J. Britt Ravnan

1.8k citations

19 papers · 1.1k indexed · h-index 12

Genetics top 2%
Pediatrics, Perinatology and Child Health top 2%
Molecular Biology
Plant Science
Cognitive Neuroscience

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
Topics: Genomic variations and chromosomal abnormalities (11 papers)Prenatal Screening and Diagnostics (9 papers)Congenital heart defects research (5 papers)
Cited by: Genetics Pediatrics, Perinatology and Child Health Molecular Biology
Journals: Journal of Molecular Biology PEDIATRICS Journal of Virology
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 of co-authors of J. Britt Ravnan

This figure shows the co-authorship network connecting the top 25 collaborators of J. Britt Ravnan. A scholar is included among the top collaborators of J. Britt Ravnan based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with J. Britt Ravnan. J. Britt Ravnan is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Experience Using a Rapid Assay for Aneuploidy and Microdeletion/Microduplication Detection in over 2,900 Prenatal Specimens 2014 ·Fetal Diagnosis and Therapy ·Jill A. Rosenfeld,(unknown),(unknown),(unknown),Lisa D. McDaniel,Roger A. Schultz,Beth S. Torchia,J. Britt Ravnan,Jay W. Ellison,Allan J. Fisher	9
2	Clinical features associated with copy number variations of the 14q32 imprinted gene cluster 2014 ·American Journal of Medical Genetics Part A ·Jill A. Rosenfeld,Joyce E. Fox,Maria Descartes,(unknown),Tracy Stroud,Jerome L. Gorski,(unknown),John B. Moeschler,(unknown),Nicholas J. Neill,Allen N. Lamb,Blake C. Ballif,Lisa G. Shaffer,J. Britt Ravnan	27
3	Experience With Microarray-Based Comparative Genomic Hybridization for Prenatal Diagnosis in Over 5000 Pregnancies 2013 ·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	4
4	Identification of a Novel 14q13.3 Deletion Involving the SLC25A21 Gene Associated with Familial Synpolydactyly 2012 ·Molecular Syndromology ·(unknown),J. Britt Ravnan,Reuben Matalon	5
5	Defining the impact of maternal cell contamination on the interpretation of prenatal microarray analysis 2012 ·Genetics in Medicine ·Allen N. Lamb,Jill A. Rosenfeld,Justine Coppinger,(unknown),Mindy Preston Dabell,Beth S. Torchia,J. Britt Ravnan,Lisa G. Shaffer,Blake C. Ballif	10
6	Experience with microarray‐based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies 2012 ·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	163
7	Clinical Utility of Chromosomal Microarray Analysis 2012 ·PEDIATRICS ·Jay W. Ellison,J. Britt Ravnan,Jill A. Rosenfeld,(unknown),Nicholas J. Neill,Marc S. Williams,(unknown),Beth S. Torchia,(unknown),Ryan N. Traylor,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Berkley R. Powell,Timothy Wilks,Lisa G. Shaffer	37
8	Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound 2012 ·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	191
9	Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems 2011 ·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	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 2011 ·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	41
11	The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes 2011 ·Prenatal Diagnosis ·Lisa G. Shaffer,Justine Coppinger,(unknown),Sarah Alliman,(unknown),Ryan N. Traylor,(unknown),(unknown),Allen N. Lamb,Roger A. Schultz,J. Britt Ravnan,Catherine D. Kashork,Beth S. Torchia,(unknown),Kyle Sundin,(unknown),(unknown),Stephanie Dallaire,Blake C. Ballif	33
12	Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders 2010 ·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	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 2006 ·Prenatal Diagnosis ·(unknown),Alan E. Donnenfeld,J. Britt Ravnan	17
14	Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities 2005 ·Journal of Medical Genetics ·J. Britt Ravnan,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown)	271
15	Chromosome 22q11.2 microdeletions in velocardiofacial syndrome patients with widely variable manifestations 1996 ·American Journal of Medical Genetics ·J. Britt Ravnan,Emily Chen,Mahin Golabi,Roger V. Lebo	38
16	Disparate Replication Properties of Integrated and Extrachromosomal Forms of Bovine Papilloma Virus in ID13 Cells 1995 ·Journal of Molecular Biology ·Kelly G. Ten Hagen,J. Britt Ravnan,Stanley N. Cohen	4
17	Transformed Mouse Cell Lines That Consist Predominantly of Cells Maintaining Bovine Papilloma Virus at High Copy Number 1995 ·Virology ·J. Britt Ravnan,(unknown)	4
18	Analysis of 22q11.2 deletions by FISH in a series of velocardiofacial syndrome patients 1994 ·The American Journal of Human Genetics ·J. Britt Ravnan,Mahin Golabi,R V Lebo	1
19	Random-choice replication of extrachromosomal bovine papillomavirus (BPV) molecules in heterogeneous, clonally derived BPV-infected cell lines 1992 ·Journal of Virology ·J. Britt Ravnan,David M. Gilbert,Kelly G. Ten Hagen,Stanley N. Cohen	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) and Congenital heart defects research (5 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.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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