Christopher N Hahn

6.0k total citations
72 papers, 2.2k citations indexed

About

Christopher N Hahn is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Christopher N Hahn has authored 72 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 30 papers in Hematology and 17 papers in Genetics. Recurrent topics in Christopher N Hahn's work include Acute Myeloid Leukemia Research (25 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (12 papers) and Chronic Myeloid Leukemia Treatments (7 papers). Christopher N Hahn is often cited by papers focused on Acute Myeloid Leukemia Research (25 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (12 papers) and Chronic Myeloid Leukemia Treatments (7 papers). Christopher N Hahn collaborates with scholars based in Australia, United States and Malaysia. Christopher N Hahn's co-authors include Hamish S. Scott, Jennifer R. Gamble, Mathew A. Vadas, Brian K. May, Pu Xia, Xiaochun Li, Anna Brown, Alessandra d’Azzo, John L. Omdahl and Maria del Pilar Martin and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Christopher N Hahn

70 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christopher N Hahn Australia 28 1.2k 325 297 290 275 72 2.2k
Andrea Kolbus Austria 26 1.4k 1.2× 277 0.9× 331 1.1× 163 0.6× 239 0.9× 39 2.5k
Akiko Kimura Japan 26 1.4k 1.1× 301 0.9× 282 0.9× 111 0.4× 252 0.9× 49 2.4k
Florian Bassermann Germany 26 1.7k 1.4× 432 1.3× 184 0.6× 319 1.1× 155 0.6× 105 2.9k
Tomoyuki Masuda Japan 28 1.5k 1.2× 304 0.9× 196 0.7× 96 0.3× 195 0.7× 160 2.8k
Anna Maria Billi Italy 32 2.0k 1.7× 521 1.6× 174 0.6× 308 1.1× 135 0.5× 93 2.6k
Marjorie Brand Canada 33 3.1k 2.5× 186 0.6× 228 0.8× 261 0.9× 303 1.1× 65 3.5k
Changwon Park United States 30 2.2k 1.9× 590 1.8× 205 0.7× 213 0.7× 145 0.5× 59 3.2k
Gerold Untergasser Austria 29 1.1k 0.9× 201 0.6× 126 0.4× 104 0.4× 165 0.6× 84 2.4k
Ming Ji China 26 1.1k 0.9× 349 1.1× 167 0.6× 87 0.3× 109 0.4× 92 2.3k
Gretchen Bain United States 28 2.2k 1.8× 254 0.8× 271 0.9× 280 1.0× 305 1.1× 55 3.9k

Countries citing papers authored by Christopher N Hahn

Since Specialization
Citations

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

Fields of papers citing papers by Christopher N Hahn

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christopher N Hahn. 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 Christopher N Hahn. The network helps show where Christopher N Hahn may publish in the future.

