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2016 4
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2019 5
2020 3
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21 results

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Page 1
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, Buxó CJ, Butali A, Adeyemo WL, Vieira AR, Shaffer JR, Murray JC, Weinberg SM, Leslie EJ, Marazita ML. Mukhopadhyay N, et al. Genet Epidemiol. 2022 Apr;46(3-4):182-198. doi: 10.1002/gepi.22447. Epub 2022 Feb 22. Genet Epidemiol. 2022. PMID: 35191549 Free PMC article.
Genetic Analyses of Enamel Hypoplasia in Multiethnic Cohorts.
Alotaibi RN, Howe BJ, Moreno Uribe LM, Sanchez C, Deleyiannis FWB, Padilla C, Poletta FA, Orioli IM, Buxó CJ, Wehby GL, Vieira AR, Murray J, Valencia-Ramírez C, Restrepo Muñeton CP, Long RE, Shaffer JR, Reis SE, Weinberg SM, Neiswanger K, McNeil DW, Marazita ML. Alotaibi RN, et al. Hum Hered. 2022 Feb 16;87(2):34-50. doi: 10.1159/000522642. Online ahead of print. Hum Hered. 2022. PMID: 35172313 Free PMC article.
Genome-Wide Association Study (GWAS) of dental caries in diverse populations.
Alotaibi RN, Howe BJ, Chernus JM, Mukhopadhyay N, Sanchez C, Deleyiannis FWB, Neiswanger K, Padilla C, Poletta FA, Orioli IM, Buxó CJ, Hecht JT, Wehby GL, Long RE, Vieira AR, Weinberg SM, Shaffer JR, Moreno Uribe LM, Marazita ML. Alotaibi RN, et al. BMC Oral Health. 2021 Jul 26;21(1):377. doi: 10.1186/s12903-021-01670-5. BMC Oral Health. 2021. PMID: 34311721 Free PMC article.
FAT4 identified as a potential modifier of orofacial cleft laterality.
Curtis SW, Chang D, Sun MR, Epstein MP, Murray JC, Feingold E, Beaty TH, Weinberg SM, Marazita ML, Lipinski RJ, Carlson JC, Leslie EJ. Curtis SW, et al. Genet Epidemiol. 2021 Oct;45(7):721-735. doi: 10.1002/gepi.22420. Epub 2021 Jun 15. Genet Epidemiol. 2021. PMID: 34130359 Free PMC article.
Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel Regions.
Mukhopadhyay N, Feingold E, Moreno-Uribe L, Wehby G, Valencia-Ramirez LC, Muñeton CPR, Padilla C, Deleyiannis F, Christensen K, Poletta FA, Orioli IM, Hecht JT, Buxó CJ, Butali A, Adeyemo WL, Vieira AR, Shaffer JR, Murray JC, Weinberg SM, Leslie EJ, Marazita ML. Mukhopadhyay N, et al. Front Cell Dev Biol. 2021 Apr 9;9:621482. doi: 10.3389/fcell.2021.621482. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 33898419 Free PMC article.
The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip.
Curtis SW, Chang D, Lee MK, Shaffer JR, Indencleef K, Epstein MP, Cutler DJ, Murray JC, Feingold E, Beaty TH, Claes P, Weinberg SM, Marazita ML, Carlson JC, Leslie EJ. Curtis SW, et al. HGG Adv. 2021 Apr 8;2(2):100025. doi: 10.1016/j.xhgg.2021.100025. HGG Adv. 2021. PMID: 33817668 Free PMC article.
Multivariate GWAS of Structural Dental Anomalies and Dental Caries in a Multi-Ethnic Cohort.
Alotaibi RN, Howe BJ, Moreno Uribe LM, Ramirez CV, Restrepo C, Deleyiannis FWB, Padilla C, Orioli IM, Buxó CJ, Hecht JT, Wehby GL, Neiswanger K, Murray JC, Shaffer JR, Weinberg SM, Marazita ML. Alotaibi RN, et al. Front Dent Med. 2021;2:771116. doi: 10.3389/fdmed.2021.771116. Epub 2022 Jan 4. Front Dent Med. 2021. PMID: 36267138 Free PMC article.
FaceBase 3: analytical tools and FAIR resources for craniofacial and dental research.
Samuels BD, Aho R, Brinkley JF, Bugacov A, Feingold E, Fisher S, Gonzalez-Reiche AS, Hacia JG, Hallgrimsson B, Hansen K, Harris MP, Ho TV, Holmes G, Hooper JE, Jabs EW, Jones KL, Kesselman C, Klein OD, Leslie EJ, Li H, Liao EC, Long H, Lu N, Maas RL, Marazita ML, Mohammed J, Prescott S, Schuler R, Selleri L, Spritz RA, Swigut T, van Bakel H, Visel A, Welsh I, Williams C, Williams TJ, Wysocka J, Yuan Y, Chai Y. Samuels BD, et al. Development. 2020 Sep 21;147(18):dev191213. doi: 10.1242/dev.191213. Development. 2020. PMID: 32958507 Free PMC article. Review.
Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21.
Mukhopadhyay N, Bishop M, Mortillo M, Chopra P, Hetmanski JB, Taub MA, Moreno LM, Valencia-Ramirez LC, Restrepo C, Wehby GL, Hecht JT, Deleyiannis F, Butali A, Weinberg SM, Beaty TH, Murray JC, Leslie EJ, Feingold E, Marazita ML. Mukhopadhyay N, et al. Hum Genet. 2020 Feb;139(2):215-226. doi: 10.1007/s00439-019-02099-1. Epub 2019 Dec 17. Hum Genet. 2020. PMID: 31848685 Free PMC article.
Leveraging Family History in Case-Control Analyses of Rare Variation.
Solis-Lemus CR, Fischer ST, Todor A, Liu C, Leslie EJ, Cutler DJ, Ghosh D, Epstein MP. Solis-Lemus CR, et al. Genetics. 2020 Feb;214(2):295-303. doi: 10.1534/genetics.119.302846. Epub 2019 Dec 16. Genetics. 2020. PMID: 31843756 Free PMC article.
21 results