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Pietzner M에 대해
20건.
Genetic studies of urinary metabolites illuminate mechanisms of detoxification and excretion in humans
Schlosser P,
Li Y,
Sekula P,
Raffler J,
Grundner-Culemann F,
Pietzner M,
Cheng Y,
Wuttke M,
Steinbrenner I,
Schultheiss UT,
Kotsis F,
Kacprowski T
외 14명 — 모두 보기
Forer L,
Hausknecht B,
Ekici AB,
Nauck M,
Völker U,
Walz G,
Oefner PJ,
Kronenberg F,
Mohney RP,
Köttgen M,
Suhre K,
Eckardt KU,
Kastenmüller G,
Köttgen A
GCKD Investigators
Nature genetics · 2020 · PMID 31959995
페이지 12개+
A cross-platform approach identifies genetic regulators of human metabolism and health
Lotta LA,
Pietzner M,
Stewart ID,
Wittemans LBL,
Li C,
Bonelli R,
Raffler J,
Biggs EK,
Oliver-Williams C,
Auyeung VPW,
Luan J,
Wheeler E
외 22명 — 모두 보기
Paige E,
Surendran P,
Michelotti GA,
Scott RA,
Burgess S,
Zuber V,
Sanderson E,
Koulman A,
Imamura F,
Forouhi NG,
Khaw KT,
Griffin JL,
Wood AM,
Kastenmüller G,
Danesh J,
Butterworth AS,
Gribble FM,
Reimann F,
Bahlo M,
Fauman E,
Wareham NJ,
Langenberg C
MacTel Consortium
Nature genetics · 2021 · PMID 33414548
페이지 12개+
Mapping the proteo-genomic convergence of human diseases
Pietzner M,
Wheeler E,
Carrasco-Zanini J,
Cortes A,
Koprulu M,
Wörheide MA,
Oerton E,
Cook J,
Stewart ID,
Kerrison ND,
Luan J,
Raffler J
외 9명 — 모두 보기
Science (New York, N.Y.) · 2021 · PMID 34648354
페이지 12개+
Mapping the serum proteome to neurological diseases using whole genome sequencing
Png G,
Barysenka A,
Repetto L,
Navarro P,
Shen X,
Pietzner M,
Wheeler E,
Wareham NJ,
Langenberg C,
Tsafantakis E,
Karaleftheri M,
Dedoussis G
외 4명 — 모두 보기
Nature communications · 2021 · PMID 34857772 · open access
페이지 12개+
Rare and common genetic determinants of metabolic individuality and their effects on human health
Surendran P,
Stewart ID,
Au Yeung VPW,
Pietzner M,
Raffler J,
Wörheide MA,
Li C,
Smith RF,
Wittemans LBL,
Bomba L,
Menni C,
Zierer J
외 24명 — 모두 보기
Rossi N,
Sheridan PA,
Watkins NA,
Mangino M,
Hysi PG,
Di Angelantonio E,
Falchi M,
Spector TD,
Soranzo N,
Michelotti GA,
Arlt W,
Lotta LA,
Denaxas S,
Hemingway H,
Gamazon ER,
Howson JMM,
Wood AM,
Danesh J,
Wareham NJ,
Kastenmüller G,
Fauman EB,
Suhre K,
Butterworth AS,
Langenberg C
Nature medicine · 2022 · PMID 36357675 · open access
페이지 12개+
Genetic architecture of routinely acquired blood tests in a British South Asian cohort
Jacobs BM,
Stow D,
Hodgson S,
Zöllner J,
Samuel M,
Kanoni S,
Bidi S,
Walter K,
Langenberg C,
Dobson R,
Finer S,
Morton C
외 5명 — 모두 보기
