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Is your paper here?
2,676 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.
6 matches for
Jiang C.
Multi-ancestry genome-wide association analyses of refractive error augment genetic discovery and polygenic prediction
Cheng FF,
Liu X,
Mi H,
Wang L,
Ma R,
Guo Y,
Sidorenko J,
Jiang C,
Islam T,
Meguro A,
Hikino K,
Ishikawa Y
and 15 more — show all
Tang S,
Li T,
Chen R,
Wang L,
Mägi R,
Metspalu A,
Takeuchi M,
Mizuki N,
Choquet H,
Jin ZB,
Chen G,
Zhou K,
Terao C,
Zeng J,
Yang J
Estonian Biobank Research Team · 23andMe Research Team
Nature genetics · 2026 · PMID 42009823 · open access
12 pages+
Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes
van der Laan CM,
Ip HF,
Schipper M,
Hottenga JJ,
St Pourcain B,
Zayats T,
Pool R,
Krapohl EML,
Brikell I,
Soler Artigas M,
Cabana-Domínguez J,
Llonga N
and 117 more — show all
Nolte IM,
Bolhuis K,
Palviainen T,
Zafarmand H,
Gordon S,
Aliev F,
Burt SA,
Wang CA,
Saunders G,
Karhunen V,
Adkins DE,
Border R,
Peterson RE,
Prinz JA,
Thiering E,
Vilor-Tejedor N,
Ahluwalia TS,
Allegrini A,
Rimfeld K,
Chen Q,
Lu Y,
Martin J,
Bosch R,
Ramos-Quiroga JA,
Neumann A,
Ensink J,
Grasby KL,
Morosoli JJ,
Tong X,
Marrington S,
Scott JG,
Shabalin AA,
Corley R,
Evans LM,
Sugden K,
Alemany S,
Sass L,
Vinding R,
Ehli EA,
Hagenbeek FA,
Derks EM,
Larsson H,
Snieder H,
Cecil C,
Whipp AM,
Korhonen T,
Vuoksimaa E,
Rose RJ,
Uitterlinden AG,
Haavik J,
Harris JR,
Helgeland Ø,
Johansson S,
Knudsen GPS,
Njolstad PR,
Lu Q,
Rodriguez A,
Henders AK,
Mamun A,
Najman JM,
Brown S,
Hopfer C,
Krauter K,
Reynolds CA,
Smolen A,
Stallings M,
Wadsworth S,
Wall TL,
Eaves L,
Silberg JL,
Miller A,
Havdahl A,
Llop S,
Lopez-Espinosa MJ,
Bønnelykke K,
Sunyer J,
Arseneault L,
Standl M,
Heinrich J,
Boden J,
Pearson J,
Horwood J,
Kennedy M,
Poulton R,
Maes HH,
Hewitt J,
Copeland WE,
Middeldorp CM,
Williams GM,
Wray N,
Järvelin MR,
McGue M,
Iacono W,
Caspi A,
Moffitt TE,
Whitehouse AJO,
Pennell CE,
Klump KL,
Jiang C,
Dick DM,
Reichborn-Kjennerud T,
Martin NG,
Medland SE,
Vrijkotte T,
Kaprio J,
Tiemeier H,
Davey Smith G,
Hartman CA,
Oldehinkel AJ,
Casas M,
Ribasés M,
Lichtenstein P,
Lundström S,
Plomin R,
Bartels M,
Nivard MG,
Boomsma DI
Nature genetics · 2025 · PMID 40962958
9 pages
Large-scale GWAS of strabismus identifies risk loci and provides support for a link with maternal smoking
He W,
van der Most PJ,
Ong JS,
Hwang LD,
Wu Y,
Magnø MS,
Vehof J,
Krebs K,
Mauring L,
Õunap K,
Abner E,
Martin NG
and 12 more — show all
Plotnikov D,
Jiang C,
Melles RB,
Gharahkhani P,
Snieder H,
Palumaa T,
Kaljurand K,
Guggenheim JA,
Mackey DA,
Engle EC,
Choquet H,
MacGregor S
Lifelines Cohort Study
Nature communications · 2025 · PMID 40849414 · open access
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
A multiethnic genome-wide analysis of 19,420 individuals identifies novel loci associated with axial length and shared genetic influences with refractive error and myopia
Jiang C,
Melles RB,
Yin J,
Fan Q,
Guo X,
Cheng CY,
He M,
Mackey DA,
Guggenheim JA,
Klaver C,
Nair KS,
Jorgenson E
and 1 more — show all
Consortium for Refractive Error and Myopia (CREAM)
Frontiers in genetics · 2023 · PMID 37351342 · open access
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.