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28 matches for
Sala C,
showing the first 8.
KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference
Schumann G,
Liu C,
O'Reilly P,
Gao H,
Song P,
Xu B,
Ruggeri B,
Amin N,
Jia T,
Preis S,
Segura Lepe M,
Akira S
and 115 more — show all
Barbieri C,
Baumeister S,
Cauchi S,
Clarke TK,
Enroth S,
Fischer K,
Hällfors J,
Harris SE,
Hieber S,
Hofer E,
Hottenga JJ,
Johansson Å,
Joshi PK,
Kaartinen N,
Laitinen J,
Lemaitre R,
Loukola A,
Luan J,
Lyytikäinen LP,
Mangino M,
Manichaikul A,
Mbarek H,
Milaneschi Y,
Moayyeri A,
Mukamal K,
Nelson C,
Nettleton J,
Partinen E,
Rawal R,
Robino A,
Rose L,
Sala C,
Satoh T,
Schmidt R,
Schraut K,
Scott R,
Smith AV,
Starr JM,
Teumer A,
Trompet S,
Uitterlinden AG,
Venturini C,
Vergnaud AC,
Verweij N,
Vitart V,
Vuckovic D,
Wedenoja J,
Yengo L,
Yu B,
Zhang W,
Zhao JH,
Boomsma DI,
Chambers J,
Chasman DI,
Daniela T,
de Geus E,
Deary I,
Eriksson JG,
Esko T,
Eulenburg V,
Franco OH,
Froguel P,
Gieger C,
Grabe HJ,
Gudnason V,
Gyllensten U,
Harris TB,
Hartikainen AL,
Heath AC,
Hocking L,
Hofman A,
Huth C,
Jarvelin MR,
Jukema JW,
Kaprio J,
Kooner JS,
Kutalik Z,
Lahti J,
Langenberg C,
Lehtimäki T,
Liu Y,
Madden PA,
Martin N,
Morrison A,
Penninx B,
Pirastu N,
Psaty B,
Raitakari O,
Ridker P,
Rose R,
Rotter JI,
Samani NJ,
Schmidt H,
Spector TD,
Stott D,
Strachan D,
Tzoulaki I,
van der Harst P,
van Duijn CM,
Marques-Vidal P,
Vollenweider P,
Wareham NJ,
Whitfield JB,
Wilson J,
Wolffenbuttel B,
Bakalkin G,
Evangelou E,
Liu Y,
Rice KM,
Desrivières S,
Kliewer SA,
Mangelsdorf DJ,
Müller CP,
Levy D,
Elliott P
Proceedings of the National Academy of Sciences of the United States of America · 2016 · PMID 27911795
3 pages
Genome-Wide Meta-Analysis Unravels Interactions between Magnesium Homeostasis and Metabolic Phenotypes
Corre T,
Arjona FJ,
Hayward C,
Youhanna S,
de Baaij JHF,
Belge H,
Nägele N,
Debaix H,
Blanchard MG,
Traglia M,
Harris SE,
Ulivi S
and 29 more — show all
Rueedi R,
Lamparter D,
Macé A,
Sala C,
Lenarduzzi S,
Ponte B,
Pruijm M,
Ackermann D,
Ehret G,
Baptista D,
Polasek O,
Rudan I,
Hurd TW,
Hastie ND,
Vitart V,
Waeber G,
Kutalik Z,
Bergmann S,
Vargas-Poussou R,
Konrad M,
Gasparini P,
Deary IJ,
Starr JM,
Toniolo D,
Vollenweider P,
Hoenderop JGJ,
Bindels RJM,
Bochud M,
Devuyst O
Journal of the American Society of Nephrology : JASN · 2018 · PMID 29093028
3 pages
A genome-wide association study of early menopause and the combined impact of identified variants
Perry JR,
Corre T,
Esko T,
Chasman DI,
Fischer K,
Franceschini N,
He C,
Kutalik Z,
Mangino M,
Rose LM,
Vernon Smith A,
Stolk L
and 54 more — show all
Sulem P,
Weedon MN,
Zhuang WV,
Arnold A,
Ashworth A,
Bergmann S,
Buring JE,
Burri A,
Chen C,
Cornelis MC,
Couper DJ,
Goodarzi MO,
Gudnason V,
Harris T,
Hofman A,
Jones M,
Kraft P,
Launer L,
Laven JS,
Li G,
McKnight B,
Masciullo C,
Milani L,
Orr N,
Psaty BM,
Ridker PM,
Rivadeneira F,
Sala C,
Salumets A,
Schoemaker M,
