J. Britt Ravnan

1.8k citations

19 papers · 1.1k indexed · h-index 12

Genetics top 2%
- Genomic variations and chromosomal abnormalities 11
- Genetic Syndromes and Imprinting 4
- Genomics and Rare Diseases 2
Pediatrics, Perinatology and Child Health top 2%
- Prenatal Screening and Diagnostics 9
Molecular Biology
- Congenital heart defects research 5
Developmental Biology
Plant Science
Immunology
- T-cell and Retrovirus Studies 2
Surgery
- Tissue Engineering and Regenerative Medicine 2
Agronomy and Crop Science
- Animal Disease Management and Epidemiology 2

Co-authors: Lisa G. Shaffer Beth S. Torchia Jill A. Rosenfeld Blake C. Ballif Jay W. Ellison Justine Coppinger Mindy Preston Dabell Allan J. Fisher
Cited by: Genetics Pediatrics, Perinatology and Child Health Molecular Biology
Journals: Journal of Molecular Biology (1 paper)PEDIATRICS (1 paper)Journal of Virology (1 paper)
Partner nations: United States Poland Germany

In The Last Decade

J. Britt Ravnan

19 papers receiving 999 citations

Peers

Countries citing papers authored by J. Britt Ravnan

Since Specialization

Citations

This map shows the geographic impact of J. Britt Ravnan's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by J. Britt Ravnan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J. Britt Ravnan more than expected).

Fields of papers citing papers by J. Britt Ravnan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J. Britt Ravnan. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by J. Britt Ravnan. The network helps show where J. Britt Ravnan may publish in the future.

Co-authorship network

The 25 scholars most cited alongside J. Britt Ravnan, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with J. Britt Ravnan Line = papers co-authored together J. Britt Ravnan links everyone, so they are left out of the graph.

