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성함이나 학술지명, PMID로 찾아보십시오.
Langefeld C에 대해
29건, 그중 9건 표시.
Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis
Hinks A,
Cobb J,
Marion MC,
Prahalad S,
Sudman M,
Bowes J,
Martin P,
Comeau ME,
Sajuthi S,
Andrews R,
Brown M,
Chen WM
외 27명 — 모두 보기
Concannon P,
Deloukas P,
Edkins S,
Eyre S,
Gaffney PM,
Guthery SL,
Guthridge JM,
Hunt SE,
James JA,
Keddache M,
Moser KL,
Nigrovic PA,
Onengut-Gumuscu S,
Onslow ML,
Rosé CD,
Rich SS,
Steel KJ,
Wakeland EK,
Wallace CA,
Wedderburn LR,
Woo P,
Bohnsack JF,
Haas JP,
Glass DN,
Langefeld CD,
Thomson W,
Thompson SD
Boston Children's JIA Registry · British Society of Paediatric and Adolescent Rheumatology (BSPAR) Study Group 외 컨소시엄 7곳
Nature genetics · 2013 · PMID 23603761 · open access
페이지 2개
Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans
Carty CL,
Keene KL,
Cheng YC,
Meschia JF,
Chen WM,
Nalls M,
Bis JC,
Kittner SJ,
Rich SS,
Tajuddin S,
Zonderman AB,
Evans MK
외 17명 — 모두 보기
Langefeld CD,
Gottesman R,
Mosley TH,
Shahar E,
Woo D,
Yaffe K,
Liu Y,
Sale MM,
Dichgans M,
Malik R,
Longstreth WT Jr,
Mitchell BD,
Psaty BM,
Kooperberg C,
Reiner A,
Worrall BB,
Fornage M
COMPASS and METASTROKE Consortia
Stroke · 2015 · PMID 26089329
페이지 2개
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification
Kavousi M,
Bos MM,
Barnes HJ,
Lino Cardenas CL,
Wong D,
Lu H,
Hodonsky CJ,
Landsmeer LPL,
Turner AW,
Kho M,
Hasbani NR,
de Vries PS
외 77명 — 모두 보기
Bowden DW,
Chopade S,
Deelen J,
Benavente ED,
Guo X,
Hofer E,
Hwang SJ,
Lutz SM,
Lyytikäinen LP,
Slenders L,
Smith AV,
Stanislawski MA,
van Setten J,
Wong Q,
Yanek LR,
Becker DM,
Beekman M,
Budoff MJ,
Feitosa MF,
Finan C,
Hilliard AT,
Kardia SLR,
Kovacic JC,
Kral BG,
Langefeld CD,
Launer LJ,
Malik S,
Hoesein FAAM,
Mokry M,
Schmidt R,
Smith JA,
Taylor KD,
Terry JG,
van der Grond J,
van Meurs J,
Vliegenthart R,
Xu J,
Young KA,
Zilhão NR,
Zweiker R,
Assimes TL,
Becker LC,
Bos D,
Carr JJ,
Cupples LA,
de Kleijn DPV,
de Winther M,
den Ruijter HM,
Fornage M,
Freedman BI,
Gudnason V,
Hingorani AD,
Hokanson JE,
Ikram MA,
Išgum I,
Jacobs DR Jr,
Kähönen M,
Lange LA,
Lehtimäki T,
Pasterkamp G,
Raitakari OT,
Schmidt H,
Slagboom PE,
Uitterlinden AG,
Vernooij MW,
Bis JC,
Franceschini N,
Psaty BM,
Post WS,
Rotter JI,
Björkegren JLM,
O'Donnell CJ,
Bielak LF,
Peyser PA,
Malhotra R,
van der Laan SW,
Miller CL
Nature genetics · 2023 · PMID 37770635
페이지 2개
A genome-wide association search for type 2 diabetes genes in African Americans
Palmer ND,
McDonough CW,
Hicks PJ,
Roh BH,
Wing MR,
An SS,
Hester JM,
Cooke JN,
Bostrom MA,
Rudock ME,
Talbert ME,
Lewis JP
외 379명 — 모두 보기
Ferrara A,
Lu L,
Ziegler JT,
Sale MM,
Divers J,
Shriner D,
Adeyemo A,
Rotimi CN,
Ng MC,
Langefeld CD,
