For researchers
Is your paper here?
2,663 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
Quaye L.
Genome-wide association study identifies 74 loci associated with educational attainment
Okbay A,
Beauchamp JP,
Fontana MA,
Lee JJ,
Pers TH,
Rietveld CA,
Turley P,
Chen GB,
Emilsson V,
Meddens SF,
Oskarsson S,
Pickrell JK
and 243 more — show all
Thom K,
Timshel P,
de Vlaming R,
Abdellaoui A,
Ahluwalia TS,
Bacelis J,
Baumbach C,
Bjornsdottir G,
Brandsma JH,
Pina Concas M,
Derringer J,
Furlotte NA,
Galesloot TE,
Girotto G,
Gupta R,
Hall LM,
Harris SE,
Hofer E,
Horikoshi M,
Huffman JE,
Kaasik K,
Kalafati IP,
Karlsson R,
Kong A,
Lahti J,
van der Lee SJ,
deLeeuw C,
Lind PA,
Lindgren KO,
Liu T,
Mangino M,
Marten J,
Mihailov E,
Miller MB,
van der Most PJ,
Oldmeadow C,
Payton A,
Pervjakova N,
Peyrot WJ,
Qian Y,
Raitakari O,
Rueedi R,
Salvi E,
Schmidt B,
Schraut KE,
Shi J,
Smith AV,
Poot RA,
St Pourcain B,
Teumer A,
Thorleifsson G,
Verweij N,
Vuckovic D,
Wellmann J,
Westra HJ,
Yang J,
Zhao W,
Zhu Z,
Alizadeh BZ,
Amin N,
Bakshi A,
Baumeister SE,
Biino G,
Bønnelykke K,
Boyle PA,
Campbell H,
Cappuccio FP,
Davies G,
De Neve JE,
Deloukas P,
Demuth I,
Ding J,
Eibich P,
Eisele L,
Eklund N,
Evans DM,
Faul JD,
Feitosa MF,
Forstner AJ,
Gandin I,
Gunnarsson B,
Halldórsson BV,
Harris TB,
Heath AC,
Hocking LJ,
Holliday EG,
Homuth G,
Horan MA,
Hottenga JJ,
de Jager PL,
Joshi PK,
Jugessur A,
Kaakinen MA,
Kähönen M,
Kanoni S,
Keltigangas-Järvinen L,
Kiemeney LA,
Kolcic I,
Koskinen S,
Kraja AT,
Kroh M,
Kutalik Z,
Latvala A,
Launer LJ,
Lebreton MP,
Levinson DF,
Lichtenstein P,
Lichtner P,
Liewald DC,
Loukola A,
Madden PA,
Mägi R,
Mäki-Opas T,
Marioni RE,
Marques-Vidal P,
Meddens GA,
McMahon G,
Meisinger C,
Meitinger T,
Milaneschi Y,
Milani L,
Montgomery GW,
Myhre R,
Nelson CP,
Nyholt DR,
Ollier WE,
Palotie A,
Paternoster L,
Pedersen NL,
Petrovic KE,
Porteous DJ,
Räikkönen K,
Ring SM,
Robino A,
Rostapshova O,
Rudan I,
Rustichini A,
Salomaa V,
Sanders AR,
Sarin AP,
Schmidt H,
Scott RJ,
Smith BH,
Smith JA,
Staessen JA,
Steinhagen-Thiessen E,
Strauch K,
Terracciano A,
Tobin MD,
Ulivi S,
Vaccargiu S,
Quaye L,
van Rooij FJ,
Venturini C,
Vinkhuyzen AA,
Völker U,
Völzke H,
Vonk JM,
Vozzi D,
Waage J,
Ware EB,
Willemsen G,
Attia JR,
Bennett DA,
Berger K,
Bertram L,
Bisgaard H,
Boomsma DI,
Borecki IB,
Bültmann U,
Chabris CF,
Cucca F,
Cusi D,
Deary IJ,
Dedoussis GV,
van Duijn CM,
Eriksson JG,
Franke B,
Franke L,
Gasparini P,
Gejman PV,
Gieger C,
Grabe HJ,
Gratten J,
Groenen PJ,
Gudnason V,
van der Harst P,
Hayward C,
Hinds DA,
Hoffmann W,
Hyppönen E,
Iacono WG,
