For researchers
Is your paper here?
2,671 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.
8 matches for
Helgason A.
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
Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis
Stacey SN,
Zink F,
Halldorsson GH,
Stefansdottir L,
Gudjonsson SA,
Einarsson G,
Hjörleifsson G,
Eiriksdottir T,
Helgadottir A,
Björnsdottir G,
Thorgeirsson TE,
Olafsdottir TA
and 19 more — show all
Jonsdottir I,
Gretarsdottir S,
Tragante V,
Magnusson MK,
Jonsson H,
Gudmundsson J,
Olafsson S,
Holm H,
Gudbjartsson DF,
Sulem P,
Helgason A,
Thorsteinsdottir U,
Tryggvadottir L,
Rafnar T,
Melsted P,
Ulfarsson MÖ,
Vidarsson B,
Thorleifsson G,
Stefansson K
Nature genetics · 2023 · PMID 37932435 · open access
4 pages
Genetic variants associated with mosaic Y chromosome loss highlight cell cycle genes and overlap with cancer susceptibility
Wright DJ,
Day FR,
Kerrison ND,
Zink F,
Cardona A,
Sulem P,
Thompson DJ,
Sigurjonsdottir S,
Gudbjartsson DF,
Helgason A,
Chapman JR,
Jackson SP
and 7 more — show all
Nature genetics · 2017 · PMID 28346444 · open access
3 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
Variants conferring risk of atrial fibrillation on chromosome 4q25
Gudbjartsson DF,
Arnar DO,
Helgadottir A,
Gretarsdottir S,
Holm H,
Sigurdsson A,
Jonasdottir A,
Baker A,
Thorleifsson G,
Kristjansson K,
Palsson A,
Blondal T
and 28 more — show all
Sulem P,
Backman VM,
Hardarson GA,
Palsdottir E,
Helgason A,
Sigurjonsdottir R,
Sverrisson JT,
Kostulas K,
Ng MC,
Baum L,
So WY,
Wong KS,
Chan JC,
Furie KL,
Greenberg SM,
Sale M,
Kelly P,
MacRae CA,
Smith EE,
Rosand J,
Hillert J,
Ma RC,
Ellinor PT,
Thorgeirsson G,
Gulcher JR,
Kong A,
Thorsteinsdottir U,
Stefansson K
Nature · 2007 · PMID 17603472
2 pages
Two newly identified genetic determinants of pigmentation in Europeans
Sulem P,
Gudbjartsson DF,
Stacey SN,
Helgason A,
Rafnar T,
Jakobsdottir M,
Steinberg S,
Gudjonsson SA,
Palsson A,
Thorleifsson G,
Pálsson S,
Sigurgeirsson B
and 13 more — show all
Thorisdottir K,
Ragnarsson R,
Benediktsdottir KR,
Aben KK,
Vermeulen SH,
Goldstein AM,
Tucker MA,
Kiemeney LA,
Olafsson JH,
Gulcher J,
Kong A,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2008 · PMID 18488028
1 page
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma
Thorleifsson G,
Walters GB,
Hewitt AW,
Masson G,
Helgason A,
DeWan A,
Sigurdsson A,
Jonasdottir A,
Gudjonsson SA,
Magnusson KP,
Stefansson H,
Lam DS
and 35 more — show all
Tam PO,
Gudmundsdottir GJ,
Southgate L,
Burdon KP,
Gottfredsdottir MS,
Aldred MA,
Mitchell P,
St Clair D,
Collier DA,
Tang N,
Sveinsson O,
Macgregor S,
Martin NG,
Cree AJ,
Gibson J,
Macleod A,
Jacob A,
Ennis S,
Young TL,
Chan JC,
Karwatowski WS,
Hammond CJ,
Thordarson K,
Zhang M,
Wadelius C,
Lotery AJ,
Trembath RC,
Pang CP,
Hoh J,
Craig JE,
Kong A,
Mackey DA,
Jonasson F,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2010 · PMID 20835238
1 page
The nature of nurture: Effects of parental genotypes
Kong A,
Thorleifsson G,
Frigge ML,
Vilhjalmsson BJ,
Young AI,
Thorgeirsson TE,
Benonisdottir S,
Oddsson A,
Halldorsson BV,
Masson G,
Gudbjartsson DF,
Helgason A
and 3 more — show all
Science (New York, N.Y.) · 2018 · PMID 29371463
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.