BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

414 related articles for article (PubMed ID: 27018475)

  • 1. Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate.
    Mangold E; Böhmer AC; Ishorst N; Hoebel AK; Gültepe P; Schuenke H; Klamt J; Hofmann A; Gölz L; Raff R; Tessmann P; Nowak S; Reutter H; Hemprich A; Kreusch T; Kramer FJ; Braumann B; Reich R; Schmidt G; Jäger A; Reiter R; Brosch S; Stavusis J; Ishida M; Seselgyte R; Moore GE; Nöthen MM; Borck G; Aldhorae KA; Lace B; Stanier P; Knapp M; Ludwig KU
    Am J Hum Genet; 2016 Apr; 98(4):755-62. PubMed ID: 27018475
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Association study between Van der Woude Syndrome causative gene GRHL3 and nonsyndromic cleft lip with or without cleft palate in a Chinese cohort.
    Wang Y; Sun Y; Huang Y; Pan Y; Jia Z; Ma L; Ma L; Lan F; Zhou Y; Shi J; Yang X; Zhang L; Jiang H; Jiang M; Yin A; Cheng J; Wang L; Yang Y; Shi B
    Gene; 2016 Aug; 588(1):69-73. PubMed ID: 27129939
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Lack of Association between Missense Variants in GRHL3 (rs2486668 and rs545809) and Susceptibility to Non-Syndromic Orofacial Clefts in a Han Chinese Population.
    He M; Bian Z
    PLoS One; 2016; 11(7):e0159940. PubMed ID: 27459192
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Whole exome sequencing identifies mutations in 10% of patients with familial non-syndromic cleft lip and/or palate in genes mutated in well-known syndromes.
    Basha M; Demeer B; Revencu N; Helaers R; Theys S; Bou Saba S; Boute O; Devauchelle B; Francois G; Bayet B; Vikkula M
    J Med Genet; 2018 Jul; 55(7):449-458. PubMed ID: 29500247
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Association and Mutation Analyses of the IRF6 Gene in Families With Nonsyndromic and Syndromic Cleft Lip and/or Cleft Palate.
    Pegelow M; Koillinen H; Magnusson M; Fransson I; Unneberg P; Kere J; Karsten A; Peyrard-Janvid M
    Cleft Palate Craniofac J; 2014 Jan; 51(1):49-55. PubMed ID: 23394314
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development.
    Peyrard-Janvid M; Leslie EJ; Kousa YA; Smith TL; Dunnwald M; Magnusson M; Lentz BA; Unneberg P; Fransson I; Koillinen HK; Rautio J; Pegelow M; Karsten A; Basel-Vanagaite L; Gordon W; Andersen B; Svensson T; Murray JC; Cornell RA; Kere J; Schutte BC
    Am J Hum Genet; 2014 Jan; 94(1):23-32. PubMed ID: 24360809
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Exploring GRHL3 polymorphisms and SNP-SNP interactions in the risk of non-syndromic oral clefts in the Brazilian population.
    Azevedo CMS; Machado RA; Martelli-Júnior H; Reis SRA; Persuhn DC; Coletta RD; Rangel ALCA
    Oral Dis; 2020 Jan; 26(1):145-151. PubMed ID: 31564061
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Association analysis of SNPs in GRHL3, FAF1, and KCNJ2 with NSCPO sub-phenotypes in Han Chinese.
    Sun JL; Shi JY; Yin B; Lin YS; Shi B; Jia ZL
    Oral Dis; 2022 Nov; 28(8):2204-2214. PubMed ID: 34255421
    [TBL] [Abstract][Full Text] [Related]  