Genes & Health Research Team
Nature communications · 2024 · PMID 39414775 · open access
페이지 12개+
A genetic map of human metabolism across the allele frequency spectrum
Zoodsma M,
Beuchel C,
Yasmeen S,
Kohleick L,
Nepal A,
Koprulu M,
Kronenberg F,
Mayr M,
Williamson A,
Pietzner M,
Langenberg C
Nature genetics · 2025 · PMID 41044249 · open access
페이지 12개+
Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions
de Vries PS,
Brown MR,
Bentley AR,
Sung YJ,
Winkler TW,
Ntalla I,
Schwander K,
Kraja AT,
Guo X,
Franceschini N,
Cheng CY,
Sim X
외 254명 — 모두 보기
Vojinovic D,
Huffman JE,
Musani SK,
Li C,
Feitosa MF,
Richard MA,
Noordam R,
Aschard H,
Bartz TM,
Bielak LF,
Deng X,
Dorajoo R,
Lohman KK,
Manning AK,
Rankinen T,
Smith AV,
Tajuddin SM,
Evangelou E,
Graff M,
Alver M,
Boissel M,
Chai JF,
Chen X,
Divers J,
Gandin I,
Gao C,
Goel A,
Hagemeijer Y,
Harris SE,
Hartwig FP,
He M,
Horimoto ARVR,
Hsu FC,
Jackson AU,
Kasturiratne A,
Komulainen P,
Kühnel B,
Laguzzi F,
Lee JH,
Luan J,
Lyytikäinen LP,
Matoba N,
Nolte IM,
Pietzner M,
Riaz M,
Said MA,
Scott RA,
Sofer T,
Stančáková A,
Takeuchi F,
Tayo BO,
van der Most PJ,
Varga TV,
Wang Y,
Ware EB,
Wen W,
Yanek LR,
Zhang W,
Zhao JH,
Afaq S,
Amin N,
Amini M,
Arking DE,
Aung T,
Ballantyne C,
Boerwinkle E,
Broeckel U,
Campbell A,
Canouil M,
Charumathi S,
Chen YI,
Connell JM,
de Faire U,
de las Fuentes L,
de Mutsert R,
de Silva HJ,
Ding J,
Dominiczak AF,
Duan Q,
Eaton CB,
Eppinga RN,
Faul JD,
Fisher V,
Forrester T,
Franco OH,
Friedlander Y,
Ghanbari M,
Giulianini F,
Grabe HJ,
Grove ML,
Gu CC,
Harris TB,
Heikkinen S,
Heng CK,
Hirata M,
Hixson JE,
Howard BV,
Ikram MA,
Jacobs DR,
Johnson C,
Jonas JB,
Kammerer CM,
Katsuya T,
Khor CC,
Kilpeläinen TO,
Koh WP,
Koistinen HA,
Kolcic I,
Kooperberg C,
Krieger JE,
Kritchevsky SB,
Kubo M,
Kuusisto J,
Lakka TA,
Langefeld CD,
Langenberg C,
Launer LJ,
Lehne B,
Lemaitre RN,
Li Y,
Liang J,
Liu J,
Liu K,
Loh M,
Louie T,
Mägi R,
Manichaikul AW,
McKenzie CA,
Meitinger T,
Metspalu A,
Milaneschi Y,
Milani L,
Mohlke KL,
Mosley TH,
Mukamal KJ,
Nalls MA,
Nauck M,
Nelson CP,
Sotoodehnia N,
O'Connell JR,
Palmer ND,
Pazoki R,
Pedersen NL,
Peters A,
Peyser PA,
Polasek O,
Poulter N,
Raffel LJ,
Raitakari OT,
Reiner AP,
Rice TK,
Rich SS,
Robino A,
Robinson JG,
Rose LM,
Rudan I,
Schmidt CO,
Schreiner PJ,
Scott WR,
Sever P,
Shi Y,
Sidney S,
Sims M,
Smith BH,
Smith JA,
Snieder H,
Starr JM,
Strauch K,
Tan N,
Taylor KD,
Teo YY,
Tham YC,
Uitterlinden AG,
van Heemst D,
Vuckovic D,
Waldenberger M,
Wang L,
Wang Y,
