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Connection

Philippe Stanier to Cleft Lip

This is a "connection" page, showing publications Philippe Stanier has written about Cleft Lip.
Connection Strength

2.064
  1. Set?-Salvia N, Stanier P. Genetics of cleft lip and/or cleft palate: association with other common anomalies. Eur J Med Genet. 2014 Aug; 57(8):381-93.
    View in: PubMed
    Score: 0.449
  2. Carta E, Pauws E, Thomas AC, Mengrelis K, Moore GE, Lees M, Stanier P. Investigation of SUMO pathway genes in the etiology of nonsyndromic cleft lip with or without cleft palate. Birth Defects Res A Clin Mol Teratol. 2012 Jun; 94(6):459-63.
    View in: PubMed
    Score: 0.390
  3. Pauws E, Stanier P. FGF signalling and SUMO modification: new players in the aetiology of cleft lip and/or palate. Trends Genet. 2007 Dec; 23(12):631-40.
    View in: PubMed
    Score: 0.287
  4. Stanier P, Moore GE. Genetics of cleft lip and palate: syndromic genes contribute to the incidence of non-syndromic clefts. Hum Mol Genet. 2004 Apr 01; 13 Spec No 1:R73-81.
    View in: PubMed
    Score: 0.220
  5. Howe LJ, Richardson TG, Arathimos R, Alvizi L, Passos-Bueno MR, Stanier P, Nohr E, Ludwig KU, Mangold E, Knapp M, Stergiakouli E, Pourcain BS, Smith GD, Sandy J, Relton CL, Lewis SJ, Hemani G, Sharp GC. Evidence for DNA methylation mediating genetic liability to non-syndromic cleft lip/palate. Epigenomics. 2019 02; 11(2):133-145.
    View in: PubMed
    Score: 0.156
  6. Alvizi L, Ke X, Brito LA, Seselgyte R, Moore GE, Stanier P, Passos-Bueno MR. Differential methylation is associated with non-syndromic cleft lip and palate and contributes to penetrance effects. Sci Rep. 2017 05 26; 7(1):2441.
    View in: PubMed
    Score: 0.139
  7. Muggenthaler MM, Chowdhury B, Hasan SN, Cross HE, Mark B, Harlalka GV, Patton MA, Ishida M, Behr ER, Sharma S, Zahka K, Faqeih E, Blakley B, Jackson M, Lees M, Dolinsky V, Cross L, Stanier P, Salter C, Baple EL, Alkuraya FS, Crosby AH, Triggs-Raine B, Chioza BA. Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndrome of Orofacial Clefting and Cor Triatriatum Sinister in Humans and Mice. PLoS Genet. 2017 Jan; 13(1):e1006470.
    View in: PubMed
    Score: 0.135
  8. Pauws E, Stanier P. Sumoylation in Craniofacial Disorders. Adv Exp Med Biol. 2017; 963:323-335.
    View in: PubMed
    Score: 0.135
  9. Stanier P, Pauws E. Development of the lip and palate: FGF signalling. Front Oral Biol. 2012; 16:71-80.
    View in: PubMed
    Score: 0.099
  10. Mangold E, B?hmer AC, Ishorst N, Hoebel AK, G?ltepe P, Schuenke H, Klamt J, Hofmann A, G?lz L, Raff R, Tessmann P, Nowak S, Reutter H, Hemprich A, Kreusch T, Kramer FJ, Braumann B, Reich R, Schmidt G, J?ger A, Reiter R, Brosch S, Stavusis J, Ishida M, Seselgyte R, Moore GE, N?then MM, Borck G, Aldhorae KA, Lace B, Stanier P, Knapp M, Ludwig KU. Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate. Am J Hum Genet. 2016 Apr 07; 98(4):755-62.
    View in: PubMed
    Score: 0.032
  11. Rooryck C, Diaz-Font A, Osborn DP, Chabchoub E, Hernandez-Hernandez V, Shamseldin H, Kenny J, Waters A, Jenkins D, Kaissi AA, Leal GF, Dallapiccola B, Carnevale F, Bitner-Glindzicz M, Lees M, Hennekam R, Stanier P, Burns AJ, Peeters H, Alkuraya FS, Beales PL. Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndrome. Nat Genet. 2011 Mar; 43(3):197-203.
    View in: PubMed
    Score: 0.022
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.