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2,649 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.
10 matches for
Johnson JA.
Genome-Wide Association Approach Identified Novel Genetic Predictors of Heart Rate Response to β-Blockers
Shahin MH,
Conrado DJ,
Gonzalez D,
Gong Y,
Lobmeyer MT,
Beitelshees AL,
Boerwinkle E,
Gums JG,
Chapman A,
Turner ST,
Cooper-DeHoff RM,
Johnson JA
Journal of the American Heart Association · 2018 · PMID 29478026 · open access
11 pages
The major genetic determinants of HIV-1 control affect HLA class I peptide presentation
Pereyra F,
Jia X,
McLaren PJ,
Telenti A,
de Bakker PI,
Walker BD,
Ripke S,
Brumme CJ,
Pulit SL,
Carrington M,
Kadie CM,
Carlson JM
and 326 more — show all
Heckerman D,
Graham RR,
Plenge RM,
Deeks SG,
Gianniny L,
Crawford G,
Sullivan J,
Gonzalez E,
Davies L,
Camargo A,
Moore JM,
Beattie N,
Gupta S,
Crenshaw A,
Burtt NP,
Guiducci C,
Gupta N,
Gao X,
Qi Y,
Yuki Y,
Piechocka-Trocha A,
Cutrell E,
Rosenberg R,
Moss KL,
Lemay P,
O'Leary J,
Schaefer T,
Verma P,
Toth I,
Block B,
Baker B,
Rothchild A,
Lian J,
Proudfoot J,
Alvino DM,
Vine S,
Addo MM,
Allen TM,
Altfeld M,
Henn MR,
Le Gall S,
Streeck H,
Haas DW,
Kuritzkes DR,
Robbins GK,
Shafer RW,
Gulick RM,
Shikuma CM,
Haubrich R,
Riddler S,
Sax PE,
Daar ES,
Ribaudo HJ,
Agan B,
Agarwal S,
Ahern RL,
Allen BL,
Altidor S,
Altschuler EL,
Ambardar S,
Anastos K,
Anderson B,
Anderson V,
Andrady U,
Antoniskis D,
Bangsberg D,
Barbaro D,
Barrie W,
Bartczak J,
Barton S,
Basden P,
Basgoz N,
Bazner S,
Bellos NC,
Benson AM,
Berger J,
Bernard NF,
Bernard AM,
Birch C,
Bodner SJ,
Bolan RK,
Boudreaux ET,
Bradley M,
Braun JF,
Brndjar JE,
Brown SJ,
Brown K,
Brown ST,
Burack J,
Bush LM,
Cafaro V,
Campbell O,
Campbell J,
Carlson RH,
Carmichael JK,
Casey KK,
Cavacuiti C,
Celestin G,
Chambers ST,
Chez N,
Chirch LM,
Cimoch PJ,
Cohen D,
Cohn LE,
Conway B,
Cooper DA,
Cornelson B,
Cox DT,
Cristofano MV,
Cuchural G Jr,
Czartoski JL,
Dahman JM,
Daly JS,
Davis BT,
Davis K,
Davod SM,
DeJesus E,
Dietz CA,
Dunham E,
Dunn ME,
Ellerin TB,
Eron JJ,
Fangman JJ,
Farel CE,
Ferlazzo H,
Fidler S,
Fleenor-Ford A,
Frankel R,
Freedberg KA,
French NK,
Fuchs JD,
Fuller JD,
Gaberman J,
Gallant JE,
Gandhi RT,
Garcia E,
Garmon D,
Gathe JC Jr,
Gaultier CR,
Gebre W,
Gilman FD,
Gilson I,
Goepfert PA,
Gottlieb MS,
Goulston C,
Groger RK,
Gurley TD,
Haber S,
Hardwicke R,
Hardy WD,
Harrigan PR,
Hawkins TN,
Heath S,
Hecht FM,
Henry WK,
Hladek M,
Hoffman RP,
Horton JM,
Hsu RK,
Huhn GD,
Hunt P,
Hupert MJ,
Illeman ML,
Jaeger H,
Jellinger RM,
John M,
Johnson JA,
Johnson KL,
