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70 matches for
Wang C,
showing the first 20.
Cross-ancestry genome-wide association studies of brain imaging phenotypes
Fu J,
Zhang Q,
Wang J,
Wang M,
Zhang B,
Zhu W,
Qiu S,
Geng Z,
Cui G,
Yu Y,
Liao W,
Zhang H
and 32 more — show all
Gao B,
Xu X,
Han T,
Yao Z,
Qin W,
Liu F,
Liang M,
Wang S,
Xu Q,
Xu J,
Zhang P,
Li W,
Shi D,
Wang C,
Lui S,
Yan Z,
Chen F,
Zhang J,
Li J,
Shen W,
Miao Y,
Wang D,
Xian J,
Gao JH,
Zhang X,
Xu K,
Zuo XN,
Zhang L,
Ye Z,
Cheng J,
Li MJ,
Yu C
CHIMGEN Consortium
Nature genetics · 2024 · PMID 38811844
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+
Cross-ancestry and sex-stratified genome-wide association analyses of amygdala and subnucleus volumes
Ji Y,
Liu N,
Yang Y,
Wang M,
Cheng J,
Zhu W,
Qiu S,
Geng Z,
Cui G,
Yu Y,
Liao W,
Zhang H
and 33 more — show all
Gao B,
Xu X,
Han T,
Yao Z,
Zhang Q,
Qin W,
Liu F,
Liang M,
Wang S,
Xu Q,
Xu J,
Fu J,
Zhang P,
Li W,
Shi D,
Wang C,
Lui S,
Yan Z,
Chen F,
Zhang J,
Shen W,
Miao Y,
Wang D,
Gao JH,
Zhang X,
Xu K,
Zuo XN,
Zhang L,
Ye Z,
Li MJ,
Xian J,
Zhang B,
Yu C
CHIMGEN Consortium
Nature genetics · 2025 · PMID 40097784
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+
Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis
Paternoster L,
Standl M,
Waage J,
Baurecht H,
Hotze M,
Strachan DP,
Curtin JA,
Bønnelykke K,
Tian C,
Takahashi A,
Esparza-Gordillo J,
Alves AC
and 140 more — show all
Thyssen JP,
den Dekker HT,
Ferreira MA,
Altmaier E,
Sleiman PM,
Xiao FL,
Gonzalez JR,
Marenholz I,
Kalb B,
Yanes MP,
Xu CJ,
Carstensen L,
Groen-Blokhuis MM,
Venturini C,
Pennell CE,
Barton SJ,
Levin AM,
Curjuric I,
Bustamante M,
Kreiner-Møller E,
Lockett GA,
Bacelis J,
Bacelis J,
Bunyavanich S,
Myers RA,
Matanovic A,
Kumar A,
Tung JY,
Hirota T,
Kubo M,
McArdle WL,
Henderson AJ,
Kemp JP,
Zheng J,
Smith GD,
Rüschendorf F,
Bauerfeind A,
Lee-Kirsch MA,
Arnold A,
Homuth G,
Schmidt CO,
Mangold E,
Cichon S,
Keil T,
Rodríguez E,
Peters A,
Peters A,
Franke A,
Lieb W,
Novak N,
Fölster-Holst R,
Horikoshi M,
Pekkanen J,
Sebert S,
Husemoen LL,
Grarup N,
de Jongste JC,
Rivadeneira F,
Hofman A,
Jaddoe VW,
Pasmans SG,
Elbert NJ,
Uitterlinden AG,
Marks GB,
Thompson PJ,
Matheson MC,
Robertson CF,
Ried JS,
Li J,
Zuo XB,
Zheng XD,
Yin XY,
Sun LD,
McAleer MA,
O'Regan GM,
Fahy CM,
Campbell LE,
Macek M,
Kurek M,
Hu D,
Eng C,
Postma DS,
Feenstra B,
Geller F,
Hottenga JJ,
Middeldorp CM,
Hysi P,
Bataille V,
Spector T,
Tiesler CM,
Thiering E,
Pahukasahasram B,
Yang JJ,
Imboden M,
Huntsman S,
Vilor-Tejedor N,
Relton CL,
Myhre R,
Nystad W,
Custovic A,
Weiss ST,
Meyers DA,
Söderhäll C,
Melén E,
Ober C,
Raby BA,
Simpson A,
Jacobsson B,
Holloway JW,
Bisgaard H,
Sunyer J,
Hensch NMP,
Williams LK,
Godfrey KM,
Wang CA,
Boomsma DI,
Melbye M,
Koppelman GH,
Jarvis D,
McLean WI,
Irvine AD,
Zhang XJ,
Hakonarson H,
Gieger C,
Burchard EG,
Martin NG,
Duijts L,
Linneberg A,
Jarvelin MR,
Noethen MM,
Lau S,
Hübner N,
Lee YA,
Tamari M,
Hinds DA,
Glass D,
Brown SJ,
Heinrich J,
Evans DM,
Weidinger S
Australian Asthma Genetics Consortium (AAGC)
Nature genetics · 2015 · PMID 26482879 · open access
