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Is your paper here?
2,655 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.
3 matches for
Newnham JP.
Genome-wide associations for birth weight and correlations with adult disease
Horikoshi M,
Beaumont RN,
Day FR,
Warrington NM,
Kooijman MN,
Fernandez-Tajes J,
Feenstra B,
van Zuydam NR,
Gaulton KJ,
Grarup N,
Bradfield JP,
Strachan DP
and 157 more — show all
Li-Gao R,
Ahluwalia TS,
Kreiner E,
Rueedi R,
Lyytikäinen LP,
Cousminer DL,
Wu Y,
Thiering E,
Wang CA,
Have CT,
Hottenga JJ,
Vilor-Tejedor N,
Joshi PK,
Boh ETH,
Ntalla I,
Pitkänen N,
Mahajan A,
van Leeuwen EM,
Joro R,
Lagou V,
Nodzenski M,
Diver LA,
Zondervan KT,
Bustamante M,
Marques-Vidal P,
Mercader JM,
Bennett AJ,
Rahmioglu N,
Nyholt DR,
Ma RCW,
Tam CHT,
Tam WH,
Ganesh SK,
van Rooij FJ,
Jones SE,
Loh PR,
Ruth KS,
Tuke MA,
Tyrrell J,
Wood AR,
Yaghootkar H,
Scholtens DM,
Paternoster L,
Prokopenko I,
Kovacs P,
Atalay M,
Willems SM,
Panoutsopoulou K,
Wang X,
Carstensen L,
Geller F,
Schraut KE,
Murcia M,
van Beijsterveldt CE,
Willemsen G,
Appel EVR,
Fonvig CE,
Trier C,
Tiesler CM,
Standl M,
Kutalik Z,
Bonas-Guarch S,
Hougaard DM,
Sánchez F,
Torrents D,
Waage J,
Hollegaard MV,
de Haan HG,
Rosendaal FR,
Medina-Gomez C,
Ring SM,
Hemani G,
McMahon G,
Robertson NR,
Groves CJ,
Langenberg C,
Luan J,
Scott RA,
Zhao JH,
Mentch FD,
MacKenzie SM,
Reynolds RM,
Lowe WL Jr,
Tönjes A,
Stumvoll M,
Lindi V,
Lakka TA,
van Duijn CM,
Kiess W,
Körner A,
Sørensen TI,
Niinikoski H,
Pahkala K,
Raitakari OT,
Zeggini E,
Dedoussis GV,
Teo YY,
Saw SM,
Melbye M,
Campbell H,
Wilson JF,
Vrijheid M,
de Geus EJ,
Boomsma DI,
Kadarmideen HN,
Holm JC,
Holm JC,
Hansen T,
Sebert S,
Hattersley AT,
Beilin LJ,
Newnham JP,
Newnham JP,
Pennell CE,
Heinrich J,
Adair LS,
Borja JB,
Mohlke KL,
Eriksson JG,
Widén EE,
Kähönen M,
Viikari JS,
Lehtimäki T,
Vollenweider P,
Vollenweider P,
Bønnelykke K,
Bisgaard H,
Mook-Kanamori DO,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
Pisinger C,
Pisinger C,
Pedersen O,
Power C,
Hyppönen E,
Wareham NJ,
Hakonarson H,
Davies E,
Walker BR,
Jaddoe VW,
Jarvelin MR,
Grant SF,
Vaag AA,
Lawlor DA,
Frayling TM,
Frayling TM,
Davey Smith G,
Morris AP,
Ong KK,
Felix JF,
Timpson NJ,
Perry JR,
Evans DM,
McCarthy MI,
McCarthy MI,
Freathy RM
CHARGE Consortium Hematology Working Group · Early Growth Genetics (EGG) Consortium
Nature · 2016 · PMID 27680694
12 pages+
A novel common variant in DCST2 is associated with length in early life and height in adulthood
van der Valk RJ,
Kreiner-Møller E,
Kooijman MN,
Guxens M,
Stergiakouli E,
Sääf A,
Bradfield JP,
Geller F,
Hayes MG,
Cousminer DL,
Körner A,
Thiering E
and 105 more — show all
Curtin JA,
Myhre R,
Huikari V,
Joro R,
Kerkhof M,
Warrington NM,
Pitkänen N,
Ntalla I,
Horikoshi M,
