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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.
11 matches for
Cai J.
Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies
Morris AP,
Le TH,
Wu H,
Akbarov A,
van der Most PJ,
Hemani G,
Smith GD,
Mahajan A,
Gaulton KJ,
Nadkarni GN,
Valladares-Salgado A,
Wacher-Rodarte N
and 60 more — show all
Mychaleckyj JC,
Dueker ND,
Guo X,
Hai Y,
Haessler J,
Kamatani Y,
Stilp AM,
Zhu G,
Cook JP,
Ärnlöv J,
Blanton SH,
de Borst MH,
Bottinger EP,
Buchanan TA,
Cechova S,
Charchar FJ,
Chu PL,
Damman J,
Eales J,
Gharavi AG,
Giedraitis V,
Heath AC,
Ipp E,
Kiryluk K,
Kramer HJ,
Kubo M,
Larsson A,
Lindgren CM,
Lu Y,
Madden PAF,
Montgomery GW,
Papanicolaou GJ,
Raffel LJ,
Sacco RL,
Sanchez E,
Stark H,
Sundstrom J,
Taylor KD,
Xiang AH,
Zivkovic A,
Lind L,
Ingelsson E,
Martin NG,
Whitfield JB,
Cai J,
Laurie CC,
Okada Y,
Matsuda K,
Kooperberg C,
Chen YI,
Rundek T,
Rich SS,
Loos RJF,
Parra EJ,
Cruz M,
Rotter JI,
Snieder H,
Tomaszewski M,
Humphreys BD,
Franceschini N
Nature communications · 2019 · PMID 30604766 · open access
12 pages+
A Genome-wide Association Study Discovers 46 Loci of the Human Metabolome in the Hispanic Community Health Study/Study of Latinos
Feofanova EV,
Chen H,
Dai Y,
Jia P,
Grove ML,
Morrison AC,
Qi Q,
Daviglus M,
Cai J,
North KE,
Laurie CC,
Kaplan RC
and 2 more — show all
American journal of human genetics · 2020 · PMID 33031748
12 pages+
Multi-ancestry genome-wide analysis identifies shared genetic effects and common genetic variants for self-reported sleep duration
Scammell BH,
Tchio C,
Song Y,
Nishiyama T,
Louie TL,
Dashti HS,
Nakatochi M,
Zee PC,
Daghlas I,
Momozawa Y,
Cai J,
Ollila HM
and 6 more — show all
Human molecular genetics · 2023 · PMID 37384397
12 pages+
Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity
Mahajan A,
Rodan AR,
Le TH,
Gaulton KJ,
Haessler J,
Stilp AM,
Kamatani Y,
Zhu G,
Sofer T,
Puri S,
Schellinger JN,
Chu PL
and 26 more — show all
Cechova S,
van Zuydam N,
Arnlov J,
Flessner MF,
Giedraitis V,
Heath AC,
Kubo M,
Larsson A,
Lindgren CM,
Madden PAF,
Montgomery GW,
Papanicolaou GJ,
Reiner AP,
Sundström J,
Thornton TA,
Lind L,
Ingelsson E,
Cai J,
Martin NG,
Kooperberg C,
Matsuda K,
Whitfield JB,
Okada Y,
Laurie CC,
Morris AP,
Franceschini N
SUMMIT Consortium · BioBank Japan Project
American journal of human genetics · 2016 · PMID 27588450 · open access
8 pages
Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations
Liang J,
Le TH,
Edwards DRV,
Tayo BO,
Gaulton KJ,
Smith JA,
Lu Y,
Jensen RA,
Chen G,
Yanek LR,
Schwander K,
Tajuddin SM
and 69 more — show all
Sofer T,
Kim W,
Kayima J,
McKenzie CA,
Fox E,
Nalls MA,
Young JH,
Sun YV,
Lane JM,
Cechova S,
Zhou J,
Tang H,
Fornage M,
Musani SK,
Wang H,
Lee J,
Adeyemo A,
Dreisbach AW,
Forrester T,
Chu PL,
Cappola A,
Evans MK,
Morrison AC,
Martin LW,
Wiggins KL,
Hui Q,
Zhao W,
Jackson RD,
Ware EB,
Faul JD,
Reiner AP,
Bray M,
