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29 matches for
Masson G,
showing the first 20.
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
Perry JR,
Day F,
Elks CE,
Sulem P,
Thompson DJ,
Ferreira T,
He C,
Chasman DI,
Esko T,
Thorleifsson G,
Albrecht E,
Ang WQ
and 186 more — show all
Corre T,
Cousminer DL,
Feenstra B,
Franceschini N,
Ganna A,
Johnson AD,
Kjellqvist S,
Lunetta KL,
McMahon G,
Nolte IM,
Paternoster L,
Porcu E,
Smith AV,
Stolk L,
Teumer A,
Tšernikova N,
Tikkanen E,
Ulivi S,
Wagner EK,
Amin N,
Bierut LJ,
Byrne EM,
Hottenga JJ,
Koller DL,
Mangino M,
Pers TH,
Yerges-Armstrong LM,
Zhao JH,
Andrulis IL,
Anton-Culver H,
Atsma F,
Bandinelli S,
Beckmann MW,
Benitez J,
Blomqvist C,
Bojesen SE,
Bolla MK,
Bonanni B,
Brauch H,
Brenner H,
Buring JE,
Chang-Claude J,
Chanock S,
Chen J,
Chenevix-Trench G,
Collée JM,
Couch FJ,
Couper D,
Coveillo AD,
Cox A,
Czene K,
D'adamo AP,
Smith GD,
De Vivo I,
Demerath EW,
Dennis J,
Devilee P,
Dieffenbach AK,
Dunning AM,
Eiriksdottir G,
Eriksson JG,
Fasching PA,
Ferrucci L,
Flesch-Janys D,
Flyger H,
Foroud T,
Franke L,
Garcia ME,
García-Closas M,
Geller F,
de Geus EE,
Giles GG,
Gudbjartsson DF,
Gudnason V,
Guénel P,
Guo S,
Hall P,
Hamann U,
Haring R,
Hartman CA,
Heath AC,
Hofman A,
Hooning MJ,
Hopper JL,
Hu FB,
Hunter DJ,
Karasik D,
Kiel DP,
Knight JA,
Kosma VM,
Kutalik Z,
Lai S,
Lambrechts D,
Lindblom A,
Mägi R,
Magnusson PK,
Mannermaa A,
Martin NG,
Masson G,
McArdle PF,
McArdle WL,
Melbye M,
Michailidou K,
Mihailov E,
Milani L,
Milne RL,
Nevanlinna H,
Neven P,
Nohr EA,
Oldehinkel AJ,
Oostra BA,
Palotie A,
Peacock M,
Pedersen NL,
Peterlongo P,
Peto J,
Pharoah PD,
Postma DS,
Pouta A,
Pylkäs K,
Radice P,
Ring S,
Rivadeneira F,
Robino A,
Rose LM,
Rudolph A,
Salomaa V,
Sanna S,
Schlessinger D,
Schmidt MK,
Southey MC,
Sovio U,
Stampfer MJ,
Stöckl D,
Storniolo AM,
Timpson NJ,
Tyrer J,
Visser JA,
Vollenweider P,
Völzke H,
Waeber G,
Waldenberger M,
Wallaschofski H,
Wang Q,
Willemsen G,
Winqvist R,
Wolffenbuttel BH,
Wright MJ,
Boomsma DI,
Econs MJ,
Khaw KT,
Loos RJ,
McCarthy MI,
Montgomery GW,
Rice JP,
Streeten EA,
Thorsteinsdottir U,
van Duijn CM,
Alizadeh BZ,
Bergmann S,
Boerwinkle E,
Boyd HA,
Crisponi L,
Gasparini P,
Gieger C,
Harris TB,
Ingelsson E,
Järvelin MR,
Kraft P,
Lawlor D,
Metspalu A,
Pennell CE,
Ridker PM,
Snieder H,
Sørensen TI,
Spector TD,
Strachan DP,
Uitterlinden AG,
Wareham NJ,
Widen E,
Zygmunt M,
Murray A,
Easton DF,
Stefansson K,
Murabito JM,
Ong KK
Australian Ovarian Cancer Study · GENICA Network and 4 more consortia
Nature · 2014 · PMID 25231870 · open access
12 pages+
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits
Rafnar T,
Gunnarsson B,
Stefansson OA,
Sulem P,
Ingason A,
Frigge ML,
Stefansdottir L,
Sigurdsson JK,
Tragante V,
Steinthorsdottir V,
Styrkarsdottir U,
Stacey SN
and 25 more — show all
Gudmundsson J,
Arnadottir GA,
Oddsson A,
Zink F,
Halldorsson G,
