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2,657 papers hold this site up. Every variant and condition page names
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17 matches for
Tobias JH.
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+
The genetic architecture of hip shape and its role in the development of hip osteoarthritis and fracture
Faber BG,
Frysz M,
Zheng J,
Lin H,
Flynn KA,
Ebsim R,
Saunders FR,
Beynon R,
Gregory JS,
Aspden RM,
Harvey NC,
Lindner C
and 7 more — show all
Human molecular genetics · 2025 · PMID 39574169 · open access
12 pages+
Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus
Medina-Gomez C,
Kemp JP,
Dimou NL,
Kreiner E,
Chesi A,
Zemel BS,
Bønnelykke K,
Boer CG,
Ahluwalia TS,
Bisgaard H,
Evangelou E,
Heppe DHM
and 22 more — show all
Bonewald LF,
Gorski JP,
Ghanbari M,
Demissie S,
Duque G,
Maurano MT,
Kiel DP,
Hsu YH,
C J van der Eerden B,
Ackert-Bicknell C,
Reppe S,
Gautvik KM,
Raastad T,
Karasik D,
van de Peppel J,
Jaddoe VWV,
Uitterlinden AG,
Tobias JH,
Grant SFA,
Bagos PG,
Evans DM,
Rivadeneira F
Nature communications · 2017 · PMID 28743860 · open access
11 pages
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations
Boer CG,
Hatzikotoulas K,
Southam L,
Stefánsdóttir L,
Zhang Y,
Coutinho de Almeida R,
Wu TT,
Zheng J,
Hartley A,
Teder-Laving M,
Skogholt AH,
Terao C
and 50 more — show all
Zengini E,
Alexiadis G,
Barysenka A,
Bjornsdottir G,
Gabrielsen ME,
Gilly A,
Ingvarsson T,
Johnsen MB,
Jonsson H,
Kloppenburg M,
Luetge A,
Lund SH,
Mägi R,
Mangino M,
Nelissen RRGHH,
Shivakumar M,
Steinberg J,
Takuwa H,
Thomas LF,
Tuerlings M,
Babis GC,
Cheung JPY,
Kang JH,
Kraft P,
Lietman SA,
Samartzis D,
Slagboom PE,
Stefansson K,
Thorsteinsdottir U,
Tobias JH,
Uitterlinden AG,
Winsvold B,
Zwart JA,
Davey Smith G,
Sham PC,
Thorleifsson G,
Gaunt TR,
Morris AP,
Valdes AM,
Tsezou A,
Cheah KSE,
Ikegawa S,
Hveem K,
Esko T,
Wilkinson JM,
Meulenbelt I,
Lee MTM,
van Meurs JBJ,
Styrkársdóttir U,
Zeggini E
arcOGEN Consortium · HUNT All-In Pain and 2 more consortia
Cell · 2021 · PMID 34450027 · 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
The identification of distinct protective and susceptibility mechanisms for hip osteoarthritis: findings from a genome-wide association study meta-analysis of minimum joint space width and Mendelian randomisation cluster analyses
Faber BG,
Frysz M,
Boer CG,
Evans DS,
Ebsim R,
Flynn KA,
Lundberg M,
Southam L,
Hartley A,
Saunders FR,
Lindner C,
Gregory JS
and 10 more — show all
EBioMedicine · 2023 · PMID 37619450 · open access
10 pages
Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances
Fatemifar G,
Hoggart CJ,
Paternoster L,
Kemp JP,
Prokopenko I,
Horikoshi M,
Wright VJ,
Tobias JH,
Richmond S,
Zhurov AI,
Toma AM,
Pouta A
and 14 more — show all
Taanila A,
Sipila K,
Lähdesmäki R,
Pillas D,
Geller F,
Feenstra B,
Melbye M,
Nohr EA,
Ring SM,
St Pourcain B,
Timpson NJ,
Davey Smith G,
Jarvelin MR,
Evans DM
Human molecular genetics · 2013 · PMID 23704328 · open access
8 pages
Femoral neck width genetic risk score is a novel independent risk factor for hip fractures
Tobias JH,
Nethander M,
Faber BG,
Heppenstall SV,
Ebsim R,
Cootes T,
Lindner C,
Saunders FR,
Gregory JS,
Aspden RM,
Harvey NC,
Kemp JP
and 2 more — show all
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2024 · PMID 38477772 · open access
8 pages
Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment
Kemp JP,
Medina-Gomez C,
Estrada K,
St Pourcain B,
Heppe DH,
Warrington NM,
Oei L,
Ring SM,
Kruithof CJ,
Timpson NJ,
Wolber LE,
Reppe S
and 21 more — show all
