For researchers
Is your paper here?
2,675 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.
98 matches for
Ni S,
showing the first 20.
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy
Mingardo E,
Beaman G,
Grote P,
Nordenskjöld A,
Newman W,
Woolf AS,
Eckstein M,
Hilger AC,
Dworschak GC,
Rösch W,
Ebert AK,
Stein R
and 54 more — show all
Brusco A,
Di Grazia M,
Tamer A,
Torres FM,
Hernandez JL,
Erben P,
Maj C,
Olmos JM,
Riancho JA,
Valero C,
Hostettler IC,
Houlden H,
Werring DJ,
Schumacher J,
Gehlen J,
Giel AS,
Buerfent BC,
Arkani S,
Åkesson E,
Rotstein E,
Ludwig M,
Holmdahl G,
Giorgio E,
Berettini A,
Keene D,
Cervellione RM,
Younsi N,
Ortlieb M,
Oswald J,
Haid B,
Promm M,
Neissner C,
Hirsch K,
Stehr M,
Schäfer FM,
Schmiedeke E,
Boemers TM,
van Rooij IALM,
Feitz WFJ,
Marcelis CLM,
Lacher M,
Nelson J,
Ure B,
Fortmann C,
Gale DP,
Chan MMY,
Ludwig KU,
Nöthen MM,
Heilmann S,
Zwink N,
Jenetzky E,
Odermatt B,
Knapp M,
Reutter H
Communications biology · 2022 · PMID 36352089 · open access
4 pages
Genomics of chronic dry cough unravels neurological pathways
Coley K,
John C,
Ghouse J,
Shepherd DJ,
Shrine N,
Izquierdo AG,
Kanoni S,
Magavern EF,
Packer R,
McGarvey L,
Smith JA,
Bundgaard H
and 11 more — show all
Ostrowski SR,
Erikstrup C,
Pedersen OBV,
van Heel DA,
Hennah W,
Marttila M,
Free RC,
Hollox EJ,
Wain LV,
Tobin MD,
Batini C
Genes and Health Research Team
The European respiratory journal · 2025 · PMID 40675770 · open access
4 pages
Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci
De Jager PL,
Jia X,
Wang J,
de Bakker PI,
Ottoboni L,
Aggarwal NT,
Piccio L,
Raychaudhuri S,
Tran D,
Aubin C,
Briskin R,
Romano S
and 21 more — show all
Baranzini SE,
McCauley JL,
Pericak-Vance MA,
Haines JL,
Gibson RA,
Naeglin Y,
Uitdehaag B,
Matthews PM,
Kappos L,
Polman C,
McArdle WL,
Strachan DP,
Evans D,
Cross AH,
Daly MJ,
Compston A,
Sawcer SJ,
Weiner HL,
Hauser SL,
Hafler DA,
Oksenberg JR
International MS Genetics Consortium
Nature genetics · 2009 · PMID 19525953
3 pages
Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes
Strawbridge RJ,
Dupuis J,
Prokopenko I,
Barker A,
Ahlqvist E,
Rybin D,
Petrie JR,
Travers ME,
Bouatia-Naji N,
Dimas AS,
Nica A,
Wheeler E
and 91 more — show all
Chen H,
Voight BF,
Taneera J,
Kanoni S,
Peden JF,
Turrini F,
Gustafsson S,
Zabena C,
Almgren P,
Barker DJ,
Barnes D,
Dennison EM,
Eriksson JG,
Eriksson P,
Eury E,
Folkersen L,
Fox CS,
Frayling TM,
Goel A,
Gu HF,
Horikoshi M,
Isomaa B,
Jackson AU,
Jameson KA,
Kajantie E,
Kerr-Conte J,
Kuulasmaa T,
Kuusisto J,
Loos RJ,
Luan J,
Makrilakis K,
Manning AK,
Martínez-Larrad MT,
Narisu N,
Nastase Mannila M,
Ohrvik J,
Osmond C,
Pascoe L,
Payne F,
Sayer AA,
Sennblad B,
Silveira A,
Stancáková A,
Stirrups K,
Swift AJ,
Syvänen AC,
Tuomi T,
van 't Hooft FM,
Walker M,
Weedon MN,
Xie W,
Zethelius B,
Ongen H,
Mälarstig A,
Hopewell JC,
Saleheen D,
Chambers J,
Parish S,
Danesh J,
Kooner J,
Ostenson CG,
Lind L,
Cooper CC,
Serrano-Ríos M,
Ferrannini E,
Forsen TJ,
Clarke R,
Franzosi MG,
Seedorf U,
Watkins H,
Froguel P,
Johnson P,
Deloukas P,
Collins FS,
Laakso M,
Dermitzakis ET,
Boehnke M,
McCarthy MI,
Wareham NJ,
Groop L,
Pattou F,
Gloyn AL,
Dedoussis GV,
Lyssenko V,
Meigs JB,
Barroso I,
Watanabe RM,
Ingelsson E,
Langenberg C,
Hamsten A,
Florez JC
DIAGRAM Consortium · GIANT Consortium and 3 more consortia
Diabetes · 2011 · PMID 21873549 · open access
