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성함이나 학술지명, PMID로 찾아보십시오.
He F에 대해
37건, 그중 20건 표시.
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Michailidou K,
Hall P,
Gonzalez-Neira A,
Ghoussaini M,
Dennis J,
Milne RL,
Schmidt MK,
Chang-Claude J,
Bojesen SE,
Bolla MK,
Wang Q,
Dicks E
외 208명 — 모두 보기
Lee A,
Turnbull C,
Rahman N,
Fletcher O,
Peto J,
Gibson L,
Dos Santos Silva I,
Nevanlinna H,
Muranen TA,
Aittomäki K,
Blomqvist C,
Czene K,
Irwanto A,
Liu J,
Waisfisz Q,
Meijers-Heijboer H,
Adank M,
van der Luijt RB,
Hein R,
Dahmen N,
Beckman L,
Meindl A,
Schmutzler RK,
Müller-Myhsok B,
Lichtner P,
Hopper JL,
Southey MC,
Makalic E,
Schmidt DF,
Uitterlinden AG,
Hofman A,
Hunter DJ,
Chanock SJ,
Vincent D,
Bacot F,
Tessier DC,
Canisius S,
Wessels LF,
Haiman CA,
Shah M,
Luben R,
Brown J,
Luccarini C,
Schoof N,
Humphreys K,
Li J,
Nordestgaard BG,
Nielsen SF,
Flyger H,
Couch FJ,
Wang X,
Vachon C,
Stevens KN,
Lambrechts D,
Moisse M,
Paridaens R,
Christiaens MR,
Rudolph A,
Nickels S,
Flesch-Janys D,
Johnson N,
Aitken Z,
Aaltonen K,
Heikkinen T,
Broeks A,
Veer LJ,
van der Schoot CE,
Guénel P,
Truong T,
Laurent-Puig P,
Menegaux F,
Marme F,
Schneeweiss A,
Sohn C,
Burwinkel B,
Zamora MP,
Perez JI,
Pita G,
Alonso MR,
Cox A,
Brock IW,
Cross SS,
Reed MW,
Sawyer EJ,
Tomlinson I,
Kerin MJ,
Miller N,
Henderson BE,
Schumacher F,
Le Marchand L,
Andrulis IL,
Knight JA,
Glendon G,
Mulligan AM,
Lindblom A,
Margolin S,
Hooning MJ,
Hollestelle A,
van den Ouweland AM,
Jager A,
Bui QM,
Stone J,
Dite GS,
Apicella C,
Tsimiklis H,
Giles GG,
Severi G,
Baglietto L,
Fasching PA,
Haeberle L,
Ekici AB,
Beckmann MW,
Brenner H,
Müller H,
Arndt V,
Stegmaier C,
Swerdlow A,
Ashworth A,
Orr N,
Jones M,
Figueroa J,
Lissowska J,
Brinton L,
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,
Bonanni B,
Devilee P,
Tollenaar RA,
Seynaeve C,
van Asperen CJ,
Jakubowska A,
Lubinski J,
Jaworska K,
Durda K,
Mannermaa A,
Kataja V,
Kosma VM,
Hartikainen JM,
Bogdanova NV,
Antonenkova NN,
Dörk T,
Kristensen VN,
Anton-Culver H,
Slager S,
Toland AE,
Edge S,
Fostira F,
Kang D,
Yoo KY,
Noh DY,
Matsuo K,
Ito H,
Iwata H,
Sueta A,
Wu AH,
Tseng CC,
Van Den Berg D,
Stram DO,
Shu XO,
Lu W,
Gao YT,
Cai H,
Teo SH,
Yip CH,
Phuah SY,
Cornes BK,
Hartman M,
Miao H,
Lim WY,
Sng JH,
Muir K,
Lophatananon A,
Stewart-Brown S,
Siriwanarangsan P,
Shen CY,
Hsiung CN,
Wu PE,
Ding SL,
Sangrajrang S,
Gaborieau V,
Brennan P,
McKay J,
Blot WJ,
Signorello LB,
Cai Q,
Zheng W,
Zheng W,
Deming-Halverson S,
Shrubsole M,
