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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.
5 matches for
Newman WG.
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations
Liu JZ,
van Sommeren S,
Huang H,
Ng SC,
Alberts R,
Takahashi A,
Ripke S,
Lee JC,
Jostins L,
Shah T,
Abedian S,
Cheon JH
and 28 more — show all
Cho J,
Dayani NE,
Franke L,
Fuyuno Y,
Hart A,
Juyal RC,
Juyal G,
Kim WH,
Morris AP,
Poustchi H,
Newman WG,
Midha V,
Orchard TR,
Vahedi H,
Sood A,
Sung JY,
Malekzadeh R,
Westra HJ,
Yamazaki K,
Yang SK,
Barrett JC,
Alizadeh BZ,
Parkes M,
Bk T,
Daly MJ,
Kubo M,
Anderson CA,
Weersma RK
International Multiple Sclerosis Genetics Consortium · International IBD Genetics Consortium
Nature genetics · 2015 · PMID 26192919
12 pages+
Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease
de Lange KM,
Moutsianas L,
Lee JC,
Lamb CA,
Luo Y,
Kennedy NA,
Jostins L,
Rice DL,
Gutierrez-Achury J,
Ji SG,
Heap G,
Nimmo ER
and 20 more — show all
Edwards C,
Henderson P,
Mowat C,
Sanderson J,
Satsangi J,
Simmons A,
Wilson DC,
Tremelling M,
Hart A,
Mathew CG,
Newman WG,
Parkes M,
Lees CW,
Uhlig H,
Hawkey C,
Prescott NJ,
Ahmad T,
Mansfield JC,
Anderson CA,
Barrett JC
Nature genetics · 2017 · PMID 28067908 · open access
12 pages+
Genome-wide and transcriptome-wide association studies of mammographic density phenotypes reveal novel loci
Chen H,
Fan S,
Stone J,
Thompson DJ,
Douglas J,
Li S,
Scott C,
Bolla MK,
Wang Q,
Dennis J,
Michailidou K,
Li C
and 44 more — show all
Peters U,
Hopper JL,
Southey MC,
Nguyen-Dumont T,
Nguyen TL,
Fasching PA,
Behrens A,
Cadby G,
Murphy RA,
Aronson K,
Howell A,
Astley S,
Couch F,
Olson J,
Milne RL,
Giles GG,
Haiman CA,
Maskarinec G,
Winham S,
John EM,
Kurian A,
Eliassen H,
Andrulis I,
Evans DG,
Newman WG,
Hall P,
Czene K,
Swerdlow A,
Jones M,
Pollan M,
Fernandez-Navarro P,
McConnell DS,
Kristensen VN,
Rothstein JH,
Wang P,
Habel LA,
Sieh W,
Dunning AM,
Pharoah PDP,
Easton DF,
Gierach GL,
Tamimi RM,
Vachon CM,
Lindström S
NBCS Investigators
Breast cancer research : BCR · 2022 · PMID 35414113 · open access
12 pages+
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
Zhang H,
Ahearn TU,
Lecarpentier J,
Barnes D,
Beesley J,
Qi G,
Jiang X,
O'Mara TA,
Zhao N,
Bolla MK,
Dunning AM,
Dennis J
and 261 more — show all
Wang Q,
Ful ZA,
Aittomäki K,
Andrulis IL,
Anton-Culver H,
Arndt V,
Aronson KJ,
Arun BK,
Auer PL,
Azzollini J,
Barrowdale D,
Becher H,
Beckmann MW,
Behrens S,
Benitez J,
Bermisheva M,
Bialkowska K,
Blanco A,
Blomqvist C,
Bogdanova NV,
Bojesen SE,
Bonanni B,
Bondavalli D,
Borg A,
Brauch H,
Brenner H,
Briceno I,
Broeks A,
Brucker SY,
Brüning T,
Burwinkel B,
Buys SS,
Byers H,
Caldés T,
Caligo MA,
Calvello M,
Campa D,
Castelao JE,
Chang-Claude J,
Chanock SJ,
Christiaens M,
Christiansen H,
Chung WK,
Claes KBM,
Clarke CL,
Cornelissen S,
Couch FJ,
Cox A,
Cross SS,
Czene K,
Daly MB,
Devilee P,
Diez O,
Domchek SM,
Dörk T,
Dwek M,
Eccles DM,
Ekici AB,
