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141 matches for
Lin M,
showing the first 20.
Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances
Fatemifar G,
Hoggart CJ,
Paternoster L,
Kemp JP,
Prokopenko I,
Horikoshi M,
Wright VJ,
Tobias JH,
Richmond S,
Zhurov AI,
Toma AM,
Pouta A
and 14 more — show all
Taanila A,
Sipila K,
Lähdesmäki R,
Pillas D,
Geller F,
Feenstra B,
Melbye M,
Nohr EA,
Ring SM,
St Pourcain B,
Timpson NJ,
Davey Smith G,
Jarvelin MR,
Evans DM
Human molecular genetics · 2013 · PMID 23704328 · open access
8 pages
Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index
Felix JF,
Bradfield JP,
Monnereau C,
van der Valk RJ,
Stergiakouli E,
Chesi A,
Gaillard R,
Feenstra B,
Thiering E,
Kreiner-Møller E,
Mahajan A,
Pitkänen N
and 99 more — show all
Joro R,
Cavadino A,
Huikari V,
Franks S,
Groen-Blokhuis MM,
Cousminer DL,
Marsh JA,
Lehtimäki T,
Curtin JA,
Vioque J,
Ahluwalia TS,
Myhre R,
Price TS,
Vilor-Tejedor N,
Yengo L,
Grarup N,
Ntalla I,
Ang W,
Atalay M,
Bisgaard H,
Blakemore AI,
Bonnefond A,
Carstensen L,
Eriksson J,
Flexeder C,
Franke L,
Geller F,
Geserick M,
Hartikainen AL,
Haworth CM,
Hirschhorn JN,
Hofman A,
Holm JC,
Horikoshi M,
Hottenga JJ,
Huang J,
Kadarmideen HN,
Kähönen M,
Kiess W,
Lakka HM,
Lakka TA,
Lewin AM,
Liang L,
Lyytikäinen LP,
Ma B,
Magnus P,
McCormack SE,
McMahon G,
Mentch FD,
Middeldorp CM,
Murray CS,
Pahkala K,
Pers TH,
Pfäffle R,
Postma DS,
Power C,
Simpson A,
Sengpiel V,
Tiesler CM,
Torrent M,
Uitterlinden AG,
van Meurs JB,
Vinding R,
Waage J,
Wardle J,
Zeggini E,
Zemel BS,
Dedoussis GV,
Pedersen O,
Froguel P,
Sunyer J,
Plomin R,
Jacobsson B,
Hansen T,
Gonzalez JR,
Custovic A,
Raitakari OT,
Pennell CE,
Widén E,
Boomsma DI,
Koppelman GH,
Sebert S,
Järvelin MR,
Hyppönen E,
McCarthy MI,
Lindi V,
Harri N,
Körner A,
Bønnelykke K,
Heinrich J,
Melbye M,
Rivadeneira F,
Hakonarson H,
Ring SM,
Smith GD,
Sørensen TI,
Timpson NJ,
Grant SF,
Jaddoe VW
Bone Mineral Density in Childhood Study (BMDCS) · Early Genetics and Lifecourse Epidemiology (EAGLE) consortium and 2 more consortia
Human molecular genetics · 2016 · PMID 26604143
8 pages
Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation
Soler Artigas M,
Wain LV,
Miller S,
Kheirallah AK,
Huffman JE,
Ntalla I,
Shrine N,
Obeidat M,
Trochet H,
McArdle WL,
Alves AC,
Hui J
and 78 more — show all
Zhao JH,
Joshi PK,
Teumer A,