Long J,
Simard J,
Garcia-Closas M,
Pharoah PD,
Chenevix-Trench G,
Dunning AM,
Benitez J,
Easton DF
Breast and Ovarian Cancer Susceptibility Collaboration · Hereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON) 외 컨소시엄 3곳
Nature genetics · 2013 · PMID 23535729
페이지 12개+
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 208370 East Asians identifies 113 susceptibility loci for systemic lupus erythematosus
Yin X,
Kim K,
Suetsugu H,
Bang SY,
Wen L,
Koido M,
Ha E,
Liu L,
Sakamoto Y,
Jo S,
Leng RX,
Otomo N
외 76명 — 모두 보기
Laurynenka V,
Kwon YC,
Sheng Y,
Sugano N,
Sugano N,
Hwang MY,
Li W,
Mukai M,
Yoon K,
Cai M,
Ishigaki K,
Chung WT,
Huang H,
Takahashi D,
Lee SS,
Wang M,
Karino K,
Shim SC,
Zheng X,
Miyamura T,
Kang YM,
Ye D,
Nakamura J,
Suh CH,
Tang Y,
Motomura G,
Park YB,
Ding H,
Kuroda T,
Choe JY,
Li C,
Niiro H,
Park Y,
Shen C,
Miyamoto T,
Ahn GY,
Fei W,
Takeuchi T,
Shin JM,
Li K,
Kawaguchi Y,
Lee YK,
Wang Y,
Amano K,
Park DJ,
Yang W,
Tada Y,
Yamaji K,
Shimizu M,
Atsumi T,
Suzuki A,
Sumida T,
Okada Y,
Matsuda K,
Matsuo K,
Kochi Y,
Kottyan LC,
Weirauch MT,
Parameswaran S,
Eswar S,
Salim H,
Chen X,
Yamamoto K,
Harley JB,
Ohmura K,
Kim TH,
Yang S,
Yamamoto T,
Kim BJ,
Shen N,
Ikegawa S,
Lee HS,
Zhang X,
Terao C,
Cui Y,
Bae SC
Japanese Research Committee on Idiopathic Osteonecrosis of the Femoral Head
Annals of the rheumatic diseases · 2021 · PMID 33272962 · open access
페이지 12개+
New insights into the genetic etiology of Alzheimer's disease and related dementias
Bellenguez C,
Küçükali F,
Jansen IE,
Kleineidam L,
Moreno-Grau S,
Amin N,
Naj AC,
Campos-Martin R,
Grenier-Boley B,
Andrade V,
Holmans PA,
Boland A
외 391명 — 모두 보기
Damotte V,
van der Lee SJ,
Costa MR,
Kuulasmaa T,
Yang Q,
de Rojas I,
Bis JC,
Yaqub A,
Prokic I,
Chapuis J,
Ahmad S,
Giedraitis V,
Aarsland D,
Garcia-Gonzalez P,
Abdelnour C,
Alarcón-Martín E,
Alcolea D,
Alegret M,
Alvarez I,
Álvarez V,
Armstrong NJ,
Tsolaki A,
Antúnez C,
Appollonio I,
Arcaro M,
Archetti S,
Pastor AA,
Arosio B,
Athanasiu L,
Bailly H,
Banaj N,
Baquero M,
Barral S,
Beiser A,
Pastor AB,
Below JE,
Benchek P,
Benussi L,
Berr C,
Besse C,
Bessi V,
Binetti G,
Bizarro A,
Blesa R,
Boada M,
Boerwinkle E,
Borroni B,
Boschi S,
Bossù P,
Bråthen G,
Bressler J,
Bresner C,
Brodaty H,
Brookes KJ,
Brusco LI,
Buiza-Rueda D,
Bûrger K,
Burholt V,
Bush WS,
Calero M,
Cantwell LB,
Chene G,
Chung J,
Cuccaro ML,
Carracedo Á,
Cecchetti R,
Cervera-Carles L,
Charbonnier C,
Chen HH,
Chillotti C,
Ciccone S,
Claassen JAHR,
Clark C,
Conti E,
Corma-Gómez A,
