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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.
7 matches for
Prokisch H.
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
Soranzo N,
Spector TD,
Mangino M,
Kühnel B,
Rendon A,
Teumer A,
Willenborg C,
Wright B,
Chen L,
Li M,
Salo P,
Voight BF
and 68 more — show all
Burns P,
Laskowski RA,
Xue Y,
Menzel S,
Altshuler D,
Bradley JR,
Bumpstead S,
Burnett MS,
Devaney J,
Döring A,
Elosua R,
Epstein SE,
Erber W,
Falchi M,
Garner SF,
Ghori MJ,
Goodall AH,
Gwilliam R,
Hakonarson HH,
Hall AS,
Hammond N,
Hengstenberg C,
Illig T,
König IR,
Knouff CW,
McPherson R,
Melander O,
Mooser V,
Nauck M,
Nieminen MS,
O'Donnell CJ,
Peltonen L,
Potter SC,
Prokisch H,
Rader DJ,
Rice CM,
Roberts R,
Salomaa V,
Sambrook J,
Schreiber S,
Schunkert H,
Schwartz SM,
Serbanovic-Canic J,
Sinisalo J,
Siscovick DS,
Stark K,
Surakka I,
Stephens J,
Thompson JR,
Völker U,
Völzke H,
Watkins NA,
Wells GA,
Wichmann HE,
Van Heel DA,
Tyler-Smith C,
Thein SL,
Kathiresan S,
Perola M,
Reilly MP,
Stewart AF,
Erdmann J,
Samani NJ,
Meisinger C,
Greinacher A,
Deloukas P,
Ouwehand WH,
Gieger C
Nature genetics · 2009 · PMID 19820697
8 pages
Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations
Kolz M,
Johnson T,
Sanna S,
Teumer A,
Vitart V,
Perola M,
Mangino M,
Albrecht E,
Wallace C,
Farrall M,
Johansson A,
Nyholt DR
and 44 more — show all
Aulchenko Y,
Beckmann JS,
Bergmann S,
Bochud M,
Brown M,
Campbell H,
Connell J,
Dominiczak A,
Homuth G,
Lamina C,
McCarthy MI,
Meitinger T,
Mooser V,
Munroe P,
Nauck M,
Peden J,
Prokisch H,
Salo P,
Salomaa V,
Samani NJ,
Schlessinger D,
Uda M,
Völker U,
Waeber G,
Waterworth D,
Wang-Sattler R,
Wright AF,
Adamski J,
Whitfield JB,
Gyllensten U,
Wilson JF,
Rudan I,
Pramstaller P,
Watkins H,
Doering A,
Wichmann HE,
Spector TD,
Peltonen L,
Völzke H,
Nagaraja R,
Vollenweider P,
Caulfield M,
Illig T,
Gieger C
EUROSPAN Consortium · ENGAGE Consortium and 3 more consortia
PLoS genetics · 2009 · PMID 19503597 · open access
3 pages
Multiple loci are associated with white blood cell phenotypes
Nalls MA,
Couper DJ,
Tanaka T,
van Rooij FJ,
Chen MH,
Smith AV,
Toniolo D,
Zakai NA,
Yang Q,
Greinacher A,
Wood AR,
Garcia M
and 81 more — show all
Gasparini P,
Liu Y,
Lumley T,
Folsom AR,
Reiner AP,
Gieger C,
Lagou V,
Felix JF,
Völzke H,
Gouskova NA,
Biffi A,
Döring A,
Völker U,
Chong S,
Wiggins KL,
Rendon A,
Dehghan A,
Moore M,
Taylor K,
Wilson JG,
Lettre G,
Hofman A,
Bis JC,
Pirastu N,
Fox CS,
Meisinger C,
Sambrook J,
Arepalli S,
Nauck M,
Prokisch H,
Stephens J,
Glazer NL,
Cupples LA,
Okada Y,
Takahashi A,
Kamatani Y,
Matsuda K,
Tsunoda T,
Tanaka T,
Kubo M,
Nakamura Y,
Yamamoto K,
Kamatani N,
Stumvoll M,
Tönjes A,
Prokopenko I,
Illig T,
Patel KV,
Garner SF,
Kuhnel B,
Mangino M,
Oostra BA,
Thein SL,
Coresh J,
Wichmann HE,
Menzel S,
Lin J,
Pistis G,
Uitterlinden AG,
Spector TD,
Teumer A,
Eiriksdottir G,
Gudnason V,
Bandinelli S,
Frayling TM,
Chakravarti A,
van Duijn CM,
Melzer D,
Ouwehand WH,
Levy D,
Boerwinkle E,
Singleton AB,
Hernandez DG,
Longo DL,
Soranzo N,
Witteman JC,
Psaty BM,
Ferrucci L,
Harris TB,
O'Donnell CJ,
Ganesh SK
PLoS genetics · 2011 · PMID 21738480 · open access
3 pages
Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease
