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Is your paper here?
2,673 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.
18 matches for
Huang Y.
Genetic determinants of daytime napping and effects on cardiometabolic health
Dashti HS,
Daghlas I,
Lane JM,
Huang Y,
Udler MS,
Wang H,
Ollila HM,
Jones SE,
Kim J,
Wood AR,
Weedon MN,
Aslibekyan S
and 2 more — show all
23andMe Research Team
Nature communications · 2021 · PMID 33568662 · open access
12 pages+
Genetic insights into biological mechanisms governing human ovarian ageing
Ruth KS,
Day FR,
Hussain J,
Martínez-Marchal A,
Aiken CE,
Azad A,
Thompson DJ,
Knoblochova L,
Abe H,
Tarry-Adkins JL,
Gonzalez JM,
Fontanillas P
and 256 more — show all
Claringbould A,
Bakker OB,
Sulem P,
Walters RG,
Terao C,
Turon S,
Horikoshi M,
Lin K,
Onland-Moret NC,
Sankar A,
Hertz EPT,
Timshel PN,
Shukla V,
Borup R,
Olsen KW,
Aguilera P,
Ferrer-Roda M,
Huang Y,
Stankovic S,
Timmers PRHJ,
Ahearn TU,
Alizadeh BZ,
Naderi E,
Andrulis IL,
Arnold AM,
Aronson KJ,
Augustinsson A,
Bandinelli S,
Barbieri CM,
Beaumont RN,
Becher H,
Beckmann MW,
Benonisdottir S,
Bergmann S,
Bochud M,
Boerwinkle E,
Bojesen SE,
Bolla MK,
Boomsma DI,
Bowker N,
Brody JA,
Broer L,
Buring JE,
Campbell A,
Campbell H,
Castelao JE,
Catamo E,
Chanock SJ,
Chenevix-Trench G,
Ciullo M,
Corre T,
Couch FJ,
Cox A,
Crisponi L,
Cross SS,
Cucca F,
Czene K,
Smith GD,
de Geus EJCN,
de Mutsert R,
De Vivo I,
Demerath EW,
Dennis J,
Dunning AM,
Dwek M,
Eriksson M,
Esko T,
Fasching PA,
Faul JD,
Ferrucci L,
Franceschini N,
Frayling TM,
Gago-Dominguez M,
Mezzavilla M,
García-Closas M,
Gieger C,
Giles GG,
Grallert H,
Gudbjartsson DF,
Gudnason V,
Guénel P,
Haiman CA,
Håkansson N,
Hall P,
Hayward C,
He C,
He W,
Heiss G,
Høffding MK,
Hopper JL,
Hottenga JJ,
Hu F,
Hunter D,
Ikram MA,
Jackson RD,
Joaquim MDR,
John EM,
Joshi PK,
Karasik D,
Kardia SLR,
Kartsonaki C,
Karlsson R,
Kitahara CM,
Kolcic I,
Kooperberg C,
Kraft P,
Kurian AW,
Kutalik Z,
La Bianca M,
LaChance G,
Langenberg C,
Launer LJ,
Laven JSE,
Lawlor DA,
Le Marchand L,
Li J,
Lindblom A,
Lindstrom S,
Lindstrom T,
Linet M,
Liu Y,
Liu S,
Luan J,
Mägi R,
Magnusson PKE,
Mangino M,
Mannermaa A,
Marco B,
Marten J,
Martin NG,
Mbarek H,
McKnight B,
Medland SE,
Meisinger C,
Meitinger T,
Menni C,
Metspalu A,
Milani L,
Milne RL,
Montgomery GW,
Mook-Kanamori DO,
Mulas A,
Mulligan AM,
Murray A,
Nalls MA,
Newman A,
Noordam R,
Nutile T,
Nyholt DR,
Olshan AF,
Olsson H,
Painter JN,
Patel AV,
Pedersen NL,
Perjakova N,
Peters A,
Peters U,
Pharoah PDP,
Polasek O,
Porcu E,
Psaty BM,
Rahman I,
Rennert G,
Rennert HS,
Ridker PM,
Ring SM,
Robino A,
Rose LM,
Rosendaal FR,
Rossouw J,
Rudan I,
Rueedi R,
Ruggiero D,
Sala CF,
Saloustros E,
Sandler DP,
Sanna S,
Sawyer EJ,
Sarnowski C,
Schlessinger D,
Schmidt MK,
Schoemaker MJ,
Schraut KE,
Scott C,
Shekari S,
Shrikhande A,
Smith AV,
Smith BH,
Smith JA,
Sorice R,
Southey MC,
Spector TD,
Spinelli JJ,
Stampfer M,
Stöckl D,
van Meurs JBJ,
Strauch K,
Styrkarsdottir U,
Swerdlow AJ,
Tanaka T,
Teras LR,
Teumer A,
Þorsteinsdottir U,
Timpson NJ,
Toniolo D,
Traglia M,
Troester MA,
