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2,673 papers hold this site up. Every variant and condition page names
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5 matches for
Atzmon G.
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci
Kenny EE,
Pe'er I,
Karban A,
Ozelius L,
Mitchell AA,
Ng SM,
Erazo M,
Ostrer H,
Abraham C,
Abreu MT,
Atzmon G,
Barzilai N
and 31 more — show all
Brant SR,
Bressman S,
Burns ER,
Chowers Y,
Clark LN,
Darvasi A,
Doheny D,
Duerr RH,
Eliakim R,
Giladi N,
Gregersen PK,
Hakonarson H,
Jones MR,
Marder K,
McGovern DP,
Mulle J,
Orr-Urtreger A,
Proctor DD,
Pulver A,
Rotter JI,
Silverberg MS,
Ullman T,
Warren ST,
Waterman M,
Zhang W,
Bergman A,
Mayer L,
Katz S,
Desnick RJ,
Cho JH,
Peter I
PLoS genetics · 2012 · PMID 22412388 · open access
6 pages
Genome-wide analysis identifies 12 loci influencing human reproductive behavior
Barban N,
Jansen R,
de Vlaming R,
Vaez A,
Mandemakers JJ,
Tropf FC,
Shen X,
Wilson JF,
Chasman DI,
Nolte IM,
Tragante V,
van der Laan SW
and 241 more — show all
Perry JR,
Kong A,
Ahluwalia TS,
Albrecht E,
Yerges-Armstrong L,
Atzmon G,
Auro K,
Ayers K,
Bakshi A,
Ben-Avraham D,
Berger K,
Bergman A,
Bertram L,
Bielak LF,
Bjornsdottir G,
Bonder MJ,
Broer L,
Bui M,
Barbieri C,
Cavadino A,
Chavarro JE,
Turman C,
Concas MP,
Cordell HJ,
Davies G,
Eibich P,
Eriksson N,
Esko T,
Eriksson J,
Falahi F,
Felix JF,
Fontana MA,
Franke L,
Gandin I,
Gaskins AJ,
Gieger C,
Gunderson EP,
Guo X,
Hayward C,
He C,
Hofer E,
Huang H,
Joshi PK,
Kanoni S,
Karlsson R,
Kiechl S,
Kifley A,
Kluttig A,
Kraft P,
Lagou V,
Lecoeur C,
Lahti J,
Li-Gao R,
Lind PA,
Liu T,
Makalic E,
Mamasoula C,
Matteson L,
Mbarek H,
McArdle PF,
McMahon G,
Meddens SF,
Mihailov E,
Miller M,
Missmer SA,
Monnereau C,
van der Most PJ,
Myhre R,
Nalls MA,
Nutile T,
Kalafati IP,
Porcu E,
Prokopenko I,
Rajan KB,
Rich-Edwards J,
Rietveld CA,
Robino A,
Rose LM,
Rueedi R,
Ryan KA,
Saba Y,
Schmidt D,
Smith JA,
Stolk L,
Streeten E,
Tönjes A,
Thorleifsson G,
Ulivi S,
Wedenoja J,
Wellmann J,
Willeit P,
Yao J,
Yengo L,
Zhao JH,
Zhao W,
Zhernakova DV,
Amin N,
Andrews H,
Balkau B,
Barzilai N,
Bergmann S,
Biino G,
Bisgaard H,
Bønnelykke K,
Boomsma DI,
Buring JE,
Campbell H,
Cappellani S,
Ciullo M,
Cox SR,
Cucca F,
Toniolo D,
Davey-Smith G,
Deary IJ,
Dedoussis G,
Deloukas P,
van Duijn CM,
de Geus EJ,
Eriksson JG,
Evans DA,
Faul JD,
Sala CF,
Froguel P,
Gasparini P,
Girotto G,
Grabe HJ,
Greiser KH,
Groenen PJ,
de Haan HG,
Haerting J,
Harris TB,
Heath AC,
Heikkilä K,
Hofman A,
Homuth G,
Holliday EG,
Hopper J,
Hyppönen E,
Jacobsson B,
Jaddoe VW,
Johannesson M,
Jugessur A,
Kähönen M,
Kajantie E,
Kardia SL,
Keavney B,
Kolcic I,
Koponen P,
