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Is your paper here?
2,665 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.
70 matches for
Sen S,
showing the first 10.
Genetic variation in <i>CFH</i> predicts phenytoin-induced maculopapular exanthema in European-descent patients
McCormack M,
Gui H,
Ingason A,
Speed D,
Wright GEB,
Zhang EJ,
Secolin R,
Yasuda C,
Kwok M,
Wolking S,
Becker F,
Rau S
and 37 more — show all
Avbersek A,
Heggeli K,
Leu C,
Depondt C,
Sills GJ,
Marson AG,
Auce P,
Brodie MJ,
Francis B,
Johnson MR,
Koeleman BPC,
Striano P,
Coppola A,
Zara F,
Kunz WS,
Sander JW,
Lerche H,
Klein KM,
Weckhuysen S,
Krenn M,
Gudmundsson LJ,
Stefánsson K,
Krause R,
Shear N,
Ross CJD,
Delanty N,
Pirmohamed M,
Carleton BC,
Cendes F,
Lopes-Cendes I,
Liao WP,
O'Brien TJ,
Sisodiya SM,
Cherny S,
Kwan P,
Baum L,
Cavalleri GL
EPIGEN Consortium; · Canadian Pharmacogenomics Network for Drug Safety; and 2 more consortia
Neurology · 2018 · PMID 29288229 · open access
1 page
NT5C2 germline variants alter thiopurine metabolism and are associated with acquired NT5C2 relapse mutations in childhood acute lymphoblastic leukaemia
Tulstrup M,
Grosjean M,
Nielsen SN,
Grell K,
Wolthers BO,
Wegener PS,
Jonsson OG,
Lund B,
Harila-Saari A,
Abrahamsson J,
Vaitkeviciene G,
Pruunsild K
and 13 more — show all
Toft N,
Holm M,
Hulegårdh E,
Liestøl S,
Griskevicius L,
Punab M,
Wang J,
Carroll WL,
Zhang Z,
Dalgaard MD,
Gupta R,
Nersting J,
Schmiegelow K
Leukemia · 2018 · PMID 30201983
1 page
A genome-wide association study of interhemispheric theta EEG coherence: implications for neural connectivity and alcohol use behavior
Meyers JL,
Zhang J,
Chorlian DB,
Pandey AK,
Kamarajan C,
Wang JC,
Wetherill L,
Lai D,
Chao M,
Chan G,
Kinreich S,
Kapoor M
and 13 more — show all
Bertelsen S,
McClintick J,
Bauer L,
Hesselbrock V,
Kuperman S,
Kramer J,
Salvatore JE,
Dick DM,
Agrawal A,
Foroud T,
Edenberg HJ,
Goate A,
Porjesz B
Molecular psychiatry · 2021 · PMID 32433515
1 page
Genome-wide association study identifies novel susceptibility loci for KIT D816V positive mastocytosis
Galatà G,
García-Montero AC,
Kristensen T,
Dawoud AAZ,
Muñoz-González JI,
Meggendorfer M,
Guglielmelli P,
Hoade Y,
Alvarez-Twose I,
Gieger C,
Strauch K,
Ferrucci L
and 15 more — show all
Tanaka T,
Bandinelli S,
Schnurr TM,
Haferlach T,
Broesby-Olsen S,
Vestergaard H,
Møller MB,
Bindslev-Jensen C,
Vannucchi AM,
Orfao A,
Radia D,
Reiter A,
Chase AJ,
Cross NCP,
Tapper WJ
American journal of human genetics · 2021 · PMID 33421400
1 page
Genome-wide association meta-analysis identifies pleiotropic risk loci for aerodigestive squamous cell cancers
Lesseur C,
Ferreiro-Iglesias A,
McKay JD,
Bossé Y,
Johansson M,
Gaborieau V,
Landi MT,
Christiani DC,
Caporaso NC,
Bojesen SE,
Amos CI,
Shete S
and 41 more — show all
Liu G,
Rennert G,
Albanes D,
Aldrich MC,
Tardon A,
Chen C,
Triantafillos L,
Field JK,
Teare MD,
Kiemeney LA,
Diergaarde B,
Ferris RL,
Zienolddiny S,
Lam S,
Olshan AF,
Weissler MC,
Lacko M,
Risch A,
Bickeböller H,
Ness AR,
Thomas S,
Le Marchand L,
Schabath MB,
Wünsch-Filho V,
Tajara EH,
Andrew AS,
Clifford GM,
Lazarus P,
Grankvist K,
Johansson M,
Arnold S,
Melander O,
Brunnström H,
Boccia S,
Cadoni G,
Timens W,
Obeidat M,
Xiao X,
Houlston RS,
Hung RJ,
Brennan P
PLoS genetics · 2021 · PMID 33667223 · open access
1 page
Genome-wide association study of cardiac troponin I in the general population
Moksnes MR,
Røsjø H,
Richmond A,
Lyngbakken MN,
Graham SE,
Hansen AF,
Wolford BN,
Gagliano Taliun SA,
