eriksson M,
Darabi H,
Brand JS,
Bojesen SE,
Nordestgaard BG,
Flyger H,
Nielsen SF,
Rahman N,
Turnbull C,
Fletcher O,
Peto J,
Gibson L,
dos-Santos-Silva I,
Chang-Claude J,
Flesch-Janys D,
Rudolph A,
Eilber U,
Behrens S,
Nevanlinna H,
Muranen TA,
Aittomäki K,
Blomqvist C,
Khan S,
Aaltonen K,
Ahsan H,
Kibriya MG,
Whittemore AS,
John EM,
Malone KE,
Gammon MD,
Santella RM,
Ursin G,
Makalic E,
Schmidt DF,
Casey G,
Hunter DJ,
Gapstur SM,
Gaudet MM,
Diver WR,
Haiman CA,
Schumacher F,
Henderson BE,
Le Marchand L,
Berg CD,
Chanock SJ,
Figueroa J,
Hoover RN,
Lambrechts D,
Neven P,
Wildiers H,
van Limbergen E,
Schmidt MK,
Broeks A,
Verhoef S,
Cornelissen S,
Couch FJ,
Olson JE,
Hallberg E,
Vachon C,
Waisfisz Q,
Meijers-Heijboer H,
Adank MA,
van der Luijt RB,
Li J,
Liu J,
Humphreys K,
Kang D,
Choi JY,
Park SK,
Yoo KY,
Matsuo K,
Ito H,
Iwata H,
Tajima K,
Guénel P,
Truong T,
Mulot C,
Sanchez M,
Burwinkel B,
Marme F,
Surowy H,
Sohn C,
Wu AH,
Tseng CC,
Van Den Berg D,
Stram DO,
González-Neira A,
Benitez J,
Zamora MP,
Perez JI,
Shu XO,
Lu W,
Gao YT,
Cai H,
Cox A,
Cross SS,
Reed MW,
Andrulis IL,
Knight JA,
Glendon G,
Mulligan AM,
Sawyer EJ,
Tomlinson I,
Kerin MJ,
Miller N,
Lindblom A,
Margolin S,
Teo SH,
Yip CH,
Taib NA,
Tan GH,
Hooning MJ,
Hollestelle A,
Martens JW,
Collée JM,
Blot W,
Signorello LB,
Cai Q,
Hopper JL,
Southey MC,
Tsimiklis H,
Apicella C,
Shen CY,
Hsiung CN,
Wu PE,
Hou MF,
Kristensen VN,
Nord S,
Alnaes GI,
Giles GG,
Milne RL,
McLean C,
Canzian F,
Trichopoulos D,
Peeters P,
Lund E,
Sund M,
Khaw KT,
Gunter MJ,
Palli D,
Mortensen LM,
Dossus L,
Huerta JM,
Meindl A,
Schmutzler RK,
Sutter C,
Yang R,
Muir K,
Lophatananon A,
Stewart-Brown S,
Siriwanarangsan P,
Hartman M,
Miao H,
Chia KS,
Chan CW,
Fasching PA,
Hein A,
Beckmann MW,
Haeberle L,
Brenner H,
Dieffenbach AK,
Arndt V,
Stegmaier C,
Ashworth A,
Orr N,
Schoemaker MJ,
Swerdlow AJ,
Brinton L,
Garcia-Closas M,
Zheng W,
Zheng W,
Halverson SL,
Shrubsole M,
Long J,
Goldberg MS,
Labrèche F,
Dumont M,
Winqvist R,
Pylkäs K,
Jukkola-Vuorinen A,
Grip M,
Brauch H,
Hamann U,
Brüning T,
Radice P,
Peterlongo P,
Manoukian S,
Bernard L,
Bogdanova NV,
Dörk T,
Mannermaa A,
Kataja V,
Kosma VM,
Hartikainen JM,
Devilee P,
Tollenaar RA,
Seynaeve C,
Van Asperen CJ,
Jakubowska A,
Lubinski J,
Jaworska K,
Huzarski T,
Sangrajrang S,
Gaborieau V,
Brennan P,
McKay J,
Slager S,
Toland AE,
Ambrosone CB,
Yannoukakos D,
Kabisch M,
Torres D,
Neuhausen SL,
Anton-Culver H,
Luccarini C,
Baynes C,
Ahmed S,
Healey CS,
Tessier DC,
Vincent D,
Bacot F,
Pita G,
Alonso MR,
Álvarez N,
Herrero D,
Simard J,
Pharoah PP,
Kraft P,
Dunning AM,
Chenevix-Trench G,
Hall P,
Easton DF
BOCS · kConFab Investigators 외 컨소시엄 3곳
Nature genetics · 2015 · PMID 25751625 · open access
페이지 12개+
Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases
Li YR,
Li J,
Zhao SD,
Bradfield JP,
Mentch FD,
Maggadottir SM,
Hou C,
Abrams DJ,
Chang D,
Gao F,
Guo Y,
Wei Z
외 54명 — 모두 보기
Connolly JJ,
Cardinale CJ,
Bakay M,
Glessner JT,
Li D,
Kao C,
Thomas KA,
Qiu H,
Chiavacci RM,
Kim CE,
Wang F,
Snyder J,
Richie MD,
Flatø B,
Førre Ø,
Denson LA,
Thompson SD,
Becker ML,
Guthery SL,
Latiano A,
Perez E,
Resnick E,
Russell RK,
Wilson DC,
Silverberg MS,
Annese V,
Lie BA,
Punaro M,
Dubinsky MC,
Monos DS,
Strisciuglio C,
Staiano A,
Miele E,
Kugathasan S,
Ellis JA,
Munro JE,
Sullivan KE,
Wise CA,
Chapel H,
Cunningham-Rundles C,
Grant SF,
Orange JS,
Sleiman PM,
Behrens EM,
Griffiths AM,
Satsangi J,
Finkel TH,
Keinan A,
Prak ET,
Polychronakos C,
Baldassano RN,
Li H,
Keating BJ,
Hakonarson H
Nature medicine · 2015 · PMID 26301688
페이지 12개+
Novel loci and biomedical consequences of iron homoeostasis variation
Allara E,
Bell S,
Smith R,
Keene SJ,
Gill D,
Gaziano L,
Morselli Gysi D,
Wang F,
Tragante V,
Mason A,