Wang Z,
Wei WB,
Williams C,
Wilson G,
Wojczynski MK,
Yao J,
Yu B,
Yu C,
Yuan JM,
Zhao W,
Zonderman AB,
Becker DM,
Boehnke M,
Bowden DW,
Chambers JC,
Deary IJ,
Esko T,
Farrall M,
Franks PW,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
Horta BL,
Kamatani Y,
Kato N,
Kooner JS,
Laakso M,
Leander K,
Lehtimäki T,
Magnusson PKE,
Penninx B,
Pereira AC,
Rauramaa R,
Samani NJ,
Scott J,
Shu XO,
van der Harst P,
Wagenknecht LE,
Wang YX,
Wareham NJ,
Watkins H,
Weir DR,
Wickremasinghe AR,
Zheng W,
Elliott P,
North KE,
Bouchard C,
Evans MK,
Gudnason V,
Liu CT,
Liu Y,
Psaty BM,
Ridker PM,
van Dam RM,
Kardia SLR,
Zhu X,
Rotimi CN,
Mook-Kanamori DO,
Fornage M,
Kelly TN,
Fox ER,
Hayward C,
van Duijn CM,
Tai ES,
Wong TY,
Liu J,
Rotter JI,
Gauderman WJ,
Province MA,
Munroe PB,
Rice K,
Chasman DI,
Cupples LA,
Rao DC,
Morrison AC
InterAct Consortium · Lifelines Cohort, Groningen, The Netherlands (Lifelines Cohort Study)
American journal of epidemiology · 2019 · PMID 30698716
페이지 8개
Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior
Cornelis MC,
Kacprowski T,
Menni C,
Gustafsson S,
Pivin E,
Adamski J,
Artati A,
Eap CB,
Ehret G,
Friedrich N,
Ganna A,
Guessous I
외 12명 — 모두 보기
Homuth G,
Lind L,
Magnusson PK,
Mangino M,
Pedersen NL,
Pietzner M,
Suhre K,
Völzke H,
Bochud M,
Spector TD,
Grabe HJ,
Ingelsson E
Swiss Kidney Project on Genes in Hypertension (SKIPOGH) team
Human molecular genetics · 2016 · PMID 27702941
페이지 7개
Lowering of Circulating Sclerostin May Increase Risk of Atherosclerosis and Its Risk Factors: Evidence From a Genome-Wide Association Meta-Analysis Followed by Mendelian Randomization
Zheng J,
Wheeler E,
Pietzner M,
Andlauer TFM,
Yau MS,
Hartley AE,
Brumpton BM,
Rasheed H,
Kemp JP,
Frysz M,
Robinson J,
Reppe S
외 25명 — 모두 보기
Prijatelj V,
Gautvik KM,
Falk L,
Maerz W,
Gergei I,
Peyser PA,
Kavousi M,
de Vries PS,
Miller CL,
Bos M,
van der Laan SW,
Malhotra R,
Herrmann M,
Scharnagl H,
Kleber M,
Dedoussis G,
Zeggini E,
Nethander M,
Ohlsson C,
Lorentzon M,
Wareham N,
Langenberg C,
Holmes MV,
Davey Smith G,
Tobias JH
Arthritis & rheumatology (Hoboken, N.J.) · 2023 · PMID 37096546
페이지 7개
Genome-Wide Association Study with Targeted and Non-targeted NMR Metabolomics Identifies 15 Novel Loci of Urinary Human Metabolic Individuality
Raffler J,
Friedrich N,
Arnold M,
Kacprowski T,
Rueedi R,
Altmaier E,
Bergmann S,
Budde K,
Gieger C,
Homuth G,
Pietzner M,
Römisch-Margl W
외 8명 — 모두 보기
PLoS genetics · 2015 · PMID 26352407 · open access
페이지 5개
