Beiraghi S - Search Results

1

Fine-Mapping of 18q21.1 Locus Identifies Single Nucleotide Polymorphisms Associated with Nonsyndromic Cleft Lip with or without Cleft Palate.

Mitra AK, Stessman HA, Schaefer RJ, Wang W, Myers CL, Van Ness BG, Beiraghi S. Mitra AK, et al. Among authors: beiraghi s. Front Genet. 2016 May 23;7:88. doi: 10.3389/fgene.2016.00088. eCollection 2016. Front Genet. 2016. PMID: 27242896 Free PMC article.

2

Autosomal dominant nonsyndromic cleft lip and palate: significant evidence of linkage at 18q21.1.

Beiraghi S, Nath SK, Gaines M, Mandhyan DD, Hutchings D, Ratnamala U, McElreavey K, Bartoloni L, Antonarakis GS, Antonarakis SE, Radhakrishna U. Beiraghi S, et al. Am J Hum Genet. 2007 Jul;81(1):180-8. doi: 10.1086/518944. Epub 2007 May 18. Am J Hum Genet. 2007. PMID: 17564975 Free PMC article.

3

Dental anomalies associated with unilateral and bilateral cleft lip and palate.

Qureshi WA, Beiraghi S, Leon-Salazar V. Qureshi WA, et al. Among authors: beiraghi s. J Dent Child (Chic). 2012 May-Aug;79(2):69-73. J Dent Child (Chic). 2012. PMID: 22828761

4

Craniofacial and intraoral phenotype of Robinow syndrome forms.

Beiraghi S, Leon-Salazar V, Larson BE, John MT, Cunningham ML, Petryk A, Lohr JL. Beiraghi S, et al. Clin Genet. 2011 Jul;80(1):15-24. doi: 10.1111/j.1399-0004.2011.01683.x. Epub 2011 May 16. Clin Genet. 2011. PMID: 21496006

5

Permanent tooth development in children with cleft lip and palate.

Borodkin AF, Feigal RJ, Beiraghi S, Moller KT, Hodges JS. Borodkin AF, et al. Among authors: beiraghi s. Pediatr Dent. 2008 Sep-Oct;30(5):408-13. Pediatr Dent. 2008. PMID: 18942600

6

Genomewide scan for nonsyndromic cleft lip and palate in multigenerational Indian families reveals significant evidence of linkage at 13q33.1-34.

Radhakrishna U, Ratnamala U, Gaines M, Beiraghi S, Hutchings D, Golla J, Husain SA, Gambhir PS, Sheth JJ, Sheth FJ, Chetan GK, Naveed M, Solanki JV, Patel UC, Master DC, Memon R, Antonarakis GS, Antonarakis SE, Nath SK. Radhakrishna U, et al. Among authors: beiraghi s. Am J Hum Genet. 2006 Sep;79(3):580-5. doi: 10.1086/507487. Epub 2006 Jul 21. Am J Hum Genet. 2006. PMID: 16909398 Free PMC article.

7

Identification and characterization of a novel gene disrupted by a pericentric inversion inv(4)(p13.1q21.1) in a family with cleft lip.

Beiraghi S, Zhou M, Talmadge CB, Went-Sumegi N, Davis JR, Huang D, Saal H, Seemayer TA, Sumegi J. Beiraghi S, et al. Gene. 2003 Apr 24;309(1):11-21. doi: 10.1016/s0378-1119(03)00461-x. Gene. 2003. PMID: 12727354

8

p53 activation by knockdown technologies.

Robu ME, Larson JD, Nasevicius A, Beiraghi S, Brenner C, Farber SA, Ekker SC. Robu ME, et al. Among authors: beiraghi s. PLoS Genet. 2007 May 25;3(5):e78. doi: 10.1371/journal.pgen.0030078. Epub 2007 Apr 10. PLoS Genet. 2007. PMID: 17530925 Free PMC article.

9

WNT5A mutations in patients with autosomal dominant Robinow syndrome.

Person AD, Beiraghi S, Sieben CM, Hermanson S, Neumann AN, Robu ME, Schleiffarth JR, Billington CJ Jr, van Bokhoven H, Hoogeboom JM, Mazzeu JF, Petryk A, Schimmenti LA, Brunner HG, Ekker SC, Lohr JL. Person AD, et al. Among authors: beiraghi s. Dev Dyn. 2010 Jan;239(1):327-37. doi: 10.1002/dvdy.22156. Dev Dyn. 2010. PMID: 19918918 Free PMC article.

10

Accuracy and precision of a 3D anthropometric facial analysis with and without landmark labeling before image acquisition.

Aynechi N, Larson BE, Leon-Salazar V, Beiraghi S. Aynechi N, et al. Among authors: beiraghi s. Angle Orthod. 2011 Mar;81(2):245-52. doi: 10.2319/041810-210.1. Angle Orthod. 2011. PMID: 21208076 Free PMC article.

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