연구자에게
내 논문이 여기 있나요?
논문 2,647편이 이 사이트를 떠받치고 있습니다. 모든 변이·질환 페이지가
자기가 어떤 연구로부터 쓰였는지 밝히며, 이것이 그 목록을 페이지들에서 모은 것입니다.
성함이나 학술지명, PMID로 찾아보십시오.
Pal S에 대해
7건.
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology
Nielsen JB,
Thorolfsdottir RB,
Fritsche LG,
Zhou W,
Skov MW,
Graham SE,
Herron TJ,
McCarthy S,
Schmidt EM,
Sveinbjornsson G,
Surakka I,
Mathis MR
외 37명 — 모두 보기
Yamazaki M,
Crawford RD,
Gabrielsen ME,
Skogholt AH,
Holmen OL,
Lin M,
Wolford BN,
Dey R,
Dalen H,
Sulem P,
Chung JH,
Backman JD,
Arnar DO,
Thorsteinsdottir U,
Baras A,
O'Dushlaine C,
Holst AG,
Wen X,
Hornsby W,
Dewey FE,
Boehnke M,
Kheterpal S,
Mukherjee B,
Lee S,
Kang HM,
Holm H,
Kitzman J,
Shavit JA,
Jalife J,
Brummett CM,
Teslovich TM,
Carey DJ,
Gudbjartsson DF,
Stefansson K,
Abecasis GR,
Hveem K,
Willer CJ
Nature genetics · 2018 · PMID 30061737
페이지 12개+
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes
van der Meer D,
Rokicki J,
Kaufmann T,
Córdova-Palomera A,
Moberget T,
Alnæs D,
Bettella F,
Frei O,
Doan NT,
Sønderby IE,
Smeland OB,
Agartz I
외 42명 — 모두 보기
Bertolino A,
Bralten J,
Brandt CL,
Buitelaar JK,
Djurovic S,
van Donkelaar M,
Dørum ES,
Espeseth T,
Faraone SV,
Fernández G,
Fisher SE,
Franke B,
Haatveit B,
Hartman CA,
Hoekstra PJ,
Håberg AK,
Jönsson EG,
Kolskår KK,
Le Hellard S,
Lund MJ,
Lundervold AJ,
Lundervold A,
Melle I,
Monereo Sánchez J,
Norbom LC,
Nordvik JE,
Nyberg L,
Oosterlaan J,
Papalino M,
Papassotiropoulos A,
Pergola G,
de Quervain DJF,
Richard G,
Sanders AM,
Selvaggi P,
Shumskaya E,
Steen VM,
Tønnesen S,
Ulrichsen KM,
Zwiers MP,
Andreassen OA,
Westlye LT
Alzheimer’s Disease Neuroimaging Initiative · Pediatric Imaging, Neurocognition and Genetics Study
Molecular psychiatry · 2020 · PMID 30279459 · open access
페이지 12개+
Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis
Graham SE,
Nielsen JB,
Zawistowski M,
Zhou W,
Fritsche LG,
Gabrielsen ME,
Skogholt AH,
Surakka I,
Hornsby WE,
Fermin D,
Larach DB,
Kheterpal S
외 9명 — 모두 보기
Nature communications · 2019 · PMID 31015462 · open access
페이지 12개+
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Trubetskoy V,
Pardiñas AF,
Qi T,
Panagiotaropoulou G,
Awasthi S,
Bigdeli TB,
Bryois J,
Chen CY,
Dennison CA,
Hall LS,
Lam M,
Watanabe K
외 422명 — 모두 보기
Frei O,
Ge T,
Harwood JC,
Koopmans F,
Magnusson S,
Richards AL,
Sidorenko J,
Wu Y,
Zeng J,
Grove J,
Kim M,
Li Z,
Voloudakis G,
Zhang W,
Adams M,
Agartz I,
