Hanxin Lin

2.7k total citations
39 papers, 1.3k citations indexed

About

Hanxin Lin is a scholar working on Genetics, Hematology and Genetics. According to data from OpenAlex, Hanxin Lin has authored 39 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 10 papers in Hematology and 9 papers in Genetics. Recurrent topics in Hanxin Lin's work include Myeloproliferative Neoplasms: Diagnosis and Treatment (8 papers), Acute Myeloid Leukemia Research (7 papers) and Genomics and Rare Diseases (7 papers). Hanxin Lin is often cited by papers focused on Myeloproliferative Neoplasms: Diagnosis and Treatment (8 papers), Acute Myeloid Leukemia Research (7 papers) and Genomics and Rare Diseases (7 papers). Hanxin Lin collaborates with scholars based in Canada, United States and China. Hanxin Lin's co-authors include Gurmit Singh, Katja Linher‐Melville, Bekim Sadiković, K. Andrew White, Peter Ainsworth, Xuesen Zhao, Erfan Aref‐Eshghi, Ju‐Tao Guo, Laila C. Schenkel and David I. Rodenhiser and has published in prestigious journals such as The EMBO Journal, Blood and PLoS ONE.

In The Last Decade

Hanxin Lin

35 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Hanxin Lin Canada	19	558	309	300	192	145	39	1.3k
Abul Bashar Mir Md. Khademul Islam Bangladesh	30	1.7k 3.0×	293 0.9×	227 0.8×	517 2.7×	76 0.5×	87	2.6k
Kuo Ping Chiu Singapore	11	1.4k 2.5×	296 1.0×	183 0.6×	290 1.5×	129 0.9×	17	1.9k
Juan José Berlanga Spain	25	1.4k 2.5×	165 0.5×	211 0.7×	87 0.5×	71 0.5×	40	2.1k
José Rivera Spain	16	911 1.6×	109 0.4×	159 0.5×	53 0.3×	109 0.8×	35	1.5k
Jung Mi Oh South Korea	6	974 1.7×	143 0.5×	369 1.2×	102 0.5×	57 0.4×	8	2.0k
Lan Chen China	21	606 1.1×	209 0.7×	106 0.4×	68 0.4×	51 0.4×	52	1.3k
Claudia Sievers Germany	11	1.3k 2.4×	116 0.4×	375 1.3×	214 1.1×	26 0.2×	19	1.9k
Jianli Dong United States	21	810 1.5×	98 0.3×	116 0.4×	237 1.2×	96 0.7×	57	1.4k
Chao Deng China	16	889 1.6×	77 0.2×	180 0.6×	169 0.9×	120 0.8×	47	1.6k
Keisuke Tabata Japan	18	750 1.3×	172 0.6×	44 0.1×	97 0.5×	90 0.6×	30	2.2k

Countries citing papers authored by Hanxin Lin

Since Specialization

Citations

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

Fields of papers citing papers by Hanxin Lin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hanxin Lin

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

All Works

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20 of 20 papers shown

Chin‐Yee, Benjamin, Ian Cheong, Michael A. Levy, et al.. (2022). Mutational Landscape of Patients Referred for Elevated Hemoglobin Level. Current Oncology. 29(10). 7209–7217.

Hsia, Cyrus C., Laila C. Schenkel, Benjamin D. Hedley, et al.. (2022). Clinical Utility of Implementing a Frontline NGS-Based DNA and RNA Fusion Panel Test for Patients with Suspected Myeloid Malignancies. Molecular Diagnosis & Therapy. 26(3). 333–343. 8 indexed citations

Chin‐Yee, Benjamin, Ian Cheong, Cyrus C. Hsia, et al.. (2022). A Rational Approach to JAK2 Mutation Testing in Patients with Elevated Hemoglobin: Results from the JAK2 Prediction Cohort (JAKPOT) Study. Journal of General Internal Medicine. 38(8). 1828–1833. 6 indexed citations

Feng, Biao, Saumik Biswas, Michael A. Levy, et al.. (2022). ANRIL regulates multiple molecules of pathogenetic significance in diabetic nephropathy. PLoS ONE. 17(8). e0270287–e0270287. 9 indexed citations

McCuaig, Jeanna, Kathleen Buckley, Kara Semotiuk, et al.. (2021). Incidental findings from cancer next generation sequencing panels. npj Genomic Medicine. 6(1). 63–63. 13 indexed citations

