For researchers
Is your paper here?
2,662 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.
4 matches for
Tucker NR.
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
Christophersen IE,
Rienstra M,
Roselli C,
Yin X,
Geelhoed B,
Barnard J,
Lin H,
Arking DE,
Smith AV,
Albert CM,
Chaffin M,
Tucker NR
and 150 more — show all
Li M,
Klarin D,
Bihlmeyer NA,
Low SK,
Weeke PE,
Müller-Nurasyid M,
Smith JG,
Brody JA,
Niemeijer MN,
Dörr M,
Trompet S,
Huffman J,
Gustafsson S,
Schurmann C,
Kleber ME,
Lyytikäinen LP,
Seppälä I,
Malik R,
Horimoto ARVR,
Perez M,
Sinisalo J,
Aeschbacher S,
Thériault S,
Yao J,
Radmanesh F,
Weiss S,
Teumer A,
Choi SH,
Weng LC,
Clauss S,
Deo R,
Rader DJ,
Shah SH,
Sun A,
Hopewell JC,
Debette S,
Chauhan G,
Yang Q,
Worrall BB,
Paré G,
Kamatani Y,
Hagemeijer YP,
Verweij N,
Siland JE,
Kubo M,
Smith JD,
Van Wagoner DR,
Bis JC,
Perz S,
Psaty BM,
Ridker PM,
Magnani JW,
Harris TB,
Launer LJ,
Shoemaker MB,
Padmanabhan S,
Haessler J,
Bartz TM,
Waldenberger M,
Lichtner P,
Arendt M,
Krieger JE,
Kähönen M,
Risch L,
Mansur AJ,
Peters A,
Smith BH,
Lind L,
Scott SA,
Lu Y,
Bottinger EB,
Hernesniemi J,
Lindgren CM,
Wong JA,
Huang J,
Eskola M,
Morris AP,
Ford I,
Reiner AP,
Delgado G,
Chen LY,
Chen YI,
Sandhu RK,
Li M,
Boerwinkle E,
Eisele L,
Lannfelt L,
Rost N,
Anderson CD,
Taylor KD,
Campbell A,
Magnusson PK,
Porteous D,
Hocking LJ,
Vlachopoulou E,
Pedersen NL,
Nikus K,
Orho-Melander M,
Hamsten A,
Heeringa J,
Denny JC,
Kriebel J,
Darbar D,
Newton-Cheh C,
Shaffer C,
Macfarlane PW,
Heilmann-Heimbach S,
Almgren P,
Huang PL,
Sotoodehnia N,
Soliman EZ,
Uitterlinden AG,
Hofman A,
Franco OH,
Völker U,
Jöckel KH,
Sinner MF,
Lin HJ,
Guo X,
Dichgans M,
Ingelsson E,
Kooperberg C,
Melander O,
Loos RJF,
Laurikka J,
Conen D,
Rosand J,
van der Harst P,
Lokki ML,
Kathiresan S,
Pereira A,
Jukema JW,
Hayward C,
Rotter JI,
März W,
Lehtimäki T,
Stricker BH,
Chung MK,
Felix SB,
Gudnason V,
Alonso A,
Roden DM,
Kääb S,
Chasman DI,
Heckbert SR,
Benjamin EJ,
Tanaka T,
Lunetta KL,
Lubitz SA,
Ellinor PT
METASTROKE Consortium of the ISGC · Neurology Working Group of the CHARGE Consortium and 1 more consortia
Nature genetics · 2017 · PMID 28416818
12 pages+
Multi-ethnic genome-wide association study for atrial fibrillation
Roselli C,
Chaffin MD,
Weng LC,
Aeschbacher S,
Ahlberg G,
Albert CM,
Almgren P,
Alonso A,
Anderson CD,
Aragam KG,
Arking DE,
Barnard J
and 206 more — show all
Bartz TM,
Benjamin EJ,
Bihlmeyer NA,
Bis JC,
Bloom HL,
Boerwinkle E,
Bottinger EB,
Brody JA,
Calkins H,
Campbell A,
Cappola TP,
Carlquist J,