Co-authorship network of co-authors of Christopher N Hahn

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher N Hahn. A scholar is included among the top collaborators of Christopher N Hahn 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 Christopher N Hahn. Christopher N Hahn 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.
Kutyna, Monika, Joanne Yu, Anna Brown, et al.. (2025). RBC transfusion dependency refines the Molecular International Prognostic Scoring System for myelodysplastic syndrome. Blood Advances. 9(16). 4244–4247. 1 indexed citations
2.
Wiseman, Thomas, Deepak Singhal, David T Yeung, et al.. (2024). Higher Rate of Red Blood Cell (RBC) Alloimmunization in RBC-Transfused Myelodysplastic Syndrome Compared to Acute Myeloid Leukemia. Blood. 144(Supplement 1). 1267–1267.
3.
Singhal, Deepak, Monika Kutyna, Christopher N Hahn, Mithun Vinod Shah, & Devendra Hiwase. (2024). Therapy-Related Myeloid Neoplasms: Complex Interactions among Cytotoxic Therapies, Genetic Factors, and Aberrant Microenvironment. Blood Cancer Discovery. 5(6). 400–416. 5 indexed citations
4.
Homan, Claire C., et al.. (2023). Transcription factor genetics and biology in predisposition to bone marrow failure and hematological malignancy. Frontiers in Oncology. 13. 1183318–1183318. 2 indexed citations
5.
Samaraweera, Saumya E., Tatjana Geukens, Débora A. Casolari, et al.. (2022). Novel modes of MPL activation in triple-negative myeloproliferative neoplasms. Pathology. 55(1). 77–85. 1 indexed citations
6.
Baranwal, Anmol, Christopher N Hahn, Mithun Vinod Shah, & Devendra Hiwase. (2022). Role of Germline Predisposition to Therapy-Related Myeloid Neoplasms. Current Hematologic Malignancy Reports. 17(6). 254–265. 13 indexed citations
7.
Saygin, Caner, Gregory W. Roloff, Christopher N Hahn, et al.. (2022). Allogeneic hematopoietic stem cell transplant outcomes in adults with inherited myeloid malignancies. Blood Advances. 7(4). 549–554. 23 indexed citations
8.
Feurstein, Simone, Christopher N Hahn, Nikita Mehta, & Lucy A. Godley. (2022). A practical guide to interpreting germline variants that drive hematopoietic malignancies, bone marrow failure, and chronic cytopenias. Genetics in Medicine. 24(4). 931–954. 9 indexed citations
9.
Homan, Claire C., Parvathy Venugopal, Peer Arts, et al.. (2021). GATA2 deficiency syndrome: A decade of discovery. Human Mutation. 42(11). 1399–1421. 29 indexed citations
10.
Venugopal, Parvathy, Lucia Gagliardi, Cecily Forsyth, et al.. (2020). Two monogenic disorders masquerading as one: severe congenital neutropenia with monocytosis and non-syndromic sensorineural hearing loss. BMC Medical Genetics. 21(1). 35–35. 2 indexed citations
11.
Brown, Anna, Christopher N Hahn, & Hamish S. Scott. (2020). Secondary leukemia in patients with germline transcription factor mutations (RUNX1, GATA2, CEBPA). Blood. 136(1). 24–35. 57 indexed citations
12.
Byrne, Alicia B., Peer Arts, Steven W. Polyak, et al.. (2019). Identification and targeted management of a neurodegenerative disorder caused by biallelic mutations in SLC5A6. npj Genomic Medicine. 4(1). 28–28. 16 indexed citations
13.
Hahn, Christopher N, et al.. (2017). Myeloid neoplasms with germline DDX41 mutation. International Journal of Hematology. 106(2). 163–174. 58 indexed citations
14.
Hahn, Christopher N, Milena Babic, Jinghua Feng, et al.. (2017). Duplication on Chromosome 14q Identified in Familial Predisposition to Myeloid Malignancies and Myeloproliferative Neoplasms. Blood. 130. 492–492. 3 indexed citations
15.
Pagani, Ilaria S., Chung Hoow Kok, Verity A Saunders, et al.. (2017). A Method for Next-Generation Sequencing of Paired Diagnostic and Remission Samples to Detect Mitochondrial DNA Mutations Associated with Leukemia. Journal of Molecular Diagnostics. 19(5). 711–721. 6 indexed citations
16.
Oftedal, Bergithe E, David Hamm, Poh‐Yi Gan, et al.. (2017). T cell receptor assessment in autoimmune disease requires access to the most adjacent immunologically active organ. Journal of Autoimmunity. 81. 24–33. 5 indexed citations
17.
Hu, Zhiqiang, Hamish S. Scott, Guangrong Qin, et al.. (2015). Revealing Missing Human Protein Isoforms Based on Ab Initio Prediction, RNA-seq and Proteomics. Scientific Reports. 5(1). 10940–10940. 22 indexed citations
18.
Gamble, Jennifer R., Wai Yan Sun, Xiaochun Li, et al.. (2009). Sphingosine Kinase-1 Associates with Integrin αVβ3 to Mediate Endothelial Cell Survival. American Journal Of Pathology. 175(5). 2217–2225. 16 indexed citations
19.
Dwivedi, Prem P., et al.. (1996). Transcriptional Synergism between Vitamin D-responsive Elements in the Rat 25-Hydroxyvitamin D3 24-Hydroxylase (CYP24) Promoter. Journal of Biological Chemistry. 271(47). 29715–29721. 99 indexed citations
20.
Hahn, Christopher N, et al.. (1993). Localization of the human vitamin D 24-hydroxylase gene (CYP24) to chromosome 20q13.2→q13.3. Cytogenetic and Genome Research. 62(4). 192–193. 20 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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