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Banasik K에 대해
24건, 그중 20건 표시.
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
Winkler TW,
Justice AE,
Graff M,
Barata L,
Feitosa MF,
Chu S,
Czajkowski J,
Esko T,
Fall T,
Kilpeläinen TO,
Lu Y,
Mägi R
외 427명 — 모두 보기
Mihailov E,
Pers TH,
Rüeger S,
Teumer A,
Ehret GB,
Ferreira T,
Heard-Costa NL,
Karjalainen J,
Lagou V,
Mahajan A,
Neinast MD,
Prokopenko I,
Simino J,
Teslovich TM,
Jansen R,
Westra HJ,
White CC,
Absher D,
Ahluwalia TS,
Ahmad S,
Albrecht E,
Alves AC,
Bragg-Gresham JL,
de Craen AJ,
Bis JC,
Bonnefond A,
Boucher G,
Cadby G,
Cheng YC,
Chiang CW,
Delgado G,
Demirkan A,
Dueker N,
Eklund N,
Eiriksdottir G,
Eriksson J,
Feenstra B,
Fischer K,
Frau F,
Galesloot TE,
Geller F,
Goel A,
Gorski M,
Grammer TB,
Gustafsson S,
Haitjema S,
Hottenga JJ,
Huffman JE,
Jackson AU,
Jacobs KB,
Johansson Å,
Kaakinen M,
Kleber ME,
Lahti J,
Mateo Leach I,
Lehne B,
Liu Y,
Lo KS,
Lorentzon M,
Luan J,
Madden PA,
Mangino M,
McKnight B,
Medina-Gomez C,
Monda KL,
Montasser ME,
Müller G,
Müller-Nurasyid M,
Nolte IM,
Panoutsopoulou K,
Pascoe L,
Paternoster L,
Rayner NW,
Renström F,
Rizzi F,
Rose LM,
Ryan KA,
Salo P,
Sanna S,
Scharnagl H,
Shi J,
Smith AV,
Southam L,
Stančáková A,
Steinthorsdottir V,
Strawbridge RJ,
Sung YJ,
Tachmazidou I,
Tanaka T,
Thorleifsson G,
Trompet S,
Pervjakova N,
Tyrer JP,
Vandenput L,
van der Laan SW,
van der Velde N,
van Setten J,
van Vliet-Ostaptchouk JV,
Verweij N,
Vlachopoulou E,
Waite LL,
Wang SR,
Wang Z,
Wild SH,
Willenborg C,
Wilson JF,
Wong A,
Yang J,
Yengo L,
Yerges-Armstrong LM,
Yu L,
Zhang W,
Zhao JH,
Andersson EA,
Bakker SJ,
Baldassarre D,
Banasik K,
Barcella M,
Barlassina C,
Bellis C,
Benaglio P,
Blangero J,
Blüher M,
Bonnet F,
Bonnycastle LL,
Boyd HA,
Bruinenberg M,
Buchman AS,
Campbell H,
Chen YD,
Chines PS,
Claudi-Boehm S,
Cole J,
Collins FS,
de Geus EJ,
de Groot LC,
Dimitriou M,
Duan J,
Enroth S,
Eury E,
Farmaki AE,
Forouhi NG,
Friedrich N,
Gejman PV,
Gigante B,
Glorioso N,
Go AS,
Gottesman O,
Gräßler J,
Grallert H,
Grarup N,
Gu YM,
Broer L,
Ham AC,
Hansen T,
Harris TB,
Hartman CA,
Hassinen M,
Hastie N,
Hattersley AT,
Heath AC,
Henders AK,
Hernandez D,
Hillege H,
Holmen O,
Hovingh KG,
Hui J,
Husemoen LL,
Hutri-Kähönen N,
Hysi PG,
Illig T,
De Jager PL,
Jalilzadeh S,
Jørgensen T,
Jukema JW,
Juonala M,
Kanoni S,
Karaleftheri M,
Khaw KT,
Kinnunen L,
Kittner SJ,
Koenig W,
Kolcic I,
Kovacs P,
Krarup NT,
Kratzer W,
Krüger J,
Kuh D,
Kumari M,
Kyriakou T,
Langenberg C,
Lannfelt L,
Lanzani C,
Lotay V,
Launer LJ,
Leander K,
Lindström J,
Linneberg A,
Liu YP,
Lobbens S,
Luben R,
Lyssenko V,
Männistö S,
Magnusson PK,
McArdle WL,
Menni C,
Merger S,
Milani L,
Montgomery GW,
Morris AP,
Narisu N,
Nelis M,
Ong KK,
Palotie A,
Pérusse L,
Pichler I,
Pilia MG,
Pouta A,
Rheinberger M,
Ribel-Madsen R,
Richards M,
Rice KM,
Rice TK,
Rivolta C,
Salomaa V,
Sanders AR,
Sarzynski MA,
Scholtens S,
Scott RA,
Scott WR,
Sebert S,
Sengupta S,
Sennblad B,
Seufferlein T,
Silveira A,
Slagboom PE,
Smit JH,
Sparsø TH,
Stirrups K,
Stolk RP,
Stringham HM,
Swertz MA,
Swift AJ,
Syvänen AC,
