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2,652 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
Landers J.
Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression
Craig JE,
Han X,
Qassim A,
Hassall M,
Cooke Bailey JN,
Kinzy TG,
Khawaja AP,
An J,
Marshall H,
Gharahkhani P,
Igo RP Jr,
Graham SL
and 47 more — show all
Healey PR,
Ong JS,
Zhou T,
Siggs O,
Law MH,
Souzeau E,
Ridge B,
Hysi PG,
Burdon KP,
Mills RA,
Landers J,
Ruddle JB,
Agar A,
Galanopoulos A,
White AJR,
Willoughby CE,
Andrew NH,
Best S,
Vincent AL,
Goldberg I,
Radford-Smith G,
Martin NG,
Montgomery GW,
Vitart V,
Hoehn R,
Wojciechowski R,
Jonas JB,
Aung T,
Pasquale LR,
Cree AJ,
Sivaprasad S,
Vallabh NA,
Viswanathan AC,
Pasutto F,
Haines JL,
Klaver CCW,
van Duijn CM,
Casson RJ,
Foster PJ,
Khaw PT,
Hammond CJ,
Mackey DA,
Mitchell P,
Lotery AJ,
Wiggs JL,
Hewitt AW,
MacGregor S
NEIGHBORHOOD consortium · UK Biobank Eye and Vision Consortium
Nature genetics · 2020 · PMID 31959993
12 pages+
Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
MacGregor S,
Ong JS,
An J,
Han X,
Zhou T,
Siggs OM,
Law MH,
Souzeau E,
Sharma S,
Lynn DJ,
Beesley J,
Sheldrick B
and 20 more — show all
Mills RA,
Landers J,
Ruddle JB,
Graham SL,
Healey PR,
White AJR,
Casson RJ,
Best S,
Grigg JR,
Goldberg I,
Powell JE,
Whiteman DC,
Radford-Smith GL,
Martin NG,
Montgomery GW,
Burdon KP,
Mackey DA,
Gharahkhani P,
Craig JE,
Hewitt AW
Nature genetics · 2018 · PMID 30054594
10 pages
Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma
Gharahkhani P,
Burdon KP,
Fogarty R,
Sharma S,
Hewitt AW,
Martin S,
Law MH,
Cremin K,
Bailey JNC,
Loomis SJ,
Pasquale LR,
Haines JL
and 30 more — show all
Hauser MA,
Viswanathan AC,
McGuffin P,
Topouzis F,
Foster PJ,
Graham SL,
Casson RJ,
Chehade M,
White AJ,
Zhou T,
Souzeau E,
Landers J,
Fitzgerald JT,
Klebe S,
Ruddle JB,
Goldberg I,
Healey PR,
Mills RA,
Wang JJ,
Montgomery GW,
Martin NG,
RadfordSmith G,
Whiteman DC,
Brown MA,
Brown MA,
Wiggs JL,
Mackey DA,
Mitchell P,
MacGregor S,
Craig JE
Wellcome Trust Case Control Consortium 2, NEIGHBORHOOD consortium
Nature genetics · 2014 · PMID 25173105 · open access
3 pages
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
van Rheenen W,
van der Spek RAA,
Bakker MK,
van Vugt JJFA,
Hop PJ,
Zwamborn RAJ,
de Klein N,
Westra HJ,
Bakker OB,
Deelen P,
Shireby G,
Hannon E
and 180 more — show all
Moisse M,
Baird D,
Restuadi R,
Dolzhenko E,
Dekker AM,
Gawor K,
Westeneng HJ,
Tazelaar GHP,
van Eijk KR,
Kooyman M,
Byrne RP,
Doherty M,
Heverin M,
Al Khleifat A,
Iacoangeli A,
Shatunov A,
Ticozzi N,
Cooper-Knock J,
Smith BN,
Gromicho M,
Chandran S,
Pal S,
Morrison KE,
Shaw PJ,
Hardy J,
Orrell RW,
Sendtner M,
Meyer T,
Başak N,
van der Kooi AJ,
Ratti A,
Fogh I,
Gellera C,
Lauria G,
Corti S,
Cereda C,
Sproviero D,
D'Alfonso S,
Sorarù G,
Siciliano G,
Filosto M,
Padovani A,
Chiò A,
Calvo A,
Moglia C,
Brunetti M,
Canosa A,
Grassano M,
Beghi E,
Pupillo E,
Logroscino G,
Nefussy B,
Osmanovic A,
Nordin A,
Lerner Y,
Zabari M,
Gotkine M,
Baloh RH,
Bell S,
Vourc'h P,
Corcia P,
Couratier P,
Millecamps S,
Meininger V,
Salachas F,
Mora Pardina JS,
Assialioui A,
Rojas-García R,
Dion PA,
Ross JP,
Ludolph AC,
Weishaupt JH,
Brenner D,
Freischmidt A,
Bensimon G,
Brice A,
Durr A,
Payan CAM,
Saker-Delye S,
Wood NW,
Topp S,
Rademakers R,
Tittmann L,
Lieb W,
Franke A,
Ripke S,
Braun A,
Kraft J,
Whiteman DC,
Olsen CM,
Uitterlinden AG,
Hofman A,
Rietschel M,
Cichon S,
Nöthen MM,
Amouyel P,
Traynor BJ,
Singleton AB,
Mitne Neto M,
Cauchi RJ,
Ophoff RA,
Wiedau-Pazos M,
Lomen-Hoerth C,
van Deerlin VM,
Grosskreutz J,
Roediger A,
Gaur N,