Kovacs P,
Kronenberg F,
Kutalik Z,
La Bianca M,
Lachance G,
Iacono WG,
Lai S,
Lehtimäki T,
Liewald DC,
Lindgren CM,
Liu Y,
Luben R,
Lucht M,
Luoto R,
Magnus P,
Magnusson PK,
Martin NG,
McGue M,
McQuillan R,
Medland SE,
Meisinger C,
Mellström D,
Metspalu A,
Traglia M,
Milani L,
Mitchell P,
Montgomery GW,
Mook-Kanamori D,
de Mutsert R,
Nohr EA,
Ohlsson C,
Olsen J,
Ong KK,
Paternoster L,
Pattie A,
Penninx BW,
Perola M,
Peyser PA,
Pirastu M,
Polasek O,
Power C,
Kaprio J,
Raffel LJ,
Räikkönen K,
Raitakari O,
Ridker PM,
Ring SM,
Roll K,
Rudan I,
Ruggiero D,
Rujescu D,
Salomaa V,
Schlessinger D,
Schmidt H,
Schmidt R,
Schupf N,
Smit J,
Sorice R,
Spector TD,
Starr JM,
Stöckl D,
Strauch K,
Stumvoll M,
Swertz MA,
Thorsteinsdottir U,
Thurik AR,
Timpson NJ,
Tung JY,
Uitterlinden AG,
Vaccargiu S,
Viikari J,
Vitart V,
Völzke H,
Vollenweider P,
Vuckovic D,
Waage J,
Wagner GG,
Wang JJ,
Wareham NJ,
Weir DR,
Willemsen G,
Willeit J,
Wright AF,
Zondervan KT,
Stefansson K,
Krueger RF,
Lee JJ,
Benjamin DJ,
Cesarini D,
Koellinger PD,
den Hoed M,
Snieder H,
Mills MC
BIOS Consortium · LifeLines Cohort Study
Nature genetics · 2016 · PMID 27798627
4 pages
GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium
Matteini AM,
Tanaka T,
Karasik D,
Atzmon G,
Chou WC,
Eicher JD,
Johnson AD,
Arnold AM,
Callisaya ML,
Davies G,
Evans DS,
Holtfreter B
and 55 more — show all
Lohman K,
Lunetta KL,
Mangino M,
Smith AV,
Smith JA,
Teumer A,
Yu L,
Arking DE,
Buchman AS,
Chibinik LB,
De Jager PL,
Evans DA,
Faul JD,
Garcia ME,
Gillham-Nasenya I,
Gudnason V,
Hofman A,
Hsu YH,
Ittermann T,
Lahousse L,
Liewald DC,
Liu Y,
Lopez L,
Rivadeneira F,
Rotter JI,
Siggeirsdottir K,
Starr JM,
Thomson R,
Tranah GJ,
Uitterlinden AG,
Völker U,
Völzke H,
Weir DR,
Yaffe K,
Zhao W,
Zhuang WV,
Zmuda JM,
Bennett DA,
Cummings SR,
Deary IJ,
Ferrucci L,
Harris TB,
Kardia SL,
Kocher T,
Kritchevsky SB,
Psaty BM,
Seshadri S,
Spector TD,
Srikanth VK,
Windham BG,
Zillikens MC,
Newman AB,
Walston JD,
Kiel DP,
Murabito JM
Aging cell · 2016 · PMID 27325353 · open access
2 pages
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Flannick J,
Mercader JM,
Fuchsberger C,
Udler MS,
Mahajan A,
Wessel J,
Teslovich TM,
Caulkins L,
Koesterer R,
Barajas-Olmos F,
Blackwell TW,
Boerwinkle E
and 152 more — show all
Brody JA,
Centeno-Cruz F,
Chen L,
Chen S,
Contreras-Cubas C,
Córdova E,
Correa A,
Cortes M,
DeFronzo RA,
Dolan L,
Drews KL,
Elliott A,
Floyd JS,
Gabriel S,
Garay-Sevilla ME,
García-Ortiz H,
Gross M,
Han S,
Heard-Costa NL,
Jackson AU,
Jørgensen ME,
Kang HM,
Kelsey M,
Kim BJ,
Koistinen HA,
Kuusisto J,
Leader JB,
Linneberg A,
Liu CT,
Liu J,
Lyssenko V,
Manning AK,
Marcketta A,
Malacara-Hernandez JM,