Karthikeyan S,
Lumbers RT
외 60명 — 모두 보기
Bonglack E,
Ouwehand W,
Roberts DJ,
Dowsett J,
Ostrowski SR,
Larsen MH,
Ullum H,
Pedersen OB,
Brunak S,
Banasik K,
Erikstrup C,
Mitchell J,
Fuchsberger C,
Pattaro C,
Pramstaller PP,
Girelli D,
Arvas M,
Toivonen J,
Molnos S,
Peters A,
Polasek O,
Rudan I,
Hayward C,
McDonnell C,
Pirastu N,
Wilson JF,
van den Hurk K,
Quee F,
Ferrucci L,
Bandinelli S,
Tanaka T,
Girotto G,
Concas MP,
Pecori A,
Verweij N,
van der Harst P,
van de Vegte YJ,
Kiemeney LA,
Sweep FC,
Galesloot TE,
Sulem P,
Gudbjartsson D,
Ferkingstad E,
Djousse L,
Cho K,
Inouye M,
Burgess S,
Benyamin B,
Oexle K,
Swinkels D,
Stefansson K,
Magnusson M,
Ganna A,
Gaziano M,
Ivey K,
Danesh J,
Pereira A,
Wood AM,
Butterworth AS,
Di Angelantonio E
DBDS Genomic Consortium · FinnGen Consortium
Communications biology · 2024 · PMID 39643614 · open access
페이지 12개+
Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases
Roselli C,
Surakka I,
Olesen MS,
Sveinbjornsson G,
Marston NA,
Choi SH,
Holm H,
Chaffin M,
Gudbjartsson D,
Hill MC,
Aegisdottir H,
Albert CM
외 145명 — 모두 보기
Alonso A,
Anderson CD,
Arking DE,
Arnar DO,
Barnard J,
Benjamin EJ,
Braunwald E,
Brumpton B,
Campbell A,
Chami N,
Chasman DI,
Cho K,
Choi EK,
Christophersen IE,
Chung MK,
Conen D,
Crijns HJ,
Cutler MJ,
Czuba T,
Damrauer SM,
Dichgans M,
Dörr M,
Dudink E,
Duong T,
Erikstrup C,
Esko T,
Fatkin D,
Faul JD,
Ferreira M,
Freitag DF,
Ganesh SK,
Gaziano JM,
Geelhoed B,
Ghouse J,
Gieger C,
Giulianini F,
Graham SE,
Gudnason V,
Guo X,
Haggerty C,
Hayward C,
Heckbert SR,
Hveem K,
Ito K,
Johnson R,
Jukema JW,
Jurgens SJ,
Kääb S,
Kane JP,
Kany S,
Kardia SLR,
Kavousi M,
Khurshid S,
Kamanu FK,
Kirchhof P,
Kleber ME,
Knight S,
Komuro I,
Krieger JE,
Launer LJ,
Li D,
Lin H,
Lin HJ,
Loos RJF,
Lotta L,
Lubitz SA,
Lunetta KL,
Macfarlane PW,
Magnusson PKE,
Malik R,
Mantineo H,
Marcus GM,
März W,
McManus DD,
Melander O,
Melloni GEM,
Meyre PB,
Miyazawa K,
Mohanty S,
Monfort LM,
Müller-Nurasyid M,
Nafissi NA,
Natale A,
Nazarian S,
Ostrowski SR,
Pak HN,
Pang S,
Pedersen OB,
Pedersen NL,
Pereira AC,
Pirruccello JP,
Preuss M,
Psaty BM,
Pullinger CR,
Rader DJ,
Rämö JT,
Ridker PM,
Rienstra M,
Risch L,
Roden DM,
Rotter JI,
Sabatine MS,
Schunkert H,
Shah SH,
Shim J,
Shoemaker MB,
Simonson B,
Sinner MF,
Smit RAJ,
Smith JA,
Smith NL,
Smith JG,
Soliman EZ,
Sørensen E,
Sotoodehnia N,
Strbian D,
Stricker BH,
Teder-Laving M,
Sun YV,
Thériault S,
Thorolfsdottir RB,
Thorsteinsdottir U,
Tveit A,
van der Harst P,
van Meurs J,
Wang B,
Weiss S,
Wells QS,
Weng LC,
Wilson PW,
Xiao L,
Yang PS,
Yao J,
Yoneda ZT,
Zeller T,
Zeng L,
Zhao W,
Zhao W,
Zhou X,
Zöllner S,
Ruff CT,
Bundgaard H,
Willer C,
Stefansson K,
Ellinor PT
BioBank Japan Project · Regeneron Genetics Center 외 컨소시엄 1곳
Nature genetics · 2025 · PMID 40050429
페이지 12개+
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
Phelan CM,
Kuchenbaecker KB,
Tyrer JP,
Kar SP,
Lawrenson K,
Winham SJ,
Dennis J,
Pirie A,
Riggan MJ,
Chornokur G,
Earp MA,
Lyra PC Jr
외 402명 — 모두 보기
Lee JM,
Coetzee S,
Beesley J,
McGuffog L,
Soucy P,
Dicks E,
Lee A,
Barrowdale D,
Lecarpentier J,
Leslie G,
Aalfs CM,
Aben KKH,
Adams M,
Adlard J,
Andrulis IL,
Anton-Culver H,
Antonenkova N,
Aravantinos G,
Arnold N,
Arun BK,
Arver B,
Azzollini J,
Balmaña J,
Banerjee SN,
Barjhoux L,
Barkardottir RB,
Bean Y,
Beckmann MW,
Beeghly-Fadiel A,
Benitez J,
Bermisheva M,
Bernardini MQ,
Birrer MJ,
Bjorge L,
Black A,
Blankstein K,
Blok MJ,
Bodelon C,
Bogdanova N,
Bojesen A,
Bonanni B,
Borg Å,
Bradbury AR,
Brenton JD,
Brewer C,
Brinton L,
Broberg P,
Brooks-Wilson A,
Bruinsma F,
Brunet J,
Buecher B,
Butzow R,
Buys SS,
Caldes T,
Caligo MA,
Campbell I,
Cannioto R,
Carney ME,
Cescon T,
Chan SB,
Chang-Claude J,
Chanock S,
Chen XQ,
Chiew YE,
Chiquette J,
