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13 matches for
van Zuydam N.
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease
Nikpay M,
Goel A,
Won HH,
Hall LM,
Willenborg C,
Kanoni S,
Saleheen D,
Kyriakou T,
Nelson CP,
Hopewell JC,
Webb TR,
Zeng L
and 139 more — show all
Dehghan A,
Alver M,
Armasu SM,
Auro K,
Bjonnes A,
Chasman DI,
Chen S,
Ford I,
Franceschini N,
Gieger C,
Grace C,
Gustafsson S,
Huang J,
Hwang SJ,
Kim YK,
Kleber ME,
Lau KW,
Lu X,
Lu Y,
Lyytikäinen LP,
Mihailov E,
Morrison AC,
Pervjakova N,
Qu L,
Rose LM,
Salfati E,
Saxena R,
Scholz M,
Smith AV,
Tikkanen E,
Uitterlinden A,
Yang X,
Zhang W,
Zhao W,
de Andrade M,
de Vries PS,
van Zuydam NR,
Anand SS,
Bertram L,
Beutner F,
Dedoussis G,
Frossard P,
Gauguier D,
Goodall AH,
Gottesman O,
Haber M,
Han BG,
Huang J,
Jalilzadeh S,
Kessler T,
König IR,
Lannfelt L,
Lieb W,
Lind L,
Lindgren CM,
Lokki ML,
Magnusson PK,
Mallick NH,
Mehra N,
Meitinger T,
Memon FU,
Morris AP,
Nieminen MS,
Pedersen NL,
Peters A,
Rallidis LS,
Rasheed A,
Samuel M,
Shah SH,
Sinisalo J,
Stirrups KE,
Trompet S,
Wang L,
Zaman KS,
Ardissino D,
Boerwinkle E,
Borecki IB,
Bottinger EP,
Buring JE,
Chambers JC,
Collins R,
Cupples LA,
Danesh J,
Demuth I,
Elosua R,
Epstein SE,
Esko T,
Feitosa MF,
Franco OH,
Franzosi MG,
Granger CB,
Gu D,
Gudnason V,
Hall AS,
Hamsten A,
Harris TB,
Hazen SL,
Hengstenberg C,
Hofman A,
Ingelsson E,
Iribarren C,
Jukema JW,
Karhunen PJ,
Kim BJ,
Kooner JS,
Kullo IJ,
Lehtimäki T,
Loos RJF,
Melander O,
Metspalu A,
März W,
Palmer CN,
Perola M,
Quertermous T,
Rader DJ,
Ridker PM,
Ripatti S,
Roberts R,
Salomaa V,
Sanghera DK,
Schwartz SM,
Seedorf U,
Stewart AF,
Stott DJ,
Thiery J,
Zalloua PA,
O'Donnell CJ,
Reilly MP,
Assimes TL,
Thompson JR,
Erdmann J,
Clarke R,
Watkins H,
Kathiresan S,
McPherson R,
Deloukas P,
Schunkert H,
Samani NJ,
Farrall M
Nature genetics · 2015 · PMID 26343387 · open access
12 pages+
Genome-wide associations for birth weight and correlations with adult disease
Horikoshi M,
Beaumont RN,
Day FR,
Warrington NM,
Kooijman MN,
Fernandez-Tajes J,
Feenstra B,
van Zuydam NR,
Gaulton KJ,
Grarup N,
Bradfield JP,
Strachan DP
and 157 more — show all
Li-Gao R,
Ahluwalia TS,
Kreiner E,
Rueedi R,
Lyytikäinen LP,
Cousminer DL,
Wu Y,
Thiering E,
Wang CA,
Have CT,
Hottenga JJ,
Vilor-Tejedor N,
Joshi PK,
Boh ETH,
Ntalla I,
Pitkänen N,
Mahajan A,
van Leeuwen EM,
Joro R,
Lagou V,
Nodzenski M,
Diver LA,
Zondervan KT,
Bustamante M,
Marques-Vidal P,
Mercader JM,
Bennett AJ,
Rahmioglu N,
Nyholt DR,
Ma RCW,
Tam CHT,
Tam WH,
Ganesh SK,
van Rooij FJ,
Jones SE,
Loh PR,
Ruth KS,
Tuke MA,
Tyrrell J,
Wood AR,
Yaghootkar H,
Scholtens DM,
Paternoster L,
Prokopenko I,
Kovacs P,
Atalay M,
Willems SM,
Panoutsopoulou K,
Wang X,
