Katrina E. Kotzer

503 total citations
12 papers, 271 citations indexed

About

Katrina E. Kotzer is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Katrina E. Kotzer has authored 12 papers receiving a total of 271 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 5 papers in Pediatrics, Perinatology and Child Health and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Katrina E. Kotzer's work include BRCA gene mutations in cancer (4 papers), Genomics and Rare Diseases (3 papers) and Connective tissue disorders research (3 papers). Katrina E. Kotzer is often cited by papers focused on BRCA gene mutations in cancer (4 papers), Genomics and Rare Diseases (3 papers) and Connective tissue disorders research (3 papers). Katrina E. Kotzer collaborates with scholars based in United States and Israel. Katrina E. Kotzer's co-authors include Linnea M. Baudhuin, Susan A. Lagerstedt, Jennifer M. Skierka, Dennis J. O’Kane, Karen E. Wain, McKinsey L. Goodenberger, Jessie H. Conta, Kimberly A. Schahl, Michael J. Ackerman and John L. Black and has published in prestigious journals such as The Journal of Pediatrics, Clinica Chimica Acta and Genetics in Medicine.

In The Last Decade

Katrina E. Kotzer

12 papers receiving 270 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Katrina E. Kotzer United States 9 162 94 80 71 54 12 271
Giuseppina Casu Italy 8 192 1.2× 44 0.5× 21 0.3× 38 0.5× 96 1.8× 13 325
Amber Hildreth United States 5 249 1.5× 33 0.4× 6 0.1× 46 0.6× 105 1.9× 10 327
Susan Rojahn United States 8 137 0.8× 8 0.1× 49 0.6× 18 0.3× 79 1.5× 13 263
Patrick Reineke United States 5 244 1.5× 45 0.5× 12 0.1× 19 0.3× 64 1.2× 10 355
Grace E. VanNoy United States 8 155 1.0× 36 0.4× 8 0.1× 47 0.7× 72 1.3× 15 232
Ives Lim Singapore 7 51 0.3× 38 0.4× 16 0.2× 55 0.8× 182 3.4× 10 241
Àngels Ulied Spain 10 105 0.6× 12 0.1× 35 0.4× 92 1.3× 82 1.5× 17 357
Paul Brennan United Kingdom 10 76 0.5× 18 0.2× 118 1.5× 14 0.2× 124 2.3× 22 331
Outi Uimari Finland 12 27 0.2× 36 0.4× 10 0.1× 47 0.7× 66 1.2× 19 442
Elisabeth Widén Finland 2 162 1.0× 14 0.1× 60 0.8× 20 0.3× 49 0.9× 2 250

Countries citing papers authored by Katrina E. Kotzer

Since Specialization
Citations

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

Fields of papers citing papers by Katrina E. Kotzer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Katrina E. Kotzer. 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 Katrina E. Kotzer. The network helps show where Katrina E. Kotzer may publish in the future.

Co-authorship network of co-authors of Katrina E. Kotzer

This figure shows the co-authorship network connecting the top 25 collaborators of Katrina E. Kotzer. A scholar is included among the top collaborators of Katrina E. Kotzer 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 Katrina E. Kotzer. Katrina E. Kotzer 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.
Peterson, Sandra E., Katrina E. Kotzer, Guilherme S. Lopes, et al.. (2022). Targeted Genotyping in Clinical Pharmacogenomics. Journal of Molecular Diagnostics. 24(3). 253–261. 22 indexed citations
2.
Baudhuin, Linnea M., et al.. (2019). Variability in gene-based knowledge impacts variant classification: an analysis of FBN1 missense variants in ClinVar. European Journal of Human Genetics. 27(10). 1550–1560. 14 indexed citations
3.
Moyer, Ann M., et al.. (2017). Clinical UGT1A1 Genetic Analysis in Pediatric Patients: Experience of a Reference Laboratory. Molecular Diagnosis & Therapy. 21(3). 327–335. 7 indexed citations
4.
Baudhuin, Linnea M., Charles Leduc, Laura Train, et al.. (2017). Technical Advances for the Clinical Genomic Evaluation of Sudden Cardiac Death. Circulation Cardiovascular Genetics. 10(6). 17 indexed citations
5.
Kotzer, Katrina E., et al.. (2016). The Genetic Counselor's Role in Managing Ethical Dilemmas Arising in the Laboratory Setting. Journal of Genetic Counseling. 25(5). 838–854. 6 indexed citations
6.
Baudhuin, Linnea M., Katrina E. Kotzer, & Susan A. Lagerstedt. (2015). Decreased frequency of FBN1 missense variants in Ghent criteria-positive Marfan syndrome and characterization of novel FBN1 variants. Journal of Human Genetics. 60(5). 241–252. 15 indexed citations
7.
Arscott, Patricia, Colleen Caleshu, Katrina E. Kotzer, et al.. (2015). A Case for Inclusion of Genetic Counselors in Cardiac Care. Cardiology in Review. 24(2). 49–55. 37 indexed citations
8.
Baudhuin, Linnea M., Katrina E. Kotzer, & Susan A. Lagerstedt. (2014). Increased frequency of FBN1 truncating and splicing variants in Marfan syndrome patients with aortic events. Genetics in Medicine. 17(3). 177–187. 69 indexed citations
9.
Donato, Leslie J., Amy K. Saenger, Laura Train, et al.. (2014). Genetic and biochemical analyses in dyslipidemic patients undergoing LDL apheresis. Journal of Clinical Apheresis. 29(5). 256–265. 4 indexed citations
10.
Kotzer, Katrina E., et al.. (2013). Genetic testing utilization and the role of the laboratory genetic counselor. Clinica Chimica Acta. 427. 193–195. 23 indexed citations
11.
Skierka, Jennifer M., Katrina E. Kotzer, Susan A. Lagerstedt, Dennis J. O’Kane, & Linnea M. Baudhuin. (2013). UGT1A1 Genetic Analysis as a Diagnostic Aid for Individuals with Unconjugated Hyperbilirubinemia. The Journal of Pediatrics. 162(6). 1146–1152.e2. 35 indexed citations
12.
Kotzer, Katrina E., et al.. (2013). Looking Back and Moving Forward: An Historical Perspective from Laboratory Genetic Counselors. Journal of Genetic Counseling. 23(3). 363–370. 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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