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성함이나 학술지명, PMID로 찾아보십시오.
Eisele L에 대해
7건.
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
Arking DE,
Pulit SL,
Crotti L,
van der Harst P,
Munroe PB,
Koopmann TT,
Sotoodehnia N,
Rossin EJ,
Morley M,
Wang X,
Johnson AD,
Lundby A
외 218명 — 모두 보기
Gudbjartsson DF,
Noseworthy PA,
Eijgelsheim M,
Bradford Y,
Tarasov KV,
Dörr M,
Müller-Nurasyid M,
Lahtinen AM,
Nolte IM,
Smith AV,
Bis JC,
Isaacs A,
Newhouse SJ,
Evans DS,
Post WS,
Waggott D,
Lyytikäinen LP,
Hicks AA,
Eisele L,
Ellinghaus D,
Hayward C,
Navarro P,
Ulivi S,
Tanaka T,
Tester DJ,
Chatel S,
Gustafsson S,
Kumari M,
Morris RW,
Naluai ÅT,
Padmanabhan S,
Kluttig A,
Strohmer B,
Panayiotou AG,
Torres M,
Knoflach M,
Hubacek JA,
Slowikowski K,
Raychaudhuri S,
Kumar RD,
Harris TB,
Launer LJ,
Shuldiner AR,
Alonso A,
Bader JS,
Ehret G,
Huang H,
Kao WH,
Strait JB,
Macfarlane PW,
Brown M,
Caulfield MJ,
Samani NJ,
Kronenberg F,
Willeit J,
Smith JG,
Greiser KH,
Meyer Zu Schwabedissen H,
Werdan K,
Carella M,
Zelante L,
Heckbert SR,
Psaty BM,
Rotter JI,
Kolcic I,
Polašek O,
Wright AF,
Griffin M,
Daly MJ,
Arnar DO,
Hólm H,
Thorsteinsdottir U,
Denny JC,
Roden DM,
Zuvich RL,
Emilsson V,
Plump AS,
Larson MG,
O'Donnell CJ,
Yin X,
Bobbo M,
D'Adamo AP,
Iorio A,
Sinagra G,
Carracedo A,
Cummings SR,
Nalls MA,
Jula A,
Kontula KK,
Marjamaa A,
Oikarinen L,
Perola M,
Porthan K,
Erbel R,
Hoffmann P,
Jöckel KH,
Kälsch H,
Nöthen MM,
den Hoed M,
Loos RJ,
Thelle DS,
Gieger C,
Meitinger T,
Perz S,
Peters A,
Prucha H,
Sinner MF,
Waldenberger M,
de Boer RA,
Franke L,
van der Vleuten PA,
Beckmann BM,
Martens E,
Bardai A,
Hofman N,
Wilde AA,
Behr ER,
Dalageorgou C,
Giudicessi JR,
Medeiros-Domingo A,
Barc J,
Kyndt F,
Probst V,
Ghidoni A,
Insolia R,
Hamilton RM,
Scherer SW,
Brandimarto J,
Margulies K,
Moravec CE,
del Greco M F,
Fuchsberger C,
O'Connell JR,
Lee WK,
Watt GC,
Campbell H,
Wild SH,
El Mokhtari NE,
Frey N,
Asselbergs FW,
Mateo Leach I,
Navis G,
van den Berg MP,
van Veldhuisen DJ,
Kellis M,
Krijthe BP,
Franco OH,
Hofman A,
Kors JA,
Uitterlinden AG,
Witteman JC,
Kedenko L,
Lamina C,
Oostra BA,
Abecasis GR,
Lakatta EG,
Mulas A,
Orrú M,
Schlessinger D,
Uda M,
Markus MR,
Völker U,
Snieder H,
Spector TD,
Ärnlöv J,
Lind L,
Sundström J,
Syvänen AC,
Kivimaki M,
Kähönen M,
Mononen N,
Raitakari OT,
Viikari JS,
Adamkova V,
Kiechl S,
Brion M,
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Paulweber B,
Haerting J,
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Nyberg F,
Whincup PH,
Hingorani AD,
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Bezzina CR,
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Wilson JF,
Rudan I,
Franke A,
Mühleisen TW,
Pramstaller PP,
Lehtimäki TJ,
Paterson AD,
Parsa A,
Liu Y,
van Duijn CM,
Siscovick DS,
Gudnason V,
Jamshidi Y,
Salomaa V,
Felix SB,
Sanna S,
Ritchie MD,
Stricker BH,
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Cappola TP,
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Schwartz PJ,
Kääb S,
Chakravarti A,
Ackerman MJ,
Pfeufer A,
de Bakker PI,
Newton-Cheh C
CARe Consortium · COGENT Consortium 외 컨소시엄 3곳
Nature genetics · 2014 · PMID 24952745 · open access
페이지 12개+
