Tina Hambuch

3.4k total citations
15 papers, 862 citations indexed

About

Tina Hambuch is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Tina Hambuch has authored 15 papers receiving a total of 862 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Tina Hambuch's work include Genomics and Rare Diseases (5 papers), Chronic Lymphocytic Leukemia Research (2 papers) and Animal Behavior and Reproduction (2 papers). Tina Hambuch is often cited by papers focused on Genomics and Rare Diseases (5 papers), Chronic Lymphocytic Leukemia Research (2 papers) and Animal Behavior and Reproduction (2 papers). Tina Hambuch collaborates with scholars based in United States, Germany and Canada. Tina Hambuch's co-authors include Charles L. Sawyers, Art Raitano, John Parsch, Zhi Zhang, Eileen A. Lacey, Eugene O. Major, Xuan Liu, Owen N. Witte, Arnold Berk and Andrei Goga and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Genetics and Evolution.

In The Last Decade

Tina Hambuch

15 papers receiving 849 citations

Peers

Tina Hambuch
Lynne Minto United Kingdom
Kathleen T. Xie United States
Grace R. Jeschke United States
Steven Roels United States
J A Lautenberger United States
Kimona Ålin United States
Joanna C. Fowler Australia
Gregory B. Peters Australia
Manfred Kraus United States
Taeko Wada Japan
Lynne Minto United Kingdom
Tina Hambuch
Citations per year, relative to Tina Hambuch Tina Hambuch (= 1×) peers Lynne Minto

Countries citing papers authored by Tina Hambuch

Since Specialization
Citations

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

Fields of papers citing papers by Tina Hambuch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tina Hambuch

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

All Works

15 of 15 papers shown
1.
Bayrak‐Toydemir, Pınar, Lora Jh Bean, Alicia Braxton, et al.. (2018). Misattributed parentage as an unanticipated finding during exome/genome sequencing: current clinical laboratory practices and an opportunity for standardization. Genetics in Medicine. 21(4). 861–866. 14 indexed citations
2.
Aradhya, Swaroop, Nila Patil, Rebecca Truty, et al.. (2017). Deep sequencing multi-gene panel analysis is a useful first-tier test with a high diagnostic yield and broad mutation spectrum detection in childhood epilepsy. Journal of the Neurological Sciences. 381. 85–85. 1 indexed citations
3.
Klein, Hanns‐Georg, Peter Bauer, & Tina Hambuch. (2014). Whole genome sequencing (WGS), whole exome sequencing (WES) and clinical exome sequencing (CES) in patient care. LaboratoriumsMedizin. 38(4). 221–230. 11 indexed citations
4.
Hwang, Kyu‐Baek, In‐Hee Lee, Jin‐Ho Park, et al.. (2014). Reducing False-Positive Incidental Findings with Ensemble Genotyping and Logistic Regression Based Variant Filtering Methods. Human Mutation. 35(8). 936–944. 10 indexed citations
5.
Tsongalis, Gregory J., Elizabeth Chao, Jill Hagenkord, Tina Hambuch, & Jason H. Moore. (2013). Bioinformatics: What the Clinical Laboratorian Needs to Know and Prepare For. Clinical Chemistry. 59(9). 1301–1305. 4 indexed citations
6.
Nakagawa, Sachiko, Wei Sun, José Carlos Ferreira, et al.. (2012). Platelet Hexosaminidase A Enzyme Assay Effectively Detects Carriers Missed by Targeted DNA Mutation Analysis. JIMD Reports. 6. 1–6. 4 indexed citations
7.
Schrijver, Iris, Nazneen Aziz, Daniel H. Farkas, et al.. (2012). Opportunities and Challenges Associated with Clinical Diagnostic Genome Sequencing. Journal of Molecular Diagnostics. 14(6). 525–540. 105 indexed citations
8.
Havasi, Viktória, Steven Keiles, Tina Hambuch, Eric J. Sorscher, & Anja Kammesheidt. (2008). The role of the F508C mutation in congenital bilateral absence of the vas deferens. Genetics in Medicine. 10(12). 910–914. 3 indexed citations
9.
Hambuch, Tina & John Parsch. (2005). Patterns of Synonymous Codon Usage in Drosophila melanogaster Genes With Sex-Biased Expression. Genetics. 170(4). 1691–1700. 62 indexed citations
10.
Zhang, Zhi, Tina Hambuch, & John Parsch. (2004). Molecular Evolution of Sex-Biased Genes in Drosophila. Molecular Biology and Evolution. 21(11). 2130–2139. 143 indexed citations
11.
Hambuch, Tina, et al.. (2004). Population Genetic Analysis ofBartonella bacilliformisIsolates from Areas of Peru Where Carrion's Disease Is Endemic and Epidemic. Journal of Clinical Microbiology. 42(8). 3675–3680. 14 indexed citations
12.
Hambuch, Tina & Eileen A. Lacey. (2002). ENHANCED SELECTION FOR MHC DIVERSITY IN SOCIAL TUCO-TUCOS. Evolution. 56(4). 841–845. 38 indexed citations
13.
Hambuch, Tina & Eileen A. Lacey. (2002). ENHANCED SELECTION FOR MHC DIVERSITY IN SOCIAL TUCO-TUCOS. Evolution. 56(4). 841–841. 1 indexed citations
14.
Goga, Andrei, Xuan Liu, Tina Hambuch, et al.. (1995). p53 dependent growth suppression by the c-Abl nuclear tyrosine kinase.. PubMed. 11(4). 791–9. 108 indexed citations
15.
Raitano, Art, et al.. (1995). The Bcr-Abl leukemia oncogene activates Jun kinase and requires Jun for transformation.. Proceedings of the National Academy of Sciences. 92(25). 11746–11750. 344 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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