Charles H. Hensel

1.8k total citations
29 papers, 1.1k citations indexed

About

Charles H. Hensel is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Charles H. Hensel has authored 29 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 13 papers in Genetics and 7 papers in Oncology. Recurrent topics in Charles H. Hensel's work include Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Autism Spectrum Disorder Research (4 papers). Charles H. Hensel is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Autism Spectrum Disorder Research (4 papers). Charles H. Hensel collaborates with scholars based in United States, Netherlands and Australia. Charles H. Hensel's co-authors include Susan L. Naylor, RuiHua Xiang, Dawn Garcia, Rui Xiang, A.Y. Sakaguchi, Maria C. Daly, Perry B. Hackett, Robert B. Petersen, Christin Tse and Albert R. Davalos and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and Journal of Molecular Biology.

In The Last Decade

Charles H. Hensel

28 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Charles H. Hensel United States	17	650	337	291	235	129	29	1.1k
Beverly A. Karpinski United States	18	742 1.1×	221 0.7×	133 0.5×	105 0.4×	101 0.8×	28	1.3k
Jami Dwyer United States	14	597 0.9×	194 0.6×	178 0.6×	265 1.1×	121 0.9×	15	1.3k
Mark D. Potter United States	16	611 0.9×	367 1.1×	147 0.5×	79 0.3×	117 0.9×	23	1.3k
Tamar Paperna Israel	21	524 0.8×	242 0.7×	124 0.4×	124 0.5×	100 0.8×	48	1.2k
Sylvie Taviaux France	21	992 1.5×	312 0.9×	213 0.7×	237 1.0×	144 1.1×	42	1.5k
Amy M. Breman United States	20	587 0.9×	713 2.1×	132 0.5×	83 0.4×	164 1.3×	47	1.4k
Karine Hovanes United States	17	978 1.5×	444 1.3×	111 0.4×	75 0.3×	93 0.7×	28	1.9k
Ariya D. Lapan United States	6	569 0.9×	182 0.5×	167 0.6×	271 1.2×	104 0.8×	6	1.5k
Camelia V. Marcos-Gutierrez Netherlands	10	857 1.3×	281 0.8×	84 0.3×	443 1.9×	62 0.5×	10	1.8k
Paul C. Lott United States	13	1.3k 2.0×	299 0.9×	95 0.3×	82 0.3×	154 1.2×	23	1.7k

Countries citing papers authored by Charles H. Hensel

Since Specialization

Citations

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

Fields of papers citing papers by Charles H. Hensel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Charles H. Hensel

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Drusbosky, Leylah, Mehmet Asım Bilen, Georges Azzi, et al.. (2021). Blood-based tumor mutational burden from circulating tumor DNA (ctDNA) across advanced solid malignancies using a commercially available liquid biopsy assay.. Journal of Clinical Oncology. 39(15_suppl). 3040–3040. 13 indexed citations

Loree, Jonathan M., Jason T. Henry, Kanwal Raghav, et al.. (2021). Serial circulating tumor DNA (ctDNA) monitoring in metastatic colorectal cancer (mCRC) reveals dynamic profile of actionable alterations.. Journal of Clinical Oncology. 39(15_suppl). 3572–3572. 1 indexed citations

Vanzo, Rena, Aparna Prasad, Charles H. Hensel, et al.. (2020). The Temple Grandin Genome: Comprehensive Analysis in a Scientist with High-Functioning Autism. Journal of Personalized Medicine. 11(1). 21–21. 3 indexed citations

Hensel, Charles H., Rena Vanzo, Megan Martin, et al.. (2019). Abnormally Methylated FMR1 in Absence of a Detectable Full Mutation in a U.S.A Patient Cohort Referred for Fragile X Testing. Scientific Reports. 9(1). 15315–15315. 8 indexed citations

Prasad, Aparna, Rena Vanzo, Patricia Mowery‐Rushton, et al.. (2018). Clinical utility of exome sequencing in individuals with large homozygous regions detected by chromosomal microarray analysis. BMC Medical Genetics. 19(1). 46–46. 19 indexed citations