Sveinbjornsson G,
Kristjansson RP,
Davidsson OB,
Salvarsdottir A,
Thoroddsen A,
Helgadottir EA,
Kristjansdottir K,
Ingthorsson O,
Gudmundsson V,
Geirsson RT,
Arnadottir R,
Gudbjartsson DF,
Masson G,
Asselbergs FW,
Jonasson JG,
Olafsson K,
Thorsteinsdottir U,
Halldorsson BV,
Thorleifsson G,
Stefansson K
Nature communications · 2018 · PMID 30194396 · open access
12 pages+
Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis
Oskarsson GR,
Oddsson A,
Magnusson MK,
Kristjansson RP,
Halldorsson GH,
Ferkingstad E,
Zink F,
Helgadottir A,
Ivarsdottir EV,
Arnadottir GA,
Jensson BO,
Katrinardottir H
and 26 more — show all
Sveinbjornsson G,
Kristinsdottir AM,
Lee AL,
Saemundsdottir J,
Stefansdottir L,
Sigurdsson JK,
Davidsson OB,
Benonisdottir S,
Jonasdottir A,
Jonasdottir A,
Jonsson S,
Gudmundsson RL,
Asselbergs FW,
Tragante V,
Gunnarsson B,
Masson G,
Thorleifsson G,
Rafnar T,
Holm H,
Olafsson I,
Onundarson PT,
Gudbjartsson DF,
Norddahl GL,
Thorsteinsdottir U,
Sulem P,
Stefansson K
Communications biology · 2020 · PMID 32327693 · open access
12 pages+
FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease
Saevarsdottir S,
Olafsdottir TA,
Ivarsdottir EV,
Halldorsson GH,
Gunnarsdottir K,
Sigurdsson A,
Johannesson A,
Sigurdsson JK,
Juliusdottir T,
Lund SH,
Arnthorsson AO,
Styrmisdottir EL
and 34 more — show all
Gudmundsson J,
Grondal GM,
Steinsson K,
Alfredsson L,
Askling J,
Benediktsson R,
Bjarnason R,
Geirsson AJ,
Gudbjornsson B,
Gudjonsson H,
Hjaltason H,
Hreidarsson AB,
Klareskog L,
Kockum I,
Kristjansdottir H,
Love TJ,
Ludviksson BR,
Olsson T,
Onundarson PT,
Orvar KB,
Padyukov L,
Sigurgeirsson B,
Tragante V,
Bjarnadottir K,
Rafnar T,
Masson G,
Sulem P,
Gudbjartsson DF,
Melsted P,
Thorleifsson G,
Norddahl GL,
Thorsteinsdottir U,
Jonsdottir I,
Stefansson K
Nature · 2020 · PMID 32581359
12 pages+
Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood
Olafsson S,
Alexandersson KF,
Gizurarson JGK,
Hauksdottir K,
Gunnarsson O,
Olafsson K,
Gudmundsson J,
Stacey SN,
Sveinbjornsson G,
Saemundsdottir J,
Bjornsson ES,
Olafsson S
and 22 more — show all
Bjornsson S,
Orvar KB,
Vikingsson A,
Geirsson AJ,
Arinbjarnarson S,
Bjornsdottir G,
Thorgeirsson TE,
Sigurdsson S,
Halldorsson GH,
Magnusson OT,
Masson G,
Holm H,
Jonsdottir I,
Sigurdardottir O,
Eyjolfsson GI,
Olafsson I,
Sulem P,
Thorsteinsdottir U,
Jonsson T,
Rafnar T,
Gudbjartsson DF,
Stefansson K
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2020 · PMID 31666285
11 pages
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
Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA
Gudmundsson J,
Sigurdsson JK,
Stefansdottir L,
Agnarsson BA,
Isaksson HJ,
Stefansson OA,
Gudjonsson SA,
Gudbjartsson DF,
Masson G,
Frigge ML,
Stacey SN,
Sulem P
and 16 more — show all
Halldorsson GH,
Tragante V,
Holm H,
Eyjolfsson GI,
Sigurdardottir O,
Olafsson I,
Jonsson T,
Jonsson E,
Barkardottir RB,
Hilmarsson R,