Carstensen L,
Geller F,
Schraut KE,
Murcia M,
van Beijsterveldt CE,
Willemsen G,
Appel EVR,
Fonvig CE,
Trier C,
Tiesler CM,
Standl M,
Kutalik Z,
Bonas-Guarch S,
Hougaard DM,
Sánchez F,
Torrents D,
Waage J,
Hollegaard MV,
de Haan HG,
Rosendaal FR,
Medina-Gomez C,
Ring SM,
Hemani G,
McMahon G,
Robertson NR,
Groves CJ,
Langenberg C,
Luan J,
Scott RA,
Zhao JH,
Mentch FD,
MacKenzie SM,
Reynolds RM,
Lowe WL Jr,
Tönjes A,
Stumvoll M,
Lindi V,
Lakka TA,
van Duijn CM,
Kiess W,
Körner A,
Sørensen TI,
Niinikoski H,
Pahkala K,
Raitakari OT,
Zeggini E,
Dedoussis GV,
Teo YY,
Saw SM,
Melbye M,
Campbell H,
Wilson JF,
Vrijheid M,
de Geus EJ,
Boomsma DI,
Kadarmideen HN,
Holm JC,
Holm JC,
Hansen T,
Sebert S,
Hattersley AT,
Beilin LJ,
Newnham JP,
Newnham JP,
Pennell CE,
Heinrich J,
Adair LS,
Borja JB,
Mohlke KL,
Eriksson JG,
Widén EE,
Kähönen M,
Viikari JS,
Lehtimäki T,
Vollenweider P,
Vollenweider P,
Bønnelykke K,
Bisgaard H,
Mook-Kanamori DO,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
Pisinger C,
Pisinger C,
Pedersen O,
Power C,
Hyppönen E,
Wareham NJ,
Hakonarson H,
Davies E,
Walker BR,
Jaddoe VW,
Jarvelin MR,
Grant SF,
Vaag AA,
Lawlor DA,
Frayling TM,
Frayling TM,
Davey Smith G,
Morris AP,
Ong KK,
Felix JF,
Timpson NJ,
Perry JR,
Evans DM,
McCarthy MI,
McCarthy MI,
Freathy RM
CHARGE Consortium Hematology Working Group · Early Growth Genetics (EGG) Consortium
Nature · 2016 · PMID 27680694
12 pages+
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
Warrington NM,
Beaumont RN,
Horikoshi M,
Day FR,
Helgeland Ø,
Laurin C,
Bacelis J,
Peng S,
Hao K,
Feenstra B,
Wood AR,
Mahajan A
and 196 more — show all
Tyrrell J,
Robertson NR,
Rayner NW,
Qiao Z,
Moen GH,
Vaudel M,
Marsit CJ,
Chen J,
Nodzenski M,
Schnurr TM,
Zafarmand MH,
Bradfield JP,
Grarup N,
Kooijman MN,
Li-Gao R,
Geller F,
Ahluwalia TS,
Paternoster L,
Rueedi R,
Huikari V,
Hottenga JJ,
Lyytikäinen LP,
Cavadino A,
Metrustry S,
Cousminer DL,
Wu Y,
Thiering E,
Wang CA,
Have CT,
Vilor-Tejedor N,
Joshi PK,
Painter JN,
Ntalla I,
Myhre R,
Pitkänen N,
van Leeuwen EM,
Joro R,
Lagou V,
Richmond RC,
Espinosa A,
Barton SJ,
Inskip HM,
Holloway JW,
Santa-Marina L,
Estivill X,
Ang W,
Marsh JA,
Reichetzeder C,
Marullo L,
Hocher B,
Lunetta KL,
Murabito JM,
Relton CL,
Kogevinas M,
Chatzi L,
Allard C,
Bouchard L,
Hivert MF,
Zhang G,
Muglia LJ,
Heikkinen J,
Morgen CS,
van Kampen AHC,
van Schaik BDC,
Mentch FD,
Langenberg C,
Luan J,
Scott RA,
Zhao JH,
Hemani G,
Ring SM,
Bennett AJ,
Gaulton KJ,
Fernandez-Tajes J,
van Zuydam NR,
Medina-Gomez C,
de Haan HG,
Rosendaal FR,
Kutalik Z,
Marques-Vidal P,
Das S,
Willemsen G,
Mbarek H,
Müller-Nurasyid M,
Standl M,
Appel EVR,
Fonvig CE,
Trier C,
van Beijsterveldt CEM,
Murcia M,
Bustamante M,
Bonas-Guarch S,
Hougaard DM,