Freedman BI,
Bowden DW,
Voight BF,
Scott LJ,
Steinthorsdottir V,
Morris AP,
Dina C,
Welch RP,
Zeggini E,
Huth C,
Aulchenko YS,
Thorleifsson G,
McCulloch LJ,
Ferreira T,
Grallert H,
Amin N,
Wu G,
Willer CJ,
Raychaudhuri S,
McCarroll SA,
Langenberg C,
Hofmann OM,
Dupuis J,
Qi L,
Segrè AV,
van Hoek M,
Navarro P,
Ardlie K,
Balkau B,
Benediktsson R,
Bennett AJ,
Blagieva R,
Boerwinkle E,
Bonnycastle LL,
Boström KB,
Bravenboer B,
Bumpstead S,
Burtt NP,
Charpentier G,
Chines PS,
Cornelis M,
Couper DJ,
Crawford G,
Doney AS,
Elliott KS,
Elliott AL,
Erdos MR,
Fox CS,
Franklin CS,
Ganser M,
Gieger C,
Grarup N,
Green T,
Griffin S,
Groves CJ,
Guiducci C,
Hadjadj S,
Hassanali N,
Herder C,
Isomaa B,
Jackson AU,
Johnson PR,
Jørgensen T,
Kao WH,
Klopp N,
Kong A,
Kraft P,
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Lauritzen T,
Li M,
Lieverse A,
Lindgren CM,
Lyssenko V,
Marre M,
Meitinger T,
Midthjell K,
Morken MA,
Narisu N,
Nilsson P,
Owen KR,
Payne F,
Perry JR,
Petersen AK,
Platou C,
Proença C,
Prokopenko I,
Rathmann W,
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Robertson NR,
Rocheleau G,
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Sampson MJ,
Saxena R,
Shields BM,
Shrader P,
Sigurdsson G,
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Strassburger K,
Stringham HM,
Sun Q,
Swift AJ,
Thorand B,
Tichet J,
Tuomi T,
van Dam RM,
van Haeften TW,
van Herpt T,
van Vliet-Ostaptchouk JV,
Walters GB,
Weedon MN,
Wijmenga C,
Witteman J,
Bergman RN,
Cauchi S,
Collins FS,
Gloyn AL,
Gyllensten U,
Hansen T,
Hide WA,
Hitman GA,
Hofman A,
Hunter DJ,
Hveem K,
Laakso M,
Mohlke KL,
Morris AD,
Palmer CN,
Pramstaller PP,
Rudan I,
Sijbrands E,
Stein LD,
Tuomilehto J,
Uitterlinden A,
Walker M,
Wareham NJ,
Watanabe RM,
Abecasis GR,
Boehm BO,
Campbell H,
Daly MJ,
Hattersley AT,
Hu FB,
Meigs JB,
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Pedersen O,
Wichmann HE,
Barroso I,
Florez JC,
Frayling TM,
Groop L,
Sladek R,
Thorsteinsdottir U,
Wilson JF,
Illig T,
Froguel P,
van Duijn CM,
Stefansson K,
Altshuler D,
Boehnke M,
McCarthy MI,
Soranzo N,
Wheeler E,
Glazer NL,
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Mägi R,
Randall J,
Johnson T,
Elliott P,
Rybin D,
Henneman P,
Dehghan A,
Hottenga JJ,
Song K,
Goel A,
Egan JM,
Lajunen T,
Doney A,
Kanoni S,
Cavalcanti-Proença C,
Kumari M,
Timpson NJ,
Zabena C,
Ingelsson E,
An P,
O'Connell J,
Luan J,
Elliott A,
McCarroll SA,
Roccasecca RM,
Pattou F,
Sethupathy P,
Ariyurek Y,
Barter P,
Beilby JP,
Ben-Shlomo Y,
Bergmann S,
Bochud M,
Bonnefond A,
Borch-Johnsen K,
Böttcher Y,
Brunner E,
Bumpstead SJ,
Chen YD,
Chines P,
Clarke R,
Coin LJ,
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Crisponi L,
Day IN,
de Geus EJ,
Delplanque J,