Costantini E,
Custodero C,
Daian D,
Dalmasso MC,
Daniele A,
Dardiotis E,
Dartigues JF,
de Deyn PP,
de Paiva Lopes K,
de Witte LD,
Debette S,
Deckert J,
Del Ser T,
Denning N,
DeStefano A,
Dichgans M,
Diehl-Schmid J,
Diez-Fairen M,
Rossi PD,
Djurovic S,
Duron E,
Düzel E,
Dufouil C,
Eiriksdottir G,
Engelborghs S,
Escott-Price V,
Espinosa A,
Ewers M,
Faber KM,
Fabrizio T,
Nielsen SF,
Fardo DW,
Farotti L,
Fenoglio C,
Fernández-Fuertes M,
Ferrari R,
Ferreira CB,
Ferri E,
Fin B,
Fischer P,
Fladby T,
Fließbach K,
Fongang B,
Fornage M,
Fortea J,
Foroud TM,
Fostinelli S,
Fox NC,
Franco-Macías E,
Bullido MJ,
Frank-García A,
Froelich L,
Fulton-Howard B,
Galimberti D,
García-Alberca JM,
García-González P,
Garcia-Madrona S,
Garcia-Ribas G,
Ghidoni R,
Giegling I,
Giorgio G,
Goate AM,
Goldhardt O,
Gomez-Fonseca D,
González-Pérez A,
Graff C,
Grande G,
Green E,
Grimmer T,
Grünblatt E,
Grunin M,
Gudnason V,
Guetta-Baranes T,
Haapasalo A,
Hadjigeorgiou G,
Haines JL,
Hamilton-Nelson KL,
Hampel H,
Hanon O,
Hardy J,
Hartmann AM,
Hausner L,
Harwood J,
Heilmann-Heimbach S,
Helisalmi S,
Heneka MT,
Hernández I,
Herrmann MJ,
Hoffmann P,
Holmes C,
Holstege H,
Vilas RH,
Hulsman M,
Humphrey J,
Biessels GJ,
Jian X,
Johansson C,
Jun GR,
Kastumata Y,
Kauwe J,
Kehoe PG,
Kilander L,
Ståhlbom AK,
Kivipelto M,
Koivisto A,
Kornhuber J,
Kosmidis MH,
Kukull WA,
Kuksa PP,
Kunkle BW,
Kuzma AB,
Lage C,
Laukka EJ,
Launer L,
Lauria A,
Lee CY,
Lehtisalo J,
Lerch O,
Lleó A,
Longstreth W Jr,
Lopez O,
de Munain AL,
Love S,
Löwemark M,
Luckcuck L,
Lunetta KL,
Ma Y,
Macías J,
MacLeod CA,
Maier W,
Mangialasche F,
Spallazzi M,
Marquié M,
Marshall R,
Martin ER,
Montes AM,
Rodríguez CM,
Masullo C,
Mayeux R,
Mead S,
Mecocci P,
Medina M,
Meggy A,
Mehrabian S,
Mendoza S,
Menéndez-González M,
Mir P,
Moebus S,
Mol M,
Molina-Porcel L,
Montrreal L,
Morelli L,
Moreno F,
Morgan K,
Mosley T,
Nöthen MM,
Muchnik C,
Mukherjee S,
Nacmias B,
Ngandu T,
Nicolas G,
Nordestgaard BG,
Olaso R,
Orellana A,
Orsini M,
Ortega G,
Padovani A,
Paolo C,
Papenberg G,
Parnetti L,
Pasquier F,
Pastor P,
Peloso G,
Pérez-Cordón A,
Pérez-Tur J,
Pericard P,
Peters O,
Pijnenburg YAL,
Pineda JA,
Piñol-Ripoll G,
Pisanu C,
Polak T,
Popp J,
Posthuma D,
Priller J,
Puerta R,
Quenez O,
Quintela I,
Thomassen JQ,
Rábano A,
Rainero I,
Rajabli F,
Ramakers I,
Real LM,
Reinders MJT,
Reitz C,
Reyes-Dumeyer D,
Ridge P,
Riedel-Heller S,
Riederer P,
Roberto N,
Rodriguez-Rodriguez E,
Rongve A,
Allende IR,
Rosende-Roca M,
Royo JL,
Rubino E,
Rujescu D,
