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49 matches for
Liu CT,
showing the first 20.
Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions
de Vries PS,
Brown MR,
Bentley AR,
Sung YJ,
Winkler TW,
Ntalla I,
Schwander K,
Kraja AT,
Guo X,
Franceschini N,
Cheng CY,
Sim X
and 254 more — show all
Vojinovic D,
Huffman JE,
Musani SK,
Li C,
Feitosa MF,
Richard MA,
Noordam R,
Aschard H,
Bartz TM,
Bielak LF,
Deng X,
Dorajoo R,
Lohman KK,
Manning AK,
Rankinen T,
Smith AV,
Tajuddin SM,
Evangelou E,
Graff M,
Alver M,
Boissel M,
Chai JF,
Chen X,
Divers J,
Gandin I,
Gao C,
Goel A,
Hagemeijer Y,
Harris SE,
Hartwig FP,
He M,
Horimoto ARVR,
Hsu FC,
Jackson AU,
Kasturiratne A,
Komulainen P,
Kühnel B,
Laguzzi F,
Lee JH,
Luan J,
Lyytikäinen LP,
Matoba N,
Nolte IM,
Pietzner M,
Riaz M,
Said MA,
Scott RA,
Sofer T,
Stančáková A,
Takeuchi F,
Tayo BO,
van der Most PJ,
Varga TV,
Wang Y,
Ware EB,
Wen W,
Yanek LR,
Zhang W,
Zhao JH,
Afaq S,
Amin N,
Amini M,
Arking DE,
Aung T,
Ballantyne C,
Boerwinkle E,
Broeckel U,
Campbell A,
Canouil M,
Charumathi S,
Chen YI,
Connell JM,
de Faire U,
de las Fuentes L,
de Mutsert R,
de Silva HJ,
Ding J,
Dominiczak AF,
Duan Q,
Eaton CB,
Eppinga RN,
Faul JD,
Fisher V,
Forrester T,
Franco OH,
Friedlander Y,
Ghanbari M,
Giulianini F,
Grabe HJ,
Grove ML,
Gu CC,
Harris TB,
Heikkinen S,
Heng CK,
Hirata M,
Hixson JE,
Howard BV,
Ikram MA,
Jacobs DR,
Johnson C,
Jonas JB,
Kammerer CM,
Katsuya T,
Khor CC,
Kilpeläinen TO,
Koh WP,
Koistinen HA,
Kolcic I,
Kooperberg C,
Krieger JE,
Kritchevsky SB,
Kubo M,
Kuusisto J,
Lakka TA,
Langefeld CD,
Langenberg C,
Launer LJ,
Lehne B,
Lemaitre RN,
Li Y,
Liang J,
Liu J,
Liu K,
Loh M,
Louie T,
Mägi R,
Manichaikul AW,
McKenzie CA,
Meitinger T,
Metspalu A,
Milaneschi Y,
Milani L,
Mohlke KL,
Mosley TH,
Mukamal KJ,
Nalls MA,
Nauck M,
Nelson CP,
Sotoodehnia N,
O'Connell JR,
Palmer ND,
Pazoki R,
Pedersen NL,
Peters A,
Peyser PA,
Polasek O,
Poulter N,
Raffel LJ,
Raitakari OT,
Reiner AP,
Rice TK,
Rich SS,
Robino A,
Robinson JG,
Rose LM,
Rudan I,
Schmidt CO,
Schreiner PJ,
Scott WR,
Sever P,
Shi Y,
Sidney S,
Sims M,
Smith BH,
Smith JA,
Snieder H,
Starr JM,
Strauch K,
Tan N,
Taylor KD,
Teo YY,
Tham YC,
Uitterlinden AG,
van Heemst D,
Vuckovic D,
Waldenberger M,
Wang L,
Wang Y,
Wang Z,
Wei WB,
Williams C,
Wilson G,
Wojczynski MK,
Yao J,
Yu B,
Yu C,
Yuan JM,
Zhao W,
Zonderman AB,
Becker DM,
Boehnke M,