Hensel, Charles H., Rena Vanzo, Megan Martin, et al.. (2017). Analytical and Clinical Validity Study of FirstStepDx PLUS: A Chromosomal Microarray Optimized for Patients with Neurodevelopmental Conditions. PLoS Currents. 9. 7 indexed citations

Ho, Karen S., E. Robert Wassman, Charles H. Hensel, et al.. (2016). Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders. International Journal of Molecular Sciences. 17(12). 2070–2070. 50 indexed citations

Ho, Karen S., Sarah T. South, Charles H. Hensel, et al.. (2016). Chromosomal microarray testing identifies a 4p terminal region associated with seizures in Wolf–Hirschhorn syndrome. Journal of Medical Genetics. 53(4). 256–263. 29 indexed citations

Matsunami, Nori, Dexter Hadley, Charles H. Hensel, et al.. (2013). Identification of Rare Recurrent Copy Number Variants in High-Risk Autism Families and Their Prevalence in a Large ASD Population. PLoS ONE. 8(1). e52239–e52239. 50 indexed citations

10.

Vijayakumar, Sapna, Dawn Garcia, Charles H. Hensel, et al.. (2005). The human Y chromosome suppresses the tumorigenicity of PC‐3, a human prostate cancer cell line, in athymic nude mice. Genes Chromosomes and Cancer. 44(4). 365–372. 40 indexed citations

11.

Camp, Nicola J., Michael Lowry, Ruth Richards, et al.. (2005). Genome‐wide linkage analyses of extended Utah pedigrees identifies loci that influence recurrent, early‐onset major depression and anxiety disorders. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 135B(1). 85–93. 80 indexed citations

12.

Xiang, RuiHua, et al.. (2002). Semaphorin 3F gene from human 3p21.3 suppresses tumor formation in nude mice.. PubMed. 62(9). 2637–43. 115 indexed citations

13.

Hunt, Steven C., Victor Abkevich, Charles H. Hensel, et al.. (2001). Linkage of body mass index to chromosome 20 in Utah pedigrees. Human Genetics. 109(3). 279–285. 42 indexed citations

14.

Xiang, RuiHua, Charles H. Hensel, Dawn Garcia, et al.. (1996). Isolation of the Human Semaphorin III/F Gene (SEMA3F) at Chromosome 3p21, a Region Deleted in Lung Cancer. Genomics. 32(1). 39–48. 135 indexed citations

15.

Daly, Maria C., Rui Xiang, Dorothy L. Buchhagen, et al.. (1994). A homozygous deletion on chromosome 3 in a small cell lung cancer cell line correlates with a region of tumor suppressor activity. Lung Cancer. 10(5-6). 401–401. 91 indexed citations

16.

Howes, Kimberly A., Armando Menéndez-Peláez, Rüssel J. Reiter, et al.. (1991). Serum Luteinizing Hormone, Prolactin, and Thyrotropin and Their Pituitary Subunit mRNA Levels during Proestrus in the Syrian Hamster. Neuroendocrinology. 54(6). 629–634. 3 indexed citations

17.

Hensel, Charles H., C L Hsieh, Adi F. Gazdar, et al.. (1991). Altered structure and expression of the human retinoblastoma susceptibility gene in small cell lung cancer. Lung Cancer. 7(3). 184–184. 130 indexed citations

18.

Naylor, Susan L., et al.. (1989). The DNF15S2 locus at 3p21 is transcribed in normal lung and small cell lung cancer. Genomics. 4(3). 355–361. 50 indexed citations

19.

Hackett, Perry B., Robert B. Petersen, Charles H. Hensel, et al.. (1986). Synthesis in vitro of a seven amino acid peptide encoded in the leader RNA of Rous sarcoma virus. Journal of Molecular Biology. 190(1). 45–57. 56 indexed citations

20.

Petersen, Robert B., Charles H. Hensel, & Perry B. Hackett. (1984). Identification of a ribosome-binding site for a leader peptide encoded by Rous sarcoma virus RNA. Journal of Virology. 51(3). 722–729. 21 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.

Explore authors with similar magnitude of impact