Johnson H,
Johnson K,
Joly J,
Jordan WC,
Kauffman CA,
Khanlou H,
Killian RK,
Kim AY,
Kim DD,
Kinder CA,
Kirchner JT,
Kogelman L,
Kojic EM,
Korthuis PT,
Kurisu W,
Kwon DS,
LaMar M,
Lampiris H,
Lanzafame M,
Lederman MM,
Lee DM,
Lee JM,
Lee MJ,
Lee ET,
Lemoine J,
Levy JA,
Llibre JM,
Liguori MA,
Little SJ,
Liu AY,
Lopez AJ,
Loutfy MR,
Loy D,
Mohammed DY,
Man A,
Mansour MK,
Marconi VC,
Markowitz M,
Marques R,
Martin JN,
Martin HL Jr,
Mayer KH,
McElrath MJ,
McGhee TA,
McGovern BH,
McGowan K,
McIntyre D,
Mcleod GX,
Menezes P,
Mesa G,
Metroka CE,
Meyer-Olson D,
Miller AO,
Montgomery K,
Mounzer KC,
Nagami EH,
Nagin I,
Nahass RG,
Nelson MO,
Nielsen C,
Norene DL,
O'Connor DH,
Ojikutu BO,
Okulicz J,
Oladehin OO,
Oldfield EC 3rd,
Olender SA,
Ostrowski M,
Owen WF Jr,
Pae E,
Parsonnet J,
Pavlatos AM,
Perlmutter AM,
Pierce MN,
Pincus JM,
Pisani L,
Price LJ,
Proia L,
Prokesch RC,
Pujet HC,
Ramgopal M,
Rathod A,
Rausch M,
Ravishankar J,
Rhame FS,
Richards CS,
Richman DD,
Rodes B,
Rodriguez M,
Rose RC 3rd,
Rosenberg ES,
Rosenthal D,
Ross PE,
Rubin DS,
Rumbaugh E,
Saenz L,
Salvaggio MR,
Sanchez WC,
Sanjana VM,
Santiago S,
Schmidt W,
Schuitemaker H,
Sestak PM,
Shalit P,
Shay W,
Shirvani VN,
Silebi VI,
Sizemore JM Jr,
Skolnik PR,
Sokol-Anderson M,
Sosman JM,
Stabile P,
Stapleton JT,
Starrett S,
Stein F,
Stellbrink HJ,
Sterman FL,
Stone VE,
Stone DR,
Tambussi G,
Taplitz RA,
Tedaldi EM,
Telenti A,
Theisen W,
Torres R,
Tosiello L,
Tremblay C,
Tribble MA,
Trinh PD,
Tsao A,
Ueda P,
Vaccaro A,
Valadas E,
Vanig TJ,
Vecino I,
Vega VM,
Veikley W,
Wade BH,
Walworth C,
Wanidworanun C,
Ward DJ,
Warner DA,
Weber RD,
Webster D,
Weis S,
Wheeler DA,
White DJ,
Wilkins E,
Winston A,
Wlodaver CG,
van't Wout A,
Wright DP,
Yang OO,
Yurdin DL,
Zabukovic BW,
Zachary KC,
Zeeman B,
Zhao M
International HIV Controllers Study
Science (New York, N.Y.) · 2010 · PMID 21051598
6 pages
Clinical Pharmacogenetics Implementation Consortium Guideline for CYP2C19 Genotype and Clopidogrel Therapy: 2022 Update
Lee CR,
Luzum JA,
Sangkuhl K,
Gammal RS,
Sabatine MS,
Stein CM,
Kisor DF,
Limdi NA,
Lee YM,
Scott SA,
Hulot JS,
Roden DM
and 5 more — show all
Clinical pharmacology and therapeutics · 2022 · PMID 35034351
4 pages
Genome-wide association analysis of common genetic variants of resistant hypertension
El Rouby N,
McDonough CW,
Gong Y,
McClure LA,
Mitchell BD,
Horenstein RB,
Talbert RL,
Crawford DC,
Gitzendanner MA,
Takahashi A,
Tanaka T,
Kubo M
and 5 more — show all
eMERGE network
The pharmacogenomics journal · 2019 · PMID 30237584
2 pages
