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21 matches for
Suhre K,
showing the first 20.
Human metabolic individuality in biomedical and pharmaceutical research
Suhre K,
Shin SY,
Petersen AK,
Mohney RP,
Meredith D,
Wägele B,
Altmaier E,
Deloukas P,
Erdmann J,
Grundberg E,
Hammond CJ,
de Angelis MH
and 21 more — show all
Kastenmüller G,
Köttgen A,
Kronenberg F,
Mangino M,
Meisinger C,
Meitinger T,
Mewes HW,
Milburn MV,
Prehn C,
Raffler J,
Ried JS,
Römisch-Margl W,
Samani NJ,
Small KS,
Wichmann HE,
Zhai G,
Illig T,
Spector TD,
Adamski J,
Soranzo N,
Gieger C
CARDIoGRAM
Nature · 2011 · PMID 21886157
12 pages+
An atlas of genetic influences on human blood metabolites
Shin SY,
Fauman EB,
Petersen AK,
Krumsiek J,
Santos R,
Huang J,
Arnold M,
Erte I,
Forgetta V,
Yang TP,
Walter K,
Menni C
and 23 more — show all
Chen L,
Vasquez L,
Valdes AM,
Hyde CL,
Wang V,
Ziemek D,
Roberts P,
Xi L,
Grundberg E,
Waldenberger M,
Richards JB,
Mohney RP,
Milburn MV,
John SL,
Trimmer J,
Theis FJ,
Overington JP,
Suhre K,
Brosnan MJ,
Gieger C,
Kastenmüller G,
Spector TD,
Soranzo N
Multiple Tissue Human Expression Resource (MuTHER) Consortium
Nature genetics · 2014 · PMID 24816252 · open access
12 pages+
Connecting genetic risk to disease end points through the human blood plasma proteome
Suhre K,
Arnold M,
Bhagwat AM,
Cotton RJ,
Engelke R,
Raffler J,
Sarwath H,
Thareja G,
Wahl A,
DeLisle RK,
Gold L,
Pezer M
and 12 more — show all
Lauc G,
El-Din Selim MA,
Mook-Kanamori DO,
Al-Dous EK,
Mohamoud YA,
Malek J,
Strauch K,
Grallert H,
Peters A,
Kastenmüller G,
Gieger C,
Graumann J
Nature communications · 2017 · PMID 28240269 · open access
12 pages+
Genomic atlas of the human plasma proteome
Sun BB,
Maranville JC,
Peters JE,
Stacey D,
Staley JR,
Blackshaw J,
Burgess S,
Jiang T,
Paige E,
Surendran P,
Oliver-Williams C,
Kamat MA
and 21 more — show all
Prins BP,
Wilcox SK,
Zimmerman ES,
Chi A,
Bansal N,
Spain SL,
Wood AM,
Morrell NW,
Bradley JR,
Janjic N,
Roberts DJ,
Ouwehand WH,
Todd JA,
Soranzo N,
Suhre K,
Paul DS,
Fox CS,
Plenge RM,
Danesh J,
Runz H,
Butterworth AS
Nature · 2018 · PMID 29875488
12 pages+
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
and 14 more — show all
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
12 pages+
Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations
Thareja G,
Belkadi A,
Arnold M,
Albagha OME,
Graumann J,
Schmidt F,
Grallert H,
Peters A,
Gieger C,
Consortium TQGPR,
Suhre K
Human molecular genetics · 2023 · PMID 36168886 · open access
12 pages+
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
and 24 more — show all
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
12 pages+
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
Shrine N,
Izquierdo AG,
Chen J,
Packer R,
Hall RJ,
Guyatt AL,
Batini C,
Thompson RJ,
Pavuluri C,
Malik V,
Hobbs BD,
Moll M
and 136 more — show all
Kim W,
Tal-Singer R,
Bakke P,
Fawcett KA,
John C,
Coley K,
Piga NN,
Pozarickij A,
Lin K,
Millwood IY,
Chen Z,
Li L,
Wijnant SRA,
Lahousse L,
Brusselle G,
Uitterlinden AG,
Manichaikul A,
Oelsner EC,
Rich SS,
Barr RG,
Kerr SM,
Vitart V,
Brown MR,
Wielscher M,
Imboden M,
Jeong A,
Bartz TM,
