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Is your paper here?
2,660 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
Service SK.
Discovery and refinement of loci associated with lipid levels
Willer CJ,
Schmidt EM,
Sengupta S,
Peloso GM,
Gustafsson S,
Kanoni S,
Ganna A,
Chen J,
Buchkovich ML,
Mora S,
Beckmann JS,
Bragg-Gresham JL
and 247 more — show all
Chang HY,
Demirkan A,
Den Hertog HM,
Do R,
Donnelly LA,
Ehret GB,
Esko T,
Feitosa MF,
Ferreira T,
Fischer K,
Fontanillas P,
Fraser RM,
Freitag DF,
Gurdasani D,
Heikkilä K,
Hyppönen E,
Isaacs A,
Jackson AU,
Johansson Å,
Johnson T,
Kaakinen M,
Kettunen J,
Kleber ME,
Li X,
Luan J,
Lyytikäinen LP,
Magnusson PKE,
Mangino M,
Mihailov E,
Montasser ME,
Müller-Nurasyid M,
Nolte IM,
O'Connell JR,
Palmer CD,
Perola M,
Petersen AK,
Sanna S,
Saxena R,
Service SK,
Shah S,
Shungin D,
Sidore C,
Song C,
Strawbridge RJ,
Surakka I,
Tanaka T,
Teslovich TM,
Thorleifsson G,
Van den Herik EG,
Voight BF,
Volcik KA,
Waite LL,
Wong A,
Wu Y,
Zhang W,
Absher D,
Asiki G,
Barroso I,
Been LF,
Bolton JL,
Bonnycastle LL,
Brambilla P,
Burnett MS,
Cesana G,
Dimitriou M,
Doney ASF,
Döring A,
Elliott P,
Epstein SE,
Ingi Eyjolfsson G,
Gigante B,
Goodarzi MO,
Grallert H,
Gravito ML,
Groves CJ,
Hallmans G,
Hartikainen AL,
Hayward C,
Hernandez D,
Hicks AA,
Holm H,
Hung YJ,
Illig T,
Jones MR,
Kaleebu P,
Kastelein JJP,
Khaw KT,
Kim E,
Klopp N,
Komulainen P,
Kumari M,
Langenberg C,
Lehtimäki T,
Lin SY,
Lindström J,
Loos RJF,
Mach F,
McArdle WL,
Meisinger C,
Mitchell BD,
Müller G,
Nagaraja R,
Narisu N,
Nieminen TVM,
Nsubuga RN,
Olafsson I,
Ong KK,
Palotie A,
Papamarkou T,
Pomilla C,
Pouta A,
Rader DJ,
Reilly MP,
Ridker PM,
Rivadeneira F,
Rudan I,
Ruokonen A,
Samani N,
Scharnagl H,
Seeley J,
Silander K,
Stančáková A,
Stirrups K,
Swift AJ,
Tiret L,
Uitterlinden AG,
van Pelt LJ,
Vedantam S,
Wainwright N,
Wijmenga C,
Wild SH,
Willemsen G,
Wilsgaard T,
Wilson JF,
Young EH,
Zhao JH,
Adair LS,
Arveiler D,
Assimes TL,
Bandinelli S,
Bennett F,
Bochud M,
Boehm BO,
Boomsma DI,
Borecki IB,
Bornstein SR,
Bovet P,
Burnier M,
Campbell H,
Chakravarti A,
Chambers JC,
Chen YI,
Collins FS,
Cooper RS,
Danesh J,
Dedoussis G,
de Faire U,
Feranil AB,
Ferrières J,
Ferrucci L,
Freimer NB,
Gieger C,
Groop LC,
Gudnason V,
Gyllensten U,
Hamsten A,
Harris TB,
Hingorani A,
Hirschhorn JN,
Hofman A,
Hovingh GK,
Hsiung CA,
Humphries SE,
Hunt SC,
Hveem K,
Iribarren C,
Järvelin MR,
Jula A,
Kähönen M,
Kaprio J,
Kesäniemi A,
Kivimaki M,
Kooner JS,
Koudstaal PJ,
Krauss RM,
Kuh D,
Kuusisto J,
Kyvik KO,
Laakso M,
Lakka TA,
Lind L,
Lindgren CM,
Martin NG,
März W,
McCarthy MI,
McKenzie CA,
Meneton P,
Metspalu A,
Moilanen L,
Morris AD,
Munroe PB,
Njølstad I,
Pedersen NL,
Power C,
Pramstaller PP,
Price JF,
Psaty BM,
Quertermous T,
Rauramaa R,
Saleheen D,
Salomaa V,
Sanghera DK,
Saramies J,
Schwarz PEH,
Sheu WH,
Shuldiner AR,
Siegbahn A,
Spector TD,
Stefansson K,
Strachan DP,
Tayo BO,
Tremoli E,
Tuomilehto J,
Uusitupa M,
van Duijn CM,
Vollenweider P,
Wallentin L,
Wareham NJ,
Whitfield JB,
Wolffenbuttel BHR,
Ordovas JM,
Boerwinkle E,
Palmer CNA,
Thorsteinsdottir U,
Chasman DI,