3 pages
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
Li R,
Brockschmidt FF,
Kiefer AK,
Stefansson H,
Nyholt DR,
Song K,
Vermeulen SH,
Kanoni S,
Glass D,
Medland SE,
Dimitriou M,
Waterworth D
and 27 more — show all
Tung JY,
Geller F,
Heilmann S,
Hillmer AM,
Bataille V,
Eigelshoven S,
Hanneken S,
Moebus S,
Herold C,
den Heijer M,
Montgomery GW,
Deloukas P,
Eriksson N,
Heath AC,
Becker T,
Sulem P,
Mangino M,
Vollenweider P,
Spector TD,
Dedoussis G,
Martin NG,
Kiemeney LA,
Mooser V,
Stefansson K,
Hinds DA,
Nöthen MM,
Richards JB
PLoS genetics · 2012 · PMID 22693459 · open access
3 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
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Lu Y,
Day FR,
Gustafsson S,
Buchkovich ML,
Na J,
Bataille V,
Cousminer DL,
Dastani Z,
Drong AW,
Esko T,
Evans DM,
Falchi M
and 247 more — show all
Feitosa MF,
Ferreira T,
Hedman ÅK,
Haring R,
Hysi PG,
Iles MM,
Justice AE,
Kanoni S,
Lagou V,
Li R,
Li X,
Locke A,
Lu C,
Mägi R,
Perry JR,
Pers TH,
Qi Q,
Sanna M,
Schmidt EM,
Scott WR,
Shungin D,
Teumer A,
Vinkhuyzen AA,
Walker RW,
Westra HJ,
Zhang M,
Zhang W,
Zhao JH,
Zhu Z,
Afzal U,
Ahluwalia TS,
Bakker SJ,
Bellis C,
Bonnefond A,
Borodulin K,
Buchman AS,
Cederholm T,
Choh AC,
Choi HJ,
Curran JE,
de Groot LC,
De Jager PL,
Dhonukshe-Rutten RA,
Enneman AW,
Eury E,
Evans DS,
Forsen T,
Friedrich N,
Fumeron F,
Garcia ME,
Gärtner S,
Han BG,
Havulinna AS,
Hayward C,
Hernandez D,
Hillege H,
Ittermann T,
Kent JW,
Kolcic I,
Laatikainen T,
Lahti J,
Mateo Leach I,
Lee CG,
Lee JY,
Liu T,
Liu Y,
Lobbens S,
Loh M,
Lyytikäinen LP,
Medina-Gomez C,
Michaëlsson K,
Nalls MA,
Nielson CM,
Oozageer L,
Pascoe L,
Paternoster L,
Polašek O,
Ripatti S,
Sarzynski MA,
Shin CS,
Narančić NS,
Spira D,
Srikanth P,
Steinhagen-Thiessen E,
Sung YJ,
Swart KM,
Taittonen L,
Tanaka T,
Tikkanen E,
van der Velde N,
van Schoor NM,
Verweij N,
Wright AF,
Yu L,
Zmuda JM,
Eklund N,
Forrester T,
Grarup N,
Jackson AU,
Kristiansson K,
Kuulasmaa T,
Kuusisto J,
Lichtner P,
Luan J,
Mahajan A,
Männistö S,
Palmer CD,
Ried JS,
Scott RA,
Stancáková A,
Wagner PJ,
Demirkan A,
Döring A,
Gudnason V,
Kiel DP,
Kühnel B,
Mangino M,
Mcknight B,
Menni C,
O'Connell JR,
Oostra BA,
Shuldiner AR,
Song K,
Vandenput L,
van Duijn CM,
Vollenweider P,
White CC,
Boehnke M,
Boettcher Y,
Cooper RS,
Forouhi NG,
Gieger C,
Grallert H,
Hingorani A,
Jørgensen T,
Jousilahti P,
Kivimaki M,
Kumari M,
Laakso M,
Langenberg C,
Linneberg A,
Luke A,
Mckenzie CA,
Palotie A,
Pedersen O,
Peters A,
Strauch K,
Tayo BO,
Wareham NJ,
Bennett DA,
Bertram L,
Blangero J,
Blüher M,
Bouchard C,
Campbell H,
Cho NH,
Cummings SR,
Czerwinski SA,
Demuth I,
Eckardt R,
Eriksson JG,
Ferrucci L,
Franco OH,
Froguel P,
Gansevoort RT,
Hansen T,
Harris TB,
Hastie N,
Heliövaara M,
Hofman A,
Jordan JM,
Jula A,
Kähönen M,
Kajantie E,
Knekt PB,
Koskinen S,
Kovacs P,
Lehtimäki T,
Lind L,
Liu Y,
Orwoll ES,
Osmond C,
Perola M,
Pérusse L,
Raitakari OT,
Rankinen T,
Rao DC,
Rice TK,
Rivadeneira F,
Rudan I,
Salomaa V,
Sørensen TI,
Stumvoll M,
Tönjes A,
Towne B,
Tranah GJ,
Tremblay A,
Uitterlinden AG,
van der Harst P,
Vartiainen E,
Viikari JS,
Vitart V,
Vohl MC,
Völzke H,
Walker M,
Wallaschofski H,
Wild S,
Wilson JF,
Yengo L,
Bishop DT,
Borecki IB,
Chambers JC,
Cupples LA,
Dehghan A,
Deloukas P,
Fatemifar G,
Fox C,
Furey TS,
Franke L,
Han J,
Hunter DJ,
Karjalainen J,
Karpe F,
