B R Pober

Summary

Affiliation: Harvard University
Country: USA

Publications

  1. pmc High prevalence of diabetes and pre-diabetes in adults with Williams syndrome
    B R Pober
    Center for Human Genetics, Simches Research Building, 185 Cambridge Street, Rm 222, Boston, MA 02115, USA
    Am J Med Genet C Semin Med Genet 154:291-8. 2010
  2. pmc A review of Donnai-Barrow and facio-oculo-acoustico-renal (DB/FOAR) syndrome: clinical features and differential diagnosis
    Barbara R Pober
    Massachusetts General Hospital, Boston, Massachusetts, USA
    Birth Defects Res A Clin Mol Teratol 85:76-81. 2009
  3. pmc Genetic aspects of human congenital diaphragmatic hernia
    B R Pober
    Center for Human Genetics, Massachusetts General Hospital, Boston, MA 02114, USA
    Clin Genet 74:1-15. 2008
  4. pmc Mechanisms and treatment of cardiovascular disease in Williams-Beuren syndrome
    Barbara R Pober
    Department of Pediatrics, MassGeneral Hospital for Children, Simches Research Building, Rm 222, 185 Cambridge St, Boston, Massachusetts 02114, USA
    J Clin Invest 118:1606-15. 2008
  5. pmc Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes
    Sibel Kantarci
    Pediatric Surgical Research Laboratories, Massachusetts General Hospital, Simches Research Building, 185 Cambridge St, Boston, Massachusetts 02114 USA
    Nat Genet 39:957-9. 2007
  6. pmc Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management
    Angela E Lin
    Genetics Unit, Department of Pediatrics, MassGeneral Hospital for Children, Boston, Massachusetts 02114, USA
    Genet Med 10:469-94. 2008
  7. pmc Donnai-Barrow syndrome (DBS/FOAR) in a child with a homozygous LRP2 mutation due to complete chromosome 2 paternal isodisomy
    Sibel Kantarci
    Pediatric Surgical Research Laboratories, Massachusetts General Hospital, Boston, Massachusetts, USA
    Am J Med Genet A 146:1842-7. 2008
  8. pmc Characterization of the chromosome 1q41q42.12 region, and the candidate gene DISP1, in patients with CDH
    Sibel Kantarci
    Pediatric Surgical Research Laboratories, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA
    Am J Med Genet A 152:2493-504. 2010
  9. pmc Congenital diaphragmatic hernia and associated cardiovascular malformations: type, frequency, and impact on management
    Angela E Lin
    Genetics Unit, MassGeneral Hospital for Children, Boston, MA 02114, USA
    Am J Med Genet C Semin Med Genet 145:201-16. 2007
  10. pmc Overview of epidemiology, genetics, birth defects, and chromosome abnormalities associated with CDH
    Barbara R Pober
    Department of Surgery, Children s Hospital of Boston, Boston, MA, USA
    Am J Med Genet C Semin Med Genet 145:158-71. 2007

