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2,657 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.
7 matches for
Louis E.
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
Franke A,
McGovern DP,
Barrett JC,
Wang K,
Radford-Smith GL,
Ahmad T,
Lees CW,
Balschun T,
Lee J,
Roberts R,
Anderson CA,
Bis JC
and 84 more — show all
Bumpstead S,
Ellinghaus D,
Festen EM,
Georges M,
Green T,
Haritunians T,
Jostins L,
Latiano A,
Mathew CG,
Montgomery GW,
Prescott NJ,
Raychaudhuri S,
Rotter JI,
Schumm P,
Sharma Y,
Simms LA,
Taylor KD,
Whiteman D,
Wijmenga C,
Baldassano RN,
Barclay M,
Bayless TM,
Brand S,
Büning C,
Cohen A,
Colombel JF,
Cottone M,
Stronati L,
Denson T,
De Vos M,
D'Inca R,
Dubinsky M,
Edwards C,
Florin T,
Franchimont D,
Gearry R,
Glas J,
Van Gossum A,
Guthery SL,
Halfvarson J,
Verspaget HW,
Hugot JP,
Karban A,
Laukens D,
Lawrance I,
Lemann M,
Levine A,
Libioulle C,
Louis E,
Mowat C,
Newman W,
Panés J,
Phillips A,
Proctor DD,
Regueiro M,
Russell R,
Rutgeerts P,
Sanderson J,
Sans M,
Seibold F,
Steinhart AH,
Stokkers PC,
Torkvist L,
Kullak-Ublick G,
Wilson D,
Walters T,
Targan SR,
Brant SR,
Rioux JD,
D'Amato M,
Weersma RK,
Kugathasan S,
Griffiths AM,
Mansfield JC,
Vermeire S,
Duerr RH,
Silverberg MS,
Satsangi J,
Schreiber S,
Cho JH,
Annese V,
Hakonarson H,
Daly MJ,
Parkes M
Nature genetics · 2010 · PMID 21102463
12 pages+
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
Anderson CA,
Boucher G,
Lees CW,
Franke A,
D'Amato M,
Taylor KD,
Lee JC,
Goyette P,
Imielinski M,
Latiano A,
Lagacé C,
Scott R
and 101 more — show all
Amininejad L,
Bumpstead S,
Baidoo L,
Baldassano RN,
Barclay M,
Bayless TM,
Brand S,
Büning C,
Colombel JF,
Denson LA,
De Vos M,
Dubinsky M,
Edwards C,
Ellinghaus D,
Fehrmann RS,
Floyd JA,
Florin T,
Franchimont D,
Franke L,
Georges M,
Glas J,
Glazer NL,
Guthery SL,
Haritunians T,
Hayward NK,
Hugot JP,
Jobin G,
Laukens D,
Lawrance I,
Lémann M,
Levine A,
Libioulle C,
Louis E,
McGovern DP,
Milla M,
Montgomery GW,
Morley KI,
Mowat C,
Ng A,
Newman W,
Ophoff RA,
Papi L,
Palmieri O,
Peyrin-Biroulet L,
Panés J,
Phillips A,
Prescott NJ,
Proctor DD,
Roberts R,
Russell R,
Rutgeerts P,
Sanderson J,
Sans M,
Schumm P,
Seibold F,
Sharma Y,
Simms LA,
Seielstad M,
Steinhart AH,
Targan SR,
van den Berg LH,
Vatn M,
Verspaget H,
Walters T,
Wijmenga C,
Wilson DC,
Westra HJ,
Xavier RJ,
Zhao ZZ,
Ponsioen CY,
Andersen V,
Torkvist L,
Gazouli M,
Anagnou NP,
Karlsen TH,
Kupcinskas L,
Sventoraityte J,
Mansfield JC,
Kugathasan S,
Silverberg MS,
Halfvarson J,
Rotter JI,
Mathew CG,
Griffiths AM,
Gearry R,
Ahmad T,
Brant SR,
Chamaillard M,
Satsangi J,
Cho JH,
Schreiber S,
Daly MJ,
Barrett JC,
Parkes M,
Annese V,
Hakonarson H,
Radford-Smith G,
Duerr RH,
Vermeire S,
Weersma RK,
Rioux JD
Nature genetics · 2011 · PMID 21297633 · open access
12 pages+
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
Jostins L,
Ripke S,
Weersma RK,
Duerr RH,
McGovern DP,
Hui KY,
Lee JC,
Schumm LP,
Sharma Y,
Anderson CA,
Essers J,
Mitrovic M
and 94 more — show all
Ning K,
Cleynen I,
Theatre E,
Spain SL,
Raychaudhuri S,
Goyette P,
Wei Z,
Abraham C,
Achkar JP,
Ahmad T,
Amininejad L,
Ananthakrishnan AN,
Andersen V,
Andrews JM,
Baidoo L,
Balschun T,
Bampton PA,
Bitton A,
Boucher G,
Brand S,
Büning C,
Cohain A,
Cichon S,
D'Amato M,
De Jong D,
Devaney KL,
Dubinsky M,
Edwards C,
Ellinghaus D,
Ferguson LR,
Franchimont D,
Fransen K,
Gearry R,
Georges M,
Gieger C,
Glas J,
Haritunians T,
Hart A,
Hawkey C,
Hedl M,
Hu X,
Karlsen TH,
Kupcinskas L,
Kugathasan S,
Latiano A,
Laukens D,
Lawrance IC,
Lees CW,
Louis E,
Mahy G,