Genome-wide association study identifies 74 loci associated with educational attainment
Okbay A,
Beauchamp JP,
Fontana MA,
Lee JJ,
Pers TH,
Rietveld CA,
Turley P,
Chen GB,
Emilsson V,
Meddens SF,
Oskarsson S,
Pickrell JK
외 243명 — 모두 보기
Thom K,
Timshel P,
de Vlaming R,
Abdellaoui A,
Ahluwalia TS,
Bacelis J,
Baumbach C,
Bjornsdottir G,
Brandsma JH,
Pina Concas M,
Derringer J,
Furlotte NA,
Galesloot TE,
Girotto G,
Gupta R,
Hall LM,
Harris SE,
Hofer E,
Horikoshi M,
Huffman JE,
Kaasik K,
Kalafati IP,
Karlsson R,
Kong A,
Lahti J,
van der Lee SJ,
deLeeuw C,
Lind PA,
Lindgren KO,
Liu T,
Mangino M,
Marten J,
Mihailov E,
Miller MB,
van der Most PJ,
Oldmeadow C,
Payton A,
Pervjakova N,
Peyrot WJ,
Qian Y,
Raitakari O,
Rueedi R,
Salvi E,
Schmidt B,
Schraut KE,
Shi J,
Smith AV,
Poot RA,
St Pourcain B,
Teumer A,
Thorleifsson G,
Verweij N,
Vuckovic D,
Wellmann J,
Westra HJ,
Yang J,
Zhao W,
Zhu Z,
Alizadeh BZ,
Amin N,
Bakshi A,
Baumeister SE,
Biino G,
Bønnelykke K,
Boyle PA,
Campbell H,
Cappuccio FP,
Davies G,
De Neve JE,
Deloukas P,
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Ding J,
Eibich P,
Eisele L,
Eklund N,
Evans DM,
Faul JD,
Feitosa MF,
Forstner AJ,
Gandin I,
Gunnarsson B,
Halldórsson BV,
Harris TB,
Heath AC,
Hocking LJ,
Holliday EG,
Homuth G,
Horan MA,
Hottenga JJ,
de Jager PL,
Joshi PK,
Jugessur A,
Kaakinen MA,
Kähönen M,
Kanoni S,
Keltigangas-Järvinen L,
Kiemeney LA,
Kolcic I,
Koskinen S,
Kraja AT,
Kroh M,
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Latvala A,
Launer LJ,
Lebreton MP,
Levinson DF,
Lichtenstein P,
Lichtner P,
Liewald DC,
Loukola A,
Madden PA,
Mägi R,
Mäki-Opas T,
Marioni RE,
Marques-Vidal P,
Meddens GA,
McMahon G,
Meisinger C,
Meitinger T,
Milaneschi Y,
Milani L,
Montgomery GW,
Myhre R,
Nelson CP,
Nyholt DR,
Ollier WE,
Palotie A,
Paternoster L,
Pedersen NL,
Petrovic KE,
Porteous DJ,
Räikkönen K,
Ring SM,
Robino A,
Rostapshova O,
Rudan I,
Rustichini A,
Salomaa V,
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Sarin AP,
Schmidt H,
Scott RJ,
Smith BH,
Smith JA,
Staessen JA,
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Strauch K,
Terracciano A,
Tobin MD,
Ulivi S,
Vaccargiu S,
Quaye L,
van Rooij FJ,
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Vozzi D,
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Attia JR,
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Berger K,
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Boomsma DI,
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Chabris CF,
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van Duijn CM,
Eriksson JG,
Franke B,
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Gieger C,
Grabe HJ,
Gratten J,
Groenen PJ,
Gudnason V,
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Hoffmann W,
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Iacono WG,
Jacobsson B,
Järvelin MR,
Jöckel KH,
Kaprio J,
Kardia SL,
Lehtimäki T,
Lehrer SF,
Magnusson PK,
Martin NG,
McGue M,
Metspalu A,
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Penninx BW,
Perola M,
Pirastu N,
Pirastu M,
Polasek O,
Posthuma D,
Power C,
Province MA,
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Schlessinger D,
Schmidt R,
Sørensen TI,
Spector TD,
Stefansson K,
Thorsteinsdottir U,
Thurik AR,
Timpson NJ,