Mercader JM,
Linneberg A,
Schraut KE,
Lind PA,
Medland SE,
Shields BM,
Knight BA,
Chai JF,
Panoutsopoulou K,
Bartels M,
Sánchez F,
Stokholm J,
Torrents D,
Vinding RK,
Willems SM,
Atalay M,
Chawes BL,
Kovacs P,
Prokopenko I,
Tuke MA,
Yaghootkar H,
Ruth KS,
Jones SE,
Loh PR,
Murray A,
Weedon MN,
Tönjes A,
Stumvoll M,
Michaelsen KF,
Eloranta AM,
Lakka TA,
van Duijn CM,
Kiess W,
Körner A,
Niinikoski H,
Pahkala K,
Raitakari OT,
Jacobsson B,
Zeggini E,
Dedoussis GV,
Teo YY,
Saw SM,
Montgomery GW,
Campbell H,
Wilson JF,
Vrijkotte TGM,
Vrijheid M,
de Geus EJCN,
Hayes MG,
Kadarmideen HN,
Holm JC,
Beilin LJ,
Pennell CE,
Heinrich J,
Adair LS,
Borja JB,
Mohlke KL,
Eriksson JG,
Widén EE,
Hattersley AT,
Spector TD,
Kähönen M,
Viikari JS,
Lehtimäki T,
Boomsma DI,
Sebert S,
Vollenweider P,
Sørensen TIA,
Bisgaard H,
Bønnelykke K,
Murray JC,
Melbye M,
Nohr EA,
Mook-Kanamori DO,
Rivadeneira F,
Hofman A,
Felix JF,
Jaddoe VWV,
Hansen T,
Pisinger C,
Vaag AA,
Pedersen O,
Uitterlinden AG,
Järvelin MR,
Power C,
Hyppönen E,
Scholtens DM,
Lowe WL Jr,
Davey Smith G,
Timpson NJ,
Morris AP,
Wareham NJ,
Hakonarson H,
Grant SFA,
Frayling TM,
Lawlor DA,
Njølstad PR,
Johansson S,
Ong KK,
McCarthy MI,
Perry JRB,
Evans DM,
Freathy RM
EGG Consortium
Nature genetics · 2019 · PMID 31043758
12 pages+
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour
Mills MC,
Tropf FC,
Brazel DM,
van Zuydam N,
Vaez A,
Pers TH,
Snieder H,
Perry JRB,
Ong KK,
den Hoed M,
Barban N,
Day FR
eQTLGen Consortium · BIOS Consortium and 1 more consortia
Nature human behaviour · 2021 · PMID 34211149 · open access
12 pages+
Genome-wide characterization of circulating metabolic biomarkers
Karjalainen MK,
Karthikeyan S,
Oliver-Williams C,
Sliz E,
Allara E,
Fung WT,
Surendran P,
Zhang W,
Jousilahti P,
Kristiansson K,
Salomaa V,
Goodwin M
and 75 more — show all
Hughes DA,
Boehnke M,
Fernandes Silva L,
Yin X,
Mahajan A,
Neville MJ,
van Zuydam NR,
de Mutsert R,
Li-Gao R,
Mook-Kanamori DO,
Demirkan A,
Liu J,
Noordam R,
Trompet S,
Chen Z,
Kartsonaki C,
Li L,
Lin K,
Hagenbeek FA,
Hottenga JJ,
Pool R,
Ikram MA,
van Meurs J,
Haller T,
Milaneschi Y,
Kähönen M,
Mishra PP,
Joshi PK,
Macdonald-Dunlop E,
Mangino M,
Zierer J,
Acar IE,
Hoyng CB,
Lechanteur YTE,
Franke L,
Kurilshikov A,
Zhernakova A,
Beekman M,
van den Akker EB,
Kolcic I,
Polasek O,
Rudan I,
Gieger C,
Waldenberger M,
Asselbergs FW,
Hayward C,
Fu J,
den Hollander AI,
Menni C,
Spector TD,
Wilson JF,
Lehtimäki T,
Raitakari OT,
Penninx BWJH,
Esko T,
Walters RG,
Jukema JW,
Sattar N,
Ghanbari M,
Willems van Dijk K,
Karpe F,
McCarthy MI,
Laakso M,
Järvelin MR,
Timpson NJ,
Perola M,
Kooner JS,
Chambers JC,
van Duijn C,
Slagboom PE,
Boomsma DI,
Danesh J,
Ala-Korpela M,
Butterworth AS,