Sáez ME,
Sakka P,
Saltvedt I,
Sanabria Á,
Sánchez-Arjona MB,
Sanchez-Garcia F,
Juan PS,
Sánchez-Valle R,
Sando SB,
Sarnowski C,
Satizabal CL,
Scamosci M,
Scarmeas N,
Scarpini E,
Scheltens P,
Scherbaum N,
Scherer M,
Schmid M,
Schneider A,
Schott JM,
Selbæk G,
Seripa D,
Serrano M,
Sha J,
Shadrin AA,
Skrobot O,
Slifer S,
Snijders GJL,
Soininen H,
Solfrizzi V,
Solomon A,
Song Y,
Sorbi S,
Sotolongo-Grau O,
Spalletta G,
Spottke A,
Squassina A,
Stordal E,
Tartan JP,
Tárraga L,
Tesí N,
Thalamuthu A,
Thomas T,
Tosto G,
Traykov L,
Tremolizzo L,
Tybjærg-Hansen A,
Uitterlinden A,
Ullgren A,
Ulstein I,
Valero S,
Valladares O,
Broeckhoven CV,
Vance J,
Vardarajan BN,
van der Lugt A,
Dongen JV,
van Rooij J,
van Swieten J,
Vandenberghe R,
Verhey F,
Vidal JS,
Vogelgsang J,
Vyhnalek M,
Wagner M,
Wallon D,
Wang LS,
Wang R,
Weinhold L,
Wiltfang J,
Windle G,
Woods B,
Yannakoulia M,
Zare H,
Zhao Y,
Zhang X,
Zhu C,
Zulaica M,
Farrer LA,
Psaty BM,
Ghanbari M,
Raj T,
Sachdev P,
Mather K,
Jessen F,
Ikram MA,
de Mendonça A,
Hort J,
Tsolaki M,
Pericak-Vance MA,
Amouyel P,
Williams J,
Frikke-Schmidt R,
Clarimon J,
Deleuze JF,
Rossi G,
Seshadri S,
Andreassen OA,
Ingelsson M,
Hiltunen M,
Sleegers K,
Schellenberg GD,
van Duijn CM,
Sims R,
van der Flier WM,
Ruiz A,
Ramirez A,
Lambert JC
EADB · GR@ACE 외 컨소시엄 7곳
Nature genetics · 2022 · PMID 35379992 · open access
페이지 9개
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
Demontis D,
Walters RK,
Martin J,
Mattheisen M,
Als TD,
Agerbo E,
Baldursson G,
Belliveau R,
Bybjerg-Grauholm J,
Bækvad-Hansen M,
Cerrato F,
Chambert K
외 69명 — 모두 보기
Churchhouse C,
Dumont A,
Eriksson N,
Gandal M,
Goldstein JI,
Grasby KL,
Grove J,
Gudmundsson OO,
Hansen CS,
Hauberg ME,
Hollegaard MV,
Howrigan DP,
Huang H,
Maller JB,
Martin AR,
Martin NG,
Moran J,
Pallesen J,
Palmer DS,
Pedersen CB,
Pedersen MG,
Poterba T,
Poulsen JB,
Ripke S,
Robinson EB,
Satterstrom FK,
Stefansson H,
Stevens C,
Turley P,
Walters GB,
Won H,
Wright MJ,
Andreassen OA,
Asherson P,
Burton CL,
Boomsma DI,
Cormand B,
Dalsgaard S,
Franke B,
Gelernter J,
Geschwind D,
Hakonarson H,
Haavik J,
Kranzler HR,
Kuntsi J,
Langley K,
Lesch KP,
Middeldorp C,
Reif A,
Rohde LA,
Roussos P,
Schachar R,
Sklar P,
Sonuga-Barke EJS,
Sullivan PF,
Thapar A,
Tung JY,
Waldman ID,
Medland SE,
Stefansson K,
Nordentoft M,
Hougaard DM,
Werge T,
Mors O,
Mortensen PB,
Daly MJ,
Faraone SV,
Børglum AD,
Neale BM
ADHD Working Group of the Psychiatric Genomics Consortium (PGC) · Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium 외 컨소시엄 1곳
