For researchers
Is your paper here?
3,070 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.
13 matches for
Johnson S.
Unique motif shared by HLA-B*59:01 and HLA-B*55:02 is associated with methazolamide-induced Stevens-Johnson syndrome and toxic epidermal necrolysis in Han Chinese
Jiang M,
Yang F,
Zhang L,
Xu D,
Jia Y,
Cheng Y,
Han S,
Wang T,
Chen Z,
Su Y,
Zhu Z,
Chen S
and 6 more — show all
Journal of the European Academy of Dermatology and Venereology : JEADV · 2022 · PMID 35122707
4 pages
GWAS meta-analysis of cerebrospinal fluid Alzheimer's biomarkers reveals loci regulating lipids, brain volume and autophagy
Timsina J,
Jiang C,
McCartney DL,
Tao F,
Dalmasso MC,
Najar J,
Anastasi F,
Ohlei O,
Puerta Fuentes R,
Yang C,
Bradley J,
Western D
and 143 more — show all
Ali M,
Wang C,
Yang C,
Wu Y,
Liu M,
Budde J,
Williams J,
Mahoney R,
Castillo Morales A,
Hohman TJ,
Dumitrescu L,
Wang TC,
Tesi N,
Kern S,
Waern M,
Skoog I,
van Harten A,
Pijnenburg YAL,
van der Flier WM,
Sánchez-Juan P,
Rodriguez-Rodriguez E,
Kleineidam L,
Peters O,
Schneider A,
Küçükali F,
Bellenguez C,
Grenier-Boley B,
Heikkinen S,
de Rojas I,
Rujescu D,
Scherbaum N,
Hausner L,
Düzel E,
Grimmer T,
Wiltfang J,
Vandenberghe R,
Engelborghs S,
Heilmann-Heimbach S,
Schmid M,
Tegos T,
Scarmeas N,
Dols-Icardo O,
Moreno F,
Pérez-Tur J,
Bullido MJ,
Sánchez-Valle R,
Álvarez V,
García-González P,
Mir P,
Real LM,
Piñol-Ripoll G,
García-Alberca JM,
Seelaar H,
Ramakers I,
Papma J,
Hulsman M,
Laske C,
Teipel S,
Priller J,
Perneczky R,
Buerger K,
Nöthen MM,
Lewczuk P,
Kornhuber J,
Hampel H,
Giegling I,
Goldhardt O,
Diehl-Schmid J,
Andrade V,
Heneka MM,
Frölich L,
Vogelgsang J,
Graff C,
Thonberg H,
Ullgren A,
Papenberg G,
Deleuze JF,
Dufouil C,
Wagner M,
Jessen F,
Holstege H,
van Duijn C,
Lebouvier T,
Hannon O,
Leinonen V,
Soininen H,
Herukka SK,
Giedraitis V,
Löwenmark M,
Kilander L,
Genius P,
Rodríguez B,
Luckett ES,
Navarro A,
Cano A,
Marquié M,
Blennow K,
Zetterberg H,
Lleo A,
Boada M,
Ruiz A,
Lee VM,
Van Deerlin VM,
Deming Y,
Johnson SC,
Engelman CD,
Pastor P,
Alvarez I,
Peskind ER,
Heslegrave AJ,
Saykin AJ,
Nho K,
Schindler SE,
Morris JC,
Holtzman DM,
McDade E,
Renton AE,
Goate A,
Ibanez L,
Riemenschneider M,
Albert MS,
Laws SM,
Porter T,
O'Brien EK,
Shaw LM,
Tijms BM,
Ingelsson M,
Visser PJ,
Hiltunen M,
Sleegers K,
Ritchie CW,
Sims R,
Belloy M,
Lambert JC,
Vilor-Tejedor N,
Fernández MV,
Li QS,
Nagle MW,
Marioni RE,
Ramirez A,
Bertram L,
van der Lee SJ,
Cruchaga C
Nature communications · 2026 · PMID 42014397 · open access
4 pages
Clinical Pharmacogenetics Implementation Consortium (CPIC) guidelines for human leukocyte antigen B (HLA-B) genotype and allopurinol dosing: 2015 update
Saito Y,
Stamp LK,
Caudle KE,
Hershfield MS,
McDonagh EM,
Callaghan JT,
Tassaneeyakul W,
Mushiroda T,
Kamatani N,
Goldspiel BR,
Phillips EJ,
Klein TE
and 1 more — show all
Clinical Pharmacogenetics Implementation Consortium
Clinical pharmacology and therapeutics · 2016 · PMID 26094938