Kaplan RC,
Kooner JS,
McCarthy MI,
Murabito JM,
Morris AP,
Bishop JA,
North KE,
Ohlsson C,
Ong KK,
Prokopenko I,
Richards JB,
Schadt EE,
Spector TD,
Widén E,
Willer CJ,
Yang J,
Ingelsson E,
Mohlke KL,
Hirschhorn JN,
Pospisilik JA,
Zillikens MC,
Lindgren C,
Kilpeläinen TO,
Loos RJ
Nature communications · 2016 · PMID 26833246 · open access
3 pages
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes
Franceschini N,
Giambartolomei C,
de Vries PS,
Finan C,
Bis JC,
Huntley RP,
Lovering RC,
Tajuddin SM,
Winkler TW,
Graff M,
Kavousi M,
Dale C
and 146 more — show all
Smith AV,
Hofer E,
van Leeuwen EM,
Nolte IM,
Lu L,
Scholz M,
Sargurupremraj M,
Pitkänen N,
Franzén O,
Joshi PK,
Noordam R,
Marioni RE,
Hwang SJ,
Musani SK,
Schminke U,
Palmas W,
Isaacs A,
Correa A,
Zonderman AB,
Hofman A,
Teumer A,
Cox AJ,
Uitterlinden AG,
Wong A,
Smit AJ,
Newman AB,
Britton A,
Ruusalepp A,
Sennblad B,
Hedblad B,
Pasaniuc B,
Penninx BW,
Langefeld CD,
Wassel CL,
Tzourio C,
Fava C,
Baldassarre D,
O'Leary DH,
Teupser D,
Kuh D,
Tremoli E,
Mannarino E,
Grossi E,
Boerwinkle E,
Schadt EE,
Ingelsson E,
Veglia F,
Rivadeneira F,
Beutner F,
Chauhan G,
Heiss G,
Snieder H,
Campbell H,
Völzke H,
Markus HS,
Deary IJ,
Jukema JW,
de Graaf J,
Price J,
Pott J,
Hopewell JC,
Liang J,
Thiery J,
Engmann J,
Gertow K,
Rice K,
Taylor KD,
Dhana K,
Kiemeney LALM,
Lind L,
Raffield LM,
Launer LJ,
Holdt LM,
Dörr M,
Dichgans M,
Traylor M,
Sitzer M,
Kumari M,
Kivimaki M,
Nalls MA,
Melander O,
Raitakari O,
Franco OH,
Rueda-Ochoa OL,
Roussos P,
Whincup PH,
Amouyel P,
Giral P,
Anugu P,
Wong Q,
Malik R,
Rauramaa R,
Burkhardt R,
Hardy R,
Schmidt R,
de Mutsert R,
Morris RW,
Strawbridge RJ,
Wannamethee SG,
Hägg S,
Shah S,
McLachlan S,
Trompet S,
Seshadri S,
Kurl S,
Heckbert SR,
Ring S,
Harris TB,
Lehtimäki T,
Galesloot TE,
Shah T,
de Faire U,
Plagnol V,
Rosamond WD,
Post W,
Zhu X,
Zhang X,
Guo X,
Saba Y,
Dehghan A,
Seldenrijk A,
Morrison AC,
Hamsten A,
Psaty BM,
van Duijn CM,
Lawlor DA,
Mook-Kanamori DO,
Bowden DW,
Schmidt H,
Wilson JF,
Wilson JG,
Rotter JI,
Wardlaw JM,
Deanfield J,
Halcox J,
Lyytikäinen LP,
Loeffler M,
Evans MK,
Debette S,
Humphries SE,
Völker U,
Gudnason V,
Hingorani AD,
Björkegren JLM,
Casas JP,
O'Donnell CJ
MEGASTROKE Consortium
Nature communications · 2018 · PMID 30510157 · open access
3 pages
Immunochip meta-analysis in European and Argentinian populations identifies two novel genetic loci associated with celiac disease
Ricaño-Ponce I,
Gutierrez-Achury J,
Costa AF,
Deelen P,
Kurilshikov A,
Zorro MM,
Platteel M,
van der Graaf A,
Sanna S,
Daffra O,
Zhernakova A,
Fu J
and 6 more — show all
Consortium for the study of genetic associations of celiac disease in Latin-America
European journal of human genetics : EJHG · 2020 · PMID 31591516
3 pages
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability
Lagou V,
Mägi R,
Hottenga JJ,
Grallert H,
Perry JRB,
Bouatia-Naji N,
Marullo L,
Rybin D,
Jansen R,
Min JL,
Dimas AS,
Ulrich A
and 192 more — show all
Zudina L,
Gådin JR,
Jiang L,
Faggian A,
Bonnefond A,
Fadista J,
Stathopoulou MG,
Isaacs A,
Willems SM,
Navarro P,
Tanaka T,
Jackson AU,
Montasser ME,
O'Connell JR,
Bielak LF,
Webster RJ,
Saxena R,
Stafford JM,
Pourcain BS,
Timpson NJ,
Salo P,
Shin SY,
Amin N,
Smith AV,
Li G,
Verweij N,
Goel A,
Ford I,
Johnson PCD,
Johnson T,
Kapur K,
Thorleifsson G,
Strawbridge RJ,
Rasmussen-Torvik LJ,
