These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

226 related articles for article (PubMed ID: 28287101)

  • 1. Identification of common non-coding variants at 1p22 that are functional for non-syndromic orofacial clefting.
    Liu H; Leslie EJ; Carlson JC; Beaty TH; Marazita ML; Lidral AC; Cornell RA
    Nat Commun; 2017 Mar; 8():14759. PubMed ID: 28287101
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Expression and mutation analyses implicate ARHGAP29 as the etiologic gene for the cleft lip with or without cleft palate locus identified by genome-wide association on chromosome 1p22.
    Leslie EJ; Mansilla MA; Biggs LC; Schuette K; Bullard S; Cooper M; Dunnwald M; Lidral AC; Marazita ML; Beaty TH; Murray JC
    Birth Defects Res A Clin Mol Teratol; 2012 Nov; 94(11):934-42. PubMed ID: 23008150
    [TBL] [Abstract][Full Text] [Related]  

  • 3. New Causal Candidate Genes and Enhancers Linked to Orofacial Clefting Identified.
    Am J Med Genet A; 2019 Aug; 179(8):1409-1410. PubMed ID: 31355538
    [No Abstract]   [Full Text] [Related]  

  • 4. Further evidence suggesting a role for variation in ARHGAP29 variants in nonsyndromic cleft lip/palate.
    Letra A; Maili L; Mulliken JB; Buchanan E; Blanton SH; Hecht JT
    Birth Defects Res A Clin Mol Teratol; 2014 Sep; 100(9):679-85. PubMed ID: 25163644
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci.
    Leslie EJ; Taub MA; Liu H; Steinberg KM; Koboldt DC; Zhang Q; Carlson JC; Hetmanski JB; Wang H; Larson DE; Fulton RS; Kousa YA; Fakhouri WD; Naji A; Ruczinski I; Begum F; Parker MM; Busch T; Standley J; Rigdon J; Hecht JT; Scott AF; Wehby GL; Christensen K; Czeizel AE; Deleyiannis FW; Schutte BC; Wilson RK; Cornell RA; Lidral AC; Weinstock GM; Beaty TH; Marazita ML; Murray JC
    Am J Hum Genet; 2015 Mar; 96(3):397-411. PubMed ID: 25704602
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Polymorphic variants near 1p22 and 20q11.2 loci and the risk of non-syndromic cleft lip and palate in South Indian population.
    Babu Gurramkonda V; Hussain Syed A; Murthy J; Chaubey G; Bhaskar Lakkakula VK
    Int J Pediatr Otorhinolaryngol; 2015 Dec; 79(12):2389-93. PubMed ID: 26586245
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Exome sequencing provides additional evidence for the involvement of ARHGAP29 in Mendelian orofacial clefting and extends the phenotypic spectrum to isolated cleft palate.
    Liu H; Busch T; Eliason S; Anand D; Bullard S; Gowans LJJ; Nidey N; Petrin A; Augustine-Akpan EA; Saadi I; Dunnwald M; Lachke SA; Zhu Y; Adeyemo A; Amendt B; Roscioli T; Cornell R; Murray J; Butali A
    Birth Defects Res; 2017 Jan; 109(1):27-37. PubMed ID: 28029220
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 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
    Hum Mol Genet; 2016 Jul; 25(13):2862-2872. PubMed ID: 27033726
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of novel susceptibility genes for non-syndromic cleft lip with or without cleft palate using NGS-based multigene panel testing.
    Dąbrowska J; Biedziak B; Szponar-Żurowska A; Budner M; Jagodziński PP; Płoski R; Mostowska A
    Mol Genet Genomics; 2022 Sep; 297(5):1315-1327. PubMed ID: 35778651
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of a Novel Variant of
    Tang JX; Xiao XS; Wang K; Jin JY; Fan LL; Xiang R
    Biomed Res Int; 2020; 2020():8790531. PubMed ID: 33150183
