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2,657 papers hold this site up. Every variant and condition page names
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16 matches for
Yang C.
A sex- and site-specific relationship between body mass index and osteoarthritis: evidence from observational and genetic analyses
Zhang L,
Zhang W,
Wu X,
Cui H,
Yan P,
Yang C,
Zhao X,
Xiao J,
Xiao C,
Tang M,
Wang Y,
Chen L
and 10 more — show all
Osteoarthritis and cartilage · 2023 · PMID 36889626
12 pages+
Using human genetics to understand the phenotypic association between chronotype and breast cancer
Wu X,
Yang C,
Zou Y,
Jones SE,
Zhao X,
Zhang L,
Han Z,
Hao Y,
Xiao J,
Xiao C,
Zhang W,
Yan P
and 10 more — show all
Journal of sleep research · 2024 · PMID 37380357
12 pages+
Proteogenomic analysis of human cerebrospinal fluid identifies neurologically relevant regulation and implicates causal proteins for Alzheimer's disease
Western D,
Timsina J,
Wang L,
Wang C,
Yang C,
Phillips B,
Wang Y,
Liu M,
Ali M,
Beric A,
Gorijala P,
Kohlfeld P
and 28 more — show all
Budde J,
Levey AI,
Morris JC,
Perrin RJ,
Ruiz A,
Marquié M,
Boada M,
de Rojas I,
Rutledge J,
Oh H,
Wilson EN,
Le Guen Y,
Reus LM,
Tijms B,
Visser PJ,
van der Lee SJ,
Pijnenburg YAL,
Teunissen CE,
Del Campo Milan M,
Alvarez I,
Aguilar M,
Greicius MD,
Pastor P,
Pulford DJ,
Ibanez L,
Wyss-Coray T,
Sung YJ,
Cruchaga C
Dominantly Inherited Alzheimer Network (DIAN) · Alzheimer’s Disease Neuroimaging Initiative (ADNI)
Nature genetics · 2024 · PMID 39528825
12 pages+
Genetic architecture of cerebrospinal fluid and brain metabolite levels and the genetic colocalization of metabolites with human traits
Wang C,
Yang C,
Western D,
Ali M,
Wang Y,
Phuah CL,
Budde J,
Wang L,
Gorijala P,
Timsina J,
Ruiz A,
Pastor P
and 14 more — show all
Fernandez MV,
Panyard DJ,
Engelman CD,
Deming Y,
Boada M,
Cano A,
Garcia-Gonzalez P,
Graff-Radford NR,
Mori H,
Lee JH,
Perrin RJ,
Ibanez L,
Sung YJ,
Cruchaga C
Dominantly Inherited Alzheimer Network (DIAN) · Alzheimer’s Disease Neuroimaging Initiative (ADNI)
Nature genetics · 2024 · PMID 39528826
12 pages+
Low overlap of plasma and CSF protein quantitative trait loci affects protein discovery for neurological disease
Western D,
Yang C,
Timsina J,
Liu M,
Wang C,
Campbell MC,
Kotzbauer P,
Perlmutter JS,
Schindler SE,
Morris JC,
Holtzman DM,
Alvarez I
and 12 more — show all
Pastor P,
Wyss-Coray T,
Marquié M,
Cano A,
Sung YJ,
de Rojas I,
Ruiz A,
Budde J,
Fernandez MV,
Tarawneh R,
Ibanez L,
Cruchaga C
Science translational medicine · 2026 · PMID 42054495
12 pages+
Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleft
Huang L,
Jia Z,
Shi Y,
Du Q,
Shi J,
Wang Z,
Mou Y,
Wang Q,
Zhang B,
Wang Q,
Ma S,
Lin H
and 15 more — show all
Duan S,
Yin B,
Lin Y,
Wang Y,
Jiang D,
Hao F,
Zhang L,
Wang H,
Jiang S,
Xu H,
Yang C,
Li C,
Li J,
Shi B,
Yang Z
PLoS genetics · 2019 · PMID 31609978 · open access
5 pages
Stroke genetics informs drug discovery and risk prediction across ancestries
Mishra A,
Malik R,
Hachiya T,
Jürgenson T,
Namba S,
Posner DC,
Kamanu FK,