Albrecht E,
Imboden M,
Rawal R,
Lopez LM,
Marten J,
Enroth S,
Surakka I,
Polasek O,
Lyytikäinen LP,
Granell R,
Hysi PG,
Flexeder C,
Mahajan A,
Beilby J,
Bossé Y,
Brandsma CA,
Campbell H,
Gieger C,
Gläser S,
González JR,
Grallert H,
Hammond CJ,
Harris SE,
Hartikainen AL,
Heliövaara M,
Henderson J,
Hocking L,
Horikoshi M,
Hutri-Kähönen N,
Ingelsson E,
Johansson Å,
Kemp JP,
Kolcic I,
Kumar A,
Lind L,
Melén E,
Musk AW,
Navarro P,
Nickle DC,
Padmanabhan S,
Raitakari OT,
Ried JS,
Ripatti S,
Schulz H,
Scott RA,
Sin DD,
Starr JM,
Viñuela A,
Völzke H,
Wild SH,
Wright AF,
Zemunik T,
Jarvis DL,
Spector TD,
Evans DM,
Lehtimäki T,
Vitart V,
Kähönen M,
Gyllensten U,
Rudan I,
Deary IJ,
Karrasch S,
Probst-Hensch NM,
Heinrich J,
Stubbe B,
Wilson JF,
Wareham NJ,
James AL,
Morris AP,
Jarvelin MR,
Hayward C,
Sayers I,
Strachan DP,
Hall IP,
Tobin MD
UK BiLEVE
Nature communications · 2015 · PMID 26635082 · open access
8 pages
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
Rahmioglu N,
Mortlock S,
Ghiasi M,
Møller PL,
Stefansdottir L,
Galarneau G,
Turman C,
Danning R,
Law MH,
Sapkota Y,
Christofidou P,
Skarp S
and 121 more — show all
Giri A,
Banasik K,
Krassowski M,
Lepamets M,
Marciniak B,
Nõukas M,
Perro D,
Sliz E,
Sobalska-Kwapis M,
Thorleifsson G,
Topbas-Selcuki NF,
Vitonis A,
Westergaard D,
Arnadottir R,
Burgdorf KS,
Campbell A,
Cheuk CSK,
Clementi C,
Cook J,
De Vivo I,
DiVasta A,
Dorien O,
Donoghue JF,
Edwards T,
Fontanillas P,
Fung JN,
Geirsson RT,
Girling JE,
Harkki P,
Harris HR,
Healey M,
Heikinheimo O,
Holdsworth-Carson S,
Hostettler IC,
Houlden H,
Houshdaran S,
Irwin JC,
Jarvelin MR,
Kamatani Y,
Kennedy SH,
Kepka E,
Kettunen J,
Kubo M,
Kulig B,
Kurra V,
Laivuori H,
Laufer MR,
Lindgren CM,
MacGregor S,
Mangino M,
Martin NG,
Matalliotaki C,
Matalliotakis M,
Murray AD,
Ndungu A,
Nezhat C,
Olsen CM,
Opoku-Anane J,
Padmanabhan S,
Paranjpe M,
Peters M,
Polak G,
Porteous DJ,
Rabban J,
Rexrode KM,
Romanowicz H,
Saare M,
Saavalainen L,
Schork AJ,
Sen S,
Shafrir AL,
Siewierska-Górska A,
Słomka M,
Smith BH,
Smolarz B,
Szaflik T,
Szyłło K,
Takahashi A,
Terry KL,
Tomassetti C,
Treloar SA,
Vanhie A,
Vincent K,
Vo KC,
Werring DJ,
Zeggini E,
Zervou MI,
Adachi S,
Buring JE,
Ridker PM,
D'Hooghe T,
Goulielmos GN,
Hapangama DK,
Hayward C,
Horne AW,
Low SK,
Martikainen H,
Chasman DI,
Rogers PAW,
Saunders PT,
Sirota M,
Spector T,
Strapagiel D,
Tung JY,