Fedson AC,
Fischer-Rosinsky A,
Forouhi NG,
Frants R,
Franzosi MG,
Galan P,
Goodarzi MO,
Graessler J,
Grundy S,
Gwilliam R,
Hallmans G,
Hammond N,
Han X,
Hartikainen AL,
Hayward C,
Heath SC,
Hercberg S,
Hicks AA,
Hillman DR,
Hingorani AD,
Hui J,
Hung J,
Jula A,
Kaakinen M,
Kaprio J,
Kesaniemi YA,
Kivimaki M,
Knight B,
Koskinen S,
Kovacs P,
Kyvik KO,
Lathrop GM,
Lawlor DA,
Le Bacquer O,
Lecoeur C,
Li Y,
Mahley R,
Mangino M,
Manning AK,
Martínez-Larrad MT,
McAteer JB,
McPherson R,
Meisinger C,
Melzer D,
Meyre D,
Mitchell BD,
Mukherjee S,
Naitza S,
Neville MJ,
Oostra BA,
Orrù M,
Pakyz R,
Paolisso G,
Pattaro C,
Pearson D,
Peden JF,
Pedersen NL,
Perola M,
Pfeiffer AF,
Pichler I,
Polasek O,
Posthuma D,
Potter SC,
Pouta A,
Province MA,
Psaty BM,
Rayner NW,
Rice K,
Ripatti S,
Rivadeneira F,
Rolandsson O,
Sandbaek A,
Sandhu M,
Sanna S,
Sayer AA,
Scheet P,
Seedorf U,
Sharp SJ,
Shields B,
Sijbrands EJ,
Silveira A,
Simpson L,
Singleton A,
Smith NL,
Sovio U,
Swift A,
Syddall H,
Syvänen AC,
Tanaka T,
Tönjes A,
Uitterlinden AG,
van Dijk KW,
Varma D,
Visvikis-Siest S,
Vitart V,
Vogelzangs N,
Waeber G,
Wagner PJ,
Walley A,
Ward KL,
Watkins H,
Wild SH,
Willemsen G,
Willemsen G,
Witteman JC,
Yarnell JW,
Zelenika D,
Zethelius B,
Zhai G,
Zhao JH,
Zillikens MC,
Borecki IB,
Loos RJ,
Meneton P,
Magnusson PK,
Nathan DM,
Williams GH,
Silander K,
Salomaa V,
Smith GD,
Bornstein SR,
Schwarz P,
Spranger J,
Karpe F,
Shuldiner AR,
Cooper C,
Dedoussis GV,
Serrano-Ríos M,
Lind L,
Palmer LJ,
Franks PW,
Ebrahim S,
Marmot M,
Kao WH,
Pramstaller PP,
Wright AF,
Stumvoll M,
Hamsten A,
Buchanan TA,
Valle TT,
Rotter JI,
Siscovick DS,
Penninx BW,
Boomsma DI,
Deloukas P,
Spector TD,
Ferrucci L,
Cao A,
Scuteri A,
Schlessinger D,
Uda M,
Ruokonen A,
Jarvelin MR,
Waterworth DM,
Vollenweider P,
Peltonen L,
Mooser V,
Sladek R
DIAGRAM Consortium · MAGIC Investigators
PloS one · 2012 · PMID 22238593 · open access
페이지 1개
Chromosome 2q31.1 associates with ESRD in women with type 1 diabetes
Sandholm N,
McKnight AJ,
Salem RM,
Brennan EP,
Forsblom C,
Harjutsalo V,
Mäkinen VP,
McKay GJ,
Sadlier DM,
Williams WW,
Martin F,
Panduru NM
외 11명 — 모두 보기
Tarnow L,
Tuomilehto J,
Tryggvason K,
Zerbini G,
Comeau ME,
Langefeld CD,
Godson C,
Hirschhorn JN,
Maxwell AP,
Florez JC,
Groop PH
FIND Consortium · FinnDiane Study Group and the GENIE Consortium
Journal of the American Society of Nephrology : JASN · 2013 · PMID 24029427
페이지 1개
Genetic variation at 16q24.2 is associated with small vessel stroke
Traylor M,
Malik R,
Nalls MA,
Cotlarciuc I,
Radmanesh F,
Thorleifsson G,
Hanscombe KB,
Langefeld C,
Saleheen D,
Rost NS,
Yet I,
Spector TD
외 55명 — 모두 보기
Bell JT,
Hannon E,
Mill J,
Chauhan G,
Debette S,
Bis JC,
Longstreth WT Jr,
Ikram MA,