Tiemeier H,
Tung JY,
Uitterlinden AG,
Vitart V,
Vollenweider P,
Weir DR,
Wilson JF,
Wright AF,
Conley DC,
Krueger RF,
Davey Smith G,
Hofman A,
Laibson DI,
Medland SE,
Meyer MN,
Yang J,
Johannesson M,
Visscher PM,
Esko T,
Koellinger PD,
Cesarini D,
Benjamin DJ
LifeLines Cohort Study
Nature · 2016 · PMID 27225129 · open access
페이지 12개+
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
Christophersen IE,
Rienstra M,
Roselli C,
Yin X,
Geelhoed B,
Barnard J,
Lin H,
Arking DE,
Smith AV,
Albert CM,
Chaffin M,
Tucker NR
외 150명 — 모두 보기
Li M,
Klarin D,
Bihlmeyer NA,
Low SK,
Weeke PE,
Müller-Nurasyid M,
Smith JG,
Brody JA,
Niemeijer MN,
Dörr M,
Trompet S,
Huffman J,
Gustafsson S,
Schurmann C,
Kleber ME,
Lyytikäinen LP,
Seppälä I,
Malik R,
Horimoto ARVR,
Perez M,
Sinisalo J,
Aeschbacher S,
Thériault S,
Yao J,
Radmanesh F,
Weiss S,
Teumer A,
Choi SH,
Weng LC,
Clauss S,
Deo R,
Rader DJ,
Shah SH,
Sun A,
Hopewell JC,
Debette S,
Chauhan G,
Yang Q,
Worrall BB,
Paré G,
Kamatani Y,
Hagemeijer YP,
Verweij N,
Siland JE,
Kubo M,
Smith JD,
Van Wagoner DR,
Bis JC,
Perz S,
Psaty BM,
Ridker PM,
Magnani JW,
Harris TB,
Launer LJ,
Shoemaker MB,
Padmanabhan S,
Haessler J,
Bartz TM,
Waldenberger M,
Lichtner P,
Arendt M,
Krieger JE,
Kähönen M,
Risch L,
Mansur AJ,
Peters A,
Smith BH,
Lind L,
Scott SA,
Lu Y,
Bottinger EB,
Hernesniemi J,
Lindgren CM,
Wong JA,
Huang J,
Eskola M,
Morris AP,
Ford I,
Reiner AP,
Delgado G,
Chen LY,
Chen YI,
Sandhu RK,
Li M,
Boerwinkle E,
Eisele L,
Lannfelt L,
Rost N,
Anderson CD,
Taylor KD,
Campbell A,
Magnusson PK,
Porteous D,
Hocking LJ,
Vlachopoulou E,
Pedersen NL,
Nikus K,
Orho-Melander M,
Hamsten A,
Heeringa J,
Denny JC,
Kriebel J,
Darbar D,
Newton-Cheh C,
Shaffer C,
Macfarlane PW,
Heilmann-Heimbach S,
Almgren P,
Huang PL,
Sotoodehnia N,
Soliman EZ,
Uitterlinden AG,
Hofman A,
Franco OH,
Völker U,
Jöckel KH,
Sinner MF,
Lin HJ,
Guo X,
Dichgans M,
Ingelsson E,
Kooperberg C,
Melander O,
Loos RJF,
Laurikka J,
Conen D,
Rosand J,
van der Harst P,
Lokki ML,
Kathiresan S,
Pereira A,
Jukema JW,
Hayward C,
Rotter JI,
März W,
Lehtimäki T,
Stricker BH,
Chung MK,
Felix SB,
Gudnason V,
Alonso A,
Roden DM,
Kääb S,
Chasman DI,
Heckbert SR,
Benjamin EJ,
Tanaka T,
Lunetta KL,
Lubitz SA,
Ellinor PT
METASTROKE Consortium of the ISGC · Neurology Working Group of the CHARGE Consortium 외 컨소시엄 1곳
Nature genetics · 2017 · PMID 28416818
페이지 12개+
Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci
Law PJ,
Sud A,
Mitchell JS,
Henrion M,
Orlando G,
Lenive O,
Broderick P,
Speedy HE,
Johnson DC,
Kaiser M,
Weinhold N,
Cooke R
외 29명 — 모두 보기
Sunter NJ,
Jackson GH,
Summerfield G,
Harris RJ,
Pettitt AR,
Allsup DJ,
Carmichael J,
Bailey JR,
Pratt G,
Rahman T,
Pepper C,
Fegan C,
von Strandmann EP,
Engert A,
Försti A,
Chen B,
Filho MI,
Thomsen H,
Hoffmann P,
Noethen MM,
Eisele L,
Jöckel KH,
Allan JM,
Swerdlow AJ,
Goldschmidt H,
Catovsky D,
Morgan GJ,
Hemminki K,
Houlston RS
Scientific reports · 2017 · PMID 28112199 · open access
페이지 3개
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk
Chubb D,
Weinhold N,
Broderick P,
Chen B,
Johnson DC,
Försti A,
Vijayakrishnan J,
Migliorini G,
Dobbins SE,
Holroyd A,
Hose D,
Walker BA
외 23명 — 모두 보기
Davies FE,
Gregory WA,
Jackson GH,