Whiteman DC,
Giudice LC,
Velez-Edwards DR,
Uimari O,
Kraft P,
Salumets A,
Nyholt DR,
Mägi R,
Stefansson K,
Becker CM,
Yurttas-Beim P,
Steinthorsdottir V,
Nyegaard M,
Missmer SA,
Montgomery GW,
Morris AP,
Zondervan KT
DBDS Genomic Consortium · FinnGen Study and 3 more consortia
Nature genetics · 2023 · PMID 36914876
8 pages
A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium
Kraja AT,
Vaidya D,
Pankow JS,
Goodarzi MO,
Assimes TL,
Kullo IJ,
Sovio U,
Mathias RA,
Sun YV,
Franceschini N,
Absher D,
Li G
and 27 more — show all
Zhang Q,
Feitosa MF,
Glazer NL,
Haritunians T,
Hartikainen AL,
Knowles JW,
North KE,
Iribarren C,
Kral B,
Yanek L,
O'Reilly PF,
McCarthy MI,
Jaquish C,
Couper DJ,
Chakravarti A,
Psaty BM,
Becker LC,
Province MA,
Boerwinkle E,
Quertermous T,
Palotie L,
Jarvelin MR,
Becker DM,
Kardia SL,
Rotter JI,
Chen YD,
Borecki IB
Diabetes · 2011 · PMID 21386085 · open access
7 pages
Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization
Bønnelykke K,
Matheson MC,
Pers TH,
Granell R,
Strachan DP,
Alves AC,
Linneberg A,
Curtin JA,
Warrington NM,
Standl M,
Kerkhof M,
Jonsdottir I
and 58 more — show all
Bukvic BK,
Kaakinen M,
Sleimann P,
Thorleifsson G,
Thorsteinsdottir U,
Schramm K,
Baltic S,
Kreiner-Møller E,
Simpson A,
St Pourcain B,
Coin L,
Hui J,
Walters EH,
Tiesler CMT,
Duffy DL,
Jones G,
Ring SM,
McArdle WL,
Price L,
Robertson CF,
Pekkanen J,
Pekkanen J,
Tang CS,
Thiering E,
Montgomery GW,
Hartikainen AL,
Dharmage SC,
Husemoen LL,
Herder C,
Kemp JP,
Elliot P,
James A,
Waldenberger M,
Abramson MJ,
Fairfax BP,
Knight JC,
Knight JC,
Gupta R,
Thompson PJ,
Holt P,
Sly P,
Hirschhorn JN,
Blekic M,
Weidinger S,
Hakonarsson H,
Stefansson K,
Heinrich J,
Postma DS,
Custovic A,
Pennell CE,
Pennell CE,
Jarvelin MR,
Koppelman GH,
Timpson N,
Ferreira MA,
Ferreira MA,
Bisgaard H,
Henderson AJ
AAGC
Nature genetics · 2013 · PMID 23817571
7 pages
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Kanoni S,
Graham SE,
Wang Y,
Surakka I,
Ramdas S,
Zhu X,
Clarke SL,
Bhatti KF,
Vedantam S,
Winkler TW,
Locke AE,
Marouli E
and 527 more — show all
Zajac GJM,
Wu KH,
Ntalla I,
Hui Q,
Klarin D,
Hilliard AT,
Wang Z,
Xue C,
Thorleifsson G,
Helgadottir A,
Gudbjartsson DF,
Holm H,
Olafsson I,
Hwang MY,
Han S,
Akiyama M,
Sakaue S,
Terao C,
Kanai M,
Zhou W,
Brumpton BM,
Rasheed H,
Havulinna AS,
Veturi Y,
Pacheco JA,
Rosenthal EA,
