연구자에게
내 논문이 여기 있나요?
논문 2,673편이 이 사이트를 떠받치고 있습니다. 모든 변이·질환 페이지가
자기가 어떤 연구로부터 쓰였는지 밝히며, 이것이 그 목록을 페이지들에서 모은 것입니다.
성함이나 학술지명, PMID로 찾아보십시오.
Ross A에 대해
12건.
Discovery of common and rare genetic risk variants for colorectal cancer
Huyghe JR,
Bien SA,
Harrison TA,
Kang HM,
Chen S,
Schmit SL,
Conti DV,
Qu C,
Jeon J,
Edlund CK,
Greenside P,
Wainberg M
외 188명 — 모두 보기
Schumacher FR,
Smith JD,
Levine DM,
Nelson SC,
Sinnott-Armstrong NA,
Albanes D,
Alonso MH,
Anderson K,
Arnau-Collell C,
Arndt V,
Bamia C,
Banbury BL,
Baron JA,
Berndt SI,
Bézieau S,
Bishop DT,
Boehm J,
Boeing H,
Brenner H,
Brezina S,
Buch S,
Buchanan DD,
Burnett-Hartman A,
Butterbach K,
Caan BJ,
Campbell PT,
Carlson CS,
Castellví-Bel S,
Chan AT,
Chang-Claude J,
Chanock SJ,
Chirlaque MD,
Cho SH,
Connolly CM,
Cross AJ,
Cuk K,
Curtis KR,
de la Chapelle A,
Doheny KF,
Duggan D,
Easton DF,
Elias SG,
Elliott F,
English DR,
Feskens EJM,
Figueiredo JC,
Fischer R,
FitzGerald LM,
Forman D,
Gala M,
Gallinger S,
Gauderman WJ,
Giles GG,
Gillanders E,
Gong J,
Goodman PJ,
Grady WM,
Grove JS,
Gsur A,
Gunter MJ,
Haile RW,
Hampe J,
Hampel H,
Harlid S,
Hayes RB,
Hofer P,
Hoffmeister M,
Hopper JL,
Hsu WL,
Huang WY,
Hudson TJ,
Hunter DJ,
Ibañez-Sanz G,
Idos GE,
Ingersoll R,
Jackson RD,
Jacobs EJ,
Jenkins MA,
Joshi AD,
Joshu CE,
Keku TO,
Key TJ,
Kim HR,
Kobayashi E,
Kolonel LN,
Kooperberg C,
Kühn T,
Küry S,
Kweon SS,
Larsson SC,
Laurie CA,
Le Marchand L,
Leal SM,
Lee SC,
Lejbkowicz F,
Lemire M,
Li CI,
Li L,
Lieb W,
Lin Y,
Lindblom A,
Lindor NM,
Ling H,
Louie TL,
Männistö S,
Markowitz SD,
Martín V,
Masala G,
McNeil CE,
Melas M,
Milne RL,
Moreno L,
Murphy N,
Myte R,
Naccarati A,
Newcomb PA,
Offit K,
Ogino S,
Onland-Moret NC,
Pardini B,
Parfrey PS,
Pearlman R,
Perduca V,
Pharoah PDP,
Pinchev M,
Platz EA,
Prentice RL,
Pugh E,
Raskin L,
Rennert G,
Rennert HS,
Riboli E,
Rodríguez-Barranco M,
Romm J,
Sakoda LC,
Schafmayer C,
Schoen RE,
Seminara D,
Shah M,
Shelford T,
Shin MH,
Shulman K,
Sieri S,
Slattery ML,
Southey MC,
Stadler ZK,
Stegmaier C,
Su YR,
Tangen CM,
Thibodeau SN,
Thomas DC,
Thomas SS,
Toland AE,
Trichopoulou A,
Ulrich CM,
Van Den Berg DJ,
van Duijnhoven FJB,
Van Guelpen B,
van Kranen H,
Vijai J,
Visvanathan K,
Vodicka P,
Vodickova L,
Vymetalkova V,
Weigl K,
Weinstein SJ,
White E,
Win AK,
Wolf CR,
Wolk A,
Woods MO,
Wu AH,
Zaidi SH,
Zanke BW,
Zhang Q,
Zheng W,
Zheng W,
Scacheri PC,
Potter JD,
Bassik MC,
Kundaje A,
Casey G,
Moreno V,
Abecasis GR,
Nickerson DA,
Gruber SB,
Hsu L,
Peters U
Nature genetics · 2019 · PMID 30510241 · open access
페이지 12개+