Tan ST,
Thorand B,
Tönjes A,
Tremblay A,
Tsafantakis E,
van der Most PJ,
Völker U,
Vohl MC,
Vonk JM,
Waldenberger M,
Walker RW,
Wennauer R,
Widén E,
Willemsen G,
Wilsgaard T,
Wright AF,
Zillikens MC,
van Dijk SC,
van Schoor NM,
Asselbergs FW,
de Bakker PI,
Beckmann JS,
Beilby J,
Bennett DA,
Bergman RN,
Bergmann S,
Böger CA,
Boehm BO,
Boerwinkle E,
Boomsma DI,
Bornstein SR,
Bottinger EP,
Bouchard C,
Chambers JC,
Chanock SJ,
Chasman DI,
Cucca F,
Cusi D,
Dedoussis G,
Erdmann J,
Eriksson JG,
Evans DA,
de Faire U,
Farrall M,
Ferrucci L,
Ford I,
Franke L,
Franks PW,
Froguel P,
Gansevoort RT,
Gieger C,
Grönberg H,
Gudnason V,
Gyllensten U,
Hall P,
Hamsten A,
van der Harst P,
Hayward C,
Heliövaara M,
Hengstenberg C,
Hicks AA,
Hingorani A,
Hofman A,
Hu F,
Huikuri HV,
Hveem K,
James AL,
Jordan JM,
Jula A,
Kähönen M,
Kajantie E,
Kathiresan S,
Kiemeney LA,
Kivimaki M,
Knekt PB,
Koistinen HA,
Kooner JS,
Koskinen S,
Kuusisto J,
Maerz W,
Martin NG,
Laakso M,
Lakka TA,
Lehtimäki T,
Lettre G,
Levinson DF,
Lind L,
Lokki ML,
Mäntyselkä P,
Melbye M,
Metspalu A,
Mitchell BD,
Moll FL,
Murray JC,
Musk AW,
Nieminen MS,
Njølstad I,
Ohlsson C,
Oldehinkel AJ,
Oostra BA,
Palmer LJ,
Pankow JS,
Pasterkamp G,
Pedersen NL,
Pedersen O,
Penninx BW,
Perola M,
Peters A,
Polašek O,
Pramstaller PP,
Psaty BM,
Qi L,
Quertermous T,
Raitakari OT,
Rankinen T,
Rauramaa R,
Ridker PM,
Rioux JD,
Rivadeneira F,
Rotter JI,
Rudan I,
den Ruijter HM,
Saltevo J,
Sattar N,
Schunkert H,
Schwarz PE,
Shuldiner AR,
Sinisalo J,
Snieder H,
Sørensen TI,
Spector TD,
Staessen JA,
Stefania B,
Thorsteinsdottir U,
Stumvoll M,
Tardif JC,
Tremoli E,
Tuomilehto J,
Uitterlinden AG,
Uusitupa M,
Verbeek AL,
Vermeulen SH,
Viikari JS,
Vitart V,
Völzke H,
Vollenweider P,
Waeber G,
Walker M,
Wallaschofski H,
Wareham NJ,
Watkins H,
Zeggini E,
Chakravarti A,
Clegg DJ,
Cupples LA,
Gordon-Larsen P,
Jaquish CE,
Rao DC,
Abecasis GR,
Assimes TL,
Barroso I,
Berndt SI,
Boehnke M,
Deloukas P,
Fox CS,
Groop LC,
Hunter DJ,
Ingelsson E,
Kaplan RC,
McCarthy MI,
Mohlke KL,
O'Connell JR,
Schlessinger D,
Strachan DP,
Stefansson K,
van Duijn CM,
Hirschhorn JN,
Lindgren CM,
Heid IM,
North KE,
Borecki IB,
Kutalik Z,
Loos RJ
CHARGE Consortium · DIAGRAM Consortium 외 컨소시엄 4곳
PLoS genetics · 2015 · PMID 26426971 · open access
페이지 12개+
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles
Hautakangas H,
Winsvold BS,
Ruotsalainen SE,
Bjornsdottir G,
Harder AVE,
Kogelman LJA,
Thomas LF,
Noordam R,
Benner C,
Gormley P,
Artto V,
Banasik K
외 59명 — 모두 보기
Bjornsdottir A,
Boomsma DI,
Brumpton BM,
Burgdorf KS,
Buring JE,
Chalmer MA,
de Boer I,
Dichgans M,
Erikstrup C,
Färkkilä M,
Garbrielsen ME,
Ghanbari M,
Hagen K,
Häppölä P,
Hottenga JJ,
Hrafnsdottir MG,
Hveem K,
Johnsen MB,
Kähönen M,
Kristoffersen ES,
Kurth T,
Lehtimäki T,
Lighart L,
Magnusson SH,
Malik R,
Pedersen OB,
Pelzer N,
Penninx BWJH,
Ran C,
Ridker PM,
Rosendaal FR,
Sigurdardottir GR,
Skogholt AH,
Sveinsson OA,
Thorgeirsson TE,
Ullum H,
Vijfhuizen LS,
Widén E,
van Dijk KW,
Aromaa A,
Belin AC,
Freilinger T,
Ikram MA,
Järvelin MR,
Raitakari OT,
Terwindt GM,
Kallela M,