Bowden DW,
Chambers JC,
Deary IJ,
Esko T,
Farrall M,
Franks PW,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
Horta BL,
Kamatani Y,
Kato N,
Kooner JS,
Laakso M,
Leander K,
Lehtimäki T,
Magnusson PKE,
Penninx B,
Pereira AC,
Rauramaa R,
Samani NJ,
Scott J,
Shu XO,
van der Harst P,
Wagenknecht LE,
Wang YX,
Wareham NJ,
Watkins H,
Weir DR,
Wickremasinghe AR,
Zheng W,
Elliott P,
North KE,
Bouchard C,
Evans MK,
Gudnason V,
Liu CT,
Liu Y,
Psaty BM,
Ridker PM,
van Dam RM,
Kardia SLR,
Zhu X,
Rotimi CN,
Mook-Kanamori DO,
Fornage M,
Kelly TN,
Fox ER,
Hayward C,
van Duijn CM,
Tai ES,
Wong TY,
Liu J,
Rotter JI,
Gauderman WJ,
Province MA,
Munroe PB,
Rice K,
Chasman DI,
Cupples LA,
Rao DC,
Morrison AC
InterAct Consortium · Lifelines Cohort, Groningen, The Netherlands (Lifelines Cohort Study)
American journal of epidemiology · 2019 · PMID 30698716
8 pages
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation
Vujkovic M,
Ramdas S,
Lorenz KM,
Guo X,
Darlay R,
Cordell HJ,
He J,
Gindin Y,
Chung C,
Myers RP,
Schneider CV,
Park J
and 78 more — show all
Lee KM,
Serper M,
Carr RM,
Kaplan DE,
Haas ME,
MacLean MT,
Witschey WR,
Zhu X,
Tcheandjieu C,
Kember RL,
Kranzler HR,
Verma A,
Giri A,
Klarin DM,
Sun YV,
Huang J,
Huffman JE,
Creasy KT,
Hand NJ,
Liu CT,
Long MT,
Yao J,
Budoff M,
Tan J,
Li X,
Lin HJ,
Chen YI,
Taylor KD,
Chang RK,
Krauss RM,
Vilarinho S,
Brancale J,
Nielsen JB,
Locke AE,
Jones MB,
Verweij N,
Baras A,
Reddy KR,
Neuschwander-Tetri BA,
Schwimmer JB,
Sanyal AJ,
Chalasani N,
Ryan KA,
Mitchell BD,
Gill D,
Wells AD,
Manduchi E,
Saiman Y,
Mahmud N,
Miller DR,
Reaven PD,
Phillips LS,
Muralidhar S,
DuVall SL,
Lee JS,
Assimes TL,
Pyarajan S,
Cho K,
Edwards TL,
Damrauer SM,
Wilson PW,
Gaziano JM,
O'Donnell CJ,
Khera AV,
Grant SFA,
Brown CD,
Tsao PS,
Saleheen D,
Lotta LA,
Bastarache L,
Anstee QM,
Daly AK,
Meigs JB,
Rotter JI,
Lynch JA,
Rader DJ,
Voight BF,
Chang KM
Regeneron Genetics Center · Geisinger-Regeneron DiscovEHR Collaboration and 2 more consortia
Nature genetics · 2022 · PMID 35654975
8 pages
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
Estrada K,
Styrkarsdottir U,
Evangelou E,
Hsu YH,
Duncan EL,
Ntzani EE,
Oei L,
Albagha OM,
Amin N,
Kemp JP,
Koller DL,
Li G
and 170 more — show all
Liu CT,
Minster RL,
Moayyeri A,
Vandenput L,
Willner D,
Xiao SM,
Yerges-Armstrong LM,
Zheng HF,
Alonso N,
Eriksson J,
Kammerer CM,
Kaptoge SK,
