Catherine Bove

590 total citations
12 papers, 441 citations indexed

About

Catherine Bove is a scholar working on Neurology, Physiology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Catherine Bove has authored 12 papers receiving a total of 441 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Neurology, 5 papers in Physiology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Catherine Bove's work include Lysosomal Storage Disorders Research (3 papers), Neurofibromatosis and Schwannoma Cases (3 papers) and Tuberous Sclerosis Complex Research (2 papers). Catherine Bove is often cited by papers focused on Lysosomal Storage Disorders Research (3 papers), Neurofibromatosis and Schwannoma Cases (3 papers) and Tuberous Sclerosis Complex Research (2 papers). Catherine Bove collaborates with scholars based in United States, Poland and Israel. Catherine Bove's co-authors include M. Priscilla Short, Vijaya Ramesh, Scott R. Plotkin, Fabio P. Nunes, Mia MacCollin, William T. Curry, James S. Acierno, Ehud Goldin, Katherine B. Sims and Bruce J. Masek and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and Movement Disorders.

In The Last Decade

Catherine Bove

12 papers receiving 431 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Catherine Bove United States 9 170 137 125 86 77 12 441
Patrick A. Lundquist United States 8 29 0.2× 238 1.7× 50 0.4× 130 1.5× 50 0.6× 16 440
Linda Manwaring United States 8 33 0.2× 83 0.6× 49 0.4× 136 1.6× 18 0.2× 15 374
Denise Griffiths United States 7 86 0.5× 157 1.1× 48 0.4× 146 1.7× 16 0.2× 8 341
Orit Neudorfer Israel 7 223 1.3× 397 2.9× 73 0.6× 117 1.4× 24 0.3× 9 583
Mario A. Cabrera-Salazar United States 10 33 0.2× 325 2.4× 100 0.8× 169 2.0× 31 0.4× 11 396
Esther Nibbeling Netherlands 10 73 0.4× 38 0.3× 22 0.2× 191 2.2× 29 0.4× 15 408
Christiane Kehrer Germany 15 41 0.2× 436 3.2× 208 1.7× 239 2.8× 45 0.6× 21 594
Heather Cahan United States 7 27 0.2× 265 1.9× 64 0.5× 119 1.4× 39 0.5× 16 418
Denise A Cloutier United States 7 27 0.2× 299 2.2× 101 0.8× 212 2.5× 38 0.5× 7 488
Johanna M. P. van den Hout Netherlands 12 47 0.3× 634 4.6× 150 1.2× 144 1.7× 38 0.5× 31 729

Countries citing papers authored by Catherine Bove

Since Specialization
Citations

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

Fields of papers citing papers by Catherine Bove

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Catherine Bove. 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 Catherine Bove. The network helps show where Catherine Bove may publish in the future.

Co-authorship network of co-authors of Catherine Bove

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

All Works

12 of 12 papers shown
1.
Plotkin, Scott R., et al.. (2011). Spinal ependymomas in neurofibromatosis Type 2: a retrospective analysis of 55 patients. Journal of Neurosurgery Spine. 14(4). 543–547. 66 indexed citations
2.
Bove, Catherine, et al.. (2008). Presymptomatic Genetic Testing in Children for Neurofibromatosis 2. Journal of Pediatric Nursing. 23(3). 183–194. 7 indexed citations
3.
Mankin, Henry J., Katherine B. Sims, & Catherine Bove. (2005). Erlenmeyer flasking of a child's bones: a diagnostic puzzle.. PubMed. 34(8). 393–5. 1 indexed citations
4.
Acierno, James S., John C. Kennedy, John Falardeau, et al.. (2001). A Physical and Transcript Map of the MCOLN1 Gene Region on Human Chromosome 19p13.3–p13.2. Genomics. 73(2). 203–210. 10 indexed citations
5.
Masek, Bruce J., et al.. (1999). Quality of life assessment in adults with type 1 Gaucher disease. Quality of Life Research. 8(3). 263–268. 58 indexed citations
6.
Slaugenhaupt, Susan, James S. Acierno, Catherine Bove, et al.. (1999). Mapping of the Mucolipidosis Type IV Gene to Chromosome 19p and Definition of Founder Haplotypes. The American Journal of Human Genetics. 65(3). 773–778. 74 indexed citations
7.
Bove, Catherine, et al.. (1998). FACTORS PERCEIVED TO INFLUENCE PARENTAL DECISION-MAKING REGARDING PRESYMPTOMATIC TESTING OF CHILDREN AT RISK FOR TREATABLE ADULT-ONSET GENETIC DISORDERS. Issues in Comprehensive Pediatric Nursing. 21(1). 19–34. 3 indexed citations
8.
Bove, Catherine, Sara T. Fry, & Deborah J. MacDonald. (1997). Presymptomatic and predisposition genetic testing: Ethical and social considerations. Seminars in Oncology Nursing. 13(2). 135–140. 16 indexed citations
9.
Wilson, Peter J., Vijaya Ramesh, Arthur G. Kristiansen, et al.. (1996). Novel Mutations Detected in the TSC2 Hene From Both Sporadic and Familial TSC Patients. Human Molecular Genetics. 5(2). 249–256. 67 indexed citations
10.
Gasser, Thomas, Catherine Bove, Laurie J. Ozelius, et al.. (1996). Haplotype analysis at the DYT1 Locus in ashkenazi jewish patients with occupational hand dystonia. Movement Disorders. 11(2). 163–166. 21 indexed citations
11.
MacCollin, M., Vijaya Ramesh, Lee B. Jacoby, et al.. (1994). Mutational analysis of patients with neurofibromatosis 2.. PubMed. 55(2). 314–20. 91 indexed citations
12.
Pashayan, Hermine M., et al.. (1982). The Angelman syndrome in two brothers. American Journal of Medical Genetics. 13(3). 295–298. 27 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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