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Is your paper here?
2,676 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
Freidin MB.
Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks
Demenais F,
Margaritte-Jeannin P,
Barnes KC,
Cookson WOC,
Altmüller J,
Ang W,
Barr RG,
Beaty TH,
Becker AB,
Beilby J,
Bisgaard H,
Bjornsdottir US
and 163 more — show all
Bleecker E,
Bønnelykke K,
Boomsma DI,
Bouzigon E,
Brightling CE,
Brossard M,
Brusselle GG,
Burchard E,
Burkart KM,
Bush A,
Chan-Yeung M,
Chung KF,
Couto Alves A,
Curtin JA,
Custovic A,
Daley D,
de Jongste JC,
Del-Rio-Navarro BE,
Donohue KM,
Duijts L,
Eng C,
Eriksson JG,
Farrall M,
Fedorova Y,
Feenstra B,
Ferreira MA,
Freidin MB,
Gajdos Z,
Gauderman J,
Gehring U,
Geller F,
Genuneit J,
Gharib SA,
Gilliland F,
Granell R,
Graves PE,
Gudbjartsson DF,
Haahtela T,
Heckbert SR,
Heederik D,
Heinrich J,
Heliövaara M,
Henderson J,
Himes BE,
Hirose H,
Hirschhorn JN,
Hofman A,
Holt P,
Hottenga J,
Hudson TJ,
Hui J,
Imboden M,
Ivanov V,
Jaddoe VWV,
James A,
Janson C,
Jarvelin MR,
Jarvis D,
Jones G,
Jonsdottir I,
Jousilahti P,
Kabesch M,
Kähönen M,
Kantor DB,
Karunas AS,
Khusnutdinova E,
Koppelman GH,
Kozyrskyj AL,
Kreiner E,
Kubo M,
Kumar R,
Kumar A,
Kuokkanen M,
Lahousse L,
Laitinen T,
Laprise C,
Lathrop M,
Lau S,
Lee YA,
Lehtimäki T,
Letort S,
Levin AM,
Li G,
Liang L,
Loehr LR,
London SJ,
Loth DW,
Manichaikul A,
Marenholz I,
Martinez FJ,
Matheson MC,
Mathias RA,
Matsumoto K,
Mbarek H,
McArdle WL,
Melbye M,
Melén E,
Meyers D,
Michel S,
Mohamdi H,
Musk AW,
Myers RA,
Nieuwenhuis MAE,
Noguchi E,
O'Connor GT,
Ogorodova LM,
Palmer CD,
Palotie A,
Park JE,
Pennell CE,
Pershagen G,
Polonikov A,
Postma DS,
Probst-Hensch N,
Puzyrev VP,
Raby BA,
Raitakari OT,
Ramasamy A,
Rich SS,
Robertson CF,
Romieu I,
Salam MT,
Salomaa V,
Schlünssen V,
Scott R,
Selivanova PA,
Sigsgaard T,
Simpson A,
Siroux V,
Smith LJ,
Solodilova M,
Standl M,
Stefansson K,
Strachan DP,
Stricker BH,
Takahashi A,
Thompson PJ,
Thorleifsson G,
Thorsteinsdottir U,
Tiesler CMT,
Torgerson DG,
Tsunoda T,
Uitterlinden AG,
van der Valk RJP,
Vaysse A,
Vedantam S,
von Berg A,
von Mutius E,
Vonk JM,
Waage J,
Wareham NJ,
Weiss ST,
White WB,
Wickman M,
Widén E,
Willemsen G,
Williams LK,
Wouters IM,
Yang JJ,
Zhao JH,
Moffatt MF,
Ober C,
Nicolae DL
Australian Asthma Genetics Consortium (AAGC) collaborators
Nature genetics · 2018 · PMID 29273806 · open access
12 pages+
Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss
Trpchevska N,
Freidin MB,
Broer L,
Oosterloo BC,
