For researchers
Is your paper here?
2,660 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.
6 matches for
Mukamal K.
Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions
de Vries PS,
Brown MR,
Bentley AR,
Sung YJ,
Winkler TW,
Ntalla I,
Schwander K,
Kraja AT,
Guo X,
Franceschini N,
Cheng CY,
Sim X
and 254 more — show all
Vojinovic D,
Huffman JE,
Musani SK,
Li C,
Feitosa MF,
Richard MA,
Noordam R,
Aschard H,
Bartz TM,
Bielak LF,
Deng X,
Dorajoo R,
Lohman KK,
Manning AK,
Rankinen T,
Smith AV,
Tajuddin SM,
Evangelou E,
Graff M,
Alver M,
Boissel M,
Chai JF,
Chen X,
Divers J,
Gandin I,
Gao C,
Goel A,
Hagemeijer Y,
Harris SE,
Hartwig FP,
He M,
Horimoto ARVR,
Hsu FC,
Jackson AU,
Kasturiratne A,
Komulainen P,
Kühnel B,
Laguzzi F,
Lee JH,
Luan J,
Lyytikäinen LP,
Matoba N,
Nolte IM,
Pietzner M,
Riaz M,
Said MA,
Scott RA,
Sofer T,
Stančáková A,
Takeuchi F,
Tayo BO,
van der Most PJ,
Varga TV,
Wang Y,
Ware EB,
Wen W,
Yanek LR,
Zhang W,
Zhao JH,
Afaq S,
Amin N,
Amini M,
Arking DE,
Aung T,
Ballantyne C,
Boerwinkle E,
Broeckel U,
Campbell A,
Canouil M,
Charumathi S,
Chen YI,
Connell JM,
de Faire U,
de las Fuentes L,
de Mutsert R,
de Silva HJ,
Ding J,
Dominiczak AF,
Duan Q,
Eaton CB,
Eppinga RN,
Faul JD,
Fisher V,
Forrester T,
Franco OH,
Friedlander Y,
Ghanbari M,
Giulianini F,
Grabe HJ,
Grove ML,
Gu CC,
Harris TB,
Heikkinen S,
Heng CK,
Hirata M,
Hixson JE,
Howard BV,
Ikram MA,
Jacobs DR,
Johnson C,
Jonas JB,
Kammerer CM,
Katsuya T,
Khor CC,
Kilpeläinen TO,
Koh WP,
Koistinen HA,
Kolcic I,
Kooperberg C,
Krieger JE,
Kritchevsky SB,
Kubo M,
Kuusisto J,
Lakka TA,
Langefeld CD,
Langenberg C,
Launer LJ,
Lehne B,
Lemaitre RN,
Li Y,
Liang J,
Liu J,
Liu K,
Loh M,
Louie T,
Mägi R,
Manichaikul AW,
McKenzie CA,
Meitinger T,
Metspalu A,
Milaneschi Y,
Milani L,
Mohlke KL,
Mosley TH,
Mukamal KJ,
Nalls MA,
Nauck M,
Nelson CP,
Sotoodehnia N,
O'Connell JR,
Palmer ND,
Pazoki R,
Pedersen NL,
Peters A,
Peyser PA,
Polasek O,
Poulter N,
Raffel LJ,
Raitakari OT,
Reiner AP,
Rice TK,
Rich SS,
Robino A,
Robinson JG,
Rose LM,
Rudan I,
Schmidt CO,
Schreiner PJ,
Scott WR,
Sever P,
Shi Y,
Sidney S,
Sims M,
Smith BH,
Smith JA,
Snieder H,
Starr JM,
Strauch K,
Tan N,
Taylor KD,
Teo YY,
Tham YC,
Uitterlinden AG,
van Heemst D,
Vuckovic D,
Waldenberger M,
Wang L,
Wang Y,
Wang Z,
Wei WB,
Williams C,
Wilson G,
Wojczynski MK,
Yao J,
Yu B,
Yu C,
Yuan JM,
Zhao W,
Zonderman AB,
Becker DM,
Boehnke M,
Bowden DW,
Chambers JC,
Deary IJ,
Esko T,
Farrall M,
Franks PW,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
Horta BL,
Kamatani Y,
Kato N,
Kooner JS,
Laakso M,
Leander K,
Lehtimäki T,
Magnusson PKE,
Penninx B,
Pereira AC,
Rauramaa R,
Samani NJ,
Scott J,
Shu XO,
van der Harst P,
Wagenknecht LE,
Wang YX,
