J K Hartsfield

Summary

Affiliation: Indiana University
Country: USA

Publications

  1. ncbi request reprint Analysis of the EPHX1 113 polymorphism and GSTM1 homozygous null polymorphism and oral clefting associated with maternal smoking
    J K Hartsfield
    Oral Facial Genetics Section, Indiana University School of Dentistry, Indianapolis, Indiana 46202 5186, USA
    Am J Med Genet 102:21-4. 2001
  2. ncbi request reprint Review of the etiologic heterogeneity of the oculo-auriculo-vertebral spectrum (Hemifacial Microsomia)
    J K Hartsfield
    Department of Orthodontics and Oral Facial Genetics, Indiana University School of Dentistry, Indianapolis, IN, USA
    Orthod Craniofac Res 10:121-8. 2007
  3. ncbi request reprint The Ephx1(d) allele encoding an Arg338Cys substitution is associated with heat lability
    J K Hartsfield
    Oral Facial Genetics Program, Department of Oral Facial Development, Indiana University School of Dentistry, 1121 W Michigan Street, DS270, Indianapolis, Indiana 46202, USA
    Mamm Genome 11:915-8. 2000
  4. ncbi request reprint Root resorption associated with orthodontic force in IL-1Beta knockout mouse
    R A Al-Qawasmi
    Indiana University School of Dentistry, Indianapolis, IN 46202, USA
    J Musculoskelet Neuronal Interact 4:383-5. 2004
  5. ncbi request reprint Assignment1 of microsomal epoxide hydrolase (EPHX1) to human chromosome 1q42.1 by in situ hybridization
    J K Hartsfield
    Division of Oral Facial Genetics, Indiana University School of Dentistry, Indianapolis IN, USA
    Cytogenet Cell Genet 83:44-5. 1998
  6. ncbi request reprint Genetic predisposition to external apical root resorption in orthodontic patients: linkage of chromosome-18 marker
    R A Al-Qawasmi
    Department of Oral Facial Development, Indiana University School of Dentistry, 1121 West Michigan Street, Indianapolis 46202 5186, USA
    J Dent Res 82:356-60. 2003
  7. ncbi request reprint Phenytoin embryopathy: effect of epoxide hydrolase inhibitor on phenytoin exposure in utero in C57BL/6J mice
    J K Hartsfield
    Department of Oral Facial Development, Indiana University, Indianapolis 46202 5186, USA
    Biochem Mol Med 56:131-43. 1995
  8. doi request reprint Comparison of reliability in anatomical landmark identification using two-dimensional digital cephalometrics and three-dimensional cone beam computed tomography in vivo
    P C Chien
    Department of Orthodontics and Oral Facial Genetics, Indiana University Shool of Dentistry, Indianapolis, IN, USA
    Dentomaxillofac Radiol 38:262-73. 2009
  9. ncbi request reprint A novel FGFR2 gene mutation in Crouzon syndrome associated with apparent nonpenetrance
    E T Everett
    Department of Oral Facial Development, Indiana University School of Dentistry, Indianapolis 46202, USA
    Cleft Palate Craniofac J 36:533-41. 1999
  10. ncbi request reprint Dentin dysplasia, type II linkage to chromosome 4q
    J A Dean
    Department of Oral Facial Development, Indiana University School of Dentistry, Indianapolis 46202 5186, USA
    J Craniofac Genet Dev Biol 17:172-7. 1997