Chasman DI,
Chen LY,
Chen YI,
Choi EK,
Choi SH,
Christophersen IE,
Chung MK,
Cole JW,
Conen D,
Cook J,
Crijns HJ,
Cutler MJ,
Damrauer SM,
Daniels BR,
Darbar D,
Delgado G,
Denny JC,
Dichgans M,
Dörr M,
Dudink EA,
Dudley SC,
Esa N,
Esko T,
Eskola M,
Fatkin D,
Felix SB,
Ford I,
Franco OH,
Geelhoed B,
Grewal RP,
Gudnason V,
Guo X,
Gupta N,
Gustafsson S,
Gutmann R,
Hamsten A,
Harris TB,
Hayward C,
Heckbert SR,
Hernesniemi J,
Hocking LJ,
Hofman A,
Horimoto ARVR,
Huang J,
Huang PL,
Huffman J,
Ingelsson E,
Ipek EG,
Ito K,
Jimenez-Conde J,
Johnson R,
Jukema JW,
Kääb S,
Kähönen M,
Kamatani Y,
Kane JP,
Kastrati A,
Kathiresan S,
Katschnig-Winter P,
Kavousi M,
Kessler T,
Kietselaer BL,
Kirchhof P,
Kleber ME,
Knight S,
Krieger JE,
Kubo M,
Launer LJ,
Laurikka J,
Lehtimäki T,
Leineweber K,
Lemaitre RN,
Li M,
Lim HE,
Lin HJ,
Lin H,
Lind L,
Lindgren CM,
Lokki ML,
London B,
Loos RJF,
Low SK,
Lu Y,
Lyytikäinen LP,
Macfarlane PW,
Magnusson PK,
Mahajan A,
Malik R,
Mansur AJ,
Marcus GM,
Margolin L,
Margulies KB,
März W,
McManus DD,
Melander O,
Mohanty S,
Montgomery JA,
Morley MP,
Morris AP,
Müller-Nurasyid M,
Natale A,
Nazarian S,
Neumann B,
Newton-Cheh C,
Niemeijer MN,
Nikus K,
Nilsson P,
Noordam R,
Oellers H,
Olesen MS,
Orho-Melander M,
Padmanabhan S,
Pak HN,
Paré G,
Pedersen NL,
Pera J,
Pereira A,
Porteous D,
Psaty BM,
Pulit SL,
Pullinger CR,
Rader DJ,
Refsgaard L,
Ribasés M,
Ridker PM,
Rienstra M,
Risch L,
Roden DM,
Rosand J,
Rosenberg MA,
Rost N,
Rotter JI,
Saba S,
Sandhu RK,
Schnabel RB,
Schramm K,
Schunkert H,
Schurman C,
Scott SA,
Seppälä I,
Shaffer C,
Shah S,
Shalaby AA,
Shim J,
Shoemaker MB,
Siland JE,
Sinisalo J,
Sinner MF,
Slowik A,
Smith AV,
Smith BH,
Smith JG,
Smith JD,
Smith NL,
Soliman EZ,
Sotoodehnia N,
Stricker BH,
Sun A,
Sun H,
Svendsen JH,
Tanaka T,
Tanriverdi K,
Taylor KD,
Teder-Laving M,
Teumer A,
Thériault S,
Trompet S,
Tucker NR,
Tveit A,
Uitterlinden AG,
Van Der Harst P,
Van Gelder IC,
Van Wagoner DR,
Verweij N,
Vlachopoulou E,
Völker U,
Wang B,
Weeke PE,
Weijs B,
Weiss R,
Weiss S,
Wells QS,
Wiggins KL,
Wong JA,
Woo D,
Worrall BB,
Yang PS,
Yao J,
Yoneda ZT,
Zeller T,
Zeng L,
Lubitz SA,
Lunetta KL,
Ellinor PT
Nature genetics · 2018 · PMID 29892015
12 pages+
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
Ntalla I,
Weng LC,
Cartwright JH,
Hall AW,
Sveinbjornsson G,
Tucker NR,
Choi SH,
Chaffin MD,
Roselli C,
Barnes MR,
Mifsud B,
Warren HR
and 175 more — show all
Hayward C,
Marten J,
Cranley JJ,
Concas MP,
Gasparini P,
Boutin T,
Kolcic I,
Polasek O,
Rudan I,
Araujo NM,
Lima-Costa MF,
Ribeiro ALP,
