Dave Viskochil

859 total citations
4 papers, 27 citations indexed

About

Dave Viskochil is a scholar working on Molecular Biology, Neurology and Surgery. According to data from OpenAlex, Dave Viskochil has authored 4 papers receiving a total of 27 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Molecular Biology, 2 papers in Neurology and 1 paper in Surgery. Recurrent topics in Dave Viskochil's work include Neuroblastoma Research and Treatments (2 papers), Neurofibromatosis and Schwannoma Cases (2 papers) and Sarcoma Diagnosis and Treatment (1 paper). Dave Viskochil is often cited by papers focused on Neuroblastoma Research and Treatments (2 papers), Neurofibromatosis and Schwannoma Cases (2 papers) and Sarcoma Diagnosis and Treatment (1 paper). Dave Viskochil collaborates with scholars based in United States and Canada. Dave Viskochil's co-authors include John C. Carey, Peter Ainsworth, Rong Mao, Rebecca L. Margraf, Jacques DʼAstous, Heather Hanson, Wei Shen, Hunter Best, Lesa Nelson and Sarah Dugan and has published in prestigious journals such as Human Molecular Genetics, Journal of Medical Genetics and American Journal of Medical Genetics.

In The Last Decade

Dave Viskochil

4 papers receiving 25 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Dave Viskochil United States	4	18	12	7	6	5	4	27
Benjamin Alexander Canada	2	9 0.5×	14 1.2×	7 1.0×	3 0.5×	9 1.8×	2	33
Vinod Varghese India	3	4 0.2×	10 0.8×	4 0.6×	6 1.0×	6 1.2×	5	33
Jeanette Buehler China	3	14 0.8×	26 2.2×	5 0.7×		8 1.6×	3	82
Kate Mowrey United States	4	6 0.3×	11 0.9×	8 1.1×	3 0.5×	9 1.8×	13	37
Melanie O’Leary United States	2	9 0.5×	17 1.4×	2 0.3×	7 1.2×	19 3.8×	5	42
Eugen Schlegel Germany	3	15 0.8×	6 0.5×	9 1.3×	2 0.3×		4	36
Amy R. Fairchild United Kingdom	2	6 0.3×	9 0.8×	2 0.3×	4 0.7×	4 0.8×	2	21
E. Hennes Austria	3	17 0.9×	5 0.4×	3 0.4×	1 0.2×	2 0.4×	4	42
Daphne J. Smits Netherlands	3	8 0.4×	12 1.0×	4 0.6×		5 1.0×	6	26
Katleen Wild Germany	3	4 0.2×	10 0.8×	8 1.1×	2 0.3×	2 0.4×	3	41

Countries citing papers authored by Dave Viskochil

Since Specialization

Citations

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

Fields of papers citing papers by Dave Viskochil

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dave Viskochil

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

All Works

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4 of 4 papers shown

1.

Shen, Wei, et al.. (2020). Detecting mosaic variants in patients with somatic overgrowth syndromes using cell-free circulating DNA and deep sequencing. Journal of Medical Genetics. 57(11). 794–796. 3 indexed citations

2.

Margraf, Rebecca L., David Sant, John C. Carey, et al.. (2017). Utilization of Whole-Exome Next-Generation Sequencing Variant Read Frequency for Detection of Lesion-Specific, Somatic Loss of Heterozygosity in a Neurofibromatosis Type 1 Cohort with Tibial Pseudarthrosis. Journal of Molecular Diagnostics. 19(3). 468–474. 5 indexed citations

3.

Viskochil, Dave. (1999). Neurofibromatosis 1. American Journal of Medical Genetics. 89(1). v–viii. 12 indexed citations

4.

Bleyl, Steven B., Peter Ainsworth, Lesa Nelson, Dave Viskochil, & Kenneth Ward. (1994). An ancient Ta subclass L1 insertion results in an intragenic polymorphism in an intron of the NF1 gene. Human Molecular Genetics. 3(3). 517–518. 7 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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