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113건, 그중 20건 표시.
The genetic architecture of hip shape and its role in the development of hip osteoarthritis and fracture
Faber BG,
Frysz M,
Zheng J,
Lin H,
Flynn KA,
Ebsim R,
Saunders FR,
Beynon R,
Gregory JS,
Aspden RM,
Harvey NC,
Lindner C
외 7명 — 모두 보기
Human molecular genetics · 2025 · PMID 39574169 · open access
페이지 12개+
Multiscale analysis and functional validation of the cellular and genetic determinants of skeletal disease
Chai RC,
Lundberg M,
Freudenthal B,
Smith JT,
Boughton AP,
Zhang Y,
Flynn KA,
Frysz M,
Corr AP,
Khoo WH,
Komla-Ebri D,
Dack MRG
외 38명 — 모두 보기
Guilfoyle SE,
Logan JG,
Butterfield NC,
Leitch VD,
Pollard AS,
Mäkitie RE,
Bradford N,
Ramos-Mucci L,
Vilas-Zornoza A,
Chen Y,
Yip RKH,
Er J,
Tan SZ,
McDonald MM,
Youlten SE,
Sergio CM,
Castro-Martinez A,
Young SG,
Skorokhodova E,
Evans DM,
Powell JE,
de Leeuw CA,
Ewing AD,
Eisman JA,
Blank RD,
Phan TG,
Lagendijk AK,
Hawkins ED,
Oh HL,
McIntyre RE,
Hessel EM,
Taylor-King JP,
Baldock PA,
Duncan EL,
Williams GR,
Bassett JHD,
Croucher PI,
Kemp JP
International Federation of Musculoskeletal Research Societies (IFMRS) Big Data Working Group
Nature genetics · 2026 · PMID 42432248 · open access
페이지 12개+
Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis
Paternoster L,
Standl M,
Waage J,
Baurecht H,
Hotze M,
Strachan DP,
Curtin JA,
Bønnelykke K,
Tian C,
Takahashi A,
Esparza-Gordillo J,
Alves AC
외 140명 — 모두 보기
Thyssen JP,
den Dekker HT,
Ferreira MA,
Altmaier E,
Sleiman PM,
Xiao FL,
Gonzalez JR,
Marenholz I,
Kalb B,
Yanes MP,
Xu CJ,
Carstensen L,
Groen-Blokhuis MM,
Venturini C,
Pennell CE,
Barton SJ,
Levin AM,
Curjuric I,
Bustamante M,
Kreiner-Møller E,
Lockett GA,
Bacelis J,
Bacelis J,
Bunyavanich S,
Myers RA,
Matanovic A,
Kumar A,
Tung JY,
Hirota T,
Kubo M,
McArdle WL,
Henderson AJ,
Kemp JP,
Zheng J,
Smith GD,
Rüschendorf F,
Bauerfeind A,
Lee-Kirsch MA,
Arnold A,
Homuth G,
Schmidt CO,
Mangold E,
Cichon S,
Keil T,
Rodríguez E,
Peters A,
Peters A,
Franke A,
Lieb W,
Novak N,
Fölster-Holst R,
Horikoshi M,
Pekkanen J,
Sebert S,
Husemoen LL,
Grarup N,
de Jongste JC,
Rivadeneira F,
Hofman A,
Jaddoe VW,
Pasmans SG,
Elbert NJ,
Uitterlinden AG,
Marks GB,
Thompson PJ,
Matheson MC,
Robertson CF,
Ried JS,
Li J,
Zuo XB,
Zheng XD,
Yin XY,
Sun LD,
McAleer MA,
O'Regan GM,
Fahy CM,
Campbell LE,
Macek M,
Kurek M,
Hu D,
Eng C,
Postma DS,
Feenstra B,
Geller F,
Hottenga JJ,
Middeldorp CM,
Hysi P,
Bataille V,
Spector T,
Tiesler CM,
Thiering E,
Pahukasahasram B,
Yang JJ,
Imboden M,
Huntsman S,
Vilor-Tejedor N,
Relton CL,
Myhre R,
Nystad W,
Custovic A,
Weiss ST,
Meyers DA,
Söderhäll C,
Melén E,
Ober C,
Raby BA,
Simpson A,
Jacobsson B,
Holloway JW,
Bisgaard H,
Sunyer J,
Hensch NMP,
Williams LK,
Godfrey KM,
Wang CA,
Boomsma DI,
Melbye M,
Koppelman GH,
