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2,651 papers hold this site up. Every variant and condition page names
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13 matches for
Gulcher JR.
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Schunkert H,
König IR,
Kathiresan S,
Reilly MP,
Assimes TL,
Holm H,
Preuss M,
Stewart AF,
Barbalic M,
Gieger C,
Absher D,
Aherrahrou Z
and 155 more — show all
Allayee H,
Altshuler D,
Anand SS,
Andersen K,
Anderson JL,
Ardissino D,
Ball SG,
Balmforth AJ,
Barnes TA,
Becker DM,
Becker LC,
Berger K,
Bis JC,
Boekholdt SM,
Boerwinkle E,
Braund PS,
Brown MJ,
Burnett MS,
Buysschaert I,
Carlquist JF,
Chen L,
Cichon S,
Codd V,
Davies RW,
Dedoussis G,
Dehghan A,
Demissie S,
Devaney JM,
Diemert P,
Do R,
Doering A,
Eifert S,
Mokhtari NE,
Ellis SG,
Elosua R,
Engert JC,
Epstein SE,
de Faire U,
Fischer M,
Folsom AR,
Freyer J,
Gigante B,
Girelli D,
Gretarsdottir S,
Gudnason V,
Gulcher JR,
Halperin E,
Hammond N,
Hazen SL,
Hofman A,
Horne BD,
Illig T,
Iribarren C,
Jones GT,
Jukema JW,
Kaiser MA,
Kaplan LM,
Kastelein JJ,
Khaw KT,
Knowles JW,
Kolovou G,
Kong A,
Laaksonen R,
Lambrechts D,
Leander K,
Lettre G,
Li M,
Lieb W,
Loley C,
Lotery AJ,
Mannucci PM,
Maouche S,
Martinelli N,
McKeown PP,
Meisinger C,
Meitinger T,
Melander O,
Merlini PA,
Mooser V,
Morgan T,
Mühleisen TW,
Muhlestein JB,
Münzel T,
Musunuru K,
Nahrstaedt J,
Nelson CP,
Nöthen MM,
Olivieri O,
Patel RS,
Patterson CC,
Peters A,
Peyvandi F,
Qu L,
Quyyumi AA,
Rader DJ,
Rallidis LS,
Rice C,
Rosendaal FR,
Rubin D,
Salomaa V,
Sampietro ML,
Sandhu MS,
Schadt E,
Schäfer A,
Schillert A,
Schreiber S,
Schrezenmeir J,
Schwartz SM,
Siscovick DS,
Sivananthan M,
Sivapalaratnam S,
Smith A,
Smith TB,
Snoep JD,
Soranzo N,
Spertus JA,
Stark K,
Stirrups K,
Stoll M,
Tang WH,
Tennstedt S,
Thorgeirsson G,
Thorleifsson G,
Tomaszewski M,
Uitterlinden AG,
van Rij AM,
Voight BF,
Wareham NJ,
Wells GA,
Wichmann HE,
Wild PS,
Willenborg C,
Witteman JC,
Wright BJ,
Ye S,
Zeller T,
Ziegler A,
Cambien F,
Goodall AH,
Cupples LA,
Quertermous T,
März W,
Hengstenberg C,
Blankenberg S,
Ouwehand WH,
Hall AS,
Deloukas P,
Thompson JR,
Stefansson K,
Roberts R,
Thorsteinsdottir U,
O'Donnell CJ,
McPherson R,
Erdmann J,
Samani NJ
Cardiogenics · CARDIoGRAM Consortium
Nature genetics · 2011 · PMID 21378990
7 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
Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer
Gudmundsson J,
Sulem P,
Rafnar T,
Bergthorsson JT,
Manolescu A,
Gudbjartsson D,
Agnarsson BA,
Sigurdsson A,
Benediktsdottir KR,
Blondal T,
Jakobsdottir M,
Stacey SN
and 59 more — show all
Kostic J,
Kristinsson KT,
Birgisdottir B,
Ghosh S,
Magnusdottir DN,
Thorlacius S,
Thorleifsson G,
Zheng SL,
Sun J,
Chang BL,
Elmore JB,
Breyer JP,
McReynolds KM,
Bradley KM,
Yaspan BL,
Wiklund F,
Stattin P,
Lindström S,
Adami HO,
McDonnell SK,
Schaid DJ,
Cunningham JM,
Wang L,
