Other search tools

About this data

The publication data currently available has been vetted by Vanderbilt faculty, staff, administrators and trainees. The data itself is retrieved directly from NCBI's PubMed and is automatically updated on a weekly basis to ensure accuracy and completeness.

If you have any questions or comments, please contact us.

Results: 1 to 10 of 23

Publication Record

Connections

Addition of H19 'loss of methylation testing' for Beckwith-Wiedemann syndrome (BWS) increases the diagnostic yield.
Lennerz JK, Timmerman RJ, Grange DK, DeBaun MR, Feinberg AP, Zehnbauer BA
(2010) J Mol Diagn 12: 576-88
MeSH Terms: Autoradiography, Base Sequence, Beckwith-Wiedemann Syndrome, Blotting, Southern, DNA Primers, Electrophoresis, Agar Gel, Humans, Methylation, RNA, Long Noncoding, RNA, Untranslated
Added November 27, 2013
1 Communities
1 Members
0 Resources
10 MeSH Terms
Children with idiopathic hemihypertrophy and beckwith-wiedemann syndrome have different constitutional epigenotypes associated with wilms tumor.
Niemitz EL, Feinberg AP, Brandenburg SA, Grundy PE, DeBaun MR
(2005) Am J Hum Genet 77: 887-91
MeSH Terms: Beckwith-Wiedemann Syndrome, Child, Chromosomes, Human, Pair 11, DNA Methylation, Genotype, Humans, Wilms Tumor
Added November 27, 2013
1 Communities
1 Members
0 Resources
7 MeSH Terms
Inheritance pattern of Beckwith-Wiedemann syndrome is heterogeneous in 291 families with an affected proband.
Wangler MF, An P, Feinberg AP, Province M, Debaun MR
(2005) Am J Med Genet A 137: 16-21
MeSH Terms: Beckwith-Wiedemann Syndrome, Family Health, Female, Genetic Heterogeneity, Humans, Inheritance Patterns, Male, Models, Genetic, Pedigree
Added November 27, 2013
1 Communities
1 Members
0 Resources
9 MeSH Terms
Factors associated with preterm delivery in mothers of children with Beckwith-Wiedemann syndrome: a case cohort study from the BWS registry.
Wangler MF, Chang AS, Moley KH, Feinberg AP, Debaun MR
(2005) Am J Med Genet A 134A: 187-91
MeSH Terms: Adolescent, Adult, Beckwith-Wiedemann Syndrome, Child, Child, Preschool, Cohort Studies, Female, Humans, Hypertension, Infant, Infant, Newborn, Logistic Models, Male, Middle Aged, Multivariate Analysis, Pregnancy, Pregnancy Complications, Premature Birth, Proteinuria, Registries, Risk Factors, Ultrasonography, Prenatal, alpha-Fetoproteins
Added November 27, 2013
1 Communities
1 Members
0 Resources
23 MeSH Terms
Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: a case series of 19 patients.
Chang AS, Moley KH, Wangler M, Feinberg AP, Debaun MR
(2005) Fertil Steril 83: 349-54
MeSH Terms: Adolescent, Adult, Beckwith-Wiedemann Syndrome, Blastomeres, Embryo Transfer, Female, Fertilization in Vitro, Humans, Infant, Newborn, Male, Ovulation Induction, Phenotype, Pregnancy, Registries, Retrospective Studies, Sperm Injections, Intracytoplasmic
Added November 27, 2013
1 Communities
1 Members
0 Resources
16 MeSH Terms
LIT1 and H19 methylation defects in isolated hemihyperplasia.
Martin RA, Grange DK, Zehnbauer B, Debaun MR
(2005) Am J Med Genet A 134A: 129-31
MeSH Terms: Abnormalities, Multiple, Adolescent, Beckwith-Wiedemann Syndrome, Body Height, Body Weight, Child, Child, Preschool, DNA Methylation, Female, Humans, Infant, Male, Membrane Proteins, Potassium Channels, Voltage-Gated, RNA, Long Noncoding, RNA, Untranslated, Uniparental Disomy
Added November 27, 2013
1 Communities
1 Members
0 Resources
17 MeSH Terms
Microdeletion of LIT1 in familial Beckwith-Wiedemann syndrome.
Niemitz EL, DeBaun MR, Fallon J, Murakami K, Kugoh H, Oshimura M, Feinberg AP
(2004) Am J Hum Genet 75: 844-9
MeSH Terms: Beckwith-Wiedemann Syndrome, Chromosomes, Human, Pair 11, Cyclin-Dependent Kinase Inhibitor p57, DNA Primers, Gene Deletion, Gene Expression, Haplotypes, Humans, In Situ Hybridization, Fluorescence, Karyotyping, Membrane Proteins, Nuclear Proteins, Potassium Channels, Voltage-Gated, Reverse Transcriptase Polymerase Chain Reaction
Added November 27, 2013
1 Communities
1 Members
0 Resources
14 MeSH Terms
Serum alpha-fetoprotein screening for hepatoblastoma in children with Beckwith-Wiedemann syndrome or isolated hemihyperplasia.
Clericuzio CL, Chen E, McNeil DE, O'Connor T, Zackai EH, Medne L, Tomlinson G, DeBaun M
(2003) J Pediatr 143: 270-2
MeSH Terms: Beckwith-Wiedemann Syndrome, Female, Hepatoblastoma, Humans, Hypertrophy, Infant, Infant, Newborn, Liver Neoplasms, Male, alpha-Fetoproteins
Added September 19, 2013
0 Communities
1 Members
0 Resources
10 MeSH Terms
Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19.
DeBaun MR, Niemitz EL, Feinberg AP
(2003) Am J Hum Genet 72: 156-60
MeSH Terms: Adult, Beckwith-Wiedemann Syndrome, Child, CpG Islands, DNA Methylation, Female, Fertilization in Vitro, Genomic Imprinting, Humans, Male, Membrane Proteins, Molecular Sequence Data, Phenotype, Potassium Channels, Voltage-Gated, RNA, Long Noncoding, RNA, Untranslated
Added November 27, 2013
1 Communities
1 Members
0 Resources
16 MeSH Terms
Neuroblastoma in a patient with the Beckwith-Wiedemann syndrome (BWS).
Yoon G, Graham G, Weksberg R, Gaul HP, DeBaun MR, Coppes MJ
(2002) Med Pediatr Oncol 38: 193-9
MeSH Terms: Alberta, Beckwith-Wiedemann Syndrome, Child, Preschool, Female, Humans, Mass Screening, Mediastinal Neoplasms, Neuroblastoma
Added November 27, 2013
1 Communities
1 Members
0 Resources
8 MeSH Terms