Jacobsson B,
Järvelin MR,
Jöckel KH,
Kaprio J,
Kardia SL,
Lehtimäki T,
Lehrer SF,
Magnusson PK,
Martin NG,
McGue M,
Metspalu A,
Pendleton N,
Penninx BW,
Perola M,
Pirastu N,
Pirastu M,
Polasek O,
Posthuma D,
Power C,
Province MA,
Samani NJ,
Schlessinger D,
Schmidt R,
Sørensen TI,
Spector TD,
Stefansson K,
Thorsteinsdottir U,
Thurik AR,
Timpson NJ,
Tiemeier H,
Tung JY,
Uitterlinden AG,
Vitart V,
Vollenweider P,
Weir DR,
Wilson JF,
Wright AF,
Conley DC,
Krueger RF,
Davey Smith G,
Hofman A,
Laibson DI,
Medland SE,
Meyer MN,
Yang J,
Johannesson M,
Visscher PM,
Esko T,
Koellinger PD,
Cesarini D,
Benjamin DJ
LifeLines Cohort Study
Nature · 2016 · PMID 27225129 · open access
12 pages+
Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults
Graff M,
Scott RA,
Justice AE,
Young KL,
Feitosa MF,
Barata L,
Winkler TW,
Chu AY,
Mahajan A,
Hadley D,
Xue L,
Workalemahu T
and 269 more — show all
Heard-Costa NL,
den Hoed M,
Ahluwalia TS,
Qi Q,
Ngwa JS,
Renström F,
Quaye L,
Eicher JD,
Hayes JE,
Cornelis M,
Kutalik Z,
Lim E,
Luan J,
Huffman JE,
Zhang W,
Zhao W,
Griffin PJ,
Haller T,
Ahmad S,
Marques-Vidal PM,
Bien S,
Yengo L,
Teumer A,
Smith AV,
Kumari M,
Harder MN,
Justesen JM,
Kleber ME,
Hollensted M,
Lohman K,
Rivera NV,
Whitfield JB,
Zhao JH,
Stringham HM,
Lyytikäinen LP,
Huppertz C,
Willemsen G,
Peyrot WJ,
Wu Y,
Kristiansson K,
Demirkan A,
Fornage M,
Hassinen M,
Bielak LF,
Cadby G,
Tanaka T,
Mägi R,
van der Most PJ,
Jackson AU,
Bragg-Gresham JL,
Vitart V,
Marten J,
Navarro P,
Bellis C,
Pasko D,
Johansson Å,
Snitker S,
Cheng YC,
Eriksson J,
Lim U,
Aadahl M,
Adair LS,
Amin N,
Balkau B,
Auvinen J,
Beilby J,
Bergman RN,
Bergmann S,
Bertoni AG,
Blangero J,
Bonnefond A,
Bonnycastle LL,
Borja JB,
Brage S,
Busonero F,
Buyske S,
Campbell H,
Chines PS,
Collins FS,
Corre T,
Smith GD,
Delgado GE,
Dueker N,
Dörr M,
Ebeling T,
Eiriksdottir G,
Esko T,
Faul JD,
Fu M,
Færch K,
Gieger C,
Gläser S,
Gong J,
Gordon-Larsen P,
Grallert H,
Grammer TB,
Grarup N,
van Grootheest G,
Harald K,
Hastie ND,
Havulinna AS,
Hernandez D,
Hindorff L,
Hocking LJ,
Holmens OL,
Holzapfel C,
Hottenga JJ,
Huang J,
Huang T,
Hui J,
Huth C,
Hutri-Kähönen N,
James AL,
Jansson JO,
Jhun MA,
Juonala M,
Kinnunen L,
Koistinen HA,
Kolcic I,
Komulainen P,
Kuusisto J,
Kvaløy K,
Kähönen M,
Lakka TA,
Launer LJ,
Lehne B,
Lindgren CM,
Lorentzon M,
Luben R,
Marre M,
Milaneschi Y,
Monda KL,
Montgomery GW,
De Moor MHM,
Mulas A,
Müller-Nurasyid M,
Musk AW,
Männikkö R,
Männistö S,
Narisu N,
Nauck M,
Nettleton JA,
Nolte IM,
Oldehinkel AJ,
Olden M,
Ong KK,
Padmanabhan S,
Paternoster L,
Perez J,
Perola M,