Asselbergs FW,
Geirsson G,
Thorsteinsdottir U,
Rafnar T,
Thorleifsson G,
Stefansson K
Nature communications · 2018 · PMID 30410027 · open access
9 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
Sequence variants associating with urinary biomarkers
Benonisdottir S,
Kristjansson RP,
Oddsson A,
Steinthorsdottir V,
Mikaelsdottir E,
Kehr B,
Jensson BO,
Arnadottir GA,
Sulem G,
Sveinbjornsson G,
Kristmundsdottir S,
Ivarsdottir EV
and 26 more — show all
Tragante V,
Gunnarsson B,
Runolfsdottir HL,
Arthur JG,
Deaton AM,
Eyjolfsson GI,
Davidsson OB,
Asselbergs FW,
Hreidarsson AB,
Rafnar T,
Thorleifsson G,
Edvardsson V,
Sigurdsson G,
Helgadottir A,
Halldorsson BV,
Masson G,
Holm H,
Onundarson PT,
Indridason OS,
Benediktsson R,
Palsson R,
Gudbjartsson DF,
Olafsson I,
Thorsteinsdottir U,
Sulem P,
Stefansson K
Human molecular genetics · 2019 · PMID 30476138 · open access
7 pages
GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures
Styrkarsdottir U,
Stefansson OA,
Gunnarsdottir K,
Thorleifsson G,
Lund SH,
Stefansdottir L,
Juliusson K,
Agustsdottir AB,
Zink F,
Halldorsson GH,
Ivarsdottir EV,
Benonisdottir S
and 40 more — show all
Jonsson H,
Gylfason A,
Norland K,
Trajanoska K,
Boer CG,
Southam L,
Leung JCS,
Tang NLS,
Kwok TCY,
Lee JSW,
Ho SC,
Byrjalsen I,
Center JR,
Lee SH,
Koh JM,
Lohmander LS,
Ho-Pham LT,
Nguyen TV,
Eisman JA,
Woo J,
Leung PC,
Loughlin J,
Zeggini E,
Christiansen C,
Rivadeneira F,
van Meurs J,
Uitterlinden AG,
Mogensen B,
Jonsson H,
Ingvarsson T,
Sigurdsson G,
Benediktsson R,
Sulem P,
Jonsdottir I,
Masson G,
Holm H,
Norddahl GL,
Thorsteinsdottir U,
Gudbjartsson DF,
Stefansson K
Nature communications · 2019 · PMID 31053729 · open access
7 pages
Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets
Grarup N,
Sulem P,
Sandholt CH,
Thorleifsson G,
Ahluwalia TS,
Steinthorsdottir V,
Bjarnason H,
Gudbjartsson DF,
Magnusson OT,
Sparsø T,
Albrechtsen A,
Kong A
and 19 more — show all
Masson G,
Tian G,
Cao H,
Nie C,
Kristiansen K,
Husemoen LL,
Thuesen B,
Li Y,
Nielsen R,
Linneberg A,
Olafsson I,
Eyjolfsson GI,
Jørgensen T,
Wang J,
Wang J,
Hansen T,
Thorsteinsdottir U,
Stefánsson K,
Pedersen O
PLoS genetics · 2013 · PMID 23754956 · open access
6 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
Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis
Olafsdottir TA,
Theodors F,
Bjarnadottir K,
Bjornsdottir US,
Agustsdottir AB,
Stefansson OA,
Ivarsdottir EV,
Sigurdsson JK,
Benonisdottir S,
Eyjolfsson GI,
Gislason D,
Gislason T
and 23 more — show all
Guðmundsdóttir S,
Gylfason A,
Halldorsson BV,
Halldorsson GH,
Juliusdottir T,
Kristinsdottir AM,
Ludviksdottir D,
Ludviksson BR,
Masson G,
Norland K,
Onundarson PT,
Olafsson I,
Sigurdardottir O,
Stefansdottir L,
Sveinbjornsson G,
Tragante V,
Gudbjartsson DF,
Thorleifsson G,
Sulem P,
Thorsteinsdottir U,
Norddahl GL,
Jonsdottir I,
Stefansson K
Nature communications · 2020 · PMID 31959851 · open access