Collaborators

Detail Information

Publications12

  1. ncbi request reprint Analysis of the EPHX1 113 polymorphism and GSTM1 homozygous null polymorphism and oral clefting associated with maternal smoking
    J K Hartsfield
    Oral Facial Genetics Section, Indiana University School of Dentistry, Indianapolis, Indiana 46202 5186, USA
    Am J Med Genet 102:21-4. 2001
    ..This suggests that when mothers smoke periconceptionally, their infants having these alleles at either (or both) loci were not at substantially increased risk for CL/P compared to infants with the wild-type alleles...
  2. ncbi request reprint Review of the etiologic heterogeneity of the oculo-auriculo-vertebral spectrum (Hemifacial Microsomia)
    J K Hartsfield
    Department of Orthodontics and Oral Facial Genetics, Indiana University School of Dentistry, Indianapolis, IN, USA
    Orthod Craniofac Res 10:121-8. 2007
    ..The same genetic-environmental factors and or etiological mechanisms may then be investigated in apparently sporadic cases...
  3. ncbi request reprint The Ephx1(d) allele encoding an Arg338Cys substitution is associated with heat lability
    J K Hartsfield
    Oral Facial Genetics Program, Department of Oral Facial Development, Indiana University School of Dentistry, 1121 W Michigan Street, DS270, Indianapolis, Indiana 46202, USA
    Mamm Genome 11:915-8. 2000
    ..5cm (lod = 10.0)...
  4. ncbi request reprint Root resorption associated with orthodontic force in IL-1Beta knockout mouse
    R A Al-Qawasmi
    Indiana University School of Dentistry, Indianapolis, IN 46202, USA
    J Musculoskelet Neuronal Interact 4:383-5. 2004
  5. ncbi request reprint Assignment1 of microsomal epoxide hydrolase (EPHX1) to human chromosome 1q42.1 by in situ hybridization
    J K Hartsfield
    Division of Oral Facial Genetics, Indiana University School of Dentistry, Indianapolis IN, USA
    Cytogenet Cell Genet 83:44-5. 1998
  6. ncbi request reprint Genetic predisposition to external apical root resorption in orthodontic patients: linkage of chromosome-18 marker
    R A Al-Qawasmi
    Department of Oral Facial Development, Indiana University School of Dentistry, 1121 West Michigan Street, Indianapolis 46202 5186, USA
    J Dent Res 82:356-60. 2003
    ..5; p = 0.02) of EARR affecting the maxillary central incisor with the microsatellite marker D18S64 (tightly linked to TNFRSF11A). This indicates that the TNFRSF11A locus, or another tightly linked gene, is associated with EARR...
  7. ncbi request reprint Phenytoin embryopathy: effect of epoxide hydrolase inhibitor on phenytoin exposure in utero in C57BL/6J mice
    J K Hartsfield
    Department of Oral Facial Development, Indiana University, Indianapolis 46202 5186, USA
    Biochem Mol Med 56:131-43. 1995
    ..This suggests either that differences in the genotypes of Swiss and C57BL/6J mice may be a contributing factor or that other teratogenic mechanisms were involved...
  8. doi request reprint Comparison of reliability in anatomical landmark identification using two-dimensional digital cephalometrics and three-dimensional cone beam computed tomography in vivo
    P C Chien
    Department of Orthodontics and Oral Facial Genetics, Indiana University Shool of Dentistry, Indianapolis, IN, USA
    Dentomaxillofac Radiol 38:262-73. 2009
    ..To compare reliability for landmark identification on patient images from three-dimensional (3D) cone beam CT (CBCT) and digital two-dimensional (2D) lateral cephalograms...
  9. ncbi request reprint A novel FGFR2 gene mutation in Crouzon syndrome associated with apparent nonpenetrance
    E T Everett
    Department of Oral Facial Development, Indiana University School of Dentistry, Indianapolis 46202, USA
    Cleft Palate Craniofac J 36:533-41. 1999
    ..To determine whether specific mutations within the fibroblast growth factor receptor 2 (FGFR2) gene that are associated with Crouzon syndrome can be present in an individual who had been assumed to be "clinically normal."..
  10. ncbi request reprint Dentin dysplasia, type II linkage to chromosome 4q
    J A Dean
    Department of Oral Facial Development, Indiana University School of Dentistry, Indianapolis 46202 5186, USA
    J Craniofac Genet Dev Biol 17:172-7. 1997
    ..1 cM, includes SPPI, D4S2691, D4S2690, D4S451, and D4S2456, and overlaps the most likely location of the DGII locus. A candidate gene for DGII should also be considered a candidate gene for dentin dysplasia, type II...
  11. ncbi request reprint The use of small titanium screws for orthodontic anchorage
    T Deguchi
    Department of Orthodontics, Okayama University Graduate School of Medicine and Dentistry, 2 5 1, Shikata cho, Japan
    J Dent Res 82:377-81. 2003
    ..Analysis of these data indicates that small titanium screws were able to function as rigid osseous anchorage against orthodontic load for 3 months with a minimal (under 3 weeks) healing period...
  12. pmc Lowe oculocerebrorenal syndrome in a female with a balanced X;20 translocation: mapping of the X chromosome breakpoint
    O T Mueller
    Department of Pediatrics, University of South Florida College of Medicine, Tampa 33612
    Am J Hum Genet 49:804-10. 1991
    ..The translocation chromosome originated from an unaffected male without a visible translocation, indicating that the most likely cause of OCRL in this patient is the de novo translocation that disrupted the OCRL locus...