Karen J. Harrison

716 total citations
17 papers, 461 citations indexed

About

Karen J. Harrison is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Karen J. Harrison has authored 17 papers receiving a total of 461 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Karen J. Harrison's work include Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (5 papers) and Acute Myeloid Leukemia Research (2 papers). Karen J. Harrison is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (5 papers) and Acute Myeloid Leukemia Research (2 papers). Karen J. Harrison collaborates with scholars based in Canada, United States and India. Karen J. Harrison's co-authors include Dagmar K. Kalousek, Brian D. Kuchinka, Irene Barrett, Brenda Lomax, Jennifer MacKenzie, Ajay Pandita, Bernice E. Morrow, Khaldoun Al‐Romaih, Margaret Lilley and Lionel Willatt and has published in prestigious journals such as SHILAP Revista de lepidopterología, Oncogene and Clinical Cancer Research.

In The Last Decade

Karen J. Harrison

17 papers receiving 445 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Karen J. Harrison 252 248 88 77 71 17 461
Shihui Yu 346 1.4× 326 1.3× 98 1.1× 101 1.3× 64 0.9× 34 627
Constance K. Stein 346 1.4× 380 1.5× 45 0.5× 95 1.2× 64 0.9× 17 666
Elizabeth Wohler 338 1.3× 266 1.1× 73 0.8× 70 0.9× 39 0.5× 40 603
Fortunato Lonardo 350 1.4× 258 1.0× 99 1.1× 30 0.4× 53 0.7× 52 645
María Palomares‐Bralo 364 1.4× 339 1.4× 105 1.2× 53 0.7× 55 0.8× 38 540
Anita S. Kulharya 452 1.8× 509 2.1× 147 1.7× 59 0.8× 106 1.5× 31 843
Olaf Rittinger 384 1.5× 433 1.7× 81 0.9× 47 0.6× 55 0.8× 40 785
Smita M. Purandare 160 0.6× 323 1.3× 34 0.4× 114 1.5× 36 0.5× 15 598
Lukrecija Brečević 479 1.9× 361 1.5× 174 2.0× 64 0.8× 161 2.3× 31 749
Aleksander Jamsheer 397 1.6× 433 1.7× 112 1.3× 41 0.5× 27 0.4× 77 731

Countries citing papers authored by Karen J. Harrison

Since Specialization
Citations

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

Fields of papers citing papers by Karen J. Harrison

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Karen J. Harrison. 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 Karen J. Harrison. The network helps show where Karen J. Harrison may publish in the future.

Co-authorship network of co-authors of Karen J. Harrison

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

All Works

17 of 17 papers shown
1.
MacKenzie, Jennifer, et al.. (2024). Sirenomelia: An anatomical assessment and genetic sex determination of two cases. Journal of Anatomy. 244(6). 1093–1101. 1 indexed citations
2.
3.
Reginold, William, et al.. (2016). Melanocortin-4 Receptor Deficiency Phenotype with an Interstitial 18q Deletion: A Case Report of Severe Childhood Obesity and Tall Stature. SHILAP Revista de lepidopterología. 2016. 1–6. 4 indexed citations
4.
Anger, G, Susan Crocker, Kerry K. Brown, et al.. (2014). X-Linked Deafness-2 (DFNX2) Phenotype Associated With a Paracentric Inversion Upstream of POU3F4. American Journal of Audiology. 23(1). 1–6. 18 indexed citations
5.
LeBrun, David P., Tara Baetz, Patricia Farmer, et al.. (2008). Predicting Outcome in Follicular Lymphoma by Using Interactive Gene Pairs. Clinical Cancer Research. 14(2). 478–487. 6 indexed citations
6.
Baetz, Tara, et al.. (2008). Primary cardiac lymphoma: molecular cytogenetic characterization of a rare entity. Cardiovascular Pathology. 18(2). 92–99. 5 indexed citations
7.
Somerville, Martin J., Lionel Willatt, Helen V. Firth, et al.. (2005). Microduplication and Triplication of 22q11.2: A Highly Variable Syndrome. The American Journal of Human Genetics. 76(5). 865–876. 170 indexed citations
8.
Andrew, Scott D., Karen J. Harrison, Sherryl A. Taylor, et al.. (2004). A model for GFRα4 function and a potential modifying role in multiple endocrine neoplasia 2. Oncogene. 24(6). 1091–1097. 9 indexed citations
9.
Bayani, Jane, Maria Zieleńska, Ajay Pandita, et al.. (2002). Spectral karyotyping identifies recurrent complex rearrangements of chromosomes 8, 17, and 20 in osteosarcomas. Genes Chromosomes and Cancer. 36(1). 7–16. 91 indexed citations
10.
Harrison, Karen J., Ikuko Teshima, Meredith M. Silver, et al.. (1998). Partial tetrasomy with triplication of chromosome (5) (p14-p15.33) in a patient with severe multiple congenital anomalies. American Journal of Medical Genetics. 79(2). 103–107. 17 indexed citations
11.
Harrison, Karen J., Ikuko Teshima, Meredith M. Silver, et al.. (1998). Partial tetrasomy with triplication of chromosome (5) (p14‐p15.33) in a patient with severe multiple congenital anomalies. American Journal of Medical Genetics. 79(2). 103–107. 2 indexed citations
12.
Kuchinka, Brian D., Dagmar K. Kalousek, Brenda Lomax, Karen J. Harrison, & Irene Barrett. (1995). Interphase cytogenetic analysis of single cell suspensions prepared from previously formalin-fixed and paraffin-embedded tissues.. PubMed. 8(2). 183–6. 30 indexed citations
13.
Harrison, Karen J., Bonnie G. Massing, Christopher R. McKenna, & Dagmar K. Kalousek. (1995). Molecular cytogenetic analysis of monosomy 7 in pediatric patients with myelodysplastic syndrome. American Journal of Hematology. 48(2). 88–91. 6 indexed citations
14.
Norman, Margaret G., Karen J. Harrison, Kenneth J. Poskitt, & Dagmar K. Kalousek. (1995). Duplication of 9P and Hyperplasia of the Choroid Plexus: A Pathologic, Radiologic, and Molecular Cytogenetics Study. Pediatric Pathology & Laboratory Medicine. 15(1). 109–120. 16 indexed citations
15.
Harrison, Karen J., et al.. (1994). Astrocytoma with a unique telomere association. Cancer Genetics and Cytogenetics. 76(1). 33–35. 11 indexed citations
16.
Lomax, Brenda, et al.. (1994). The utilization of interphase cytogenetic analysis for the detection of mosaicism. Human Genetics. 93(3). 243–247. 39 indexed citations
17.
Harrison, Karen J., Irene Barrett, Brenda Lomax, Brian D. Kuchinka, & Dagmar K. Kalousek. (1993). Detection of confined placental mosaicism in trisomy 18 conceptions using interphase cytogenetic analysis. Human Genetics. 92(4). 353–358. 22 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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