Karin E. Finberg

5.2k total citations
52 papers, 3.2k citations indexed

About

Karin E. Finberg is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Karin E. Finberg has authored 52 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 15 papers in Hematology and 14 papers in Genetics. Recurrent topics in Karin E. Finberg's work include Iron Metabolism and Disorders (15 papers), Hemoglobinopathies and Related Disorders (14 papers) and Ion Transport and Channel Regulation (10 papers). Karin E. Finberg is often cited by papers focused on Iron Metabolism and Disorders (15 papers), Hemoglobinopathies and Related Disorders (14 papers) and Ion Transport and Channel Regulation (10 papers). Karin E. Finberg collaborates with scholars based in United States, Switzerland and United Kingdom. Karin E. Finberg's co-authors include Richard P. Lifton, Carsten A. Wagner, John P. Geibel, Nancy C. Andrews, Mark D. Fleming, Matthew M. Heeney, Dennis Brown, Sylvie Breton, Petra Ross‐Macdonald and M Snyder and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Karin E. Finberg

50 papers receiving 3.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Karin E. Finberg United States 26 1.6k 889 779 487 408 52 3.2k
David G. Motto United States 31 1.4k 0.9× 992 1.1× 390 0.5× 86 0.2× 157 0.4× 58 3.9k
Claude Gazin France 11 2.2k 1.4× 486 0.5× 103 0.1× 138 0.3× 172 0.4× 13 2.9k
Antonio Porcellini Italy 38 2.2k 1.4× 343 0.4× 280 0.4× 91 0.2× 250 0.6× 152 4.6k
Saghi Ghaffari United States 36 2.6k 1.7× 1.2k 1.4× 866 1.1× 79 0.2× 181 0.4× 80 4.6k
Stephan M. Tanner United States 23 1.4k 0.9× 539 0.6× 279 0.4× 51 0.1× 141 0.3× 44 2.4k
Weiping Yuan China 30 2.1k 1.3× 644 0.7× 230 0.3× 68 0.1× 160 0.4× 141 3.3k
GL Semenza United States 9 1.7k 1.1× 408 0.5× 292 0.4× 49 0.1× 192 0.5× 9 3.2k
Waihay J. Wong United States 15 1.3k 0.8× 470 0.5× 451 0.6× 31 0.1× 234 0.6× 26 2.8k
Gang Huang United States 32 2.1k 1.3× 1.4k 1.6× 545 0.7× 126 0.3× 155 0.4× 112 3.5k
David A. Sweetser United States 27 1.9k 1.2× 599 0.7× 188 0.2× 137 0.3× 65 0.2× 62 3.0k

Countries citing papers authored by Karin E. Finberg

Since Specialization
Citations

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

Fields of papers citing papers by Karin E. Finberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karin E. Finberg

