Robert H. Wharton

1.1k total citations
20 papers, 810 citations indexed

About

Robert H. Wharton is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Robert H. Wharton has authored 20 papers receiving a total of 810 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 5 papers in Molecular Biology and 3 papers in Surgery. Recurrent topics in Robert H. Wharton's work include Genetic Syndromes and Imprinting (8 papers), Genomic variations and chromosomal abnormalities (4 papers) and Media Influence and Health (2 papers). Robert H. Wharton is often cited by papers focused on Genetic Syndromes and Imprinting (8 papers), Genomic variations and chromosomal abnormalities (4 papers) and Media Influence and Health (2 papers). Robert H. Wharton collaborates with scholars based in United States and Tunisia. Robert H. Wharton's co-authors include David Haig, Samuel A. Latt, Lawrence C. Kaplan, Richard Barnum, John M. Graham, Robert D. Nicholls, Richard Famularo, Doris H. Wurster‐Hill, John M. Opitz and Ellen Roy Elias and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PEDIATRICS and Developmental Medicine & Child Neurology.

In The Last Decade

Robert H. Wharton

20 papers receiving 776 citations

Peers

Robert H. Wharton

GENET

PPCH

EPIDE

Carl A. Huether United States

Sarah Marsh United States

Shona M. Kerr United Kingdom

Sara Stinson United States

Jon Stene Denmark

J. Fernando Arena United States

M. H. Y. Tang China

David Mutton United Kingdom

Florence P. Haseltine United States

R Lew United States

Carl A. Huether United States

Robert H. Wharton

237 ×0.5

GENET

177 ×0.6

293 ×1.1

PPCH

20 ×0.3

51 ×0.7

EPIDE

Citations per year, relative to Robert H. Wharton Robert H. Wharton (= 1×) peers Carl A. Huether

Countries citing papers authored by Robert H. Wharton

Since Specialization

Citations

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

Fields of papers citing papers by Robert H. Wharton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert H. Wharton. 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 Robert H. Wharton. The network helps show where Robert H. Wharton may publish in the future.

Co-authorship network of co-authors of Robert H. Wharton

This figure shows the co-authorship network connecting the top 25 collaborators of Robert H. Wharton. A scholar is included among the top collaborators of Robert H. Wharton 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 Robert H. Wharton. Robert H. Wharton 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

Allen, George P., David C. Bolin, Uneeda K. Bryant, et al.. (2008). Prevalence of latent, neuropathogenic equine herpesvirus‐1 in the Thoroughbred broodmare population of central Kentucky. Equine Veterinary Journal. 40(2). 105–110. 72 indexed citations

Haig, David & Robert H. Wharton. (2003). Prader‐Willi syndrome and the evolution of human childhood. American Journal of Human Biology. 15(3). 320–329. 89 indexed citations

Wharton, Robert H., et al.. (2003). Living as a Cancer Surpriser: A Doctor Tells His Story. The Oncologist. 8(1). 108–122. 10 indexed citations

Nicholls, Robert D., R. Scott Frayo, Robert H. Wharton, et al.. (2003). Mouse Models for Prader-Willi and Angelman Syndromes offer Insights into Novel Obesity Mechanisms. 6 indexed citations

Wharton, Robert H.. (2002). Sleeping with the Enemy: Treatment of Fatigue in Individuals with Cancer. The Oncologist. 7(2). 96–99. 2 indexed citations

Wharton, Robert H., et al.. (2000). Williams Syndrome and Happiness. American Journal on Mental Retardation. 105(5). 363–363. 11 indexed citations

Wharton, Robert H., et al.. (1997). Acute idiopathic gastric dilatation with gastric necrosis in individuals with Prader-Willi syndrome. American Journal of Medical Genetics. 73(4). 437–441. 52 indexed citations

Wharton, Robert H., et al.. (1996). Advanced Care Planning for Children With Special Health Care Needs: A Survey of Parental Attitudes. PEDIATRICS. 97(5). 682–687. 64 indexed citations

Wharton, Robert H. & Karen J. Loechner. (1996). Genetic and clinical advances in Prader-Willi syndrome. Current Opinion in Pediatrics. 8(6). 618–624. 21 indexed citations

10.

Wharton, Robert H., et al.. (1993). Pediatrician's Role After Hospital-Based Death and Permanent Disability in School-Aged Children. Clinical Pediatrics. 32(11). 675–680. 1 indexed citations

11.

Baird, Inga S., et al.. (1990). Joint Venture Success: A Sino–U.S. Perspective. International Studies of Management and Organization. 20(1-2). 125–134. 19 indexed citations

12.

Wharton, Robert H. & Michael J. Bresnan. (1989). NEONATAL RESPIRATORY DEPRESSION AND DELAY IN DIAGNOSIS IN PRADER‐WILLI SYNDROME. Developmental Medicine & Child Neurology. 31(2). 231–236. 27 indexed citations

13.

Nicholls, Robert D., Joan H.M. Knoll, Karen A. Glatt, et al.. (1989). Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader‐Willi syndrome. American Journal of Medical Genetics. 33(1). 66–77. 127 indexed citations

14.

Tantravahi, Umadevi, Robert D. Nicholls, Helene Stroh, et al.. (1989). Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader‐Willi syndrome. American Journal of Medical Genetics. 33(1). 78–87. 61 indexed citations

15.

Hollis, Michael, et al.. (1988). A repressor heterodimer binds to a chimeric operator.. Proceedings of the National Academy of Sciences. 85(16). 5834–5838. 23 indexed citations

16.

Kaplan, Lawrence C., Robert H. Wharton, Ellen Roy Elias, et al.. (1987). Clinical heterogeneity associated with deletions in the long arm of chromosome 15: Report of 3 new cases and their possible genetic significance. American Journal of Medical Genetics. 28(1). 45–53. 141 indexed citations

17.

Famularo, Richard, et al.. (1986). Alcoholism and severe child maltreatment.. American Journal of Orthopsychiatry. 56(3). 481–485. 76 indexed citations

18.

Wharton, Robert H. & Frederick Mandell. (1986). Violence on television and imitative behavior: impact on parenting practices. Journal of the American Academy of Child Psychiatry. 25(1). 150–150. 1 indexed citations

19.

Latt, S.A., M. Lalande, Tim Donlon, et al.. (1986). DNA-based Detection of Chromosome Deletion and Amplification: Diagnostic and Mechanistic Significance. Cold Spring Harbor Symposia on Quantitative Biology. 51(0). 299–307. 2 indexed citations

20.

Wharton, Robert H. & Frederick Mandell. (1985). Violence on Television and Imitative Behavior: Impact on Parenting Practices. PEDIATRICS. 75(6). 1120–1123. 5 indexed citations

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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