Chung WK,
Claes KBM,
Conner T,
Cook LS,
Cook J,
Cramer DW,
Cunningham JM,
D'Aloisio AA,
Daly MB,
Damiola F,
Damirovna SD,
Dansonka-Mieszkowska A,
Dao F,
Davidson R,
DeFazio A,
Delnatte C,
Doheny KF,
Diez O,
Ding YC,
Doherty JA,
Domchek SM,
Dorfling CM,
Dörk T,
Dossus L,
Duran M,
Dürst M,
Dworniczak B,
Eccles D,
Edwards T,
Eeles R,
Eilber U,
Ejlertsen B,
Ekici AB,
Ellis S,
Elvira M,
Eng KH,
Engel C,
Evans DG,
Fasching PA,
Ferguson S,
Ferrer SF,
Flanagan JM,
Fogarty ZC,
Fortner RT,
Fostira F,
Foulkes WD,
Fountzilas G,
Fridley BL,
Friebel TM,
Friedman E,
Frost D,
Ganz PA,
Garber J,
García MJ,
Garcia-Barberan V,
Gehrig A,
Gentry-Maharaj A,
Gerdes AM,
Giles GG,
Glasspool R,
Glendon G,
Godwin AK,
Goldgar DE,
Goranova T,
Gore M,
Greene MH,
Gronwald J,
Gruber S,
Hahnen E,
Haiman CA,
Håkansson N,
Hamann U,
Hansen TVO,
Harrington PA,
Harris HR,
Hauke J,
Hein A,
Henderson A,
Hildebrandt MAT,
Hillemanns P,
Hodgson S,
Høgdall CK,
Høgdall E,
Hogervorst FBL,
Holland H,
Hooning MJ,
Hosking K,
Huang RY,
Hulick PJ,
Hung J,
Hunter DJ,
Huntsman DG,
Huzarski T,
Imyanitov EN,
Isaacs C,
Iversen ES,
Izatt L,
Izquierdo A,
Jakubowska A,
James P,
Janavicius R,
Jernetz M,
Jensen A,
Jensen UB,
John EM,
Johnatty S,
Jones ME,
Kannisto P,
Karlan BY,
Karnezis A,
Kast K,
Kennedy CJ,
Khusnutdinova E,
Kiemeney LA,
Kiiski JI,
Kim SW,
Kjaer SK,
Köbel M,
Kopperud RK,
Kruse TA,
Kupryjanczyk J,
Kwong A,
Laitman Y,
Lambrechts D,
Larrañaga N,
Larson MC,
Lazaro C,
Le ND,
Le Marchand L,
Lee JW,
Lele SB,
Leminen A,
Leroux D,
Lester J,
Lesueur F,
Levine DA,
Liang D,
Liebrich C,
Lilyquist J,
Lipworth L,
Lissowska J,
Lu KH,
Lubinński J,
Luccarini C,
Lundvall L,
Mai PL,
Mendoza-Fandiño G,
Manoukian S,
Massuger LFAG,
May T,
Mazoyer S,
McAlpine JN,
McGuire V,
McLaughlin JR,
McNeish I,
Meijers-Heijboer H,
Meindl A,
Menon U,
Mensenkamp AR,
Merritt MA,
Milne RL,
Mitchell G,
Modugno F,
Moes-Sosnowska J,
Moffitt M,
Montagna M,
Moysich KB,
Mulligan AM,
Musinsky J,
Nathanson KL,
Nedergaard L,
Ness RB,
Neuhausen SL,
Nevanlinna H,
Niederacher D,
Nussbaum RL,
Odunsi K,
Olah E,
Olopade OI,
Olsson H,
Olswold C,
O'Malley DM,
Ong KR,
Onland-Moret NC,
Orr N,
Orsulic S,
Osorio A,
Palli D,
Papi L,
Park-Simon TW,
Paul J,
Pearce CL,
Pedersen IS,
Peeters PHM,
Peissel B,
Peixoto A,
Pejovic T,
Pelttari LM,
Permuth JB,
Peterlongo P,
Pezzani L,
Pfeiler G,
Phillips KA,
Piedmonte M,
Pike MC,
Piskorz AM,
Poblete SR,
Pocza T,
Poole EM,
Poppe B,
Porteous ME,
Prieur F,
Prokofyeva D,
Pugh E,
Pujana MA,
Pujol P,
Radice P,
Rantala J,
Rappaport-Fuerhauser C,
Rennert G,
Rhiem K,
Rice P,
Richardson A,
Robson M,
Rodriguez GC,
Rodríguez-Antona C,
Romm J,
Rookus MA,
Rossing MA,
Rothstein JH,
Rudolph A,
Runnebaum IB,
Salvesen HB,
Sandler DP,
Schoemaker MJ,
Senter L,
Setiawan VW,
Severi G,
Sharma P,
Shelford T,
Siddiqui N,
Side LE,
Sieh W,
Singer CF,
Sobol H,
Song H,
Southey MC,
Spurdle AB,
Stadler Z,
Steinemann D,
Stoppa-Lyonnet D,
Sucheston-Campbell LE,
Sukiennicki G,
Sutphen R,
Sutter C,
Swerdlow AJ,
Szabo CI,
Szafron L,
Tan YY,
Taylor JA,
Tea MK,
Teixeira MR,
Teo SH,
Terry KL,
Thompson PJ,
Thomsen LCV,
Thull DL,
Tihomirova L,
Tinker AV,
Tischkowitz M,
Tognazzo S,
Toland AE,
Tone A,
Trabert B,
Travis RC,
Trichopoulou A,
Tung N,
Tworoger SS,
van Altena AM,
Van Den Berg D,
van der Hout AH,
van der Luijt RB,
Van Heetvelde M,
Van Nieuwenhuysen E,
van Rensburg EJ,
Vanderstichele A,
Varon-Mateeva R,
Vega A,
Edwards DV,
Vergote I,
Vierkant RA,
Vijai J,
Vratimos A,
Walker L,
Walsh C,
Wand D,
Wang-Gohrke S,
Wappenschmidt B,
Webb PM,
Weinberg CR,
Weitzel JN,
Wentzensen N,
Whittemore AS,
Wijnen JT,
Wilkens LR,
Wolk A,
Woo M,
Wu X,
Wu AH,
Yang H,
Yannoukakos D,
Ziogas A,
Zorn KK,
Narod SA,
Easton DF,
Amos CI,
Schildkraut JM,
Ramus SJ,
Ottini L,
Goodman MT,