Irving JA,
Pratt G,
Fegan C,
Fenton JA,
Neben K,
Hoffmann P,
Nöthen MM,
Mühleisen TW,
Eisele L,
Ross FM,
Straka C,
Einsele H,
Langer C,
Dörner E,
Allan JM,
Jauch A,
Morgan GJ,
Hemminki K,
Houlston RS,
Goldschmidt H
Nature genetics · 2013 · PMID 23955597 · open access
페이지 2개
Common variation at 10p12.31 near MLLT10 influences meningioma risk
Dobbins SE,
Broderick P,
Melin B,
Feychting M,
Johansen C,
Andersson U,
Brännström T,
Schramm J,
Olver B,
Lloyd A,
Ma YP,
Hosking FJ
외 15명 — 모두 보기
Lönn S,
Ahlbom A,
Henriksson R,
Schoemaker MJ,
Hepworth SJ,
Hoffmann P,
Mühleisen TW,
Nöthen MM,
Moebus S,
Eisele L,
Kosteljanetz M,
Muir K,
Swerdlow A,
Simon M,
Houlston RS
Nature genetics · 2011 · PMID 21804547 · open access
페이지 1개
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
Scott RA,
Scott LJ,
Mägi R,
Marullo L,
Gaulton KJ,
Kaakinen M,
Pervjakova N,
Pers TH,
Johnson AD,
Eicher JD,
Jackson AU,
Ferreira T
외 163명 — 모두 보기
Lee Y,
Ma C,
Steinthorsdottir V,
Thorleifsson G,
Qi L,
Van Zuydam NR,
Mahajan A,
Chen H,
Almgren P,
Voight BF,
Grallert H,
Müller-Nurasyid M,
Ried JS,
Rayner NW,
Robertson N,
Karssen LC,
van Leeuwen EM,
Willems SM,
Fuchsberger C,
Kwan P,
Teslovich TM,
Chanda P,
Li M,
Lu Y,
Dina C,
Thuillier D,
Yengo L,
Jiang L,
Sparso T,
Kestler HA,
Chheda H,
Eisele L,
Gustafsson S,
Frånberg M,
Strawbridge RJ,
Benediktsson R,
Hreidarsson AB,
Kong A,
Sigurðsson G,
Kerrison ND,
Luan J,
Liang L,
Meitinger T,
Roden M,
Thorand B,
Esko T,
Mihailov E,
Fox C,
Liu CT,
Rybin D,
Isomaa B,
Lyssenko V,
Tuomi T,
Couper DJ,
Pankow JS,
Grarup N,
Have CT,
Jørgensen ME,
Jørgensen T,
Linneberg A,
Cornelis MC,
van Dam RM,
Hunter DJ,
Kraft P,
Sun Q,
Edkins S,
Owen KR,
Perry JRB,
Wood AR,
Zeggini E,
Tajes-Fernandes J,
Abecasis GR,
Bonnycastle LL,
Chines PS,
Stringham HM,
Koistinen HA,
Kinnunen L,
Sennblad B,
Mühleisen TW,
Nöthen MM,
Pechlivanis S,
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Gertow K,
Humphries SE,
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Steinbach G,
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Scapoli C,
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Hamsten A,
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Deloukas P,
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Ripatti S,
Salomaa V,
Pedersen NL,
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Bergman RN,
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Mohlke KL,
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Hansen T,
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Lannfelt L,
Ingelsson E,
Lind L,
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Loos RJF,
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Boeing H,
Franks PW,
Barricarte Gurrea A,
Palli D,
van der Schouw YT,
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Sijbrands E,
van Duijn CM,
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Strauch K,
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Morris AD,
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DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium
Diabetes · 2017 · PMID 28566273
페이지 1개
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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.