Kettunen J
China Kadoorie Biobank Collaborative Group · Estonian Biobank Research Team and 1 more consortia
Nature · 2024 · PMID 38448586 · open access
12 pages+
Exome-wide association study of plasma lipids in >300,000 individuals
Liu DJ,
Peloso GM,
Yu H,
Butterworth AS,
Wang X,
Mahajan A,
Saleheen D,
Emdin C,
Alam D,
Alves AC,
Amouyel P,
Di Angelantonio E
and 215 more — show all
Arveiler D,
Assimes TL,
Auer PL,
Baber U,
Ballantyne CM,
Bang LE,
Benn M,
Bis JC,
Boehnke M,
Boerwinkle E,
Bork-Jensen J,
Bottinger EP,
Brandslund I,
Brown M,
Busonero F,
Caulfield MJ,
Chambers JC,
Chasman DI,
Chen YE,
Chen YI,
Chowdhury R,
Christensen C,
Chu AY,
Connell JM,
Cucca F,
Cupples LA,
Damrauer SM,
Davies G,
Deary IJ,
Dedoussis G,
Denny JC,
Dominiczak A,
Dubé MP,
Ebeling T,
Eiriksdottir G,
Esko T,
Farmaki AE,
Feitosa MF,
Ferrario M,
Ferrieres J,
Ford I,
Fornage M,
Franks PW,
Frayling TM,
Frikke-Schmidt R,
Fritsche LG,
Frossard P,
Fuster V,
Ganesh SK,
Gao W,
Garcia ME,
Gieger C,
Giulianini F,
Goodarzi MO,
Grallert H,
Grarup N,
Groop L,
Grove ML,
Gudnason V,
Hansen T,
Harris TB,
Hayward C,
Hirschhorn JN,
Holmen OL,
Huffman J,
Huo Y,
Hveem K,
Jabeen S,
Jackson AU,
Jakobsdottir J,
Jarvelin MR,
Jensen GB,
Jørgensen ME,
Jukema JW,
Justesen JM,
Kamstrup PR,
Kanoni S,
Karpe F,
Kee F,
Khera AV,
Klarin D,
Koistinen HA,
Kooner JS,
Kooperberg C,
Kuulasmaa K,
Kuusisto J,
Laakso M,
Lakka T,
Langenberg C,
Langsted A,
Launer LJ,
Lauritzen T,
Liewald DCM,
Lin LA,
Linneberg A,
Loos RJF,
Lu Y,
Lu X,
Mägi R,
Malarstig A,
Manichaikul A,
Manning AK,
Mäntyselkä P,
Marouli E,
Masca NGD,
Maschio A,
Meigs JB,
Melander O,
Metspalu A,
Morris AP,
Morrison AC,
Mulas A,
Müller-Nurasyid M,
Munroe PB,
Neville MJ,
Nielsen JB,
Nielsen SF,
Nordestgaard BG,
Ordovas JM,
Mehran R,
O'Donnell CJ,
Orho-Melander M,
Molony CM,
Muntendam P,
Padmanabhan S,
Palmer CNA,
Pasko D,
Patel AP,
Pedersen O,
Perola M,
Peters A,
Pisinger C,
Pistis G,
Polasek O,
Poulter N,
Psaty BM,
Rader DJ,
Rasheed A,
Rauramaa R,
Reilly DF,
Reiner AP,
Renström F,
Rich SS,
Ridker PM,
Rioux JD,
Robertson NR,
Roden DM,
Rotter JI,
Rudan I,
Salomaa V,
Samani NJ,
Sanna S,
Sattar N,
Schmidt EM,
Scott RA,
Sever P,
Sevilla RS,
Shaffer CM,
Sim X,
Sivapalaratnam S,
Small KS,
Smith AV,
Smith BH,
Somayajula S,
Southam L,
Spector TD,
Speliotes EK,
Starr JM,
Stirrups KE,
Stitziel N,
Strauch K,
Stringham HM,
Surendran P,
Tada H,
Tall AR,
Tang H,
Tardif JC,
Taylor KD,
Trompet S,
Tsao PS,
Tuomilehto J,
Tybjaerg-Hansen A,
van Zuydam NR,
Varbo A,
Varga TV,
Virtamo J,
Waldenberger M,
Wang N,
Wareham NJ,
Warren HR,
Weeke PE,
Weinstock J,
Wessel J,
Wilson JG,
Wilson PWF,
Xu M,
Yaghootkar H,
Young R,
Zeggini E,
Zhang H,
Zheng NS,
Zhang W,
Zhang Y,
Zhou W,
Zhou Y,
Zoledziewska M,