LeFaive J,
Rasheed H,
Thomas LF,
Zhou W
and 18 more — show all
Aung N,
Surakka I,
Douville NJ,
Campbell A,
Porteous DJ,
Petersen SE,
Munroe PB,
Welsh P,
Sattar N,
Smith GD,
Fritsche LG,
Nielsen JB,
Åsvold BO,
Hveem K,
Hayward C,
Willer CJ,
Brumpton BM,
Omland T
Human molecular genetics · 2021 · PMID 33961016 · open access
1 page
Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information
Maihofer AX,
Choi KW,
Coleman JRI,
Daskalakis NP,
Denckla CA,
Ketema E,
Morey RA,
Polimanti R,
Ratanatharathorn A,
Torres K,
Wingo AP,
Zai CC
and 169 more — show all
Aiello AE,
Almli LM,
Amstadter AB,
Andersen SB,
Andreassen OA,
Arbisi PA,
Ashley-Koch AE,
Austin SB,
Avdibegović E,
Borglum AD,
Babić D,
Bækvad-Hansen M,
Baker DG,
Beckham JC,
Bierut LJ,
Bisson JI,
Boks MP,
Bolger EA,
Bradley B,
Brashear M,
Breen G,
Bryant RA,
Bustamante AC,
Bybjerg-Grauholm J,
Calabrese JR,
Caldas-de-Almeida JM,
Chen CY,
Dale AM,
Dalvie S,
Deckert J,
Delahanty DL,
Dennis MF,
Disner SG,
Domschke K,
Duncan LE,
Džubur Kulenović A,
Erbes CR,
Evans A,
Farrer LA,
Feeny NC,
Flory JD,
Forbes D,
Franz CE,
Galea S,
Garrett ME,
Gautam A,
Gelaye B,
Gelernter J,
Geuze E,
Gillespie CF,
Goçi A,
Gordon SD,
Guffanti G,
Hammamieh R,
Hauser MA,
Heath AC,
Hemmings SMJ,
Hougaard DM,
Jakovljević M,
Jett M,
Johnson EO,
Jones I,
Jovanovic T,
Qin XJ,
Karstoft KI,
Kaufman ML,
Kessler RC,
Khan A,
Kimbrel NA,
King AP,
Koen N,
Kranzler HR,
Kremen WS,
Lawford BR,
Lebois LAM,
Lewis C,
Liberzon I,
Linnstaedt SD,
Logue MW,
Lori A,
Lugonja B,
Luykx JJ,
Lyons MJ,
Maples-Keller JL,
Marmar C,
Martin NG,
Maurer D,
Mavissakalian MR,
McFarlane A,
McGlinchey RE,
McLaughlin KA,
McLean SA,
Mehta D,
Mellor R,
Michopoulos V,
Milberg W,
Miller MW,
Morris CP,
Mors O,
Mortensen PB,
Nelson EC,
Nordentoft M,
Norman SB,
O'Donnell M,
Orcutt HK,
Panizzon MS,
Peters ES,
Peterson AL,
Peverill M,
Pietrzak RH,
Polusny MA,
Rice JP,
Risbrough VB,
Roberts AL,
Rothbaum AO,
Rothbaum BO,
Roy-Byrne P,
Ruggiero KJ,
Rung A,
Rutten BPF,
Saccone NL,
Sanchez SE,
Schijven D,
Seedat S,
Seligowski AV,
Seng JS,
Sheerin CM,
Silove D,
Smith AK,
Smoller JW,
Sponheim SR,
Stein DJ,
Stevens JS,
Teicher MH,
Thompson WK,
Trapido E,
Uddin M,
Ursano RJ,
van den Heuvel LL,
Van Hooff M,
Vermetten E,
Vinkers CH,
Voisey J,
Wang Y,
Wang Z,
Werge T,
Williams MA,
Williamson DE,
Winternitz S,
Wolf C,
Wolf EJ,
Yehuda R,
Young KA,
Young RM,
Zhao H,
Zoellner LA,
Haas M,
Lasseter H,
Provost AC,
Salem RM,
Sebat J,
Shaffer RA,
Wu T,
Ripke S,
Daly MJ,
Ressler KJ,
Koenen KC,
Stein MB,
Nievergelt CM
Biological psychiatry · 2022 · PMID 34865855 · open access
1 page
Established risk loci for systemic lupus erythematosus at NCF2, STAT4, TNPO3, IRF5 and ITGAM associate with distinct clinical manifestations: A Danish genome-wide association study
Leffers HCB,
Westergaard D,
Saevarsdottir S,
Jonsdottir I,
Pedersen OB,
Troldborg A,
Voss A,
Kristensen S,
Lindhardsen J,
Kumar P,
Linauskas A,
Juul L
and 12 more — show all
Krogh NS,
Deleuran B,
Dreyer L,
Schwinn M,
Thørner LW,
Hindhede L,
Erikstrup C,
Ullum H,
Brunak S,
Stefansson K,
Banasik K,
Jacobsen S
DBDS genomic consortium
Joint bone spine · 2022 · PMID 35167971
1 page
Coenzyme Q10 Supplementation in Statin Treated Patients: A Double-Blinded Randomized Placebo-Controlled Trial
Dohlmann TL,
Kuhlman AB,
Morville T,
Dahl M,
Asping M,
Orlando P,
Silvestri S,
Tiano L,
Helge JW,
Dela F,
Larsen S
Antioxidants (Basel, Switzerland) · 2022 · PMID 36139772 · 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.