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error
Fan Q,
Pozarickij A,
Tan NYQ,
Guo X,
Verhoeven VJM,
Vitart V,
Guggenheim JA,
Miyake M,
Tideman JWL,
Khawaja AP,
Zhang L,
MacGregor S
외 46명 — 모두 보기
Höhn R,
Chen P,
Biino G,
Wedenoja J,
Saffari SE,
Tedja MS,
Xie J,
Lanca C,
Wang YX,
Sahebjada S,
Mazur J,
Mirshahi A,
Martin NG,
Yazar S,
Pennell CE,
Yap M,
Haarman AEG,
Enthoven CA,
Polling J,
Hewitt AW,
Jaddoe VWV,
van Duijn CM,
Hayward C,
Polasek O,
Tai ES,
Yoshikatsu H,
Hysi PG,
Young TL,
Tsujikawa A,
Wang JJ,
Mitchell P,
Pfeiffer N,
Pärssinen O,
Foster PJ,
Fossarello M,
Yip SP,
Williams C,
Hammond CJ,
Jonas JB,
He M,
Mackey DA,
Wong TY,
Klaver CCW,
Saw SM,
Baird PN,
Cheng CY
Consortium for Refractive Error and Myopia (CREAM) · UK Biobank Eye and Vision Consortium
Communications biology · 2020 · PMID 32193507 · open access
페이지 12개+
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Gharahkhani P,
Jorgenson E,
Hysi P,
Khawaja AP,
Pendergrass S,
Han X,
Ong JS,
Hewitt AW,
Segrè AV,
Rouhana JM,
Hamel AR,
Igo RP Jr
외 67명 — 모두 보기
Choquet H,
Qassim A,
Josyula NS,
Cooke Bailey JN,
Bonnemaijer PWM,
Iglesias A,
Siggs OM,
Young TL,
Vitart V,
Thiadens AAHJ,
Karjalainen J,
Uebe S,
Melles RB,
Nair KS,
Luben R,
Simcoe M,
Amersinghe N,
Cree AJ,
Hohn R,
Poplawski A,
Chen LJ,
Rong SS,
Aung T,
Vithana EN,
Tamiya G,
Shiga Y,
Yamamoto M,
Nakazawa T,
Currant H,
Birney E,
Wang X,
Auton A,
Lupton MK,
Martin NG,
Ashaye A,
Olawoye O,
Williams SE,
Akafo S,
Ramsay M,
Hashimoto K,
Kamatani Y,
Akiyama M,
Momozawa Y,
Foster PJ,
Khaw PT,
Morgan JE,
Strouthidis NG,
Kraft P,
Kang JH,
Pang CP,
Pasutto F,
Mitchell P,
Lotery AJ,
Palotie A,
van Duijn C,
Haines JL,
Hammond C,
Pasquale LR,
Klaver CCW,
Hauser M,
Khor CC,
Mackey DA,
Kubo M,
Cheng CY,
Craig JE,
MacGregor S,
Wiggs JL
NEIGHBORHOOD consortium · ANZRAG consortium 외 컨소시엄 5곳
Nature communications · 2021 · PMID 33627673 · open access
페이지 12개+
Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries
Gorman BR,
Voloudakis G,
Igo RP Jr,
Kinzy T,
Halladay CW,
Bigdeli TB,
Zeng B,
Venkatesh S,
Cooke Bailey JN,
Crawford DC,
Markianos K,
Dong F
외 26명 — 모두 보기
Schreiner PA,
Zhang W,
Hadi T,
Anger MD,
Stockwell A,
Melles RB,
Yin J,
Choquet H,
Kaye R,
Patasova K,
Patel PJ,
Yaspan BL,
Jorgenson E,
Hysi PG,
Lotery AJ,
Gaziano JM,
Tsao PS,
Fliesler SJ,
Sullivan JM,
Greenberg PB,
Wu WC,
Assimes TL,
Pyarajan S,
Roussos P,
Peachey NS,
Iyengar SK
VA Million Veteran Program · International AMD Genomics Consortium (IAMDGC)
Nature genetics · 2024 · PMID 39623103
페이지 12개+