Jörk A,
Barthel T,
Theele E,
Ilse B,
Stubendorff B,
Witte OW,
Steinbach R,
Hübner CA,
Graff C,
Brylev L,
Fominykh V,
Demeshonok V,
Ataulina A,
Rogelj B,
Koritnik B,
Zidar J,
Ravnik-Glavač M,
Glavač D,
Stević Z,
Drory V,
Povedano M,
Blair IP,
Kiernan MC,
Benyamin B,
Henderson RD,
Furlong S,
Mathers S,
McCombe PA,
Needham M,
Ngo ST,
Nicholson GA,
Pamphlett R,
Rowe DB,
Steyn FJ,
Williams KL,
Mather KA,
Sachdev PS,
Henders AK,
Wallace L,
de Carvalho M,
Pinto S,
Petri S,
Weber M,
Rouleau GA,
Silani V,
Curtis CJ,
Breen G,
Glass JD,
Brown RH Jr,
Landers JE,
Shaw CE,
Andersen PM,
Groen EJN,
van Es MA,
Pasterkamp RJ,
Fan D,
Garton FC,
McRae AF,
Davey Smith G,
Gaunt TR,
Eberle MA,
Mill J,
McLaughlin RL,
Hardiman O,
Kenna KP,
Wray NR,
Tsai E,
Runz H,
Franke L,
Al-Chalabi A,
Van Damme P,
van den Berg LH,
Veldink JH
SLALOM Consortium · PARALS Consortium and 2 more consortia
Nature genetics · 2021 · PMID 34873335 · open access
3 pages
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis
Fogh I,
Ratti A,
Gellera C,
Lin K,
Tiloca C,
Moskvina V,
Corrado L,
Sorarù G,
Cereda C,
Corti S,
Gentilini D,
Calini D
and 53 more — show all
Castellotti B,
Mazzini L,
Querin G,
Gagliardi S,
Del Bo R,
Conforti FL,
Siciliano G,
Inghilleri M,
Saccà F,
Bongioanni P,
Penco S,
Corbo M,
Sorbi S,
Filosto M,
Ferlini A,
Di Blasio AM,
Signorini S,
Shatunov A,
Jones A,
Shaw PJ,
Morrison KE,
Farmer AE,
Van Damme P,
Robberecht W,
Chiò A,
Traynor BJ,
Sendtner M,
Melki J,
Meininger V,
Hardiman O,
Andersen PM,
Leigh NP,
Glass JD,
Overste D,
Diekstra FP,
Veldink JH,
van Es MA,
Shaw CE,
Weale ME,
Lewis CM,
Williams J,
Brown RH,
Landers JE,
Ticozzi N,
Ceroni M,
Pegoraro E,
Comi GP,
D'Alfonso S,
van den Berg LH,
Taroni F,
Al-Chalabi A,
Powell J,
Silani V
SLAGEN Consortium and Collaborators
Human molecular genetics · 2014 · PMID 24256812
2 pages
Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process
Springelkamp H,
Höhn R,
Mishra A,
Hysi PG,
Khor CC,
Loomis SJ,
Bailey JN,
Gibson J,
Thorleifsson G,
Janssen SF,
Luo X,
Ramdas WD
and 66 more — show all
Vithana E,
Nongpiur ME,
Montgomery GW,
Xu L,
Mountain JE,
Gharahkhani P,
Lu Y,
Amin N,
Karssen LC,
Sim KS,
van Leeuwen EM,
Iglesias AI,
Verhoeven VJ,
Hauser MA,
Loon SC,
Despriet DD,
Nag A,
Venturini C,
Sanfilippo PG,
Schillert A,
Kang JH,
Landers J,
Jonasson F,
Cree AJ,
van Koolwijk LM,
Rivadeneira F,
Souzeau E,
Jonsson V,
Menon G,
Weinreb RN,
de Jong PT,
Oostra BA,
Uitterlinden AG,
Hofman A,
Ennis S,
Thorsteinsdottir U,
Burdon KP,
Spector TD,
Mirshahi A,
Saw SM,
Vingerling JR,
Teo YY,
Haines JL,
Wolfs RC,
Lemij HG,
Tai ES,
Jansonius NM,
Jonas JB,
Cheng CY,
Aung T,
Viswanathan AC,
Klaver CC,
Craig JE,
Macgregor S,
Mackey DA,
Lotery AJ,
Stefansson K,
Bergen AA,
Young TL,
Wiggs JL,
Pfeiffer N,
Wong TY,
Pasquale LR,
Hewitt AW,
van Duijn CM,
Hammond CJ
Blue Mountains Eye Study—GWAS group · NEIGHBORHOOD Consortium and 1 more consortia
Nature communications · 2014 · PMID 25241763 · open access
2 pages
Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Gharahkhani P,
Burdon KP,
Cooke Bailey JN,
Hewitt AW,
Law MH,
Pasquale LR,
Kang JH,
Haines JL,
Souzeau E,
Zhou T,
Siggs OM,
Landers J
and 27 more — show all
Awadalla M,
Sharma S,
Mills RA,
Ridge B,
Lynn D,
Casson R,
Graham SL,
Goldberg I,
White A,
Healey PR,
Grigg J,
Lawlor M,
Mitchell P,
Ruddle J,
Coote M,
Walland M,
Best S,
Vincent A,
Gale J,
RadfordSmith G,
Whiteman DC,
Montgomery GW,
Martin NG,
Mackey DA,
Wiggs JL,
MacGregor S,
Craig JE
NEIGHBORHOOD consortium
Scientific reports · 2018 · PMID 29449654 · 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.