Koido M,
Le Grand Q,
Shi M,
He Y,
Georgakis MK
and 175 more — show all
Caro I,
Krebs K,
Liaw YC,
Vaura FC,
Lin K,
Winsvold BS,
Srinivasasainagendra V,
Parodi L,
Bae HJ,
Chauhan G,
Chong MR,
Tomppo L,
Akinyemi R,
Roshchupkin GV,
Habib N,
Jee YH,
Thomassen JQ,
Abedi V,
Cárcel-Márquez J,
Nygaard M,
Leonard HL,
Yang C,
Yonova-Doing E,
Knol MJ,
Lewis AJ,
Judy RL,
Ago T,
Amouyel P,
Armstrong ND,
Bakker MK,
Bartz TM,
Bennett DA,
Bis JC,
Bordes C,
Børte S,
Cain A,
Ridker PM,
Cho K,
Chen Z,
Cruchaga C,
Cole JW,
de Jager PL,
de Cid R,
Endres M,
Ferreira LE,
Geerlings MI,
Gasca NC,
Gudnason V,
Hata J,
He J,
Heath AK,
Ho YL,
Havulinna AS,
Hopewell JC,
Hyacinth HI,
Inouye M,
Jacob MA,
Jeon CE,
Jern C,
Kamouchi M,
Keene KL,
Kitazono T,
Kittner SJ,
Konuma T,
Kumar A,
Lacaze P,
Launer LJ,
Lee KJ,
Lepik K,
Li J,
Li L,
Manichaikul A,
Markus HS,
Marston NA,
Meitinger T,
Mitchell BD,
Montellano FA,
Morisaki T,
Mosley TH,
Nalls MA,
Nordestgaard BG,
O'Donnell MJ,
Okada Y,
Onland-Moret NC,
Ovbiagele B,
Peters A,
Psaty BM,
Rich SS,
Rosand J,
Sabatine MS,
Sacco RL,
Saleheen D,
Sandset EC,
Salomaa V,
Sargurupremraj M,
Sasaki M,
Satizabal CL,
Schmidt CO,
Shimizu A,
Smith NL,
Sloane KL,
Sutoh Y,
Sun YV,
Tanno K,
Tiedt S,
Tatlisumak T,
Torres-Aguila NP,
Tiwari HK,
Trégouët DA,
Trompet S,
Tuladhar AM,
Tybjærg-Hansen A,
van Vugt M,
Vibo R,
Verma SS,
Wiggins KL,
Wennberg P,
Woo D,
Wilson PWF,
Xu H,
Yang Q,
Yoon K,
Millwood IY,
Gieger C,
Ninomiya T,
Grabe HJ,
Jukema JW,
Rissanen IL,
Strbian D,
Kim YJ,
Chen PH,
Mayerhofer E,
Howson JMM,
Irvin MR,
Adams H,
Wassertheil-Smoller S,
Christensen K,
Ikram MA,
Rundek T,
Worrall BB,
Lathrop GM,
Riaz M,
Simonsick EM,
Kõrv J,
França PHC,
Zand R,
Prasad K,
Frikke-Schmidt R,
de Leeuw FE,
Liman T,
Haeusler KG,
Ruigrok YM,
Heuschmann PU,
Longstreth WT,
Jung KJ,
Bastarache L,
Paré G,
Damrauer SM,
Chasman DI,
Rotter JI,
Anderson CD,
Zwart JA,
Niiranen TJ,
Fornage M,
Liaw YP,
Seshadri S,
Fernández-Cadenas I,
Walters RG,
Ruff CT,
Owolabi MO,
Huffman JE,
Milani L,
Kamatani Y,
Dichgans M,
Debette S
COMPASS Consortium · INVENT Consortium and 13 more consortia
Nature · 2022 · PMID 36180795 · open access
5 pages
Genome-wide association analysis reveals insights into the genetic architecture of right ventricular structure and function
Aung N,
Vargas JD,
Yang C,
Fung K,
Sanghvi MM,
Piechnik SK,
Neubauer S,
Manichaikul A,
Rotter JI,
Taylor KD,
Lima JAC,
Bluemke DA
and 3 more — show all
Nature genetics · 2022 · PMID 35697868
4 pages
Proteo-genomics of soluble TREM2 in cerebrospinal fluid provides novel insights and identifies novel modulators for Alzheimer's disease
Wang L,
Nykänen NP,
Western D,
Gorijala P,
Timsina J,
Li F,
Wang Z,
Ali M,
Yang C,
Liu M,
Brock W,
Marquié M
and 21 more — show all
Boada M,
Alvarez I,
Aguilar M,
Pastor P,
Ruiz A,
Puerta R,
Orellana A,
Rutledge J,
Oh H,
Greicius MD,
Le Guen Y,
Perrin RJ,
Wyss-Coray T,
Jefferson A,
Hohman TJ,
Graff-Radford N,
Mori H,
Goate A,
Levin J,
Sung YJ,
Cruchaga C
Molecular neurodegeneration · 2024 · PMID 38172904 · 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