Genome-wide association study of prostate-specific antigen levels in 392,522 men identifies new loci and improves prediction across ancestry groups
Hoffmann TJ,
Graff RE,
Madduri RK,
Rodriguez AA,
Cario CL,
Feng K,
Jiang Y,
Wang A,
Klein RJ,
Pierce BL,
Eggener S,
Tong L
외 37명 — 모두 보기
Blot W,
Long J,
Goss LB,
Darst BF,
Rebbeck T,
Lachance J,
Andrews C,
Adebiyi AO,
Adusei B,
Aisuodionoe-Shadrach OI,
Fernandez PW,
Jalloh M,
Janivara R,
Chen WC,
Mensah JE,
Agalliu I,
Berndt SI,
Shelley JP,
Schaffer K,
Machiela MJ,
Freedman ND,
Huang WY,
Li SA,
Goodman PJ,
Till C,
Thompson I,
Lilja H,
Ranatunga DK,
Presti J,
Van Den Eeden SK,
Chanock SJ,
Mosley JD,
Conti DV,
Haiman CA,
Justice AC,
Kachuri L,
Witte JS
Nature genetics · 2025 · PMID 39930085 · open access
페이지 12개+
MRI-Based Genetic Studies Reveal Specific Genetic Variants and Disease Risks Associated With Fat Distribution Across Anatomical Sites
Ahmed A,
Cule M,
Naz A,
Thanaj M,
Sorokin EP,
Odoemelam CS,
Whitcher B,
Sattar N,
Bell JD,
Thomas EL,
Yaghootkar H
Journal of obesity · 2025 · PMID 40922984 · open access
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
Genetic architectures of proximal and distal colorectal cancer are partly distinct
Huyghe JR,
Harrison TA,
Bien SA,
Hampel H,
Figueiredo JC,
Schmit SL,
Conti DV,
Chen S,
Qu C,
Lin Y,
Barfield R,
Baron JA
외 129명 — 모두 보기
Cross AJ,
Diergaarde B,
Duggan D,
Harlid S,
Imaz L,
Kang HM,
Levine DM,
Perduca V,
Perez-Cornago A,
Sakoda LC,
Schumacher FR,
Slattery ML,
Toland AE,
van Duijnhoven FJB,
Van Guelpen B,
Agudo A,
Albanes D,
Alonso MH,
Anderson K,
Arnau-Collell C,
Arndt V,
Banbury BL,
Bassik MC,
Berndt SI,
Bézieau S,
Bishop DT,
Boehm J,
Boeing H,
Boutron-Ruault MC,
Brenner H,
Brezina S,
Buch S,
Buchanan DD,
Burnett-Hartman A,
Caan BJ,
Campbell PT,
Carr PR,
Castells A,
Castellví-Bel S,
Chan AT,
Chang-Claude J,
Chanock SJ,
Curtis KR,
de la Chapelle A,
Easton DF,
English DR,
Feskens EJM,
Gala M,
Gallinger SJ,
Gauderman WJ,
Giles GG,
Goodman PJ,
Grady WM,
Grove JS,
Gsur A,
Gunter MJ,
Haile RW,
Hampe J,
Hoffmeister M,
Hopper JL,
Hsu WL,
Huang WY,
Hudson TJ,
Jenab M,
Jenkins MA,
Joshi AD,
Keku TO,
Kooperberg C,
Kühn T,
Küry S,
Le Marchand L,
Lejbkowicz F,
Li CI,
Li L,
Lieb W,
Lindblom A,
Lindor NM,
Männistö S,
Markowitz SD,
Milne RL,
Moreno L,
Murphy N,
Nassir R,
Offit K,
Ogino S,
Panico S,
Parfrey PS,
Pearlman R,
Pharoah PDP,
Phipps AI,
Platz EA,
Potter JD,
Prentice RL,
Qi L,
Raskin L,
Rennert G,
Rennert HS,
Riboli E,
Schafmayer C,
Schoen RE,
Seminara D,
Song M,
Su YR,
Tangen CM,
Thibodeau SN,
Thomas DC,
Trichopoulou A,