  • 9. IRF6 mutation screening in non-syndromic orofacial clefting: analysis of 1521 families.
    Leslie EJ; Koboldt DC; Kang CJ; Ma L; Hecht JT; Wehby GL; Christensen K; Czeizel AE; Deleyiannis FW; Fulton RS; Wilson RK; Beaty TH; Schutte BC; Murray JC; Marazita ML
    Clin Genet; 2016 Jul; 90(1):28-34. PubMed ID: 26346622
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Van der Woude syndrome: a review of 11 cases seen at the Lagos University Teaching Hospital.
    James O; Adeyemo WL; Emeka CI; Ogunlewe MO; Ladeinde AL; Butali A
    Afr J Paediatr Surg; 2014; 11(1):52-5. PubMed ID: 24647295
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Two rare variants reveal the significance of Grainyhead-like 3 Arginine 391 underlying non-syndromic cleft palate only.
    Huang W; He Q; Li M; Ding Y; Liang W; Li W; Lin J; Zhao H; Chen F
    Oral Dis; 2023 May; 29(4):1632-1643. PubMed ID: 35189007
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Loss-of-Function GRHL3 Variants Detected in African Patients with Isolated Cleft Palate.
    Eshete MA; Liu H; Li M; Adeyemo WL; Gowans LJJ; Mossey PA; Busch T; Deressa W; Donkor P; Olaitan PB; Aregbesola BS; Braimah RO; Oseni GO; Oginni F; Audu R; Onwuamah C; James O; Augustine-Akpan E; Rahman LA; Ogunlewe MO; Arthur FKN; Bello SA; Agbenorku P; Twumasi P; Abate F; Hailu T; Demissie Y; Hailu A; Plange-Rhule G; Obiri-Yeboah S; Dunnwald MM; Gravem PE; Marazita ML; Adeyemo AA; Murray JC; Cornell RA; Butali A
    J Dent Res; 2018 Jan; 97(1):41-48. PubMed ID: 28886269
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Toward an orofacial gene regulatory network.
    Kousa YA; Schutte BC
    Dev Dyn; 2016 Mar; 245(3):220-32. PubMed ID: 26332872
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome Sequencing.
    Hoebel AK; Drichel D; van de Vorst M; Böhmer AC; Sivalingam S; Ishorst N; Klamt J; Gölz L; Alblas M; Maaser A; Keppler K; Zink AM; Dixon MJ; Dixon J; Hemprich A; Kruse T; Graf I; Dunsche A; Schmidt G; Daratsianos N; Nowak S; Aldhorae KA; Nöthen MM; Knapp M; Thiele H; Gilissen C; Reutter H; Hoischen A; Mangold E; Ludwig KU
    J Dent Res; 2017 Oct; 96(11):1314-1321. PubMed ID: 28767323
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel IRF6 Mutations Detected in Orofacial Cleft Patients by Targeted Massively Parallel Sequencing.
    Khandelwal KD; Ishorst N; Zhou H; Ludwig KU; Venselaar H; Gilissen C; Thonissen M; van Rooij IA; Dreesen K; Steehouwer M; van de Vorst M; Bloemen M; van Beusekom E; Roosenboom J; Borstlap W; Admiraal R; Dormaar T; Schoenaers J; Vander Poorten V; Hens G; Verdonck A; Bergé S; Roeleveldt N; Vriend G; Devriendt K; Brunner HG; Mangold E; Hoischen A; van Bokhoven H; Carels CE
    J Dent Res; 2017 Feb; 96(2):179-185. PubMed ID: 27834299
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genome-wide Analyses Identify a Novel Risk Locus for Nonsyndromic Cleft Palate.
    He M; Zuo X; Liu H; Wang W; Zhang Y; Fu Y; Zhen Q; Yu Y; Pan Y; Qin C; Li B; Yang R; Wu J; Huang Z; Ge H; Wu H; Xu Q; Zuo Y; Chen W; Qin Y; Liu Z; Chen S; Zhang H; Zhou F; Yan H; Yu Y; Yong L; Chen G; Liang B; Cornell RA; Zong L; Wang L; Zou D; Sun L; Bian Z
    J Dent Res; 2020 Dec; 99(13):1461-1468. PubMed ID: 32758111
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Strong association of variants around FOXE1 and orofacial clefting.
    Ludwig KU; Böhmer AC; Rubini M; Mossey PA; Herms S; Nowak S; Reutter H; Alblas MA; Lippke B; Barth S; Paredes-Zenteno M; Muñoz-Jimenez SG; Ortiz-Lopez R; Kreusch T; Hemprich A; Martini M; Braumann B; Jäger A; Pötzsch B; Molloy A; Peterlin B; Hoffmann P; Nöthen MM; Rojas-Martinez A; Knapp M; Steegers-Theunissen RP; Mangold E
    J Dent Res; 2014 Apr; 93(4):376-81. PubMed ID: 24563486
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Nonsyndromic cleft palate: An association study at GWAS candidate loci in a multiethnic sample.
    Ishorst N; Francheschelli P; Böhmer AC; Khan MFJ; Heilmann-Heimbach S; Fricker N; Little J; Steegers-Theunissen RPM; Peterlin B; Nowak S; Martini M; Kruse T; Dunsche A; Kreusch T; Gölz L; Aldhorae K; Halboub E; Reutter H; Mossey P; Nöthen MM; Rubini M; Ludwig KU; Knapp M; Mangold E
    Birth Defects Res; 2018 Jun; 110(10):871-882. PubMed ID: 29498243
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 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
    Am J Hum Genet; 2016 Apr; 98(4):744-54. PubMed ID: 27018472
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of susceptibility loci for nonsyndromic orofacial clefting in a European trio sample.
    Böhmer AC; Mangold E; Tessmann P; Mossey PA; Steegers-Theunissen RP; Lindemans J; Bouwman-Both M; Rubini M; Franceschelli P; Aiello V; Peterlin B; Molloy AM; Nöthen MM; Knapp M; Ludwig KU
    Am J Med Genet A; 2013 Oct; 161A(10):2545-9. PubMed ID: 24038802
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 21.