Atkinson EG,
Agerbo E,
Al Eissa M,
Albus M,
Alexander M,
Alizadeh BZ,
Alptekin K,
Als TD,
Amin F,
Arolt V,
Arrojo M,
Athanasiu L,
Azevedo MH,
Bacanu SA,
Bass NJ,
Begemann M,
Belliveau RA,
Bene J,
Benyamin B,
Bergen SE,
Blasi G,
Bobes J,
Bonassi S,
Braun A,
Bressan RA,
Bromet EJ,
Bruggeman R,
Buckley PF,
Buckner RL,
Bybjerg-Grauholm J,
Cahn W,
Cairns MJ,
Calkins ME,
Carr VJ,
Castle D,
Catts SV,
Chambert KD,
Chan RCK,
Chaumette B,
Cheng W,
Cheung EFC,
Chong SA,
Cohen D,
Consoli A,
Cordeiro Q,
Costas J,
Curtis C,
Davidson M,
Davis KL,
de Haan L,
Degenhardt F,
DeLisi LE,
Demontis D,
Dickerson F,
Dikeos D,
Dinan T,
Djurovic S,
Duan J,
Ducci G,
Dudbridge F,
Eriksson JG,
Fañanás L,
Faraone SV,
Fiorentino A,
Forstner A,
Frank J,
Freimer NB,
Fromer M,
Frustaci A,
Gadelha A,
Genovese G,
Gershon ES,
Giannitelli M,
Giegling I,
Giusti-Rodríguez P,
Godard S,
Goldstein JI,
González Peñas J,
González-Pinto A,
Gopal S,
Gratten J,
Green MF,
Greenwood TA,
Guillin O,
Gülöksüz S,
Gur RE,
Gur RC,
Gutiérrez B,
Hahn E,
Hakonarson H,
Haroutunian V,
Hartmann AM,
Harvey C,
Hayward C,
Henskens FA,
Herms S,
Hoffmann P,
Howrigan DP,
Ikeda M,
Iyegbe C,
Joa I,
Julià A,
Kähler AK,
Kam-Thong T,
Kamatani Y,
Karachanak-Yankova S,
Kebir O,
Keller MC,
Kelly BJ,
Khrunin A,
Kim SW,
Klovins J,
Kondratiev N,
Konte B,
Kraft J,
Kubo M,
Kučinskas V,
Kučinskiene ZA,
Kusumawardhani A,
Kuzelova-Ptackova H,
Landi S,
Lazzeroni LC,
Lee PH,
Legge SE,
Lehrer DS,
Lencer R,
Lerer B,
Li M,
Lieberman J,
Light GA,
Limborska S,
Liu CM,
Lönnqvist J,
Loughland CM,
Lubinski J,
Luykx JJ,
Lynham A,
Macek M Jr,
Mackinnon A,
Magnusson PKE,
Maher BS,
Maier W,
Malaspina D,
Mallet J,
Marder SR,
Marsal S,
Martin AR,
Martorell L,
Mattheisen M,
McCarley RW,
McDonald C,
McGrath JJ,
Medeiros H,
Meier S,
Melegh B,
Melle I,
Mesholam-Gately RI,
Metspalu A,
Michie PT,
Milani L,
Milanova V,
Mitjans M,
Molden E,
Molina E,
Molto MD,
Mondelli V,
Moreno C,
Morley CP,
Muntané G,
Murphy KC,
Myin-Germeys I,
Nenadić I,
Nestadt G,
Nikitina-Zake L,
Noto C,
Nuechterlein KH,
O'Brien NL,
O'Neill FA,
Oh SY,
Olincy A,
Ota VK,
Pantelis C,
Papadimitriou GN,
Parellada M,
Paunio T,
Pellegrino R,
Periyasamy S,
Perkins DO,
Pfuhlmann B,
Pietiläinen O,
Pimm J,
Porteous D,
Powell J,
Quattrone D,
Quested D,
Radant AD,
Rampino A,
Rapaport MH,
Rautanen A,
Reichenberg A,
Roe C,
Roffman JL,
Roth J,
Rothermundt M,
Rutten BPF,
Saker-Delye S,
Salomaa V,