Denny JC,
Mosley TH,
Palmas W,
Guo X,
Papanicolaou GJ,
Penman AD,
Polak JF,
Rice K,
Rice K,
Taylor KD,
Boerwinkle E,
Bottinger EP,
Liu K,
Risch N,
Hunt SC,
Kooperberg C,
Zonderman AB,
Laurie CC,
Becker DM,
Cai J,
Loos RJF,
Psaty BM,
Weir DR,
Kardia SLR,
Arnett DK,
Won S,
Edwards TL,
Redline S,
Cooper RS,
Rao DC,
Rotter JI,
Rotimi C,
Levy D,
Chakravarti A,
Zhu X,
Franceschini N,
Franceschini N
PLoS genetics · 2017 · PMID 28498854 · open access
8 pages
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements
Scholz M,
Horn K,
Pott J,
Wuttke M,
Kühnapfel A,
Nasr MK,
Kirsten H,
Li Y,
Hoppmann A,
Gorski M,
Ghasemi S,
Li M
and 147 more — show all
Tin A,
Chai JF,
Cocca M,
Wang J,
Nutile T,
Akiyama M,
Åsvold BO,
Bansal N,
Biggs ML,
Boutin T,
Brenner H,
Brumpton B,
Burkhardt R,
Cai J,
Campbell A,
Campbell H,
Chalmers J,
Chasman DI,
Chee ML,
Chee ML,
Chen X,
Cheng CY,
Cifkova R,
Daviglus M,
Delgado G,
Dittrich K,
Edwards TL,
Endlich K,
Michael Gaziano J,
Giri A,
Giulianini F,
Gordon SD,
Gudbjartsson DF,
Hallan S,
Hamet P,
Hartman CA,
Hayward C,
Heid IM,
Hellwege JN,
Holleczek B,
Holm H,
Hutri-Kähönen N,
Hveem K,
Isermann B,
Jonas JB,
Joshi PK,
Kamatani Y,
Kanai M,
Kastarinen M,
Khor CC,
Kiess W,
Kleber ME,
Körner A,
Kovacs P,
Krajcoviechova A,
Kramer H,
Krämer BK,
Kuokkanen M,
Kähönen M,
Lange LA,
Lash JP,
Lehtimäki T,
Li H,
Lin BM,
Liu J,
Loeffler M,
Lyytikäinen LP,
Magnusson PKE,
Martin NG,
Matsuda K,
Milaneschi Y,
Mishra PP,
Mononen N,
Montgomery GW,
Mook-Kanamori DO,
Mychaleckyj JC,
März W,
Nauck M,
Nikus K,
Nolte IM,
Noordam R,
Okada Y,
Olafsson I,
Oldehinkel AJ,
Penninx BWJH,
Perola M,
Pirastu N,
Polasek O,
Porteous DJ,
Poulain T,
Psaty BM,
Rabelink TJ,
Raffield LM,
Raitakari OT,
Rasheed H,
Reilly DF,
Rice KM,
Richmond A,
Ridker PM,
Rotter JI,
Rudan I,
Sabanayagam C,
Salomaa V,
Schneiderman N,
Schöttker B,
Sims M,
Snieder H,
Stark KJ,
Stefansson K,
Stocker H,
Stumvoll M,
Sulem P,
Sveinbjornsson G,
Svensson PO,
Tai ES,
Taylor KD,
Tayo BO,
Teren A,
Tham YC,
Thiery J,
Thio CHL,
Thomas LF,
Tremblay J,
Tönjes A,
van der Most PJ,
Vitart V,
Völker U,
Wang YX,
Wang C,
Wei WB,
Whitfield JB,
Wild SH,
Wilson JF,
Winkler TW,
Wong TY,
Woodward M,
Sim X,
Chu AY,
Feitosa MF,
Thorsteinsdottir U,
Hung AM,
Teumer A,
Franceschini N,
Parsa A,
Köttgen A,
Schlosser P,
Pattaro C
Nature communications · 2024 · PMID 38233393 · open access
8 pages
Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas
Hughes O,
Bentley AR,
Breeze CE,
Aguet F,
Xu X,
Nadkarni G,
Sun Q,
Lin BM,
Gilliland T,
Meyer MC,
Du J,
Raffield LM
and 62 more — show all
Kramer H,
Morton RW,
Gouveia MH,
Atkinson EG,
Valladares-Salgado A,
Wacher-Rodarte N,
Dueker ND,
Guo X,
Hai Y,
Adeyemo A,
Best LG,
Cai J,
Chen G,
Chong M,
Doumatey A,
Eales J,
Goodarzi MO,
Ipp E,
Irvin MR,
Jiang M,
Jones AC,
Kooperberg C,
Krieger JE,
Lange EM,
Lanktree MB,
Lash JP,
Lotufo PA,
Loos RJF,
Ha My VT,
Peralta-Romero J,
Qi L,