Gharib SA,
Flexeder C,
Karrasch S,
Gieger C,
Peters A,
Stubbe B,
Hu X,
Ortega VE,
Meyers DA,
Bleecker ER,
Gabriel SB,
Gupta N,
Smith AV,
Luan J,
Zhao JH,
Hansen AF,
Langhammer A,
Willer C,
Bhatta L,
Porteous D,
Smith BH,
Campbell A,
Sofer T,
Lee J,
Daviglus ML,
Yu B,
Lim E,
Xu H,
O'Connor GT,
Thareja G,
Albagha OME,
Suhre K,
Granell R,
Faquih TO,
Hiemstra PS,
Slats AM,
Mullin BH,
Hui J,
James A,
Beilby J,
Patasova K,
Hysi P,
Koskela JT,
Wyss AB,
Jin J,
Sikdar S,
Lee M,
May-Wilson S,
Pirastu N,
Kentistou KA,
Joshi PK,
Timmers PRHJ,
Williams AT,
Free RC,
Wang X,
Morrison JL,
Gilliland FD,
Chen Z,
Wang CA,
Foong RE,
Harris SE,
Taylor A,
Redmond P,
Cook JP,
Mahajan A,
Lind L,
Palviainen T,
Lehtimäki T,
Raitakari OT,
Kaprio J,
Rantanen T,
Pietiläinen KH,
Cox SR,
Pennell CE,
Hall GL,
Gauderman WJ,
Brightling C,
Wilson JF,
Vasankari T,
Laitinen T,
Salomaa V,
Mook-Kanamori DO,
Timpson NJ,
Zeggini E,
Dupuis J,
Hayward C,
Brumpton B,
Langenberg C,
Weiss S,
Homuth G,
Schmidt CO,
Probst-Hensch N,
Jarvelin MR,
Morrison AC,
Polasek O,
Rudan I,
Lee JH,
Sayers I,
Rawlins EL,
Dudbridge F,
Silverman EK,
Strachan DP,
Walters RG,
Morris AP,
London SJ,
Cho MH,
Wain LV,
Hall IP,
Tobin MD
China Kadoorie Biobank Collaborative Group · Qatar Genome Program Research (QGPR) Consortium
Nature genetics · 2023 · PMID 36914875 · open access
12 pages+
A genome-wide association study in 10,000 individuals links plasma N-glycome to liver disease and anti-inflammatory proteins
Sharapov S,
Timoshchuk A,
Zaytseva O,
Maslov DE,
Soplenkova A,
Elgaeva EE,
Tiys ES,
Mangino M,
Wittenbecher C,
Karssen L,
Timofeeva M,
Nostaeva A
and 19 more — show all
Vuckovic F,
Trbojević-Akmačić I,
Štambuk T,
Feoktistova S,
Potapova NA,
Voroshilova V,
Williams F,
Primorac D,
Van Zundert J,
Georges M,
Suhre K,
Allegri M,
Chaturvedi N,
Dunlop M,
Schulze MB,
Spector T,
Tsepilov YA,
Lauc G,
Aulchenko YS
Nature communications · 2025 · PMID 40593539 · open access
12 pages+
A genome-wide association study of mass spectrometry proteomics using a nanoparticle enrichment platform
Suhre K,
Chen Q,
Halama A,
Mendez K,
Dahlin A,
Stephan N,
Thareja G,
Sarwath H,
Guturu H,
Dwaraka VB,
Smith R,
Batzoglou S
and 2 more — show all
Nature genetics · 2025 · PMID 41310232 · open access
12 pages+
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
and 12 more — show all
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
7 pages
A genome-wide perspective of genetic variation in human metabolism
Illig T,
Gieger C,
Zhai G,
Römisch-Margl W,
Wang-Sattler R,
Prehn C,
Altmaier E,
Kastenmüller G,
Kato BS,
Mewes HW,
Meitinger T,
de Angelis MH
and 6 more — show all
Nature genetics · 2010 · PMID 20037589
6 pages
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
and 8 more — show all
PLoS genetics · 2015 · PMID 26352407 · open access
5 pages
A genome-wide association study of metabolic traits in human urine
Suhre K,
Wallaschofski H,
Raffler J,
Friedrich N,
Haring R,
Michael K,
Wasner C,
Krebs A,
Kronenberg F,
Chang D,
Meisinger C,
Wichmann HE
and 12 more — show all
Hoffmann W,
Völzke H,
Völker U,
Teumer A,
Biffar R,
Kocher T,
Felix SB,
Illig T,
Kroemer HK,
Gieger C,