Traglia M,
Waeber G,
Chanock SJ,
Demerath EW,
Garcia M,
Hankinson SE,
Hu FB,
Hunter DJ,
Lunetta KL,
Metspalu A,
Montgomery GW,
Murabito JM,
Newman AB,
Ong KK,
Spector TD,
Stefansson K,
Swerdlow AJ,
Thorsteinsdottir U,
Van Dam RM,
Uitterlinden AG,
Visser JA,
Vollenweider P,
Toniolo D,
Murray A
ReproGen Consortium
Human molecular genetics · 2013 · PMID 23307926 · open access
2 pages
Common variants in UMOD associate with urinary uromodulin levels: a meta-analysis
Olden M,
Corre T,
Hayward C,
Toniolo D,
Ulivi S,
Gasparini P,
Pistis G,
Hwang SJ,
Bergmann S,
Campbell H,
Cocca M,
Gandin I
and 18 more — show all
Girotto G,
Glaudemans B,
Hastie ND,
Loffing J,
Polasek O,
Rampoldi L,
Rudan I,
Sala C,
Traglia M,
Vollenweider P,
Vuckovic D,
Youhanna S,
Weber J,
Wright AF,
Kutalik Z,
Bochud M,
Fox CS,
Devuyst O
Journal of the American Society of Nephrology : JASN · 2014 · PMID 24578125
2 pages
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
Kato N,
Loh M,
Takeuchi F,
Verweij N,
Wang X,
Zhang W,
Kelly TN,
Saleheen D,
Lehne B,
Leach IM,
Drong AW,
Abbott J
and 233 more — show all
Wahl S,
Tan ST,
Scott WR,
Campanella G,
Chadeau-Hyam M,
Afzal U,
Ahluwalia TS,
Bonder MJ,
Chen P,
Dehghan A,
Edwards TL,
Esko T,
Go MJ,
Harris SE,
Hartiala J,
Kasela S,
Kasturiratne A,
Khor CC,
Kleber ME,
Li H,
Yu Mok Z,
Nakatochi M,
Sapari NS,
Saxena R,
Stewart AFR,
Stolk L,
Tabara Y,
Teh AL,
Wu Y,
Wu JY,
Zhang Y,
Aits I,
Da Silva Couto Alves A,
Das S,
Dorajoo R,
Hopewell JC,
Kim YK,
Koivula RW,
Luan J,
Lyytikäinen LP,
Nguyen QN,
Pereira MA,
Postmus I,
Raitakari OT,
Scannell Bryan M,
Scott RA,
Sorice R,
Tragante V,
Traglia M,
White J,
Yamamoto K,
Zhang Y,
Adair LS,
Ahmed A,
Akiyama K,
Asif R,
Aung T,
Barroso I,
Bjonnes A,
Braun TR,
Cai H,
Chang LC,
Chen CH,
Cheng CY,
Chong YS,
Collins R,
Courtney R,
Davies G,
Delgado G,
Do LD,
Doevendans PA,
Gansevoort RT,
Gao YT,
Grammer TB,
Grarup N,
Grewal J,
Gu D,
Wander GS,
Hartikainen AL,
Hazen SL,
He J,
Heng CK,
Hixson JE,
Hofman A,
Hsu C,
Huang W,
Husemoen LLN,
Hwang JY,
Ichihara S,
Igase M,
Isono M,
Justesen JM,
Katsuya T,
Kibriya MG,
Kim YJ,
Kishimoto M,
Koh WP,
Kohara K,
Kumari M,
Kwek K,
Lee NR,
Lee J,
Liao J,
Lieb W,
Liewald DCM,
Matsubara T,
Matsushita Y,
Meitinger T,
Mihailov E,
Milani L,
Mills R,
Mononen N,
Müller-Nurasyid M,
Nabika T,
Nakashima E,
Ng HK,
Nikus K,
Nutile T,
Ohkubo T,
Ohnaka K,
Parish S,
Paternoster L,
Peng H,
Peters A,
Pham ST,
Pinidiyapathirage MJ,
Rahman M,
Rakugi H,
Rolandsson O,
Ann Rozario M,
Ruggiero D,
Sala CF,
Sarju R,
Shimokawa K,
Snieder H,
Sparsø T,
Spiering W,
Starr JM,
Stott DJ,
Stram DO,
Sugiyama T,
Szymczak S,
Tang WHW,
Tong L,
Trompet S,
Turjanmaa V,
Ueshima H,
Uitterlinden AG,
Umemura S,
Vaarasmaki M,
van Dam RM,
van Gilst WH,
van Veldhuisen DJ,
Viikari JS,
Waldenberger M,
Wang Y,
Wang A,
Wilson R,
Wong TY,
Xiang YB,
Yamaguchi S,
Ye X,
Young RD,
Young TL,
Yuan JM,
Zhou X,
Asselbergs FW,
Ciullo M,
Clarke R,
Deloukas P,
Franke A,
Franks PW,