Esko T,
Mihailov E,
Fall T,
Fraser RM,
Mahajan A,
Kanoni S,
Giedraitis V,
Kleber ME,
Silbernagel G,
Meyer J,
Müller-Nurasyid M,
Ganna A,
Sarin AP,
Yengo L,
Shungin D,
Luan J,
Horikoshi M,
An P,
Sanna S,
Boettcher Y,
Rayner NW,
Nolte IM,
Zemunik T,
Iperen EV,
Kovacs P,
Hastie ND,
Wild SH,
McLachlan S,
Campbell S,
Polasek O,
Carlson O,
Egan J,
Kiess W,
Willemsen G,
Kuusisto J,
Laakso M,
Dimitriou M,
Hicks AA,
Rauramaa R,
Bandinelli S,
Thorand B,
Liu Y,
Miljkovic I,
Lind L,
Doney A,
Perola M,
Hingorani A,
Kivimaki M,
Kumari M,
Bennett AJ,
Groves CJ,
Herder C,
Koistinen HA,
Kinnunen L,
Faire U,
Bakker SJL,
Uusitupa M,
Palmer CNA,
Jukema JW,
Sattar N,
Pouta A,
Snieder H,
Boerwinkle E,
Pankow JS,
Magnusson PK,
Krus U,
Scapoli C,
de Geus EJCN,
Blüher M,
Wolffenbuttel BHR,
Province MA,
Abecasis GR,
Meigs JB,
Hovingh GK,
Lindström J,
Wilson JF,
Wright AF,
Dedoussis GV,
Bornstein SR,
Schwarz PEH,
Tönjes A,
Winkelmann BR,
Boehm BO,
März W,
Metspalu A,
Price JF,
Deloukas P,
Körner A,
Lakka TA,
Keinanen-Kiukaanniemi SM,
Saaristo TE,
Bergman RN,
Tuomilehto J,
Wareham NJ,
Langenberg C,
Männistö S,
Franks PW,
Hayward C,
Vitart V,
Kaprio J,
Visvikis-Siest S,
Balkau B,
Altshuler D,
Rudan I,
Stumvoll M,
Campbell H,
van Duijn CM,
Gieger C,
Illig T,
Ferrucci L,
Pedersen NL,
Pramstaller PP,
Boehnke M,
Frayling TM,
Shuldiner AR,
Peyser PA,
Kardia SLR,
Palmer LJ,
Penninx BW,
Meneton P,
Harris TB,
Navis G,
Harst PV,
Smith GD,
Forouhi NG,
Loos RJF,
Salomaa V,
Soranzo N,
Boomsma DI,
Groop L,
Tuomi T,
Hofman A,
Munroe PB,
Gudnason V,
Siscovick DS,
Watkins H,
Lecoeur C,
Vollenweider P,
Franco-Cereceda A,
Eriksson P,
Jarvelin MR,
Stefansson K,
Hamsten A,
Nicholson G,
Karpe F,
Dermitzakis ET,
Lindgren CM,
McCarthy MI,
Froguel P,
Kaakinen MA,
Lyssenko V,
Watanabe RM,
Ingelsson E,
Florez JC,
Dupuis J,
Barroso I,
Morris AP,
Prokopenko I
Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC)
Nature communications · 2021 · PMID 33402679 · open access
3 pages
Discovery of 42 genome-wide significant loci associated with dyslexia
Doust C,
Fontanillas P,
Eising E,
Gordon SD,
Wang Z,
Alagöz G,
Molz B,
Pourcain BS,
Francks C,
Marioni RE,
Zhao J,
Paracchini S
and 15 more — show all
Talcott JB,
Monaco AP,
Stein JF,
Gruen JR,
Olson RK,
Willcutt EG,
DeFries JC,
Pennington BF,
Smith SD,
Wright MJ,
Martin NG,
Auton A,
Bates TC,
Fisher SE,
Luciano M
23andMe Research Team · Quantitative Trait Working Group of the GenLang Consortium
Nature genetics · 2022 · PMID 36266505 · open access
3 pages
Genetic determinants of zinc homeostasis and its role in cardiometabolic diseases
Sadler MC,
Ghobril JP,
Borisov O,
Perrais M,
Schiano G,
Petrovic D,
Ha E,
Ponte B,
Li Y,
Rodriguez-Hernandez Z,
Pruijm M,
Ackermann D
and 20 more — show all
Guessous I,
Stringhini S,
Ehret G,
Corre T,
Vogt B,
Martin PY,
Ongen H,
Dermitzakis E,
Williams JE,
Murdoch BM,
McGuire MK,
Meehan CL,
Lenglet S,
Susztak K,
Vaucher J,
Thomas A,
Devuyst O,
Köttgen A,
Bochud M,
Kutalik Z
INSPIRE Consortium
PLoS genetics · 2025 · PMID 41325371 · open access
3 pages
Genome-wide association study identifies five susceptibility loci for glioma
Shete S,
Hosking FJ,
Robertson LB,
Dobbins SE,
Sanson M,
Malmer B,
Simon M,
Marie Y,
Boisselier B,
Delattre JY,
Hoang-Xuan K,
El Hallani S
and 25 more — show all
Idbaih A,
Zelenika D,
Andersson U,
Henriksson R,
Bergenheim AT,
Feychting M,
Lönn S,
Ahlbom A,
