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J. Britt Ravnan

Observed names: J B Ravnan, J.B. Ravnan, JULIE-BRITT RAVNAN, Julie-Britt Ravnan
OpenAlex ID: A5013949573
Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities
2005 · J B Ravnan, J H Tepperberg, et al. · Journal of Medical Genetics · 413
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Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound
2012 · Lisa G. Shaffer, Jill A. Rosenfeld, et al. · Prenatal Diagnosis · 267
Experience with microarray‐based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies
2012 · Lisa G. Shaffer, Mindy P. Dabell, et al. · Prenatal Diagnosis · 243
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Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders
2010 · Jill A. Rosenfeld, Blake C. Ballif, et al. · Genetics in Medicine · 168
High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44
2011 · Blake C. Ballif, Jill A. Rosenfeld, et al. · Human Genetics · 152
Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems
2011 · Trilochan Sahoo, Aaron Theisen, et al. · Genetics in Medicine · 115
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Prenatal diagnosis of an unexpected interstitial 22q11.2 deletion causing truncus arteriosus and thymic hypoplasia in a ring 22 chromosome derived from a maternally inherited paracentric inversion
2006 · Jennifer McClarren, Alan E. Donnenfeld, et al. · Prenatal Diagnosis · 77
Recurrence, submicroscopic complexity, and potential clinical relevance of copy gains detected by array CGH that are shown to be unbalanced insertions by FISH
2011 · Nicholas J. Neill, Blake C. Ballif, et al. · Genome Research · 56
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Clinical Utility of Chromosomal Microarray Analysis
2012 · Jay W. Ellison, J. Britt Ravnan, et al. · PEDIATRICS · 53
Clinical features associated with copy number variations of the 14q32 imprinted gene cluster
2014 · Jill A. Rosenfeld, Joyce E. Fox, et al. · American Journal of Medical Genetics Part A · 52
Recurrent HERV-H-Mediated 3q13.2-q13.31 Deletions Cause a Syndrome of Hypotonia and Motor, Language, and Cognitive Delays
2013 · Andrey Shuvarikov, Ian M. Campbell, et al. · Human Mutation · 48
Chromosome 22q11.2 microdeletions in velocardiofacial syndrome patients with widely variable manifestations
1996 · J. Britt Ravnan, Emily Chen, et al. · American Journal of Medical Genetics · 45
The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes
2011 · Lisa G. Shaffer, Justine Coppinger, et al. · Prenatal Diagnosis · 44
Random-choice replication of extrachromosomal bovine papillomavirus (BPV) molecules in heterogeneous, clonally derived BPV-infected cell lines
1992 · J B Ravnan, D M Gilbert, et al. · Journal of Virology · 44
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Defining the impact of maternal cell contamination on the interpretation of prenatal microarray analysis
2012 · Allen N. Lamb, Jill A. Rosenfeld, et al. · Genetics in Medicine · 19
Experience Using a Rapid Assay for Aneuploidy and Microdeletion/Microduplication Detection in over 2,900 Prenatal Specimens
2014 · Jill A. Rosenfeld, S. Anne Morton, et al. · Fetal Diagnosis and Therapy · 10
Experience With Microarray-Based Comparative Genomic Hybridization for Prenatal Diagnosis in Over 5000 Pregnancies
2013 · Lisa G. Shaffer, Mindy P. Dabell, et al. · Obstetrical & Gynecological Survey · 9
Novel clinical features in a child with partial deletion of chromosome 11 [del(11)(q24.2)]: Further evidence for phenotypic heterogeneity
2006 · Philip F. Giampietro, Deepti Babu, et al. · American Journal of Medical Genetics Part A · 8
Disparate Replication Properties of Integrated and Extrachromosomal Forms of Bovine Papilloma Virus in ID13 Cells
1995 · Kelly G. Ten Hagen, Julie-Britt Ravnan, et al. · Journal of Molecular Biology · 7
Identification of a Novel 14q13.3 Deletion Involving the SLC25A21 Gene Associated with Familial Synpolydactyly
2012 · K. Meyertholen, J.B. Ravnan, et al. · Molecular Syndromology · 6
Transformed Mouse Cell Lines That Consist Predominantly of Cells Maintaining Bovine Papilloma Virus at High Copy Number
1995 · JULIE-BRITT RAVNAN, STANLEY N. COHEN · Virology · 4
Analysis of 22q11.2 deletions by FISH in a series of velocardiofacial syndrome patients
1994 · J. Britt Ravnan, Mahin Golabi, et al. · The American Journal of Human Genetics · 1
Erratum
2014 · Scott G. Sulpizio, S. Anne Morton, et al. · Fetal Diagnosis and Therapy
Erratum
2014 · Scott G. Sulpizio, S. Anne Morton, et al. · Fetal Diagnosis and Therapy
Front & Back Matter
2012 · E. Athanasakis, A. Fabretto, et al. · Molecular Syndromology
Works count: 28
Citation count: 1,840
H-index: 15
I10-index: 16
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