Nature genetics · 2019 · PMID 30478444
페이지 8개
GWAS for systemic sclerosis identifies six novel susceptibility loci including one in the Fcγ receptor region
Ishikawa Y,
Tanaka N,
Asano Y,
Kodera M,
Shirai Y,
Akahoshi M,
Hasegawa M,
Matsushita T,
Saito K,
Motegi SI,
Yoshifuji H,
Yoshizaki A
외 60명 — 모두 보기
Kohmoto T,
Takagi K,
Oka A,
Kanda M,
Tanaka Y,
Ito Y,
Nakano K,
Kasamatsu H,
Utsunomiya A,
Sekiguchi A,
Niiro H,
Jinnin M,
Makino K,
Makino T,
Ihn H,
Yamamoto M,
Suzuki C,
Takahashi H,
Nishida E,
Morita A,
Yamamoto T,
Fujimoto M,
Kondo Y,
Goto D,
Sumida T,
Ayuzawa N,
Yanagida H,
Horita T,
Atsumi T,
Endo H,
Shima Y,
Kumanogoh A,
Hirata J,
Otomo N,
Suetsugu H,
Koike Y,
Tomizuka K,
Yoshino S,
Liu X,
Ito S,
Hikino K,
Suzuki A,
Momozawa Y,
Ikegawa S,
Tanaka Y,
Ishikawa O,
Takehara K,
Torii T,
Sato S,
Okada Y,
Mimori T,
Matsuda F,
Matsuda K,
Amariuta T,
Imoto I,
Matsuo K,
Kuwana M,
Kawaguchi Y,
Ohmura K,
Terao C
Nature communications · 2024 · PMID 38296975 · open access
페이지 7개
Attention-deficit/hyperactivity disorder and lifetime cannabis use: genetic overlap and causality
Soler Artigas M,
Sánchez-Mora C,
Rovira P,
Richarte V,
Garcia-Martínez I,
Pagerols M,
Demontis D,
Stringer S,
Vink JM,
Børglum AD,
Neale BM,
Franke B
외 4명 — 모두 보기
ADHD Group of the Psychiatric Genomics Consortium, International Cannabis Consortium
Molecular psychiatry · 2020 · PMID 30610198
페이지 5개
A genome-wide association study of plasma total IgE concentrations in the Framingham Heart Study
Granada M,
Wilk JB,
Tuzova M,
Strachan DP,
Weidinger S,
Albrecht E,
Gieger C,
Heinrich J,
Himes BE,
Hunninghake GM,
Celedón JC,
Weiss ST
외 4명 — 모두 보기
The Journal of allergy and clinical immunology · 2012 · PMID 22075330
페이지 3개
Genome-wide analysis of insomnia disorder
Stein MB,
McCarthy MJ,
Chen CY,
Jain S,
Gelernter J,
He F,
Heeringa SG,
Kessler RC,
Nock MK,
Ripke S,
Sun X,
Wynn GH
외 2명 — 모두 보기
Molecular psychiatry · 2018 · PMID 29520036 · open access
페이지 3개
The First Genome-Wide Association Study for Type 2 Diabetes in Youth: The Progress in Diabetes Genetics in Youth (ProDiGY) Consortium
Srinivasan S,
Chen L,
Todd J,
Divers J,
Gidding S,
Chernausek S,
Gubitosi-Klug RA,
Kelsey MM,
Shah R,
Black MH,
Wagenknecht LE,
Manning A
외 5명 — 모두 보기
ProDiGY Consortium
Diabetes · 2021 · PMID 33479058 · open access
페이지 3개
Genome wide association analysis and association of genetic risk and lifestyle with upper gastrointestinal cancer among an endoscopy-screened cohort in China
He F,
