For researchers
Is your paper here?
2,673 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.
5 matches for
Hoffman JD.
Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data
Tachmazidou I,
Hatzikotoulas K,
Southam L,
Esparza-Gordillo J,
Haberland V,
Zheng J,
Johnson T,
Koprulu M,
Zengini E,
Steinberg J,
Wilkinson JM,
Bhatnagar S
and 9 more — show all
arcOGEN Consortium
Nature genetics · 2019 · PMID 30664745 · open access
12 pages+
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries
Shrine N,
Guyatt AL,
Erzurumluoglu AM,
Jackson VE,
Hobbs BD,
Melbourne CA,
Batini C,
Fawcett KA,
Song K,
Sakornsakolpat P,
Li X,
Boxall R
and 99 more — show all
Reeve NF,
Obeidat M,
Zhao JH,
Wielscher M,
Weiss S,
Kentistou KA,
Kentistou KA,
Cook JP,
Sun BB,
Zhou J,
Hui J,
Karrasch S,
Imboden M,
Harris SE,
Marten J,
Enroth S,
Kerr SM,
Surakka I,
Vitart V,
Lehtimäki T,
Allen RJ,
Bakke PS,
Beaty TH,
Bleecker ER,
Bossé Y,
Brandsma CA,
Chen Z,
Crapo JD,
Danesh J,
DeMeo DL,
Dudbridge F,
Ewert R,
Gieger C,
Gulsvik A,
Hansell AL,
Hao K,
Hoffman JD,
Hokanson JE,
Homuth G,
Joshi PK,
Joubert P,
Langenberg C,
Li X,
Li L,
Lin K,
Lind L,
Locantore N,
Luan J,
Mahajan A,
Maranville JC,
Murray A,
Nickle DC,
Packer R,
Parker MM,
Paynton ML,
Porteous DJ,
Porteous DJ,
Prokopenko D,
Qiao D,
Rawal R,
Runz H,
Sayers I,
Sin DD,
Smith BH,
Soler Artigas M,
Sparrow D,
Tal-Singer R,
Timmers PRHJ,
Van den Berge M,
Whittaker JC,
Woodruff PG,
Yerges-Armstrong LM,
Troyanskaya OG,
Raitakari OT,
Kähönen M,
Polašek O,
Gyllensten U,
Rudan I,
Deary IJ,
Probst-Hensch NM,
Schulz H,
James AL,
Wilson JF,
Stubbe B,
Zeggini E,
Jarvelin MR,
Wareham N,
Silverman EK,
Hayward C,
Morris AP,
Butterworth AS,
Scott RA,
Walters RG,
Meyers DA,
Cho MH,
Strachan DP,
Hall IP,
Tobin MD,
Wain LV
Understanding Society Scientific Group
Nature genetics · 2019 · PMID 30804560 · open access
12 pages+
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts
Rashkin SR,
Graff RE,
Kachuri L,
Thai KK,
Alexeeff SE,
Blatchins MA,
Cavazos TB,
Corley DA,
Emami NC,
Hoffman JD,
Jorgenson E,
Kushi LH
and 7 more — show all
Nature communications · 2020 · PMID 32887889 · open access
12 pages+
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology
Ferreira MA,
Vonk JM,
Baurecht H,
Marenholz I,
Tian C,
Hoffman JD,
Helmer Q,
Tillander A,
Ullemar V,
van Dongen J,
Lu Y,
Rüschendorf F
and 54 more — show all
Esparza-Gordillo J,
Medway CW,
Mountjoy E,
Burrows K,
Hummel O,
Grosche S,
Brumpton BM,
Witte JS,
Hottenga JJ,
Willemsen G,
Zheng J,
Rodríguez E,
Hotze M,
Franke A,
Revez JA,
Beesley J,
Matheson MC,
Dharmage SC,
Bain LM,
Fritsche LG,
Gabrielsen ME,
Balliu B,
Nielsen JB,
Zhou W,
Hveem K,
Langhammer A,
Holmen OL,
Løset M,
Abecasis GR,
Willer CJ,
Arnold A,
Homuth G,
Schmidt CO,
Thompson PJ,
Martin NG,
Duffy DL,
Novak N,
Schulz H,
Karrasch S,
Gieger C,
Strauch K,
Melles RB,
Hinds DA,
Hübner N,
Weidinger S,
Magnusson PKE,
Jansen R,
Jorgenson E,
Lee YA,
Boomsma DI,
Almqvist C,
Karlsson R,
Koppelman GH,
Paternoster L
23andMe Research Team · AAGC collaborators and 2 more consortia
Nature genetics · 2017 · PMID 29083406 · open access
10 pages
Age-of-onset information helps identify 76 genetic variants associated with allergic disease
Ferreira MAR,
Vonk JM,
Baurecht H,
Marenholz I,
Tian C,
Hoffman JD,
Helmer Q,
Tillander A,
Ullemar V,
Lu Y,
Grosche S,
Rüschendorf F
and 28 more — show all
Granell R,
Brumpton BM,
Fritsche LG,
Bhatta L,
Gabrielsen ME,
Nielsen JB,
Zhou W,
Hveem K,
Langhammer A,
Holmen OL,
Løset M,
Abecasis GR,
Willer CJ,
Emami NC,
Cavazos TB,
Witte JS,
Szwajda A,
Hinds DA,
Hübner N,
Weidinger S,
Magnusson PK,
Jorgenson E,
Karlsson R,
Paternoster L,
Boomsma DI,
Almqvist C,
Lee YA,
Koppelman GH
23andMe Research Team · collaborators of the SHARE study
PLoS genetics · 2020 · PMID 32603359 · open access
7 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.