Launer LJ,
Seshadri S,
Hamilton-Bruce MA,
Jimenez-Conde J,
Cole JW,
Schmidt R,
Słowik A,
Lemmens R,
Lindgren A,
Melander O,
Grewal RP,
Sacco RL,
Rundek T,
Rexrode K,
Arnett DK,
Johnson JA,
Benavente OR,
Wasssertheil-Smoller S,
Lee JM,
Pulit SL,
Wong Q,
Rich SS,
de Bakker PI,
McArdle PF,
Woo D,
Anderson CD,
Xu H,
Heitsch L,
Fornage M,
Jern C,
Stefansson K,
Thorsteinsdottir U,
Gretarsdottir S,
Lewis CM,
Sharma P,
Sudlow CL,
Rothwell PM,
Boncoraglio GB,
Thijs V,
Levi C,
Meschia JF,
Rosand J,
Kittner SJ,
Mitchell BD,
Dichgans M,
Worrall BB,
Markus HS
METASTROKE, UK Young Lacunar DNA Study, NINDS Stroke Genetics Network, Neurology Working Group of the CHARGE Consortium · International Stroke Genetics Consortium
Annals of neurology · 2017 · PMID 27997041 · open access
페이지 1개
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
Bentley AR,
Sung YJ,
Brown MR,
Winkler TW,
Kraja AT,
Ntalla I,
Schwander K,
Chasman DI,
Lim E,
Deng X,
Guo X,
Liu J
외 290명 — 모두 보기
Lu Y,
Cheng CY,
Sim X,
Vojinovic D,
Huffman JE,
Musani SK,
Li C,
Feitosa MF,
Richard MA,
Noordam R,
Baker J,
Chen G,
Aschard H,
Bartz TM,
Ding J,
Dorajoo R,
Manning AK,
Rankinen T,
Smith AV,
Tajuddin SM,
Zhao W,
Graff M,
Alver M,
Boissel M,
Chai JF,
Chen X,
Divers J,
Evangelou E,
Gao C,
Goel A,
Hagemeijer Y,
Harris SE,
Hartwig FP,
He M,
Horimoto ARVR,
Hsu FC,
Hung YJ,
Jackson AU,
Kasturiratne A,
Komulainen P,
Kühnel B,
Leander K,
Lin KH,
Luan J,
Lyytikäinen LP,
Matoba N,
Nolte IM,
Pietzner M,
Prins B,
Riaz M,
Robino A,
Said MA,
Schupf N,
Scott RA,
Sofer T,
Stancáková A,
Takeuchi F,
Tayo BO,
van der Most PJ,
Varga TV,
Wang TD,
Wang Y,
Ware EB,
Wen W,
Xiang YB,
Yanek LR,
Zhang W,
Zhao JH,
Adeyemo A,
Afaq S,
Amin N,
Amini M,
Arking DE,
Arzumanyan Z,
Aung T,
Ballantyne C,
Barr RG,
Bielak LF,
Boerwinkle E,
Bottinger EP,
Broeckel U,
Brown M,
Cade BE,
Campbell A,
Canouil M,
Charumathi S,
Chen YI,
Christensen K,
Concas MP,
Connell JM,
de las Fuentes L,
de Silva HJ,
de Vries PS,
Doumatey A,
Duan Q,
Eaton CB,
Eppinga RN,
Faul JD,
Floyd JS,
Forouhi NG,
Forrester T,
Friedlander Y,
Gandin I,
Gao H,
Ghanbari M,
Gharib SA,
Gigante B,
Giulianini F,
Grabe HJ,
Gu CC,
Harris TB,
Heikkinen S,
Heng CK,
Hirata M,
Hixson JE,
Ikram MA,
Jia Y,
Joehanes R,
Johnson C,
Jonas JB,
Justice AE,
Katsuya T,
Khor CC,
Kilpeläinen TO,
Koh WP,
Kolcic I,
Kooperberg C,
Krieger JE,
Kritchevsky SB,
Kubo M,
Kuusisto J,
Lakka TA,
Langefeld CD,
Langenberg C,
Launer LJ,
Lehne B,
Lewis CE,
Li Y,
Liang J,
Lin S,
Liu CT,
Liu J,
Liu K,
Loh M,
Lohman KK,
Louie T,
Luzzi A,
Mägi R,
Mahajan A,
Manichaikul AW,
McKenzie CA,
Meitinger T,
Metspalu A,
Milaneschi Y,
Milani L,
Mohlke KL,
Momozawa Y,
Morris AP,
Murray AD,
Nalls MA,
Nauck M,
Nelson CP,
North KE,
O'Connell JR,
Palmer ND,