Martínez-Hernández A,
Matsuo K,
Mayer-Davis E,
Mendoza-Caamal E,
Mohlke KL,
Morrison AC,
Ndungu A,
Ng MCY,
O'Dushlaine C,
Payne AJ,
Pihoker C,
Post WS,
Preuss M,
Psaty BM,
Vasan RS,
Rayner NW,
Reiner AP,
Revilla-Monsalve C,
Robertson NR,
Santoro N,
Schurmann C,
So WY,
Soberón X,
Stringham HM,
Strom TM,
Tam CHT,
Thameem F,
Tomlinson B,
Torres JM,
Tracy RP,
van Dam RM,
Vujkovic M,
Wang S,
Welch RP,
Witte DR,
Wong TY,
Atzmon G,
Barzilai N,
Blangero J,
Bonnycastle LL,
Bowden DW,
Chambers JC,
Chan E,
Cheng CY,
Cho YS,
Collins FS,
de Vries PS,
Duggirala R,
Glaser B,
Gonzalez C,
Gonzalez ME,
Groop L,
Kooner JS,
Kwak SH,
Laakso M,
Lehman DM,
Nilsson P,
Spector TD,
Tai ES,
Tuomi T,
Tuomilehto J,
Wilson JG,
Aguilar-Salinas CA,
Bottinger E,
Burke B,
Carey DJ,
Chan JCN,
Dupuis J,
Frossard P,
Heckbert SR,
Hwang MY,
Kim YJ,
Kirchner HL,
Lee JY,
Lee J,
Loos RJF,
Ma RCW,
Morris AD,
O'Donnell CJ,
Palmer CNA,
Pankow J,
Park KS,
Rasheed A,
Saleheen D,
Sim X,
Small KS,
Teo YY,
Haiman C,
Hanis CL,
Henderson BE,
Orozco L,
Tusié-Luna T,
Dewey FE,
Baras A,
Gieger C,
Meitinger T,
Strauch K,
Lange L,
Grarup N,
Hansen T,
Pedersen O,
Zeitler P,
Dabelea D,
Abecasis G,
Bell GI,
Cox NJ,
Seielstad M,
Sladek R,
Meigs JB,
Rich SS,
Rotter JI,
Altshuler D,
Burtt NP,
Scott LJ,
Morris AP,
Florez JC,
McCarthy MI,
Boehnke M
Broad Genomics Platform · DiscovEHR Collaboration and 8 more consortia
Nature · 2019 · PMID 31118516 · open access
2 pages
A meta-analysis of genome-wide association studies identifies multiple longevity genes
Deelen J,
Evans DS,
Arking DE,
Tesi N,
Nygaard M,
Liu X,
Wojczynski MK,
Biggs ML,
van der Spek A,
Atzmon G,
Ware EB,
Sarnowski C
and 72 more — show all
Smith AV,
Seppälä I,
Cordell HJ,
Dose J,
Amin N,
Arnold AM,
Ayers KL,
Barzilai N,
Becker EJ,
Beekman M,
Blanché H,
Christensen K,
Christiansen L,
Collerton JC,
Cubaynes S,
Cummings SR,
Davies K,
Debrabant B,
Deleuze JF,
Duncan R,
Faul JD,
Franceschi C,
Galan P,
Gudnason V,
Harris TB,
Huisman M,
Hurme MA,
Jagger C,
Jansen I,
Jylhä M,
Kähönen M,
Karasik D,
Kardia SLR,
Kingston A,
Kirkwood TBL,
Launer LJ,
Lehtimäki T,
Lieb W,
Lyytikäinen LP,
Martin-Ruiz C,
Min J,
Nebel A,
Newman AB,
Nie C,
Nohr EA,
Orwoll ES,
Perls TT,
Province MA,
Psaty BM,
Raitakari OT,
Reinders MJT,
Robine JM,
Rotter JI,
Sebastiani P,
Smith J,
Sørensen TIA,
Taylor KD,
Uitterlinden AG,
van der Flier W,
van der Lee SJ,
van Duijn CM,
van Heemst D,
Vaupel JW,
Weir D,
Ye K,
Zeng Y,
Zheng W,
Holstege H,
Kiel DP,
Lunetta KL,
Slagboom PE,
Murabito JM
Nature communications · 2019 · PMID 31413261 · open access
1 page
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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.