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

All Works

20 of 20 papers shown
1.
Li, Xiuqi & Karin E. Finberg. (2025). Iron Deficiency Anemia. Advances in experimental medicine and biology. 1480. 163–178.
2.
Li, Xiuqi, et al.. (2023). Bone marrow sinusoidal endothelial cells are a site of Fgf23 upregulation in a mouse model of iron deficiency anemia. Blood Advances. 7(17). 5156–5171. 4 indexed citations
3.
Irshaid, Lina, Mitchell Clark, Oluwole Fadare, Karin E. Finberg, & Vinita Parkash. (2021). Endometrial Carcinoma as the Presenting Malignancy in a Teenager With a Pathogenic TP53 Germline Mutation: A Case Report and Literature Review. International Journal of Gynecological Pathology. 41(3). 258–267. 2 indexed citations
4.
Jenkins, Sarah, Xiuqi Li, Tracy Nelson, et al.. (2020). IL-1β Drives Production of FGF-23 at the Onset of Chronic Kidney Disease in Mice. Journal of Bone and Mineral Research. 35(7). 1352–1362. 25 indexed citations
5.
Li, Xiuqi, Abitha Sukumaran, Luis Gonzalez, et al.. (2020). NCOA4 is Regulated by HIF and Mediates Mobilization of Murine Hepatic Iron Stores After Blood Loss. Blood. 136(23). 2691–2702. 59 indexed citations
6.
O’Malley, Dennis P., et al.. (2019). EBV-Positive Primary Large B-Cell Lymphoma: The Role of Immunohistochemistry and XPO1 in the Diagnosis of Mediastinal Lymphomas. Applied immunohistochemistry & molecular morphology. 28(10). 725–730. 10 indexed citations
7.
Le, Long P., Lilit Garibyan, Karin E. Finberg, et al.. (2012). Fibrosis-Associated Single-Nucleotide Polymorphisms in TGFB1 and CAV1 Are Not Associated With the Development of Nephrogenic Systemic Fibrosis. American Journal of Dermatopathology. 35(3). 351–356. 4 indexed citations
8.
Farris, Alton B., Elizabeth G. Demicco, Karin E. Finberg, et al.. (2011). Clinicopathologic and Molecular Profiles of Microsatellite Unstable Barrett Esophagus-associated Adenocarcinoma. The American Journal of Surgical Pathology. 35(5). 647–655. 45 indexed citations
9.
Finberg, Karin E., et al.. (2009). Tmprss6 Is a Genetic Modifier of the Hfe-Hemochromatosis Phenotype in Mice.. Blood. 114(22). 625–625. 1 indexed citations
10.
Finberg, Karin E., Matthew M. Heeney, Dean R. Campagna, et al.. (2008). Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA). Nature Genetics. 40(5). 569–571. 484 indexed citations
11.
Finberg, Karin E., Lecia V. Sequist, Victoria A. Joshi, et al.. (2007). Mucinous Differentiation Correlates with Absence of EGFR Mutation and Presence of KRAS Mutation in Lung Adenocarcinomas with Bronchioloalveolar Features. Journal of Molecular Diagnostics. 9(3). 320–326. 158 indexed citations
12.
Nahed, Brian V., Aşkın Şeker, Bülent Güçlü, et al.. (2004). Mapping a Mendelian Form of Intracranial Aneurysm to 1p34.3-p36.13. The American Journal of Human Genetics. 76(1). 172–179. 62 indexed citations
13.
Wagner, Carsten A., Karin E. Finberg, Sylvie Breton, et al.. (2004). Renal Vacuolar H+-ATPase. Physiological Reviews. 84(4). 1263–1314. 333 indexed citations
14.
Dou, Hongwei, Karin E. Finberg, Emma Lou Cardell, Richard P. Lifton, & Daniel Choo. (2003). Mice lacking the B1 subunit of H+-ATPase have normal hearing. Hearing Research. 180(1-2). 76–84. 42 indexed citations
15.
Stehberger, Paul A., Nicole Schulz, Karin E. Finberg, et al.. (2003). Localization and Regulation of the ATP6V0A4 (a4) Vacuolar H+-ATPase Subunit Defective in an Inherited Form of Distal Renal Tubular Acidosis. Journal of the American Society of Nephrology. 14(12). 3027–3038. 72 indexed citations
16.
Finberg, Karin E., Carsten A. Wagner, Paul A. Stehberger, John P. Geibel, & Richard P. Lifton. (2003). Molecular cloning and characterization of Atp6v1b1, the murine vacuolar H+-ATPase B1-subunit. Gene. 318. 25–34. 30 indexed citations
17.
Smith, Annabel N., Karin E. Finberg, Carsten A. Wagner, et al.. (2001). Molecular Cloning and Characterization of Atp6n1b. Journal of Biological Chemistry. 276(45). 42382–42388. 83 indexed citations
18.
Karet, Fiona E., Karin E. Finberg, Ahmet Nayır, et al.. (1999). Localization of a Gene for Autosomal Recessive Distal Renal Tubular Acidosis with Normal Hearing (rdRTA2) to 7q33-34. The American Journal of Human Genetics. 65(6). 1656–1665. 69 indexed citations
19.
Günel, Murat, et al.. (1996). Genetic Heterogeneity of Inherited Cerebral Cavernous Malformation. Neurosurgery. 38(6). 1265–1271. 94 indexed citations
20.
Günel, Murat, Issam A. Awad, Karin E. Finberg, et al.. (1996). A Founder Mutation as a Cause of Cerebral Cavernous Malformation in Hispanic Americans. New England Journal of Medicine. 334(15). 946–951. 161 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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