Li, Xinglin, et al.. (2021). Cell Entry of Animal Coronaviruses. Viruses. 13(10). 1977–1977. 15 indexed citations

Kawata, Eri, Benjamin D. Hedley, Benjamin Chin‐Yee, et al.. (2021). Reducing cytogenetic testing in the era of next generation sequencing: Are we choosing wisely?. International Journal of Laboratory Hematology. 44(2). 333–341. 2 indexed citations

Turashvili, Gulisa, et al.. (2021). Lynch Syndrome Screening of Women with Endometrial Cancer: Feasibility and Outcomes in a Community Program. Journal of Obstetrics and Gynaecology Canada. 44(2). 142–147. 1 indexed citations

Chin‐Yee, Benjamin, Ian Cheong, Cyrus C. Hsia, et al.. (2021). A Prediction Rule to Guide JAK2 Testing in Patients with Suspected Polycythemia Vera. Blood. 138(Supplement 1). 4635–4635.

10.

Levy, Michael A., Kathleen Rooney, Deanna Alexis Carere, et al.. (2021). Analysis of Sequence and Copy Number Variants in Canadian Patient Cohort With Familial Cancer Syndromes Using a Unique Next Generation Sequencing Based Approach. Frontiers in Genetics. 12. 698595–698595. 2 indexed citations

11.

Kawata, Eri, Alejandro Lazo‐Langner, Anargyros Xenocostas, et al.. (2020). Clinical value of next‐generation sequencing compared to cytogenetics in patients with suspected myelodysplastic syndrome. British Journal of Haematology. 192(4). 729–736. 8 indexed citations

12.

Aref‐Eshghi, Erfan, Danielle K. Bourque, Jennifer Kerkhof, et al.. (2019). Genome‐wide DNA methylation and RNA analyses enable reclassification of two variants of uncertain significance in a patient with clinical Kabuki syndrome. Human Mutation. 40(10). 1684–1689. 19 indexed citations

13.

Aref‐Eshghi, Erfan, David I. Rodenhiser, Laila C. Schenkel, et al.. (2018). Genomic DNA Methylation Signatures Enable Concurrent Diagnosis and Clinical Genetic Variant Classification in Neurodevelopmental Syndromes. The American Journal of Human Genetics. 102(1). 156–174. 90 indexed citations

14.

Aref‐Eshghi, Erfan, Laila C. Schenkel, Peter Ainsworth, et al.. (2018). Genomic DNA Methylation-Derived Algorithm Enables Accurate Detection of Malignant Prostate Tissues. Frontiers in Oncology. 8. 100–100. 34 indexed citations

15.

Schenkel, Laila C., Erfan Aref‐Eshghi, Cindy Skinner, et al.. (2018). Peripheral blood epi-signature of Claes-Jensen syndrome enables sensitive and specific identification of patients and healthy carriers with pathogenic mutations in KDM5C. Clinical Epigenetics. 10(1). 21–21. 35 indexed citations

16.

Aref‐Eshghi, Erfan, Laila C. Schenkel, Hanxin Lin, et al.. (2017). Clinical Validation of a Genome-Wide DNA Methylation Assay for Molecular Diagnosis of Imprinting Disorders. Journal of Molecular Diagnostics. 19(6). 848–856. 26 indexed citations

17.

Kerkhof, Jennifer, Laila C. Schenkel, Jack Reilly, et al.. (2017). Clinical Validation of Copy Number Variant Detection from Targeted Next-Generation Sequencing Panels. Journal of Molecular Diagnostics. 19(6). 905–920. 94 indexed citations

18.

Linher‐Melville, Katja, et al.. (2015). Expression of xCT and activity of system xc− are regulated by NRF2 in human breast cancer cells in response to oxidative stress. Redox Biology. 5. 33–42. 212 indexed citations

19.

Fazzari, Jennifer, et al.. (2015). Inhibitors of glutamate release from breast cancer cells; new targets for cancer-induced bone-pain. Scientific Reports. 5(1). 8380–8380. 40 indexed citations

20.

Lin, Hanxin & K. Andrew White. (2004). A complex network of RNA–RNA interactions controls subgenomic mRNA transcription in a tombusvirus. The EMBO Journal. 23(16). 3365–3374. 54 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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