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Is your paper here?
2,661 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
Helgason H.
Physical and neurobehavioral determinants of reproductive onset and success
Day FR,
Helgason H,
Chasman DI,
Rose LM,
Loh PR,
Scott RA,
Helgason A,
Kong A,
Masson G,
Magnusson OT,
Gudbjartsson D,
Thorsteinsdottir U
and 6 more — show all
Nature genetics · 2016 · PMID 27089180
10 pages
New basal cell carcinoma susceptibility loci
Stacey SN,
Helgason H,
Gudjonsson SA,
Thorleifsson G,
Zink F,
Sigurdsson A,
Kehr B,
Gudmundsson J,
Sulem P,
Sigurgeirsson B,
Benediktsdottir KR,
Thorisdottir K
and 31 more — show all
Ragnarsson R,
Fuentelsaz V,
Corredera C,
Gilaberte Y,
Grasa M,
Planelles D,
Sanmartin O,
Rudnai P,
Gurzau E,
Koppova K,
Nexø BA,
Tjønneland A,
Overvad K,
Jonasson JG,
Tryggvadottir L,
Johannsdottir H,
Kristinsdottir AM,
Stefansson H,
Masson G,
Magnusson OT,
Halldorsson BV,
Kong A,
Rafnar T,
Thorsteinsdottir U,
Vogel U,
Kumar R,
Nagore E,
Mayordomo JI,
Gudbjartsson DF,
Olafsson JH,
Stefansson K
Nature communications · 2015 · PMID 25855136 · open access
7 pages
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase
Kristjansson RP,
Oddsson A,
Helgason H,
Sveinbjornsson G,
Arnadottir GA,
Jensson BO,
Jonasdottir A,
Jonasdottir A,
Bragi Walters G,
Sulem G,
Oskarsdottir A,
Benonisdottir S
and 12 more — show all
Davidsson OB,
Masson G,
Magnusson OT,
Holm H,
Sigurdardottir O,
Jonsdottir I,
Eyjolfsson GI,
Olafsson I,
Gudbjartsson DF,
Thorsteinsdottir U,
Sulem P,
Stefansson K
Nature communications · 2016 · PMID 26838040 · open access
6 pages
Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and Naming
Gisladottir RS,
Ivarsdottir EV,
Helgason A,
Jonsson L,
Hannesdottir NK,
Rutsdottir G,
Arnadottir GA,
Skuladottir A,
Jonsson BA,
Norddahl GL,
Ulfarsson MO,
Helgason H
and 16 more — show all
Halldorsson BV,
Nawaz MS,
Tragante V,
Sveinbjornsson G,
Thorgeirsson T,
Oddsson A,
Kristjansson RP,
Bjornsdottir G,
Thorgeirsson G,
Jonsdottir I,
Holm H,
Gudbjartsson DF,
Thorsteinsdottir U,
Stefansson H,
Sulem P,
Stefansson K
Current biology : CB · 2020 · PMID 33035477
3 pages
Common and rare variants associated with kidney stones and biochemical traits
Oddsson A,
Sulem P,
Helgason H,
Edvardsson VO,
Thorleifsson G,
Sveinbjörnsson G,
Haraldsdottir E,
Eyjolfsson GI,
Sigurdardottir O,
Olafsson I,
Masson G,
Holm H
and 5 more — show all
Nature communications · 2015 · PMID 26272126 · open access
2 pages
A genome-wide association study yields five novel thyroid cancer risk loci
Gudmundsson J,
Thorleifsson G,
Sigurdsson JK,
Stefansdottir L,
Jonasson JG,
Gudjonsson SA,
Gudbjartsson DF,
Masson G,
Johannsdottir H,
Halldorsson GH,
Stacey SN,
Helgason H
and 28 more — show all
Sulem P,
Senter L,
He H,
Liyanarachchi S,
Ringel MD,
Aguillo E,
Panadero A,
Prats E,
Garcia-Castaño A,
De Juan A,
Rivera F,
Xu L,
Kiemeney LA,
Eyjolfsson GI,
Sigurdardottir O,
Olafsson I,