Wessman M,
Olesen J,
Chasman DI,
Nyholt DR,
Stefánsson H,
Stefansson K,
van den Maagdenberg AMJM,
Hansen TF,
Ripatti S,
Zwart JA,
Palotie A,
Pirinen M
International Headache Genetics Consortium · HUNT All-in Headache 외 컨소시엄 1곳
Nature genetics · 2022 · PMID 35115687 · open access
페이지 12개+
A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome
Skuladottir AT,
Bjornsdottir G,
Ferkingstad E,
Einarsson G,
Stefansdottir L,
Nawaz MS,
Oddsson A,
Olafsdottir TA,
Saevarsdottir S,
Walters GB,
Magnusson SH,
Bjornsdottir A
외 18명 — 모두 보기
Sveinsson OA,
Vikingsson A,
Hansen TF,
Jacobsen RL,
Erikstrup C,
Schwinn M,
Brunak S,
Banasik K,
Ostrowski SR,
Troelsen A,
Henkel C,
Pedersen OB,
Jonsdottir I,
Gudbjartsson DF,
Sulem P,
Thorgeirsson TE,
Stefansson H,
Stefansson K
DBDS Genetic Consortium
Nature communications · 2022 · PMID 35332129 · open access
페이지 12개+
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis
Ghouse J,
Sveinbjörnsson G,
Vujkovic M,
Seidelin AS,
Gellert-Kristensen H,
Ahlberg G,
Tragante V,
Rand SA,
Brancale J,
Vilarinho S,
Lundegaard PR,
Sørensen E
외 39명 — 모두 보기
Erikstrup C,
Bruun MT,
Jensen BA,
Brunak S,
Banasik K,
Ullum H,
Verweij N,
Lotta L,
Baras A,
Mirshahi T,
Carey DJ,
Kaplan DE,
Lynch J,
Morgan T,
Schwantes-An TH,
Dochtermann DR,
Pyarajan S,
Tsao PS,
Laisk T,
Mägi R,
Kozlitina J,
Tybjærg-Hansen A,
Jones D,
Knowlton KU,
Nadauld L,
Ferkingstad E,
Björnsson ES,
Ulfarsson MO,
Sturluson Á,
Sulem P,
Pedersen OB,
Ostrowski SR,
Gudbjartsson DF,
Stefansson K,
Olesen MS,
Chang KM,
Holm H,
Bundgaard H,
Stender S
DBDS Genomic Consortium · Regeneron Genetics Center 외 컨소시엄 3곳
Nature genetics · 2024 · PMID 38632349 · open access
페이지 12개+
Translational genomics of osteoarthritis in 1,962,069 individuals
Hatzikotoulas K,
Southam L,
Stefansdottir L,
Boer CG,
McDonald ML,
Pett JP,
Park YC,
Tuerlings M,
Mulders R,
Barysenka A,
Arruda AL,
Tragante V
외 162명 — 모두 보기
Rocco A,
Bittner N,
Chen S,
Horn S,
Srinivasasainagendra V,
To K,
Katsoula G,
Kreitmaier P,
Tenghe AMM,
Gilly A,
Arbeeva L,
Chen LG,
de Pins AM,
Dochtermann D,
Henkel C,
Höijer J,
Ito S,
Lind PA,
Lukusa-Sawalena B,
Minn AKK,
Mola-Caminal M,
Narita A,
Nguyen C,
Reimann E,
Silberstein MD,
Skogholt AH,
Tiwari HK,
Yau MS,
Yue M,
Zhao W,
Zhao W,
Zhou JJ,
Alexiadis G,
Banasik K,
Brunak S,
Campbell A,
Cheung JTS,
Dowsett J,
Faquih T,
Faul JD,
Fei L,
Fenstad AM,
Funayama T,
Gabrielsen ME,
Gocho C,
Gromov K,
Hansen T,
Hudjashov G,
Ingvarsson T,
Johnson JS,
Jonsson H,
Kakehi S,
Karjalainen J,
Kasbohm E,
Lemmelä S,
Lin K,
Liu X,
Loef M,
Mangino M,
McCartney D,
Millwood IY,
Richman J,
Roberts MB,
Ryan KA,
Samartzis D,
Shivakumar M,
Skou ST,
Sugimoto S,
Suzuki K,
Takuwa H,
Teder-Laving M,
Thomas L,
Tomizuka K,
Turman C,
Weiss S,
Wu TT,
Zengini E,
Zhang Y,
Ferreira MAR,
Babis G,
Baras A,
Barker T,
Carey DJ,
Cheah KSE,
Chen Z,
Cheung JP,
Daly M,
de Mutsert R,
Eaton CB,
Erikstrup C,
Furnes ON,
Golightly YM,
Gudbjartsson DF,
Hailer NP,
Hayward C,
Hochberg MC,
Homuth G,
Huckins LM,
Hveem K,
Ikegawa S,
Ishijima M,
Isomura M,
Jones M,
Kang JH,
Kardia SLR,
Kloppenburg M,
Kraft P,
Kumahashi N,