Peters A,
Peters U,
Peyser PA,
Prokopenko I,
Puolijoki H,
Raitakari OT,
Rankinen T,
Rasmussen-Torvik LJ,
Rawal R,
Ridker PM,
Rose LM,
Rudan I,
Sarti C,
Sarzynski MA,
Savonen K,
Scott WR,
Sanna S,
Shuldiner AR,
Sidney S,
Silbernagel G,
Smith BH,
Smith JA,
Snieder H,
Stančáková A,
Sternfeld B,
Swift AJ,
Tammelin T,
Tan ST,
Thorand B,
Thuillier D,
Vandenput L,
Vestergaard H,
van Vliet-Ostaptchouk JV,
Vohl MC,
Völker U,
Waeber G,
Walker M,
Wild S,
Wong A,
Wright AF,
Zillikens MC,
Zubair N,
Haiman CA,
Lemarchand L,
Gyllensten U,
Ohlsson C,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
Pérusse L,
Wilson JF,
Hayward C,
Polasek O,
Cucca F,
Hveem K,
Hartman CA,
Tönjes A,
Bandinelli S,
Palmer LJ,
Kardia SLR,
Rauramaa R,
Sørensen TIA,
Tuomilehto J,
Salomaa V,
Penninx BWJH,
de Geus EJC,
Boomsma DI,
Lehtimäki T,
Mangino M,
Laakso M,
Bouchard C,
Martin NG,
Kuh D,
Liu Y,
Linneberg A,
März W,
Strauch K,
Kivimäki M,
Harris TB,
Gudnason V,
Völzke H,
Qi L,
Järvelin MR,
Chambers JC,
Kooner JS,
Froguel P,
Kooperberg C,
Vollenweider P,
Hallmans G,
Hansen T,
Pedersen O,
Metspalu A,
Wareham NJ,
Langenberg C,
Weir DR,
Porteous DJ,
Boerwinkle E,
Chasman DI,
Abecasis GR,
Barroso I,
McCarthy MI,
Frayling TM,
O'Connell JR,
van Duijn CM,
Boehnke M,
Heid IM,
Mohlke KL,
Strachan DP,
Fox CS,
Liu CT,
Hirschhorn JN,
Klein RJ,
Johnson AD,
Borecki IB,
Franks PW,
North KE,
Cupples LA,
Loos RJF,
Kilpeläinen TO
CHARGE Consortium · EPIC-InterAct Consortium and 1 more consortia
PLoS genetics · 2017 · PMID 28448500 · open access
12 pages+
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
Okbay A,
Baselmans BM,
De Neve JE,
Turley P,
Nivard MG,
Fontana MA,
Meddens SF,
Linnér RK,
Rietveld CA,
Derringer J,
Gratten J,
Lee JJ
and 180 more — show all
Liu JZ,
de Vlaming R,
Ahluwalia TS,
Buchwald J,
Cavadino A,
Frazier-Wood AC,
Furlotte NA,
Garfield V,
Geisel MH,
Gonzalez JR,
Haitjema S,
Karlsson R,
van der Laan SW,
Ladwig KH,
Lahti J,
van der Lee SJ,
Lind PA,
Liu T,
Matteson L,
Mihailov E,
Miller MB,
Minica CC,
Nolte IM,
Mook-Kanamori D,
van der Most PJ,
Oldmeadow C,
Qian Y,
Raitakari O,
Rawal R,
Realo A,
Rueedi R,
Schmidt B,
Smith AV,
Stergiakouli E,
Tanaka T,
Taylor K,
Thorleifsson G,
Wedenoja J,
Wellmann J,
Westra HJ,
Willems SM,
Zhao W,
Amin N,
Bakshi A,
Bergmann S,
Bjornsdottir G,
Boyle PA,
Cherney S,
Cox SR,
Davies G,
Davis OS,
Ding J,
Direk N,
Eibich P,
Eibich P,
Emeny RT,
Fatemifar G,
Faul JD,
Ferrucci L,
Ferrucci L,
Forstner AJ,
Gieger C,
Gupta R,
Harris TB,
Harris JM,
Holliday EG,
Hottenga JJ,
De Jager PL,
Kaakinen MA,
Kajantie E,
Karhunen V,
Kolcic I,
Kumari M,