Wareham NJ,
Watkins H,
Weir DR,
Wickremasinghe AR,
Zheng W,
Elliott P,
North KE,
Bouchard C,
Evans MK,
Gudnason V,
Liu CT,
Liu Y,
Psaty BM,
Ridker PM,
van Dam RM,
Kardia SLR,
Zhu X,
Rotimi CN,
Mook-Kanamori DO,
Fornage M,
Kelly TN,
Fox ER,
Hayward C,
van Duijn CM,
Tai ES,
Wong TY,
Liu J,
Rotter JI,
Gauderman WJ,
Province MA,
Munroe PB,
Rice K,
Chasman DI,
Cupples LA,
Rao DC,
Morrison AC
InterAct Consortium · Lifelines Cohort, Groningen, The Netherlands (Lifelines Cohort Study)
American journal of epidemiology · 2019 · PMID 30698716
8 pages
KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference
Schumann G,
Liu C,
O'Reilly P,
Gao H,
Song P,
Xu B,
Ruggeri B,
Amin N,
Jia T,
Preis S,
Segura Lepe M,
Akira S
and 115 more — show all
Barbieri C,
Baumeister S,
Cauchi S,
Clarke TK,
Enroth S,
Fischer K,
Hällfors J,
Harris SE,
Hieber S,
Hofer E,
Hottenga JJ,
Johansson Å,
Joshi PK,
Kaartinen N,
Laitinen J,
Lemaitre R,
Loukola A,
Luan J,
Lyytikäinen LP,
Mangino M,
Manichaikul A,
Mbarek H,
Milaneschi Y,
Moayyeri A,
Mukamal K,
Nelson C,
Nettleton J,
Partinen E,
Rawal R,
Robino A,
Rose L,
Sala C,
Satoh T,
Schmidt R,
Schraut K,
Scott R,
Smith AV,
Starr JM,
Teumer A,
Trompet S,
Uitterlinden AG,
Venturini C,
Vergnaud AC,
Verweij N,
Vitart V,
Vuckovic D,
Wedenoja J,
Yengo L,
Yu B,
Zhang W,
Zhao JH,
Boomsma DI,
Chambers J,
Chasman DI,
Daniela T,
de Geus E,
Deary I,
Eriksson JG,
Esko T,
Eulenburg V,
Franco OH,
Froguel P,
Gieger C,
Grabe HJ,
Gudnason V,
Gyllensten U,
Harris TB,
Hartikainen AL,
Heath AC,
Hocking L,
Hofman A,
Huth C,
Jarvelin MR,
Jukema JW,
Kaprio J,
Kooner JS,
Kutalik Z,
Lahti J,
Langenberg C,
Lehtimäki T,
Liu Y,
Madden PA,
Martin N,
Morrison A,
Penninx B,
Pirastu N,
Psaty B,
Raitakari O,
Ridker P,
Rose R,
Rotter JI,
Samani NJ,
Schmidt H,
Spector TD,
Stott D,
Strachan D,
Tzoulaki I,
van der Harst P,
van Duijn CM,
Marques-Vidal P,
Vollenweider P,
Wareham NJ,
Whitfield JB,
Wilson J,
Wolffenbuttel B,
Bakalkin G,
Evangelou E,
Liu Y,
Rice KM,
Desrivières S,
Kliewer SA,
Mangelsdorf DJ,
Müller CP,
Levy D,
Elliott P
Proceedings of the National Academy of Sciences of the United States of America · 2016 · PMID 27911795
3 pages
Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption
Cornelis MC,
Byrne EM,
Esko T,
Nalls MA,
Ganna A,
Paynter N,
Monda KL,
Amin N,
Fischer K,
Renstrom F,
Ngwa JS,
Huikari V
and 142 more — show all
Cavadino A,
Nolte IM,
Teumer A,
Yu K,
Marques-Vidal P,
Rawal R,
Manichaikul A,
Wojczynski MK,
Vink JM,
Zhao JH,
Burlutsky G,
Lahti J,
Mikkilä V,
Lemaitre RN,
Eriksson J,
Musani SK,
Tanaka T,
Geller F,
Luan J,
Hui J,
Mägi R,
Dimitriou M,
Garcia ME,
Ho WK,
Wright MJ,
Rose LM,
Magnusson PK,
Pedersen NL,
Couper D,
Oostra BA,
Hofman A,
Ikram MA,
