For researchers
Is your paper here?
2,663 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.
19 matches for
Zhu Z.
Genome-wide association study identifies 74 loci associated with educational attainment
Okbay A,
Beauchamp JP,
Fontana MA,
Lee JJ,
Pers TH,
Rietveld CA,
Turley P,
Chen GB,
Emilsson V,
Meddens SF,
Oskarsson S,
Pickrell JK
and 243 more — show all
Thom K,
Timshel P,
de Vlaming R,
Abdellaoui A,
Ahluwalia TS,
Bacelis J,
Baumbach C,
Bjornsdottir G,
Brandsma JH,
Pina Concas M,
Derringer J,
Furlotte NA,
Galesloot TE,
Girotto G,
Gupta R,
Hall LM,
Harris SE,
Hofer E,
Horikoshi M,
Huffman JE,
Kaasik K,
Kalafati IP,
Karlsson R,
Kong A,
Lahti J,
van der Lee SJ,
deLeeuw C,
Lind PA,
Lindgren KO,
Liu T,
Mangino M,
Marten J,
Mihailov E,
Miller MB,
van der Most PJ,
Oldmeadow C,
Payton A,
Pervjakova N,
Peyrot WJ,
Qian Y,
Raitakari O,
Rueedi R,
Salvi E,
Schmidt B,
Schraut KE,
Shi J,
Smith AV,
Poot RA,
St Pourcain B,
Teumer A,
Thorleifsson G,
Verweij N,
Vuckovic D,
Wellmann J,
Westra HJ,
Yang J,
Zhao W,
Zhu Z,
Alizadeh BZ,
Amin N,
Bakshi A,
Baumeister SE,
Biino G,
Bønnelykke K,
Boyle PA,
Campbell H,
Cappuccio FP,
Davies G,
De Neve JE,
Deloukas P,
Demuth I,
Ding J,
Eibich P,
Eisele L,
Eklund N,
Evans DM,
Faul JD,
Feitosa MF,
Forstner AJ,
Gandin I,
Gunnarsson B,
Halldórsson BV,
Harris TB,
Heath AC,
Hocking LJ,
Holliday EG,
Homuth G,
Horan MA,
Hottenga JJ,
de Jager PL,
Joshi PK,
Jugessur A,
Kaakinen MA,
Kähönen M,
Kanoni S,
Keltigangas-Järvinen L,
Kiemeney LA,
Kolcic I,
Koskinen S,
Kraja AT,
Kroh M,
Kutalik Z,
Latvala A,
Launer LJ,
Lebreton MP,
Levinson DF,
Lichtenstein P,
Lichtner P,
Liewald DC,
Loukola A,
Madden PA,
Mägi R,
Mäki-Opas T,
Marioni RE,
Marques-Vidal P,
Meddens GA,
McMahon G,
Meisinger C,
Meitinger T,
Milaneschi Y,
Milani L,
Montgomery GW,
Myhre R,
Nelson CP,
Nyholt DR,
Ollier WE,
Palotie A,
Paternoster L,
Pedersen NL,
Petrovic KE,
Porteous DJ,
Räikkönen K,
Ring SM,
Robino A,
Rostapshova O,
Rudan I,
Rustichini A,
Salomaa V,
Sanders AR,
Sarin AP,
Schmidt H,
Scott RJ,
Smith BH,
Smith JA,
Staessen JA,
Steinhagen-Thiessen E,
Strauch K,
Terracciano A,
Tobin MD,
Ulivi S,
Vaccargiu S,
Quaye L,
van Rooij FJ,
Venturini C,
Vinkhuyzen AA,
Völker U,
Völzke H,
Vonk JM,
Vozzi D,
Waage J,
Ware EB,
Willemsen G,
Attia JR,
Bennett DA,
Berger K,
Bertram L,
Bisgaard H,
Boomsma DI,
Borecki IB,
Bültmann U,
Chabris CF,
Cucca F,
Cusi D,
Deary IJ,
Dedoussis GV,
van Duijn CM,
Eriksson JG,
Franke B,
Franke L,
Gasparini P,
Gejman PV,
Gieger C,
Grabe HJ,
Gratten J,
Groenen PJ,
Gudnason V,
van der Harst P,
Hayward C,
Hinds DA,
Hoffmann W,
Hyppönen E,
Iacono WG,
Jacobsson B,
Järvelin MR,
Jöckel KH,
Kaprio J,
Kardia SL,
Lehtimäki T,
Lehrer SF,
Magnusson PK,
Martin NG,
McGue M,
Metspalu A,
Pendleton N,
Penninx BW,
Perola M,
Pirastu N,
Pirastu M,
Polasek O,
Posthuma D,
Power C,
Province MA,
Samani NJ,
Schlessinger D,
Schmidt R,
Sørensen TI,
