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2,657 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
Forgetta V.
An atlas of genetic influences on human blood metabolites
Shin SY,
Fauman EB,
Petersen AK,
Krumsiek J,
Santos R,
Huang J,
Arnold M,
Erte I,
Forgetta V,
Yang TP,
Walter K,
Menni C
and 23 more — show all
Chen L,
Vasquez L,
Valdes AM,
Hyde CL,
Wang V,
Ziemek D,
Roberts P,
Xi L,
Grundberg E,
Waldenberger M,
Richards JB,
Mohney RP,
Milburn MV,
John SL,
Trimmer J,
Theis FJ,
Overington JP,
Suhre K,
Brosnan MJ,
Gieger C,
Kastenmüller G,
Spector TD,
Soranzo N
Multiple Tissue Human Expression Resource (MuTHER) Consortium
Nature genetics · 2014 · PMID 24816252 · open access
12 pages+
Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis
Manousaki D,
Dudding T,
Haworth S,
Hsu YH,
Liu CT,
Medina-Gómez C,
Voortman T,
van der Velde N,
Melhus H,
Robinson-Cohen C,
Cousminer DL,
Nethander M
and 41 more — show all
Vandenput L,
Noordam R,
Forgetta V,
Greenwood CMT,
Biggs ML,
Psaty BM,
Rotter JI,
Zemel BS,
Mitchell JA,
Taylor B,
Lorentzon M,
Karlsson M,
Jaddoe VVW,
Tiemeier H,
Campos-Obando N,
Franco OH,
Utterlinden AG,
Broer L,
van Schoor NM,
Ham AC,
Ikram MA,
Karasik D,
de Mutsert R,
Rosendaal FR,
den Heijer M,
Wang TJ,
Lind L,
Orwoll ES,
Mook-Kanamori DO,
Michaëlsson K,
Kestenbaum B,
Ohlsson C,
Mellström D,
de Groot LCPGM,
Grant SFA,
Kiel DP,
Zillikens MC,
Rivadeneira F,
Sawcer S,
Timpson NJ,
Richards JB
American journal of human genetics · 2017 · PMID 28757204
12 pages+
Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis
Kemp JP,
Morris JA,
Medina-Gomez C,
Forgetta V,
Warrington NM,
Youlten SE,
Zheng J,
Gregson CL,
Grundberg E,
Trajanoska K,
Logan JG,
Pollard AS
and 26 more — show all
Sparkes PC,
Ghirardello EJ,
Allen R,
Leitch VD,
Butterfield NC,
Komla-Ebri D,
Adoum AT,
Curry KF,
White JK,
Kussy F,
Greenlaw KM,
Xu C,
Harvey NC,
Cooper C,
Adams DJ,
Greenwood CMT,
Maurano MT,
Kaptoge S,
Rivadeneira F,
Tobias JH,
Croucher PI,
Ackert-Bicknell CL,
Bassett JHD,
Williams GR,
Richards JB,
Evans DM
Nature genetics · 2017 · PMID 28869591 · open access
12 pages+
Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects
Medina-Gomez C,
Kemp JP,
Trajanoska K,
Luan J,
Chesi A,
Ahluwalia TS,
Mook-Kanamori DO,
Ham A,
Hartwig FP,
Evans DS,
Joro R,
Nedeljkovic I
and 77 more — show all
Zheng HF,
Zhu K,
Atalay M,
Liu CT,
Nethander M,
Broer L,
Porleifsson G,
Mullin BH,
Handelman SK,
Nalls MA,
Jessen LE,
Heppe DHM,
Richards JB,
Wang C,
Chawes B,
Schraut KE,
Amin N,
Wareham N,
Karasik D,
Van der Velde N,
Ikram MA,
Zemel BS,
Zhou Y,
Carlsson CJ,
Liu Y,
McGuigan FE,
Boer CG,
Bønnelykke K,
Ralston SH,
Robbins JA,
Walsh JP,
Zillikens MC,
Langenberg C,
Li-Gao R,
Williams FMK,
Harris TB,
Akesson K,
Jackson RD,
Sigurdsson G,
den Heijer M,
van der Eerden BCJ,
van de Peppel J,
Spector TD,
Pennell C,
Horta BL,
Felix JF,
Zhao JH,
Wilson SG,
de Mutsert R,
Bisgaard H,
