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8 matches for
Walsh JP.
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+
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation
Teumer A,
Chaker L,
Groeneweg S,
Li Y,
Di Munno C,
Barbieri C,
Schultheiss UT,
Traglia M,
Ahluwalia TS,
Akiyama M,
Appel EVR,
Arking DE
and 116 more — show all
Arnold A,
Astrup A,
Beekman M,
Beilby JP,
Bekaert S,
Boerwinkle E,
Brown SJ,
De Buyzere M,
Campbell PJ,
Ceresini G,
Cerqueira C,
Cucca F,
Deary IJ,
Deelen J,
Eckardt KU,
Ekici AB,
Eriksson JG,
Ferrrucci L,
Fiers T,
Fiorillo E,
Ford I,
Fox CS,
Fuchsberger C,
Galesloot TE,
Gieger C,
Gögele M,
De Grandi A,
Grarup N,
Greiser KH,
Haljas K,
Hansen T,
Harris SE,
van Heemst D,
den Heijer M,
Hicks AA,
den Hollander W,
Homuth G,
Hui J,
Ikram MA,
Ittermann T,
Jensen RA,
Jing J,
Jukema JW,
Kajantie E,
Kamatani Y,
Kasbohm E,
Kaufman JM,
Kiemeney LA,
Kloppenburg M,
Kronenberg F,
Kubo M,
Lahti J,
Lapauw B,
Li S,
Liewald DCM,
Lim EM,
Linneberg A,
Marina M,
Mascalzoni D,
Matsuda K,
Medenwald D,
Meisinger C,
Meulenbelt I,
De Meyer T,
Meyer Zu Schwabedissen HE,
Mikolajczyk R,
Moed M,
Netea-Maier RT,
Nolte IM,
Okada Y,
Pala M,
Pattaro C,
Pedersen O,
Petersmann A,
Porcu E,
Postmus I,
Pramstaller PP,
Psaty BM,
Ramos YFM,
Rawal R,
Redmond P,
Richards JB,
Rietzschel ER,
Rivadeneira F,
Roef G,
Rotter JI,
Sala CF,
Schlessinger D,
Selvin E,
Slagboom PE,
Soranzo N,
Sørensen TIA,
Spector TD,
Starr JM,
Stott DJ,
Taes Y,
Taliun D,
Tanaka T,
Thuesen B,
Tiller D,
Toniolo D,
Uitterlinden AG,
Visser WE,
Walsh JP,
Wilson SG,
Wolffenbuttel BHR,
Yang Q,
Zheng HF,
Cappola A,
Peeters RP,
Naitza S,
Völzke H,
Sanna S,
Köttgen A,
Visser TJ,
Medici M
Lifelines Cohort Study
Nature communications · 2018 · PMID 30367059 · open access
12 pages+
A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function
Porcu E,
Medici M,
Pistis G,
Volpato CB,
Wilson SG,
Cappola AR,
Bos SD,
Deelen J,
den Heijer M,
Freathy RM,
Lahti J,
Liu C
and 82 more — show all
Lopez LM,
Nolte IM,
O'Connell JR,
Tanaka T,
Trompet S,
Arnold A,
Bandinelli S,
Beekman M,
Böhringer S,
Brown SJ,
Buckley BM,
Camaschella C,
de Craen AJ,
Davies G,
de Visser MC,
Ford I,
Forsen T,
Frayling TM,
Fugazzola L,
Gögele M,
Hattersley AT,
Hermus AR,
Hofman A,
Houwing-Duistermaat JJ,
Jensen RA,
Kajantie E,
Kloppenburg M,
Lim EM,
Masciullo C,
Mariotti S,
Minelli C,
Mitchell BD,
Nagaraja R,
Netea-Maier RT,
Palotie A,
Persani L,
Piras MG,
Psaty BM,
Räikkönen K,
Richards JB,
Rivadeneira F,
Sala C,
Sabra MM,
Sattar N,
Shields BM,
Soranzo N,
Starr JM,
Stott DJ,
Sweep FC,
Usala G,
van der Klauw MM,
van Heemst D,
van Mullem A,
Vermeulen SH,
Visser WE,
Walsh JP,
Westendorp RG,
Widen E,
Zhai G,
Cucca F,
Deary IJ,
Eriksson JG,
Ferrucci L,
Fox CS,
Jukema JW,
Kiemeney LA,
Pramstaller PP,
Schlessinger D,