Leo PJ,
Thorleifsson G,
Wilson SG,
Wilson JF,
Aalto V,
Alen M,
Aragaki AK,
Aspelund T,
Center JR,
Dailiana Z,
Duggan DJ,
Garcia M,
Garcia-Giralt N,
Giroux S,
Hallmans G,
Hocking LJ,
Husted LB,
Jameson KA,
Khusainova R,
Kim GS,
Kooperberg C,
Koromila T,
Kruk M,
Laaksonen M,
Lacroix AZ,
Lee SH,
Leung PC,
Lewis JR,
Masi L,
Mencej-Bedrac S,
Nguyen TV,
Nogues X,
Nogues X,
Patel MS,
Prezelj J,
Rose LM,
Scollen S,
Siggeirsdottir K,
Smith AV,
Svensson O,
Trompet S,
Trummer O,
van Schoor NM,
Woo J,
Zhu K,
Balcells S,
Brandi ML,
Buckley BM,
Cheng S,
Christiansen C,
Cooper C,
Dedoussis G,
Ford I,
Frost M,
Goltzman D,
González-Macías J,
Kähönen M,
Karlsson M,
Khusnutdinova E,
Koh JM,
Kollia P,
Langdahl BL,
Leslie WD,
Lips P,
Ljunggren Ö,
Lorenc RS,
Marc J,
Mellström D,
Obermayer-Pietsch B,
Olmos JM,
Pettersson-Kymmer U,
Reid DM,
Riancho JA,
Ridker PM,
Rousseau F,
Slagboom PE,
Tang NL,
Urreizti R,
Van Hul W,
Viikari J,
Zarrabeitia MT,
Aulchenko YS,
Castano-Betancourt M,
Grundberg E,
Herrera L,
Ingvarsson T,
Johannsdottir H,
Kwan T,
Li R,
Luben R,
Medina-Gómez C,
Palsson ST,
Reppe S,
Rotter JI,
Sigurdsson G,
van Meurs JB,
Verlaan D,
Williams FM,
Wood AR,
Zhou Y,
Gautvik KM,
Pastinen T,
Raychaudhuri S,
Cauley JA,
Chasman DI,
Clark GR,
Cummings SR,
Danoy P,
Dennison EM,
Eastell R,
Eisman JA,
Gudnason V,
Hofman A,
Jackson RD,
Jones G,
Jukema JW,
Khaw KT,
Lehtimäki T,
Liu Y,
Lorentzon M,
McCloskey E,
Mitchell BD,
Nandakumar K,
Nicholson GC,
Oostra BA,
Peacock M,
Pols HA,
Prince RL,
Raitakari O,
Reid IR,
Robbins J,
Sambrook PN,
Sham PC,
Shuldiner AR,
Tylavsky FA,
van Duijn CM,
Wareham NJ,
Cupples LA,
Econs MJ,
Evans DM,
Harris TB,
Kung AW,
Psaty BM,
Reeve J,
Spector TD,
Streeten EA,
Zillikens MC,
Thorsteinsdottir U,
Ohlsson C,
Karasik D,
Richards JB,
Brown MA,
Stefansson K,
Uitterlinden AG,
Ralston SH,
Ioannidis JP,
Kiel DP,
Rivadeneira F
Nature genetics · 2012 · PMID 22504420 · open access
7 pages
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture
Zheng HF,
Forgetta V,
Hsu YH,
Estrada K,
Rosello-Diez A,
Leo PJ,
Dahia CL,
Park-Min KH,
Tobias JH,
Kooperberg C,
Kleinman A,
Styrkarsdottir U
and 146 more — show all
Liu CT,
Uggla C,
Evans DS,
Nielson CM,
Walter K,
Pettersson-Kymmer U,
McCarthy S,
Eriksson J,
Kwan T,
Jhamai M,
Trajanoska K,
Memari Y,
Min J,
Huang J,
Danecek P,
Wilmot B,
Li R,
Chou WC,
Mokry LE,
Moayyeri A,
Claussnitzer M,
Cheng CH,