Römisch-Margl W,
Nauck M
Nature genetics · 2011 · PMID 21572414
3 pages
Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels
Draisma HHM,
Pool R,
Kobl M,
Jansen R,
Petersen AK,
Vaarhorst AAM,
Yet I,
Haller T,
Demirkan A,
Esko T,
Zhu G,
Böhringer S
and 36 more — show all
Beekman M,
van Klinken JB,
Römisch-Margl W,
Prehn C,
Adamski J,
de Craen AJM,
van Leeuwen EM,
Amin N,
Dharuri H,
Westra HJ,
Franke L,
de Geus EJC,
Hottenga JJ,
Willemsen G,
Henders AK,
Montgomery GW,
Nyholt DR,
Whitfield JB,
Penninx BW,
Spector TD,
Metspalu A,
Slagboom PE,
van Dijk KW,
't Hoen PAC,
Strauch K,
Martin NG,
van Ommen GB,
Illig T,
Bell JT,
Mangino M,
Suhre K,
McCarthy MI,
Gieger C,
Isaacs A,
van Duijn CM,
Boomsma DI
Nature communications · 2015 · PMID 26068415
3 pages
A genome-wide metabolic QTL analysis in Europeans implicates two loci shaped by recent positive selection
Nicholson G,
Rantalainen M,
Li JV,
Maher AD,
Malmodin D,
Ahmadi KR,
Faber JH,
Barrett A,
Min JL,
Rayner NW,
Toft H,
Krestyaninova M
and 17 more — show all
Viksna J,
Neogi SG,
Dumas ME,
Sarkans U,
Donnelly P,
Illig T,
Adamski J,
Suhre K,
Allen M,
Zondervan KT,
Spector TD,
Nicholson JK,
Lindon JC,
Baunsgaard D,
Holmes E,
McCarthy MI,
Holmes CC
MolPAGE Consortium
PLoS genetics · 2011 · PMID 21931564 · open access
2 pages
Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease
Yao C,
Chen G,
Song C,
Keefe J,
Mendelson M,
Huan T,
Sun BB,
Laser A,
Maranville JC,
Wu H,
Ho JE,
Courchesne P
and 12 more — show all
Lyass A,
Larson MG,
Gieger C,
Graumann J,
Johnson AD,
Danesh J,
Runz H,
Hwang SJ,
Liu C,
Butterworth AS,
Suhre K,
Levy D
Nature communications · 2018 · PMID 30111768 · open access
2 pages
Defining the genetic control of human blood plasma N-glycome using genome-wide association study
Sharapov SZ,
Tsepilov YA,
Klaric L,
Mangino M,
Thareja G,
Shadrina AS,
Simurina M,
Dagostino C,
Dmitrieva J,
Vilaj M,
Vuckovic F,
Pavic T
and 20 more — show all
Stambuk J,
Stambuk J,
Trbojevic-Akmacic I,
Kristic J,
Simunovic J,
Momcilovic A,
Campbell H,
Doherty M,
Dunlop MG,
Farrington SM,
Pucic-Bakovic M,
Gieger C,
Allegri M,
Louis E,
Georges M,
Suhre K,
Spector T,
Williams FMK,
Lauc G,
Aulchenko YS
Human molecular genetics · 2019 · PMID 31163085
1 page
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Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
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Because a study that needed 622 people is a different kind of study from one that
needed four, and "et al." erases that. Twelve names show and the rest are one click
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that person exists and may be looking for it.
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Tell us and it is fixed. Names come from the public record and initials are
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My paper is not here. Does that mean you rejected it?
No. This catalogue is assembled from what a small team could read, and it is
thinnest outside European-ancestry cohorts. A paper is absent because nobody has got
to it, not because it was assessed and turned down.
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