Ulrich CM,
Visvanathan K,
Vodicka P,
Vodickova L,
Vymetalkova V,
Weigl K,
Weinstein SJ,
White E,
Wolk A,
Woods MO,
Wu AH,
Abecasis GR,
Nickerson DA,
Scacheri PC,
Kundaje A,
Casey G,
Gruber SB,
Hsu L,
Moreno V,
Hayes RB,
Newcomb PA,
Peters U
Gut · 2021 · PMID 33632709 · open access
페이지 5개
Stroke genetics informs drug discovery and risk prediction across ancestries
Mishra A,
Malik R,
Hachiya T,
Jürgenson T,
Namba S,
Posner DC,
Kamanu FK,
Koido M,
Le Grand Q,
Shi M,
He Y,
Georgakis MK
외 175명 — 모두 보기
Caro I,
Krebs K,
Liaw YC,
Vaura FC,
Lin K,
Winsvold BS,
Srinivasasainagendra V,
Parodi L,
Bae HJ,
Chauhan G,
Chong MR,
Tomppo L,
Akinyemi R,
Roshchupkin GV,
Habib N,
Jee YH,
Thomassen JQ,
Abedi V,
Cárcel-Márquez J,
Nygaard M,
Leonard HL,
Yang C,
Yonova-Doing E,
Knol MJ,
Lewis AJ,
Judy RL,
Ago T,
Amouyel P,
Armstrong ND,
Bakker MK,
Bartz TM,
Bennett DA,
Bis JC,
Bordes C,
Børte S,
Cain A,
Ridker PM,
Cho K,
Chen Z,
Cruchaga C,
Cole JW,
de Jager PL,
de Cid R,
Endres M,
Ferreira LE,
Geerlings MI,
Gasca NC,
Gudnason V,
Hata J,
He J,
Heath AK,
Ho YL,
Havulinna AS,
Hopewell JC,
Hyacinth HI,
Inouye M,
Jacob MA,
Jeon CE,
Jern C,
Kamouchi M,
Keene KL,
Kitazono T,
Kittner SJ,
Konuma T,
Kumar A,
Lacaze P,
Launer LJ,
Lee KJ,
Lepik K,
Li J,
Li L,
Manichaikul A,
Markus HS,
Marston NA,
Meitinger T,
Mitchell BD,
Montellano FA,
Morisaki T,
Mosley TH,
Nalls MA,
Nordestgaard BG,
O'Donnell MJ,
Okada Y,
Onland-Moret NC,
Ovbiagele B,
Peters A,
Psaty BM,
Rich SS,
Rosand J,
Sabatine MS,
Sacco RL,
Saleheen D,
Sandset EC,
Salomaa V,
Sargurupremraj M,
Sasaki M,
Satizabal CL,
Schmidt CO,
Shimizu A,
Smith NL,
Sloane KL,
Sutoh Y,
Sun YV,
Tanno K,
Tiedt S,
Tatlisumak T,
Torres-Aguila NP,
Tiwari HK,
Trégouët DA,
Trompet S,
Tuladhar AM,
Tybjærg-Hansen A,
van Vugt M,
Vibo R,
Verma SS,
Wiggins KL,
Wennberg P,
Woo D,
Wilson PWF,
Xu H,
Yang Q,
Yoon K,
Millwood IY,
Gieger C,
Ninomiya T,
Grabe HJ,
Jukema JW,
Rissanen IL,
Strbian D,
Kim YJ,
Chen PH,
Mayerhofer E,
Howson JMM,
Irvin MR,
Adams H,
Wassertheil-Smoller S,
Christensen K,
Ikram MA,
Rundek T,
Worrall BB,
Lathrop GM,
Riaz M,
Simonsick EM,
Kõrv J,
França PHC,
Zand R,
Prasad K,
Frikke-Schmidt R,
de Leeuw FE,
Liman T,
Haeusler KG,
Ruigrok YM,
Heuschmann PU,
Longstreth WT,
Jung KJ,
Bastarache L,
Paré G,
Damrauer SM,
Chasman DI,
Rotter JI,
Anderson CD,
Zwart JA,
Niiranen TJ,
Fornage M,
Liaw YP,
Seshadri S,
Fernández-Cadenas I,
Walters RG,
Ruff CT,
Owolabi MO,
Huffman JE,
Milani L,
Kamatani Y,
Dichgans M,
Debette S
COMPASS Consortium · INVENT Consortium 외 컨소시엄 13곳
Nature · 2022 · PMID 36180795 · open access