Park SK,
Kelemen LE,
Risch HA,
Thomassen M,
Offit K,
Simard J,
Schmutzler RK,
Hazelett D,
Monteiro AN,
Couch FJ,
Berchuck A,
Chenevix-Trench G,
Goode EL,
Sellers TA,
Gayther SA,
Antoniou AC,
Pharoah PDP
AOCS study group · EMBRACE Study 외 컨소시엄 4곳
Nature genetics · 2017 · PMID 28346442
페이지 9개
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Schunkert H,
König IR,
Kathiresan S,
Reilly MP,
Assimes TL,
Holm H,
Preuss M,
Stewart AF,
Barbalic M,
Gieger C,
Absher D,
Aherrahrou Z
외 155명 — 모두 보기
Allayee H,
Altshuler D,
Anand SS,
Andersen K,
Anderson JL,
Ardissino D,
Ball SG,
Balmforth AJ,
Barnes TA,
Becker DM,
Becker LC,
Berger K,
Bis JC,
Boekholdt SM,
Boerwinkle E,
Braund PS,
Brown MJ,
Burnett MS,
Buysschaert I,
Carlquist JF,
Chen L,
Cichon S,
Codd V,
Davies RW,
Dedoussis G,
Dehghan A,
Demissie S,
Devaney JM,
Diemert P,
Do R,
Doering A,
Eifert S,
Mokhtari NE,
Ellis SG,
Elosua R,
Engert JC,
Epstein SE,
de Faire U,
Fischer M,
Folsom AR,
Freyer J,
Gigante B,
Girelli D,
Gretarsdottir S,
Gudnason V,
Gulcher JR,
Halperin E,
Hammond N,
Hazen SL,
Hofman A,
Horne BD,
Illig T,
Iribarren C,
Jones GT,
Jukema JW,
Kaiser MA,
Kaplan LM,
Kastelein JJ,
Khaw KT,
Knowles JW,
Kolovou G,
Kong A,
Laaksonen R,
Lambrechts D,
Leander K,
Lettre G,
Li M,
Lieb W,
Loley C,
Lotery AJ,
Mannucci PM,
Maouche S,
Martinelli N,
McKeown PP,
Meisinger C,
Meitinger T,
Melander O,
Merlini PA,
Mooser V,
Morgan T,
Mühleisen TW,
Muhlestein JB,
Münzel T,
Musunuru K,
Nahrstaedt J,
Nelson CP,
Nöthen MM,
Olivieri O,
Patel RS,
Patterson CC,
Peters A,
Peyvandi F,
Qu L,
Quyyumi AA,
Rader DJ,
Rallidis LS,
Rice C,
Rosendaal FR,
Rubin D,
Salomaa V,
Sampietro ML,
Sandhu MS,
Schadt E,
Schäfer A,
Schillert A,
Schreiber S,
Schrezenmeir J,
Schwartz SM,
Siscovick DS,
Sivananthan M,
Sivapalaratnam S,
Smith A,
Smith TB,
Snoep JD,
Soranzo N,
Spertus JA,
Stark K,
Stirrups K,
Stoll M,
Tang WH,
Tennstedt S,
Thorgeirsson G,
Thorleifsson G,
Tomaszewski M,
Uitterlinden AG,
van Rij AM,
Voight BF,
Wareham NJ,
Wells GA,
Wichmann HE,
Wild PS,
Willenborg C,
Witteman JC,
Wright BJ,
Ye S,
Zeller T,
Ziegler A,
Cambien F,
Goodall AH,
Cupples LA,
Quertermous T,
März W,
Hengstenberg C,
Blankenberg S,
Ouwehand WH,
Hall AS,
Deloukas P,
Thompson JR,
Stefansson K,
Roberts R,
Thorsteinsdottir U,
O'Donnell CJ,
McPherson R,
Erdmann J,
Samani NJ
Cardiogenics · CARDIoGRAM Consortium
Nature genetics · 2011 · PMID 21378990
페이지 7개
Novel Susceptibility Loci for Moyamoya Disease Revealed by a Genome-Wide Association Study
Duan L,
Wei L,
Tian Y,
Zhang Z,
Hu P,
Wei Q,
Liu S,
Zhang J,
Wang Y,
Li D,
Yang W,
Zong R
외 25명 — 모두 보기
Xian P,
Han C,
Bao X,
Zhao F,
Feng J,
Liu W,
Cao W,
Zhou G,
Zhu C,
Yu F,
Yang W,
Meng Y,
Wang J,
Chen X,
Wang Y,
Shen B,
Zhao B,
Wan J,
Zhang F,
Zhao G,
Xu A,
Zhang X,
Liu J,
Zuo X,
Wang K
Stroke · 2018 · PMID 29273593
페이지 6개
Identification of nine new susceptibility loci for endometrial cancer
O'Mara TA,
Glubb DM,
Amant F,
Annibali D,
Ashton K,
Attia J,
Auer PL,
Beckmann MW,
Black A,
Bolla MK,
Brauch H,
Brenner H
외 114명 — 모두 보기
Brinton L,
Buchanan DD,
Burwinkel B,
Chang-Claude J,
Chanock SJ,
Chen C,
Chen MM,
Cheng THT,
Clarke CL,
Clendenning M,
Cook LS,
Couch FJ,
Cox A,
Crous-Bous M,
Czene K,
Day F,
Dennis J,
Depreeuw J,
Doherty JA,
Dörk T,
Dowdy SC,
Dürst M,
Ekici AB,
Fasching PA,
Fridley BL,
Friedenreich CM,
Fritschi L,
Fung J,
García-Closas M,
Gaudet MM,
Giles GG,
Goode EL,
Gorman M,
Haiman CA,
Hall P,
Hankison SE,
Healey CS,
Hein A,
Hillemanns P,
Hodgson S,
Hoivik EA,
Holliday EG,
Hopper JL,
Hunter DJ,
Jones A,
Krakstad C,
Kristensen VN,
Lambrechts D,
Marchand LL,
Liang X,
Lindblom A,
Lissowska J,
Long J,
Lu L,
Magliocco AM,
Martin L,
McEvoy M,
Meindl A,
Michailidou K,
Milne RL,
Mints M,
Montgomery GW,
Nassir R,
Olsson H,
Orlow I,