Schramm J,
Linnebank M,
Hemminki K,
Kumar R,
Hepworth SJ,
Price A,
Armstrong G,
Liu Y,
Gu X,
Yu R,
Lau C,
Schoemaker M,
Muir K,
Swerdlow A,
Lathrop M,
Bondy M,
Houlston RS
Nature genetics · 2009 · PMID 19578367
2 pages
Genome-wide association studies of the PR interval in African Americans
Smith JG,
Magnani JW,
Palmer C,
Meng YA,
Soliman EZ,
Musani SK,
Kerr KF,
Schnabel RB,
Lubitz SA,
Sotoodehnia N,
Redline S,
Pfeufer A
and 16 more — show all
Müller M,
Evans DS,
Nalls MA,
Liu Y,
Newman AB,
Zonderman AB,
Evans MK,
Deo R,
Ellinor PT,
Paltoo DN,
Newton-Cheh C,
Benjamin EJ,
Mehra R,
Alonso A,
Heckbert SR,
Fox ER
Candidate-gene Association Resource (CARe) Consortium
PLoS genetics · 2011 · PMID 21347284 · open access
2 pages
New susceptibility loci associated with kidney disease in type 1 diabetes
Sandholm N,
Salem RM,
McKnight AJ,
Brennan EP,
Forsblom C,
Isakova T,
McKay GJ,
Williams WW,
Sadlier DM,
Mäkinen VP,
Swan EJ,
Palmer C
and 80 more — show all
Boright AP,
Ahlqvist E,
Deshmukh HA,
Keller BJ,
Huang H,
Ahola AJ,
Fagerholm E,
Gordin D,
Harjutsalo V,
He B,
Heikkilä O,
Hietala K,
Kytö J,
Lahermo P,
Lehto M,
Lithovius R,
Osterholm AM,
Parkkonen M,
Pitkäniemi J,
Rosengård-Bärlund M,
Saraheimo M,
Sarti C,
Söderlund J,
Soro-Paavonen A,
Syreeni A,
Thorn LM,
Tikkanen H,
Tolonen N,
Tryggvason K,
Tuomilehto J,
Wadén J,
Gill GV,
Prior S,
Guiducci C,
Mirel DB,
Taylor A,
Hosseini SM,
Parving HH,
Rossing P,
Tarnow L,
Ladenvall C,
Alhenc-Gelas F,
Lefebvre P,
Rigalleau V,
Roussel R,
Tregouet DA,
Maestroni A,
Maestroni S,
Falhammar H,
Gu T,
Möllsten A,
Cimponeriu D,
Ioana M,
Mota M,
Mota E,
Serafinceanu C,
Stavarachi M,
Hanson RL,
Nelson RG,
Kretzler M,
Colhoun HM,
Panduru NM,
Gu HF,
Brismar K,
Zerbini G,
Hadjadj S,
Marre M,
Groop L,
Lajer M,
Bull SB,
Waggott D,
Paterson AD,
Savage DA,
Bain SC,
Martin F,
Hirschhorn JN,
Godson C,
Florez JC,
Groop PH,
Maxwell AP
DCCT/EDIC Research Group
PLoS genetics · 2012 · PMID 23028342 · open access
2 pages
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations
Franceschini N,
Fox E,
Zhang Z,
Edwards TL,
Nalls MA,
Sung YJ,
Tayo BO,
Sun YV,
Gottesman O,
Adeyemo A,
Johnson AD,
Young JH
and 94 more — show all
Rice K,
Duan Q,
Chen F,
Li Y,
Tang H,
Fornage M,
Keene KL,
Andrews JS,
Smith JA,
Faul JD,
Guangfa Z,
Guo W,
Liu Y,
Murray SS,
Musani SK,
Srinivasan S,
Velez Edwards DR,
Wang H,
Becker LC,
Bovet P,
Bochud M,
Broeckel U,
Burnier M,
Carty C,
Chasman DI,
Ehret G,
Chen WM,
Chen G,
Chen W,
Ding J,
Dreisbach AW,
Evans MK,
Guo X,
Garcia ME,
Jensen R,
Keller MF,
Lettre G,
Lotay V,
Martin LW,
Moore JH,
Morrison AC,
Mosley TH,
Ogunniyi A,
Palmas W,
Papanicolaou G,
Penman A,
Polak JF,
Ridker PM,
Salako B,
Singleton AB,
Shriner D,
Taylor KD,
Vasan R,
Wiggins K,
Williams SM,
Yanek LR,
Zhao W,
Zonderman AB,
Becker DM,
Berenson G,
Boerwinkle E,
Bottinger E,
Cushman M,
Eaton C,
Nyberg F,
Heiss G,
Hirschhron JN,
Howard VJ,
Karczewsk KJ,
Lanktree MB,
Liu K,
Liu Y,
Loos R,
Margolis K,
Snyder M,
Psaty BM,
Schork NJ,
Weir DR,
Rotimi CN,
Sale MM,
Harris T,
Kardia SL,
Hunt SC,
Arnett D,
Redline S,
Cooper RS,
Risch NJ,
Rao DC,
Rotter JI,
Chakravarti A,
Reiner AP,
Levy D,
Keating BJ,
Zhu X
Asian Genetic Epidemiology Network Consortium
American journal of human genetics · 2013 · PMID 23972371
2 pages
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error
Cheng CY,
Schache M,
Ikram MK,
