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2,665 papers hold this site up. Every variant and condition page names
the research it was written from, and this is that list, gathered from the pages themselves.
Search your name, your journal, or a PMID.
4 matches for
Postmus I.
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation
Teumer A,
Chaker L,
Groeneweg S,
Li Y,
Di Munno C,
Barbieri C,
Schultheiss UT,
Traglia M,
Ahluwalia TS,
Akiyama M,
Appel EVR,
Arking DE
and 116 more — show all
Arnold A,
Astrup A,
Beekman M,
Beilby JP,
Bekaert S,
Boerwinkle E,
Brown SJ,
De Buyzere M,
Campbell PJ,
Ceresini G,
Cerqueira C,
Cucca F,
Deary IJ,
Deelen J,
Eckardt KU,
Ekici AB,
Eriksson JG,
Ferrrucci L,
Fiers T,
Fiorillo E,
Ford I,
Fox CS,
Fuchsberger C,
Galesloot TE,
Gieger C,
Gögele M,
De Grandi A,
Grarup N,
Greiser KH,
Haljas K,
Hansen T,
Harris SE,
van Heemst D,
den Heijer M,
Hicks AA,
den Hollander W,
Homuth G,
Hui J,
Ikram MA,
Ittermann T,
Jensen RA,
Jing J,
Jukema JW,
Kajantie E,
Kamatani Y,
Kasbohm E,
Kaufman JM,
Kiemeney LA,
Kloppenburg M,
Kronenberg F,
Kubo M,
Lahti J,
Lapauw B,
Li S,
Liewald DCM,
Lim EM,
Linneberg A,
Marina M,
Mascalzoni D,
Matsuda K,
Medenwald D,
Meisinger C,
Meulenbelt I,
De Meyer T,
Meyer Zu Schwabedissen HE,
Mikolajczyk R,
Moed M,
Netea-Maier RT,
Nolte IM,
Okada Y,
Pala M,
Pattaro C,
Pedersen O,
Petersmann A,
Porcu E,
Postmus I,
Pramstaller PP,
Psaty BM,
Ramos YFM,
Rawal R,
Redmond P,
Richards JB,
Rietzschel ER,
Rivadeneira F,
Roef G,
Rotter JI,
Sala CF,
Schlessinger D,
Selvin E,
Slagboom PE,
Soranzo N,
Sørensen TIA,
Spector TD,
Starr JM,
Stott DJ,
Taes Y,
Taliun D,
Tanaka T,
Thuesen B,
Tiller D,
Toniolo D,
Uitterlinden AG,
Visser WE,
Walsh JP,
Wilson SG,
Wolffenbuttel BHR,
Yang Q,
Zheng HF,
Cappola A,
Peeters RP,
Naitza S,
Völzke H,
Sanna S,
Köttgen A,
Visser TJ,
Medici M
Lifelines Cohort Study
Nature communications · 2018 · PMID 30367059 · open access
12 pages+
Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age
Deelen J,
Beekman M,
Uh HW,
Broer L,
Ayers KL,
Tan Q,
Kamatani Y,
Bennet AM,
Tamm R,
Trompet S,
Guðbjartsson DF,
Flachsbart F
and 75 more — show all
Rose G,
Viktorin A,
Fischer K,
Nygaard M,
Cordell HJ,
Crocco P,
van den Akker EB,
Böhringer S,
Helmer Q,
Nelson CP,
Saunders GI,
Alver M,
Andersen-Ranberg K,
Breen ME,
van der Breggen R,
Caliebe A,
Capri M,
Cevenini E,
Collerton JC,
Dato S,
Davies K,
Ford I,
Gampe J,
Garagnani P,
de Geus EJ,
Harrow J,
van Heemst D,
Heijmans BT,
Heinsen FA,
Hottenga JJ,
Hofman A,
Jeune B,
Jonsson PV,
Lathrop M,
Lechner D,
Martin-Ruiz C,
Mcnerlan SE,
Mihailov E,
Montesanto A,
Mooijaart SP,
Murphy A,
Nohr EA,
Paternoster L,
Postmus I,
Rivadeneira F,
Ross OA,
Salvioli S,
Sattar N,
Schreiber S,
Stefánsson H,
Stott DJ,
Tiemeier H,
Uitterlinden AG,
Westendorp RG,
Willemsen G,
Samani NJ,
Galan P,
Sørensen TI,
Boomsma DI,
Jukema JW,
Rea IM,
Passarino G,
de Craen AJ,
Christensen K,
Nebel A,
Stefánsson K,
Metspalu A,
Magnusson P,
Blanché H,
Christiansen L,
Kirkwood TB,
van Duijn CM,
Franceschi C,
Houwing-Duistermaat JJ,
Slagboom PE
Human molecular genetics · 2014 · PMID 24688116 · open access
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
Meta-analysis of genome-wide association studies of HDL cholesterol response to statins
Postmus I,
Warren HR,
Trompet S,
Arsenault BJ,
Avery CL,
Bis JC,
Chasman DI,
de Keyser CE,
Deshmukh HA,
Evans DS,
Feng Q,
Li X
and 76 more — show all
Smit RA,
Smith AV,
Sun F,
Taylor KD,
Arnold AM,
Barnes MR,
Barratt BJ,
Betteridge J,
Boekholdt SM,
Boerwinkle E,
Buckley BM,
Chen YI,
de Craen AJ,
Cummings SR,
Denny JC,
Dubé MP,
Durrington PN,
Eiriksdottir G,
Ford I,
Guo X,
Harris TB,
Heckbert SR,
Hofman A,
Hovingh GK,
Kastelein JJ,
Launer LJ,
Liu CT,
Liu Y,
Lumley T,
McKeigue PM,
Munroe PB,
Neil A,
Nickerson DA,
Nyberg F,
O'Brien E,
O'Donnell CJ,
Post W,
Poulter N,
Vasan RS,
Rice K,
Rich SS,
Rivadeneira F,
Sattar N,
Sever P,
Shaw-Hawkins S,
Shields DC,
Slagboom PE,
Smith NL,
Smith JD,
Sotoodehnia N,
Stanton A,
Stott DJ,
Stricker BH,
Stürmer T,
Uitterlinden AG,
Wei WQ,
Westendorp RG,
Whitsel EA,
Wiggins KL,
Wilke RA,
Ballantyne CM,
Colhoun HM,
Cupples LA,
Franco OH,
Gudnason V,
Hitman G,
Palmer CN,
Psaty BM,
Ridker PM,
Stafford JM,
Stein CM,
Tardif JC,
Caulfield MJ,
Jukema JW,
Rotter JI,
Krauss RM
Journal of medical genetics · 2016 · PMID 27587472
2 pages
Questions about this list
Why is my paper here? I never gave you permission.
Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
cites your work, and links to the paper on PubMed — which is what a citation is.
Your title and author list come from Europe PMC, the same public record a library
catalogue uses.
Why are all the authors listed instead of "et al."?
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
away. Everyone is searchable, including the 187th name on a consortium paper —
that person exists and may be looking for it.
My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
inconsistent across databases; where two people share a form of a name we cannot
separate them, and we would rather be corrected than guess.
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.
Which pages rest on a paper?
Each row lists them, up to six, and links to each one. The count beside a row is
how many pages cite it in total.
How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
resting on it and disappears if that page stops — there is no separate list to
keep in step, because the citation lives on the page that makes the claim.