Kuwata S,
Lee MTM,
Lee PH,
Lerner R,
Li L,
Lietman SA,
Lotta L,
Lupton MK,
Mägi R,
Martin NG,
McAlindon TE,
Medland SE,
Michaëlsson K,
Mitchell BD,
Mook-Kanamori DO,
Morris AP,
Nabika T,
Nagami F,
Nelson AE,
Ostrowski SR,
Palotie A,
Pedersen OB,
Rosendaal FR,
Sakurai-Yageta M,
Schmidt CO,
Sham PC,
Singh JA,
Smelser DT,
Smith JA,
Song YQ,
Sørensen E,
Tamiya G,
Tamura Y,
Terao C,
Thorleifsson G,
Troelsen A,
Tsezou A,
Uchio Y,
Uitterlinden AG,
Ullum H,
Valdes AM,
van Heel DA,
Walters RG,
Weir DR,
Wilkinson JM,
Winsvold BS,
Yamamoto M,
Zwart JA,
Stefansson K,
Meulenbelt I,
Teichmann SA,
van Meurs JBJ,
Styrkarsdottir U,
Zeggini E
arcOGEN Consortium · ARGO Consortium 외 컨소시엄 7곳
Nature · 2025 · PMID 40205036 · open access
페이지 12개+
Genome-wide analyses identify 25 infertility loci and relationships with reproductive traits across the allele frequency spectrum
Venkatesh SS,
Wittemans LBL,
Palmer DS,
Baya NA,
Ferreira T,
Hill B,
Lassen FH,
Parker MJ,
Reibe S,
Elhakeem A,
Banasik K,
Bruun MT
외 39명 — 모두 보기
Erikstrup C,
Aagard Jensen B,
Juul A,
Mikkelsen C,
Nielsen HS,
Ostrowski SR,
Pedersen OB,
Rohde PD,
Sørensen E,
Ullum H,
Westergaard D,
Haraldsson A,
Holm H,
Jonsdottir I,
Olafsson I,
Steingrimsdottir T,
Steinthorsdottir V,
Thorleifsson G,
Figueredo J,
Karjalainen MK,
Pasanen A,
Jacobs BM,
Kalantzis G,
Hubers N,
Lippincott M,
Fraser A,
Lawlor DA,
Timpson NJ,
Nyegaard M,
Stefansson K,
Magi R,
Laivuori H,
van Heel DA,
Boomsma DI,
Balasubramanian R,
Seminara SB,
Chan YM,
Laisk T,
Lindgren CM
Genes & Health Research Team · Estonian Biobank Research Team 외 컨소시엄 3곳
Nature genetics · 2025 · PMID 40229599 · open access
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 11개
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
Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology
Bjornsdottir G,
Stefansdottir L,
Thorleifsson G,
Sulem P,
Norland K,
Ferkingstad E,
Oddsson A,
Zink F,
Lund SH,
Nawaz MS,
Bragi Walters G,
Skuladottir AT
외 32명 — 모두 보기
Gudjonsson SA,
Einarsson G,
Halldorsson GH,
Bjarnadottir V,
Sveinbjornsson G,
Helgadottir A,
Styrkarsdottir U,
Gudmundsson LJ,
Pedersen OB,
Hansen TF,
Werge T,
Banasik K,
Troelsen A,
Skou ST,
Thørner LW,
Erikstrup C,
Nielsen KR,
Mikkelsen S,
Jonsdottir I,
Bjornsson A,
Olafsson IH,
Ulfarsson E,
Blondal J,
Vikingsson A,
Brunak S,
Ostrowski SR,
Ullum H,
Thorsteinsdottir U,
Stefansson H,
Gudbjartsson DF,
Thorgeirsson TE,
Stefansson K
DBDS Genetic Consortium · GO Consortium
Nature communications · 2022 · PMID 35110524 · open access
페이지 8개
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
Rahmioglu N,
Mortlock S,
Ghiasi M,
Møller PL,
Stefansdottir L,
Galarneau G,
Turman C,
Danning R,
Law MH,
Sapkota Y,
Christofidou P,
Skarp S
외 121명 — 모두 보기
Giri A,
Banasik K,
Krassowski M,
Lepamets M,
Marciniak B,
Nõukas M,
Perro D,
Sliz E,
Sobalska-Kwapis M,
Thorleifsson G,
Topbas-Selcuki NF,
Vitonis A,
Westergaard D,
Arnadottir R,
Burgdorf KS,
Campbell A,
Cheuk CSK,
Clementi C,
Cook J,
De Vivo I,
DiVasta A,
Dorien O,
Donoghue JF,
Edwards T,
Fontanillas P,
Fung JN,
Geirsson RT,
Girling JE,
Harkki P,