Yao S,
Zhou Y,
Vona B,
Bishop C,
Bizaki-Vallaskangas A,
Canlon B,
Castellana F,
Chasman DI
and 54 more — show all
Cherny S,
Christensen K,
Concas MP,
Correa A,
Elkon R,
Mengel-From J,
Gao Y,
Giersch ABS,
Girotto G,
Gudjonsson A,
Gudnason V,
Heard-Costa NL,
Hertzano R,
Hjelmborg JVB,
Hjerling-Leffler J,
Hoffman HJ,
Kaprio J,
Kettunen J,
Krebs K,
Kähler AK,
Lallemend F,
Launer LJ,
Lee IM,
Leonard H,
Li CM,
Lowenheim H,
Magnusson PKE,
van Meurs J,
Milani L,
Morton CC,
Mäkitie A,
Nalls MA,
Nardone GG,
Nygaard M,
Palviainen T,
Pratt S,
Quaranta N,
Rämö J,
Saarentaus E,
Sardone R,
Satizabal CL,
Schweinfurth JM,
Seshadri S,
Shiroma E,
Shulman E,
Simonsick E,
Spankovich C,
Tropitzsch A,
Lauschke VM,
Sullivan PF,
Goedegebure A,
Cederroth CR,
Williams FMK,
Nagtegaal AP
Estonian Biobank Research Team
American journal of human genetics · 2022 · PMID 35580588 · open access
12 pages+
Meta-analysis identifies seven susceptibility loci involved in the atopic march
Marenholz I,
Esparza-Gordillo J,
Rüschendorf F,
Bauerfeind A,
Strachan DP,
Spycher BD,
Baurecht H,
Margaritte-Jeannin P,
Sääf A,
Kerkhof M,
Ege M,
Baltic S
and 61 more — show all
Matheson MC,
Li J,
Michel S,
Ang WQ,
McArdle W,
Arnold A,
Homuth G,
Demenais F,
Bouzigon E,
Söderhäll C,
Pershagen G,
de Jongste JC,
Postma DS,
Braun-Fahrländer C,
Horak E,
Ogorodova LM,
Puzyrev VP,
Bragina EY,
Hudson TJ,
Morin C,
Duffy DL,
Marks GB,
Robertson CF,
Montgomery GW,
Musk B,
Thompson PJ,
Martin NG,
James A,
Sleiman P,
Toskala E,
Rodriguez E,
Fölster-Holst R,
Franke A,
Lieb W,
Gieger C,
Heinzmann A,
Rietschel E,
Keil T,
Cichon S,
Nöthen MM,
Pennell CE,
Sly PD,
Schmidt CO,
Matanovic A,
Schneider V,
Heinig M,
Hübner N,
Holt PG,
Lau S,
Kabesch M,
Weidinger S,
Hakonarson H,
Ferreira MAR,
Laprise C,
Freidin MB,
Genuneit J,
Koppelman GH,
Melén E,
Dizier MH,
Henderson AJ,
Lee YA
Nature communications · 2015 · PMID 26542096 · open access
3 pages
Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain
Suri P,
Palmer MR,
Tsepilov YA,
Freidin MB,
Boer CG,
Yau MS,
Evans DS,
Gelemanovic A,
Bartz TM,
Nethander M,
Arbeeva L,
Karssen L
and 25 more — show all
Neogi T,
Campbell A,
Mellstrom D,
Ohlsson C,
Marshall LM,
Orwoll E,
Uitterlinden A,
Rotter JI,
Lauc G,
Psaty BM,
Karlsson MK,
Lane NE,
Jarvik GP,
Polasek O,
Hochberg M,
Jordan JM,
Van Meurs JBJ,
Jackson R,
Nielson CM,
Mitchell BD,
Smith BH,
Hayward C,
Smith NL,
Aulchenko YS,
Williams FMK
PLoS genetics · 2018 · PMID 30261039 · open access
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.