Launer LJ,
Franke L,
Franke L,
Li-Gao R,
Liewald DC,
Koini M,
Loukola A,
Marques-Vidal P,
Montgomery GW,
Mosing MA,
Paternoster L,
Pattie A,
Petrovic KE,
Pulkki-Råback L,
Quaye L,
Räikkönen K,
Rudan I,
Scott RJ,
Smith JA,
Sutin AR,
Trzaskowski M,
Vinkhuyzen AE,
Yu L,
Zabaneh D,
Attia JR,
Bennett DA,
Berger K,
Bertram L,
Boomsma DI,
Snieder H,
Chang SC,
Cucca F,
Deary IJ,
van Duijn CM,
Eriksson JG,
Bültmann U,
de Geus EJ,
Groenen PJ,
Gudnason V,
Hansen T,
Hartman CA,
Haworth CM,
Haworth CM,
Hayward C,
Heath AC,
Hinds DA,
Hyppönen E,
Iacono WG,
Järvelin MR,
Jöckel KH,
Kaprio J,
Kardia SL,
Keltikangas-Järvinen L,
Kraft P,
Kubzansky LD,
Lehtimäki T,
Magnusson PK,
Martin NG,
McGue M,
Metspalu A,
Mills M,
de Mutsert R,
Oldehinkel AJ,
Pasterkamp G,
Pedersen NL,
Plomin R,
Polasek O,
Power C,
Rich SS,
Rosendaal FR,
den Ruijter HM,
Schlessinger D,
Schmidt H,
Svento R,
Schmidt R,
Alizadeh BZ,
Sørensen TI,
Spector TD,
Starr JM,
Stefansson K,
Steptoe A,
Terracciano A,
Thorsteinsdottir U,
Thurik AR,
Timpson NJ,
Tiemeier H,
Uitterlinden AG,
Vollenweider P,
Vollenweider P,
Wagner GG,
Weir DR,
Yang J,
Conley DC,
Smith GD,
Hofman A,
Johannesson M,
Laibson DI,
Medland SE,
Meyer MN,
Pickrell JK,
Esko T,
Krueger RF,
Beauchamp JP,
Koellinger PD,
Benjamin DJ,
Bartels M,
Cesarini D
LifeLines Cohort Study
Nature genetics · 2016 · PMID 27089181 · open access
10 pages
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
Gormley P,
Anttila V,
Winsvold BS,
Palta P,
Esko T,
Pers TH,
Farh KH,
Cuenca-Leon E,
Muona M,
Furlotte NA,
Kurth T,
Ingason A
and 95 more — show all
McMahon G,
Ligthart L,
Terwindt GM,
Kallela M,
Freilinger TM,
Ran C,
Gordon SG,
Stam AH,
Steinberg S,
Borck G,
Koiranen M,
Quaye L,
Adams HH,
Lehtimäki T,
Sarin AP,
Wedenoja J,
Hinds DA,
Buring JE,
Schürks M,
Ridker PM,
Hrafnsdottir MG,
Stefansson H,
Ring SM,
Hottenga JJ,
Penninx BW,
Färkkilä M,
Artto V,
Kaunisto M,
Vepsäläinen S,
Malik R,
Heath AC,
Madden PA,
Martin NG,
Montgomery GW,
Kurki MI,
Kals M,
Mägi R,
Pärn K,
Hämäläinen E,
Huang H,
Byrnes AE,
Franke L,
Huang J,
Stergiakouli E,
Lee PH,
Sandor C,
Webber C,
Cader Z,
Muller-Myhsok B,
Schreiber S,
Meitinger T,
Eriksson JG,
Salomaa V,
Heikkilä K,
Loehrer E,
Uitterlinden AG,
Hofman A,
van Duijn CM,
Cherkas L,
Pedersen LM,
Stubhaug A,
Nielsen CS,
Männikkö M,
Mihailov E,
Milani L,
Göbel H,
Esserlind AL,
Christensen AF,
Hansen TF,
Werge T,
Kaprio J,
Aromaa AJ,
Raitakari O,
Ikram MA,
Spector T,
Järvelin MR,
Metspalu A,
Kubisch C,
Strachan DP,
Ferrari MD,
Belin AC,
Dichgans M,
Wessman M,
van den Maagdenberg AM,
Zwart JA,
Boomsma DI,
Smith GD,