Howson JMM,
Danesh J,
McCarthy MI,
Cowan CA,
Abecasis G,
Deloukas P,
Musunuru K,
Willer CJ,
Kathiresan S
Charge Diabetes Working Group · EPIC-InterAct Consortium and 3 more consortia
Nature genetics · 2017 · PMID 29083408 · open access
11 pages
Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity
Mahajan A,
Rodan AR,
Le TH,
Gaulton KJ,
Haessler J,
Stilp AM,
Kamatani Y,
Zhu G,
Sofer T,
Puri S,
Schellinger JN,
Chu PL
and 26 more — show all
Cechova S,
van Zuydam N,
Arnlov J,
Flessner MF,
Giedraitis V,
Heath AC,
Kubo M,
Larsson A,
Lindgren CM,
Madden PAF,
Montgomery GW,
Papanicolaou GJ,
Reiner AP,
Sundström J,
Thornton TA,
Lind L,
Ingelsson E,
Cai J,
Martin NG,
Kooperberg C,
Matsuda K,
Whitfield JB,
Okada Y,
Laurie CC,
Morris AP,
Franceschini N
SUMMIT Consortium · BioBank Japan Project
American journal of human genetics · 2016 · PMID 27588450 · open access
8 pages
Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen
Salem RM,
Todd JN,
Sandholm N,
Cole JB,
Chen WM,
Andrews D,
Pezzolesi MG,
McKeigue PM,
Hiraki LT,
Qiu C,
Nair V,
Di Liao C
and 76 more — show all
Cao JJ,
Valo E,
Onengut-Gumuscu S,
Smiles AM,
McGurnaghan SJ,
Haukka JK,
Harjutsalo V,
Brennan EP,
van Zuydam N,
Ahlqvist E,
Doyle R,
Ahluwalia TS,
Lajer M,
Hughes MF,
Park J,
Skupien J,
Spiliopoulou A,
Liu A,
Menon R,
Boustany-Kari CM,
Kang HM,
Nelson RG,
Klein R,
Klein BE,
Lee KE,
Gao X,
Mauer M,
Maestroni S,
Caramori ML,
de Boer IH,
Miller RG,
Guo J,
Boright AP,
Tregouet D,
Gyorgy B,
Snell-Bergeon JK,
Maahs DM,
Bull SB,
Canty AJ,
Palmer CNA,
Stechemesser L,
Paulweber B,
Weitgasser R,
Sokolovska J,
Rovīte V,
Pīrāgs V,
Prakapiene E,
Radzeviciene L,
Verkauskiene R,
Panduru NM,
Groop LC,
McCarthy MI,
Gu HF,
Möllsten A,
Falhammar H,
Brismar K,
Martin F,
Rossing P,
Costacou T,
Zerbini G,
Marre M,
Hadjadj S,
McKnight AJ,
Forsblom C,
McKay G,
Godson C,
Maxwell AP,
Kretzler M,
Susztak K,
Colhoun HM,
Krolewski A,
Paterson AD,
Groop PH,
Rich SS,
Hirschhorn JN,
Florez JC
SUMMIT Consortium, DCCT/EDIC Research Group, GENIE Consortium
Journal of the American Society of Nephrology : JASN · 2019 · PMID 31537649
5 pages
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies
Traylor M,
Farrall M,
Holliday EG,
Sudlow C,
Hopewell JC,
Cheng YC,
Fornage M,
Ikram MA,
Malik R,
Bevan S,
Thorsteinsdottir U,
Nalls MA
and 70 more — show all
Longstreth W,
Wiggins KL,
Yadav S,
Parati EA,
Destefano AL,
Worrall BB,
Kittner SJ,
Khan MS,
Reiner AP,
Helgadottir A,
Achterberg S,
Fernandez-Cadenas I,
Abboud S,
Schmidt R,
Walters M,
Chen WM,
Ringelstein EB,
O'Donnell M,
Ho WK,
Pera J,
Lemmens R,
Norrving B,
Higgins P,
Benn M,
Sale M,
Kuhlenbäumer G,
Doney AS,
Vicente AM,
Delavaran H,
Algra A,
Davies G,
Oliveira SA,
Palmer CN,
Deary I,
Schmidt H,