6 pages
Identification of sequence variants influencing immunoglobulin levels
Jonsson S,
Sveinbjornsson G,
de Lapuente Portilla AL,
Swaminathan B,
Plomp R,
Dekkers G,
Ajore R,
Ali M,
Bentlage AEH,
Elmér E,
Eyjolfsson GI,
Gudjonsson SA
and 26 more — show all
Gullberg U,
Gylfason A,
Halldorsson BV,
Hansson M,
Holm H,
Johansson Å,
Johnsson E,
Jonasdottir A,
Ludviksson BR,
Oddsson A,
Olafsson I,
Olafsson S,
Sigurdardottir O,
Sigurdsson A,
Stefansdottir L,
Masson G,
Sulem P,
Wuhrer M,
Wihlborg AK,
Thorleifsson G,
Gudbjartsson DF,
Thorsteinsdottir U,
Vidarsson G,
Jonsdottir I,
Nilsson B,
Stefansson K
Nature genetics · 2017 · PMID 28628107
5 pages
Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis
Styrkarsdottir U,
Lund SH,
Thorleifsson G,
Zink F,
Stefansson OA,
Sigurdsson JK,
Juliusson K,
Bjarnadottir K,
Sigurbjornsdottir S,
Jonsson S,
Norland K,
Stefansdottir L
and 17 more — show all
Sigurdsson A,
Sveinbjornsson G,
Oddsson A,
Bjornsdottir G,
Gudmundsson RL,
Halldorsson GH,
Rafnar T,
Jonsdottir I,
Steingrimsson E,
Norddahl GL,
Masson G,
Sulem P,
Jonsson H,
Ingvarsson T,
Gudbjartsson DF,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2018 · PMID 30374069
5 pages
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis
Kristjansson RP,
Benonisdottir S,
Davidsson OB,
Oddsson A,
Tragante V,
Sigurdsson JK,
Stefansdottir L,
Jonsson S,
Jensson BO,
Arthur JG,
Arnadottir GA,
Sulem G
and 28 more — show all
Halldorsson BV,
Gunnarsson B,
Halldorsson GH,
Stefansson OA,
Oskarsson GR,
Deaton AM,
Olafsson I,
Eyjolfsson GI,
Sigurdardottir O,
Onundarson PT,
Gislason D,
Gislason T,
Ludviksson BR,
Ludviksdottir D,
Olafsdottir TA,
Rafnar T,
Masson G,
Zink F,
Bjornsdottir G,
Magnusson OT,
Bjornsdottir US,
Thorleifsson G,
Norddahl GL,
Gudbjartsson DF,
Thorsteinsdottir U,
Jonsdottir I,
Sulem P,
Stefansson K
Nature genetics · 2019 · PMID 30643255
5 pages
Genetic correction of PSA values using sequence variants associated with PSA levels
Gudmundsson J,
Besenbacher S,
Sulem P,
Gudbjartsson DF,
Olafsson I,
Arinbjarnarson S,
Agnarsson BA,
Benediktsdottir KR,
Isaksson HJ,
Kostic JP,
Gudjonsson SA,
Stacey SN
and 37 more — show all
Gylfason A,
Sigurdsson A,
Holm H,
Bjornsdottir US,
Eyjolfsson GI,
Navarrete S,
Fuertes F,
Garcia-Prats MD,
Polo E,
Checherita IA,
Jinga M,
Badea P,
Aben KK,
Schalken JA,
van Oort IM,
Sweep FC,
Helfand BT,
Davis M,
Donovan JL,
Hamdy FC,
Kristjansson K,
Gulcher JR,
Masson G,
Kong A,
Catalona WJ,
Mayordomo JI,
Geirsson G,
Einarsson GV,
Barkardottir RB,
Jonsson E,
Jinga V,
Mates D,
Kiemeney LA,
Neal DE,
Thorsteinsdottir U,
Rafnar T,
Stefansson K
Science translational medicine · 2010 · PMID 21160077
4 pages
Discovery of common variants associated with low TSH levels and thyroid cancer risk
Gudmundsson J,
Sulem P,
Gudbjartsson DF,
Jonasson JG,
Masson G,
He H,
Jonasdottir A,
Sigurdsson A,
Stacey SN,
Johannsdottir H,
Helgadottir HT,
Li W