Stefansson K,
Eriksson N,
Daly MJ,
Neale BM,
Olesen J,
Chasman DI,
Nyholt DR,
Palotie A
International Headache Genetics Consortium
Nature genetics · 2016 · PMID 27322543
9 pages
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment
Rietveld CA,
Medland SE,
Derringer J,
Yang J,
Esko T,
Martin NW,
Westra HJ,
Shakhbazov K,
Abdellaoui A,
Agrawal A,
Albrecht E,
Alizadeh BZ
and 191 more — show all
Amin N,
Barnard J,
Baumeister SE,
Benke KS,
Bielak LF,
Boatman JA,
Boyle PA,
Davies G,
de Leeuw C,
Eklund N,
Evans DS,
Ferhmann R,
Fischer K,
Gieger C,
Gjessing HK,
Hägg S,
Harris JR,
Hayward C,
Holzapfel C,
Ibrahim-Verbaas CA,
Ingelsson E,
Jacobsson B,
Joshi PK,
Jugessur A,
Kaakinen M,
Kanoni S,
Karjalainen J,
Kolcic I,
Kristiansson K,
Kutalik Z,
Lahti J,
Lee SH,
Lin P,
Lind PA,
Liu Y,
Lohman K,
Loitfelder M,
McMahon G,
Vidal PM,
Meirelles O,
Milani L,
Myhre R,
Nuotio ML,
Oldmeadow CJ,
Petrovic KE,
Peyrot WJ,
Polasek O,
Quaye L,
Reinmaa E,
Rice JP,
Rizzi TS,
Schmidt H,
Schmidt R,
Smith AV,
Smith JA,
Tanaka T,
Terracciano A,
van der Loos MJ,
Vitart V,
Völzke H,
Wellmann J,
Yu L,
Zhao W,
Allik J,
Attia JR,
Bandinelli S,
Bastardot F,
Beauchamp J,
Bennett DA,
Berger K,
Bierut LJ,
Boomsma DI,
Bültmann U,
Campbell H,
Chabris CF,
Cherkas L,
Chung MK,
Cucca F,
de Andrade M,
De Jager PL,
De Neve JE,
Deary IJ,
Dedoussis GV,
Deloukas P,
Dimitriou M,
Eiríksdóttir G,
Elderson MF,
Eriksson JG,
Evans DM,
Faul JD,
Ferrucci L,
Garcia ME,
Grönberg H,
Guðnason V,
Hall P,
Harris JM,
Harris TB,
Hastie ND,
Heath AC,
Hernandez DG,
Hoffmann W,
Hofman A,
Holle R,
Holliday EG,
Hottenga JJ,
Iacono WG,
Illig T,
Järvelin MR,
Kähönen M,
Kaprio J,
Kirkpatrick RM,
Kowgier M,
Latvala A,
Launer LJ,
Lawlor DA,
Lehtimäki T,
Li J,
Lichtenstein P,
Lichtner P,
Liewald DC,
Madden PA,
Magnusson PK,
Mäkinen TE,
Masala M,
McGue M,
Metspalu A,
Mielck A,
Miller MB,
Montgomery GW,
Mukherjee S,
Nyholt DR,
Oostra BA,
Palmer LJ,
Palotie A,
Penninx BW,
Perola M,
Peyser PA,
Preisig M,
Räikkönen K,
Raitakari OT,
Realo A,
Ring SM,
Ripatti S,
Rivadeneira F,
Rudan I,
Rustichini A,
Salomaa V,
Sarin AP,
Schlessinger D,
Scott RJ,
Snieder H,
St Pourcain B,
Starr JM,
Sul JH,
Surakka I,
Svento R,
Teumer A,
Tiemeier H,
van Rooij FJ,
Van Wagoner DR,
Vartiainen E,
Viikari J,
Vollenweider P,
Vonk JM,
Waeber G,
Weir DR,
Wichmann HE,
Widen E,
Willemsen G,
Wilson JF,
Wright AF,
Conley D,
Davey-Smith G,
Franke L,
Groenen PJ,
Hofman A,
Johannesson M,
Kardia SL,
Krueger RF,
Laibson D,
Martin NG,
Meyer MN,
Posthuma D,
Thurik AR,
Timpson NJ,
Uitterlinden AG,
van Duijn CM,
Visscher PM,
Benjamin DJ,
Cesarini D,