Ran X,
Jiang H,
Fan Z,
Zhang Y,
Wang J,
Hao C,
Song G,
Gong Y,
Li Y,
Li X,
Chen R
외 5명 — 모두 보기
Science bulletin · 2026 · PMID 41963194
페이지 3개
Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits
Scuteri A,
Sanna S,
Chen WM,
Uda M,
Albai G,
Strait J,
Najjar S,
Nagaraja R,
Orrú M,
Usala G,
Dei M,
Lai S
외 13명 — 모두 보기
Maschio A,
Busonero F,
Mulas A,
Ehret GB,
Fink AA,
Weder AB,
Cooper RS,
Galan P,
Chakravarti A,
Schlessinger D,
Cao A,
Lakatta E,
Abecasis GR
PLoS genetics · 2007 · PMID 17658951 · open access
페이지 2개
Genome-wide association study identifies 1p36.22 as a new susceptibility locus for hepatocellular carcinoma in chronic hepatitis B virus carriers
Zhang H,
Zhai Y,
Hu Z,
Wu C,
Qian J,
Jia W,
Ma F,
Huang W,
Yu L,
Yue W,
Wang Z,
Li P
외 20명 — 모두 보기
Zhang Y,
Liang R,
Wei Z,
Cui Y,
Xie W,
Cai M,
Yu X,
Yuan Y,
Xia X,
Zhang X,
Yang H,
Qiu W,
Yang J,
Gong F,
Chen M,
Shen H,
Lin D,
Zeng YX,
He F,
Zhou G
Nature genetics · 2010 · PMID 20676096
페이지 2개
Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation
Lauc G,
Essafi A,
Huffman JE,
Hayward C,
Knežević A,
Kattla JJ,
Polašek O,
Gornik O,
Vitart V,
Abrahams JL,
Pučić M,
Novokmet M
외 14명 — 모두 보기
Redžić I,
Campbell S,
Wild SH,
Borovečki F,
Wang W,
Kolčić I,
Zgaga L,
Gyllensten U,
Wilson JF,
Wright AF,
Hastie ND,
Campbell H,
Rudd PM,
Rudan I
PLoS genetics · 2010 · PMID 21203500 · open access
페이지 2개
A genome-wide association study of saturated, mono- and polyunsaturated red blood cell fatty acids in the Framingham Heart Offspring Study
Tintle NL,
Pottala JV,
Lacey S,
Ramachandran V,
Westra J,
Rogers A,
Clark J,
Olthoff B,
Larson M,
Harris W,
Shearer GC
Prostaglandins, leukotrienes, and essential fatty acids · 2015 · PMID 25500335
페이지 2개
The first genome-wide association study identifying new susceptibility loci for obstetric antiphospholipid syndrome
Sugiura-Ogasawara M,
Omae Y,
Kawashima M,
Toyo-Oka L,
Khor SS,
Sawai H,
Horita T,
Atsumi T,
Murashima A,
Fujita D,
Fujita T,
Morimoto S
외 6명 — 모두 보기
Journal of human genetics · 2017 · PMID 28424481
페이지 2개
Genome-wide association study identifies two risk loci for tuberculosis in Han Chinese
Zheng R,
Li Z,
He F,
Liu H,
Chen J,
Chen J,
Xie X,
Zhou J,
Chen H,
Wu X,
Wu J,
Chen B
외 21명 — 모두 보기
Liu Y,
Cui H,
Fan L,
Sha W,
Liu Y,
Wang J,
Huang X,
Zhang L,
Xu F,
Wang J,
Feng Y,
Qin L,
Yang H,
Liu Z,
Cui Z,
Liu F,
Chen X,
Gao S,
Sun S,
Shi Y,
Ge B
Nature communications · 2018 · PMID 30287856 · open access
페이지 2개
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