Franks S,
Friedlander Y,
Gross MD,
Guo Z,
Hansen T,
Jarvelin MR,
Jørgensen T,
Jukema JW,
Kähönen M,
Kajio H,
Kivimaki M,
Lee JY,
Lehtimäki T,
Linneberg A,
Miki T,
Pedersen O,
Samani NJ,
Sørensen TIA,
Takayanagi R,
Toniolo D,
Ahsan H,
Allayee H,
Chen YT,
Danesh J,
Deary IJ,
Franco OH,
Franke L,
Heijman BT,
Holbrook JD,
Isaacs A,
Kim BJ,
Lin X,
Liu J,
März W,
Metspalu A,
Mohlke KL,
Sanghera DK,
Shu XO,
van Meurs JBJ,
Vithana E,
Wickremasinghe AR,
Wijmenga C,
Wolffenbuttel BHW,
Yokota M,
Zheng W,
Zheng W,
Zhu D,
Vineis P,
Kyrtopoulos SA,
Kleinjans JCS,
McCarthy MI,
Soong R,
Gieger C,
Scott J,
Teo YY,
He J,
Elliott P,
Tai ES,
van der Harst P,
Kooner JS,
Chambers JC
BIOS-consortium · CARDIo GRAMplusCD and 2 more consortia
Nature genetics · 2015 · PMID 26390057
2 pages
Six Novel Loci Associated with Circulating VEGF Levels Identified by a Meta-analysis of Genome-Wide Association Studies
Choi SH,
Ruggiero D,
Sorice R,
Song C,
Nutile T,
Vernon Smith A,
Concas MP,
Traglia M,
Barbieri C,
Ndiaye NC,
Stathopoulou MG,
Lagou V
and 20 more — show all
Maestrale GB,
Sala C,
Debette S,
Kovacs P,
Lind L,
Lamont J,
Fitzgerald P,
Tönjes A,
Gudnason V,
Toniolo D,
Pirastu M,
Bellenguez C,
Vasan RS,
Ingelsson E,
Leutenegger AL,
Johnson AD,
DeStefano AL,
Visvikis-Siest S,
Seshadri S,
Ciullo M
PLoS genetics · 2016 · PMID 26910538 · open access
2 pages
Modulation of genetic associations with serum urate levels by body-mass-index in humans
Huffman JE,
Albrecht E,
Teumer A,
Mangino M,
Kapur K,
Johnson T,
Kutalik Z,
Pirastu N,
Pistis G,
Lopez LM,
Haller T,
Salo P
and 108 more — show all
Goel A,
Li M,
Tanaka T,
Dehghan A,
Ruggiero D,
Malerba G,
Smith AV,
Nolte IM,
Portas L,
Phipps-Green A,
Boteva L,
Navarro P,
Johansson A,
Hicks AA,
Polasek O,
Esko T,
Peden JF,
Harris SE,
Murgia F,
Wild SH,
Tenesa A,
Tin A,
Mihailov E,
Grotevendt A,
Gislason GK,
Coresh J,
D'Adamo P,
Ulivi S,
Vollenweider P,
Waeber G,
Campbell S,
Kolcic I,
Fisher K,
Viigimaa M,
Metter JE,
Masciullo C,
Trabetti E,
Bombieri C,
Sorice R,
Döring A,
Reischl E,
Strauch K,
Hofman A,
Uitterlinden AG,
Waldenberger M,
Wichmann HE,
Davies G,
Gow AJ,
Dalbeth N,
Stamp L,
Smit JH,
Kirin M,
Nagaraja R,
Nauck M,
Schurmann C,
Budde K,
Farrington SM,
Theodoratou E,
Jula A,
Salomaa V,
Sala C,
Hengstenberg C,
Burnier M,
Mägi R,
Klopp N,
Kloiber S,
Schipf S,
Ripatti S,
Cabras S,
Soranzo N,
Homuth G,
Nutile T,
Munroe PB,
Hastie N,
Campbell H,
Rudan I,
Cabrera C,
Haley C,
Franco OH,
Merriman TR,
Gudnason V,
Pirastu M,
Penninx BW,
Snieder H,
Metspalu A,
Ciullo M,
Pramstaller PP,
van Duijn CM,
Ferrucci L,
Gambaro G,
Deary IJ,
Dunlop MG,
Wilson JF,
Gasparini P,
Gyllensten U,
Spector TD,
Wright AF,
Hayward C,
Watkins H,
Perola M,
Bochud M,
Kao WH,
Caulfield M,
Toniolo D,
Völzke H,
Gieger C,
Köttgen A,
Vitart V
PloS one · 2015 · PMID 25811787 · open access
1 page
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
Day FR,
Thompson DJ,
Helgason H,
Chasman DI,
Finucane H,
Sulem P,