11 pages
Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis
Medina-Gomez C,
Mullin BH,
Chesi A,
Prijatelj V,
Kemp JP,
Shochat-Carvalho C,
Trajanoska K,
Wang C,
Joro R,
Evans TE,
Schraut KE,
Li-Gao R
and 46 more — show all
Ahluwalia TS,
Zillikens MC,
Zhu K,
Mook-Kanamori DO,
Evans DS,
Nethander M,
Knol MJ,
Thorleifsson G,
Prokic I,
Zemel B,
Broer L,
McGuigan FE,
van Schoor NM,
Reppe S,
Pawlak MA,
Ralston SH,
van der Velde N,
Lorentzon M,
Stefansson K,
Adams HHH,
Wilson SG,
Ikram MA,
Walsh JP,
Lakka TA,
Gautvik KM,
Wilson JF,
Orwoll ES,
van Duijn CM,
Bønnelykke K,
Uitterlinden AG,
Styrkársdóttir U,
Akesson KE,
Spector TD,
Tobias JH,
Ohlsson C,
Felix JF,
Bisgaard H,
Grant SFA,
Richards JB,
Evans DM,
van der Eerden B,
van de Peppel J,
Ackert-Bicknell C,
Karasik D,
Kague E,
Rivadeneira F
Communications biology · 2023 · PMID 37402774 · open access
11 pages
Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth
Beaumont RN,
Flatley C,
Vaudel M,
Wu X,
Chen J,
Moen GH,
Skotte L,
Helgeland Ø,
Solé-Navais P,
Banasik K,
Albiñana C,
Ronkainen J
and 76 more — show all
Fadista J,
Stinson SE,
Trajanoska K,
Wang CA,
Westergaard D,
Srinivasan S,
Sánchez-Soriano C,
Bilbao JR,
Allard C,
Groleau M,
Kuulasmaa T,
Leirer DJ,
White F,
Jacques PÉ,
Cheng H,
Hao K,
Andreassen OA,
Åsvold BO,
Atalay M,
Bhatta L,
Bouchard L,
Brumpton BM,
Brunak S,
Bybjerg-Grauholm J,
Ebbing C,
Elliott P,
Engelbrechtsen L,
Erikstrup C,
Estarlich M,
Franks S,
Gaillard R,
Geller F,
Grove J,
Hougaard DM,
Kajantie E,
Morgen CS,
Nohr EA,
Nyegaard M,
Palmer CNA,
Pedersen OB,
Rivadeneira F,
Sebert S,
Shields BM,
Stoltenberg C,
Surakka I,
Thørner LW,
Ullum H,
Vaarasmaki M,
Vilhjalmsson BJ,
Willer CJ,
Lakka TA,
Gybel-Brask D,
Bustamante M,
Hansen T,
Pearson ER,
Reynolds RM,
Ostrowski SR,
Pennell CE,
Jaddoe VWV,
Felix JF,
Hattersley AT,
Melbye M,
Lawlor DA,
Hveem K,
Werge T,
Nielsen HS,
Magnus P,
Evans DM,
Jacobsson B,
Järvelin MR,
Zhang G,
Hivert MF,
Johansson S,
Freathy RM,
Feenstra B,
Njølstad PR
Early Growth Genetics (EGG) Consortium
Nature genetics · 2023 · PMID 37798380 · open access
10 pages
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
Mahajan A,
Go MJ,
Zhang W,
Below JE,
Gaulton KJ,
Ferreira T,
Horikoshi M,
Johnson AD,
Ng MC,
Prokopenko I,
Saleheen D,
Wang X
and 322 more — show all
Zeggini E,
Abecasis GR,
Adair LS,
Almgren P,
Atalay M,
Aung T,
Baldassarre D,
Balkau B,
Bao Y,
Barnett AH,
Barroso I,
Basit A,
Been LF,
Beilby J,
Bell GI,
Benediktsson R,
Bergman RN,
Boehm BO,
Boerwinkle E,
Bonnycastle LL,
Burtt N,
Cai Q,
Campbell H,
Carey J,
Cauchi S,
Caulfield M,
Chan JC,
Chang LC,
Chang TJ,
Chang YC,
Charpentier G,
Chen CH,
Chen H,
Chen YT,
Chia KS,
Chidambaram M,
Chines PS,
Cho NH,
Cho YM,
Chuang LM,
Chuang LM,
Collins FS,
Cornelis MC,
Couper DJ,
Crenshaw AT,
van Dam RM,
Danesh J,
Das D,
de Faire U,
Dedoussis G,
Deloukas P,
Dimas AS,
Dina C,
Doney AS,
Donnelly PJ,
Dorkhan M,
van Duijn C,
Dupuis J,
Edkins S,
Elliott P,
Emilsson V,
Erbel R,
Eriksson JG,
Escobedo J,
Esko T,
Eury E,
Florez JC,
Fontanillas P,
Forouhi NG,
Forsen T,
Fox C,
Fraser RM,
Frayling TM,