Otton G,
Palles C,
Perry JRB,
Peto J,
Pooler L,
Prescott J,
Proietto T,
Rebbeck TR,
Risch HA,
Rogers PAW,
Rübner M,
Runnebaum I,
Sacerdote C,
Sarto GE,
Schumacher F,
Scott RJ,
Setiawan VW,
Shah M,
Sheng X,
Shu XO,
Southey MC,
Swerdlow AJ,
Tham E,
Trovik J,
Turman C,
Tyrer JP,
Vachon C,
VanDen Berg D,
Vanderstichele A,
Wang Z,
Webb PM,
Wentzensen N,
Werner HMJ,
Winham SJ,
Wolk A,
Xia L,
Xiang YB,
Yang HP,
Yu H,
Zheng W,
Zheng W,
Pharoah PDP,
Dunning AM,
Kraft P,
De Vivo I,
Tomlinson I,
Easton DF,
Spurdle AB,
Thompson DJ
Nature communications · 2018 · PMID 30093612 · open access
페이지 6개
Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer
Wolpin BM,
Rizzato C,
Kraft P,
Kooperberg C,
Petersen GM,
Wang Z,
Arslan AA,
Beane-Freeman L,
Bracci PM,
Buring J,
Canzian F,
Duell EJ
외 106명 — 모두 보기
Gallinger S,
Giles GG,
Goodman GE,
Goodman PJ,
Jacobs EJ,
Kamineni A,
Klein AP,
Kolonel LN,
Kulke MH,
Li D,
Malats N,
Olson SH,
Risch HA,
Sesso HD,
Visvanathan K,
White E,
Zheng W,
Zheng W,
Abnet CC,
Albanes D,
Andreotti G,
Austin MA,
Barfield R,
Basso D,
Berndt SI,
Boutron-Ruault MC,
Brotzman M,
Büchler MW,
Bueno-de-Mesquita HB,
Bugert P,
Burdette L,
Campa D,
Caporaso NE,
Capurso G,
Chung C,
Cotterchio M,
Costello E,
Elena J,
Funel N,
Gaziano JM,
Giese NA,
Giovannucci EL,
Goggins M,
Gorman MJ,
Gross M,
Haiman CA,
Hassan M,
Helzlsouer KJ,
Henderson BE,
Holly EA,
Hu N,
Hunter DJ,
Innocenti F,
Jenab M,
Kaaks R,
Key TJ,
Khaw KT,
Klein EA,
Kogevinas M,
Krogh V,
Kupcinskas J,
Kurtz RC,
LaCroix A,
Landi MT,
Landi S,
Le Marchand L,
Mambrini A,
Mannisto S,
Milne RL,
Nakamura Y,
Oberg AL,
Owzar K,
Patel AV,
Peeters PH,
Peters U,
Pezzilli R,
Piepoli A,
Porta M,
Real FX,
Riboli E,
Rothman N,
Scarpa A,
Shu XO,
Silverman DT,
Soucek P,
Sund M,
Talar-Wojnarowska R,
Taylor PR,
Theodoropoulos GE,
Thornquist M,
Tjønneland A,
Tobias GS,
Trichopoulos D,
Vodicka P,
Wactawski-Wende J,
Wentzensen N,
Wu C,
Yu H,
Yu K,
Zeleniuch-Jacquotte A,
Hoover R,
Hartge P,
Fuchs C,
Chanock SJ,
Stolzenberg-Solomon RS,
Amundadottir LT
Nature genetics · 2014 · PMID 25086665 · open access
페이지 5개
Novel genetic loci affecting facial shape variation in humans
Xiong Z,
Dankova G,
Howe LJ,
Lee MK,
Hysi PG,
de Jong MA,
Zhu G,
Adhikari K,
Li D,
Li Y,
Pan B,
Feingold E
외 37명 — 모두 보기
Marazita ML,
Shaffer JR,
McAloney K,
Xu SH,
Jin L,
Wang S,
de Vrij FM,
Lendemeijer B,
Richmond S,
Zhurov A,
Lewis S,
Sharp GC,
Paternoster L,
Thompson H,
Gonzalez-Jose R,
Bortolini MC,
Canizales-Quinteros S,
Gallo C,
Poletti G,
Bedoya G,
Rothhammer F,
Uitterlinden AG,
Ikram MA,
Wolvius E,
Kushner SA,
Nijsten TE,
Palstra RT,
Boehringer S,
Medland SE,
Tang K,
Ruiz-Linares A,
Martin NG,
Spector TD,
Stergiakouli E,
Weinberg SM,
Liu F,
Kayser M
International Visible Trait Genetics (VisiGen) Consortium
eLife · 2019 · PMID 31763980 · open access
페이지 5개
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Kathiresan S,
Voight BF,
Purcell S,
Musunuru K,
Ardissino D,
Mannucci PM,
Anand S,
Engert JC,
Samani NJ,
Schunkert H,
Erdmann J,
Reilly MP
외 174명 — 모두 보기
Rader DJ,
Morgan T,
Spertus JA,
Stoll M,
Girelli D,
McKeown PP,
Patterson CC,
Siscovick DS,
O'Donnell CJ,
Elosua R,
Peltonen L,
Salomaa V,
Schwartz SM,
Melander O,
Altshuler D,
Ardissino D,
Merlini PA,
Berzuini C,
Bernardinelli L,
Peyvandi F,
Tubaro M,
Celli P,
Ferrario M,
Fetiveau R,
Marziliano N,
Casari G,
Galli M,
Ribichini F,
Rossi M,
Bernardi F,
Zonzin P,
Piazza A,
Mannucci PM,
Schwartz SM,
Siscovick DS,
Yee J,
Friedlander Y,
Elosua R,
Marrugat J,
Lucas G,
Subirana I,
Sala J,
Ramos R,
Kathiresan S,
Meigs JB,
Williams G,
Nathan DM,
MacRae CA,
O'Donnell CJ,
Salomaa V,
Havulinna AS,
Peltonen L,
Melander O,
Berglund G,
Voight BF,
Kathiresan S,
Hirschhorn JN,
Asselta R,
Duga S,
Spreafico M,
Musunuru K,
