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Search your name, your journal, or a PMID.
7 matches for
INVENT Consortium.
Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels
Sabater-Lleal M,
Huffman JE,
de Vries PS,
Marten J,
Mastrangelo MA,
Song C,
Pankratz N,
Ward-Caviness CK,
Yanek LR,
Trompet S,
Delgado GE,
Guo X
and 64 more — show all
Bartz TM,
Martinez-Perez A,
Germain M,
de Haan HG,
Ozel AB,
Polasek O,
Smith AV,
Eicher JD,
Reiner AP,
Tang W,
Davies NM,
Stott DJ,
Rotter JI,
Tofler GH,
Boerwinkle E,
de Maat MPM,
Kleber ME,
Welsh P,
Brody JA,
Chen MH,
Vaidya D,
Soria JM,
Suchon P,
van Hylckama Vlieg A,
Desch KC,
Kolcic I,
Joshi PK,
Launer LJ,
Harris TB,
Campbell H,
Rudan I,
Becker DM,
Li JZ,
Rivadeneira F,
Uitterlinden AG,
Hofman A,
Franco OH,
Cushman M,
Psaty BM,
Morange PE,
McKnight B,
Chong MR,
Fernandez-Cadenas I,
Rosand J,
Lindgren A,
Gudnason V,
Wilson JF,
Hayward C,
Ginsburg D,
Fornage M,
Rosendaal FR,
Souto JC,
Becker LC,
Jenny NS,
März W,
Jukema JW,
Dehghan A,
Trégouët DA,
Morrison AC,
Johnson AD,
O'Donnell CJ,
Strachan DP,
Lowenstein CJ,
Smith NL
INVENT Consortium; MEGASTROKE Consortium of the International Stroke Genetics Consortium (ISGC)
Circulation · 2019 · PMID 30586737
8 pages
A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology
de Vries PS,
Sabater-Lleal M,
Huffman JE,
Marten J,
Song C,
Pankratz N,
Bartz TM,
de Haan HG,
Delgado GE,
Eicher JD,
Martinez-Perez A,
Ward-Caviness CK
and 33 more — show all
Brody JA,
Chen MH,
de Maat MPM,
Frånberg M,
Gill D,
Kleber ME,
Rivadeneira F,
Soria JM,
Tang W,
Tofler GH,
Uitterlinden AG,
van Hylckama Vlieg A,
Seshadri S,
Boerwinkle E,
Davies NM,
Giese AK,
Ikram MK,
Kittner SJ,
McKnight B,
Psaty BM,
Reiner AP,
Sargurupremraj M,
Taylor KD,
Fornage M,
Hamsten A,
März W,
Rosendaal FR,
Souto JC,
Dehghan A,
Johnson AD,
Morrison AC,
O'Donnell CJ,
Smith NL
INVENT Consortium · MEGASTROKE Consortium of the International Stroke Genetics Consortium
Blood · 2019 · PMID 30642921
8 pages
Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease
Klarin D,
Busenkell E,
Judy R,
Lynch J,
Levin M,
Haessler J,
Aragam K,
Chaffin M,
Haas M,
Lindström S,
Assimes TL,
Huang J
and 30 more — show all
Min Lee K,
Shao Q,
Huffman JE,
Kabrhel C,
Huang Y,
Sun YV,
Vujkovic M,
Saleheen D,
Miller DR,
Reaven P,
DuVall S,
Boden WE,
Pyarajan S,
Reiner AP,
Trégouët DA,
Henke P,
Kooperberg C,
Gaziano JM,
Concato J,
Rader DJ,
Cho K,
Chang KM,
Wilson PWF,
Smith NL,
O'Donnell CJ,
Tsao PS,
Kathiresan S,
Obi A,
Damrauer SM,
Natarajan P
INVENT Consortium · Veterans Affairs’ Million Veteran Program
Nature genetics · 2019 · PMID 31676865 · open access
7 pages
Stroke genetics informs drug discovery and risk prediction across ancestries
Mishra A,
Malik R,
Hachiya T,
Jürgenson T,
Namba S,
Posner DC,
Kamanu FK,
Koido M,
Le Grand Q,
Shi M,
He Y,
Georgakis MK
and 175 more — show all
Caro I,
Krebs K,
Liaw YC,
Vaura FC,
Lin K,
Winsvold BS,
Srinivasasainagendra V,
Parodi L,
Bae HJ,
Chauhan G,
Chong MR,
Tomppo L,
Akinyemi R,
Roshchupkin GV,
Habib N,
Jee YH,
Thomassen JQ,
Abedi V,
Cárcel-Márquez J,
Nygaard M,