Lingren T,
Feng Q,
Kullo IJ,
Narita A,
Takayama J,
Martin HC,
Hunt KA,
Trivedi B,
Haessler J,
Giulianini F,
Bradford Y,
Miller JE,
Campbell A,
Lin K,
Millwood IY,
Rasheed A,
Hindy G,
Faul JD,
Zhao W,
Weir DR,
Turman C,
Huang H,
Graff M,
Choudhury A,
Sengupta D,
Mahajan A,
Brown MR,
Zhang W,
Yu K,
Schmidt EM,
Pandit A,
Gustafsson S,
Yin X,
Luan J,
Zhao JH,
Matsuda F,
Jang HM,
Yoon K,
Medina-Gomez C,
Pitsillides A,
Hottenga JJ,
Wood AR,
Ji Y,
Gao Z,
Haworth S,
Yousri NA,
Mitchell RE,
Chai JF,
Aadahl M,
Bjerregaard AA,
Yao J,
Manichaikul A,
Hwu CM,
Hung YJ,
Warren HR,
Ramirez J,
Bork-Jensen J,
Kårhus LL,
Goel A,
Sabater-Lleal M,
Noordam R,
Mauro P,
Matteo F,
McDaid AF,
Marques-Vidal P,
Wielscher M,
Trompet S,
Sattar N,
Møllehave LT,
Munz M,
Zeng L,
Huang J,
Yang B,
Poveda A,
Kurbasic A,
Lamina C,
Forer L,
Scholz M,
Galesloot TE,
Bradfield JP,
Ruotsalainen SE,
Daw E,
Zmuda JM,
Mitchell JS,
Fuchsberger C,
Christensen H,
Brody JA,
Vazquez-Moreno M,
Feitosa MF,
Wojczynski MK,
Wang Z,
Preuss MH,
Mangino M,
Christofidou P,
Verweij N,
Benjamins JW,
Engmann J,
Tsao NL,
Verma A,
Slieker RC,
Lo KS,
Zilhao NR,
Le P,
Kleber ME,
Delgado GE,
Huo S,
Ikeda DD,
Iha H,
Yang J,
Liu J,
Demirkan A,
Leonard HL,
Marten J,
Frank M,
Schmidt B,
Smyth LJ,
Cañadas-Garre M,
Wang C,
Nakatochi M,
Wong A,
Hutri-Kähönen N,
Sim X,
Xia R,
Huerta-Chagoya A,
Fernandez-Lopez JC,
Lyssenko V,
Nongmaithem SS,
Bayyana S,
Stringham HM,
Irvin MR,
Oldmeadow C,
Kim HN,
Ryu S,
Timmers PRHJ,
Arbeeva L,
Dorajoo R,
Lange LA,
Prasad G,
Lorés-Motta L,
Pauper M,
Long J,
Li X,
Theusch E,
Takeuchi F,
Spracklen CN,
Loukola A,
Bollepalli S,
Warner SC,
Wang YX,
Wei WB,
Nutile T,
Ruggiero D,
Sung YJ,
Chen S,
Liu F,
Yang J,
Kentistou KA,
Banas B,
Nardone GG,
Meidtner K,
Bielak LF,
Smith JA,
Hebbar P,
Farmaki AE,
Hofer E,
Lin M,
Concas MP,
Vaccargiu S,
van der Most PJ,
Pitkänen N,
Cade BE,
van der Laan SW,
Chitrala KN,
Weiss S,
Bentley AR,
Doumatey AP,
Adeyemo AA,
Lee JY,
Petersen ERB,
Nielsen AA,
Choi HS,
Nethander M,
Freitag-Wolf S,
Southam L,
Rayner NW,
Wang CA,
Lin SY,
Wang JS,
Couture C,
Lyytikäinen LP,
Nikus K,
Cuellar-Partida G,
Vestergaard H,
Hidalgo B,
Giannakopoulou O,
Cai Q,
Obura MO,
van Setten J,
Li X,
Liang J,
Tang H,
Terzikhan N,
Shin JH,
Jackson RD,
Reiner AP,
Martin LW,
Chen Z,
Li L,
Kawaguchi T,
Thiery J,
Bis JC,
Launer LJ,
Li H,
Nalls MA,
Raitakari OT,
Ichihara S,