페이지 5개
Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci
De Jager PL,
Jia X,
Wang J,
de Bakker PI,
Ottoboni L,
Aggarwal NT,
Piccio L,
Raychaudhuri S,
Tran D,
Aubin C,
Briskin R,
Romano S
외 21명 — 모두 보기
Baranzini SE,
McCauley JL,
Pericak-Vance MA,
Haines JL,
Gibson RA,
Naeglin Y,
Uitdehaag B,
Matthews PM,
Kappos L,
Polman C,
McArdle WL,
Strachan DP,
Evans D,
Cross AH,
Daly MJ,
Compston A,
Sawcer SJ,
Weiner HL,
Hauser SL,
Hafler DA,
Oksenberg JR
International MS Genetics Consortium
Nature genetics · 2009 · PMID 19525953
페이지 3개
Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease
Medici M,
Porcu E,
Pistis G,
Teumer A,
Brown SJ,
Jensen RA,
Rawal R,
Roef GL,
Plantinga TS,
Vermeulen SH,
Lahti J,
Simmonds MJ
외 106명 — 모두 보기
Husemoen LL,
Freathy RM,
Shields BM,
Pietzner D,
Nagy R,
Broer L,
Chaker L,
Korevaar TI,
Plia MG,
Sala C,
Völker U,
Richards JB,
Sweep FC,
Gieger C,
Corre T,
Kajantie E,
Thuesen B,
Taes YE,
Visser WE,
Hattersley AT,
Kratzsch J,
Hamilton A,
Li W,
Homuth G,
Lobina M,
Mariotti S,
Soranzo N,
Cocca M,
Nauck M,
Spielhagen C,
Ross A,
Arnold A,
van de Bunt M,
Liyanarachchi S,
Heier M,
Grabe HJ,
Masciullo C,
Galesloot TE,
Lim EM,
Reischl E,
Leedman PJ,
Lai S,
Delitala A,
Bremner AP,
Philips DI,
Beilby JP,
Mulas A,
Vocale M,
Abecasis G,
Forsen T,
James A,
Widen E,
Hui J,
Prokisch H,
Rietzschel EE,
Palotie A,
Feddema P,
Fletcher SJ,
Schramm K,
Rotter JI,
Kluttig A,
Radke D,
Traglia M,
Surdulescu GL,
He H,
Franklyn JA,
Tiller D,
Vaidya B,
de Meyer T,
Jørgensen T,
Eriksson JG,
O'Leary PC,
Wichmann E,
Hermus AR,
Psaty BM,
Ittermann T,
Hofman A,
Bosi E,
Schlessinger D,
Wallaschofski H,
Pirastu N,
Aulchenko YS,
de la Chapelle A,
Netea-Maier RT,
Gough SC,
Meyer Zu Schwabedissen H,
Frayling TM,
Kaufman JM,
Linneberg A,
Räikkönen K,
Smit JW,
Kiemeney LA,
Rivadeneira F,
Uitterlinden AG,
Walsh JP,
Meisinger C,
den Heijer M,
Visser TJ,
Spector TD,
Wilson SG,
Völzke H,
Cappola A,
Toniolo D,
Sanna S,
Naitza S,
Peeters RP
PLoS genetics · 2014 · PMID 24586183 · open access
페이지 3개
Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease
Tang CS,
Gui H,
Kapoor A,
Kim JH,
Luzón-Toro B,
Pelet A,
Burzynski G,
Lantieri F,
So MT,
Berrios C,
Shin HD,
Fernández RM
외 20명 — 모두 보기
Le TL,
Verheij JB,
Matera I,
Cherny SS,
Nandakumar P,
Cheong HS,
Antiñolo G,
Amiel J,
Seo JM,
Kim DY,
Oh JT,
Lyonnet S,
Borrego S,
Ceccherini I,
Hofstra RM,
Chakravarti A,
Kim HY,
Sham PC,
Tam PK,
Garcia-Barceló MM
Human molecular genetics · 2016 · PMID 27702942
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.