For researchers
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.
5 matches for
Bhangale T.
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Lango Allen H,
Estrada K,
Lettre G,
Berndt SI,
Weedon MN,
Rivadeneira F,
Willer CJ,
Jackson AU,
Vedantam S,
Raychaudhuri S,
Ferreira T,
Wood AR
and 281 more — show all
Weyant RJ,
Segrè AV,
Speliotes EK,
Wheeler E,
Soranzo N,
Park JH,
Yang J,
Gudbjartsson D,
Heard-Costa NL,
Randall JC,
Qi L,
Vernon Smith A,
Mägi R,
Pastinen T,
Liang L,
Heid IM,
Luan J,
Thorleifsson G,
Winkler TW,
Goddard ME,
Sin Lo K,
Palmer C,
Workalemahu T,
Aulchenko YS,
Johansson A,
Zillikens MC,
Feitosa MF,
Esko T,
Johnson T,
Ketkar S,
Kraft P,
Mangino M,
Prokopenko I,
Absher D,
Albrecht E,
Ernst F,
Glazer NL,
Hayward C,
Hottenga JJ,
Jacobs KB,
Knowles JW,
Kutalik Z,
Monda KL,
Polasek O,
Preuss M,
Rayner NW,
Robertson NR,
Steinthorsdottir V,
Tyrer JP,
Voight BF,
Wiklund F,
Xu J,
Zhao JH,
Nyholt DR,
Pellikka N,
Perola M,
Perry JR,
Surakka I,
Tammesoo ML,
Altmaier EL,
Amin N,
Aspelund T,
Bhangale T,
Boucher G,
Chasman DI,
Chen C,
Coin L,
Cooper MN,
Dixon AL,
Gibson Q,
Grundberg E,
Hao K,
Juhani Junttila M,
Kaplan LM,
Kettunen J,
König IR,
Kwan T,
Lawrence RW,
Levinson DF,
Lorentzon M,
McKnight B,
Morris AP,
Müller M,
Suh Ngwa J,
Purcell S,
Rafelt S,
Salem RM,
Salvi E,
Sanna S,
Shi J,
Sovio U,
Thompson JR,
Turchin MC,
Vandenput L,
Verlaan DJ,
Vitart V,
White CC,
Ziegler A,
Almgren P,
Balmforth AJ,
Campbell H,
Citterio L,
De Grandi A,
Dominiczak A,
Duan J,
Elliott P,
Elosua R,
Eriksson JG,
Freimer NB,
Geus EJ,
Glorioso N,
Haiqing S,
Hartikainen AL,
Havulinna AS,
Hicks AA,
Hui J,
Igl W,
Illig T,
Jula A,
Kajantie E,
Kilpeläinen TO,
Koiranen M,
Kolcic I,
Koskinen S,
Kovacs P,
Laitinen J,
Liu J,
Lokki ML,
Marusic A,
Maschio A,
Meitinger T,
Mulas A,
Paré G,
Parker AN,
Peden JF,
Petersmann A,
Pichler I,
Pietiläinen KH,
Pouta A,
Ridderstråle M,
Rotter JI,
Sambrook JG,
Sanders AR,
Schmidt CO,
Sinisalo J,
Smit JH,
Stringham HM,
Bragi Walters G,
Widen E,
Wild SH,
Willemsen G,
Zagato L,
Zgaga L,
Zitting P,
Alavere H,
Farrall M,
McArdle WL,
Nelis M,
Peters MJ,
Ripatti S,
van Meurs JB,
Aben KK,
Ardlie KG,
Beckmann JS,
Beilby JP,
Bergman RN,
Bergmann S,
Collins FS,
Cusi D,
den Heijer M,
Eiriksdottir G,
Gejman PV,
Hall AS,
Hamsten A,
Huikuri HV,
Iribarren C,
Kähönen M,
Kaprio J,
Kathiresan S,
Kiemeney L,
Kocher T,
Launer LJ,
Lehtimäki T,
Melander O,
Mosley TH Jr,
Musk AW,
Nieminen MS,
O'Donnell CJ,
Ohlsson C,
Oostra B,
Palmer LJ,
Raitakari O,
Ridker PM,
Rioux JD,
Rissanen A,
Rivolta C,
Schunkert H,
Shuldiner AR,
Siscovick DS,
Stumvoll M,
Tönjes A,
Tuomilehto J,
van Ommen GJ,
Viikari J,
Heath AC,
Martin NG,
Montgomery GW,
Province MA,
Kayser M,
Arnold AM,
Atwood LD,
Boerwinkle E,
Chanock SJ,
Deloukas P,
Gieger C,
Grönberg H,
Hall P,
Hattersley AT,
Hengstenberg C,
Hoffman W,
Lathrop GM,
Salomaa V,
Schreiber S,
Uda M,
Waterworth D,
Wright AF,
Assimes TL,
Barroso I,
Hofman A,
Mohlke KL,
Boomsma DI,
Caulfield MJ,
Cupples LA,
Erdmann J,
Fox CS,
Gudnason V,
Gyllensten U,