Collaborators

Detail Information

Publications22

  1. pmc High prevalence of diabetes and pre-diabetes in adults with Williams syndrome
    B R Pober
    Center for Human Genetics, Simches Research Building, 185 Cambridge Street, Rm 222, Boston, MA 02115, USA
    Am J Med Genet C Semin Med Genet 154:291-8. 2010
    ..Syntaxin-1A is a prime candidate gene based on its location in the WSCR, its role in insulin release, and the presence of abnormal glucose metabolism in mouse models with aberrantly expressed Stx-1a...
  2. pmc A review of Donnai-Barrow and facio-oculo-acoustico-renal (DB/FOAR) syndrome: clinical features and differential diagnosis
    Barbara R Pober
    Massachusetts General Hospital, Boston, Massachusetts, USA
    Birth Defects Res A Clin Mol Teratol 85:76-81. 2009
    ..Although several conditions to consider in the differential diagnosis are highlighted, the diagnosis of DB/FOAR syndrome should not be difficult to establish as its constellation of findings is strikingly characteristic...
  3. pmc Genetic aspects of human congenital diaphragmatic hernia
    B R Pober
    Center for Human Genetics, Massachusetts General Hospital, Boston, MA 02114, USA
    Clin Genet 74:1-15. 2008
    ....
  4. pmc Mechanisms and treatment of cardiovascular disease in Williams-Beuren syndrome
    Barbara R Pober
    Department of Pediatrics, MassGeneral Hospital for Children, Simches Research Building, Rm 222, 185 Cambridge St, Boston, Massachusetts 02114, USA
    J Clin Invest 118:1606-15. 2008
    ....
  5. pmc Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes
    Sibel Kantarci
    Pediatric Surgical Research Laboratories, Massachusetts General Hospital, Simches Research Building, 185 Cambridge St, Boston, Massachusetts 02114 USA
    Nat Genet 39:957-9. 2007
    ..LRP2 encodes megalin, a multiligand uptake receptor that regulates levels of diverse circulating compounds. This work implicates a pathway with potential pharmacological therapeutic targets...
  6. pmc Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management
    Angela E Lin
    Genetics Unit, Department of Pediatrics, MassGeneral Hospital for Children, Boston, Massachusetts 02114, USA
    Genet Med 10:469-94. 2008
    ..New data are also provided about the cardiac status of adults with a 22q11.2 deletion and with Down syndrome...
  7. pmc Donnai-Barrow syndrome (DBS/FOAR) in a child with a homozygous LRP2 mutation due to complete chromosome 2 paternal isodisomy
    Sibel Kantarci
    Pediatric Surgical Research Laboratories, Massachusetts General Hospital, Boston, Massachusetts, USA
    Am J Med Genet A 146:1842-7. 2008
    ..This report highlights the importance of parental genotyping in order to give accurate genetic counseling for autosomal recessive disorders...
  8. pmc Characterization of the chromosome 1q41q42.12 region, and the candidate gene DISP1, in patients with CDH
    Sibel Kantarci
    Pediatric Surgical Research Laboratories, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA
    Am J Med Genet A 152:2493-504. 2010
    ....
  9. pmc Congenital diaphragmatic hernia and associated cardiovascular malformations: type, frequency, and impact on management
    Angela E Lin
    Genetics Unit, MassGeneral Hospital for Children, Boston, MA 02114, USA
    Am J Med Genet C Semin Med Genet 145:201-16. 2007
    ..Irrespective of the type of severity of CVMs in patients with CDH, the degree of pulmonary hypoplasia and pulmonary vascular disease predicts outcome...
  10. pmc Overview of epidemiology, genetics, birth defects, and chromosome abnormalities associated with CDH
    Barbara R Pober
    Department of Surgery, Children s Hospital of Boston, Boston, MA, USA
    Am J Med Genet C Semin Med Genet 145:158-71. 2007
    ....
  11. pmc Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes
    Shinji Kondo
    Department of Pediatrics, The University of Iowa, Iowa City, Iowa 52242, USA
    Nat Genet 32:285-9. 2002
    ..Our observations demonstrate that haploinsufficiency of IRF6 disrupts orofacial development and are consistent with dominant-negative mutations disturbing development of the skin and genitalia...
  12. pmc Infants with Bochdalek diaphragmatic hernia: sibling precurrence and monozygotic twin discordance in a hospital-based malformation surveillance program
