For researchers
Is your paper here?
2,663 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.
6 matches for
Klaric L.
Genome-Wide Association Study on Immunoglobulin G Glycosylation Patterns
Wahl A,
van den Akker E,
Klaric L,
Štambuk J,
Benedetti E,
Plomp R,
Razdorov G,
Trbojević-Akmačić I,
Deelen J,
van Heemst D,
Slagboom PE,
Vučković F
and 10 more — show all
Frontiers in immunology · 2018 · PMID 29535710 · open access
12 pages+
GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19
Pairo-Castineira E,
Rawlik K,
Bretherick AD,
Qi T,
Wu Y,
Nassiri I,
McConkey GA,
Zechner M,
Klaric L,
Griffiths F,
Oosthuyzen W,
Kousathanas A
and 43 more — show all
Richmond A,
Millar J,
Russell CD,
Malinauskas T,
Thwaites R,
Morrice K,
Keating S,
Maslove D,
Nichol A,
Semple MG,
Knight J,
Shankar-Hari M,
Summers C,
Hinds C,
Horby P,
Ling L,
McAuley D,
Montgomery H,
Openshaw PJM,
Begg C,
Walsh T,
Tenesa A,
Flores C,
Riancho JA,
Rojas-Martinez A,
Lapunzina P,
Yang J,
Ponting CP,
Wilson JF,
Vitart V,
Abedalthagafi M,
Luchessi AD,
Parra EJ,
Cruz R,
Carracedo A,
Fawkes A,
Murphy L,
Rowan K,
Pereira AC,
Law A,
Fairfax B,
Hendry SC,
Baillie JK
GenOMICC Investigators · SCOURGE Consortium and 2 more consortia
Nature · 2023 · PMID 37198478 · open access
12 pages+
Whole-genome sequencing reveals host factors underlying critical COVID-19
Kousathanas A,
Pairo-Castineira E,
Rawlik K,
Stuckey A,
Odhams CA,
Walker S,
Russell CD,
Malinauskas T,
Wu Y,
Millar J,
Shen X,
Elliott KS
and 64 more — show all
Griffiths F,
Oosthuyzen W,
Morrice K,
Keating S,
Wang B,
Rhodes D,
Klaric L,
Zechner M,
Parkinson N,
Siddiq A,
Goddard P,
Donovan S,
Maslove D,
Nichol A,
Semple MG,
Zainy T,
Maleady-Crowe F,
Todd L,
Salehi S,
Knight J,
Elgar G,
Chan G,
Arumugam P,
Patch C,
Rendon A,
Bentley D,
Kingsley C,
Kosmicki JA,
Horowitz JE,
Baras A,
Abecasis GR,
Ferreira MAR,
Justice A,
Mirshahi T,
Oetjens M,
Rader DJ,
Ritchie MD,
Verma A,
Fowler TA,
Shankar-Hari M,
Summers C,
Hinds C,
Horby P,
Ling L,
McAuley D,
Montgomery H,
Openshaw PJM,
Elliott P,
Walsh T,
Tenesa A,
Fawkes A,
Murphy L,
Rowan K,
Ponting CP,
Vitart V,
Wilson JF,
Yang J,
Bretherick AD,
Scott RH,
Hendry SC,
Moutsianas L,
Law A,
Caulfield MJ,
Baillie JK
GenOMICC investigators · 23andMe investigators and 1 more consortia
Nature · 2022 · PMID 35255492 · open access
5 pages
Genetic mechanisms of critical illness in COVID-19
Pairo-Castineira E,
Clohisey S,
Klaric L,
Bretherick AD,
Rawlik K,
Pasko D,
Walker S,
Parkinson N,
Fourman MH,
Russell CD,
Furniss J,
Richmond A
and 54 more — show all
Gountouna E,
Wrobel N,
Harrison D,
Wang B,
Wu Y,
Meynert A,
Griffiths F,
Oosthuyzen W,
Kousathanas A,
Moutsianas L,
Yang Z,
Zhai R,
Zheng C,
Grimes G,
Beale R,
Millar J,
Shih B,
Keating S,
Zechner M,
Haley C,
Porteous DJ,
Hayward C,
Yang J,
Knight J,
Summers C,
Shankar-Hari M,
Klenerman P,
Turtle L,
Ho A,
Moore SC,
Hinds C,
Horby P,
Nichol A,
Maslove D,
Ling L,
McAuley D,
Montgomery H,
Walsh T,
Pereira AC,
Renieri A,
Shen X,
Ponting CP,
Fawkes A,
Tenesa A,
Caulfield M,
Scott R,
Rowan K,
Murphy L,
Openshaw PJM,
Semple MG,
Law A,
Vitart V,
Wilson JF,
Baillie JK
GenOMICC Investigators · ISARIC4C Investigators and 4 more consortia
Nature · 2021 · PMID 33307546
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
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.