Leonard HL,
Yang C,
Yonova-Doing E,
Knol MJ,
Lewis AJ,
Judy RL,
Ago T,
Amouyel P,
Armstrong ND,
Bakker MK,
Bartz TM,
Bennett DA,
Bis JC,
Bordes C,
Børte S,
Cain A,
Ridker PM,
Cho K,
Chen Z,
Cruchaga C,
Cole JW,
de Jager PL,
de Cid R,
Endres M,
Ferreira LE,
Geerlings MI,
Gasca NC,
Gudnason V,
Hata J,
He J,
Heath AK,
Ho YL,
Havulinna AS,
Hopewell JC,
Hyacinth HI,
Inouye M,
Jacob MA,
Jeon CE,
Jern C,
Kamouchi M,
Keene KL,
Kitazono T,
Kittner SJ,
Konuma T,
Kumar A,
Lacaze P,
Launer LJ,
Lee KJ,
Lepik K,
Li J,
Li L,
Manichaikul A,
Markus HS,
Marston NA,
Meitinger T,
Mitchell BD,
Montellano FA,
Morisaki T,
Mosley TH,
Nalls MA,
Nordestgaard BG,
O'Donnell MJ,
Okada Y,
Onland-Moret NC,
Ovbiagele B,
Peters A,
Psaty BM,
Rich SS,
Rosand J,
Sabatine MS,
Sacco RL,
Saleheen D,
Sandset EC,
Salomaa V,
Sargurupremraj M,
Sasaki M,
Satizabal CL,
Schmidt CO,
Shimizu A,
Smith NL,
Sloane KL,
Sutoh Y,
Sun YV,
Tanno K,
Tiedt S,
Tatlisumak T,
Torres-Aguila NP,
Tiwari HK,
Trégouët DA,
Trompet S,
Tuladhar AM,
Tybjærg-Hansen A,
van Vugt M,
Vibo R,
Verma SS,
Wiggins KL,
Wennberg P,
Woo D,
Wilson PWF,
Xu H,
Yang Q,
Yoon K,
Millwood IY,
Gieger C,
Ninomiya T,
Grabe HJ,
Jukema JW,
Rissanen IL,
Strbian D,
Kim YJ,
Chen PH,
Mayerhofer E,
Howson JMM,
Irvin MR,
Adams H,
Wassertheil-Smoller S,
Christensen K,
Ikram MA,
Rundek T,
Worrall BB,
Lathrop GM,
Riaz M,
Simonsick EM,
Kõrv J,
França PHC,
Zand R,
Prasad K,
Frikke-Schmidt R,
de Leeuw FE,
Liman T,
Haeusler KG,
Ruigrok YM,
Heuschmann PU,
Longstreth WT,
Jung KJ,
Bastarache L,
Paré G,
Damrauer SM,
Chasman DI,
Rotter JI,
Anderson CD,
Zwart JA,
Niiranen TJ,
Fornage M,
Liaw YP,
Seshadri S,
Fernández-Cadenas I,
Walters RG,
Ruff CT,
Owolabi MO,
Huffman JE,
Milani L,
Kamatani Y,
Dichgans M,
Debette S
COMPASS Consortium · INVENT Consortium and 13 more consortia
Nature · 2022 · PMID 36180795 · open access
5 pages
Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis
Hinds DA,
Buil A,
Ziemek D,
Martinez-Perez A,
Malik R,
Folkersen L,
Germain M,
Mälarstig A,
Brown A,
Soria JM,
Dichgans M,
Bing N
and 7 more — show all
METASTROKE Consortium, INVENT Consortium
Human molecular genetics · 2016 · PMID 26908601
2 pages
Genome-wide analysis identifies novel susceptibility loci for myocardial infarction
Hartiala JA,
Han Y,
Jia Q,
Hilser JR,
Huang P,
Gukasyan J,
Schwartzman WS,
Cai Z,
Biswas S,
Trégouët DA,
Smith NL,
Seldin M
and 47 more — show all
Pan C,
Mehrabian M,
Lusis AJ,
Bazeley P,
Sun YV,
Liu C,
Quyyumi AA,
Scholz M,
Thiery J,
Delgado GE,
Kleber ME,
März W,
Howe LJ,
Asselbergs FW,
van Vugt M,
Vlachojannis GJ,
Patel RS,
Lyytikäinen LP,
Kähönen M,
Lehtimäki T,
Nieminen TVM,
Kuukasjärvi P,
Laurikka JO,
Chang X,
Heng CK,
Jiang R,
Kraus WE,
Hauser ER,
Ferguson JF,
Reilly MP,
Ito K,
Koyama S,
Kamatani Y,
Komuro I,
Stolze LK,
Romanoski CE,
Khan MD,
Turner AW,
Miller CL,
Aherrahrou R,
Civelek M,
Ma L,
Björkegren JLM,
Kumar SR,
Tang WHW,
Hazen SL,
Allayee H
INVENT Consortium · CHARGE Consortium Hemostasis Working Group and 2 more consortia
European heart journal · 2021 · PMID 33532862
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.