Sanjuan J,
Santoro ML,
Savitz A,
Schall U,
Scott RJ,
Seidman LJ,
Sharp SI,
Shi J,
Siever LJ,
Sigurdsson E,
Sim K,
Skarabis N,
Slominsky P,
So HC,
Sobell JL,
Söderman E,
Stain HJ,
Steen NE,
Steixner-Kumar AA,
Stögmann E,
Stone WS,
Straub RE,
Streit F,
Strengman E,
Stroup TS,
Subramaniam M,
Sugar CA,
Suvisaari J,
Svrakic DM,
Swerdlow NR,
Szatkiewicz JP,
Ta TMT,
Takahashi A,
Terao C,
Thibaut F,
Toncheva D,
Tooney PA,
Torretta S,
Tosato S,
Tura GB,
Turetsky BI,
Üçok A,
Vaaler A,
van Amelsvoort T,
van Winkel R,
Veijola J,
Waddington J,
Walter H,
Waterreus A,
Webb BT,
Weiser M,
Williams NM,
Witt SH,
Wormley BK,
Wu JQ,
Xu Z,
Yolken R,
Zai CC,
Zhou W,
Zhu F,
Zimprich F,
Atbaşoğlu EC,
Ayub M,
Benner C,
Bertolino A,
Black DW,
Bray NJ,
Breen G,
Buccola NG,
Byerley WF,
Chen WJ,
Cloninger CR,
Crespo-Facorro B,
Donohoe G,
Freedman R,
Galletly C,
Gandal MJ,
Gennarelli M,
Hougaard DM,
Hwu HG,
Jablensky AV,
McCarroll SA,
Moran JL,
Mors O,
Mortensen PB,
Müller-Myhsok B,
Neil AL,
Nordentoft M,
Pato MT,
Petryshen TL,
Pirinen M,
Pulver AE,
Schulze TG,
Silverman JM,
Smoller JW,
Stahl EA,
Tsuang DW,
Vilella E,
Wang SH,
Xu S,
Adolfsson R,
Arango C,
Baune BT,
Belangero SI,
Børglum AD,
Braff D,
Bramon E,
Buxbaum JD,
Campion D,
Cervilla JA,
Cichon S,
Collier DA,
Corvin A,
Curtis D,
Forti MD,
Domenici E,
Ehrenreich H,
Escott-Price V,
Esko T,
Fanous AH,
Gareeva A,
Gawlik M,
Gejman PV,
Gill M,
Glatt SJ,
Golimbet V,
Hong KS,
Hultman CM,
Hyman SE,
Iwata N,
Jönsson EG,
Kahn RS,
Kennedy JL,
Khusnutdinova E,
Kirov G,
Knowles JA,
Krebs MO,
Laurent-Levinson C,
Lee J,
Lencz T,
Levinson DF,
Li QS,
Liu J,
Malhotra AK,
Malhotra D,
McIntosh A,
McQuillin A,
Menezes PR,
Morgan VA,
Morris DW,
Mowry BJ,
Murray RM,
Nimgaonkar V,
Nöthen MM,
Ophoff RA,
Paciga SA,
Palotie A,
Pato CN,
Qin S,
Rietschel M,
Riley BP,
Rivera M,
Rujescu D,
Saka MC,
Sanders AR,
Schwab SG,
Serretti A,
Sham PC,
Shi Y,
St Clair D,
Stefánsson H,
Stefansson K,
Tsuang MT,
van Os J,
Vawter MP,
Weinberger DR,
Werge T,
Wildenauer DB,
Yu X,
Yue W,
Holmans PA,
Pocklington AJ,
Roussos P,
Vassos E,
Verhage M,
Visscher PM,
Yang J,
Posthuma D,
Andreassen OA,
Kendler KS,
Owen MJ,
Wray NR,
Daly MJ,
Huang H,
Neale BM,
Sullivan PF,
Ripke S,
Walters JTR,
O'Donovan MC
Indonesia Schizophrenia Consortium · PsychENCODE 외 컨소시엄 3곳
Nature · 2022 · PMID 35396580
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