Cerhan JR,
St Sauver JL,
Isaacs SD,
Wiley KE,
Partin AW,
Walsh PC,
Polo S,
Ruiz-Echarri M,
Navarrete S,
Fuertes F,
Saez B,
Godino J,
Weijerman PC,
Swinkels DW,
Aben KK,
Witjes JA,
Suarez BK,
Helfand BT,
Frigge ML,
Kristjansson K,
Ober C,
Jonsson E,
Einarsson GV,
Xu J,
Gronberg H,
Smith JR,
Thibodeau SN,
Isaacs WB,
Catalona WJ,
Mayordomo JI,
Kiemeney LA,
Barkardottir RB,
Gulcher JR,
Thorsteinsdottir U,
Kong A,
Stefansson K
Nature genetics · 2008 · PMID 18264098
3 pages
Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility
Gudmundsson J,
Sulem P,
Gudbjartsson DF,
Blondal T,
Gylfason A,
Agnarsson BA,
Benediktsdottir KR,
Magnusdottir DN,
Orlygsdottir G,
Jakobsdottir M,
Stacey SN,
Sigurdsson A
and 32 more — show all
Wahlfors T,
Tammela T,
Breyer JP,
McReynolds KM,
Bradley KM,
Saez B,
Godino J,
Navarrete S,
Fuertes F,
Murillo L,
Polo E,
Aben KK,
van Oort IM,
Suarez BK,
Helfand BT,
Kan D,
Zanon C,
Frigge ML,
Kristjansson K,
Gulcher JR,
Einarsson GV,
Jonsson E,
Catalona WJ,
Mayordomo JI,
Kiemeney LA,
Smith JR,
Schleutker J,
Barkardottir RB,
Kong A,
Thorsteinsdottir U,
Rafnar T,
Stefansson K
Nature genetics · 2009 · PMID 19767754
3 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
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
Multiple genetic loci for bone mineral density and fractures
Styrkarsdottir U,
Halldorsson BV,
Gretarsdottir S,
Gudbjartsson DF,
Walters GB,
Ingvarsson T,
Jonsdottir T,
Saemundsdottir J,
Center JR,
Nguyen TV,
Bagger Y,
Gulcher JR
and 6 more — show all
The New England journal of medicine · 2008 · PMID 18445777
2 pages
Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations
Gudmundsson J,
Sulem P,
Gudbjartsson DF,
Jonasson JG,
Sigurdsson A,
Bergthorsson JT,
He H,
Blondal T,
Geller F,
Jakobsdottir M,
Magnusdottir DN,
Matthiasdottir S
and 26 more — show all
Stacey SN,
Skarphedinsson OB,
Helgadottir H,
Li W,
Nagy R,
Aguillo E,
Faure E,
Prats E,
Saez B,
Martinez M,
Eyjolfsson GI,
Bjornsdottir US,
Holm H,
Kristjansson K,
Frigge ML,
Kristvinsson H,
Gulcher JR,
Jonsson T,
Rafnar T,
Hjartarsson H,
Mayordomo JI,
de la Chapelle A,
Hrafnkelsson J,
Thorsteinsdottir U,
Kong A,
Stefansson K
Nature genetics · 2009 · PMID 19198613
2 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,
Melle I,
Djurovic S,
Abramova L,
Kaleda V,
Sanjuan J,
de Frutos R,
Bramon E,
Vassos E,
Fraser G,
Ettinger U,
Picchioni M,
Walker N,
Toulopoulou T,
Need AC,
Ge D,
Yoon JL,
Shianna KV,
Freimer NB,
Cantor RM,
Murray R,
Kong A,
Golimbet V,
Carracedo A,
Arango C,
Costas J,
Jönsson EG,
Terenius L,
Agartz I,
Petursson H,
Nöthen MM,
Rietschel M,
Matthews PM,
Muglia P,
Peltonen L,
St Clair D,
Goldstein DB,
Stefansson K,
Collier DA
Genetic Risk and Outcome in Psychosis (GROUP)
Nature · 2009 · PMID 19571808
2 pages
A genetic risk factor for periodic limb movements in sleep
Stefansson H,
Rye DB,
Hicks A,
Petursson H,
Ingason A,