Harris TB,
Hayes RB,
Jarvelin MR,
Mooser V,
Munroe PB,
Ouwehand WH,
Penninx BW,
Pramstaller PP,
Quertermous T,
Rudan I,
Samani NJ,
Spector TD,
Völzke H,
Watkins H,
Wilson JF,
Groop LC,
Haritunians T,
Hu FB,
Kaplan RC,
Metspalu A,
North KE,
Schlessinger D,
Wareham NJ,
Hunter DJ,
O'Connell JR,
Strachan DP,
Wichmann HE,
Borecki IB,
van Duijn CM,
Schadt EE,
Thorsteinsdottir U,
Peltonen L,
Uitterlinden AG,
Visscher PM,
Chatterjee N,
Loos RJ,
Boehnke M,
McCarthy MI,
Ingelsson E,
Lindgren CM,
Abecasis GR,
Stefansson K,
Frayling TM,
Hirschhorn JN
Nature · 2010 · PMID 20881960 · open access
12 pages+
Genetics of rheumatoid arthritis contributes to biology and drug discovery
Okada Y,
Wu D,
Trynka G,
Raj T,
Terao C,
Ikari K,
Kochi Y,
Ohmura K,
Suzuki A,
Yoshida S,
Graham RR,
Manoharan A
and 83 more — show all
Ortmann W,
Bhangale T,
Denny JC,
Carroll RJ,
Eyler AE,
Greenberg JD,
Kremer JM,
Pappas DA,
Jiang L,
Yin J,
Ye L,
Su DF,
Yang J,
Xie G,
Keystone E,
Westra HJ,
Esko T,
Metspalu A,
Zhou X,
Gupta N,
Mirel D,
Stahl EA,
Diogo D,
Cui J,
Liao K,
Guo MH,
Myouzen K,
Kawaguchi T,
Coenen MJ,
van Riel PL,
van de Laar MA,
Guchelaar HJ,
Huizinga TW,
Dieudé P,
Mariette X,
Bridges SL Jr,
Zhernakova A,
Toes RE,
Tak PP,
Miceli-Richard C,
Bang SY,
Lee HS,
Martin J,
Gonzalez-Gay MA,
Rodriguez-Rodriguez L,
Rantapää-Dahlqvist S,
Arlestig L,
Choi HK,
Kamatani Y,
Galan P,
Lathrop M,
Eyre S,
Bowes J,
Barton A,
de Vries N,
Moreland LW,
Criswell LA,
Karlson EW,
Taniguchi A,
Yamada R,
Kubo M,
Liu JS,
Bae SC,
Worthington J,
Padyukov L,
Klareskog L,
Gregersen PK,
Raychaudhuri S,
Stranger BE,
De Jager PL,
Franke L,
Visscher PM,
Brown MA,
Yamanaka H,
Mimori T,
Takahashi A,
Xu H,
Behrens TW,
Siminovitch KA,
Momohara S,
Matsuda F,
Yamamoto K,
Plenge RM
RACI consortium · GARNET consortium
Nature · 2014 · PMID 24390342 · open access
12 pages+
A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci
Chang D,
Nalls MA,
Hallgrímsdóttir IB,
Hunkapiller J,
van der Brug M,
Cai F,
Kerchner GA,
Ayalon G,
Bingol B,
Sheng M,
Hinds D,
Behrens TW
and 3 more — show all
International Parkinson's Disease Genomics Consortium · 23andMe Research Team
Nature genetics · 2017 · PMID 28892059
3 pages
Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes
Sobrin L,
Ripke S,
Yu Y,
Fagerness J,
Bhangale TR,
Tan PL,
Souied EH,
Buitendijk GH,
Merriam JE,
Richardson AJ,
Raychaudhuri S,
Reynolds R
and 22 more — show all
Chin KA,
Lee AY,
Leveziel N,
Zack DJ,
Campochiaro P,
Smith RT,
Barile GR,
Hogg RE,
Chakravarthy U,
Behrens TW,
Uitterlinden AG,
van Duijn CM,
Vingerling JR,
Brantley MA Jr,
Baird PN,
Klaver CC,
Allikmets R,
Katsanis N,
Graham RR,
Ioannidis JP,
Daly MJ,
Seddon JM
Ophthalmology · 2012 · PMID 22705344
2 pages
Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency
Bronson PG,
Chang D,
Bhangale T,
Seldin MF,
Ortmann W,
Ferreira RC,
Urcelay E,
Pereira LF,
Martin J,
Plebani A,
Lougaris V,
Friman V
and 7 more — show all
Nature genetics · 2016 · PMID 27723758 · open access
2 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.