Genome-wide association meta-analysis in Chinese and European individuals identifies ten new loci associated with systemic lupus erythematosus
Morris DL,
Sheng Y,
Zhang Y,
Wang YF,
Zhu Z,
Tombleson P,
Chen L,
Cunninghame Graham DS,
Bentham J,
Roberts AL,
Chen R,
Zuo X
and 20 more — show all
Wang T,
Wen L,
Yang C,
Liu L,
Yang L,
Li F,
Huang Y,
Yin X,
Yang S,
Rönnblom L,
Fürnrohr BG,
Voll RE,
Schett G,
Costedoat-Chalumeau N,
Gaffney PM,
Lau YL,
Zhang X,
Yang W,
Cui Y,
Vyse TJ
Nature genetics · 2016 · PMID 27399966
3 pages
Epidemiological and Genetic Analyses of Schizophrenia and Breast Cancer
Tang M,
Wu X,
Zhang W,
Cui H,
Zhang L,
Yan P,
Yang C,
Wang Y,
Chen L,
Xiao C,
Liu Y,
Zou Y
and 7 more — show all
Schizophrenia bulletin · 2024 · PMID 37467357
3 pages
Genome-wide association study identifies two new susceptibility loci for atopic dermatitis in the Chinese Han population
Sun LD,
Xiao FL,
Li Y,
Zhou WM,
Tang HY,
Tang XF,
Zhang H,
Schaarschmidt H,
Zuo XB,
Foelster-Holst R,
He SM,
Shi M
and 55 more — show all
Liu Q,
Lv YM,
Chen XL,
Zhu KJ,
Guo YF,
Hu DY,
Li M,
Li M,
Zhang YH,
Zhang X,
Tang JP,
Guo BR,
Wang H,
Liu Y,
Zou XY,
Zhou FS,
Liu XY,
Chen G,
Ma L,
Zhang SM,
Jiang AP,
Zheng XD,
Gao XH,
Li P,
Tu CX,
Yin XY,
Han XP,
Ren YQ,
Song SP,
Lu ZY,
Zhang XL,
Cui Y,
Chang J,
Gao M,
Luo XY,
Wang PG,
Dai X,
Su W,
Li H,
Shen CP,
Liu SX,
Feng XB,
Yang CJ,
Lin GS,
Wang ZX,
Huang JQ,
Fan X,
Wang Y,
Bao YX,
Yang S,
Liu JJ,
Franke A,
Weidinger S,
Yao ZR,
Zhang XJ
Nature genetics · 2011 · PMID 21666691
2 pages
Genome-wide association studies and fine-mapping identify genomic loci for n-3 and n-6 polyunsaturated fatty acids in Hispanic American and African American cohorts
Yang C,
Veenstra J,
Bartz TM,
Pahl MC,
Hallmark B,
Chen YI,
Westra J,
Steffen LM,
Brown CD,
Siscovick D,
Tsai MY,
Wood AC
and 9 more — show all
Communications biology · 2023 · PMID 37587153 · open access
2 pages
Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus
Han JW,
Zheng HF,
Cui Y,
Sun LD,
Ye DQ,
Hu Z,
Xu JH,
Cai ZM,
Huang W,
Zhao GP,
Xie HF,
Fang H
and 55 more — show all
Lu QJ,
Xu JH,
Li XP,
Pan YF,
Deng DQ,
Zeng FQ,
Ye ZZ,
Zhang XY,
Wang QW,
Hao F,
Ma L,
Zuo XB,
Zhou FS,
Du WH,
Cheng YL,
Yang JQ,
Shen SK,
Li J,
Sheng YJ,
Zuo XX,
Zhu WF,
Gao F,
Zhang PL,
Guo Q,
Li B,
Gao M,
Xiao FL,
Quan C,
Zhang C,
Zhang Z,
Zhu KJ,
Li Y,
Hu DY,
Lu WS,
Huang JL,
Liu SX,
Li H,
Ren YQ,
Wang ZX,
Yang CJ,
Wang PG,
Zhou WM,
Lv YM,
Zhang AP,
Zhang SQ,
Lin D,
Li Y,
Low HQ,
Shen M,
Zhai ZF,
Wang Y,
Zhang FY,
Yang S,
Liu JJ,
Zhang XJ
Nature genetics · 2009 · PMID 19838193
1 page
Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population
Shi Y,
Qu J,
Zhang D,
Zhao P,
Zhang Q,
Tam POS,
Sun L,
Zuo X,
Zhou X,
Xiao X,
Hu J,
Li Y
and 30 more — show all
Cai L,
Liu X,
Lu F,
Liao S,
Chen B,
He F,
Gong B,
Lin H,
Ma S,
Cheng J,
Zhang J,
Chen Y,
Zhao F,
Yang X,
Chen Y,
Yang C,
Lam DSC,
Li X,
Shi F,
Wu Z,
Lin Y,
Yang J,
Li S,
Ren Y,
Xue A,
Fan Y,
Li D,
Pang CP,
Zhang X,
Yang Z
American journal of human genetics · 2011 · PMID 21640322
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.