Genome-wide studies reveal factors associated with circulating uromodulin and its relationships to complex diseases
Li Y,
Cheng Y,
Consolato F,
Schiano G,
Chong MR,
Pietzner M,
Nguyen NQH,
Scherer N,
Biggs ML,
Kleber ME,
Haug S,
Göçmen B
외 31명 — 모두 보기
Pigeyre M,
Sekula P,
Steinbrenner I,
Schlosser P,
Joseph CB,
Brody JA,
Grams ME,
Hayward C,
Schultheiss UT,
Krämer BK,
Kronenberg F,
Peters A,
Seissler J,
Steubl D,
Then C,
Wuttke M,
März W,
Eckardt KU,
Gieger C,
Boerwinkle E,
Psaty BM,
Coresh J,
Oefner PJ,
Pare G,
Langenberg C,
Scherberich JE,
Yu B,
Akilesh S,
Devuyst O,
Rampoldi L,
Köttgen A
JCI insight · 2022 · PMID 35446786 · open access
페이지 4개
Plasma Vitamin C and Type 2 Diabetes: Genome-Wide Association Study and Mendelian Randomization Analysis in European Populations
Zheng JS,
Luan J,
Sofianopoulou E,
Imamura F,
Stewart ID,
Day FR,
Pietzner M,
Wheeler E,
Lotta LA,
Gundersen TE,
Amiano P,
Ardanaz E
외 30명 — 모두 보기
Chirlaque MD,
Fagherazzi G,
Franks PW,
Kaaks R,
Laouali N,
Mancini FR,
Nilsson PM,
Onland-Moret NC,
Olsen A,
Overvad K,
Panico S,
Palli D,
Ricceri F,
Rolandsson O,
Spijkerman AMW,
Sánchez MJ,
Schulze MB,
Sala N,
Sieri S,
Tjønneland A,
Tumino R,
van der Schouw YT,
Weiderpass E,
Riboli E,
Danesh J,
Butterworth AS,
Sharp SJ,
Langenberg C,
Forouhi NG,
Wareham NJ
Diabetes care · 2021 · PMID 33203707 · open access
페이지 2개
Genetic Landscape of the ACE2 Coronavirus Receptor
Yang Z,
Macdonald-Dunlop E,
Chen J,
Zhai R,
Li T,
Richmond A,
Klarić L,
Pirastu N,
Ning Z,
Zheng C,
Wang Y,
Huang T
외 57명 — 모두 보기
He Y,
Guo H,
Ying K,
Gustafsson S,
Prins B,
Ramisch A,
Dermitzakis ET,
Png G,
Eriksson N,
Haessler J,
Hu X,
Zanetti D,
Boutin T,
Hwang SJ,
Wheeler E,
Pietzner M,
Raffield LM,
Kalnapenkis A,
Peters JE,
Viñuela A,
Gilly A,
Elmståhl S,
Dedoussis G,
Petrie JR,
Polašek O,
Folkersen L,
Chen Y,
Yao C,
Võsa U,
Pairo-Castineira E,
Clohisey S,
Bretherick AD,
Rawlik K,
Esko T,
Enroth S,
Johansson Å,
Gyllensten U,
Langenberg C,
Levy D,
Hayward C,
Assimes TL,
Kooperberg C,
Manichaikul AW,
Siegbahn A,
Wallentin L,
Lind L,
Zeggini E,
Schwenk JM,
Butterworth AS,
Michaëlsson K,
Pawitan Y,
Joshi PK,
Baillie JK,
Mälarstig A,
Reiner AP,
Wilson JF,
Shen X
GenOMICC Consortium† · IMI-DIRECT Consortium†
Circulation · 2022 · PMID 35387486 · open access
페이지 2개
Genome-wide association analysis and Mendelian randomization proteomics identify drug targets for heart failure
Rasooly D,
Peloso GM,
Pereira AC,
Dashti H,
Giambartolomei C,
Wheeler E,
Aung N,
Ferolito BR,
Pietzner M,
Farber-Eger EH,
Wells QS,