Cheung W,
Medina-Gómez C,
Ge B,
Chen SH,
Choi K,
Oei L,
Fraser J,
Kraaij R,
Hibbs MA,
Gregson CL,
Paquette D,
Hofman A,
Wibom C,
Tranah GJ,
Marshall M,
Gardiner BB,
Cremin K,
Auer P,
Hsu L,
Ring S,
Tung JY,
Thorleifsson G,
Enneman AW,
van Schoor NM,
de Groot LC,
van der Velde N,
Melin B,
Kemp JP,
Christiansen C,
Sayers A,
Zhou Y,
Calderari S,
van Rooij J,
Carlson C,
Peters U,
Berlivet S,
Dostie J,
Uitterlinden AG,
Williams SR,
Farber C,
Grinberg D,
LaCroix AZ,
Haessler J,
Chasman DI,
Giulianini F,
Rose LM,
Ridker PM,
Eisman JA,
Nguyen TV,
Center JR,
Nogues X,
Nogues X,
Garcia-Giralt N,
Launer LL,
Gudnason V,
Mellström D,
Vandenput L,
Amin N,
van Duijn CM,
Karlsson MK,
Ljunggren Ö,
Svensson O,
Hallmans G,
Rousseau F,
Giroux S,
Bussière J,
Arp PP,
Koromani F,
Prince RL,
Lewis JR,
Langdahl BL,
Hermann AP,
Jensen JE,
Kaptoge S,
Khaw KT,
Reeve J,
Formosa MM,
Xuereb-Anastasi A,
Åkesson K,
McGuigan FE,
Garg G,
Olmos JM,
Zarrabeitia MT,
Riancho JA,
Ralston SH,
Alonso N,
Jiang X,
Goltzman D,
Pastinen T,
Grundberg E,
Gauguier D,
Orwoll ES,
Karasik D,
Davey-Smith G,
Smith AV,
Smith AV,
Siggeirsdottir K,
Harris TB,
Zillikens MC,
van Meurs JB,
Thorsteinsdottir U,
Maurano MT,
Timpson NJ,
Soranzo N,
Durbin R,
Wilson SG,
Ntzani EE,
Brown MA,
Stefansson K,
Hinds DA,
Spector T,
Cupples LA,
Ohlsson C,
Greenwood CM,
Jackson RD,
Rowe DW,
Loomis CA,
Evans DM,
Ackert-Bicknell CL,
Joyner AL,
Duncan EL,
Kiel DP,
Rivadeneira F,
Richards JB
AOGC Consortium · UK10K Consortium
Nature · 2015 · PMID 26367794
7 pages
Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation
Chu AY,
Deng X,
Fisher VA,
Drong A,
Zhang Y,
Feitosa MF,
Liu CT,
Weeks O,
Choh AC,
Duan Q,
Dyer TD,
Eicher JD
and 56 more — show all
Guo X,
Heard-Costa NL,
Kacprowski T,
Kent JW Jr,
Lange LA,
Liu X,
Lohman K,
Lu L,
Mahajan A,
O'Connell JR,
Parihar A,
Peralta JM,
Smith AV,
Zhang Y,
Homuth G,
Kissebah AH,
Kullberg J,
Laqua R,
Launer LJ,
Nauck M,
Olivier M,
Peyser PA,
Terry JG,
Wojczynski MK,
Yao J,
Bielak LF,
Blangero J,
Borecki IB,
Bowden DW,
Carr JJ,
Czerwinski SA,
Ding J,
Friedrich N,
Gudnason V,
Harris TB,
Ingelsson E,
Johnson AD,
Kardia SL,
Langefeld CD,
Lind L,
Liu Y,
Mitchell BD,
Morris AP,
Mosley TH Jr,
Rotter JI,
Shuldiner AR,
Towne B,
Völzke H,
Wallaschofski H,
Wilson JG,
Allison M,
Lindgren CM,
Goessling W,
Cupples LA,
Steinhauser ML,
Fox CS
Nature genetics · 2017 · PMID 27918534
