For researchers
Is your paper here?
2,665 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
Reutter H.
Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformations
van de Putte R,
Wijers CHW,
Reutter H,
Vermeulen SH,
Marcelis CLM,
Brosens E,
Broens PMA,
Homberg M,
Ludwig M,
Jenetzky E,
Zwink N,
Sloots CEJ
and 16 more — show all
de Klein A,
Brooks AS,
Hofstra RMW,
Holsink SAC,
van der Zanden LFM,
Galesloot TE,
Tam PK,
Steehouwer M,
Acuna-Hidalgo R,
Vorst MV,
Kiemeney LA,
Garcia-Barceló MM,
de Blaauw I,
Brunner HG,
Roeleveld N,
van Rooij IALM
PloS one · 2019 · PMID 31136621 · open access
8 pages
Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci
Ludwig KU,
Mangold E,
Herms S,
Nowak S,
Reutter H,
Paul A,
Becker J,
Herberz R,
AlChawa T,
Nasser E,
Böhmer AC,
Mattheisen M
and 27 more — show all
Alblas MA,
Barth S,
Kluck N,
Lauster C,
Braumann B,
Reich RH,
Hemprich A,
Pötzsch S,
Blaumeiser B,
Daratsianos N,
Kreusch T,
Murray JC,
Marazita ML,
Ruczinski I,
Scott AF,
Beaty TH,
Kramer FJ,
Wienker TF,
Steegers-Theunissen RP,
Rubini M,
Mossey PA,
Hoffmann P,
Lange C,
Cichon S,
Propping P,
Knapp M,
Nöthen MM
Nature genetics · 2012 · PMID 22863734
6 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
Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24
Birnbaum S,
Ludwig KU,
Reutter H,
Herms S,
Steffens M,
Rubini M,
Baluardo C,
Ferrian M,
Almeida de Assis N,
Alblas MA,
Barth S,
Freudenberg J
and 22 more — show all
Lauster C,
Schmidt G,
Scheer M,
Braumann B,
Bergé SJ,
Reich RH,
Schiefke F,
Hemprich A,
Pötzsch S,
Steegers-Theunissen RP,
Pötzsch B,
Moebus S,
Horsthemke B,
Kramer FJ,
Wienker TF,
Mossey PA,
Propping P,
Cichon S,
Hoffmann P,
Knapp M,
Nöthen MM,
Mangold E
Nature genetics · 2009 · PMID 19270707
2 pages
Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate
Mangold E,
Ludwig KU,
Birnbaum S,
Baluardo C,
Ferrian M,
Herms S,
Reutter H,
de Assis NA,
Chawa TA,
Mattheisen M,
Steffens M,
Barth S
and 26 more — show all
Kluck N,
Paul A,
Becker J,
Lauster C,
Schmidt G,
Braumann B,
Scheer M,
Reich RH,
Hemprich A,
Pötzsch S,
Blaumeiser B,
Moebus S,
Krawczak M,
Schreiber S,
Meitinger T,
Wichmann HE,
Steegers-Theunissen RP,
Kramer FJ,
Cichon S,
Propping P,
Wienker TF,
Knapp M,
Rubini M,
Mossey PA,
Hoffmann P,
Nöthen MM
Nature genetics · 2010 · PMID 20023658
2 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
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.