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16 matches for
Thiering E.
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+
Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis
Waage J,
Standl M,
Curtin JA,
Jessen LE,
Thorsen J,
Tian C,
Schoettler N,
Flores C,
Abdellaoui A,
Ahluwalia TS,
Alves AC,
Amaral AFS
and 76 more — show all
Antó JM,
Arnold A,
Barreto-Luis A,
Baurecht H,
van Beijsterveldt CEM,
Bleecker ER,
Bonàs-Guarch S,
Boomsma DI,
Brix S,
Bunyavanich S,
Burchard EG,
Chen Z,
Curjuric I,
Custovic A,
den Dekker HT,
Dharmage SC,
Dmitrieva J,
Duijts L,
Ege MJ,
Gauderman WJ,
Georges M,
Gieger C,
Gilliland F,
Granell R,
Gui H,
Hansen T,
Heinrich J,
Henderson J,
Hernandez-Pacheco N,
Holt P,
Imboden M,
Jaddoe VWV,
Jarvelin MR,
Jarvis DL,
Jensen KK,
Jónsdóttir I,
Kabesch M,
Kaprio J,
Kumar A,
Lee YA,
Levin AM,
Li X,
Lorenzo-Diaz F,
Melén E,
Mercader JM,
Meyers DA,
Myers R,
Nicolae DL,
Nohr EA,
Palviainen T,
Paternoster L,
Pennell CE,
Pershagen G,
Pino-Yanes M,
Probst-Hensch NM,
Rüschendorf F,
Simpson A,
Stefansson K,
Sunyer J,
Sveinbjornsson G,
Thiering E,
Thompson PJ,
Torrent M,
Torrents D,
Tung JY,
Wang CA,
Weidinger S,
Weiss S,
Willemsen G,
Williams LK,
Ober C,
Hinds DA,
Ferreira MA,
Bisgaard H,
Strachan DP,
Bønnelykke K
23andMe Research Team · AAGC collaborators
Nature genetics · 2018 · PMID 30013184
12 pages+
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders
Ligthart S,
Vaez A,
Võsa U,
Stathopoulou MG,
de Vries PS,
Prins BP,
Van der Most PJ,
Tanaka T,
Naderi E,
Rose LM,
Wu Y,
Karlsson R
and 274 more — show all
Barbalic M,
Lin H,
Pool R,
Zhu G,
Macé A,
Sidore C,
Trompet S,
Mangino M,
Sabater-Lleal M,
Kemp JP,
Abbasi A,
Kacprowski T,
Verweij N,
Smith AV,
Huang T,
Marzi C,
Feitosa MF,
Lohman KK,
Kleber ME,
Milaneschi Y,
Mueller C,
Huq M,
Vlachopoulou E,
Lyytikäinen LP,
Oldmeadow C,
Deelen J,
Perola M,
Zhao JH,
Feenstra B,
Amini M,
Lahti J,
Schraut KE,
Fornage M,
Suktitipat B,
Chen WM,
Li X,
Nutile T,
Malerba G,
Luan J,
Bak T,
Schork N,
Del Greco M F,
Thiering E,
Mahajan A,
Marioni RE,
Mihailov E,
Eriksson J,
Ozel AB,
Zhang W,
Nethander M,
Cheng YC,
Aslibekyan S,
Ang W,
Gandin I,
Yengo L,
Portas L,
Kooperberg C,
Hofer E,
Rajan KB,
Schurmann C,
den Hollander W,
Ahluwalia TS,
Zhao J,
Draisma HHM,
Ford I,
Timpson N,
Teumer A,
Huang H,
Wahl S,
Liu Y,
Huang J,
Uh HW,
Geller F,
Joshi PK,
Yanek LR,
Trabetti E,
Lehne B,
Vozzi D,
Verbanck M,
Biino G,
Saba Y,
Meulenbelt I,
O'Connell JR,
Laakso M,
Giulianini F,
Magnusson PKE,
Ballantyne CM,
Hottenga JJ,
Montgomery GW,
Rivadineira F,
Rueedi R,
Steri M,
Herzig KH,
Stott DJ,
Menni C,
Frånberg M,
St Pourcain B,
Felix SB,
Pers TH,
Bakker SJL,
Kraft P,
Peters A,
Vaidya D,
Delgado G,
Smit JH,
Großmann V,
Sinisalo J,
Seppälä I,
Williams SR,
Holliday EG,
Moed M,
Langenberg C,
Räikkönen K,
Ding J,
Campbell H,
Sale MM,
Chen YI,
James AL,
Ruggiero D,
Soranzo N,
Hartman CA,
Smith EN,
Berenson GS,
Fuchsberger C,
Hernandez D,
Tiesler CMT,
Giedraitis V,
Liewald D,
Fischer K,
Mellström D,
Larsson A,
Wang Y,
Scott WR,
Lorentzon M,
Beilby J,
Ryan KA,
Pennell CE,
Vuckovic D,
Balkau B,
Concas MP,
Schmidt R,
Mendes de Leon CF,
Bottinger EP,