Harris HR,
Healey M,
Heikinheimo O,
Holdsworth-Carson S,
Hostettler IC,
Houlden H,
Houshdaran S,
Irwin JC,
Jarvelin MR,
Kamatani Y,
Kennedy SH,
Kepka E,
Kettunen J,
Kubo M,
Kulig B,
Kurra V,
Laivuori H,
Laufer MR,
Lindgren CM,
MacGregor S,
Mangino M,
Martin NG,
Matalliotaki C,
Matalliotakis M,
Murray AD,
Ndungu A,
Nezhat C,
Olsen CM,
Opoku-Anane J,
Padmanabhan S,
Paranjpe M,
Peters M,
Polak G,
Porteous DJ,
Rabban J,
Rexrode KM,
Romanowicz H,
Saare M,
Saavalainen L,
Schork AJ,
Sen S,
Shafrir AL,
Siewierska-Górska A,
Słomka M,
Smith BH,
Smolarz B,
Szaflik T,
Szyłło K,
Takahashi A,
Terry KL,
Tomassetti C,
Treloar SA,
Vanhie A,
Vincent K,
Vo KC,
Werring DJ,
Zeggini E,
Zervou MI,
Adachi S,
Buring JE,
Ridker PM,
D'Hooghe T,
Goulielmos GN,
Hapangama DK,
Hayward C,
Horne AW,
Low SK,
Martikainen H,
Chasman DI,
Rogers PAW,
Saunders PT,
Sirota M,
Spector T,
Strapagiel D,
Tung JY,
Whiteman DC,
Giudice LC,
Velez-Edwards DR,
Uimari O,
Kraft P,
Salumets A,
Nyholt DR,
Mägi R,
Stefansson K,
Becker CM,
Yurttas-Beim P,
Steinthorsdottir V,
Nyegaard M,
Missmer SA,
Montgomery GW,
Morris AP,
Zondervan KT
DBDS Genomic Consortium · FinnGen Study 외 컨소시엄 3곳
Nature genetics · 2023 · PMID 36914876
페이지 8개
Genome-wide meta-analysis identifies genetic drivers of bile acid metabolism in intrahepatic cholestasis of pregnancy
Tyrmi JS,
Karjalainen J,
Venkatesh SS,
Benoit-Pilven C,
Lemmelä SM,
Brunak S,
Aagaard B,
Bruun MT,
Erikstrup C,
Ullum H,
Pedersen OB,
Banasik K
외 19명 — 모두 보기
Sørensen E,
Mikkelsen C,
Schwinn M,
Sturluson A,
Ostrowski SR,
Kettunen J,
Nielsen HS,
Nyegaard M,
Westergaard D,
Rafnar T,
Sulem P,
Stefansson K,
Palta P,
Laisk T,
Tukiainen T,
Lindgren CM,
Daly M,
Havulinna AS,
Laivuori HM
FinnGen · Estonian Biobank research team 외 컨소시엄 1곳
Nature communications · 2026 · PMID 42178310 · open access
페이지 8개
GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis
Skuladottir AT,
Stefansdottir L,
Halldorsson GH,
Stefansson OA,
Bjornsdottir A,
Jonsson P,
Palmadottir V,
Thorgeirsson TE,
Walters GB,
Gisladottir RS,
Bjornsdottir G,
Jonsdottir GA
외 20명 — 모두 보기
Sulem P,
Gudbjartsson DF,
Knowlton KU,
Jones DA,
Ottas A,
Pedersen OB,
Didriksen M,
Brunak S,
Banasik K,
Hansen TF,
Erikstrup C,
Haavik J,
Andreassen OA,
Rye D,
Igland J,
Ostrowski SR,
Milani LA,
Nadauld LD,
Stefansson H,
Stefansson K
Estonian Biobank · DBDS Genomic Consortium
Communications biology · 2024 · PMID 38671141 · open access
페이지 7개
Genetic insight into sick sinus syndrome
Thorolfsdottir RB,
Sveinbjornsson G,
Aegisdottir HM,
Benonisdottir S,
Stefansdottir L,
Ivarsdottir EV,
Halldorsson GH,
Sigurdsson JK,
Torp-Pedersen C,
Weeke PE,
Brunak S,
Westergaard D
외 32명 — 모두 보기
Pedersen OB,
Sorensen E,
Nielsen KR,
Burgdorf KS,
Banasik K,
Brumpton B,
Zhou W,
Oddsson A,
Tragante V,
Hjorleifsson KE,
Davidsson OB,
Rajamani S,
Jonsson S,
Torfason B,
Valgardsson AS,
Thorgeirsson G,
Frigge ML,
Thorleifsson G,
Norddahl GL,
Helgadottir A,
Gretarsdottir S,
Sulem P,
Jonsdottir I,
Willer CJ,
Hveem K,
Bundgaard H,
Ullum H,
Arnar DO,
Thorsteinsdottir U,
Gudbjartsson DF,
Holm H,
Stefansson K
DBDS Genomic Consortium