Froguel P,
Frossard P,
Gao Y,
Gertow K,
Gieger C,
Gigante B,
Grallert H,
Grant GB,
Grrop LC,
Groves CJ,
Grundberg E,
Guiducci C,
Hamsten A,
Han BG,
Hara K,
Hassanali N,
Hattersley AT,
Hayward C,
Hedman AK,
Herder C,
Hofman A,
Holmen OL,
Hovingh K,
Hreidarsson AB,
Hu C,
Hu FB,
Hui J,
Humphries SE,
Hunt SE,
Hunter DJ,
Hveem K,
Hydrie ZI,
Ikegami H,
Illig T,
Ingelsson E,
Islam M,
Isomaa B,
Jackson AU,
Jafar T,
James A,
Jia W,
Jöckel KH,
Jonsson A,
Jowett JB,
Kadowaki T,
Kang HM,
Kanoni S,
Kao WH,
Kathiresan S,
Kato N,
Katulanda P,
Keinanen-Kiukaanniemi KM,
Kelly AM,
Khan H,
Khaw KT,
Khor CC,
Kim HL,
Kim S,
Kim YJ,
Kinnunen L,
Klopp N,
Kong A,
Korpi-Hyövälti E,
Kowlessur S,
Kraft P,
Kravic J,
Kristensen MM,
Krithika S,
Kumar A,
Kumate J,
Kuusisto J,
Kwak SH,
Laakso M,
Lagou V,
Lakka TA,
Langenberg C,
Langford C,
Lawrence R,
Leander K,
Lee JM,
Lee NR,
Li M,
Li X,
Li Y,
Liang J,
Liju S,
Lim WY,
Lind L,
Lindgren CM,
Lindholm E,
Liu CT,
Liu JJ,
Lobbens S,
Long J,
Loos RJ,
Lu W,
Luan J,
Lyssenko V,
Ma RC,
Maeda S,
Mägi R,
Männisto S,
Matthews DR,
Meigs JB,
Melander O,
Metspalu A,
Meyer J,
Mirza G,
Mihailov E,
Moebus S,
Mohan V,
Mohlke KL,
Morris AD,
Mühleisen TW,
Müller-Nurasyid M,
Musk B,
Nakamura J,
Nakashima E,
Navarro P,
Ng PK,
Nica AC,
Nilsson PM,
Njølstad I,
Nöthen MM,
Ohnaka K,
Ong TH,
Owen KR,
Palmer CN,
Pankow JS,
Park KS,
Parkin M,
Pechlivanis S,
Pedersen NL,
Peltonen L,
Perry JR,
Peters A,
Pinidiyapathirage JM,
Platou CG,
Potter S,
Price JF,
Qi L,
Radha V,
Rallidis L,
Rasheed A,
Rathman W,
Rauramaa R,
Raychaudhuri S,
Rayner NW,
Rees SD,
Rehnberg E,
Ripatti S,
Robertson N,
Roden M,
Rossin EJ,
Rudan I,
Rybin D,
Saaristo TE,
Salomaa V,
Saltevo J,
Samuel M,
Sanghera DK,
Saramies J,
Scott J,
Scott LJ,
Scott RA,
Segrè AV,
Sehmi J,
Sennblad B,
Shah N,
Shah S,
Shera AS,
Shu XO,
Shuldiner AR,
Sigurđsson G,
Sijbrands E,
Silveira A,
Sim X,
Sivapalaratnam S,
Small KS,
So WY,
Stančáková A,
Stefansson K,
Steinbach G,
Steinthorsdottir V,
Stirrups K,
Strawbridge RJ,
Stringham HM,
Sun Q,
Suo C,
Syvänen AC,
Takayanagi R,
Takeuchi F,
Tay WT,
Teslovich TM,
Thorand B,
Thorleifsson G,
Thorsteinsdottir U,
Tikkanen E,
Trakalo J,
Tremoli E,
Trip MD,
Tsai FJ,
Tuomi T,
Tuomilehto J,
Uitterlinden AG,
Valladares-Salgado A,
Vedantam S,
Veglia F,
Voight BF,
Wang C,
Wareham NJ,
Wennauer R,
Wickremasinghe AR,
Wilsgaard T,
Wilson JF,
Wiltshire S,
Winckler W,
Wong TY,
Wood AR,
Wu JY,
Wu Y,
Yamamoto K,
Yamauchi T,
Yang M,
Yengo L,
Yokota M,
Young R,
Zabaneh D,
Zhang F,
Zhang R,
Zheng W,
Zheng W,
Zimmet PZ,
Altshuler D,
Bowden DW,
Cho YS,
Cox NJ,
Cruz M,
Hanis CL,
Kooner J,
Lee JY,
Seielstad M,
Teo YY,
Boehnke M,
Parra EJ,
Chambers JC,
Tai ES,
McCarthy MI,
Morris AP
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Asian Genetic Epidemiology Network Type 2 Diabetes (AGEN-T2D) Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24509480 · open access
9 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
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
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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.