Spector TD,
Stefansson K,
Thorsteinsdottir U,
Thurik AR,
Timpson NJ,
Tiemeier H,
Tung JY,
Uitterlinden AG,
Vitart V,
Vollenweider P,
Weir DR,
Wilson JF,
Wright AF,
Conley DC,
Krueger RF,
Davey Smith G,
Hofman A,
Laibson DI,
Medland SE,
Meyer MN,
Yang J,
Johannesson M,
Visscher PM,
Esko T,
Koellinger PD,
Cesarini D,
Benjamin DJ
LifeLines Cohort Study
Nature · 2016 · PMID 27225129 · open access
12 pages+
Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes
Xue A,
Wu Y,
Zhu Z,
Zhang F,
Kemper KE,
Zheng Z,
Yengo L,
Lloyd-Jones LR,
Sidorenko J,
Wu Y,
McRae AF,
Visscher PM
and 2 more — show all
eQTLGen Consortium
Nature communications · 2018 · PMID 30054458 · open access
12 pages+
Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration
Revez JA,
Lin T,
Qiao Z,
Xue A,
Holtz Y,
Zhu Z,
Zeng J,
Wang H,
Sidorenko J,
Kemper KE,
Vinkhuyzen AAE,
Frater J
and 9 more — show all
Nature communications · 2020 · PMID 32242144 · open access
12 pages+
A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic aetiology with obesity
Zhu Z,
Li J,
Si J,
Ma B,
Shi H,
Lv J,
Cao W,
Guo Y,
Millwood IY,
Walters RG,
Lin K,
Yang L
and 12 more — show all
Chen Y,
Du H,
Yu B,
Hasegawa K,
Camargo CA Jr,
Moffatt MF,
Cookson WOC,
Chen J,
Chen Z,
Li L,
Yu C,
Liang L
The European respiratory journal · 2021 · PMID 33766948
12 pages+
The correlates of neonatal complement component 3 and 4 protein concentrations with a focus on psychiatric and autoimmune disorders
Borbye-Lorenzen N,
Zhu Z,
Agerbo E,
Albiñana C,
Benros ME,
Bian B,
Børglum AD,
Bulik CM,
Debost JPG,
Grove J,
Hougaard DM,
McRae AF
and 12 more — show all
Mors O,
Mortensen PB,
Musliner KL,
Nordentoft M,
Petersen LV,
Privé F,
Sidorenko J,
Skogstrand K,
Werge T,
Wray NR,
Vilhjálmsson BJ,
McGrath JJ
Cell genomics · 2023 · PMID 38116117 · open access
12 pages+
Shared genetic and experimental links between obesity-related traits and asthma subtypes in UK Biobank
Zhu Z,
Guo Y,
Shi H,
Liu CL,
Panganiban RA,
Chung W,
O'Connor LJ,
Himes BE,
Gazal S,
Hasegawa K,
Camargo CA Jr,
Qi L
and 5 more — show all
The Journal of allergy and clinical immunology · 2020 · PMID 31669095
6 pages
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Lu Y,
Day FR,
Gustafsson S,
Buchkovich ML,
Na J,
Bataille V,
Cousminer DL,
Dastani Z,
Drong AW,
Esko T,
Evans DM,
Falchi M
and 247 more — show all
Feitosa MF,
Ferreira T,
Hedman ÅK,
Haring R,
Hysi PG,
Iles MM,
Justice AE,
Kanoni S,
Lagou V,
Li R,
Li X,
Locke A,
Lu C,
Mägi R,
Perry JR,
Pers TH,
Qi Q,
Sanna M,
Schmidt EM,
Scott WR,
Shungin D,
Teumer A,
Vinkhuyzen AA,
Walker RW,
Westra HJ,
Zhang M,
Zhang W,
Zhao JH,
Zhu Z,
Afzal U,
Ahluwalia TS,
Bakker SJ,
Bellis C,
Bonnefond A,
Borodulin K,
Buchman AS,
Cederholm T,
Choh AC,
Choi HJ,
Curran JE,
de Groot LC,
De Jager PL,
Dhonukshe-Rutten RA,
Enneman AW,
Eury E,
Evans DS,
Forsen T,
Friedrich N,
Fumeron F,
Garcia ME,