European heart journal · 2021 · PMID 33580673 · open access
페이지 5개
Detailed stratified GWAS analysis for severe COVID-19 in four European populations
Degenhardt F,
Ellinghaus D,
Juzenas S,
Lerga-Jaso J,
Wendorff M,
Maya-Miles D,
Uellendahl-Werth F,
ElAbd H,
Rühlemann MC,
Arora J,
Özer O,
Lenning OB
외 317명 — 모두 보기
Myhre R,
Vadla MS,
Wacker EM,
Wienbrandt L,
Blandino Ortiz A,
de Salazar A,
Garrido Chercoles A,
Palom A,
Ruiz A,
Garcia-Fernandez AE,
Blanco-Grau A,
Mantovani A,
Zanella A,
Holten AR,
Mayer A,
Bandera A,
Cherubini A,
Protti A,
Aghemo A,
Gerussi A,
Ramirez A,
Braun A,
Nebel A,
Barreira A,
Lleo A,
Teles A,
Kildal AB,
Biondi A,
Caballero-Garralda A,
Ganna A,
Gori A,
Glück A,
Lind A,
Tanck A,
Hinney A,
Carreras Nolla A,
Fracanzani AL,
Peschuck A,
Cavallero A,
Dyrhol-Riise AM,
Ruello A,
Julià A,
Muscatello A,
Pesenti A,
Voza A,
Rando-Segura A,
Solier A,
Schmidt A,
Cortes B,
Mateos B,
Nafria-Jimenez B,
Schaefer B,
Jensen B,
Bellinghausen C,
Maj C,
Ferrando C,
de la Horra C,
Quereda C,
Skurk C,
Thibeault C,
Scollo C,
Herr C,
Spinner CD,
Gassner C,
Lange C,
Hu C,
Paccapelo C,
Lehmann C,
Angelini C,
Cappadona C,
Azuure C,
Bianco C,
Cea C,
Sancho C,
Hoff DAL,
Galimberti D,
Prati D,
Haschka D,
Jiménez D,
Pestaña D,
Toapanta D,
Muñiz-Diaz E,
Azzolini E,
Sandoval E,
Binatti E,
Scarpini E,
Helbig ET,
Casalone E,
Urrechaga E,
Paraboschi EM,
Pontali E,
Reverter E,
Calderón EJ,
Navas E,
Solligård E,
Contro E,
Arana-Arri E,
Aziz F,
Garcia F,
García Sánchez F,
Ceriotti F,
Martinelli-Boneschi F,
Peyvandi F,
Kurth F,
Blasi F,
Malvestiti F,
Medrano FJ,
Mesonero F,
Rodriguez-Frias F,
Hanses F,
Müller F,
Hemmrich-Stanisak G,
Bellani G,
Grasselli G,
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Costantino G,
Albano G,
Cardamone G,
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Foti G,
Lamorte G,
Matullo G,
Baselli G,
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Neb H,
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de Rojas I,
Galván-Femenia I,
Holter JC,
Afset JE,
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Kässens J,
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Schröder J,
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Sumoy L,
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Lippert LJ,
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Kogevinas M,
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Berger MM,
Schaefer M,
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Gutiérrez-Stampa MA,
Carrabba M,
Figuera Basso ME,
Valsecchi MG,
Hernandez-Tejero M,
Vehreschild MJGT,
Manunta M,
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Grimsrud MM,
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Marquié M,
Castoldi M,
Cordioli M,
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Augustin M,
Tomasi M,
Boada M,
Dreher M,
Seilmaier MJ,
Joannidis M,
Wittig M,
Mazzocco M,
Ciccarelli M,
Rodríguez-Gandía M,
Bocciolone M,
Miozzo M,
Imaz Ayo N,
Blay N,
Chueca N,
Montano N,
Braun N,
Ludwig N,
Marx N,
Martínez N,
Cornely OA,
Witzke O,
Palmieri O,
Faverio P,
Preatoni P,
Bonfanti P,