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts.
    Shaffer JR; LeClair J; Carlson JC; Feingold E; Buxó CJ; Christensen K; Deleyiannis FWB; Field LL; Hecht JT; Moreno L; Orioli IM; Padilla C; Vieira AR; Wehby GL; Murray JC; Weinberg SM; Marazita ML; Leslie EJ
    Am J Med Genet A; 2019 Mar; 179(3):467-474. PubMed ID: 30582786
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Gene-gene interaction of single nucleotide polymorphisms in 16p13.3 may contribute to the risk of non-syndromic cleft lip with or without cleft palate in Chinese case-parent trios.
    Liu D; Wang H; Schwender H; Marazita ML; Wang Z; Yuan Y; Wang P; Liang KY; Wu-Chou YH; Wang M; Shi B; Zhu H; Wu T; Beaty TH
    Am J Med Genet A; 2017 Jun; 173(6):1489-1494. PubMed ID: 28402597
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss-of-function vs missense variants.
    Savastano CP; Brito LA; Faria ÁC; Setó-Salvia N; Peskett E; Musso CM; Alvizi L; Ezquina SA; James C; GOSgene ; Beales P; Lees M; Moore GE; Stanier P; Passos-Bueno MR
    Clin Genet; 2017 May; 91(5):683-689. PubMed ID: 27350171
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association between single-nucleotide polymorphisms on chromosome 1p22 and 20q12 and nonsyndromic cleft lip with or without cleft palate: new data in Han Chinese and meta-analysis.
    Huang E; Cheng H; Xu M; Shu S; Tang S
    Birth Defects Res A Clin Mol Teratol; 2012 Jun; 94(6):469-76. PubMed ID: 22522387
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Brazilian population with high African ancestry.
    do Rego Borges A; Sá J; Hoshi R; Viena CS; Mariano LC; de Castro Veiga P; Medrado AP; Machado RA; de Aquino SN; Messetti AC; Spritz RA; Coletta RD; Reis SR
    Am J Med Genet A; 2015 Oct; 167A(10):2344-9. PubMed ID: 26198054
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of novel susceptibility loci for non-syndromic cleft lip with or without cleft palate.
    Ma L; Lou S; Miao Z; Yao S; Yu X; Kan S; Zhu G; Yang F; Zhang C; Zhang W; Wang M; Wang L; Pan Y
    J Cell Mol Med; 2020 Dec; 24(23):13669-13678. PubMed ID: 33108691
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Evaluating eight newly identified susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population.
    Ludwig KU; Wahle P; Reutter H; Paredes-Zenteno M; Muñoz-Jimenez SG; Ortiz-Lopez R; Böhmer AC; Tessmann P; Nowak S; Nöthen MM; Knapp M; Rojas-Martinez A; Mangold E
    Birth Defects Res A Clin Mol Teratol; 2014 Jan; 100(1):43-7. PubMed ID: 24382704
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes.
    Carlson JC; Standley J; Petrin A; Shaffer JR; Butali A; Buxó CJ; Castilla E; Christensen K; Deleyiannis FW; Hecht JT; Field LL; Garidkhuu A; Moreno Uribe LM; Nagato N; Orioli IM; Padilla C; Poletta F; Suzuki S; Vieira AR; Wehby GL; Weinberg SM; Beaty TH; Feingold E; Murray JC; Marazita ML; Leslie EJ
    Genet Epidemiol; 2017 Dec; 41(8):887-897. PubMed ID: 29124805
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association of CDKAL1 nucleotide variants with the risk of non-syndromic cleft lip with or without cleft palate.
    Gaczkowska A; Żukowski K; Biedziak B; Hozyasz KK; Wójcicki P; Zadurska M; Budner M; Lasota A; Szponar-Żurowska A; Jagodziński PP; Mostowska A
    J Hum Genet; 2018 Apr; 63(4):397-406. PubMed ID: 29403086
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.