Gärtner S,
Han BG,
Havulinna AS,
Hayward C,
Hernandez D,
Hillege H,
Ittermann T,
Kent JW,
Kolcic I,
Laatikainen T,
Lahti J,
Mateo Leach I,
Lee CG,
Lee JY,
Liu T,
Liu Y,
Lobbens S,
Loh M,
Lyytikäinen LP,
Medina-Gomez C,
Michaëlsson K,
Nalls MA,
Nielson CM,
Oozageer L,
Pascoe L,
Paternoster L,
Polašek O,
Ripatti S,
Sarzynski MA,
Shin CS,
Narančić NS,
Spira D,
Srikanth P,
Steinhagen-Thiessen E,
Sung YJ,
Swart KM,
Taittonen L,
Tanaka T,
Tikkanen E,
van der Velde N,
van Schoor NM,
Verweij N,
Wright AF,
Yu L,
Zmuda JM,
Eklund N,
Forrester T,
Grarup N,
Jackson AU,
Kristiansson K,
Kuulasmaa T,
Kuusisto J,
Lichtner P,
Luan J,
Mahajan A,
Männistö S,
Palmer CD,
Ried JS,
Scott RA,
Stancáková A,
Wagner PJ,
Demirkan A,
Döring A,
Gudnason V,
Kiel DP,
Kühnel B,
Mangino M,
Mcknight B,
Menni C,
O'Connell JR,
Oostra BA,
Shuldiner AR,
Song K,
Vandenput L,
van Duijn CM,
Vollenweider P,
White CC,
Boehnke M,
Boettcher Y,
Cooper RS,
Forouhi NG,
Gieger C,
Grallert H,
Hingorani A,
Jørgensen T,
Jousilahti P,
Kivimaki M,
Kumari M,
Laakso M,
Langenberg C,
Linneberg A,
Luke A,
Mckenzie CA,
Palotie A,
Pedersen O,
Peters A,
Strauch K,
Tayo BO,
Wareham NJ,
Bennett DA,
Bertram L,
Blangero J,
Blüher M,
Bouchard C,
Campbell H,
Cho NH,
Cummings SR,
Czerwinski SA,
Demuth I,
Eckardt R,
Eriksson JG,
Ferrucci L,
Franco OH,
Froguel P,
Gansevoort RT,
Hansen T,
Harris TB,
Hastie N,
Heliövaara M,
Hofman A,
Jordan JM,
Jula A,
Kähönen M,
Kajantie E,
Knekt PB,
Koskinen S,
Kovacs P,
Lehtimäki T,
Lind L,
Liu Y,
Orwoll ES,
Osmond C,
Perola M,
Pérusse L,
Raitakari OT,
Rankinen T,
Rao DC,
Rice TK,
Rivadeneira F,
Rudan I,
Salomaa V,
Sørensen TI,
Stumvoll M,
Tönjes A,
Towne B,
Tranah GJ,
Tremblay A,
Uitterlinden AG,
van der Harst P,
Vartiainen E,
Viikari JS,
Vitart V,
Vohl MC,
Völzke H,
Walker M,
Wallaschofski H,
Wild S,
Wilson JF,
Yengo L,
Bishop DT,
Borecki IB,
Chambers JC,
Cupples LA,
Dehghan A,
Deloukas P,
Fatemifar G,
Fox C,
Furey TS,
Franke L,
Han J,
Hunter DJ,
Karjalainen J,
Karpe F,
Kaplan RC,
Kooner JS,
McCarthy MI,
Murabito JM,
Morris AP,
Bishop JA,
North KE,
Ohlsson C,
Ong KK,
Prokopenko I,
Richards JB,
Schadt EE,
Spector TD,
Widén E,
Willer CJ,
Yang J,
Ingelsson E,
Mohlke KL,
Hirschhorn JN,
Pospisilik JA,
Zillikens MC,
Lindgren C,
Kilpeläinen TO,
Loos RJ
Nature communications · 2016 · PMID 26833246 · open access
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
A Functional SNP in BNC2 Is Associated with Adolescent Idiopathic Scoliosis
Ogura Y,
Kou I,
Miura S,
Takahashi A,
Xu L,
Takeda K,
Takahashi Y,
Kono K,
Kawakami N,
Uno K,
Ito M,
Minami S
and 23 more — show all
Yonezawa I,
Yanagida H,
Taneichi H,
Zhu Z,
Tsuji T,
Suzuki T,
Sudo H,
Kotani T,
Watanabe K,
Hosogane N,
Okada E,
Iida A,
Nakajima M,
Sudo A,
Chiba K,
Hiraki Y,
Toyama Y,
Qiu Y,
Shukunami C,
Kamatani Y,
Kubo M,
Matsumoto M,
Ikegawa S
American journal of human genetics · 2015 · PMID 26211971