Mansfield J,
Morgan AR,
Mowat C,
Newman W,
Palmieri O,
Ponsioen CY,
Potocnik U,
Prescott NJ,
Regueiro M,
Rotter JI,
Russell RK,
Sanderson JD,
Sans M,
Satsangi J,
Schreiber S,
Simms LA,
Sventoraityte J,
Targan SR,
Taylor KD,
Tremelling M,
Verspaget HW,
De Vos M,
Wijmenga C,
Wilson DC,
Winkelmann J,
Xavier RJ,
Zeissig S,
Zhang B,
Zhang CK,
Zhao H,
Silverberg MS,
Annese V,
Hakonarson H,
Brant SR,
Radford-Smith G,
Mathew CG,
Rioux JD,
Schadt EE,
Daly MJ,
Franke A,
Parkes M,
Vermeire S,
Barrett JC,
Cho JH
International IBD Genetics Consortium (IIBDGC)
Nature · 2012 · PMID 23128233 · open access
12 pages+
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
Barrett JC,
Hansoul S,
Nicolae DL,
Cho JH,
Duerr RH,
Rioux JD,
Brant SR,
Silverberg MS,
Taylor KD,
Barmada MM,
Bitton A,
Dassopoulos T
and 49 more — show all
Datta LW,
Green T,
Griffiths AM,
Kistner EO,
Murtha MT,
Regueiro MD,
Rotter JI,
Schumm LP,
Steinhart AH,
Targan SR,
Xavier RJ,
Libioulle C,
Sandor C,
Lathrop M,
Belaiche J,
Dewit O,
Gut I,
Heath S,
Laukens D,
Mni M,
Rutgeerts P,
Van Gossum A,
Zelenika D,
Franchimont D,
Hugot JP,
de Vos M,
Vermeire S,
Louis E,
Cardon LR,
Anderson CA,
Drummond H,
Nimmo E,
Ahmad T,
Prescott NJ,
Onnie CM,
Fisher SA,
Marchini J,
Ghori J,
Bumpstead S,
Gwilliam R,
Tremelling M,
Deloukas P,
Mansfield J,
Jewell D,
Satsangi J,
Mathew CG,
Parkes M,
Georges M,
Daly MJ
NIDDK IBD Genetics Consortium · Belgian-French IBD Consortium and 1 more consortia
Nature genetics · 2008 · PMID 18587394
11 pages
Genome-wide association study in essential tremor identifies three new loci
Müller SH,
Girard SL,
Hopfner F,
Merner ND,
Bourassa CV,
Lorenz D,
Clark LN,
Tittmann L,
Soto-Ortolaza AI,
Klebe S,
Hallett M,
Schneider SA
and 37 more — show all
Hodgkinson CA,
Lieb W,
Wszolek ZK,
Pendziwiat M,
Lorenzo-Betancor O,
Poewe W,
Ortega-Cubero S,
Seppi K,
Rajput A,
Hussl A,
Rajput AH,
Berg D,
Dion PA,
Wurster I,
Shulman JM,
Srulijes K,
Haubenberger D,
Pastor P,
Vilariño-Güell C,
Postuma RB,
Bernard G,
Ladwig KH,
Dupré N,
Jankovic J,
Strauch K,
Panisset M,
Winkelmann J,
Testa CM,
Reischl E,
Zeuner KE,
Ross OA,
Arzberger T,
Chouinard S,
Deuschl G,
Louis ED,
Kuhlenbäumer G,
Rouleau GA
Brain : a journal of neurology · 2016 · PMID 27797806 · open access
4 pages
Defining the genetic control of human blood plasma N-glycome using genome-wide association study
Sharapov SZ,
Tsepilov YA,
Klaric L,
Mangino M,
Thareja G,
Shadrina AS,
Simurina M,
Dagostino C,
Dmitrieva J,
Vilaj M,
Vuckovic F,
Pavic T
and 20 more — show all
Stambuk J,
Stambuk J,
Trbojevic-Akmacic I,
Kristic J,
Simunovic J,
Momcilovic A,
Campbell H,
Doherty M,
Dunlop MG,
Farrington SM,
Pucic-Bakovic M,
Gieger C,
Allegri M,
Louis E,
Georges M,
Suhre K,
Spector T,
Williams FMK,
Lauc G,
Aulchenko YS
Human molecular genetics · 2019 · PMID 31163085
1 page
Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis
Liao C,
Castonguay CE,
Heilbron K,
Vuokila V,
Medeiros M,
Houle G,
Akçimen F,
Ross JP,
Catoire H,
Diez-Fairen M,
Kang J,
Mueller SH
and 36 more — show all
Girard SL,
Hopfner F,
Lorenz D,
Clark LN,
Soto-Beasley AI,
Klebe S,
Hallett M,
Wszolek ZK,
Pendziwiat M,
Lorenzo-Betancor O,
Seppi K,
Berg D,
Vilariño-Güell C,
Postuma RB,
Bernard G,
Dupré N,
Jankovic J,
Testa CM,
Ross OA,
Arzberger T,
Chouinard S,
Louis ED,
Mandich P,
Vitale C,
Barone P,
García-Martín E,
Alonso-Navarro H,
Agúndez JAG,
Jiménez-Jiménez FJ,
Pastor P,
Rajput A,
Deuschl G,
Kuhlenbaümer G,
Meijer IA,
Dion PA,
Rouleau GA
23andMe Research Team
JAMA neurology · 2022 · PMID 34982113 · 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.