Styrkársdóttir U,
Jaddoe VW,
Orwoll E,
Lakka TA,
Scott R,
Grant SFA,
Lorentzon M,
van Duijn CM,
Wilson JF,
Stefansson K,
Psaty BM,
Kiel DP,
Ohlsson C,
Ntzani E,
van Wijnen AJ,
Forgetta V,
Ghanbari M,
Logan JG,
Williams GR,
Bassett JHD,
Croucher PI,
Evangelou E,
Uitterlinden AG,
Ackert-Bicknell CL,
Tobias JH,
Evans DM,
Rivadeneira F
American journal of human genetics · 2018 · PMID 29304378
12 pages+
An atlas of genetic influences on osteoporosis in humans and mice
Morris JA,
Kemp JP,
Youlten SE,
Laurent L,
Logan JG,
Chai RC,
Vulpescu NA,
Forgetta V,
Kleinman A,
Mohanty ST,
Sergio CM,
Quinn J
and 47 more — show all
Nguyen-Yamamoto L,
Luco AL,
Vijay J,
Simon MM,
Pramatarova A,
Medina-Gomez C,
Trajanoska K,
Ghirardello EJ,
Butterfield NC,
Curry KF,
Leitch VD,
Sparkes PC,
Adoum AT,
Mannan NS,
Komla-Ebri DSK,
Pollard AS,
Dewhurst HF,
Hassall TAD,
Beltejar MG,
Adams DJ,
Vaillancourt SM,
Kaptoge S,
Baldock P,
Cooper C,
Reeve J,
Ntzani EE,
Evangelou E,
Ohlsson C,
Karasik D,
Rivadeneira F,
Kiel DP,
Tobias JH,
Gregson CL,
Harvey NC,
Grundberg E,
Goltzman D,
Adams DJ,
Lelliott CJ,
Hinds DA,
Ackert-Bicknell CL,
Hsu YH,
Maurano MT,
Croucher PI,
Williams GR,
Bassett JHD,
Evans DM,
Richards JB
23andMe Research Team
Nature genetics · 2019 · PMID 30598549 · open access
12 pages+
Genome-wide Association Study for Vitamin D Levels Reveals 69 Independent Loci
Manousaki D,
Mitchell R,
Dudding T,
Haworth S,
Harroud A,
Forgetta V,
Shah RL,
Luan J,
Langenberg C,
Timpson NJ,
Richards JB
American journal of human genetics · 2020 · PMID 32059762
12 pages+
Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases
Chen Y,
Lu T,
Pettersson-Kymmer U,
Stewart ID,
Butler-Laporte G,
Nakanishi T,
Cerani A,
Liang KYH,
Yoshiji S,
Willett JDS,
Su CY,
Raina P
and 7 more — show all
Nature genetics · 2023 · PMID 36635386
12 pages+
Whole-genome sequence-based analysis of thyroid function
Taylor PN,
Porcu E,
Chew S,
Campbell PJ,
Traglia M,
Brown SJ,
Mullin BH,
Shihab HA,
Min J,
Walter K,
Memari Y,
Huang J
and 38 more — show all
Barnes MR,
Beilby JP,
Charoen P,
Danecek P,
Dudbridge F,
Forgetta V,
Greenwood C,
Grundberg E,
Johnson AD,
Hui J,
Lim EM,
McCarthy S,
Muddyman D,
Panicker V,
Perry JR,
Bell JT,
Yuan W,
Relton C,
Gaunt T,
Schlessinger D,
Abecasis G,
Cucca F,
Surdulescu GL,
Woltersdorf W,
Zeggini E,
Zheng HF,
Toniolo D,
Dayan CM,
Naitza S,
Walsh JP,
Spector T,
Davey Smith G,
Durbin R,
Richards JB,
Sanna S,
Soranzo N,
Timpson NJ,
Wilson SG
UK0K Consortium
Nature communications · 2015 · PMID 25743335 · 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
Rare Genetic Variants of Large Effect Influence Risk of Type 1 Diabetes
Forgetta V,
Manousaki D,
Istomine R,
Ross S,
Tessier MC,
Marchand L,
Li M,
Qu HQ,
Bradfield JP,
Grant SFA,
Hakonarson H,
Paterson AD
and 3 more — show all
DCCT/EDIC Research Group
Diabetes · 2020 · PMID 32005708 · 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.