2 pages
Genome-wide association study identifies new susceptibility loci for adolescent idiopathic scoliosis in Chinese girls
Zhu Z,
Tang NL,
Xu L,
Qin X,
Mao S,
Song Y,
Liu L,
Li F,
Liu P,
Yi L,
Chang J,
Jiang L
and 25 more — show all
Ng BK,
Shi B,
Zhang W,
Qiao J,
Sun X,
Qiu X,
Wang Z,
Wang F,
Xie D,
Chen L,
Chen Z,
Jin M,
Han X,
Hu Z,
Zhang Z,
Liu Z,
Zhu F,
Qian BP,
Yu Y,
Wang B,
Lee KM,
Lee WYW,
Lam TP,
Qiu Y,
Cheng JC
Nature communications · 2015 · PMID 26394188 · open access
2 pages
A genome-wide association study identifies six novel risk loci for primary biliary cholangitis
Qiu F,
Tang R,
Zuo X,
Shi X,
Wei Y,
Zheng X,
Dai Y,
Gong Y,
Wang L,
Xu P,
Zhu X,
Wu J
and 78 more — show all
Han C,
Gao Y,
Zhang K,
Jiang Y,
Zhou J,
Shao Y,
Hu Z,
Tian Y,
Zhang H,
Dai N,
Liu L,
Wu X,
Zhao W,
Zhang X,
Zang Z,
Nie J,
Sun W,
Zhao Y,
Mao Y,
Jiang P,
Ji H,
Dong Q,
Li J,
Li Z,
Bai X,
Li L,
Lin M,
Dong M,
Li J,
Zhu P,
Wang C,
Zhang Y,
Jiang P,
Wang Y,
Jawed R,
Xu J,
Zhang Y,
Wang Q,
Yang Y,
Yang F,
Lian M,
Jiang X,
Xiao X,
Li Y,
Fang J,
Qiu D,
Zhu Z,
Qiu H,
Zhang J,
Tian W,
Chen S,
Jiang L,
Ji B,
Li P,
Chen G,
Wu T,
Sun Y,
Yu J,
Tang H,
He M,
Xia M,
Pei H,
Huang L,
Qing Z,
Wu J,
Huang Q,
Han J,
Xie W,
Sun Z,
Guo J,
He G,
Eric Gershwin M,
Lian Z,
Liu X,
Seldin MF,
Liu X,
Chen W,
Ma X
Nature communications · 2017 · PMID 28425483 · open access
2 pages
Association Study and Fine-Mapping Major Histocompatibility Complex Analysis of Pemphigus Vulgaris in a Han Chinese Population
Gao J,
Zhu C,
Zhang Y,
Sheng Y,
Yang F,
Wang W,
Qian W,
Chen S,
Zhu Q,
Zuo X,
Tang H,
Tang X
and 13 more — show all
Li Y,
Cheng H,
Zhou F,
Liu S,
Chen G,
Zheng X,
Zhu Z,
Wang Z,
Yang S,
Luo X,
Ye D,
Zhang X,
Sun L
The Journal of investigative dermatology · 2018 · PMID 29857070
2 pages
Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity
Yu Y,
Zuo X,
He M,
Gao J,
Fu Y,
Qin C,
Meng L,
Wang W,
Song Y,
Cheng Y,
Zhou F,
Chen G
and 18 more — show all
Zheng X,
Wang X,
Liang B,
Zhu Z,
Fu X,
Sheng Y,
Hao J,
Liu Z,
Yan H,
Mangold E,
Ruczinski I,
Liu J,
Marazita ML,
Ludwig KU,
Beaty TH,
Zhang X,
Sun L,
Bian Z
Nature communications · 2017 · PMID 28232668 · open access
1 page
Genome-wide Association Studies of Specific Antinuclear Autoantibody Subphenotypes in Primary Biliary Cholangitis
Wang C,
Zheng X,
Jiang P,
Tang R,
Gong Y,
Dai Y,
Wang L,
Xu P,
Sun W,
Wang L,
Han C,
Jiang Y
and 39 more — show all
Wei Y,
Zhang K,
Wu J,
Shao Y,
Gao Y,
Yu J,
Hu Z,
Zang Z,
Zhao Y,
Wu X,
Dai N,
Liu L,
Nie J,
Jiang B,
Lin M,
Li L,
Li Y,
Chen S,
Shu L,
Qiu F,
Wu Q,
Zhang M,
Chen R,
Jawed R,
Zhang Y,
Shi X,
Zhu Z,
Pei H,
Huang L,
Zhao W,
Tian Y,
Zhu X,
Qiu H,
Gershwin ME,
Chen W,
Seldin MF,
Liu X,
Sun L,
Ma X
Hepatology (Baltimore, Md.) · 2019 · PMID 30854688 · open access
1 page
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
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.