Omodei P,
Tentorio P,
Castro P,
Rodrigues PM,
España PP,
Hoffmann P,
Rosenstiel P,
Schommers P,
Suwalski P,
de Pablo R,
Ferrer R,
Bals R,
Gualtierotti R,
Gallego-Durán R,
Nieto R,
Carpani R,
Morilla R,
Badalamenti S,
Haider S,
Ciesek S,
May S,
Bombace S,
Marsal S,
Pigazzini S,
Klein S,
Pelusi S,
Wilfling S,
Bosari S,
Volland S,
Brunak S,
Raychaudhuri S,
Schreiber S,
Heilmann-Heimbach S,
Aliberti S,
Ripke S,
Dudman S,
Wesse T,
Zheng T,
Bahmer T,
Eggermann T,
Illig T,
Brenner T,
Pumarola T,
Feldt T,
Folseraas T,
Gonzalez Cejudo T,
Landmesser U,
Protzer U,
Hehr U,
Rimoldi V,
Monzani V,
Skogen V,
Keitel V,
Kopfnagel V,
Friaza V,
Andrade V,
Moreno V,
Albrecht W,
Peter W,
Poller W,
Farre X,
Yi X,
Wang X,
Khodamoradi Y,
Karadeniz Z,
Latiano A,
Goerg S,
Bacher P,
Koehler P,
Tran F,
Zoller H,
Schulte EC,
Heidecker B,
Ludwig KU,
Fernández J,
Romero-Gómez M,
Albillos A,
Invernizzi P,
Buti M,
Duga S,
Bujanda L,
Hov JR,
Lenz TL,
Asselta R,
de Cid R,
Valenti L,
Karlsen TH,
Cáceres M,
Franke A
COVICAT study group, Aachen Study (COVAS) · Norwegian SARS-CoV-2 Study group 외 컨소시엄 2곳
Human molecular genetics · 2022 · PMID 35848942 · open access
페이지 5개
Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease
Zheng T,
Ellinghaus D,
Juzenas S,
Cossais F,
Burmeister G,
Mayr G,
Jørgensen IF,
Teder-Laving M,
Skogholt AH,
Chen S,
Strege PR,
Ito G
외 73명 — 모두 보기
Banasik K,
Becker T,
Bokelmann F,
Brunak S,
Buch S,
Clausnitzer H,
Datz C,
Degenhardt F,
Doniec M,
Erikstrup C,
Esko T,
Forster M,
Frey N,
Fritsche LG,
Gabrielsen ME,
Gräßle T,
Gsur A,
Gross J,
Hampe J,
Hendricks A,
Hinz S,
Hveem K,
Jongen J,
Junker R,
Karlsen TH,
Hemmrich-Stanisak G,
Kruis W,
Kupcinskas J,
Laubert T,
Rosenstiel PC,
Röcken C,
Laudes M,
Leendertz FH,
Lieb W,
Limperger V,
Margetis N,
Mätz-Rensing K,
Németh CG,
Ness-Jensen E,
Nowak-Göttl U,
Pandit A,
Pedersen OB,
Peleikis HG,
Peuker K,
Rodriguez CL,
Rühlemann MC,
Schniewind B,
Schulzky M,
Skieceviciene J,
Tepel J,
Thomas L,
Uellendahl-Werth F,
Ullum H,
Vogel I,
Volzke H,
von Fersen L,
von Schönfels W,
Vanderwerff B,
Wilking J,
Wittig M,
Zeissig S,
Zobel M,
Zawistowski M,
Vacic V,
Sazonova O,
Noblin ES,
Farrugia G,
Beyder A,
Wedel T,
Kahlke V,
Schafmayer C,
D'Amato M,
Franke A
DBDS Consortium · 23andMe Research Team
Gut · 2021 · PMID 33888516 · open access
페이지 4개
Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genes
Skotte L,
Fadista J,
Bybjerg-Grauholm J,
Appadurai V,
Hildebrand MS,
Hansen TF,
Banasik K,
Grove J,
Albiñana C,
Geller F,
Bjurström CF,
Vilhjálmsson BJ
외 27명 — 모두 보기
Coleman M,
Damiano JA,
Burgess R,
Scheffer IE,
Pedersen OBV,
Erikstrup C,
Westergaard D,
Nielsen KR,
Sørensen E,
Bruun MT,
Liu X,
Hjalgrim H,
Pers TH,
Mortensen PB,
Mors O,
Nordentoft M,
Dreier JW,
Børglum AD,
Christensen J,
Hougaard DM,
Buil A,
Hviid A,
Melbye M,
Ullum H,
Berkovic SF,
Werge T,
Feenstra B
Brain : a journal of neurology · 2022 · PMID 35022648 · open access
페이지 4개
Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis
Hindy G,
Tyrrell DJ,
Vasbinder A,
Wei C,
Presswalla F,
Wang H,
Blakely P,
Ozel AB,
Graham S,
Holton GH,
Dowsett J,