Kloppenburg M,
Paternoster L,
Boehnke M,
Musk AW,
Willemsen G,
Evans DM,
Madden PAF,
Kähönen M,
Kutalik Z,
Zoledziewska M,
Karhunen V,
Kritchevsky SB,
Sattar N,
Lachance G,
Clarke R,
Harris TB,
Raitakari OT,
Attia JR,
van Heemst D,
Kajantie E,
Sorice R,
Gambaro G,
Scott RA,
Hicks AA,
Ferrucci L,
Standl M,
Lindgren CM,
Starr JM,
Karlsson M,
Lind L,
Li JZ,
Chambers JC,
Mori TA,
de Geus EJCN,
Heath AC,
Martin NG,
Auvinen J,
Buckley BM,
de Craen AJM,
Waldenberger M,
Strauch K,
Meitinger T,
Scott RJ,
McEvoy M,
Beekman M,
Bombieri C,
Ridker PM,
Mohlke KL,
Pedersen NL,
Morrison AC,
Boomsma DI,
Whitfield JB,
Strachan DP,
Hofman A,
Vollenweider P,
Cucca F,
Jarvelin MR,
Jukema JW,
Spector TD,
Hamsten A,
Zeller T,
Uitterlinden AG,
Nauck M,
Gudnason V,
Qi L,
Grallert H,
Borecki IB,
Rotter JI,
März W,
Wild PS,
Lokki ML,
Boyle M,
Salomaa V,
Melbye M,
Eriksson JG,
Wilson JF,
Penninx BWJH,
Becker DM,
Worrall BB,
Gibson G,
Krauss RM,
Ciullo M,
Zaza G,
Wareham NJ,
Oldehinkel AJ,
Palmer LJ,
Murray SS,
Pramstaller PP,
Bandinelli S,
Heinrich J,
Ingelsson E,
Deary IJ,
Mägi R,
Vandenput L,
van der Harst P,
Desch KC,
Kooner JS,
Ohlsson C,
Hayward C,
Lehtimäki T,
Shuldiner AR,
Arnett DK,
Beilin LJ,
Robino A,
Froguel P,
Pirastu M,
Jess T,
Koenig W,
Loos RJF,
Evans DA,
Schmidt H,
Smith GD,
Slagboom PE,
Eiriksdottir G,
Morris AP,
Psaty BM,
Tracy RP,
Nolte IM,
Boerwinkle E,
Visvikis-Siest S,
Reiner AP,
Gross M,
Bis JC,
Franke L,
Franco OH,
Benjamin EJ,
Chasman DI,
Dupuis J,
Snieder H,
Dehghan A,
Alizadeh BZ
LifeLines Cohort Study · CHARGE Inflammation Working Group
American journal of human genetics · 2018 · PMID 30388399
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+
European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation
Budu-Aggrey A,
Kilanowski A,
Sobczyk MK,
Shringarpure SS,
Mitchell R,
Reis K,
Reigo A,
Mägi R,
Nelis M,
Tanaka N,
Brumpton BM,
Thomas LF
and 120 more — show all
Sole-Navais P,
Flatley C,
Espuela-Ortiz A,
Herrera-Luis E,
Lominchar JVT,
Bork-Jensen J,
Marenholz I,
Arnau-Soler A,
Jeong A,
Fawcett KA,
Baurecht H,
Rodriguez E,
Alves AC,
Kumar A,
Sleiman PM,
Chang X,
Medina-Gomez C,
Hu C,
Xu CJ,
Qi C,
El-Heis S,
Titcombe P,
Antoun E,
Fadista J,
Wang CA,
Thiering E,
Wu B,
Kress S,
Kothalawala DM,
Kadalayil L,
Duan J,
Zhang H,
Hadebe S,
Hoffmann T,
Jorgenson E,
Choquet H,
Risch N,
Njølstad P,
Andreassen OA,
Johansson S,
Almqvist C,
Gong T,
Ullemar V,
Karlsson R,
Magnusson PKE,
Szwajda A,
Burchard EG,
Thyssen JP,
Hansen T,
Kårhus LL,
Dantoft TM,
Jeanrenaud ACSN,
Ghauri A,
Arnold A,
Homuth G,
Lau S,
Nöthen MM,
Hübner N,
Imboden M,
Visconti A,
Falchi M,
Bataille V,
Hysi P,
Ballardini N,
Boomsma DI,
Hottenga JJ,
Müller-Nurasyid M,
Ahluwalia TS,
Stokholm J,
Chawes B,
Schoos AM,
Esplugues A,
Bustamante M,
Raby B,
Arshad S,
German C,
Esko T,
Milani LA,
Metspalu A,
Terao C,
Abuabara K,
Løset M,
Hveem K,
Jacobsson B,
Pino-Yanes M,
Strachan DP,
Grarup N,
Linneberg A,
Lee YA,
Probst-Hensch N,
Weidinger S,
Jarvelin MR,
Melén E,
Hakonarson H,
Irvine AD,
Jarvis D,
Nijsten T,
Duijts L,
Vonk JM,
Koppelmann GH,
Godfrey KM,
Barton SJ,
Feenstra B,
Pennell CE,
Sly PD,
Holt PG,
Williams LK,