Jarvis D,
McLean WI,
Irvine AD,
Zhang XJ,
Hakonarson H,
Gieger C,
Burchard EG,
Martin NG,
Duijts L,
Linneberg A,
Jarvelin MR,
Noethen MM,
Lau S,
Hübner N,
Lee YA,
Tamari M,
Hinds DA,
Glass D,
Brown SJ,
Heinrich J,
Evans DM,
Weidinger S
Australian Asthma Genetics Consortium (AAGC)
Nature genetics · 2015 · PMID 26482879 · open access
페이지 11개
Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus
Medina-Gomez C,
Kemp JP,
Dimou NL,
Kreiner E,
Chesi A,
Zemel BS,
Bønnelykke K,
Boer CG,
Ahluwalia TS,
Bisgaard H,
Evangelou E,
Heppe DHM
외 22명 — 모두 보기
Bonewald LF,
Gorski JP,
Ghanbari M,
Demissie S,
Duque G,
Maurano MT,
Kiel DP,
Hsu YH,
C J van der Eerden B,
Ackert-Bicknell C,
Reppe S,
Gautvik KM,
Raastad T,
Karasik D,
van de Peppel J,
Jaddoe VWV,
Uitterlinden AG,
Tobias JH,
Grant SFA,
Bagos PG,
Evans DM,
Rivadeneira F
Nature communications · 2017 · PMID 28743860 · open access
페이지 11개
Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis
Medina-Gomez C,
Mullin BH,
Chesi A,
Prijatelj V,
Kemp JP,
Shochat-Carvalho C,
Trajanoska K,
Wang C,
Joro R,
Evans TE,
Schraut KE,
Li-Gao R
외 46명 — 모두 보기
Ahluwalia TS,
Zillikens MC,
Zhu K,
Mook-Kanamori DO,
Evans DS,
Nethander M,
Knol MJ,
Thorleifsson G,
Prokic I,
Zemel B,
Broer L,
McGuigan FE,
van Schoor NM,
Reppe S,
Pawlak MA,
Ralston SH,
van der Velde N,
Lorentzon M,
Stefansson K,
Adams HHH,
Wilson SG,
Ikram MA,
Walsh JP,
Lakka TA,
Gautvik KM,
Wilson JF,
Orwoll ES,
van Duijn CM,
Bønnelykke K,
Uitterlinden AG,
Styrkársdóttir U,
Akesson KE,
Spector TD,
Tobias JH,
Ohlsson C,
Felix JF,
Bisgaard H,
Grant SFA,
Richards JB,
Evans DM,
van der Eerden B,
van de Peppel J,
Ackert-Bicknell C,
Karasik D,
Kague E,
Rivadeneira F
Communications biology · 2023 · PMID 37402774 · open access
페이지 11개
Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error
Fan Q,
Verhoeven VJ,
Wojciechowski R,
Barathi VA,
Hysi PG,
Guggenheim JA,
Höhn R,
Vitart V,
Khawaja AP,
Yamashiro K,
Hosseini SM,
Lehtimäki T
외 142명 — 모두 보기
Lu Y,
Haller T,
Xie J,
Delcourt C,
Pirastu M,
Wedenoja J,
Gharahkhani P,
Venturini C,
Miyake M,
Hewitt AW,
Guo X,
Mazur J,
Huffman JE,
Williams KM,
Polasek O,
Campbell H,
Rudan I,
Vatavuk Z,
Wilson JF,
Joshi PK,
McMahon G,
St Pourcain B,
Evans DM,
Simpson CL,
Schwantes-An TH,
Igo RP,
Mirshahi A,
Cougnard-Gregoire A,
Bellenguez C,
Blettner M,
Raitakari O,
Kähönen M,
Seppala I,
Zeller T,
Meitinger T,
Ried JS,
Gieger C,
Portas L,
van Leeuwen EM,
Amin N,
Uitterlinden AG,
Rivadeneira F,
Hofman A,
Vingerling JR,
Wang YX,
Wang X,
Tai-Hui Boh E,
Ikram MK,
Sabanayagam C,
Gupta P,
Tan V,
Zhou L,
Ho CE,
Lim W,
Beuerman RW,
Siantar R,
Tai ES,
Vithana E,
Mihailov E,
Khor CC,
Hayward C,
Luben RN,
Foster PJ,
Klein BE,
Klein R,
Wong HS,
Mitchell P,
Metspalu A,
Aung T,
Young TL,
He M,
Pärssinen O,
van Duijn CM,
Jin Wang J,
Williams C,