Evans DG,
Fasching PA,
Figueroa J,
Foretova L,
Fostira F,
Friedman E,
Frost D,
Gago-Dominguez M,
Gapstur SM,
Garber J,
García-Sáenz JA,
Gaudet MM,
Gayther SA,
Giles GG,
Godwin AK,
Goldberg MS,
Goldgar DE,
González-Neira A,
Greene MH,
Gronwald J,
Guénel P,
Häberle L,
Hahnen E,
Haiman CA,
Hake CR,
Hall P,
Hamann U,
Harkness EF,
Heemskerk-Gerritsen BAM,
Hillemanns P,
Hogervorst FBL,
Holleczek B,
Hollestelle A,
Hooning MJ,
Hoover RN,
Hopper JL,
Howell A,
Huebner H,
Hulick PJ,
Imyanitov EN,
Isaacs C,
Izatt L,
Jager A,
Jakimovska M,
Jakubowska A,
James P,
Janavicius R,
Janni W,
John EM,
Jones ME,
Jung A,
Kaaks R,
Kapoor PM,
Karlan BY,
Keeman R,
Khan S,
Khusnutdinova E,
Kitahara CM,
Ko YD,
Konstantopoulou I,
Koppert LB,
Koutros S,
Kristensen VN,
Laenkholm AV,
Lambrechts D,
Larsson SC,
Laurent-Puig P,
Lazaro C,
Lazarova E,
Lejbkowicz F,
Leslie G,
Lesueur F,
Lindblom A,
Lissowska J,
Lo WY,
Loud JT,
Lubinski J,
Lukomska A,
MacInnis RJ,
Mannermaa A,
Manoochehri M,
Manoukian S,
Margolin S,
Martinez ME,
Matricardi L,
McGuffog L,
McLean C,
Mebirouk N,
Meindl A,
Menon U,
Miller A,
Mingazheva E,
Montagna M,
Mulligan AM,
Mulot C,
Muranen TA,
Nathanson KL,
Neuhausen SL,
Nevanlinna H,
Neven P,
Newman WG,
Nielsen FC,
Nikitina-Zake L,
Nodora J,
Offit K,
Olah E,
Olopade OI,
Olsson H,
Orr N,
Papi L,
Papp J,
Park-Simon TW,
Parsons MT,
Peissel B,
Peixoto A,
Peshkin B,
Peterlongo P,
Peto J,
Phillips KA,
Piedmonte M,
Plaseska-Karanfilska D,
Prajzendanc K,
Prentice R,
Prokofyeva D,
Rack B,
Radice P,
Ramus SJ,
Rantala J,
Rashid MU,
Rennert G,
Rennert HS,
Risch HA,
Romero A,
Rookus MA,
Rübner M,
Rüdiger T,
Saloustros E,
Sampson S,
Sandler DP,
Sawyer EJ,
Scheuner MT,
Schmutzler RK,
Schneeweiss A,
Schoemaker MJ,
Schöttker B,
Schürmann P,
Senter L,
Sharma P,
Sherman ME,
Shu XO,
Singer CF,
Smichkoska S,
Soucy P,
Southey MC,
Spinelli JJ,
Stone J,
Stoppa-Lyonnet D,
Swerdlow AJ,
Szabo CI,
Tamimi RM,
Tapper WJ,
Taylor JA,
Teixeira MR,
Terry M,
Thomassen M,
Thull DL,
Tischkowitz M,
Toland AE,
Tollenaar RAEM,
Tomlinson I,
Torres D,
Troester MA,
Truong T,
Tung N,
Untch M,
Vachon CM,
van den Ouweland AMW,
van der Kolk LE,
van Veen EM,
vanRensburg EJ,
Vega A,
Wappenschmidt B,
Weinberg CR,
Weitzel JN,
Wildiers H,
Winqvist R,
Wolk A,
Yang XR,
Yannoukakos D,
Zheng W,
Zheng W,
Zorn KK,
Milne RL,
Kraft P,
Simard J,
Pharoah PDP,
Michailidou K,
Antoniou AC,
Schmidt MK,
Chenevix-Trench G,
Easton DF,
Chatterjee N,
García-Closas M
kConFab Investigators · ABCTB Investigators and 2 more consortia
Nature genetics · 2020 · PMID 32424353 · open access
2 pages
Clinical Pharmacogenetics Implementation Consortium Guideline for the Use of Aminoglycosides Based on MT-RNR1 Genotype
McDermott JH,
Wolf J,
Hoshitsuki K,
Huddart R,
Caudle KE,
Whirl-Carrillo M,
Steyger PS,
Smith RJH,
Cody N,
Rodriguez-Antona C,
Klein TE,
Newman WG
Clinical pharmacology and therapeutics · 2022 · PMID 34032273
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.