For researchers
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.
6 matches for
Romitti PA.
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 meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis
Fadista J,
Skotte L,
Geller F,
Bybjerg-Grauholm J,
Gørtz S,
Romitti PA,
Caggana M,
Kay DM,
Matsson H,
Boyd HA,
Hougaard DM,
Nordenskjöld A
and 3 more — show all
Human molecular genetics · 2019 · PMID 30281099 · open access
3 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
A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9
Justice CM,
Yagnik G,
Kim Y,
Peter I,
Jabs EW,
Erazo M,
Ye X,
Ainehsazan E,
Shi L,
Cunningham ML,
Kimonis V,
Roscioli T
and 21 more — show all
Wall SA,
Wilkie AO,
Stoler J,
Richtsmeier JT,
Heuzé Y,
Sanchez-Lara PA,
Buckley MF,
Druschel CM,
Mills JL,
Caggana M,
Romitti PA,
Kay DM,
Senders C,
Taub PJ,
Klein OD,
Boggan J,
Zwienenberg-Lee M,
Naydenov C,
Kim J,
Wilson AF,
Boyadjiev SA
Nature genetics · 2012 · PMID 23160099
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
A genome-wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study
Rashkin SR,
Cleves M,
Shaw GM,
Nembhard WN,
Nestoridi E,
Jenkins MM,
Romitti PA,
Lou XY,
Browne ML,
Mitchell LE,
Olshan AF,
Lomangino K
and 3 more — show all
National Birth Defects Prevention Study
American journal of medical genetics. Part A · 2022 · PMID 35451555
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.