Daly MJ,
Purcell S,
Voight BF,
Purcell S,
Nemesh J,
Korn JM,
McCarroll SA,
Schwartz SM,
Yee J,
Kathiresan S,
Lucas G,
Subirana I,
Elosua R,
Surti A,
Guiducci C,
Gianniny L,
Mirel D,
Parkin M,
Burtt N,
Gabriel SB,
Samani NJ,
Thompson JR,
Braund PS,
Wright BJ,
Balmforth AJ,
Ball SG,
Hall A,
Schunkert H,
Erdmann J,
Linsel-Nitschke P,
Lieb W,
Ziegler A,
König I,
Hengstenberg C,
Fischer M,
Stark K,
Grosshennig A,
Preuss M,
Wichmann HE,
Schreiber S,
Schunkert H,
Samani NJ,
Erdmann J,
Ouwehand W,
Hengstenberg C,
Deloukas P,
Scholz M,
Cambien F,
Reilly MP,
Li M,
Chen Z,
Wilensky R,
Matthai W,
Qasim A,
Hakonarson HH,
Devaney J,
Burnett MS,
Pichard AD,
Kent KM,
Satler L,
Lindsay JM,
Waksman R,
Knouff CW,
Waterworth DM,
Walker MC,
Mooser V,
Epstein SE,
Rader DJ,
Scheffold T,
Berger K,
Stoll M,
Huge A,
Girelli D,
Martinelli N,
Olivieri O,
Corrocher R,
Morgan T,
Spertus JA,
McKeown P,
Patterson CC,
Schunkert H,
Erdmann E,
Linsel-Nitschke P,
Lieb W,
Ziegler A,
König IR,
Hengstenberg C,
Fischer M,
Stark K,
Grosshennig A,
Preuss M,
Wichmann HE,
Schreiber S,
Hólm H,
Thorleifsson G,
Thorsteinsdottir U,
Stefansson K,
Engert JC,
Do R,
Xie C,
Anand S,
Kathiresan S,
Ardissino D,
Mannucci PM,
Siscovick D,
O'Donnell CJ,
Samani NJ,
Melander O,
Elosua R,
Peltonen L,
Salomaa V,
Schwartz SM,
Altshuler D
Myocardial Infarction Genetics Consortium · Wellcome Trust Case Control Consortium
Nature genetics · 2009 · PMID 19198609
페이지 4개
Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer
Klein AP,
Wolpin BM,
Risch HA,
Stolzenberg-Solomon RZ,
Mocci E,
Zhang M,
Canzian F,
Childs EJ,
Hoskins JW,
Jermusyk A,
Zhong J,
Chen F
외 112명 — 모두 보기
Albanes D,
Andreotti G,
Arslan AA,
Babic A,
Bamlet WR,
Beane-Freeman L,
Berndt SI,
Blackford A,
Borges M,
Borgida A,
Bracci PM,
Brais L,
Brennan P,
Brenner H,
Bueno-de-Mesquita B,
Buring J,
Campa D,
Capurso G,
Cavestro GM,
Chaffee KG,
Chung CC,
Cleary S,
Cotterchio M,
Dijk F,
Duell EJ,
Foretova L,
Fuchs C,
Funel N,
Gallinger S,
M Gaziano JM,
Gazouli M,
Giles GG,
Giovannucci E,
Goggins M,
Goodman GE,
Goodman PJ,
Hackert T,
Haiman C,
Hartge P,
Hasan M,
Hegyi P,
Helzlsouer KJ,
Herman J,
Holcatova I,
Holly EA,
Hoover R,
Hung RJ,
Jacobs EJ,
Jamroziak K,
Janout V,
Kaaks R,
Khaw KT,
Klein EA,
Kogevinas M,
Kooperberg C,
Kulke MH,
Kupcinskas J,
Kurtz RJ,
Laheru D,
Landi S,
Lawlor RT,
Lee IM,
LeMarchand L,
Lu L,
Malats N,
Mambrini A,
Mannisto S,
Milne RL,
Mohelníková-Duchoňová B,
Neale RE,
Neoptolemos JP,
Oberg AL,
Olson SH,
Orlow I,
Pasquali C,
Patel AV,
Peters U,
Pezzilli R,
Porta M,
Real FX,
Rothman N,
Scelo G,
Sesso HD,
Severi G,
Shu XO,
Silverman D,
Smith JP,
Soucek P,
Sund M,
Talar-Wojnarowska R,
Tavano F,
Thornquist MD,
Tobias GS,
Van Den Eeden SK,
Vashist Y,
Visvanathan K,
Vodicka P,
Wactawski-Wende J,
Wang Z,
Wentzensen N,
White E,
Yu H,
Yu K,
Zeleniuch-Jacquotte A,
Zheng W,
Zheng W,
Kraft P,
Li D,
Chanock S,
Obazee O,
Petersen GM,
Amundadottir LT
Nature communications · 2018 · PMID 29422604 · open access
페이지 4개
Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length
Li C,
Stoma S,
Lotta LA,
Warner S,
Albrecht E,
Allione A,
Arp PP,
Broer L,
Buxton JL,
Da Silva Couto Alves A,
Deelen J,
Fedko IO
외 84명 — 모두 보기
Gordon SD,
Jiang T,
Karlsson R,
Kerrison N,
Loe TK,
Mangino M,
Milaneschi Y,
Miraglio B,
Pervjakova N,
Russo A,
Surakka I,
van der Spek A,
Verhoeven JE,
Amin N,
Beekman M,
Blakemore AI,
Canzian F,
Hamby SE,
Hottenga JJ,
Jones PD,
Jousilahti P,
Mägi R,
Medland SE,
Montgomery GW,
Nyholt DR,
Perola M,
Pietiläinen KH,
Salomaa V,
Sillanpää E,
Suchiman HE,
van Heemst D,
Willemsen G,
Agudo A,
Boeing H,
Boomsma DI,
Chirlaque MD,
Fagherazzi G,
Ferrari P,
Franks P,
Gieger C,
Eriksson JG,
Gunter M,
Hägg S,
Hovatta I,
Imaz L,
Kaprio J,
Kaaks R,
Key T,
Krogh V,
Martin NG,