Jonas JB,
Teo YY,
Mackey DA,
Oexle K,
Yoshimura N,
Paterson AD,
Pfeiffer N,
Wong TY,
Baird PN,
Stambolian D,
Wilson JE,
Cheng CY,
Hammond CJ,
Klaver CC,
Saw SM,
Rahi JS,
Korobelnik JF,
Kemp JP,
Timpson NJ,
Smith GD,
Craig JE,
Burdon KP,
Fogarty RD,
Iyengar SK,
Chew E,
Janmahasatian S,
Martin NG,
MacGregor S,
Xu L,
Schache M,
Nangia V,
Panda-Jonas S,
Wright AF,
Fondran JR,
Lass JH,
Feng S,
Zhao JH,
Khaw KT,
Wareham NJ,
Rantanen T,
Kaprio J,
Pang CP,
Chen LJ,
Tam PO,
Jhanji V,
Young AL,
Döring A,
Raffel LJ,
Cotch MF,
Li X,
Yip SP,
Yap MK,
Biino G,
Vaccargiu S,
Fossarello M,
Fleck B,
Yazar S,
Tideman JW,
Tedja M,
Deangelis MM,
Morrison M,
Farrer L,
Zhou X,
Chen W,
Mizuki N,
Meguro A,
Mäkelä KM
Consortium for Refractive Error and Myopia
Nature communications · 2016 · PMID 27020472 · open access
페이지 10개
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
Wheeler E,
Leong A,
Liu CT,
Hivert MF,
Strawbridge RJ,
Podmore C,
Li M,
Yao J,
Sim X,
Hong J,
Chu AY,
Zhang W
외 203명 — 모두 보기
Wang X,
Chen P,
Maruthur NM,
Porneala BC,
Sharp SJ,
Jia Y,
Kabagambe EK,
Chang LC,
Chen WM,
Elks CE,
Evans DS,
Fan Q,
Giulianini F,
Go MJ,
Hottenga JJ,
Hu Y,
Jackson AU,
Kanoni S,
Kim YJ,
Kleber ME,
Ladenvall C,
Lecoeur C,
Lim SH,
Lu Y,
Mahajan A,
Marzi C,
Nalls MA,
Navarro P,
Nolte IM,
Rose LM,
Rybin DV,
Sanna S,
Shi Y,
Stram DO,
Takeuchi F,
Tan SP,
van der Most PJ,
Van Vliet-Ostaptchouk JV,
Wong A,
Yengo L,
Zhao W,
Goel A,
Martinez Larrad MT,
Radke D,
Salo P,
Tanaka T,
van Iperen EPA,
Abecasis G,
Afaq S,
Alizadeh BZ,
Bertoni AG,
Bonnefond A,
Böttcher Y,
Bottinger EP,
Campbell H,
Carlson OD,
Chen CH,
Cho YS,
Garvey WT,
Gieger C,
Goodarzi MO,
Grallert H,
Hamsten A,
Hartman CA,
Herder C,
Hsiung CA,
Huang J,
Igase M,
Isono M,
Katsuya T,
Khor CC,
Kiess W,
Kohara K,
Kovacs P,
Lee J,
Lee WJ,
Lehne B,
Li H,
Liu J,
Lobbens S,
Luan J,
Lyssenko V,
Meitinger T,
Miki T,
Miljkovic I,
Moon S,
Mulas A,
Müller G,
Müller-Nurasyid M,
Nagaraja R,
Nauck M,
Pankow JS,
Polasek O,
Prokopenko I,
Ramos PS,
Rasmussen-Torvik L,
Rathmann W,
Rich SS,
Robertson NR,
Roden M,
Roussel R,
Rudan I,
Scott RA,
Scott WR,
Sennblad B,
Siscovick DS,
Strauch K,
Sun L,
Swertz M,
Tajuddin SM,
Taylor KD,
Teo YY,
Tham YC,
Tönjes A,
Wareham NJ,
Willemsen G,
Wilsgaard T,
Hingorani AD,
Egan J,
Ferrucci L,
Hovingh GK,
Jula A,
Kivimaki M,
Kumari M,
Njølstad I,
Palmer CNA,
Serrano Ríos M,
Stumvoll M,
Watkins H,
Aung T,
Blüher M,
Boehnke M,
Boomsma DI,
Bornstein SR,
Chambers JC,
Chasman DI,
Chen YI,
Chen YT,
Cheng CY,
Cucca F,
de Geus EJC,
Deloukas P,
Evans MK,
Fornage M,
Friedlander Y,
Froguel P,
Groop L,
Gross MD,
Harris TB,
Hayward C,
Heng CK,
Ingelsson E,
Kato N,
Kim BJ,
Koh WP,
Kooner JS,
Körner A,
Kuh D,
Kuusisto J,
Laakso M,
Lin X,
Liu Y,
Loos RJF,
Magnusson PKE,
März W,
McCarthy MI,
Oldehinkel AJ,
Ong KK,