    Barbara R Pober
    Genetics and Teratology, MassGeneral Hospital for Children, Boston, Massachusetts, USA
    Am J Med Genet A 138:81-8. 2005
    ..The twin data also raise the possibility that epigenetic abnormalities contribute to the development of CDH...
  13. ncbi request reprint Cardiovascular malformations in Fryns syndrome: is there a pathogenic role for neural crest cells?
    Angela E Lin
    Teratology Unit, Pediatric Service, MassGeneral Hospital for Children, Boston, Massachusetts 02115, USA
    Am J Med Genet A 139:186-93. 2005
    ....
  14. pmc Findings from aCGH in patients with congenital diaphragmatic hernia (CDH): a possible locus for Fryns syndrome
    S Kantarci
    Pediatric Surgical Research Laboratories, MassGeneral Hospital for Children, Harvard Medical School, 300 Longwood Avenue, Boston, MA 02115, USA
    Am J Med Genet A 140:17-23. 2006
    ..12 that was confirmed by FISH. Given prior reports of CDH in association with cytogenetic abnormalities in this region, we propose that this represents a locus for Fryns syndrome, a Fryns syndrome phenocopy, or CDH...
  15. pmc Unknown syndrome in sibs: pili torti, growth delay, developmental delay, and mild neurological abnormalities
    S K Shapira
    Division of Genetics, Children s Hospital, Boston, MA 02115
    J Med Genet 29:509-10. 1992
    ..The features of the cases presented here have not been noted in the previously reported clinical syndromes in which pili torti may be found...
  16. pmc Pulmonary function and emphysema in Williams-Beuren syndrome
    Emily S Wan
    Channing Laboratory, Department of Medicine, Brigham and Women s Hospital, Boston, Massachusetts, USA
    Am J Med Genet A 152:653-6. 2010
    ..Further investigation may elucidate the pathogenesis of non-smoking-related emphysema...
  17. ncbi request reprint Diagnosis and management of medical problems in adults with Williams-Beuren syndrome
    Barbara R Pober
    Harvard Medical School, Boston, USA
    Am J Med Genet C Semin Med Genet 145:280-90. 2007
    ..There is no evidence for decline in cognitive ability over time, but adaptive functioning may be improved with treatment of anxiety by both behavior and medical modalities...
  18. pmc Congenital diaphragmatic hernia and pulmonary hypoplasia: new insights from developmental biology and genetics
    Kate G Ackerman
    Division of Genetics, Brigham and Women s Hospital, Harvard Medical School, Boston, MA 02115, USA
    Am J Med Genet C Semin Med Genet 145:105-8. 2007
  19. doi request reprint Nutrient intakes in women and congenital diaphragmatic hernia in their offspring
    Wei Yang
    March of Dimes, California Research Division, Oakland, California 94609, USA
    Birth Defects Res A Clin Mol Teratol 82:131-8. 2008
    ..The etiologies of CDH remain unknown, although experimental animal data suggest dietary factors might play a role. This study examined whether maternal nutrient intakes were associated with delivering infants with CDH...
  20. ncbi request reprint Karyotype-phenotype insights from 11q14.1-q23.2 interstitial deletions: FZD4 haploinsufficiency and exudative vitreoretinopathy in a patient with a complex chromosome rearrangement
    Peining Li
    Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA
    Am J Med Genet A 140:2721-9. 2006
    ..These results provide insight into karyotype-phenotype correlations and prompt a rational analytic approach to cases with interstitial deletions of the 11q14-q23 region...
  21. ncbi request reprint Multisystem study of 20 older adults with Williams syndrome
    Elizabeth M Cherniske
    Child Study Center, Yale School of Medicine, New Haven, Connecticut, USA
    Am J Med Genet A 131:255-64. 2004
    ..We provide monitoring guidelines to assist in the comprehensive care of adults with WS...
  22. ncbi request reprint Fetal stroke
    Koray Ozduman
    Department of Radiology, Stanford University School of Medicine, Stanford, California, USA
    Pediatr Neurol 30:151-62. 2004
    ..A better understanding of those risk factors predisposing a fetus to cerebral infarction may provide a basis for future therapeutic intervention trials. Ozduman K, Pober BR, Barnes P, Copel JA, Ogle EA, Duncan CC, Ment LR. Fetal stroke...