Pandolfo M,
Montaner J,
Carty C,
de Bakker PI,
Kostulas K,
Ferro JM,
van Zuydam NR,
Valdimarsson E,
Nordestgaard BG,
Lindgren A,
Thijs V,
Slowik A,
Saleheen D,
Paré G,
Berger K,
Thorleifsson G,
Hofman A,
Mosley TH,
Mitchell BD,
Furie K,
Clarke R,
Levi C,
Seshadri S,
Gschwendtner A,
Boncoraglio GB,
Sharma P,
Bis JC,
Gretarsdottir S,
Psaty BM,
Rothwell PM,
Rosand J,
Meschia JF,
Stefansson K,
Dichgans M,
Markus HS
Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) · International Stroke Genetics Consortium
The Lancet. Neurology · 2012 · PMID 23041239 · open access
4 pages
Genome-Wide Association Study of Peripheral Artery Disease
van Zuydam NR,
Stiby A,
Abdalla M,
Austin E,
Dahlström EH,
Dahlström EH,
McLachlan S,
Vlachopoulou E,
Ahlqvist E,
Di Liao C,
Sandholm N,
Forsblom C
and 21 more — show all
Mahajan A,
Robertson NR,
Rayner NW,
Lindholm E,
Sinisalo J,
Perola M,
Kallio M,
Weiss E,
Price J,
Paterson A,
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GoLEAD Consortium, SUMMIT Consortium†
Circulation. Genomic and precision medicine · 2021 · PMID 34601942 · open access
3 pages
Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease
Sandholm N,
Cole JB,
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Sheng X,
Liu H,
Ahlqvist E,
van Zuydam N,
Dahlström EH,
Fermin D,
Smyth LJ,
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Forsblom C
and 19 more — show all
Valo E,
Harjutsalo V,
Brennan EP,
McKay GJ,
Andrews D,
Doyle R,
Looker HC,
Nelson RG,
Palmer C,
McKnight AJ,
Godson C,
Maxwell AP,
Groop L,
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Susztak K,
Hirschhorn JN,
Florez JC,
Groop PH
GENIE Consortium
Diabetologia · 2022 · PMID 35763030 · open access
2 pages
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
Scott RA,
Scott LJ,
Mägi R,
Marullo L,
Gaulton KJ,
Kaakinen M,
Pervjakova N,
Pers TH,
Johnson AD,
Eicher JD,
Jackson AU,
Ferreira T
and 163 more — show all
Lee Y,
Ma C,
Steinthorsdottir V,
Thorleifsson G,
Qi L,
Van Zuydam NR,
Mahajan A,
Chen H,
Almgren P,
Voight BF,
Grallert H,
Müller-Nurasyid M,
Ried JS,
Rayner NW,
Robertson N,
Karssen LC,
van Leeuwen EM,
Willems SM,
Fuchsberger C,
Kwan P,
Teslovich TM,
Chanda P,
Li M,
Lu Y,
Dina C,
Thuillier D,
Yengo L,
Jiang L,
Sparso T,
Kestler HA,
Chheda H,
Eisele L,
Gustafsson S,
Frånberg M,
Strawbridge RJ,
Benediktsson R,
Hreidarsson AB,
Kong A,
Sigurðsson G,
Kerrison ND,
Luan J,
Liang L,
Meitinger T,
Roden M,
Thorand B,
Esko T,
Mihailov E,
Fox C,
Liu CT,
Rybin D,
Isomaa B,
Lyssenko V,
Tuomi T,
Couper DJ,
Pankow JS,
Grarup N,
Have CT,
Jørgensen ME,
Jørgensen T,
Linneberg A,
Cornelis MC,
van Dam RM,
Hunter DJ,
Kraft P,
Sun Q,
Edkins S,
Owen KR,
Perry JRB,
Wood AR,
Zeggini E,
Tajes-Fernandes J,
Abecasis GR,
