Virginia P. Johnson

1.6k total citations
31 papers, 1.1k citations indexed

About

Virginia P. Johnson is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Virginia P. Johnson has authored 31 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 16 papers in Pediatrics, Perinatology and Child Health and 14 papers in Molecular Biology. Recurrent topics in Virginia P. Johnson's work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (9 papers) and Genetic Syndromes and Imprinting (4 papers). Virginia P. Johnson is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (9 papers) and Genetic Syndromes and Imprinting (4 papers). Virginia P. Johnson collaborates with scholars based in United States, Germany and Canada. Virginia P. Johnson's co-authors include Yutaka Satō, Nancy C. Andreasen, Victor W. Swayze, Jay N. Giedd, Joseph Piven, Diane Mosnik, James W. Hanson, Ellen Roy Elias, Gerald Salen and Mira Irons and has published in prestigious journals such as Proceedings of the National Academy of Sciences, American Journal of Psychiatry and PEDIATRICS.

In The Last Decade

Virginia P. Johnson

31 papers receiving 1.1k citations

Peers

Countries citing papers authored by Virginia P. Johnson

Since Specialization

Citations

This map shows the geographic impact of Virginia P. Johnson'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 Virginia P. Johnson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Virginia P. Johnson more than expected).

Fields of papers citing papers by Virginia P. Johnson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Virginia P. Johnson. 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 Virginia P. Johnson. The network helps show where Virginia P. Johnson may publish in the future.

Co-authorship network of co-authors of Virginia P. Johnson

This figure shows the co-authorship network connecting the top 25 collaborators of Virginia P. Johnson. A scholar is included among the top collaborators of Virginia P. Johnson 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 Virginia P. Johnson. Virginia P. Johnson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	New syndrome of spondylospinal thoracic dysostosis with multiple pterygia and arthrogryposis 1997 ·American Journal of Medical Genetics ·Virginia P. Johnson, Laura Davis Keppen, (unknown), Brad Randall, (unknown)	6
2	Delimiting the Wolf-Hirschhorn syndrome critical region to 750 kilobase pairs 1997 ·American Journal of Medical Genetics ·Michael R. Altherr, Tracy J. Wright, (unknown), Ana V. Perez-Castro, Virginia P. Johnson	20
3	Treatment of Smith‐Lemli‐Opitz syndrome: Results of a multicenter trial 1997 ·American Journal of Medical Genetics ·Mira Irons, Ellen Roy Elias, (unknown), Marilyn J. Bull, Carol L. Greene, Virginia P. Johnson, Laura Davis Keppen, Carolyn Schanen, G S Tint, Gerald Salen	13
4	Fetal alcohol syndrome: Craniofacial and central nervous system manifestations 1996 ·American Journal of Medical Genetics ·Virginia P. Johnson, Victor W. Swayze, Yutaka Satō, Nancy C. Andreasen	97
5	Uniparental isodisomy of chromosome 14 in two cases: An abnormal child and a normal adult 1996 ·American Journal of Medical Genetics ·Peter Papenhausen, O. Thomas Mueller, Maxine J. Sutcliffe, (unknown), Boris G. Kousseff, Virginia P. Johnson	8
6	The detection of contiguous gene deletions at the neurofibromatosis 1 locus with fluorescence in situ hybridization 1996 ·Cytogenetic and Genome Research ·Kathleen A. Leppig, David Viskochil, (unknown), Allan E. Rubenstein, Virginia P. Johnson, Xue‐Xue Zhu, Arthur R. Brothman, Karen Stephens	44
7	Distinct 15q genotypes in Russell‐Silver and ring 15 syndromes 1996 ·American Journal of Medical Genetics ·Peter K. Rogan, James R. Seip, Daniel J. Driscoll, Peter Papenhausen, Virginia P. Johnson, Salmo Raskin, Amy Woodward, Merlin G. Butler	3
8	Distinct 15q genotypes in Russell‐Silver and ring 15 syndromes 1996 ·American Journal of Medical Genetics ·Peter K. Rogan, James R. Seip, Daniel J. Driscoll, Peter Papenhausen, Virginia P. Johnson, Salmo Raskin, Amy Woodward, Merlin G. Butler	36
9	Correlation of severity and outcome with plasma sterol levels in variants of the Smith-Lemli-Opitz syndrome 1995 ·The Journal of Pediatrics ·G. Stephen Tint, Gerald Salen, Ashok K. Batta, Sarah Shefer, Mira Irons, Ellen Roy Elias, Dianne Abuelo, Virginia P. Johnson, Marie Lambert, Richard A. Lutz, Carolyn Schanen, Colleen A. Morris, George Hoganson, (unknown)	117
10	FISH detection of Wolf‐Hirschhorn syndorem: Exclusion of D4F26 as critical site 1994 ·American Journal of Medical Genetics ·Virginia P. Johnson, Michael R. Altherr, (unknown), Laura Davis Keppen	19
11	Duplication 10q confirmed by DNA in situ hybridization 1994 ·American Journal of Medical Genetics ·Virginia P. Johnson, (unknown)	4
12	Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity. 1994 ·Proceedings of the National Academy of Sciences ·Maximilian Muenke, Fiorella Gurrieri, Christiane Bay, Yi Duan, Amanda Collins, Virginia P. Johnson, Raoul C. M. Hennekam, G. Bradley Schaefer, LuAnn Weik, Mark Lubinsky	97
13	Natural history of mosaic trisomy 14 syndrome 1992 ·American Journal of Medical Genetics ·Atsuko Fujimoto, Judith Allanson, Carol A. Crowe, Mark Lipson, Virginia P. Johnson	37
14	Molecular detection of a 4p deletion using PCR‐based polymorphisms: A technique for the rapid detection of the Wolf–Hirschhorn syndrome 1992 ·American Journal of Medical Genetics ·Michael R. Altherr, James F. Gusella, John J. Wasmuth, (unknown), (unknown), Virginia P. Johnson	7
15	Duplication of the distal part of the long arm of chromosome 1 1991 ·American Journal of Medical Genetics ·Virginia P. Johnson	24
16	Sex chromosome marker: Clinical significance and DNA characterization 1991 ·American Journal of Medical Genetics ·Virginia P. Johnson, Paul G. McDonough, Sau Wai Cheung, Li Sun	7
17	Martin–Bell syndrome segregating in a large kindred with normal transmitting males: Clinical, cytogenetic, and linkage study 1991 ·American Journal of Medical Genetics ·Virginia P. Johnson, Nancy J. Carpenter, (unknown)	5
18	Holoprosencephaly: A developmental field defect 1989 ·American Journal of Medical Genetics ·Virginia P. Johnson	38
19	Alpha‐fetoprotein and acetylcholinesterase in twins discordant for neural tube defect 1989 ·Prenatal Diagnosis ·Virginia P. Johnson, (unknown), Nancy Wilson, (unknown)	2
20	The Wolf‐Hirschhorn (4p‐) syndrome 1976 ·Clinical Genetics ·Virginia P. Johnson, (unknown), (unknown)	62

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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