Gautvik K,
Grundberg E,
Ge B,
van der Eerden B,
van de Peppel J,
Hibbs MA,
Ackert-Bicknell CL,
Choi K,
Koller DL,
Econs MJ,
Williams FM,
Foroud T,
Zillikens MC,
Ohlsson C,
Hofman A,
Uitterlinden AG,
Davey Smith G,
Jaddoe VW,
Tobias JH,
Rivadeneira F,
Evans DM
PLoS genetics · 2014 · PMID 24945404 · 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
Lowering of Circulating Sclerostin May Increase Risk of Atherosclerosis and Its Risk Factors: Evidence From a Genome-Wide Association Meta-Analysis Followed by Mendelian Randomization
Zheng J,
Wheeler E,
Pietzner M,
Andlauer TFM,
Yau MS,
Hartley AE,
Brumpton BM,
Rasheed H,
Kemp JP,
Frysz M,
Robinson J,
Reppe S
and 25 more — show all
Prijatelj V,
Gautvik KM,
Falk L,
Maerz W,
Gergei I,
Peyser PA,
Kavousi M,
de Vries PS,
Miller CL,
Bos M,
van der Laan SW,
Malhotra R,
Herrmann M,
Scharnagl H,
Kleber M,
Dedoussis G,
Zeggini E,
Nethander M,
Ohlsson C,
Lorentzon M,
Wareham N,
Langenberg C,
Holmes MV,
Davey Smith G,
Tobias JH
Arthritis & rheumatology (Hoboken, N.J.) · 2023 · PMID 37096546
7 pages
Identification of Novel Loci Associated With Hip Shape: A Meta-Analysis of Genomewide Association Studies
Baird DA,
Evans DS,
Kamanu FK,
Gregory JS,
Saunders FR,
Giuraniuc CV,
Barr RJ,
Aspden RM,
Jenkins D,
Kiel DP,
Orwoll ES,
Cummings SR
and 18 more — show all
Lane NE,
Mullin BH,
Williams FM,
Richards JB,
Wilson SG,
Spector TD,
Faber BG,
Lawlor DA,
Grundberg E,
Ohlsson C,
Pettersson-Kymmer U,
Capellini TD,
Richard D,
Beck TJ,
Evans DM,
Paternoster L,
Karasik D,
Tobias JH
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2019 · PMID 30320955 · open access
4 pages
GWAS meta-analysis followed by Mendelian randomization revealed potential control mechanisms for circulating α-Klotho levels
Gergei I,
Zheng J,
Andlauer TFM,
Brandenburg V,
Mirza-Schreiber N,
Müller-Myhsok B,
Krämer BK,
Richard D,
Falk L,
Movérare-Skrtic S,
Ohlsson C,
Davey Smith G
and 3 more — show all
Human molecular genetics · 2022 · PMID 34542150 · open access
2 pages
Genome-wide association meta-analysis of cortical bone mineral density unravels allelic heterogeneity at the RANKL locus and potential pleiotropic effects on bone
Paternoster L,
Lorentzon M,
Vandenput L,
Karlsson MK,
Ljunggren O,
Kindmark A,
Mellstrom D,
Kemp JP,
Jarett CE,
Holly JM,
Sayers A,
St Pourcain B
and 7 more — show all
PLoS genetics · 2010 · PMID 21124946 · open access
1 page
Meta-analysis of genome-wide scans for total body BMD in children and adults reveals allelic heterogeneity and age-specific effects at the WNT16 locus
Medina-Gomez C,
Kemp JP,
Estrada K,
Eriksson J,
Liu J,
Reppe S,
Evans DM,
Heppe DH,
Vandenput L,
Herrera L,
Ring SM,
Kruithof CJ
and 16 more — show all
Timpson NJ,
Zillikens MC,
Olstad OK,
Zheng HF,
Richards JB,
St Pourcain B,
Hofman A,
Jaddoe VW,
Smith GD,
Lorentzon M,
Gautvik KM,
Uitterlinden AG,
Brommage R,
Ohlsson C,
Tobias JH,
Rivadeneira F
PLoS genetics · 2012 · PMID 22792070 · open access
1 page
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Why is my paper here? I never gave you permission.
Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
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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
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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
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How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
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keep in step, because the citation lives on the page that makes the claim.