Medici M,
Porcu E,
Pistis G,
Teumer A,
Brown SJ,
Jensen RA,
Rawal R,
Roef GL,
Plantinga TS,
Vermeulen SH,
Lahti J,
Simmonds MJ
and 106 more — show all
Husemoen LL,
Freathy RM,
Shields BM,
Pietzner D,
Nagy R,
Broer L,
Chaker L,
Korevaar TI,
Plia MG,
Sala C,
Völker U,
Richards JB,
Sweep FC,
Gieger C,
Corre T,
Kajantie E,
Thuesen B,
Taes YE,
Visser WE,
Hattersley AT,
Kratzsch J,
Hamilton A,
Li W,
Homuth G,
Lobina M,
Mariotti S,
Soranzo N,
Cocca M,
Nauck M,
Spielhagen C,
Ross A,
Arnold A,
van de Bunt M,
Liyanarachchi S,
Heier M,
Grabe HJ,
Masciullo C,
Galesloot TE,
Lim EM,
Reischl E,
Leedman PJ,
Lai S,
Delitala A,
Bremner AP,
Philips DI,
Beilby JP,
Mulas A,
Vocale M,
Abecasis G,
Forsen T,
James A,
Widen E,
Hui J,
Prokisch H,
Rietzschel EE,
Palotie A,
Feddema P,
Fletcher SJ,
Schramm K,
Rotter JI,
Kluttig A,
Radke D,
Traglia M,
Surdulescu GL,
He H,
Franklyn JA,
Tiller D,
Vaidya B,
de Meyer T,
Jørgensen T,
Eriksson JG,
O'Leary PC,
Wichmann E,
Hermus AR,
Psaty BM,
Ittermann T,
Hofman A,
Bosi E,
Schlessinger D,
Wallaschofski H,
Pirastu N,
Aulchenko YS,
de la Chapelle A,
Netea-Maier RT,
Gough SC,
Meyer Zu Schwabedissen H,
Frayling TM,
Kaufman JM,
Linneberg A,
Räikkönen K,
Smit JW,
Kiemeney LA,
Rivadeneira F,
Uitterlinden AG,
Walsh JP,
Meisinger C,
den Heijer M,
Visser TJ,
Spector TD,
Wilson SG,
Völzke H,
Cappola A,
Toniolo D,
Sanna S,
Naitza S,
Peeters RP
PLoS genetics · 2014 · PMID 24586183 · open access
3 pages
Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1
Winkelmann J,
Czamara D,
Schormair B,
Knauf F,
Schulte EC,
Trenkwalder C,
Dauvilliers Y,
Polo O,
Högl B,
Berger K,
Fuhs A,
Gross N
and 45 more — show all
Stiasny-Kolster K,
Oertel W,
Bachmann CG,
Paulus W,
Xiong L,
Montplaisir J,
Rouleau GA,
Fietze I,
Vávrová J,
Kemlink D,
Sonka K,
Nevsimalova S,
Lin SC,
Wszolek Z,
Vilariño-Güell C,
Farrer MJ,
Gschliesser V,
Frauscher B,
Falkenstetter T,
Poewe W,
Allen RP,
Earley CJ,
Ondo WG,
Le WD,
Spieler D,
Kaffe M,
Zimprich A,
Kettunen J,
Perola M,
Silander K,
Cournu-Rebeix I,
Francavilla M,
Fontenille C,
Fontaine B,
Vodicka P,
Prokisch H,
Lichtner P,
Peppard P,
Faraco J,
Mignot E,
Gieger C,
Illig T,
Wichmann HE,
Müller-Myhsok B,
Meitinger T
PLoS genetics · 2011 · PMID 21779176 · open access
2 pages
Identification of genetic loci associated with Helicobacter pylori serologic status
Mayerle J,
den Hoed CM,
Schurmann C,
Stolk L,
Homuth G,
Peters MJ,
Capelle LG,
Zimmermann K,
Rivadeneira F,
Gruska S,
Völzke H,
de Vries AC
and 14 more — show all
Völker U,
Teumer A,
van Meurs JB,
Steinmetz I,
Nauck M,
Ernst F,
Weiss FU,
Hofman A,
Zenker M,
Kroemer HK,
Prokisch H,
Uitterlinden AG,
Lerch MM,
Kuipers EJ
JAMA · 2013 · PMID 23652523
2 pages
Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus
Weidinger S,
Gieger C,
Rodriguez E,
Baurecht H,
Mempel M,
Klopp N,
Gohlke H,
Wagenpfeil S,
Ollert M,
Ring J,
Behrendt H,
Heinrich J
and 20 more — show all
Novak N,
Bieber T,
Krämer U,
Berdel D,
von Berg A,
Bauer CP,
Herbarth O,
Koletzko S,
Prokisch H,
Mehta D,
Mehta D,
Meitinger T,
Depner M,
von Mutius E,
Liang L,
Moffatt M,
Cookson W,
Kabesch M,
Wichmann HE,
Illig T
PLoS genetics · 2008 · PMID 18846228 · 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.