Truong T,
Tyrrell J,
Uitterlinden AG,
Ulivi S,
Vachon CM,
Vitart V,
Völker U,
Vollenweider P,
Völzke H,
Wang Q,
Wareham NJ,
Weinberg CR,
Weir DR,
Wilcox AN,
van Dijk KW,
Willemsen G,
Wilson JF,
Wolffenbuttel BHR,
Wolk A,
Wood AR,
Zhao W,
Zygmunt M,
Chen Z,
Li L,
Franke L,
Burgess S,
Deelen P,
Pers TH,
Grøndahl ML,
Andersen CY,
Pujol A,
Lopez-Contreras AJ,
Daniel JA,
Stefansson K,
Chang-Claude J,
van der Schouw YT,
Lunetta KL,
Chasman DI,
Easton DF,
Visser JA,
Ozanne SE,
Namekawa SH,
Solc P,
Murabito JM,
Ong KK,
Hoffmann ER,
Murray A,
Roig I,
Perry JRB
Biobank-based Integrative Omics Study (BIOS) Consortium · eQTLGen Consortium and 6 more consortia
Nature · 2021 · PMID 34349265
12 pages+
Genomics and phenomics of body mass index reveals a complex disease network
Huang J,
Huffman JE,
Huang Y,
Do Valle Í,
Assimes TL,
Raghavan S,
Voight BF,
Liu C,
Barabási AL,
Huang RDL,
Hui Q,
Nguyen XT
and 26 more — show all
Ho YL,
Djousse L,
Lynch JA,
Vujkovic M,
Tcheandjieu C,
Tang H,
Damrauer SM,
Reaven PD,
Miller D,
Phillips LS,
Ng MCY,
Graff M,
Haiman CA,
Loos RJF,
North KE,
Yengo L,
Smith GD,
Saleheen D,
Gaziano JM,
Rader DJ,
Tsao PS,
Cho K,
Chang KM,
Wilson PWF,
Sun YV,
O'Donnell CJ
VA Million Veteran Program
Nature communications · 2022 · PMID 36581621 · open access
12 pages+
Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease
Klarin D,
Busenkell E,
Judy R,
Lynch J,
Levin M,
Haessler J,
Aragam K,
Chaffin M,
Haas M,
Lindström S,
Assimes TL,
Huang J
and 30 more — show all
Min Lee K,
Shao Q,
Huffman JE,
Kabrhel C,
Huang Y,
Sun YV,
Vujkovic M,
Saleheen D,
Miller DR,
Reaven P,
DuVall S,
Boden WE,
Pyarajan S,
Reiner AP,
Trégouët DA,
Henke P,
Kooperberg C,
Gaziano JM,
Concato J,
Rader DJ,
Cho K,
Chang KM,
Wilson PWF,
Smith NL,
O'Donnell CJ,
Tsao PS,
Kathiresan S,
Obi A,
Damrauer SM,
Natarajan P
INVENT Consortium · Veterans Affairs’ Million Veteran Program
Nature genetics · 2019 · PMID 31676865 · open access
7 pages
Rare-variant association analysis reveals known and new age-related hearing loss genes
Cornejo-Sanchez DM,
Li G,
Fabiha T,
Wang R,
Acharya A,
Everard JL,
Kadlubowska MK,
Huang Y,
Schrauwen I,
Wang GT,
DeWan AT,
Leal SM
European journal of human genetics : EJHG · 2023 · PMID 36788145
7 pages
Genome-wide meta-analysis identifies ancestry-specific loci for Alzheimer's disease
Ge YJ,
Chen SD,
Wu BS,
Zhang YR,
Wang J,
He XY,
Liu WS,
Chen YL,
Ou YN,
Shen XN,
Huang YY,
Gan YH
and 12 more — show all
Yang L,
Ma LZ,
Ma YH,
Chen KL,
Chen SF,
Cui M,
Tan L,
Dong Q,
Zhao QH,
Wang YJ,
Jia JP,
Yu JT
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024 · PMID 39023044 · open access
4 pages
Genome-wide association study identifies a new susceptibility locus for cleft lip with or without a cleft palate
Sun Y,
Huang Y,
Yin A,
Pan Y,
Wang Y,
Wang C,
Du Y,
Wang M,
Lan F,
Hu Z,
Wang G,
Jiang M
and 17 more — show all
Ma J,
Zhang X,
Ma H,
Ma J,
Zhang W,
Huang Q,
Zhou Z,
Ma L,
Li Y,
Jiang H,
Xie L,
Jiang Y,
Shi B,
Cheng J,
Shen H,
Wang L,
Yang Y
Nature communications · 2015 · PMID 25775280
3 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
Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic
Han F,
Faraco J,
Dong XS,
Ollila HM,
Lin L,
Li J,
An P,
Wang S,
Jiang KW,
Gao ZC,
Zhao L,
Yan H
and 13 more — show all
Liu YN,
Li QH,
Zhang XZ,
Hu Y,
Wang JY,
Lu YH,
Lu CJ,
Zhou W,
Hallmayer J,
Huang YS,
Strohl KP,
Pollmächer T,
Mignot E
PLoS genetics · 2013 · PMID 24204295 · open access
2 pages
Two new susceptibility loci 1q24.2 and 11p11.2 confer risk to severe acne
He L,
Wu WJ,
Yang JK,
Cheng H,
Zuo XB,
Lai W,
Gao TW,
Ma CL,
Luo N,
Huang JQ,
Lu FY,
Liu YQ
and 22 more — show all
Huang YJ,
Lu QJ,
Zhang HL,
Wang L,
Wang WZ,
Wang MM,
Xiao SX,
Sun Q,
Li CY,
Bai YP,
Li H,
Zhou ZC,
Zhou FS,
Chen G,
Liang B,
Qi J,
Yang XY,
Yang T,
Zheng X,
Sun LD,
Zhang XJ,
Zhang YP
Nature communications · 2014 · PMID 24399259
2 pages
Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study
Noth I,
Zhang Y,
Ma SF,
Flores C,
Barber M,
Huang Y,
Broderick SM,
Wade MS,
Hysi P,
Scuirba J,
Richards TJ,
Juan-Guardela BM
and 9 more — show all
The Lancet. Respiratory medicine · 2013 · PMID 24429156
2 pages
A genetic variant in IL-6 lowering its expression is protective for critical patients with COVID-19
Gong B,
Huang L,
He Y,
Xie W,
Yin Y,
Shi Y,
Xiao J,
Zhong L,
Zhang Y,
Jiang Z,
Hao F,
Zhou Y
and 11 more — show all
Li H,
Jiang L,
Yang X,
Song X,
Kang Y,
Tuo L,
Huang Y,
Shuai P,
Liu Y,
Zheng F,
Yang Z
Signal transduction and targeted therapy · 2022 · PMID 35368020 · open access
2 pages
Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy
Ollila HM,
Sharon E,
Lin L,
Sinnott-Armstrong N,
Ambati A,
Yogeshwar SM,
Hillary RP,
Jolanki O,
Faraco J,
Einen M,
Luo G,
Zhang J
and 78 more — show all
Han F,
Yan H,
Dong XS,
Li J,
Zhang J,
Hong SC,
Kim TW,
Dauvilliers Y,
Barateau L,
Lammers GJ,
Fronczek R,
Mayer G,
Santamaria J,
Arnulf I,
Knudsen-Heier S,
Bredahl MKL,
Thorsby PM,
Plazzi G,
Pizza F,
Moresco M,
Crowe C,
Van den Eeden SK,
Lecendreux M,
Bourgin P,
Kanbayashi T,
Martínez-Orozco FJ,
Peraita-Adrados R,
Benetó A,
Montplaisir J,
Desautels A,
Huang YS,
Jennum P,
Nevsimalova S,
Kemlink D,
Iranzo A,
Overeem S,
Wierzbicka A,
Geisler P,
Sonka K,
Honda M,
Högl B,
Stefani A,
Coelho FM,
Mantovani V,
Feketeova E,
Wadelius M,
Eriksson N,
Smedje H,
Hallberg P,
Hesla PE,
Rye D,
Pelin Z,
Ferini-Strambi L,
Bassetti CL,
Mathis J,
Khatami R,
Aran A,
Nampoothiri S,
Olsson T,
Kockum I,
Partinen M,
Perola M,
Kornum BR,
Rueger S,
Winkelmann J,
Miyagawa T,
Toyoda H,
Khor SS,
Shimada M,
Tokunaga K,
Rivas M,
Pritchard JK,
Risch N,
Kutalik Z,
O'Hara R,
Hallmayer J,
Ye CJ,
Mignot EJ
FinnGen
Nature communications · 2023 · PMID 37188663 · open access
2 pages
Genome-wide association study of B cell non-Hodgkin lymphoma identifies 3q27 as a susceptibility locus in the Chinese population
Tan DE,
Foo JN,
Bei JX,
Chang J,
Peng R,
Zheng X,
Wei L,
Huang Y,
Lim WY,
Li J,
Cui Q,
Chew SH
and 15 more — show all
Ebstein RP,
Kuperan P,
Lim ST,
Tao M,
Tan SH,
Wong A,
Wong GC,
Tan SY,
Ng SB,
Zeng YX,
Khor CC,
Lin D,
Seow AL,
Jia WH,
Liu J
Nature genetics · 2013 · PMID 23749188
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.