Rotter JI,
Franks PW,
Ripatti S,
Cupples LA,
Sandhu MS,
Rich SS,
Boehnke M,
Deloukas P,
Kathiresan S,
Mohlke KL,
Ingelsson E,
Abecasis GR
Global Lipids Genetics Consortium
Nature genetics · 2013 · PMID 24097068 · open access
12 pages+
Genetic architecture of human plasma lipidome and its link to cardiovascular disease
Tabassum R,
Rämö JT,
Ripatti P,
Koskela JT,
Kurki M,
Karjalainen J,
Palta P,
Hassan S,
Nunez-Fontarnau J,
Kiiskinen TTJ,
Söderlund S,
Matikainen N
and 16 more — show all
Gerl MJ,
Surma MA,
Klose C,
Stitziel NO,
Laivuori H,
Havulinna AS,
Service SK,
Salomaa V,
Pirinen M,
Jauhiainen M,
Daly MJ,
Freimer NB,
Palotie A,
Taskinen MR,
Simons K,
Ripatti S
FinnGen Project
Nature communications · 2019 · PMID 31551469 · open access
12 pages+
Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci
Yin X,
Chan LS,
Bose D,
Jackson AU,
VandeHaar P,
Locke AE,
Fuchsberger C,
Stringham HM,
Welch R,
Yu K,
Fernandes Silva L,
Service SK
and 25 more — show all
Zhang D,
Hector EC,
Young E,
Ganel L,
Das I,
Abel H,
Erdos MR,
Bonnycastle LL,
Kuusisto J,
Stitziel NO,
Hall IM,
Wagner GR,
Kang J,
Morrison J,
Burant CF,
Collins FS,
Ripatti S,
Palotie A,
Freimer NB,
Mohlke KL,
Scott LJ,
Wen X,
Fauman EB,
Laakso M,
Boehnke M
FinnGen
Nature communications · 2022 · PMID 35347128 · open access
12 pages+
Genome-wide association analysis of metabolic traits in a birth cohort from a founder population
Sabatti C,
Service SK,
Hartikainen AL,
Pouta A,
Ripatti S,
Brodsky J,
Jones CG,
Zaitlen NA,
Varilo T,
Kaakinen M,
Sovio U,
Ruokonen A
and 13 more — show all
Laitinen J,
Jakkula E,
Coin L,
Hoggart C,
Collins A,
Turunen H,
Gabriel S,
Elliot P,
McCarthy MI,
Daly MJ,
Järvelin MR,
Freimer NB,
Peltonen L
Nature genetics · 2009 · PMID 19060910
2 pages
Genome-wide association study of Tourette's syndrome
Scharf JM,
Yu D,
Mathews CA,
Neale BM,
Stewart SE,
Fagerness JA,
Evans P,
Gamazon E,
Edlund CK,
Service SK,
Tikhomirov A,
Osiecki L
and 86 more — show all
Illmann C,
Pluzhnikov A,
Konkashbaev A,
Davis LK,
Han B,
Crane J,
Moorjani P,
Crenshaw AT,
Parkin MA,
Reus VI,
Lowe TL,
Rangel-Lugo M,
Chouinard S,
Dion Y,
Girard S,
Cath DC,
Smit JH,
King RA,
Fernandez TV,
Leckman JF,
Kidd KK,
Kidd JR,
Pakstis AJ,
State MW,
Herrera LD,
Romero R,
Fournier E,
Sandor P,
Barr CL,
Phan N,
Gross-Tsur V,
Benarroch F,
Pollak Y,
Budman CL,
Bruun RD,
Erenberg G,
Naarden AL,
Lee PC,
Weiss N,
Kremeyer B,
Berrío GB,
Campbell DD,
Cardona Silgado JC,
Ochoa WC,
Mesa Restrepo SC,
Muller H,
Valencia Duarte AV,
Lyon GJ,
Leppert M,
Morgan J,
Weiss R,
Grados MA,
Anderson K,
Davarya S,
Singer H,
Walkup J,
Jankovic J,
Tischfield JA,
Heiman GA,
Gilbert DL,
Hoekstra PJ,
Robertson MM,
Kurlan R,
Liu C,
Gibbs JR,
Singleton A,
Hardy J,
Strengman E,
Ophoff RA,
Wagner M,
Moessner R,
Mirel DB,
Posthuma D,
Sabatti C,
Eskin E,
Conti DV,
Knowles JA,
Ruiz-Linares A,
Rouleau GA,
Purcell S,
Heutink P,
Oostra BA,
McMahon WM,
Freimer NB,
Cox NJ,
Pauls DL
North American Brain Expression Consortium · UK Human Brain Expression Database
Molecular psychiatry · 2013 · PMID 22889924 · 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.