All Works

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19 of 19 papers shown

#	Work
1	Experience Using a Rapid Assay for Aneuploidy and Microdeletion/Microduplication Detection in over 2,900 Prenatal Specimens Fetal Diagnosis and Therapy ·Jill A. Rosenfeld,S. Anne Morton,Cathryn Hummel,Scott G. Sulpizio,Lisa D. McDaniel,Roger A. Schultz,Beth S. Torchia,J. Britt Ravnan,Jay W. Ellison,Allan J. Fisher	2014	9
2	Clinical features associated with copy number variations of the 14q32 imprinted gene cluster American Journal of Medical Genetics Part A ·Jill A. Rosenfeld,Joyce E. Fox,Maria Descartes,Fallon Brewer,Tracy Stroud,Jerome L. Gorski,Sheila Upton,John B. Moeschler,Berrin Monteleone,Nicholas J. Neill,Allen N. Lamb,Blake C. Ballif,Lisa G. Shaffer,J. Britt Ravnan	2014	27
3	Experience With Microarray-Based Comparative Genomic Hybridization for Prenatal Diagnosis in Over 5000 Pregnancies Obstetrical & Gynecological Survey ·Lisa G. Shaffer,Mindy Preston Dabell,Allan J. Fisher,Justine Coppinger,Anne M. Bandholz,Jay W. Ellison,J. Britt Ravnan,Beth S. Torchia,Blake C. Ballif,Jill A. Rosenfeld	2013	4
4	Identification of a Novel 14q13.3 Deletion Involving the SLC25A21 Gene Associated with Familial Synpolydactyly Molecular Syndromology ·K. Meyertholen,J. Britt Ravnan,Reuben Matalon	2012	5
5	Defining the impact of maternal cell contamination on the interpretation of prenatal microarray analysis Genetics in Medicine ·Allen N. Lamb,Jill A. Rosenfeld,Justine Coppinger,Erin T. Dodge,Mindy Preston Dabell,Beth S. Torchia,J. Britt Ravnan,Lisa G. Shaffer,Blake C. Ballif	2012	10
6	Experience with microarray‐based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies Prenatal Diagnosis ·Lisa G. Shaffer,Mindy Preston Dabell,Allan J. Fisher,Justine Coppinger,Anne M. Bandholz,Jay W. Ellison,J. Britt Ravnan,Beth S. Torchia,Blake C. Ballif,Jill A. Rosenfeld	2012	163
7	Clinical Utility of Chromosomal Microarray Analysis PEDIATRICS ·Jay W. Ellison,J. Britt Ravnan,Jill A. Rosenfeld,S. Annie Morton,Nicholas J. Neill,Marc S. Williams,J. Lewis,Beth S. Torchia,Cathryn Walker,Ryan N. Traylor,Kimberly J. Moles,Elizabeth Miller,Jennifer Lantz,Caitlin Valentin,Sara L. Minier,Kimberly A. Leiser,Berkley R. Powell,Timothy Wilks,Lisa G. Shaffer	2012	37
8	Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound Prenatal Diagnosis ·Lisa G. Shaffer,Jill A. Rosenfeld,Mindy Preston Dabell,Justine Coppinger,Anne M. Bandholz,Jay W. Ellison,J. Britt Ravnan,Beth S. Torchia,Blake C. Ballif,Allan J. Fisher	2012	191
9	Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems Genetics in Medicine ·Trilochan Sahoo,Aaron Theisen,Jill A. Rosenfeld,Allen N. Lamb,J. Britt Ravnan,Roger A. Schultz,Beth S. Torchia,Nicholas J. Neill,Ian Casci,Bassem A. Bejjani,Lisa G. Shaffer	2011	75
10	Recurrence, submicroscopic complexity, and potential clinical relevance of copy gains detected by array CGH that are shown to be unbalanced insertions by FISH Genome Research ·Nicholas J. Neill,Blake C. Ballif,Allen N. Lamb,Sumit Parikh,J. Britt Ravnan,Roger A. Schultz,Beth S. Torchia,Jill A. Rosenfeld,Lisa G. Shaffer	2011	41
11	The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes Prenatal Diagnosis ·Lisa G. Shaffer,Justine Coppinger,S. Annie Morton,Sarah Alliman,Jessica Burleson,Ryan N. Traylor,Cathryn Walker,Steve Byerly,Allen N. Lamb,Roger A. Schultz,J. Britt Ravnan,Catherine D. Kashork,Beth S. Torchia,Scott G. Sulpizio,Kyle Sundin,Mack Schermer,Karl Adler,Stephanie Dallaire,Blake C. Ballif	2011	33
12	Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders Genetics in Medicine ·Jill A. Rosenfeld,Blake C. Ballif,Beth S. Torchia,Trilochan Sahoo,J. Britt Ravnan,Roger A. Schultz,Allen N. Lamb,Bassem A. Bejjani,Lisa G. Shaffer	2010	92
13	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 Prenatal Diagnosis ·Jennifer McClarren,Alan E. Donnenfeld,J. Britt Ravnan	2006	17
14	Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities Journal of Medical Genetics ·J. Britt Ravnan,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown)	2005	271
15	Chromosome 22q11.2 microdeletions in velocardiofacial syndrome patients with widely variable manifestations American Journal of Medical Genetics ·J. Britt Ravnan,Emily Chen,Mahin Golabi,Roger V. Lebo	1996	38
16	Disparate Replication Properties of Integrated and Extrachromosomal Forms of Bovine Papilloma Virus in ID13 Cells Journal of Molecular Biology ·Kelly G. Ten Hagen,J. Britt Ravnan,Stanley N. Cohen	1995	4
17	Transformed Mouse Cell Lines That Consist Predominantly of Cells Maintaining Bovine Papilloma Virus at High Copy Number Virology ·J. Britt Ravnan,STANLEY N. COHEN	1995	4
18	Analysis of 22q11.2 deletions by FISH in a series of velocardiofacial syndrome patients The American Journal of Human Genetics ·J. Britt Ravnan,Mahin Golabi,R V Lebo	1994	1
19	Random-choice replication of extrachromosomal bovine papillomavirus (BPV) molecules in heterogeneous, clonally derived BPV-infected cell lines Journal of Virology ·J. Britt Ravnan,David M. Gilbert,Kelly G. Ten Hagen,Stanley N. Cohen	1992	35

About J. Britt Ravnan

J. Britt Ravnan is a scholar working on Genetics, Developmental Biology and Pediatrics, Perinatology and Child Health, having authored 19 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (9 papers), Congenital heart defects research (5 papers), Genetic Syndromes and Imprinting (4 papers), Genomics and Rare Diseases (2 papers), T-cell and Retrovirus Studies (2 papers), Tissue Engineering and Regenerative Medicine (2 papers) and Animal Disease Management and Epidemiology (2 papers). The work is most often cited by research in Genetics (811 citations), Pediatrics, Perinatology and Child Health (494 citations) and Molecular Biology (408 citations). J. Britt Ravnan has collaborated with scholars based in United States, Poland and Germany. Frequent co-authors include Lisa G. Shaffer, Beth S. Torchia, Jill A. Rosenfeld, Blake C. Ballif, Jay W. Ellison, Justine Coppinger, Mindy Preston Dabell, Allan J. Fisher, Anne M. Bandholz and Allen N. Lamb. Their work appears in journals such as Journal of Molecular Biology, PEDIATRICS and Journal of Virology.

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