Souza RP,
Tarazona-Santos E,
Giedraitis V,
Ingelsson E,
Mahajan A,
Morris AP,
Del Greco M F,
Foco L,
Gögele M,
Hicks AA,
Cook JP,
Lind L,
Lindgren CM,
Sundström J,
Nelson CP,
Riaz MB,
Samani NJ,
Sinagra G,
Ulivi S,
Kähönen M,
Mishra PP,
Mononen N,
Nikus K,
Caulfield MJ,
Dominiczak A,
Padmanabhan S,
Montasser ME,
O'Connell JR,
Ryan K,
Shuldiner AR,
Aeschbacher S,
Conen D,
Risch L,
Thériault S,
Hutri-Kähönen N,
Lehtimäki T,
Lyytikäinen LP,
Raitakari OT,
Barnes CLK,
Campbell H,
Joshi PK,
Wilson JF,
Isaacs A,
Kors JA,
van Duijn CM,
Huang PL,
Gudnason V,
Harris TB,
Launer LJ,
Smith AV,
Bottinger EP,
Loos RJF,
Nadkarni GN,
Preuss MH,
Correa A,
Mei H,
Wilson J,
Meitinger T,
Müller-Nurasyid M,
Peters A,
Waldenberger M,
Mangino M,
Spector TD,
Rienstra M,
van de Vegte YJ,
van der Harst P,
Verweij N,
Kääb S,
Schramm K,
Sinner MF,
Strauch K,
Cutler MJ,
Fatkin D,
London B,
Olesen M,
Roden DM,
Benjamin Shoemaker M,
Gustav Smith J,
Biggs ML,
Bis JC,
Brody JA,
Psaty BM,
Rice K,
Sotoodehnia N,
De Grandi A,
Fuchsberger C,
Pattaro C,
Pramstaller PP,
Ford I,
Wouter Jukema J,
Macfarlane PW,
Trompet S,
Dörr M,
Felix SB,
Völker U,
Weiss S,
Havulinna AS,
Jula A,
Sääksjärvi K,
Salomaa V,
Guo X,
Heckbert SR,
Lin HJ,
Rotter JI,
Taylor KD,
Yao J,
de Mutsert R,
Maan AC,
Mook-Kanamori DO,
Noordam R,
Cucca F,
Ding J,
Lakatta EG,
Qian Y,
Tarasov KV,
Levy D,
Lin H,
Newton-Cheh CH,
Lunetta KL,
Murray AD,
Porteous DJ,
Smith BH,
Stricker BH,
Uitterlinden A,
van den Berg ME,
Haessler J,
Jackson RD,
Kooperberg C,
Peters U,
Reiner AP,
Whitsel EA,
Alonso A,
Arking DE,
Boerwinkle E,
Ehret GB,
Soliman EZ,
Avery CL,
Gogarten SM,
Kerr KF,
Laurie CC,
Seyerle AA,
Stilp A,
Assa S,
Abdullah Said M,
Yldau van der Ende M,
Lambiase PD,
Orini M,
Ramirez J,
Van Duijvenboden S,
Arnar DO,
Gudbjartsson DF,
Holm H,
Sulem P,
Thorleifsson G,
Thorolfsdottir RB,
Thorsteinsdottir U,
Benjamin EJ,
Tinker A,
Stefansson K,
Ellinor PT,
Jamshidi Y,
Lubitz SA,
Munroe PB
Nature communications · 2020 · PMID 32439900 · open access
12 pages+
Deep learning enables genetic analysis of the human thoracic aorta
Pirruccello JP,
Chaffin MD,
Chou EL,
Fleming SJ,
Lin H,
Nekoui M,
Khurshid S,
Friedman SF,
Bick AG,
Arduini A,
Weng LC,
Choi SH
and 18 more — show all
Akkad AD,
Batra P,
Tucker NR,
Hall AW,
Roselli C,
Benjamin EJ,
Vellarikkal SK,
Gupta RM,
Stegmann CM,
Juric D,
Stone JR,
Vasan RS,
Ho JE,
Hoffmann U,
Lubitz SA,
Philippakis AA,
Lindsay ME,
Ellinor PT
Nature genetics · 2022 · PMID 34837083 · open access
12 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.