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Is your paper here?
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.
15 matches for
Shaffer JR.
Insights into the genetic architecture of the human face
White JD,
Indencleef K,
Naqvi S,
Eller RJ,
Hoskens H,
Roosenboom J,
Lee MK,
Li J,
Mohammed J,
Richmond S,
Quillen EE,
Norton HL
and 11 more — show all
Feingold E,
Swigut T,
Marazita ML,
Peeters H,
Hens G,
Shaffer JR,
Wysocka J,
Walsh S,
Weinberg SM,
Shriver MD,
Claes P
Nature genetics · 2021 · PMID 33288918 · open access
12 pages+
Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data
Shungin D,
Haworth S,
Divaris K,
Agler CS,
Kamatani Y,
Keun Lee M,
Grinde K,
Hindy G,
Alaraudanjoki V,
Pesonen P,
Teumer A,
Holtfreter B
and 26 more — show all
Sakaue S,
Hirata J,
Yu YH,
Ridker PM,
Giulianini F,
Chasman DI,
Magnusson PKE,
Sudo T,
Okada Y,
Völker U,
Kocher T,
Anttonen V,
Laitala ML,
Orho-Melander M,
Sofer T,
Shaffer JR,
Vieira A,
Marazita ML,
Kubo M,
Furuichi Y,
North KE,
Offenbacher S,
Ingelsson E,
Franks PW,
Timpson NJ,
Johansson I
Nature communications · 2019 · PMID 31235808 · open access
5 pages
Novel genetic loci affecting facial shape variation in humans
Xiong Z,
Dankova G,
Howe LJ,
Lee MK,
Hysi PG,
de Jong MA,
Zhu G,
Adhikari K,
Li D,
Li Y,
Pan B,
Feingold E
and 37 more — show all
Marazita ML,
Shaffer JR,
McAloney K,
Xu SH,
Jin L,
Wang S,
de Vrij FM,
Lendemeijer B,
Richmond S,
Zhurov A,
Lewis S,
Sharp GC,
Paternoster L,
Thompson H,
Gonzalez-Jose R,
Bortolini MC,
Canizales-Quinteros S,
Gallo C,
Poletti G,
Bedoya G,
Rothhammer F,
Uitterlinden AG,
Ikram MA,
Wolvius E,
Kushner SA,
Nijsten TE,
Palstra RT,
Boehringer S,
Medland SE,
Tang K,
Ruiz-Linares A,
Martin NG,
Spector TD,
Stergiakouli E,
Weinberg SM,
Liu F,
Kayser M
International Visible Trait Genetics (VisiGen) Consortium
eLife · 2019 · PMID 31763980 · open access
5 pages
Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape
Goovaerts S,
Hoskens H,
Eller RJ,
Herrick N,
Musolf AM,
Justice CM,
Yuan M,
Naqvi S,
Lee MK,
Vandermeulen D,
Szabo-Rogers HL,
Romitti PA
and 8 more — show all
Nature communications · 2023 · PMID 37973980 · open access
4 pages
Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology
Shaffer JR,
Orlova E,
Lee MK,
Leslie EJ,
Raffensperger ZD,
Heike CL,
Cunningham ML,
Hecht JT,
Kau CH,
Nidey NL,
Moreno LM,
Wehby GL
and 14 more — show all
Murray JC,
Laurie CA,
Laurie CC,
Cole J,
Ferrara T,
Ferrara T,
Santorico S,
Klein O,
Mio W,
Feingold E,
Hallgrimsson B,
Spritz RA,
Marazita ML,
Weinberg SM
PLoS genetics · 2016 · PMID 27560520 · open access
3 pages
GWAS Identifies New Loci for Painful Temporomandibular Disorder: Hispanic Community Health Study/Study of Latinos
Sanders AE,
Jain D,
Sofer T,
Kerr KF,
Laurie CC,
Shaffer JR,
Marazita ML,
Kaste LM,
Slade GD,
Fillingim RB,
Ohrbach R,
Maixner W
and 15 more — show all
Kocher T,
Bernhardt O,
Teumer A,
Schwahn C,
Sipilä K,
Lähdesmäki R,
Männikkö M,
Pesonen P,
Järvelin M,
Rizzatti-Barbosa CM,
Meloto CB,
Ribeiro-Dasilva M,
Diatchenko L,
Serrano P,
Smith SB
Journal of dental research · 2017 · PMID 28081371
3 pages
Genome-wide association study identifies four loci associated with eruption of permanent teeth
Geller F,
Feenstra B,
Zhang H,
Shaffer JR,
Hansen T,
Esserlind AL,
Boyd HA,
Nohr EA,
Timpson NJ,
Fatemifar G,
Paternoster L,
Evans DM