7 pages
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
Sung YJ,
Winkler TW,
de las Fuentes L,
Bentley AR,
Brown MR,
Kraja AT,
Schwander K,
Ntalla I,
Guo X,
Franceschini N,
Lu Y,
Cheng CY
and 286 more — show all
Sim X,
Vojinovic D,
Marten J,
Musani SK,
Li C,
Feitosa MF,
Kilpeläinen TO,
Richard MA,
Noordam R,
Aslibekyan S,
Aschard H,
Bartz TM,
Dorajoo R,
Liu Y,
Manning AK,
Rankinen T,
Smith AV,
Tajuddin SM,
Tayo BO,
Warren HR,
Zhao W,
Zhou Y,
Matoba N,
Sofer T,
Alver M,
Amini M,
Boissel M,
Chai JF,
Chen X,
Divers J,
Gandin I,
Gao C,
Giulianini F,
Goel A,
Harris SE,
Hartwig FP,
Horimoto ARVR,
Hsu FC,
Jackson AU,
Kähönen M,
Kasturiratne A,
Kühnel B,
Leander K,
Lee WJ,
Lin KH,
'an Luan J,
McKenzie CA,
Meian H,
Nelson CP,
Rauramaa R,
Schupf N,
Scott RA,
Sheu WHH,
Stančáková A,
Takeuchi F,
van der Most PJ,
Varga TV,
Wang H,
Wang Y,
Ware EB,
Weiss S,
Wen W,
Yanek LR,
Zhang W,
Zhao JH,
Afaq S,
Alfred T,
Amin N,
Arking D,
Aung T,
Barr RG,
Bielak LF,
Boerwinkle E,
Bottinger EP,
Braund PS,
Brody JA,
Broeckel U,
Cabrera CP,
Cade B,
Caizheng Y,
Campbell A,
Canouil M,
Chakravarti A,
Chauhan G,
Christensen K,
Cocca M,
Collins FS,
Connell JM,
de Mutsert R,
de Silva HJ,
Debette S,
Dörr M,
Duan Q,
Eaton CB,
Ehret G,
Evangelou E,
Faul JD,
Fisher VA,
Forouhi NG,
Franco OH,
Friedlander Y,
Gao H,
Gigante B,
Graff M,
Gu CC,
Gu D,
Gupta P,
Hagenaars SP,
Harris TB,
He J,
Heikkinen S,
Heng CK,
Hirata M,
Hofman A,
Howard BV,
Hunt S,
Irvin MR,
Jia Y,
Joehanes R,
Justice AE,
Katsuya T,
Kaufman J,
Kerrison ND,
Khor CC,
Koh WP,
Koistinen HA,
Komulainen P,
Kooperberg C,
Krieger JE,
Kubo M,
Kuusisto J,
Langefeld CD,
Langenberg C,
Launer LJ,
Lehne B,
Lewis CE,
Li Y,
Lim SH,
Lin S,
Liu CT,
Liu J,
Liu J,
Liu K,
Liu Y,
Loh M,
Lohman KK,
Long J,
Louie T,
Mägi R,
Mahajan A,
Meitinger T,
Metspalu A,
Milani L,
Momozawa Y,
Morris AP,
Mosley TH Jr,
Munson P,
Murray AD,
Nalls MA,
Nasri U,
Norris JM,
North K,
Ogunniyi A,
Padmanabhan S,
Palmas WR,
Palmer ND,
Pankow JS,
Pedersen NL,
Peters A,
Peyser PA,
Polasek O,
Raitakari OT,
Renström F,
Rice TK,
Ridker PM,
Robino A,
Robinson JG,
Rose LM,
Rudan I,
Sabanayagam C,
Salako BL,
Sandow K,
Schmidt CO,
Schreiner PJ,
Scott WR,
Seshadri S,
Sever P,
Sitlani CM,
Smith JA,
Snieder H,
Starr JM,
Strauch K,
Tang H,
Taylor KD,
Teo YY,
Tham YC,
Uitterlinden AG,
Waldenberger M,
Wang L,
Wang YX,
Wei WB,
Williams C,
Wilson G,
Wojczynski MK,