Tiemeier HW,
Uitterlinden AG,
van Rooij FJ,
Barroso I,
Johansson I,
Xue L,
Kaakinen M,
Milani L,
Power C,
Snieder H,
Stolk RP,
Baumeister SE,
Biffar R,
Gu F,
Bastardot F,
Kutalik Z,
Jacobs DR Jr,
Forouhi NG,
Mihailov E,
Lind L,
Lindgren C,
Michaëlsson K,
Morris A,
Jensen M,
Khaw KT,
Luben RN,
Wang JJ,
Männistö S,
Perälä MM,
Kähönen M,
Lehtimäki T,
Viikari J,
Mozaffarian D,
Mukamal K,
Psaty BM,
Döring A,
Heath AC,
Montgomery GW,
Dahmen N,
Carithers T,
Tucker KL,
Ferrucci L,
Boyd HA,
Melbye M,
Treur JL,
Mellström D,
Hottenga JJ,
Prokopenko I,
Tönjes A,
Deloukas P,
Kanoni S,
Lorentzon M,
Houston DK,
Liu Y,
Danesh J,
Rasheed A,
Mason MA,
Zonderman AB,
Franke L,
Kristal BS,
Karjalainen J,
Reed DR,
Westra HJ,
Evans MK,
Saleheen D,
Harris TB,
Dedoussis G,
Curhan G,
Stumvoll M,
Beilby J,
Pasquale LR,
Feenstra B,
Bandinelli S,
Ordovas JM,
Chan AT,
Peters U,
Ohlsson C,
Gieger C,
Martin NG,
Waldenberger M,
Siscovick DS,
Raitakari O,
Eriksson JG,
Mitchell P,
Hunter DJ,
Kraft P,
Rimm EB,
Boomsma DI,
Borecki IB,
Loos RJ,
Wareham NJ,
Vollenweider P,
Caporaso N,
Grabe HJ,
Neuhouser ML,
Wolffenbuttel BH,
Hu FB,
Hyppönen E,
Järvelin MR,
Cupples LA,
Franks PW,
Ridker PM,
van Duijn CM,
Heiss G,
Metspalu A,
North KE,
Ingelsson E,
Nettleton JA,
van Dam RM,
Chasman DI
Coffee and Caffeine Genetics Consortium · International Parkinson’s Disease Genomics Consortium (IPDGC) and 2 more consortia
Molecular psychiatry · 2015 · PMID 25288136
2 pages
Meta-analysis of genome-wide association studies identifies ancestry-specific associations underlying circulating total tau levels
Sarnowski C,
Ghanbari M,
Bis JC,
Logue M,
Fornage M,
Mishra A,
Ahmad S,
Beiser AS,
Boerwinkle E,
Bouteloup V,
Chouraki V,
Cupples LA
and 24 more — show all
Damotte V,
DeCarli CS,
DeStefano AL,
Djoussé L,
Fohner AE,
Franz CE,
Kautz TF,
Lambert JC,
Lyons MJ,
Mosley TH,
Mukamal KJ,
Pase MP,
Portilla Fernandez EC,
Rissman RA,
Satizabal CL,
Vasan RS,
Yaqub A,
Debette S,
Dufouil C,
Launer LJ,
Kremen WS,
Longstreth WT,
Ikram MA,
Seshadri S
Communications biology · 2022 · PMID 35396452 · open access
1 page
Genome-wide association study meta-analysis of neurofilament light (NfL) levels in blood reveals novel loci related to neurodegeneration
Ahmad S,
Imtiaz MA,
Mishra A,
Wang R,
Herrera-Rivero M,
Bis JC,
Fornage M,
Roshchupkin G,
Hofer E,
Logue M,
Longstreth WT Jr,
Xia R
and 22 more — show all
Bouteloup V,
Mosley T,
Launer LJ,
Khalil M,
Kuhle J,
Rissman RA,
Chene G,
Dufouil C,
Djoussé L,
Lyons MJ,
Mukamal KJ,
Kremen WS,
Franz CE,
Schmidt R,
Debette S,
Breteler MMB,
Berger K,
Yang Q,
Seshadri S,
Aziz NA,
Ghanbari M,
Ikram MA
Communications biology · 2024 · PMID 39251807 · 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.