and 10 more — show all
PLoS genetics · 2011 · PMID 21931568 · open access
2 pages
Genome-wide association study of primary dentition pit-and-fissure and smooth surface caries
Zeng Z,
Feingold E,
Wang X,
Weeks DE,
Lee M,
Cuenco DT,
Broffitt B,
Weyant RJ,
Crout R,
McNeil DW,
Levy SM,
Marazita ML
and 1 more — show all
Caries research · 2014 · PMID 24556642
2 pages
A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13
Leslie EJ,
Carlson JC,
Shaffer JR,
Feingold E,
Wehby G,
Laurie CA,
Jain D,
Laurie CC,
Doheny KF,
McHenry T,
Resick J,
Sanchez C
and 43 more — show all
Jacobs J,
Emanuele B,
Vieira AR,
Neiswanger K,
Lidral AC,
Valencia-Ramirez LC,
Lopez-Palacio AM,
Valencia DR,
Arcos-Burgos M,
Czeizel AE,
Field LL,
Padilla CD,
Cutiongco-de la Paz EM,
Deleyiannis F,
Christensen K,
Munger RG,
Lie RT,
Wilcox A,
Romitti PA,
Castilla EE,
Mereb JC,
Poletta FA,
Orioli IM,
Carvalho FM,
Hecht JT,
Blanton SH,
Buxó CJ,
Butali A,
Mossey PA,
Adeyemo WL,
James O,
Braimah RO,
Aregbesola BS,
Eshete MA,
Abate F,
Koruyucu M,
Seymen F,
Ma L,
de Salamanca JE,
Weinberg SM,
Moreno L,
Murray JC,
Marazita ML
Human molecular genetics · 2016 · PMID 27033726
2 pages
Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course
Graff M,
Ngwa JS,
Workalemahu T,
Homuth G,
Schipf S,
Teumer A,
Völzke H,
Wallaschofski H,
Abecasis GR,
Edward L,
Francesco C,
Sanna S
and 37 more — show all
Scheet P,
Schlessinger D,
Sidore C,
Xiao X,
Wang Z,
Chanock SJ,
Jacobs KB,
Hayes RB,
Hu F,
Van Dam RM,
Crout RJ,
Marazita ML,
Shaffer JR,
Atwood LD,
Fox CS,
Heard-Costa NL,
White C,
Choh AC,
Czerwinski SA,
Demerath EW,
Dyer TD,
Towne B,
Amin N,
Oostra BA,
Van Duijn CM,
Zillikens MC,
Esko T,
Nelis M,
Nikopensius T,
Metspalu A,
Strachan DP,
Monda K,
Qi L,
North KE,
Cupples LA,
Gordon-Larsen P,
Berndt SI
GIANT Consortium
Human molecular genetics · 2013 · PMID 23669352
1 page
A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3
Leslie EJ,
Liu H,
Carlson JC,
Shaffer JR,
Feingold E,
Wehby G,
Laurie CA,
Jain D,
Laurie CC,
Doheny KF,
McHenry T,
Resick J
and 46 more — show all
Sanchez C,
Jacobs J,
Emanuele B,
Vieira AR,
Neiswanger K,
Standley J,
Czeizel AE,
Deleyiannis F,
Christensen K,
Munger RG,
Lie RT,
Wilcox A,
Romitti PA,
Field LL,
Padilla CD,
Cutiongco-de la Paz EM,
Lidral AC,
Valencia-Ramirez LC,
Lopez-Palacio AM,
Valencia DR,
Arcos-Burgos M,
Castilla EE,
Mereb JC,
Poletta FA,
Orioli IM,
Carvalho FM,
Hecht JT,
Blanton SH,
Buxó CJ,
Butali A,
Mossey PA,
Adeyemo WL,
James O,
Braimah RO,
Aregbesola BS,
Eshete MA,
Deribew M,
Koruyucu M,
Seymen F,
Ma L,
de Salamanca JE,
Weinberg SM,
Moreno L,
Cornell RA,
Murray JC,
Marazita ML
American journal of human genetics · 2016 · PMID 27018472
1 page
Investigating the shared genetics of non-syndromic cleft lip/palate and facial morphology
Howe LJ,
Lee MK,
Sharp GC,
Davey Smith G,
St Pourcain B,
Shaffer JR,
Ludwig KU,
Mangold E,
Marazita ML,
Feingold E,
Zhurov A,
Stergiakouli E
and 5 more — show all
PLoS genetics · 2018 · PMID 30067744 · open access
1 page
Genome-wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes
Mukhopadhyay N,
Feingold E,
Moreno-Uribe L,
Wehby G,
Valencia-Ramirez LC,
Restrepo Muñeton CP,
Padilla C,
Deleyiannis F,
Christensen K,
Poletta FA,
Orioli IM,
Hecht JT
and 9 more — show all
Genetic epidemiology · 2022 · PMID 35191549
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.