Papanicolau GJ,
Pedersen NL,
Peters A,
Peyser PA,
Polasek O,
Poulter N,
Raitakari OT,
Reiner AP,
Renström F,
Rice TK,
Rich SS,
Robinson JG,
Rose LM,
Rosendaal FR,
Rudan I,
Schmidt CO,
Schreiner PJ,
Scott WR,
Sever P,
Shi Y,
Sidney S,
Sims M,
Smith JA,
Snieder H,
Starr JM,
Strauch K,
Stringham HM,
Tan NYQ,
Tang H,
Taylor KD,
Teo YY,
Tham YC,
Tiemeier H,
Turner ST,
Uitterlinden AG,
van Heemst D,
Waldenberger M,
Wang H,
Wang L,
Wang L,
Wei WB,
Williams CA,
Wilson G Sr,
Wojczynski MK,
Yao J,
Young K,
Yu C,
Yuan JM,
Zhou J,
Zonderman AB,
Becker DM,
Boehnke M,
Bowden DW,
Chambers JC,
Cooper RS,
de Faire U,
Deary IJ,
Elliott P,
Esko T,
Farrall M,
Franks PW,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
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Juang JJ,
Kamatani Y,
Kammerer CM,
Kato N,
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Laakso M,
Laurie CC,
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Lehtimäki T,
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Penninx BWJH,
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Wang YX,
Wareham NJ,
Watkins H,
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Zeggini E,
Zheng W,
Zheng W,
Bouchard C,
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Kardia SLR,
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Psaty BM,
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Fornage M,
Province MA,
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Hayward C,
van Duijn CM,
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COGENT-Kidney Consortium · EPIC-InterAct Consortium 외 컨소시엄 2곳
Nature genetics · 2019 · PMID 30926973 · open access
페이지 1개
Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke
Keene KL,
Hyacinth HI,
Bis JC,
Kittner SJ,
Mitchell BD,
Cheng YC,
Pare G,
Chong M,
O'Donnell M,
Meschia JF,
Chen WM,
Sale MM
외 35명 — 모두 보기
Rich SS,
Nalls MA,
Zonderman AB,
Evans MK,
Wilson JG,
Correa A,
Markus HS,
Traylor M,
Lewis CM,
Carty CL,
Reiner A,
Haessler J,
Langefeld CD,
Gottesman R,
Mosley TH,
Woo D,
Yaffe K,
Liu Y,
Longstreth WT,
Psaty BM,
Kooperberg C,
Lange LA,
Sacco R,
Rundek T,
Lee JM,
Cruchaga C,
Furie KL,
Arnett DK,
Benavente OR,
Grewal RP,
Peddareddygari LR,
Dichgans M,
Malik R,
Worrall BB,
Fornage M
COMPASS, SiGN, and METASTROKE Consortia
Stroke · 2020 · PMID 32693751
페이지 1개
COVID-19 and systemic lupus erythematosus genetics: A balance between autoimmune disease risk and protection against infection
Wang Y,
Guga S,
Wu K,
Khaw Z,
Tzoumkas K,
Tombleson P,
Comeau ME,
Langefeld CD,
Cunninghame Graham DS,
Morris DL,
Vyse TJ
PLoS genetics · 2022 · PMID 36327221 · open access
페이지 1개
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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.