Raffel LJ,
Rich SS,
Rodriquez EJ,
Tarazona-Santos E,
Taylor KD,
Umans JG,
Wen J,
Young BA,
Yu Z,
Zhang Y,
Ida Chen YD,
Rundek T,
Rotter JI,
Cruz M,
Fornage M,
Lima-Costa MF,
Pereira AC,
Paré G,
Natarajan P,
Cole SA,
Carson AP,
Lange LA,
Li Y,
Perez-Stable EJ,
Do R,
Charchar FJ,
Tomaszewski M,
Mychaleckyj JC,
Rotimi C,
Morris AP,
Franceschini N
Cell genomics · 2024 · PMID 38190104 · open access
5 pages
Novel Risk Loci Associated With Genetic Risk for Bipolar Disorder Among Han Chinese Individuals: A Genome-Wide Association Study and Meta-analysis
Li HJ,
Zhang C,
Hui L,
Zhou DS,
Li Y,
Zhang CY,
Wang C,
Wang L,
Li W,
Yang Y,
Qu N,
Tang J
and 37 more — show all
He Y,
Zhou J,
Yang Z,
Li X,
Cai J,
Yang L,
Chen J,
Fan W,
Tang W,
Tang W,
Jia QF,
Liu W,
Zhuo C,
Song X,
Liu F,
Bai Y,
Zhong BL,
Zhang SF,
Chen J,
Xia B,
Lv L,
Liu Z,
Hu S,
Li XY,
Liu JW,
Cai X,
Yao YG,
Zhang Y,
Yan H,
Chang S,
Zhao JP,
Yue WH,
Luo XJ,
Chen X,
Xiao X,
Fang Y,
Li M
GeseDNA Research Team
JAMA psychiatry · 2021 · PMID 33263727
4 pages
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
Kowalski MH,
Qian H,
Hou Z,
Rosen JD,
Tapia AL,
Shan Y,
Jain D,
Argos M,
Arnett DK,
Avery C,
Barnes KC,
Becker LC
and 66 more — show all
Bien SA,
Bis JC,
Blangero J,
Boerwinkle E,
Bowden DW,
Buyske S,
Cai J,
Cho MH,
Choi SH,
Choquet H,
Cupples LA,
Cushman M,
Daya M,
de Vries PS,
Ellinor PT,
Faraday N,
Fornage M,
Gabriel S,
Ganesh SK,
Graff M,
Gupta N,
He J,
Heckbert SR,
Hidalgo B,
Hodonsky CJ,
Irvin MR,
Johnson AD,
Jorgenson E,
Kaplan R,
Kardia SLR,
Kelly TN,
Kooperberg C,
Lasky-Su JA,
Loos RJF,
Lubitz SA,
Mathias RA,
McHugh CP,
Montgomery C,
Moon JY,
Morrison AC,
Palmer ND,
Pankratz N,
Papanicolaou GJ,
Peralta JM,
Peyser PA,
Rich SS,
Rotter JI,
Silverman EK,
Smith JA,
Smith NL,
Taylor KD,
Thornton TA,
Tiwari HK,
Tracy RP,
Wang T,
Weiss ST,
Weng LC,
Wiggins KL,
Wilson JG,
Yanek LR,
Zöllner S,
North KE,
Auer PL,
Raffield LM,
Reiner AP,
Li Y
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium · TOPMed Hematology & Hemostasis Working Group
PLoS genetics · 2019 · PMID 31869403 · open access
3 pages
Genetic and functional insights into the fractal structure of the heart
Meyer HV,
Dawes TJW,
Serrani M,
Bai W,
Tokarczuk P,
Cai J,
de Marvao A,
Henry A,
Lumbers RT,
Gierten J,
Thumberger T,
Wittbrodt J
and 8 more — show all
Nature · 2020 · PMID 32814899
2 pages
A Genome-Wide Association Study Identifies Blood Disorder-Related Variants Influencing Hemoglobin A<sub>1c</sub> With Implications for Glycemic Status in U.S. Hispanics/Latinos
Moon JY,
Louie TL,
Jain D,
Sofer T,
Schurmann C,
Below JE,
Lai CQ,
Aviles-Santa ML,
Talavera GA,
Smith CE,
Petty LE,
Bottinger EP
and 13 more — show all
Chen YI,
Taylor KD,
Daviglus ML,
Cai J,
Wang T,
Tucker KL,
Ordovás JM,
Hanis CL,
Loos RJF,
Schneiderman N,
Rotter JI,
Kaplan RC,
Qi Q
Diabetes care · 2019 · PMID 31213470
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.