Kristvinsson H,
Netea-Maier RT,
Jonsson T,
Mayordomo JI,
Plantinga TS,
Hjartarson H,
Hrafnkelsson J,
Sturgis EM,
Thorsteinsdottir U,
Rafnar T,
de la Chapelle A,
Stefansson K
Nature communications · 2017 · PMID 28195142 · open access
1 page
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
Day FR,
Thompson DJ,
Helgason H,
Chasman DI,
Finucane H,
Sulem P,
Ruth KS,
Whalen S,
Sarkar AK,
Albrecht E,
Altmaier E,
Amini M
and 204 more — show all
Barbieri CM,
Boutin T,
Campbell A,
Demerath E,
Giri A,
He C,
Hottenga JJ,
Karlsson R,
Kolcic I,
Loh PR,
Lunetta KL,
Mangino M,
Marco B,
McMahon G,
Medland SE,
Nolte IM,
Noordam R,
Nutile T,
Paternoster L,
Perjakova N,
Porcu E,
Rose LM,
Schraut KE,
Segrè AV,
Smith AV,
Stolk L,
Teumer A,
Andrulis IL,
Bandinelli S,
Beckmann MW,
Benitez J,
Bergmann S,
Bochud M,
Boerwinkle E,
Bojesen SE,
Bolla MK,
Brand JS,
Brauch H,
Brenner H,
Broer L,
Brüning T,
Buring JE,
Campbell H,
Catamo E,
Chanock S,
Chenevix-Trench G,
Corre T,
Couch FJ,
Cousminer DL,
Cox A,
Crisponi L,
Czene K,
Davey Smith G,
de Geus EJCN,
de Mutsert R,
De Vivo I,
Dennis J,
Devilee P,
Dos-Santos-Silva I,
Dunning AM,
Eriksson JG,
Fasching PA,
Fernández-Rhodes L,
Ferrucci L,
Flesch-Janys D,
Franke L,
Gabrielson M,
Gandin I,
Giles GG,
Grallert H,
Gudbjartsson DF,
Guénel P,
Hall P,
Hallberg E,
Hamann U,
Harris TB,
Hartman CA,
Heiss G,
Hooning MJ,
Hopper JL,
Hu F,
Hunter DJ,
Ikram MA,
Im HK,
Järvelin MR,
Joshi PK,
Karasik D,
Kellis M,
Kutalik Z,
LaChance G,
Lambrechts D,
Langenberg C,
Launer LJ,
Laven JSE,
Lenarduzzi S,
Li J,
Lind PA,
Lindstrom S,
Liu Y,
Luan J,
Mägi R,
Mannermaa A,
Mbarek H,
McCarthy MI,
Meisinger C,
Meitinger T,
Menni C,
Metspalu A,
Michailidou K,
Milani L,
Milne RL,
Montgomery GW,
Mulligan AM,
Nalls MA,
Navarro P,
Nevanlinna H,
Nyholt DR,
Oldehinkel AJ,
O'Mara TA,
Padmanabhan S,
Palotie A,
Pedersen N,
Peters A,
Peto J,
Pharoah PDP,
Pouta A,
Radice P,
Rahman I,
Ring SM,
Robino A,
Rosendaal FR,
Rudan I,
Rueedi R,
Ruggiero D,
Sala CF,
Schmidt MK,
Scott RA,
Shah M,
Sorice R,
Southey MC,
Sovio U,
Stampfer M,
Steri M,
Strauch K,
Tanaka T,
Tikkanen E,
Timpson NJ,
Traglia M,
Truong T,
Tyrer JP,
Uitterlinden AG,
Edwards DRV,
Vitart V,
Völker U,
Vollenweider P,
Wang Q,
Widen E,
van Dijk KW,
Willemsen G,
Winqvist R,
Wolffenbuttel BHR,
Zhao JH,
Zoledziewska M,
Zygmunt M,
Alizadeh BZ,
Boomsma DI,
Ciullo M,
Cucca F,
Esko T,
Franceschini N,
Gieger C,
Gudnason V,
Hayward C,
Kraft P,
Lawlor DA,
Magnusson PKE,
Martin NG,
Mook-Kanamori DO,
Nohr EA,
Polasek O,
Porteous D,
Price AL,
Ridker PM,
Snieder H,
Spector TD,
Stöckl D,
Toniolo D,
Ulivi S,
Visser JA,
Völzke H,
Wareham NJ,
Wilson JF,
Spurdle AB,
Thorsteindottir U,
Pollard KS,
Easton DF,
Tung JY,
Chang-Claude J,
Hinds D,
Murray A,
Murabito JM,
Stefansson K,
Ong KK,
Perry JRB
LifeLines Cohort Study · InterAct Consortium and 4 more consortia
Nature genetics · 2017 · PMID 28436984
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.