Veijola R,
Freathy RM,
Teo YY,
Barton SJ,
Evans DM,
Kemp JP,
St Pourcain B,
Ring SM,
Davey Smith G,
Bergström A,
Kull I,
Hakonarson H,
Mentch FD,
Bisgaard H,
Chawes B,
Stokholm J,
Waage J,
Eriksen P,
Sevelsted A,
Melbye M,
van Duijn CM,
Medina-Gomez C,
Hofman A,
de Jongste JC,
Taal HR,
Uitterlinden AG,
Armstrong LL,
Eriksson J,
Palotie A,
Bustamante M,
Estivill X,
Gonzalez JR,
Llop S,
Kiess W,
Mahajan A,
Flexeder C,
Tiesler CM,
Murray CS,
Simpson A,
Magnus P,
Sengpiel V,
Hartikainen AL,
Keinanen-Kiukaanniemi S,
Lewin A,
Da Silva Couto Alves A,
Blakemore AI,
Buxton JL,
Kaakinen M,
Rodriguez A,
Sebert S,
Vaarasmaki M,
Lakka T,
Lindi V,
Gehring U,
Postma DS,
Ang W,
Newnham JP,
Lyytikäinen LP,
Pahkala K,
Raitakari OT,
Panoutsopoulou K,
Zeggini E,
Boomsma DI,
Groen-Blokhuis M,
Ilonen J,
Franke L,
Hirschhorn JN,
Pers TH,
Liang L,
Huang J,
Hocher B,
Knip M,
Saw SM,
Holloway JW,
Melén E,
Grant SF,
Feenstra B,
Lowe WL,
Widén E,
Sergeyev E,
Grallert H,
Custovic A,
Jacobsson B,
Jarvelin MR,
Atalay M,
Koppelman GH,
Pennell CE,
Niinikoski H,
Dedoussis GV,
Mccarthy MI,
Frayling TM,
Sunyer J,
Timpson NJ,
Rivadeneira F,
Bønnelykke K,
Jaddoe VW
Early Genetics and Lifecourse Epidemiology (EAGLE) Consortium · Genetic Investigation of ANthropometric Traits (GIANT) Consortium and 1 more consortia
Human molecular genetics · 2015 · PMID 25281659 · open access
2 pages
Common variants at 12q15 and 12q24 are associated with infant head circumference
Taal HR,
Pourcain BS,
Thiering E,
Das S,
Mook-Kanamori DO,
Warrington NM,
Kaakinen M,
Kreiner-Møller E,
Bradfield JP,
Freathy RM,
Geller F,
Guxens M
and 74 more — show all
Cousminer DL,
Kerkhof M,
Timpson NJ,
Ikram MA,
Beilin LJ,
Bønnelykke K,
Buxton JL,
Charoen P,
Chawes BLK,
Eriksson J,
Evans DM,
Hofman A,
Kemp JP,
Kim CE,
Klopp N,
Lahti J,
Lye SJ,
McMahon G,
Mentch FD,
Müller M,
O'Reilly PF,
Prokopenko I,
Rivadeneira F,
Steegers EAP,
Sunyer J,
Tiesler C,
Yaghootkar H,
Breteler MMB,
Debette S,
Fornage M,
Gudnason V,
Launer LJ,
van der Lugt A,
Mosley TH,
Seshadri S,
Smith AV,
Vernooij MW,
Blakemore AI,
Chiavacci RM,
Feenstra B,
Fernandez-Benet J,
Grant SFA,
Hartikainen AL,
van der Heijden AJ,
Iñiguez C,
Lathrop M,
McArdle WL,
Mølgaard A,
Newnham JP,
Palmer LJ,
Palotie A,
Palotie A,
Pouta A,
Ring SM,
Sovio U,
Standl M,
Uitterlinden AG,
Wichmann HE,
Vissing NH,
DeCarli C,
van Duijn CM,
McCarthy MI,
Koppelman GH,
Estivill X,
Hattersley AT,
Melbye M,
Bisgaard H,
Pennell CE,
Widen E,
Hakonarson H,
Smith GD,
Heinrich J,
Jarvelin MR,
Jaddoe VWV
Cohorts for Heart and Aging Research in Genetic Epidemiology (CHARGE) Consortium · Early Genetics & Lifecourse Epidemiology (EAGLE) consortium and 1 more consortia
Nature genetics · 2012 · PMID 22504419
1 page
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.