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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.
8 matches for
Breteler MMB.
Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities
Francis CM,
Futschik ME,
Huang J,
Bai W,
Sargurupremraj M,
Teumer A,
Breteler MMB,
Petretto E,
Ho ASR,
Amouyel P,
Engelter ST,
Bülow R
and 11 more — show all
Völker U,
Völzke H,
Dörr M,
Imtiaz MA,
Aziz NA,
Lohner V,
Ware JS,
Debette S,
Elliott P,
Dehghan A,
Matthews PM
Nature communications · 2022 · PMID 35922433 · open access
12 pages+
Genome-wide association studies of missing metabolite measures from two population-based studies
Faquih TO,
Imtiaz MA,
Talevi V,
Landstra EN,
van Hylckama Vlieg A,
Li-Gao R,
Rosendaal FR,
Noordam R,
van Heemst D,
Mook-Kanamori DO,
Breteler MMB,
Aziz NA
and 1 more — show all
Genome biology · 2026 · PMID 42426908 · open access
12 pages+
Genome-wide association study identifies 48 common genetic variants associated with handedness
Cuellar-Partida G,
Tung JY,
Eriksson N,
Albrecht E,
Aliev F,
Andreassen OA,
Barroso I,
Beckmann JS,
Boks MP,
Boomsma DI,
Boyd HA,
Breteler MMB
and 106 more — show all
Campbell H,
Chasman DI,
Cherkas LF,
Davies G,
de Geus EJC,
Deary IJ,
Deloukas P,
Dick DM,
Duffy DL,
Eriksson JG,
Esko T,
Feenstra B,
Geller F,
Gieger C,
Giegling I,
Gordon SD,
Han J,
Hansen TF,
Hartmann AM,
Hayward C,
Heikkilä K,
Hicks AA,
Hirschhorn JN,
Hottenga JJ,
Huffman JE,
Hwang LD,
Ikram MA,
Kaprio J,
Kemp JP,
Khaw KT,
Klopp N,
Konte B,
Kutalik Z,
Lahti J,
Li X,
Loos RJF,
Luciano M,
Magnusson SH,
Mangino M,
Marques-Vidal P,
Martin NG,
McArdle WL,
McCarthy MI,
Medina-Gomez C,
Melbye M,
Melville SA,
Metspalu A,
Milani L,
Mooser V,
Nelis M,
Nyholt DR,
O'Connell KS,
Ophoff RA,
Palmer C,
Palotie A,
Palviainen T,
Pare G,
Paternoster L,
Peltonen L,
Penninx BWJH,
Polasek O,
Pramstaller PP,
Prokopenko I,
Raikkonen K,
Ripatti S,
Rivadeneira F,
Rudan I,
Rujescu D,
Smit JH,
Smith GD,
Smoller JW,
Soranzo N,
Spector TD,
Pourcain BS,
Starr JM,
Stefánsson H,
Steinberg S,
Teder-Laving M,
Thorleifsson G,
Stefánsson K,
Timpson NJ,
Uitterlinden AG,
van Duijn CM,
van Rooij FJA,
Vink JM,
Vollenweider P,
Vuoksimaa E,
Waeber G,
Wareham NJ,
Warrington N,
Waterworth D,
Werge T,
Wichmann HE,
Widen E,
Willemsen G,
Wright AF,
Wright MJ,
Xu M,
Zhao JH,
Kraft P,
Hinds DA,
Lindgren CM,
Mägi R,
Neale BM,
Evans DM,
Medland SE
Nature human behaviour · 2021 · PMID 32989287
7 pages
Genome-wide association meta-analysis of human olfactory identification discovers sex-specific and sex-differential genetic variants
Förster F,
Emmert D,
Horn K,
Pott J,
Frasnelli J,
Imtiaz MA,
Melas K,
Talevi V,
Chen H,
Engel C,
Filosi M,
Fornage M
and 11 more — show all
Gögele M,
Löffler M,
Mosley TH,
Pattaro C,
Pramstaller P,
Shrestha S,
Aziz NA,
Breteler MMB,
Wirkner K,
Scholz M,
Fuchsberger C
Nature communications · 2025 · PMID 40593737 · open access
2 pages
Common variants at 12q15 and 12q24 are associated with infant head circumference
Taal HR,
Pourcain BS,
Thiering E,
Das S,
Mook-Kanamori DO,
Warrington NM,
Kaakinen M,
Kreiner-Møller E,
Bradfield JP,
Freathy RM,
Geller F,
Guxens M
and 74 more — show all
Cousminer DL,
Kerkhof M,
Timpson NJ,
Ikram MA,
Beilin LJ,
Bønnelykke K,
Buxton JL,
Charoen P,
Chawes BLK,
Eriksson J,
Evans DM,
Hofman A,
Kemp JP,
Kim CE,
Klopp N,
Lahti J,
Lye SJ,
McMahon G,
Mentch FD,
Müller M,
O'Reilly PF,
Prokopenko I,
Rivadeneira F,
Steegers EAP,
Sunyer J,
Tiesler C,
Yaghootkar H,
Breteler MMB,
Debette S,
Fornage M,
Gudnason V,
Launer LJ,
van der Lugt A,
Mosley TH,
Seshadri S,
Smith AV,
Vernooij MW,
Blakemore AI,
Chiavacci RM,
Feenstra B,
Fernandez-Benet J,
Grant SFA,
Hartikainen AL,
van der Heijden AJ,
Iñiguez C,
Lathrop M,
McArdle WL,
Mølgaard A,
Newnham JP,
Palmer LJ,
Palotie A,
Palotie A,
Pouta A,
Ring SM,
Sovio U,
Standl M,
Uitterlinden AG,
Wichmann HE,
Vissing NH,
DeCarli C,
van Duijn CM,
McCarthy MI,
Koppelman GH,
Estivill X,
Hattersley AT,
Melbye M,
Bisgaard H,
Pennell CE,
Widen E,
Hakonarson H,
Smith GD,
Heinrich J,
Jarvelin MR,
Jaddoe VWV
Cohorts for Heart and Aging Research in Genetic Epidemiology (CHARGE) Consortium · Early Genetics & Lifecourse Epidemiology (EAGLE) consortium and 1 more consortia
Nature genetics · 2012 · PMID 22504419
1 page
Genome-wide association study meta-analysis of neurofilament light (NfL) levels in blood reveals novel loci related to neurodegeneration
Ahmad S,
Imtiaz MA,
Mishra A,
Wang R,
Herrera-Rivero M,
Bis JC,
Fornage M,
Roshchupkin G,
Hofer E,
Logue M,
Longstreth WT Jr,
Xia R
and 22 more — show all
Bouteloup V,
Mosley T,
Launer LJ,
Khalil M,
Kuhle J,
Rissman RA,
Chene G,
Dufouil C,
Djoussé L,
Lyons MJ,
Mukamal KJ,
Kremen WS,
Franz CE,
Schmidt R,
Debette S,
Breteler MMB,
Berger K,
Yang Q,
Seshadri S,
Aziz NA,
Ghanbari M,
Ikram MA
Communications biology · 2024 · PMID 39251807 · open access
1 page
Genome-wide association study meta-analysis uncovers novel genetic variants associated with olfactory dysfunction
Imtiaz MA,
Melas K,
Tin A,
Talevi V,
Chen H,
Fornage M,
Shrestha S,
Gögele M,
Emmert D,
Pattaro C,
Pramstaller P,
Förster F
and 6 more — show all
BMC genomic data · 2025 · PMID 40963118 · 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.