Koellinger PD
LifeLines Cohort Study
Science (New York, N.Y.) · 2013 · PMID 23722424
3 pages
Genome-wide meta-analysis identifies new susceptibility loci for migraine
Anttila V,
Winsvold BS,
Gormley P,
Kurth T,
Bettella F,
McMahon G,
Kallela M,
Malik R,
de Vries B,
Terwindt G,
Medland SE,
Todt U
and 85 more — show all
McArdle WL,
Quaye L,
Koiranen M,
Ikram MA,
Lehtimäki T,
Stam AH,
Ligthart L,
Wedenoja J,
Dunham I,
Neale BM,
Palta P,
Hamalainen E,
Schürks M,
Rose LM,
Buring JE,
Ridker PM,
Steinberg S,
Stefansson H,
Jakobsson F,
Lawlor DA,
Evans DM,
Ring SM,
Färkkilä M,
Artto V,
Kaunisto MA,
Freilinger T,
Schoenen J,
Frants RR,
Pelzer N,
Weller CM,
Zielman R,
Heath AC,
Madden PAF,
Montgomery GW,
Martin NG,
Borck G,
Göbel H,
Heinze A,
Heinze-Kuhn K,
Williams FMK,
Hartikainen AL,
Pouta A,
van den Ende J,
Uitterlinden AG,
Hofman A,
Amin N,
Hottenga JJ,
Vink JM,
Heikkilä K,
Alexander M,
Muller-Myhsok B,
Schreiber S,
Meitinger T,
Wichmann HE,
Aromaa A,
Eriksson JG,
Traynor B,
Trabzuni D,
Rossin E,
Lage K,
Jacobs SBR,
Jacobs SBR,
Gibbs JR,
Birney E,
Kaprio J,
Penninx BW,
Boomsma DI,
van Duijn C,
van Duijn C,
Raitakari O,
Jarvelin MR,
Zwart JA,
Cherkas L,
Strachan DP,
Kubisch C,
Ferrari MD,
van den Maagdenberg AMJM,
Dichgans M,
Wessman M,
Smith GD,
Stefansson K,
Daly MJ,
Nyholt DR,
Chasman D,
Palotie A
North American Brain Expression Consortium · UK Brain Expression Consortium
Nature genetics · 2013 · PMID 23793025 · open access
3 pages
Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study
Gottlieb DJ,
Hek K,
Chen TH,
Watson NF,
Eiriksdottir G,
Byrne EM,
Cornelis M,
Warby SC,
Bandinelli S,
Cherkas L,
Evans DS,
Grabe HJ
and 74 more — show all
Lahti J,
Li M,
Lehtimäki T,
Lumley T,
Marciante KD,
Pérusse L,
Psaty BM,
Robbins J,
Tranah GJ,
Vink JM,
Wilk JB,
Stafford JM,
Bellis C,
Biffar R,
Bouchard C,
Cade B,
Curhan GC,
Eriksson JG,
Ewert R,
Ferrucci L,
Fülöp T,
Gehrman PR,
Goodloe R,
Harris TB,
Heath AC,
Hernandez D,
Hofman A,
Hottenga JJ,
Hunter DJ,
Jensen MK,
Johnson AD,
Kähönen M,
Kao L,
Kraft P,
Larkin EK,
Lauderdale DS,
Luik AI,
Medici M,
Montgomery GW,
Palotie A,
Patel SR,
Pistis G,
Porcu E,
Quaye L,
Raitakari O,
Redline S,
Rimm EB,
Rotter JI,
Smith AV,
Spector TD,
Teumer A,
Uitterlinden AG,
Vohl MC,
Widen E,
Willemsen G,
Young T,
Zhang X,
Liu Y,
Blangero J,
Boomsma DI,
Gudnason V,
Hu F,
Mangino M,
Martin NG,
O'Connor GT,
Stone KL,
Tanaka T,
Viikari J,
Gharib SA,
Punjabi NM,
Räikkönen K,
Völzke H,
Mignot E,
Tiemeier H
Molecular psychiatry · 2015 · PMID 25469926 · open access
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.