Fahed AC
외 30명 — 모두 보기
Amadi KM,
Erne GK,
Tekmulla A,
Ismail A,
Launius C,
Sotoodehnia N,
Pankow JS,
Thørner LW,
Erikstrup C,
Pedersen OB,
Banasik K,
Brunak S,
Ullum H,
Eugen-Olsen J,
Ostrowski SR,
Haas ME,
Nielsen JB,
Lotta LA,
Engström G,
Melander O,
Orho-Melander M,
Zhao L,
Murthy VL,
Pinsky DJ,
Willer CJ,
Heckbert SR,
Reiser J,
Goldstein DR,
Desch KC,
Hayek SS
DBDS Consortium · Regeneron Genetics Center
The Journal of clinical investigation · 2022 · PMID 36194491 · open access
페이지 4개
Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset
Saevarsdottir S,
Stefansdottir L,
Sulem P,
Thorleifsson G,
Ferkingstad E,
Rutsdottir G,
Glintborg B,
Westerlind H,
Grondal G,
Loft IC,
Sorensen SB,
Lie BA
외 66명 — 모두 보기
Brink M,
Ärlestig L,
Arnthorsson AO,
Baecklund E,
Banasik K,
Bank S,
Bjorkman LI,
Ellingsen T,
Erikstrup C,
Frei O,
Gjertsson I,
Gudbjartsson DF,
Gudjonsson SA,
Halldorsson GH,
Hendricks O,
Hillert J,
Hogdall E,
Jacobsen S,
Jensen DV,
Jonsson H,
Kastbom A,
Kockum I,
Kristensen S,
Kristjansdottir H,
Larsen MH,
Linauskas A,
Hauge EM,
Loft AG,
Ludviksson BR,
Lund SH,
Markusson T,
Masson G,
Melsted P,
Moore KHS,
Munk H,
Nielsen KR,
Norddahl GL,
Oddsson A,
Olafsdottir TA,
Olason PI,
Olsson T,
Ostrowski SR,
Hørslev-Petersen K,
Rognvaldsson S,
Sanner H,
Silberberg GN,
Stefansson H,
Sørensen E,
Sørensen IJ,
Turesson C,
Bergman T,
Alfredsson L,
Kvien TK,
Brunak S,
Steinsson K,
Andersen V,
Andreassen OA,
Rantapää-Dahlqvist S,
Hetland ML,
Klareskog L,
Askling J,
Padyukov L,
Pedersen OB,
Thorsteinsdottir U,
Jonsdottir I,
Stefansson K
Members of the DBDS Genomic Consortium · Danish RA Genetics Working Group 외 컨소시엄 1곳
Annals of the rheumatic diseases · 2022 · PMID 35470158 · open access
페이지 3개
A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants
Wood AR,
Jonsson A,
Jackson AU,
Wang N,
van Leewen N,
Palmer ND,
Kobes S,
Deelen J,
Boquete-Vilarino L,
Paananen J,
Stančáková A,
Boomsma DI
외 40명 — 모두 보기
de Geus EJC,
Eekhoff EMW,
Fritsche A,
Kramer M,
Nijpels G,
Simonis-Bik A,
van Haeften TW,
Mahajan A,
Boehnke M,
Bergman RN,
Tuomilehto J,
Collins FS,
Mohlke KL,
Banasik K,
Groves CJ,
McCarthy MI,
Pearson ER,
Natali A,
Mari A,
Buchanan TA,
Taylor KD,
Xiang AH,
Xiang AH,
Gjesing AP,
Grarup N,
Eiberg H,
Pedersen O,
Chen YD,
Laakso M,
Norris JM,
Smith U,
Wagenknecht LE,
Baier L,
Bowden DW,
Hansen T,
Walker M,
Watanabe RM,
't Hart LM,
Hanson RL,
Frayling TM
Diabetes Research on Patient Stratification (DIRECT)
Diabetes · 2017 · PMID 28490609 · open access
페이지 2개
Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci
Ghouse J,
Tragante V,
Muhammad A,
Ahlberg G,
Skov MW,
Roden DM,
Jonsdottir I,
Andreasen L,
Lundegaard PR,
Trudsø LC,
Banasik K,
Brunak S
외 15명 — 모두 보기
Ostrowski SR,
Torp-Pedersen C,
Pedersen OV,
Sørensen E,
Køber L,
Iversen K,
Thorsteinsdottir U,
Thorgeirsson G,
Ullum H,
Gudbjartsson DF,
Mosley JD,
Holm H,
Stefansson K,
Bundgaard H,
Olesen MS
eMERGE consortium
European heart journal · 2022 · PMID 35751511
페이지 2개
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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.