Yao J,
Yuan JM,
Zonderman AB,
Becker DM,
Boehnke M,
Bowden DW,
Chambers JC,
Chen YI,
de Faire U,
Deary IJ,
Esko T,
Farrall M,
Forrester T,
Franks PW,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
Horta BL,
Hung YJ,
Jonas JB,
Kato N,
Kooner JS,
Laakso M,
Lehtimäki T,
Liang KW,
Magnusson PKE,
Newman AB,
Oldehinkel AJ,
Pereira AC,
Redline S,
Rettig R,
Samani NJ,
Scott J,
Shu XO,
van der Harst P,
Wagenknecht LE,
Wareham NJ,
Watkins H,
Weir DR,
Wickremasinghe AR,
Wu T,
Zheng W,
Zheng W,
Kamatani Y,
Laurie CC,
Bouchard C,
Cooper RS,
Evans MK,
Gudnason V,
Kardia SLR,
Kritchevsky SB,
Levy D,
O'Connell JR,
Psaty BM,
van Dam RM,
Sims M,
Arnett DK,
Mook-Kanamori DO,
Kelly TN,
Fox ER,
Hayward C,
Fornage M,
Rotimi CN,
Province MA,
van Duijn CM,
Tai ES,
Wong TY,
Loos RJF,
Reiner AP,
Rotter JI,
Zhu X,
Bierut LJ,
Gauderman WJ,
Caulfield MJ,
Elliott P,
Rice K,
Munroe PB,
Morrison AC,
Cupples LA,
Rao DC,
Chasman DI
CHARGE Neurology Working Group · COGENT-Kidney Consortium and 2 more consortia
American journal of human genetics · 2018 · PMID 29455858
7 pages
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals
Dastani Z,
Hivert MF,
Timpson N,
Perry JR,
Yuan X,
Scott RA,
Henneman P,
Heid IM,
Kizer JR,
Lyytikäinen LP,
Fuchsberger C,
Tanaka T
and 548 more — show all
Morris AP,
Small K,
Isaacs A,
Beekman M,
Coassin S,
Lohman K,
Qi L,
Kanoni S,
Pankow JS,
Uh HW,
Wu Y,
Bidulescu A,
Rasmussen-Torvik LJ,
Greenwood CM,
Ladouceur M,
Grimsby J,
Manning AK,
Liu CT,
Kooner J,
Mooser VE,
Vollenweider P,
Kapur KA,
Chambers J,
Wareham NJ,
Langenberg C,
Frants R,
Willems-Vandijk K,
Oostra BA,
Willems SM,
Lamina C,
Winkler TW,
Psaty BM,
Tracy RP,
Brody J,
Chen I,
Viikari J,
Kähönen M,
Pramstaller PP,
Evans DM,
St Pourcain B,
Sattar N,
Wood AR,
Bandinelli S,
Carlson OD,
Egan JM,
Böhringer S,
van Heemst D,
Kedenko L,
Kristiansson K,
Nuotio ML,
Loo BM,
Harris T,
Garcia M,
Kanaya A,
Haun M,
Klopp N,
Wichmann HE,
Deloukas P,
Katsareli E,
Couper DJ,
Duncan BB,
Kloppenburg M,
Adair LS,
Borja JB,
Wilson JG,
Musani S,
Guo X,
Johnson T,
Semple R,
Teslovich TM,
Allison MA,
Redline S,
Buxbaum SG,
Mohlke KL,
Meulenbelt I,
Ballantyne CM,
Dedoussis GV,
Hu FB,
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Biobank Japan Project · Lifelines Cohort Study,
HGG advances · 2026 · PMID 41520179 · open access
2 pages
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.