Young TL,
Guggenheim JA,
Vitart V,
MacGregor S,
Verhoeven VJ,
Barathi VA,
Liao J,
Hysi PG,
Bailey-Wilson JE
and 96 more — show all
St Pourcain B,
Kemp JP,
McMahon G,
Timpson NJ,
Evans DM,
Montgomery GW,
Mishra A,
Wang YX,
Wang JJ,
Rochtchina E,
Polasek O,
Wright AF,
Amin N,
van Leeuwen EM,
Wilson JF,
Pennell CE,
van Duijn CM,
de Jong PT,
Vingerling JR,
Zhou X,
Chen P,
Li R,
Tay WT,
Zheng Y,
Chew M,
Burdon KP,
Craig JE,
Iyengar SK,
Igo RP Jr,
Lass JH Jr,
Chew EY,
Haller T,
Mihailov E,
Metspalu A,
Wedenoja J,
Simpson CL,
Wojciechowski R,
Höhn R,
Mirshahi A,
Zeller T,
Pfeiffer N,
Lackner KJ,
Bettecken T,
Meitinger T,
Oexle K,
Pirastu M,
Portas L,
Nag A,
Williams KM,
Yonova-Doing E,
Klein R,
Klein BE,
Hosseini SM,
Paterson AD,
Makela KM,
Lehtimaki T,
Kahonen M,
Raitakari O,
Yoshimura N,
Matsuda F,
Chen LJ,
Pang CP,
Yip SP,
Yap MK,
Meguro A,
Mizuki N,
Inoko H,
Foster PJ,
Zhao JH,
Vithana E,
Tai ES,
Fan Q,
Xu L,
Campbell H,
Fleck B,
Rudan I,
Aung T,
Hofman A,
Uitterlinden AG,
Bencic G,
Khor CC,
Forward H,
Pärssinen O,
Mitchell P,
Rivadeneira F,
Hewitt AW,
Williams C,
Oostra BA,
Teo YY,
Hammond CJ,
Stambolian D,
Mackey DA,
Klaver CC,
Wong TY,
Saw SM,
Baird PN
Consortium for Refractive Error and Myopia · Fuchs' Genetics Multi-Center Study Group and 2 more consortia
American journal of human genetics · 2013 · PMID 24144296
2 pages
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis
Fogh I,
Ratti A,
Gellera C,
Lin K,
Tiloca C,
Moskvina V,
Corrado L,
Sorarù G,
Cereda C,
Corti S,
Gentilini D,
Calini D
and 53 more — show all
Castellotti B,
Mazzini L,
Querin G,
Gagliardi S,
Del Bo R,
Conforti FL,
Siciliano G,
Inghilleri M,
Saccà F,
Bongioanni P,
Penco S,
Corbo M,
Sorbi S,
Filosto M,
Ferlini A,
Di Blasio AM,
Signorini S,
Shatunov A,
Jones A,
Shaw PJ,
Morrison KE,
Farmer AE,
Van Damme P,
Robberecht W,
Chiò A,
Traynor BJ,
Sendtner M,
Melki J,
Meininger V,
Hardiman O,
Andersen PM,
Leigh NP,
Glass JD,
Overste D,
Diekstra FP,
Veldink JH,
van Es MA,
Shaw CE,
Weale ME,
Lewis CM,
Williams J,
Brown RH,
Landers JE,
Ticozzi N,
Ceroni M,
Pegoraro E,
Comi GP,
D'Alfonso S,
van den Berg LH,
Taroni F,
Al-Chalabi A,
Powell J,
Silani V
SLAGEN Consortium and Collaborators
Human molecular genetics · 2014 · PMID 24256812
2 pages
Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption
Cornelis MC,
Byrne EM,
Esko T,
Nalls MA,
Ganna A,
Paynter N,
Monda KL,
Amin N,
Fischer K,
Renstrom F,
Ngwa JS,
Huikari V
and 142 more — show all
Cavadino A,
Nolte IM,
Teumer A,
Yu K,
Marques-Vidal P,
Rawal R,
Manichaikul A,
Wojczynski MK,
Vink JM,
Zhao JH,
Burlutsky G,
Lahti J,
Mikkilä V,
Lemaitre RN,
Eriksson J,
Musani SK,
Tanaka T,
Geller F,
Luan J,
Hui J,
Mägi R,
Dimitriou M,
Garcia ME,
Ho WK,
Wright MJ,
Rose LM,
Magnusson PK,
Pedersen NL,
Couper D,
Oostra BA,
Hofman A,
Ikram MA,
Tiemeier HW,
Uitterlinden AG,
van Rooij FJ,
Barroso I,
Johansson I,
Xue L,
Kaakinen M,
Milani L,
Power C,
Snieder H,
Stolk RP,
Baumeister SE,
Biffar R,
Gu F,
Bastardot F,
Kutalik Z,
Jacobs DR Jr,
Forouhi NG,
Mihailov E,
Lind L,
Lindgren C,
Michaëlsson K,
Morris A,
Jensen M,
Khaw KT,
Luben RN,
Wang JJ,
Männistö S,
Perälä MM,
Kähönen M,
Lehtimäki T,
Viikari J,
Mozaffarian D,
Mukamal K,
Psaty BM,
Döring A,
Heath AC,
Montgomery GW,
Dahmen N,
Carithers T,
Tucker KL,
Ferrucci L,
Boyd HA,
Melbye M,
Treur JL,
Mellström D,
Hottenga JJ,
Prokopenko I,
Tönjes A,
Deloukas P,