Bonnycastle LL,
Chines PS,
Stringham HM,
Koistinen HA,
Kinnunen L,
Sennblad B,
Mühleisen TW,
Nöthen MM,
Pechlivanis S,
Baldassarre D,
Gertow K,
Humphries SE,
Tremoli E,
Klopp N,
Meyer J,
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Eriksson JG,
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Lobbens S,
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Leander K,
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Bottinger EP,
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Ruderfer D,
Blüher M,
Kovacs P,
Tonjes A,
Maruthur NM,
Scapoli C,
Erbel R,
Jöckel KH,
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Hamsten A,
Stumvoll M,
Deloukas P,
Donnelly PJ,
Frayling TM,
Hattersley AT,
Ripatti S,
Salomaa V,
Pedersen NL,
Boehm BO,
Bergman RN,
Collins FS,
Mohlke KL,
Tuomilehto J,
Hansen T,
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Barroso I,
Lannfelt L,
Ingelsson E,
Lind L,
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Palli D,
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Groop LC,
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DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium
Diabetes · 2017 · PMID 28566273
1 page
A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes
van Zuydam NR,
Ahlqvist E,
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Valo E
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Forsblom C,
Harjutsalo V,
Perna A,
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Marcovecchio ML,
Igo RP Jr,
Salem RM,
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Jiang G,
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So WY,
Chan JCN,
Ang SF,
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Wang L,
Clara TSH,
McKnight AJ,
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Marre M,
Gyorgy B,
Hadjadj S,
Hiraki LT,
Ahluwalia TS,
Almgren P,
Schulz CA,
Orho-Melander M,
Linneberg A,
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Witte DR,
Grarup N,
Brandslund I,
Melander O,
Paterson AD,
Tregouet D,
Maxwell AP,
Lim SC,
Ma RCW,
Tai ES,
Maeda S,
Lyssenko V,
Tuomi T,
Krolewski AS,
Rich SS,
Hirschhorn JN,
Florez JC,
Dunger D,
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Hansen T,
Rossing P,
Remuzzi G,
Brosnan MJ,
Palmer CNA,
Groop PH,
Colhoun HM,
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Finnish Diabetic Nephropathy Study (FinnDiane) · Hong Kong Diabetes Registry Theme-based Research Scheme Project Group and 4 more consortia
Diabetes · 2018 · PMID 29703844
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
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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
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