Wild SH,
Nelson CP,
Campbell H,
Jäger S,
Nabika T,
Al-Mulla F,
Niinikoski H,
Braund PS,
Kolcic I,
Kovacs P,
Giardoglou T,
Katsuya T,
de Kleijn D,
de Borst GJ,
Kim EK,
Adams HHH,
Ikram MA,
Zhu X,
Asselbergs FW,
Kraaijeveld AO,
Beulens JWJ,
Shu XO,
Rallidis LS,
Pedersen O,
Hansen T,
Mitchell P,
Hewitt AW,
Kähönen M,
Pérusse L,
Bouchard C,
Tönjes A,
Chen YI,
Pennell CE,
Mori TA,
Lieb W,
Franke A,
Ohlsson C,
Mellström D,
Cho YS,
Lee H,
Yuan JM,
Koh WP,
Rhee SY,
Woo JT,
Heid IM,
Stark KJ,
Zimmermann ME,
Völzke H,
Homuth G,
Evans MK,
Zonderman AB,
Polasek O,
Pasterkamp G,
Hoefer IE,
Redline S,
Pahkala K,
Oldehinkel AJ,
Snieder H,
Biino G,
Schmidt R,
Schmidt H,
Bandinelli S,
Dedoussis G,
Thanaraj TA,
Kardia SLR,
Peyser PA,
Kato N,
Schulze MB,
Girotto G,
Böger CA,
Jung B,
Joshi PK,
Bennett DA,
De Jager PL,
Lu X,
Mamakou V,
Brown M,
Caulfield MJ,
Munroe PB,
Guo X,
Ciullo M,
Jonas JB,
Samani NJ,
Kaprio J,
Pajukanta P,
Tusié-Luna T,
Aguilar-Salinas CA,
Adair LS,
Bechayda SA,
de Silva HJ,
Wickremasinghe AR,
Krauss RM,
Wu JY,
Zheng W,
Hollander AI,
Bharadwaj D,
Correa A,
Wilson JG,
Lind L,
Heng CK,
Nelson AE,
Golightly YM,
Wilson JF,
Penninx B,
Kim HL,
Attia J,
Scott RJ,
Rao DC,
Arnett DK,
Hunt SC,
Walker M,
Koistinen HA,
Chandak GR,
Mercader JM,
Costanzo MC,
Jang D,
Burtt NP,
Villalpando CG,
Orozco L,
Fornage M,
Tai E,
van Dam RM,
Lehtimäki T,
Chaturvedi N,
Yokota M,
Liu J,
Reilly DF,
McKnight AJ,
Kee F,
Jöckel KH,
McCarthy MI,
Palmer CNA,
Vitart V,
Hayward C,
Simonsick E,
van Duijn CM,
Jin ZB,
Qu J,
Hishigaki H,
Lin X,
März W,
Gudnason V,
Tardif JC,
Lettre G,
Hart LM',
Elders PJM,
Damrauer SM,
Kumari M,
Kivimaki M,
van der Harst P,
Spector TD,
Loos RJF,
Province MA,
Parra EJ,
Cruz M,
Psaty BM,
Brandslund I,
Pramstaller PP,
Rotimi CN,
Christensen K,
Ripatti S,
Widén E,
Hakonarson H,
Grant SFA,
Kiemeney LALM,
de Graaf J,
Loeffler M,
Kronenberg F,
Gu D,
Erdmann J,
Schunkert H,
Franks PW,
Linneberg A,
Jukema JW,
Khera AV,
Männikkö M,
Jarvelin MR,
Kutalik Z,
Francesco C,
Mook-Kanamori DO,
van Dijk KW,
Watkins H,
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Poulter N,
Chuang LM,
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Dantoft TM,
Karpe F,
Neville MJ,
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Cheng CY,
Wong TY,
Khor CC,
Li H,
Sabanayagam C,
Peters A,
Gieger C,
Hattersley AT,
Pedersen NL,
Magnusson PKE,
