Soraya Beiraghi

Summary

Affiliation: University of Minnesota
Country: USA

Publications

  1. doi Craniofacial and intraoral phenotype of Robinow syndrome forms
    S Beiraghi
    Department of Developmental and Surgical Sciences, University of Minnesota School of Dentistry, Minneapolis, MN 55455, USA
    Clin Genet 80:15-24. 2011
  2. ncbi Oral manifestations of a possible new periodic fever syndrome
    Soraya Beiraghi
    Department of Developmental and Surgical Science, Division of Pediatric Dentistry, University of Minnesota School of Medicine, Minneapolis, Minn, USA
    Pediatr Dent 29:323-6. 2007
  3. ncbi Cleft lip and palate: association with other congenital malformations
    Soraya Beriaghi
    Cleft Palate and Craniofacial Clinic, Division of Pediatric Dentistry School of Dentistry, University of Minnesota, Minneapolis, MN 55455, USA
    J Clin Pediatr Dent 33:207-10. 2009
  4. ncbi Identification and characterization of a novel gene disrupted by a pericentric inversion inv(4)(p13.1q21.1) in a family with cleft lip
    Soraya Beiraghi
    Division of Pediatric Dentistry, University of Minnesota, 6 150 Moos Tower, 515 Delaware Street SE, Minneapolis, MN 55455, USA
    Gene 309:11-21. 2003
  5. doi WNT5A mutations in patients with autosomal dominant Robinow syndrome
    Anthony D Person
    Department of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, Minnesota, USA
    Dev Dyn 239:327-37. 2010
  6. ncbi Dental anomalies associated with unilateral and bilateral cleft lip and palate
    Wafa A Qureshi
    School of Dentistry, University of Minnesota, Minneapolis, Minn, USA
    J Dent Child (Chic) 79:69-73. 2012
  7. ncbi Autosomal recessive Robinow syndrome: a case report
    Ronald Grothe
    Division of Pediatric Dentistry, Department of Developmental and Surgical Sciences, School of Dentistry, University of Minnesota, Minneapolis, Minn, USA
    J Dent Child (Chic) 75:48-54. 2008
  8. ncbi Permanent tooth development in children with cleft lip and palate
    Adena F Borodkin
    School of Dentistry, University of Minnesota, Minneapolis, Minn, USA
    Pediatr Dent 30:408-13. 2008
  9. pmc Autosomal dominant nonsyndromic cleft lip and palate: significant evidence of linkage at 18q21.1
    Soraya Beiraghi
    Division of Pediatric Dentistry, University of Minnesota, Minneapolis, MN, USA
    Am J Hum Genet 81:180-8. 2007
  10. pmc Genomewide scan for nonsyndromic cleft lip and palate in multigenerational Indian families reveals significant evidence of linkage at 13q33.1-34
    Uppala Radhakrishna
    Green Cross Blood Bank and Genetic Research Centre, Paldi, India
    Am J Hum Genet 79:580-5. 2006

Collaborators

Detail Information

Publications10

  1. doi Craniofacial and intraoral phenotype of Robinow syndrome forms
    S Beiraghi
    Department of Developmental and Surgical Sciences, University of Minnesota School of Dentistry, Minneapolis, MN 55455, USA
    Clin Genet 80:15-24. 2011
    ..We propose that the difference in the alveolar ridge deformation pattern and severity of other intraoral characteristics could enhance the differential diagnosis of the two forms of this syndrome...
  2. ncbi Oral manifestations of a possible new periodic fever syndrome
    Soraya Beiraghi
    Department of Developmental and Surgical Science, Division of Pediatric Dentistry, University of Minnesota School of Medicine, Minneapolis, Minn, USA
    Pediatr Dent 29:323-6. 2007
    ..This may represent the first known reported case in the literature of a periodic fever syndrome presenting with such unusual recurring oral findings...
  3. ncbi Cleft lip and palate: association with other congenital malformations
    Soraya Beriaghi
    Cleft Palate and Craniofacial Clinic, Division of Pediatric Dentistry School of Dentistry, University of Minnesota, Minneapolis, MN 55455, USA
    J Clin Pediatr Dent 33:207-10. 2009
    ..Orofacial clefts are frequently associated with other congenital malformations. Studies vary in incidence and types of anomalies...
  4. ncbi Identification and characterization of a novel gene disrupted by a pericentric inversion inv(4)(p13.1q21.1) in a family with cleft lip
    Soraya Beiraghi
    Division of Pediatric Dentistry, University of Minnesota, 6 150 Moos Tower, 515 Delaware Street SE, Minneapolis, MN 55455, USA
    Gene 309:11-21. 2003
    ..5 kDa. The protein is highly similar to acyl-CoA desaturases from Drosophila melanogaster to Homo sapiens. The catalytically essential histidine clusters and the potential transmembrane domains are well conserved...
  5. doi WNT5A mutations in patients with autosomal dominant Robinow syndrome
    Anthony D Person
    Department of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, Minnesota, USA
    Dev Dyn 239:327-37. 2010
    ..This work suggests that a WNT5A/ROR2 signal transduction pathway is important in human craniofacial and skeletal development and that proper formation and growth of these structures is sensitive to variations in WNT5A function...
  6. ncbi Dental anomalies associated with unilateral and bilateral cleft lip and palate
    Wafa A Qureshi
    School of Dentistry, University of Minnesota, Minneapolis, Minn, USA
    J Dent Child (Chic) 79:69-73. 2012
    ..The purpose of this study was to compare the prevalence of dental anomalies in the primary and permanent dentition of patients with unilateral (UCLP) and bilateral (BCLP) cleft lip with or without palate...
  7. ncbi Autosomal recessive Robinow syndrome: a case report
    Ronald Grothe
    Division of Pediatric Dentistry, Department of Developmental and Surgical Sciences, School of Dentistry, University of Minnesota, Minneapolis, Minn, USA
    J Dent Child (Chic) 75:48-54. 2008
    ..Of special interest was the extent to which the patient's hyperplastic gingival tissues impeded both normal tooth eruption and orthodontic tooth movement...
  8. ncbi Permanent tooth development in children with cleft lip and palate
    Adena F Borodkin
    School of Dentistry, University of Minnesota, Minneapolis, Minn, USA
    Pediatr Dent 30:408-13. 2008
    ....
  9. pmc Autosomal dominant nonsyndromic cleft lip and palate: significant evidence of linkage at 18q21.1
    Soraya Beiraghi
    Division of Pediatric Dentistry, University of Minnesota, Minneapolis, MN, USA
    Am J Hum Genet 81:180-8. 2007
    ..Thus, a novel genomic region on 18q21.1 was identified that most likely harbors a high-risk variant for NSCL/P in this family; we propose to name this locus "OFC11" (orofacial cleft 11)...
  10. pmc Genomewide scan for nonsyndromic cleft lip and palate in multigenerational Indian families reveals significant evidence of linkage at 13q33.1-34
    Uppala Radhakrishna
    Green Cross Blood Bank and Genetic Research Centre, Paldi, India
    Am J Hum Genet 79:580-5. 2006
    ..17 cM (7.42 Mb) between SNPs rs951095 and rs726455. Thus, we have identified a novel genomic region on 13q33.1-34 that harbors a high-risk variant for CL-P in these Indian families...