2 pages
Genome-wide association study using the ethnicity-specific Japonica array: identification of new susceptibility loci for cold medicine-related Stevens-Johnson syndrome with severe ocular complications
Ueta M,
Sawai H,
Shingaki R,
Kawai Y,
Sotozono C,
Kojima K,
Yoon KC,
Kim MK,
Seo KY,
Joo CK,
Nagasaki M,
Kinoshita S
and 1 more — show all
Journal of human genetics · 2017 · PMID 28100913
2 pages
Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations
Panyard DJ,
Kim KM,
Darst BF,
Deming YK,
Zhong X,
Wu Y,
Kang H,
Carlsson CM,
Johnson SC,
Asthana S,
Engelman CD,
Lu Q
Communications biology · 2021 · PMID 33437055 · open access
2 pages
Genomewide meta-analysis identifies loci associated with IGF-I and IGFBP-3 levels with impact on age-related traits
Teumer A,
Qi Q,
Nethander M,
Aschard H,
Bandinelli S,
Beekman M,
Berndt SI,
Bidlingmaier M,
Broer L,
Cappola A,
Ceda GP,
Chanock S
and 74 more — show all
Chen MH,
Chen TC,
Chen YD,
Chung J,
Del Greco Miglianico F,
Eriksson J,
Ferrucci L,
Friedrich N,
Gnewuch C,
Goodarzi MO,
Grarup N,
Guo T,
Hammer E,
Hayes RB,
Hicks AA,
Hofman A,
Houwing-Duistermaat JJ,
Hu F,
Hunter DJ,
Husemoen LL,
Isaacs A,
Jacobs KB,
Janssen JA,
Jansson JO,
Jehmlich N,
Johnson S,
Juul A,
Karlsson M,
Kilpelainen TO,
Kovacs P,
Kraft P,
Li C,
Linneberg A,
Liu Y,
Loos RJ,
Lorentzon M,
Lu Y,
Maggio M,
Magi R,
Meigs J,
Mellström D,
Nauck M,
Newman AB,
Pollak MN,
Pramstaller PP,
Prokopenko I,
Psaty BM,
Reincke M,
Rimm EB,
Rotter JI,
Saint Pierre A,
Schurmann C,
Seshadri S,
Sjögren K,
Slagboom PE,
Strickler HD,
Stumvoll M,
Suh Y,
Sun Q,
Zhang C,
Svensson J,
Tanaka T,
Tare A,
Tönjes A,
Uh HW,
van Duijn CM,
van Heemst D,
Vandenput L,
Vasan RS,
Völker U,
Willems SM,
Ohlsson C,
Wallaschofski H,
Kaplan RC
CHARGE Longevity Working Group · Body Composition Genetics Consortium
Aging cell · 2016 · PMID 27329260 · open access
1 page
Clinical Pharmacogenetics Implementation Consortium Guideline for HLA Genotype and Use of Carbamazepine and Oxcarbazepine: 2017 Update
Phillips EJ,
Sukasem C,
Whirl-Carrillo M,
Müller DJ,
Dunnenberger HM,
Chantratita W,
Goldspiel B,
Chen YT,
Carleton BC,
George AL Jr,
Mushiroda T,
Klein T
and 2 more — show all
Clinical pharmacology and therapeutics · 2018 · PMID 29392710
1 page
Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for CYP2C9 and HLA-B Genotypes and Phenytoin Dosing: 2020 Update
Karnes JH,
Rettie AE,
Somogyi AA,
Huddart R,
Fohner AE,
Formea CM,
Ta Michael Lee M,
Llerena A,
Whirl-Carrillo M,
Klein TE,
Phillips EJ,
Mintzer S
and 3 more — show all
Clinical pharmacology and therapeutics · 2021 · PMID 32779747
1 page
APOE4 homozygozity represents a distinct genetic form of Alzheimer's disease
Fortea J,
Pegueroles J,
Alcolea D,
Belbin O,
Dols-Icardo O,
Vaqué-Alcázar L,
Videla L,
Gispert JD,
Suárez-Calvet M,
Johnson SC,
Sperling R,
Bejanin A
and 2 more — show all
Nature medicine · 2024 · PMID 38710950
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.