Boomsma DI,
Willemsen AHM,
Cupples L,
van Meurs JBJ,
Ghanbari M,
Gordon-Larsen P,
Huang W,
Kim YJ,
Tabara Y,
Wareham NJ,
Langenberg C,
Zeggini E,
Kuusisto J,
Laakso M,
Ingelsson E,
Abecasis G,
Chambers JC,
Kooner JS,
de Vries PS,
Morrison AC,
Hazelhurst S,
Ramsay M,
North KE,
Daviglus M,
Kraft P,
Martin NG,
Whitfield JB,
Abbas S,
Saleheen D,
Walters RG,
Holmes MV,
Black C,
Smith BH,
Baras A,
Justice AE,
Buring JE,
Ridker PM,
Chasman DI,
Kooperberg C,
Tamiya G,
Yamamoto M,
van Heel DA,
Trembath RC,
Wei WQ,
Jarvik GP,
Namjou B,
Hayes MG,
Ritchie MD,
Jousilahti P,
Salomaa V,
Hveem K,
Åsvold BO,
Kubo M,
Kamatani Y,
Okada Y,
Murakami Y,
Kim BJ,
Thorsteinsdottir U,
Stefansson K,
Zhang J,
Chen Y,
Ho YL,
Lynch JA,
Rader DJ,
Tsao PS,
Chang KM,
Cho K,
O'Donnell CJ,
Gaziano JM,
Wilson PWF,
Frayling TM,
Hirschhorn JN,
Kathiresan S,
Mohlke KL,
Sun YV,
Morris AP,
Boehnke M,
Brown CD,
Natarajan P,
Deloukas P,
Willer CJ,
Assimes TL,
Peloso GM
Genome biology · 2022 · PMID 36575460 · open access
7 pages
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
Wain LV,
Verwoert GC,
O'Reilly PF,
Shi G,
Johnson T,
Johnson AD,
Bochud M,
Rice KM,
Henneman P,
Smith AV,
Ehret GB,
Amin N
and 214 more — show all
Larson MG,
Mooser V,
Hadley D,
Dörr M,
Bis JC,
Aspelund T,
Esko T,
Janssens AC,
Zhao JH,
Heath S,
Laan M,
Fu J,
Pistis G,
Luan J,
Arora P,
Lucas G,
Pirastu N,
Pichler I,
Jackson AU,
Webster RJ,
Zhang F,
Peden JF,
Schmidt H,
Tanaka T,
Campbell H,
Igl W,
Milaneschi Y,
Hottenga JJ,
Vitart V,
Chasman DI,
Trompet S,
Bragg-Gresham JL,
Alizadeh BZ,
Chambers JC,
Guo X,
Lehtimäki T,
Kühnel B,
Lopez LM,
Polašek O,
Boban M,
Nelson CP,
Morrison AC,
Pihur V,
Ganesh SK,
Hofman A,
Kundu S,
Mattace-Raso FU,
Rivadeneira F,
Sijbrands EJ,
Uitterlinden AG,
Hwang SJ,
Vasan RS,
Wang TJ,
Bergmann S,
Vollenweider P,
Waeber G,
Laitinen J,
Pouta A,
Zitting P,
McArdle WL,
Kroemer HK,
Völker U,
Völzke H,
Glazer NL,
Taylor KD,
Harris TB,
Alavere H,
Haller T,
Keis A,
Tammesoo ML,
Aulchenko Y,
Barroso I,
Khaw KT,
Galan P,
Hercberg S,
Lathrop M,
Eyheramendy S,
Org E,
Org E,
Sõber S,
Lu X,
Nolte IM,
Penninx BW,
Corre T,
Masciullo C,
Sala C,
Groop L,
Voight BF,
Melander O,
O'Donnell CJ,
Salomaa V,
d'Adamo AP,
Fabretto A,
Faletra F,
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Nature genetics · 2010 · PMID 20383146
4 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.