Melander O,
Metspalu A,
Moreno C,
Onland-Moret NC,
Nilsson P,
Ong KK,
Overvad K,
Palli D,
Panico S,
Pedersen NL,
Penninx BWJH,
Quirós JR,
Jarvelin MR,
Rodríguez-Barranco M,
Scott RA,
Severi G,
Slagboom PE,
Spector TD,
Tjonneland A,
Trichopoulou A,
Tumino R,
Uitterlinden AG,
van der Schouw YT,
van Duijn CM,
Weiderpass E,
Denchi EL,
Matullo G,
Butterworth AS,
Danesh J,
Samani NJ,
Wareham NJ,
Nelson CP,
Langenberg C,
Codd V
American journal of human genetics · 2020 · PMID 32109421 · open access
페이지 4개
Sex-Dimorphic Analyses Identify Novel and Sex-Specific Genetic Associations in Inflammatory Bowel Disease
Khrom M,
Li D,
Naito T,
Lee HS,
Botwin GJ,
Potdar AA,
Boucher G,
Yang S,
Mengesha E,
Dube S,
Song K,
McGovern DPB
외 1명 — 모두 보기
NIDDK Inflammatory Bowel Disease Genetics Consortium · International Inflammatory Bowel Disease Genetics Consortium
Inflammatory bowel diseases · 2023 · PMID 37262302
페이지 4개
Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer
Amundadottir L,
Kraft P,
Stolzenberg-Solomon RZ,
Fuchs CS,
Petersen GM,
Arslan AA,
Bueno-de-Mesquita HB,
Gross M,
Helzlsouer K,
Jacobs EJ,
LaCroix A,
Zheng W
외 60명 — 모두 보기
Zheng W,
Albanes D,
Bamlet W,
Berg CD,
Berrino F,
Bingham S,
Buring JE,
Bracci PM,
Canzian F,
Clavel-Chapelon F,
Clipp S,
Cotterchio M,
de Andrade M,
Duell EJ,
Fox JW Jr,
Gallinger S,
Gaziano JM,
Giovannucci EL,
Goggins M,
González CA,
Hallmans G,
Hankinson SE,
Hassan M,
Holly EA,
Hunter DJ,
Hutchinson A,
Jackson R,
Jacobs KB,
Jenab M,
Kaaks R,
Klein AP,
Kooperberg C,
Kurtz RC,
Li D,
Lynch SM,
Mandelson M,
McWilliams RR,
Mendelsohn JB,
Michaud DS,
Olson SH,
Overvad K,
Patel AV,
Peeters PH,
Rajkovic A,
Riboli E,
Risch HA,
Shu XO,
Thomas G,
Tobias GS,
Trichopoulos D,
Van Den Eeden SK,
Virtamo J,
Wactawski-Wende J,
Wolpin BM,
Yu H,
Yu K,
Zeleniuch-Jacquotte A,
Chanock SJ,
Hartge P,
Hoover RN
Nature genetics · 2009 · PMID 19648918
페이지 3개
Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer
Childs EJ,
Mocci E,
Campa D,
Bracci PM,
Gallinger S,
Goggins M,
Li D,
Neale RE,
Olson SH,
Scelo G,
Amundadottir LT,
Bamlet WR
외 50명 — 모두 보기
Bijlsma MF,
Blackford A,
Borges M,
Brennan P,
Brenner H,
Bueno-de-Mesquita HB,
Canzian F,
Capurso G,
Cavestro GM,
Chaffee KG,
Chanock SJ,
Cleary SP,
Cotterchio M,
Foretova L,
Fuchs C,
Funel N,
Gazouli M,
Hassan M,
Herman JM,
Holcatova I,
Holly EA,
Hoover RN,
Hung RJ,
Janout V,
Key TJ,
Kupcinskas J,
Kurtz RC,
Landi S,
Lu L,
Malecka-Panas E,
Mambrini A,
Mohelnikova-Duchonova B,
Neoptolemos JP,
Oberg AL,
Orlow I,
Pasquali C,
Pezzilli R,
Rizzato C,
Saldia A,
Scarpa A,
Stolzenberg-Solomon RZ,
Strobel O,
Tavano F,
Vashist YK,
Vodicka P,
Wolpin BM,
Yu H,
Petersen GM,
Risch HA,
Klein AP
Nature genetics · 2015 · PMID 26098869 · open access
페이지 3개
Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21
Zhang M,
Wang Z,
Obazee O,
Jia J,
Childs EJ,
Hoskins J,
Figlioli G,
Mocci E,
Collins I,
Chung CC,
Hautman C,
Arslan AA
외 112명 — 모두 보기
Beane-Freeman L,
Bracci PM,
Buring J,
Duell EJ,
Gallinger S,
Giles GG,
Goodman GE,
Goodman PJ,
Kamineni A,
Kolonel LN,
Kulke MH,
Malats N,
Olson SH,
Sesso HD,
Visvanathan K,
White E,
Zheng W,
Zheng W,
Abnet CC,
Albanes D,
Andreotti G,
Brais L,
Bueno-de-Mesquita HB,
Basso D,
Berndt SI,
Boutron-Ruault MC,
Bijlsma MF,
Brenner H,
Burdette L,
Campa D,
Caporaso NE,
Capurso G,
Cavestro GM,
Cotterchio M,
Costello E,
Elena J,
Boggi U,
Gaziano JM,
Gazouli M,
Giovannucci EL,
Goggins M,
Gross M,
Haiman CA,
Hassan M,
Helzlsouer KJ,
Hu N,
Hunter DJ,
Iskierka-Jazdzewska E,
Jenab M,
Kaaks R,
Key TJ,
Khaw KT,
Klein EA,
Kogevinas M,
Krogh V,
Kupcinskas J,
Kurtz RC,
Landi MT,
Landi S,
Le Marchand L,
Mambrini A,
Mannisto S,
Milne RL,
Neale RE,
Oberg AL,
Panico S,
Patel AV,
Peeters PH,
Peters U,
Pezzilli R,
Porta M,