Ruth KS,
Whalen S,
Sarkar AK,
Albrecht E,
Altmaier E,
Amini M
and 204 more — show all
Barbieri CM,
Boutin T,
Campbell A,
Demerath E,
Giri A,
He C,
Hottenga JJ,
Karlsson R,
Kolcic I,
Loh PR,
Lunetta KL,
Mangino M,
Marco B,
McMahon G,
Medland SE,
Nolte IM,
Noordam R,
Nutile T,
Paternoster L,
Perjakova N,
Porcu E,
Rose LM,
Schraut KE,
Segrè AV,
Smith AV,
Stolk L,
Teumer A,
Andrulis IL,
Bandinelli S,
Beckmann MW,
Benitez J,
Bergmann S,
Bochud M,
Boerwinkle E,
Bojesen SE,
Bolla MK,
Brand JS,
Brauch H,
Brenner H,
Broer L,
Brüning T,
Buring JE,
Campbell H,
Catamo E,
Chanock S,
Chenevix-Trench G,
Corre T,
Couch FJ,
Cousminer DL,
Cox A,
Crisponi L,
Czene K,
Davey Smith G,
de Geus EJCN,
de Mutsert R,
De Vivo I,
Dennis J,
Devilee P,
Dos-Santos-Silva I,
Dunning AM,
Eriksson JG,
Fasching PA,
Fernández-Rhodes L,
Ferrucci L,
Flesch-Janys D,
Franke L,
Gabrielson M,
Gandin I,
Giles GG,
Grallert H,
Gudbjartsson DF,
Guénel P,
Hall P,
Hallberg E,
Hamann U,
Harris TB,
Hartman CA,
Heiss G,
Hooning MJ,
Hopper JL,
Hu F,
Hunter DJ,
Ikram MA,
Im HK,
Järvelin MR,
Joshi PK,
Karasik D,
Kellis M,
Kutalik Z,
LaChance G,
Lambrechts D,
Langenberg C,
Launer LJ,
Laven JSE,
Lenarduzzi S,
Li J,
Lind PA,
Lindstrom S,
Liu Y,
Luan J,
Mägi R,
Mannermaa A,
Mbarek H,
McCarthy MI,
Meisinger C,
Meitinger T,
Menni C,
Metspalu A,
Michailidou K,
Milani L,
Milne RL,
Montgomery GW,
Mulligan AM,
Nalls MA,
Navarro P,
Nevanlinna H,
Nyholt DR,
Oldehinkel AJ,
O'Mara TA,
Padmanabhan S,
Palotie A,
Pedersen N,
Peters A,
Peto J,
Pharoah PDP,
Pouta A,
Radice P,
Rahman I,
Ring SM,
Robino A,
Rosendaal FR,
Rudan I,
Rueedi R,
Ruggiero D,
Sala CF,
Schmidt MK,
Scott RA,
Shah M,
Sorice R,
Southey MC,
Sovio U,
Stampfer M,
Steri M,
Strauch K,
Tanaka T,
Tikkanen E,
Timpson NJ,
Traglia M,
Truong T,
Tyrer JP,
Uitterlinden AG,
Edwards DRV,
Vitart V,
Völker U,
Vollenweider P,
Wang Q,
Widen E,
van Dijk KW,
Willemsen G,
Winqvist R,
Wolffenbuttel BHR,
Zhao JH,
Zoledziewska M,
Zygmunt M,
Alizadeh BZ,
Boomsma DI,
Ciullo M,
Cucca F,
Esko T,
Franceschini N,
Gieger C,
Gudnason V,
Hayward C,
Kraft P,
Lawlor DA,
Magnusson PKE,
Martin NG,
Mook-Kanamori DO,
Nohr EA,
Polasek O,
Porteous D,
Price AL,
Ridker PM,
Snieder H,
Spector TD,
Stöckl D,
Toniolo D,
Ulivi S,
Visser JA,
Völzke H,
Wareham NJ,
Wilson JF,
Spurdle AB,
Thorsteindottir U,
Pollard KS,
Easton DF,
Tung JY,
Chang-Claude J,
Hinds D,
Murray A,
Murabito JM,
Stefansson K,
Ong KK,
Perry JRB
LifeLines Cohort Study · InterAct Consortium and 4 more consortia
Nature genetics · 2017 · PMID 28436984
1 page
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Your title and author list come from Europe PMC, the same public record a library
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Because a study that needed 622 people is a different kind of study from one that
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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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