Kanoni S,
Lorentzon M,
Houston DK,
Liu Y,
Danesh J,
Rasheed A,
Mason MA,
Zonderman AB,
Franke L,
Kristal BS,
Karjalainen J,
Reed DR,
Westra HJ,
Evans MK,
Saleheen D,
Harris TB,
Dedoussis G,
Curhan G,
Stumvoll M,
Beilby J,
Pasquale LR,
Feenstra B,
Bandinelli S,
Ordovas JM,
Chan AT,
Peters U,
Ohlsson C,
Gieger C,
Martin NG,
Waldenberger M,
Siscovick DS,
Raitakari O,
Eriksson JG,
Mitchell P,
Hunter DJ,
Kraft P,
Rimm EB,
Boomsma DI,
Borecki IB,
Loos RJ,
Wareham NJ,
Vollenweider P,
Caporaso N,
Grabe HJ,
Neuhouser ML,
Wolffenbuttel BH,
Hu FB,
Hyppönen E,
Järvelin MR,
Cupples LA,
Franks PW,
Ridker PM,
van Duijn CM,
Heiss G,
Metspalu A,
North KE,
Ingelsson E,
Nettleton JA,
van Dam RM,
Chasman DI
Coffee and Caffeine Genetics Consortium · International Parkinson’s Disease Genomics Consortium (IPDGC) and 2 more consortia
Molecular psychiatry · 2015 · PMID 25288136
2 pages
Genetic studies of body mass index yield new insights for obesity biology
Locke AE,
Kahali B,
Berndt SI,
Justice AE,
Pers TH,
Day FR,
Powell C,
Vedantam S,
Buchkovich ML,
Yang J,
Croteau-Chonka DC,
Esko T
and 470 more — show all
Fall T,
Ferreira T,
Gustafsson S,
Kutalik Z,
Luan J,
Mägi R,
Randall JC,
Winkler TW,
Wood AR,
Workalemahu T,
Faul JD,
Smith JA,
Zhao JH,
Zhao W,
Chen J,
Fehrmann R,
Hedman ÅK,
Karjalainen J,
Schmidt EM,
Absher D,
Amin N,
Anderson D,
Beekman M,
Bolton JL,
Bragg-Gresham JL,
Buyske S,
Demirkan A,
Deng G,
Ehret GB,
Feenstra B,
Feitosa MF,
Fischer K,
Goel A,
Gong J,
Jackson AU,
Kanoni S,
Kleber ME,
Kristiansson K,
Lim U,
Lotay V,
Mangino M,
Leach IM,
Medina-Gomez C,
Medland SE,
Nalls MA,
Palmer CD,
Pasko D,
Pechlivanis S,
Peters MJ,
Prokopenko I,
Shungin D,
Stančáková A,
Strawbridge RJ,
Sung YJ,
Tanaka T,
Teumer A,
Trompet S,
van der Laan SW,
van Setten J,
Van Vliet-Ostaptchouk JV,
Wang Z,
Yengo L,
Zhang W,
Isaacs A,
Albrecht E,
Ärnlöv J,
Arscott GM,
Attwood AP,
Bandinelli S,
Barrett A,
Bas IN,
Bellis C,
Bennett AJ,
Berne C,
Blagieva R,
Blüher M,
Böhringer S,
Bonnycastle LL,
Böttcher Y,
Boyd HA,
Bruinenberg M,
Caspersen IH,
Chen YI,
Clarke R,
Daw EW,
de Craen AJM,
Delgado G,
Dimitriou M,
Doney ASF,
Eklund N,
Estrada K,
Eury E,
Folkersen L,
Fraser RM,
Garcia ME,
Geller F,
Giedraitis V,
Gigante B,
Go AS,
Golay A,
Goodall AH,
Gordon SD,
Gorski M,
Grabe HJ,
Grallert H,
Grammer TB,
Gräßler J,
Grönberg H,
Groves CJ,
Gusto G,
Haessler J,
Hall P,
Haller T,
Hallmans G,
Hartman CA,
Hassinen M,
Hayward C,
Heard-Costa NL,
Helmer Q,
Hengstenberg C,
Holmen O,
Hottenga JJ,
James AL,
Jeff JM,
Johansson Å,
Jolley J,
Juliusdottir T,
Kinnunen L,
Koenig W,
Koskenvuo M,
Kratzer W,
Laitinen J,
Lamina C,
Leander K,
Lee NR,
Lichtner P,
Lind L,
Lindström J,
Lo KS,
Lobbens S,
Lorbeer R,
Lu Y,
Mach F,
Magnusson PKE,
Mahajan A,
McArdle WL,
McLachlan S,
Menni C,
Merger S,
Mihailov E,
Milani L,
Moayyeri A,
Monda KL,
Morken MA,
Mulas A,
Müller G,
Müller-Nurasyid M,
Musk AW,
Nagaraja R,
Nöthen MM,
Nolte IM,
Pilz S,
Rayner NW,
Renstrom F,
Rettig R,
Ried JS,
Ripke S,
Robertson NR,
Rose LM,
Sanna S,
Scharnagl H,
Scholtens S,
Schumacher FR,
Scott WR,
Seufferlein T,
Shi J,
Smith AV,
Smolonska J,
Stanton AV,
Steinthorsdottir V,
Stirrups K,
Stringham HM,
Sundström J,
Swertz MA,
Swift AJ,
Syvänen AC,
Tan ST,
Tayo BO,
Thorand B,
Thorleifsson G,
Tyrer JP,
Uh HW,
Vandenput L,
Verhulst FC,
Vermeulen SH,
Verweij N,
Vonk JM,
Waite LL,
Warren HR,
Waterworth D,