Bisgaard H,
Bønnelykke K,
Curtin J,
Simpson A,
Murray C,
Schikowski T,
Bunyavanich S,
Weiss ST,
Holloway JW,
Min JL,
Brown SJ,
Standl M,
Paternoster L
23andMe Research Team · Estonian Biobank Research Team
Nature communications · 2023 · PMID 37794016 · open access
12 pages+
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Speliotes EK,
Willer CJ,
Berndt SI,
Monda KL,
Thorleifsson G,
Jackson AU,
Lango Allen H,
Lindgren CM,
Luan J,
Mägi R,
Randall JC,
Vedantam S
and 366 more — show all
Winkler TW,
Qi L,
Workalemahu T,
Heid IM,
Steinthorsdottir V,
Stringham HM,
Weedon MN,
Wheeler E,
Wood AR,
Ferreira T,
Weyant RJ,
Segrè AV,
Estrada K,
Liang L,
Nemesh J,
Park JH,
Gustafsson S,
Kilpeläinen TO,
Yang J,
Bouatia-Naji N,
Esko T,
Feitosa MF,
Kutalik Z,
Mangino M,
Raychaudhuri S,
Scherag A,
Smith AV,
Welch R,
Zhao JH,
Aben KK,
Absher DM,
Amin N,
Dixon AL,
Fisher E,
Glazer NL,
Goddard ME,
Heard-Costa NL,
Hoesel V,
Hottenga JJ,
Johansson A,
Johnson T,
Ketkar S,
Lamina C,
Li S,
Moffatt MF,
Myers RH,
Narisu N,
Perry JR,
Peters MJ,
Preuss M,
Ripatti S,
Rivadeneira F,
Sandholt C,
Scott LJ,
Timpson NJ,
Tyrer JP,
van Wingerden S,
Watanabe RM,
White CC,
Wiklund F,
Barlassina C,
Chasman DI,
Cooper MN,
Jansson JO,
Lawrence RW,
Pellikka N,
Prokopenko I,
Shi J,
Thiering E,
Alavere H,
Alibrandi MT,
Almgren P,
Arnold AM,
Aspelund T,
Atwood LD,
Balkau B,
Balmforth AJ,
Bennett AJ,
Ben-Shlomo Y,
Bergman RN,
Bergmann S,
Biebermann H,
Blakemore AI,
Boes T,
Bonnycastle LL,
Bornstein SR,
Brown MJ,
Buchanan TA,
Busonero F,
Campbell H,
Cappuccio FP,
Cavalcanti-Proença C,
Chen YD,
Chen CM,
Chines PS,
Clarke R,
Coin L,
Connell J,
Day IN,
den Heijer M,
Duan J,
Ebrahim S,
Elliott P,
Elliott P,
Elosua R,
Eiriksdottir G,
Erdos MR,
Eriksson JG,
Facheris MF,
Felix SB,
Fischer-Posovszky P,
Folsom AR,
Friedrich N,
Freimer NB,
Fu M,
Gaget S,
Gejman PV,
Geus EJ,
Gieger C,
Gjesing AP,
Goel A,
Goyette P,
Grallert H,
Grässler J,
Greenawalt DM,
Groves CJ,
Gudnason V,
Guiducci C,
Hartikainen AL,
Hassanali N,
Hall AS,
Havulinna AS,
Hayward C,
Heath AC,
Hengstenberg C,
Hicks AA,
Hinney A,
Hofman A,
Homuth G,
Hui J,
Igl W,
Iribarren C,
Isomaa B,
Jacobs KB,
Jarick I,
Jewell E,
John U,
Jørgensen T,
Jousilahti P,
Jula A,
Kaakinen M,
Kajantie E,
Kaplan LM,
Kathiresan S,
Kettunen J,
Kinnunen L,
Knowles JW,
Kolcic I,
König IR,
Koskinen S,
Kovacs P,
Kuusisto J,
Kraft P,
Kvaløy K,
Laitinen J,
Lantieri O,
Lanzani C,
Launer LJ,
Lecoeur C,
Lehtimäki T,
Lettre G,
Liu J,
Lokki ML,
Lorentzon M,
Luben RN,
Ludwig B,
Manunta P,
Marek D,
Marre M,
Martin NG,
McArdle WL,
McCarthy A,
McKnight B,
Meitinger T,
Melander O,
Meyre D,
Midthjell K,
Montgomery GW,
Morken MA,
Morris AP,
Mulic R,
Ngwa JS,
Nelis M,
Neville MJ,
Nyholt DR,
O'Donnell CJ,
O'Rahilly S,
Ong KK,
Oostra B,
Paré G,
Parker AN,
Perola M,
Pichler I,
Pietiläinen KH,
Platou CG,
Polasek O,
Pouta A,
Rafelt S,
Raitakari O,
Rayner NW,
Ridderstråle M,
Rief W,
Ruokonen A,
Robertson NR,
Rzehak P,
Salomaa V,
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CHARGE Inflammation Working Group
Human molecular genetics · 2021 · PMID 33517400 · 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.