Pedersen NL,
Pereira MA,
Peters A,
Ridker PM,
Sabanayagam C,
Sale M,
Saleheen D,
Saltevo J,
Schwarz PE,
Sheu WHH,
Snieder H,
Spector TD,
Tabara Y,
Tuomilehto J,
van Dam RM,
Wilson JG,
Wilson JF,
Wolffenbuttel BHR,
Wong TY,
Wu JY,
Yuan JM,
Zonderman AB,
Soranzo N,
Guo X,
Roberts DJ,
Florez JC,
Sladek R,
Dupuis J,
Morris AP,
Tai ES,
Selvin E,
Rotter JI,
Langenberg C,
Barroso I,
Meigs JB
EPIC-CVD Consortium · EPIC-InterAct Consortium 외 컨소시엄 1곳
PLoS medicine · 2017 · PMID 28898252 · open access
페이지 10개
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
Hysi PG,
Valdes AM,
Liu F,
Furlotte NA,
Evans DM,
Bataille V,
Visconti A,
Hemani G,
McMahon G,
Ring SM,
Smith GD,
Duffy DL
외 32명 — 모두 보기
Zhu G,
Gordon SD,
Medland SE,
Lin BD,
Willemsen G,
Jan Hottenga J,
Vuckovic D,
Girotto G,
Gandin I,
Sala C,
Concas MP,
Brumat M,
Gasparini P,
Toniolo D,
Cocca M,
Robino A,
Yazar S,
Hewitt AW,
Chen Y,
Zeng C,
Uitterlinden AG,
Ikram MA,
Hamer MA,
van Duijn CM,
Nijsten T,
Mackey DA,
Falchi M,
Boomsma DI,
Martin NG,
Hinds DA,
Kayser M,
Spector TD
International Visible Trait Genetics Consortium
Nature genetics · 2018 · PMID 29662168 · open access
페이지 10개
The identification of distinct protective and susceptibility mechanisms for hip osteoarthritis: findings from a genome-wide association study meta-analysis of minimum joint space width and Mendelian randomisation cluster analyses
Faber BG,
Frysz M,
Boer CG,
Evans DS,
Ebsim R,
Flynn KA,
Lundberg M,
Southam L,
Hartley A,
Saunders FR,
Lindner C,
Gregory JS
외 10명 — 모두 보기
EBioMedicine · 2023 · PMID 37619450 · open access
페이지 10개
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
Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans
Evans DS,
Avery CL,
Nalls MA,
Li G,
Barnard J,
Smith EN,
Tanaka T,
Butler AM,
Buxbaum SG,
Alonso A,
Arking DE,
Berenson GS
외 49명 — 모두 보기
Bis JC,
Buyske S,
Carty CL,
Chen W,
Chung MK,
Cummings SR,
Deo R,
Eaton CB,
Fox ER,
Heckbert SR,
Heiss G,
Hindorff LA,
Hsueh WC,
Isaacs A,
Jamshidi Y,
Kerr KF,
Liu F,
Liu Y,
Lohman KK,
Magnani JW,
Maher JF,
Mehra R,
Meng YA,
Musani SK,
Newton-Cheh C,
North KE,
Psaty BM,
Redline S,
Rotter JI,
Schnabel RB,
Schork NJ,
Shohet RV,
Singleton AB,
Smith JD,
Soliman EZ,
Srinivasan SR,
Taylor HA Jr,
Van Wagoner DR,
Wilson JG,
Young T,
Zhang ZM,
Zonderman AB,
Evans MK,
Ferrucci L,
Murray SS,
Tranah GJ,
Whitsel EA,
Reiner AP,
Sotoodehnia N
CHARGE QRS Consortium
Human molecular genetics · 2016 · PMID 27577874
페이지 9개
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,
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외 170명 — 모두 보기
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페이지 8개
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페이지 8개
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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.