Weedon MN,
Wilkens LR,
Willenborg C,
Wilsgaard T,
Wojczynski MK,
Wong A,
Wright AF,
Zhang Q,
Brennan EP,
Choi M,
Dastani Z,
Drong AW,
Eriksson P,
Franco-Cereceda A,
Gådin JR,
Gharavi AG,
Goddard ME,
Handsaker RE,
Huang J,
Karpe F,
Kathiresan S,
Keildson S,
Kiryluk K,
Kubo M,
Lee JY,
Liang L,
Lifton RP,
Ma B,
McCarroll SA,
McKnight AJ,
Min JL,
Moffatt MF,
Montgomery GW,
Murabito JM,
Nicholson G,
Nyholt DR,
Okada Y,
Perry JRB,
Dorajoo R,
Reinmaa E,
Salem RM,
Sandholm N,
Scott RA,
Stolk L,
Takahashi A,
Tanaka T,
van 't Hooft FM,
Vinkhuyzen AAE,
Westra HJ,
Zheng W,
Zondervan KT,
Heath AC,
Arveiler D,
Bakker SJL,
Beilby J,
Bergman RN,
Blangero J,
Bovet P,
Campbell H,
Caulfield MJ,
Cesana G,
Chakravarti A,
Chasman DI,
Chines PS,
Collins FS,
Crawford DC,
Cupples LA,
Cusi D,
Danesh J,
de Faire U,
den Ruijter HM,
Dominiczak AF,
Erbel R,
Erdmann J,
Eriksson JG,
Farrall M,
Felix SB,
Ferrannini E,
Ferrières J,
Ford I,
Forouhi NG,
Forrester T,
Franco OH,
Gansevoort RT,
Gejman PV,
Gieger C,
Gottesman O,
Gudnason V,
Gyllensten U,
Hall AS,
Harris TB,
Hattersley AT,
Hicks AA,
Hindorff LA,
Hingorani AD,
Hofman A,
Homuth G,
Hovingh GK,
Humphries SE,
Hunt SC,
Hyppönen E,
Illig T,
Jacobs KB,
Jarvelin MR,
Jöckel KH,
Johansen B,
Jousilahti P,
Jukema JW,
Jula AM,
Kaprio J,
Kastelein JJP,
Keinanen-Kiukaanniemi SM,
Kiemeney LA,
Knekt P,
Kooner JS,
Kooperberg C,
Kovacs P,
Kraja AT,
Kumari M,
Kuusisto J,
Lakka TA,
Langenberg C,
Marchand LL,
Lehtimäki T,
Lyssenko V,
Männistö S,
Marette A,
Matise TC,
McKenzie CA,
McKnight B,
Moll FL,
Morris AD,
Morris AP,
Murray JC,
Nelis M,
Ohlsson C,
Oldehinkel AJ,
Ong KK,
Madden PAF,
Pasterkamp G,
Peden JF,
Peters A,
Postma DS,
Pramstaller PP,
Price JF,
Qi L,
Raitakari OT,
Rankinen T,
Rao DC,
Rice TK,
Ridker PM,
Rioux JD,
Ritchie MD,
Rudan I,
Salomaa V,
Samani NJ,
Saramies J,
Sarzynski MA,
Schunkert H,
Schwarz PEH,
Sever P,
Shuldiner AR,
Sinisalo J,
Stolk RP,
Strauch K,
Tönjes A,
Trégouët DA,
Tremblay A,
Tremoli E,
Virtamo J,
Vohl MC,
Völker U,
Waeber G,
Willemsen G,
Witteman JC,
Zillikens MC,
Adair LS,
Amouyel P,
Asselbergs FW,
Assimes TL,
Bochud M,
Boehm BO,
Boerwinkle E,
Bornstein SR,
Bottinger EP,
Bouchard C,
Cauchi S,
Chambers JC,
Chanock SJ,
Cooper RS,
de Bakker PIW,
Dedoussis G,
Ferrucci L,
Franks PW,
Froguel P,
Groop LC,
Haiman CA,
Hamsten A,
Hui J,
Hunter DJ,
Hveem K,
Kaplan RC,
Kivimaki M,
Kuh D,
Laakso M,
Liu Y,
Martin NG,
März W,
Melbye M,
Metspalu A,
Moebus S,
Munroe PB,
Njølstad I,
Oostra BA,
Palmer CNA,
Pedersen NL,
Perola M,
Pérusse L,
Peters U,
Power C,
Quertermous T,
Rauramaa R,
Rivadeneira F,
Saaristo TE,
Saleheen D,
Sattar N,
Schadt EE,
Schlessinger D,
Slagboom PE,
Snieder H,
Spector TD,
Thorsteinsdottir U,
Stumvoll M,
Tuomilehto J,
Uitterlinden AG,
Uusitupa M,
van der Harst P,
Walker M,
Wallaschofski H,
Wareham NJ,
Watkins H,
Weir DR,
Wichmann HE,
Wilson JF,
Zanen P,
Borecki IB,
Deloukas P,
Fox CS,
Heid IM,
O'Connell JR,
Strachan DP,
Stefansson K,
van Duijn CM,
Abecasis GR,
Franke L,
Frayling TM,
McCarthy MI,
Visscher PM,
Scherag A,
Willer CJ,
Boehnke M,
Mohlke KL,
Lindgren CM,
Beckmann JS,
Barroso I,
North KE,
Ingelsson E,
Hirschhorn JN,
Loos RJF,
Speliotes EK
LifeLines Cohort Study · ADIPOGen Consortium and 12 more consortia
Nature · 2015 · PMID 25673413
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
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.