and 35 more — show all
Nagy R,
Ringel MD,
Kloos RT,
de Visser MC,
Plantinga TS,
den Heijer M,
Aguillo E,
Panadero A,
Prats E,
Garcia-Castaño A,
De Juan A,
Rivera F,
Walters GB,
Bjarnason H,
Tryggvadottir L,
Eyjolfsson GI,
Bjornsdottir US,
Holm H,
Olafsson I,
Kristjansson K,
Kristvinsson H,
Magnusson OT,
Thorleifsson G,
Gulcher JR,
Kong A,
Kiemeney LA,
Jonsson T,
Hjartarson H,
Mayordomo JI,
Netea-Maier RT,
de la Chapelle A,
Hrafnkelsson J,
Thorsteinsdottir U,
Rafnar T,
Stefansson K
Nature genetics · 2012 · PMID 22267200
3 pages
Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset
Saevarsdottir S,
Stefansdottir L,
Sulem P,
Thorleifsson G,
Ferkingstad E,
Rutsdottir G,
Glintborg B,
Westerlind H,
Grondal G,
Loft IC,
Sorensen SB,
Lie BA
and 66 more — show all
Brink M,
Ärlestig L,
Arnthorsson AO,
Baecklund E,
Banasik K,
Bank S,
Bjorkman LI,
Ellingsen T,
Erikstrup C,
Frei O,
Gjertsson I,
Gudbjartsson DF,
Gudjonsson SA,
Halldorsson GH,
Hendricks O,
Hillert J,
Hogdall E,
Jacobsen S,
Jensen DV,
Jonsson H,
Kastbom A,
Kockum I,
Kristensen S,
Kristjansdottir H,
Larsen MH,
Linauskas A,
Hauge EM,
Loft AG,
Ludviksson BR,
Lund SH,
Markusson T,
Masson G,
Melsted P,
Moore KHS,
Munk H,
Nielsen KR,
Norddahl GL,
Oddsson A,
Olafsdottir TA,
Olason PI,
Olsson T,
Ostrowski SR,
Hørslev-Petersen K,
Rognvaldsson S,
Sanner H,
Silberberg GN,
Stefansson H,
Sørensen E,
Sørensen IJ,
Turesson C,
Bergman T,
Alfredsson L,
Kvien TK,
Brunak S,
Steinsson K,
Andersen V,
Andreassen OA,
Rantapää-Dahlqvist S,
Hetland ML,
Klareskog L,
Askling J,
Padyukov L,
Pedersen OB,
Thorsteinsdottir U,
Jonsdottir I,
Stefansson K
Members of the DBDS Genomic Consortium · Danish RA Genetics Working Group and 1 more consortia
Annals of the rheumatic diseases · 2022 · PMID 35470158 · open access
3 pages
Common variants conferring risk of schizophrenia
Stefansson H,
Ophoff RA,
Steinberg S,
Andreassen OA,
Cichon S,
Rujescu D,
Werge T,
Pietiläinen OP,
Mors O,
Mortensen PB,
Sigurdsson E,
Gustafsson O
and 75 more — show all
Nyegaard M,
Tuulio-Henriksson A,
Ingason A,
Hansen T,
Suvisaari J,
Lonnqvist J,
Paunio T,
Børglum AD,
Hartmann A,
Fink-Jensen A,
Nordentoft M,
Hougaard D,
Norgaard-Pedersen B,
Böttcher Y,
Olesen J,
Breuer R,
Möller HJ,
Giegling I,
Rasmussen HB,
Timm S,
Mattheisen M,
Bitter I,
Réthelyi JM,
Magnusdottir BB,
Sigmundsson T,
Olason P,
Masson G,
Gulcher JR,
Haraldsson M,
Fossdal R,
Thorgeirsson TE,
Thorsteinsdottir U,
Ruggeri M,
Tosato S,
Franke B,
Strengman E,
Kiemeney LA,
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Genetic Risk and Outcome in Psychosis (GROUP)
Nature · 2009 · PMID 19571808
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
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How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
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keep in step, because the citation lives on the page that makes the claim.