Shuldiner AR,
Slagboom EP,
Uitterlinden AG,
Vaidya B,
Visser TJ,
Wolffenbuttel BH,
Meulenbelt I,
Rotter JI,
Spector TD,
Hicks AA,
Toniolo D,
Sanna S,
Peeters RP,
Naitza S
PLoS genetics · 2013 · PMID 23408906 · open access
10 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
10 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
Genome-wide association identifies three new susceptibility loci for Paget's disease of bone
Albagha OM,
Wani SE,
Visconti MR,
Alonso N,
Goodman K,
Brandi ML,
Cundy T,
Chung PY,
Dargie R,
Devogelaer JP,
Falchetti A,
Fraser WD
and 17 more — show all
Gennari L,
Gianfrancesco F,
Hooper MJ,
Van Hul W,
Isaia G,
Nicholson GC,
Nuti R,
Papapoulos S,
Montes Jdel P,
Ratajczak T,
Rea SL,
Rendina D,
Gonzalez-Sarmiento R,
Di Stefano M,
Ward LC,
Walsh JP,
Ralston SH
Genetic Determinants of Paget's Disease (GDPD) Consortium
Nature genetics · 2011 · PMID 21623375
4 pages
Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease
Medici M,
Porcu E,
Pistis G,
Teumer A,
Brown SJ,
Jensen RA,
Rawal R,
Roef GL,
Plantinga TS,
Vermeulen SH,
Lahti J,
Simmonds MJ
and 106 more — show all
Husemoen LL,
Freathy RM,
Shields BM,
Pietzner D,
Nagy R,
Broer L,
Chaker L,
Korevaar TI,
Plia MG,
Sala C,
Völker U,
Richards JB,
Sweep FC,
Gieger C,
Corre T,
Kajantie E,
Thuesen B,
Taes YE,
Visser WE,
Hattersley AT,
Kratzsch J,
Hamilton A,
Li W,
Homuth G,
Lobina M,
Mariotti S,
Soranzo N,
Cocca M,
Nauck M,
Spielhagen C,
Ross A,
Arnold A,
van de Bunt M,
Liyanarachchi S,
Heier M,
Grabe HJ,
Masciullo C,
Galesloot TE,
Lim EM,
Reischl E,
Leedman PJ,
Lai S,
Delitala A,
Bremner AP,
Philips DI,
Beilby JP,
Mulas A,
Vocale M,
Abecasis G,
Forsen T,
James A,
Widen E,
Hui J,
Prokisch H,
Rietzschel EE,
Palotie A,
Feddema P,
Fletcher SJ,
Schramm K,
Rotter JI,
Kluttig A,
Radke D,
Traglia M,
Surdulescu GL,
He H,
Franklyn JA,
Tiller D,
Vaidya B,
de Meyer T,
Jørgensen T,
Eriksson JG,
O'Leary PC,
Wichmann E,
Hermus AR,
Psaty BM,
Ittermann T,
Hofman A,
Bosi E,
Schlessinger D,
Wallaschofski H,
Pirastu N,
Aulchenko YS,
de la Chapelle A,
Netea-Maier RT,
Gough SC,
Meyer Zu Schwabedissen H,
Frayling TM,
Kaufman JM,
Linneberg A,
Räikkönen K,
Smit JW,
Kiemeney LA,
Rivadeneira F,
Uitterlinden AG,
Walsh JP,
Meisinger C,
den Heijer M,
Visser TJ,
Spector TD,
Wilson SG,
Völzke H,
Cappola A,
Toniolo D,
Sanna S,
Naitza S,
Peeters RP
PLoS genetics · 2014 · PMID 24586183 · open access
3 pages
Genome-wide analysis of thyroid function in Australian adolescents highlights SERPINA7 and NCOA3
Nolan J,
Campbell PJ,
Brown SJ,
Zhu G,
Gordon S,
Lim EM,
Joseph J,
Cross SM,
Panicker V,
Medland SE,
Melton PE,
Beilin LJ
and 8 more — show all
European journal of endocrinology · 2021 · PMID 34524976
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
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.