Purdue M,
Quiros JR,
Riboli E,
Rothman N,
Scarpa A,
Scelo G,
Shu XO,
Silverman DT,
Soucek P,
Strobel O,
Sund M,
Małecka-Panas E,
Taylor PR,
Tavano F,
Travis RC,
Thornquist M,
Tjønneland A,
Tobias GS,
Trichopoulos D,
Vashist Y,
Vodicka P,
Wactawski-Wende J,
Wentzensen N,
Yu H,
Yu K,
Zeleniuch-Jacquotte A,
Kooperberg C,
Risch HA,
Jacobs EJ,
Li D,
Fuchs C,
Hoover R,
Hartge P,
Chanock SJ,
Petersen GM,
Stolzenberg-Solomon RS,
Wolpin BM,
Kraft P,
Klein AP,
Canzian F,
Amundadottir LT
Oncotarget · 2016 · PMID 27579533 · open access
페이지 3개
Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses
Painter JN,
O'Mara TA,
Morris AP,
Cheng THT,
Gorman M,
Martin L,
Hodson S,
Jones A,
Martin NG,
Gordon S,
Henders AK,
Attia J
외 65명 — 모두 보기
McEvoy M,
Holliday EG,
Scott RJ,
Webb PM,
Fasching PA,
Beckmann MW,
Ekici AB,
Hein A,
Rübner M,
Hall P,
Czene K,
Dörk T,
Dürst M,
Hillemanns P,
Runnebaum I,
Lambrechts D,
Lambrechts D,
Amant F,
Annibali D,
Depreeuw J,
Vanderstichele A,
Goode EL,
Cunningham JM,
Dowdy SC,
Winham SJ,
Trovik J,
Hoivik E,
Werner HMJ,
Krakstad C,
Ashton K,
Otton G,
Proietto T,
Tham E,
Mints M,
Ahmed S,
Healey CS,
Shah M,
Pharoah PDP,
Dunning AM,
Dennis J,
Bolla MK,
Michailidou K,
Wang Q,
Tyrer JP,
Hopper JL,
Peto J,
Swerdlow AJ,
Burwinkel B,
Brenner H,
Meindl A,
Brauch H,
Lindblom A,
Chang-Claude J,
Couch FJ,
Giles GG,
Kristensen VN,
Cox A,
Zondervan KT,
Nyholt DR,
MacGregor S,
Montgomery GW,
Tomlinson I,
Easton DF,
Thompson DJ,
Spurdle AB
Cancer medicine · 2018 · PMID 29608257 · open access
페이지 3개
Novel Common Genetic Susceptibility Loci for Colorectal Cancer
Schmit SL,
Edlund CK,
Schumacher FR,
Gong J,
Harrison TA,
Huyghe JR,
Qu C,
Melas M,
Van Den Berg DJ,
Wang H,
Tring S,
Plummer SJ
외 171명 — 모두 보기
Albanes D,
Alonso MH,
Amos CI,
Anton K,
Aragaki AK,
Arndt V,
Barry EL,
Berndt SI,
Bezieau S,
Bien S,
Bloomer A,
Boehm J,
Boutron-Ruault MC,
Brenner H,
Brezina S,
Buchanan DD,
Butterbach K,
Caan BJ,
Campbell PT,
Carlson CS,
Castelao JE,
Chan AT,
Chang-Claude J,
Chanock SJ,
Cheng I,
Cheng YW,
Chin LS,
Church JM,
Church T,
Coetzee GA,
Cotterchio M,
Cruz Correa M,
Curtis KR,
Duggan D,
Easton DF,
English D,
Feskens EJM,
Fischer R,
FitzGerald LM,
Fortini BK,
Fritsche LG,
Fuchs CS,
Gago-Dominguez M,
Gala M,
Gallinger SJ,
Gauderman WJ,
Giles GG,
Giovannucci EL,
Gogarten SM,
Gonzalez-Villalpando C,
Gonzalez-Villalpando EM,
Grady WM,
Greenson JK,
Gsur A,
Gunter M,
Haiman CA,
Hampe J,
Harlid S,
Harju JF,
Hayes RB,
Hofer P,
Hoffmeister M,
Hopper JL,
Huang SC,
Huerta JM,
Hudson TJ,
Hunter DJ,
Idos GE,
Iwasaki M,
Jackson RD,
Jacobs EJ,
Jee SH,
Jenkins MA,
Jia WH,
Jiao S,
Joshi AD,
Kolonel LN,
Kono S,
Kooperberg C,
Krogh V,
Kuehn T,
Küry S,
LaCroix A,
Laurie CA,
Lejbkowicz F,
Lemire M,
Lenz HJ,
Levine D,
Li CI,
Li L,
Lieb W,
Lin Y,
Lindor NM,
Liu YR,
Loupakis F,
Lu Y,
Luh F,
Ma J,
Mancao C,
Manion FJ,
Markowitz SD,
Martin V,
Matsuda K,
Matsuo K,
McDonnell KJ,
McNeil CE,
Milne R,
Molina AJ,
Mukherjee B,
Murphy N,
Newcomb PA,
Offit K,
Omichessan H,
Palli D,
Cotoré JPP,
Pérez-Mayoral J,
Pharoah PD,
Potter JD,
Qu C,
Raskin L,
Rennert G,
Rennert HS,
Riggs BM,
Schafmayer C,
Schoen RE,
Sellers TA,
Seminara D,
Severi G,
Shi W,
Shibata D,
Shu XO,
Siegel EM,
Slattery ML,
Southey M,
Stadler ZK,
Stern MC,
Stintzing S,
Taverna D,
Thibodeau SN,
Thomas DC,
Trichopoulou A,
Tsugane S,
Ulrich CM,
van Duijnhoven FJB,
van Guelpan B,
Vijai J,
Virtamo J,
Weinstein SJ,
White E,
Win AK,
Wolk A,
Woods M,
Wu AH,
Wu K,
Xiang YB,
Yen Y,
Zanke BW,
Zeng YX,
Zhang B,
Zubair N,
Kweon SS,
Figueiredo JC,
Zheng W,
Marchand LL,
Lindblom A,
Moreno V,
Peters U,
Casey G,
Hsu L,
Conti DV,
Gruber SB
Journal of the National Cancer Institute · 2019 · PMID 29917119
페이지 3개
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.