Kosik NM
외 22명 — 모두 보기
Gaziano L,
Posner DC,
Bento AP,
Hui Q,
Liu C,
Aragam K,
Wang Z,
Charest B,
Huffman JE,
Wilson PWF,
Phillips LS,
Whittaker J,
Munroe PB,
Petersen SE,
Cho K,
Leach AR,
Magariños MP,
Gaziano JM,
Langenberg C,
Sun YV,
Joseph J,
Casas JP
VA Million Veteran Program
Nature communications · 2023 · PMID 37429843 · open access
페이지 2개
Genome-wide association study of 1,5-anhydroglucitol identifies novel genetic loci linked to glucose metabolism
Li M,
Maruthur NM,
Loomis SJ,
Pietzner M,
North KE,
Mei H,
Morrison AC,
Friedrich N,
Pankow JS,
Nauck M,
Boerwinkle E,
Teumer A
외 2명 — 모두 보기
Scientific reports · 2017 · PMID 28588231 · 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,
Horta BL,
Juang JJ,
Kamatani Y,
Kammerer CM,
Kato N,
Kooner JS,
Laakso M,
Laurie CC,
Lee IT,
Lehtimäki T,
Magnusson PKE,
Oldehinkel AJ,
Penninx BWJH,
Pereira AC,
Rauramaa R,
Redline S,
Samani NJ,
Scott J,
Shu XO,
van der Harst P,
Wagenknecht LE,
Wang JS,
Wang YX,
Wareham NJ,
Watkins H,
Weir DR,
Wickremasinghe AR,
Wu T,
Zeggini E,
Zheng W,
Zheng W,
Bouchard C,
Evans MK,
Gudnason V,
Kardia SLR,
Liu Y,
Psaty BM,
Ridker PM,
van Dam RM,
Mook-Kanamori DO,
Fornage M,
Province MA,
Kelly TN,
Fox ER,
Hayward C,
van Duijn CM,
Tai ES,
Wong TY,
Loos RJF,
Franceschini N,
Rotter JI,
Zhu X,
Bierut LJ,
Gauderman WJ,
Rice K,
Munroe PB,
Morrison AC,
Rao DC,
Rotimi CN,
Cupples LA
COGENT-Kidney Consortium · EPIC-InterAct Consortium 외 컨소시엄 2곳
Nature genetics · 2019 · PMID 30926973 · open access
페이지 1개
Genome-wide scan identifies novel genetic loci regulating salivary metabolite levels
Nag A,
Kurushima Y,
Bowyer RCE,
Wells PM,
Weiss S,
Pietzner M,
Kocher T,
Raffler J,
Völker U,
Mangino M,
Spector TD,
Milburn MV
외 5명 — 모두 보기
Human molecular genetics · 2020 · PMID 31960908 · open access
페이지 1개
Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism
Iglesias MJ,
Sanchez-Rivera L,
Ibrahim-Kosta M,
Naudin C,
Munsch G,
Goumidi L,
Farm M,
Smith PM,
Thibord F,
Kral-Pointner JB,
Hong MG,
Suchon P
외 31명 — 모두 보기
Germain M,
Schrottmaier W,
Dusart P,
Boland A,
Kotol D,
Edfors F,
Koprulu M,
Pietzner M,
Langenberg C,
Damrauer SM,
Johnson AD,
Klarin DM,
Smith NL,
Smadja DM,
Holmström M,
Magnusson M,
Silveira A,
Uhlén M,
Renné T,
Martinez-Perez A,
Emmerich J,
Deleuze JF,
Antovic J,
Soria Fernandez JM,
Assinger A,
Schwenk JM,
Souto Andres JC,
Morange PE,
Butler LM,
Trégouët DA,
Odeberg J
Nature communications · 2023 · PMID 37286573 · open access
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