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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.
6 matches for
Heilmann S.
Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors
Melin BS,
Barnholtz-Sloan JS,
Wrensch MR,
Johansen C,
Il'yasova D,
Kinnersley B,
Ostrom QT,
Labreche K,
Chen Y,
Armstrong G,
Liu Y,
Eckel-Passow JE
and 51 more — show all
Decker PA,
Labussière M,
Idbaih A,
Hoang-Xuan K,
Di Stefano AL,
Mokhtari K,
Delattre JY,
Broderick P,
Galan P,
Gousias K,
Schramm J,
Schoemaker MJ,
Fleming SJ,
Herms S,
Heilmann S,
Nöthen MM,
Wichmann HE,
Schreiber S,
Swerdlow A,
Lathrop M,
Simon M,
Sanson M,
Andersson U,
Rajaraman P,
Chanock S,
Linet M,
Wang Z,
Yeager M,
Wiencke JK,
Hansen H,
McCoy L,
Rice T,
Kosel ML,
Sicotte H,
Amos CI,
Bernstein JL,
Davis F,
Lachance D,
Lau C,
Merrell RT,
Shildkraut J,
Ali-Osman F,
Sadetzki S,
Scheurer M,
Shete S,
Lai RK,
Claus EB,
Olson SH,
Jenkins RB,
Houlston RS,
Bondy ML
GliomaScan Consortium
Nature genetics · 2017 · PMID 28346443
10 pages
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy
Mingardo E,
Beaman G,
Grote P,
Nordenskjöld A,
Newman W,
Woolf AS,
Eckstein M,
Hilger AC,
Dworschak GC,
Rösch W,
Ebert AK,
Stein R
and 54 more — show all
Brusco A,
Di Grazia M,
Tamer A,
Torres FM,
Hernandez JL,
Erben P,
Maj C,
Olmos JM,
Riancho JA,
Valero C,
Hostettler IC,
Houlden H,
Werring DJ,
Schumacher J,
Gehlen J,
Giel AS,
Buerfent BC,
Arkani S,
Åkesson E,
Rotstein E,
Ludwig M,
Holmdahl G,
Giorgio E,
Berettini A,
Keene D,
Cervellione RM,
Younsi N,
Ortlieb M,
Oswald J,
Haid B,
Promm M,
Neissner C,
Hirsch K,
Stehr M,
Schäfer FM,
Schmiedeke E,
Boemers TM,
van Rooij IALM,
Feitz WFJ,
Marcelis CLM,
Lacher M,
Nelson J,
Ure B,
Fortmann C,
Gale DP,
Chan MMY,
Ludwig KU,
Nöthen MM,
Heilmann S,
Zwink N,
Jenetzky E,
Odermatt B,
Knapp M,
Reutter H
Communications biology · 2022 · PMID 36352089 · open access
4 pages
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
Li R,
Brockschmidt FF,
Kiefer AK,
Stefansson H,
Nyholt DR,
Song K,
Vermeulen SH,
Kanoni S,
Glass D,
Medland SE,
Dimitriou M,
Waterworth D
and 27 more — show all
Tung JY,
Geller F,
Heilmann S,
Hillmer AM,
Bataille V,
Eigelshoven S,
Hanneken S,
Moebus S,
Herold C,
den Heijer M,
Montgomery GW,
Deloukas P,
Eriksson N,
Heath AC,
Becker T,
Sulem P,
Mangino M,
Vollenweider P,
Spector TD,
Dedoussis G,
Martin NG,
Kiemeney LA,
Mooser V,
Stefansson K,
Hinds DA,
Nöthen MM,
Richards JB
PLoS genetics · 2012 · PMID 22693459 · open access
3 pages
Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci
Betz RC,
Petukhova L,
Ripke S,
Huang H,
Menelaou A,
Redler S,
Becker T,
Heilmann S,
Yamany T,
Duvic M,
Hordinsky M,
Norris D
and 21 more — show all
Price VH,
Mackay-Wiggan J,
de Jong A,
DeStefano GM,
Moebus S,
Böhm M,
Blume-Peytavi U,
Wolff H,
Lutz G,
Kruse R,
Bian L,
Amos CI,
Lee A,
Gregersen PK,
Blaumeiser B,
Altshuler D,
Clynes R,
de Bakker PIW,
Nöthen MM,
Daly MJ,
Christiano AM
Nature communications · 2015 · PMID 25608926 · open access
3 pages
Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophy
Draaken M,
Knapp M,
Pennimpede T,
Schmidt JM,
Ebert AK,
Rösch W,
Stein R,
Utsch B,
Hirsch K,
Boemers TM,
Mangold E,
Heilmann S
and 9 more — show all
PLoS genetics · 2015 · PMID 25763902 · open access
2 pages
Genome-wide association study identifies multiple susceptibility loci for glioma
Kinnersley B,
Labussière M,
Holroyd A,
Di Stefano AL,
Broderick P,
Vijayakrishnan J,
Mokhtari K,
Delattre JY,
Gousias K,
Schramm J,
Schoemaker MJ,
Fleming SJ
and 11 more — show all
Herms S,
Heilmann S,
Schreiber S,
Wichmann HE,
Nöthen MM,
Swerdlow A,
Lathrop M,
Simon M,
Bondy M,
Sanson M,
Houlston RS
Nature communications · 2015 · PMID 26424050 · 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.