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
van Rheenen W,
van der Spek RAA,
Bakker MK,
van Vugt JJFA,
Hop PJ,
Zwamborn RAJ,
de Klein N,
Westra HJ,
Bakker OB,
Deelen P,
Shireby G,
Hannon E
외 180명 — 모두 보기
Moisse M,
Baird D,
Restuadi R,
Dolzhenko E,
Dekker AM,
Gawor K,
Westeneng HJ,
Tazelaar GHP,
van Eijk KR,
Kooyman M,
Byrne RP,
Doherty M,
Heverin M,
Al Khleifat A,
Iacoangeli A,
Shatunov A,
Ticozzi N,
Cooper-Knock J,
Smith BN,
Gromicho M,
Chandran S,
Pal S,
Morrison KE,
Shaw PJ,
Hardy J,
Orrell RW,
Sendtner M,
Meyer T,
Başak N,
van der Kooi AJ,
Ratti A,
Fogh I,
Gellera C,
Lauria G,
Corti S,
Cereda C,
Sproviero D,
D'Alfonso S,
Sorarù G,
Siciliano G,
Filosto M,
Padovani A,
Chiò A,
Calvo A,
Moglia C,
Brunetti M,
Canosa A,
Grassano M,
Beghi E,
Pupillo E,
Logroscino G,
Nefussy B,
Osmanovic A,
Nordin A,
Lerner Y,
Zabari M,
Gotkine M,
Baloh RH,
Bell S,
Vourc'h P,
Corcia P,
Couratier P,
Millecamps S,
Meininger V,
Salachas F,
Mora Pardina JS,
Assialioui A,
Rojas-García R,
Dion PA,
Ross JP,
Ludolph AC,
Weishaupt JH,
Brenner D,
Freischmidt A,
Bensimon G,
Brice A,
Durr A,
Payan CAM,
Saker-Delye S,
Wood NW,
Topp S,
Rademakers R,
Tittmann L,
Lieb W,
Franke A,
Ripke S,
Braun A,
Kraft J,
Whiteman DC,
Olsen CM,
Uitterlinden AG,
Hofman A,
Rietschel M,
Cichon S,
Nöthen MM,
Amouyel P,
Traynor BJ,
Singleton AB,
Mitne Neto M,
Cauchi RJ,
Ophoff RA,
Wiedau-Pazos M,
Lomen-Hoerth C,
van Deerlin VM,
Grosskreutz J,
Roediger A,
Gaur N,
Jörk A,
Barthel T,
Theele E,
Ilse B,
Stubendorff B,
Witte OW,
Steinbach R,
Hübner CA,
Graff C,
Brylev L,
Fominykh V,
Demeshonok V,
Ataulina A,
Rogelj B,
Koritnik B,
Zidar J,
Ravnik-Glavač M,
Glavač D,
Stević Z,
Drory V,
Povedano M,
Blair IP,
Kiernan MC,
Benyamin B,
Henderson RD,
Furlong S,
Mathers S,
McCombe PA,
Needham M,
Ngo ST,
Nicholson GA,
Pamphlett R,
Rowe DB,
Steyn FJ,
Williams KL,
Mather KA,
Sachdev PS,
Henders AK,
Wallace L,
de Carvalho M,
Pinto S,
Petri S,
Weber M,
Rouleau GA,
Silani V,
Curtis CJ,
Breen G,
Glass JD,
Brown RH Jr,
Landers JE,
Shaw CE,
Andersen PM,
Groen EJN,
van Es MA,
Pasterkamp RJ,
Fan D,
Garton FC,
McRae AF,
Davey Smith G,
Gaunt TR,
Eberle MA,
Mill J,
McLaughlin RL,
Hardiman O,
Kenna KP,
Wray NR,
Tsai E,
Runz H,
Franke L,
Al-Chalabi A,
Van Damme P,
van den Berg LH,
Veldink JH
SLALOM Consortium · PARALS Consortium 외 컨소시엄 2곳
Nature genetics · 2021 · PMID 34873335 · open access
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.