Genome-wide association study of warfarin maintenance dose in a Brazilian sample
Parra EJ,
Botton MR,
Perini JA,
Krithika S,
Bourgeois S,
Johnson TA,
Tsunoda T,
Pirmohamed M,
Wadelius M,
Limdi NA,
Cavallari LH,
Burmester JK
and 5 more — show all
Pharmacogenomics · 2015 · PMID 26265036
1 page
Genetic variation at 16q24.2 is associated with small vessel stroke
Traylor M,
Malik R,
Nalls MA,
Cotlarciuc I,
Radmanesh F,
Thorleifsson G,
Hanscombe KB,
Langefeld C,
Saleheen D,
Rost NS,
Yet I,
Spector TD
and 55 more — show all
Bell JT,
Hannon E,
Mill J,
Chauhan G,
Debette S,
Bis JC,
Longstreth WT Jr,
Ikram MA,
Launer LJ,
Seshadri S,
Hamilton-Bruce MA,
Jimenez-Conde J,
Cole JW,
Schmidt R,
Słowik A,
Lemmens R,
Lindgren A,
Melander O,
Grewal RP,
Sacco RL,
Rundek T,
Rexrode K,
Arnett DK,
Johnson JA,
Benavente OR,
Wasssertheil-Smoller S,
Lee JM,
Pulit SL,
Wong Q,
Rich SS,
de Bakker PI,
McArdle PF,
Woo D,
Anderson CD,
Xu H,
Heitsch L,
Fornage M,
Jern C,
Stefansson K,
Thorsteinsdottir U,
Gretarsdottir S,
Lewis CM,
Sharma P,
Sudlow CL,
Rothwell PM,
Boncoraglio GB,
Thijs V,
Levi C,
Meschia JF,
Rosand J,
Kittner SJ,
Mitchell BD,
Dichgans M,
Worrall BB,
Markus HS
METASTROKE, UK Young Lacunar DNA Study, NINDS Stroke Genetics Network, Neurology Working Group of the CHARGE Consortium · International Stroke Genetics Consortium
Annals of neurology · 2017 · PMID 27997041 · open access
1 page
Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for Pharmacogenetics-Guided Warfarin Dosing: 2017 Update
Johnson JA,
Caudle KE,
Gong L,
Whirl-Carrillo M,
Stein CM,
Scott SA,
Lee MT,
Gage BF,
Kimmel SE,
Perera MA,
Anderson JL,
Pirmohamed M
and 4 more — show all
Clinical pharmacology and therapeutics · 2017 · PMID 28198005
1 page
Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for CYP2C19 and Proton Pump Inhibitor Dosing
Lima JJ,
Thomas CD,
Barbarino J,
Desta Z,
Van Driest SL,
El Rouby N,
Johnson JA,
Cavallari LH,
Shakhnovich V,
Thacker DL,
Scott SA,
Schwab M
and 8 more — show all
Clinical pharmacology and therapeutics · 2021 · PMID 32770672
1 page
Meta-analysis of genome-wide association studies of stable warfarin dose in patients of African ancestry
Asiimwe IG,
Blockman M,
Cavallari LH,
Cohen K,
Cupido C,
Dandara C,
Davis BH,
Jacobson B,
Johnson JA,
Lamorde M,
Limdi NA,
Morgan J
and 15 more — show all
Mouton JP,
Muyambo S,
Nakagaayi D,
Ndadza A,
Okello E,
Perera MA,
Schapkaitz E,
Sekaggya-Wiltshire C,
Semakula JR,
Tatz G,
Waitt C,
Yang G,
Zhang EJ,
Jorgensen AL,
Pirmohamed M
Blood advances · 2024 · PMID 39163621 · 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.