For researchers
Is your paper here?
2,657 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
Montgomery C.
High-Density Genetic Mapping Identifies New Susceptibility Variants in Sarcoidosis Phenotypes and Shows Genomic-driven Phenotypic Differences
Rivera NV,
Ronninger M,
Shchetynsky K,
Franke A,
Nöthen MM,
Müller-Quernheim J,
Schreiber S,
Adrianto I,
Karakaya B,
van Moorsel CH,
Navratilova Z,
Kolek V
and 9 more — show all
American journal of respiratory and critical care medicine · 2016 · PMID 26651848
9 pages
Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjögren's syndrome
Lessard CJ,
Li H,
Adrianto I,
Ice JA,
Rasmussen A,
Grundahl KM,
Kelly JA,
Dozmorov MG,
Miceli-Richard C,
Bowman S,
Lester S,
Eriksson P
and 48 more — show all
Eloranta ML,
Brun JG,
Gøransson LG,
Harboe E,
Guthridge JM,
Kaufman KM,
Kvarnström M,
Jazebi H,
Cunninghame Graham DS,
Grandits ME,
Nazmul-Hossain AN,
Patel K,
Adler AJ,
Maier-Moore JS,
Farris AD,
Brennan MT,
Lessard JA,
Chodosh J,
Gopalakrishnan R,
Hefner KS,
Houston GD,
Huang AJ,
Hughes PJ,
Lewis DM,
Radfar L,
Rohrer MD,
Stone DU,
Wren JD,
Vyse TJ,
Gaffney PM,
James JA,
Omdal R,
Wahren-Herlenius M,
Illei GG,
Witte T,
Jonsson R,
Rischmueller M,
Rönnblom L,
Nordmark G,
Ng WF,
Mariette X,
Anaya JM,
Rhodus NL,
Segal BM,
Scofield RH,
Montgomery CG,
Harley JB,
Sivils KL
UK Primary Sjögren's Syndrome Registry
Nature genetics · 2013 · PMID 24097067 · open access
4 pages
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
Kowalski MH,
Qian H,
Hou Z,
Rosen JD,
Tapia AL,
Shan Y,
Jain D,
Argos M,
Arnett DK,
Avery C,
Barnes KC,
Becker LC
and 66 more — show all
Bien SA,
Bis JC,
Blangero J,
Boerwinkle E,
Bowden DW,
Buyske S,
Cai J,
Cho MH,
Choi SH,
Choquet H,
Cupples LA,
Cushman M,
Daya M,
de Vries PS,
Ellinor PT,
Faraday N,
Fornage M,
Gabriel S,
Ganesh SK,
Graff M,
Gupta N,
He J,
Heckbert SR,
Hidalgo B,
Hodonsky CJ,
Irvin MR,
Johnson AD,
Jorgenson E,
Kaplan R,
Kardia SLR,
Kelly TN,
Kooperberg C,
Lasky-Su JA,
Loos RJF,
Lubitz SA,
Mathias RA,
McHugh CP,
Montgomery C,
Moon JY,
Morrison AC,
Palmer ND,
Pankratz N,
Papanicolaou GJ,
Peralta JM,
Peyser PA,
Rich SS,
Rotter JI,
Silverman EK,
Smith JA,
Smith NL,
Taylor KD,
Thornton TA,
Tiwari HK,
Tracy RP,
Wang T,
Weiss ST,
Weng LC,
Wiggins KL,
Wilson JG,
Yanek LR,
Zöllner S,
North KE,
Auer PL,
Raffield LM,
Reiner AP,
Li Y
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium · TOPMed Hematology & Hemostasis Working Group
PLoS genetics · 2019 · PMID 31869403 · open access
3 pages
Identification of Immune-Relevant Factors Conferring Sarcoidosis Genetic Risk
Fischer A,
Ellinghaus D,
Nutsua M,
Hofmann S,
Montgomery CG,
Iannuzzi MC,
Rybicki BA,
Petrek M,
Mrazek F,
Pabst S,
Grohé C,
Grunewald J
and 23 more — show all
Ronninger M,
Eklund A,
Padyukov L,
Mihailovic-Vucinic V,
Jovanovic D,
Sterclova M,
Homolka J,
Nöthen MM,
Herms S,
Gieger C,
Strauch K,
Winkelmann J,
Boehm BO,
Brand S,
Büning C,
Schürmann M,
Ellinghaus E,
Baurecht H,
Lieb W,
Nebel A,
Müller-Quernheim J,
Franke A,
Schreiber S
GenPhenReSa Consortium
American journal of respiratory and critical care medicine · 2015 · PMID 26051272
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.