Thorgeirsson TE,
Palsson S,
Sigmundsson T,
Sigurdsson AP,
Eiriksdottir I,
Soebech E,
Bliwise D
and 14 more — show all
Beck JM,
Rosen A,
Waddy S,
Trotti LM,
Iranzo A,
Thambisetty M,
Hardarson GA,
Kristjansson K,
Gudmundsson LJ,
Thorsteinsdottir U,
Kong A,
Gulcher JR,
Gudbjartsson D,
Stefansson K
The New England journal of medicine · 2007 · PMID 17634447
1 page
A variant associated with nicotine dependence, lung cancer and peripheral arterial disease
Thorgeirsson TE,
Geller F,
Sulem P,
Rafnar T,
Wiste A,
Magnusson KP,
Manolescu A,
Thorleifsson G,
Stefansson H,
Ingason A,
Stacey SN,
Bergthorsson JT
and 45 more — show all
Thorlacius S,
Gudmundsson J,
Jonsson T,
Jakobsdottir M,
Saemundsdottir J,
Olafsdottir O,
Gudmundsson LJ,
Bjornsdottir G,
Kristjansson K,
Skuladottir H,
Isaksson HJ,
Gudbjartsson T,
Jones GT,
Mueller T,
Gottsäter A,
Flex A,
Aben KKH,
de Vegt F,
Mulders PFA,
Isla D,
Vidal MJ,
Asin L,
Saez B,
Murillo L,
Blondal T,
Kolbeinsson H,
Stefansson JG,
Hansdottir I,
Runarsdottir V,
Pola R,
Lindblad B,
van Rij AM,
Dieplinger B,
Haltmayer M,
Mayordomo JI,
Kiemeney LA,
Matthiasson SE,
Oskarsson H,
Tyrfingsson T,
Gudbjartsson DF,
Gulcher JR,
Jonsson S,
Thorsteinsdottir U,
Kong A,
Stefansson K
Nature · 2008 · PMID 18385739
1 page
New sequence variants associated with bone mineral density
Styrkarsdottir U,
Halldorsson BV,
Gretarsdottir S,
Gudbjartsson DF,
Walters GB,
Ingvarsson T,
Jonsdottir T,
Saemundsdottir J,
Snorradóttir S,
Center JR,
Nguyen TV,
Alexandersen P
and 7 more — show all
Nature genetics · 2009 · PMID 19079262
1 page
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior
Thorgeirsson TE,
Gudbjartsson DF,
Surakka I,
Vink JM,
Amin N,
Geller F,
Sulem P,
Rafnar T,
Esko T,
Walter S,
Gieger C,
Rawal R
and 82 more — show all
Mangino M,
Prokopenko I,
Mägi R,
Keskitalo K,
Gudjonsdottir IH,
Gretarsdottir S,
Stefansson H,
Thompson JR,
Aulchenko YS,
Nelis M,
Aben KK,
den Heijer M,
Dirksen A,
Ashraf H,
Soranzo N,
Valdes AM,
Steves C,
Uitterlinden AG,
Hofman A,
Tönjes A,
Kovacs P,
Hottenga JJ,
Willemsen G,
Vogelzangs N,
Döring A,
Dahmen N,
Nitz B,
Pergadia ML,
Saez B,
De Diego V,
Lezcano V,
Garcia-Prats MD,
Ripatti S,
Perola M,
Kettunen J,
Hartikainen AL,
Pouta A,
Laitinen J,
Isohanni M,
Huei-Yi S,
Allen M,
Krestyaninova M,
Hall AS,
Jones GT,
van Rij AM,
Mueller T,
Dieplinger B,
Haltmayer M,
Jonsson S,
Matthiasson SE,
Oskarsson H,
Tyrfingsson T,
Kiemeney LA,
Mayordomo JI,
Lindholt JS,
Pedersen JH,
Franklin WA,
Wolf H,
Montgomery GW,
Heath AC,
Martin NG,
Madden PA,
Giegling I,
Rujescu D,
Järvelin MR,
Salomaa V,
Stumvoll M,
Spector TD,
Wichmann HE,
Metspalu A,
Samani NJ,
Penninx BW,
Oostra BA,
Boomsma DI,
Tiemeier H,
van Duijn CM,
Kaprio J,
Gulcher JR,
McCarthy MI,
Peltonen L,
Thorsteinsdottir U,
Stefansson K
ENGAGE Consortium
Nature genetics · 2010 · PMID 20418888
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.