Michael J. Hafez

1.6k total citations
24 papers, 1.2k citations indexed

About

Michael J. Hafez is a scholar working on Hematology, Molecular Biology and Cancer Research. According to data from OpenAlex, Michael J. Hafez has authored 24 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Hematology, 7 papers in Molecular Biology and 7 papers in Cancer Research. Recurrent topics in Michael J. Hafez's work include Acute Myeloid Leukemia Research (6 papers), Prenatal Screening and Diagnostics (5 papers) and Cancer Genomics and Diagnostics (5 papers). Michael J. Hafez is often cited by papers focused on Acute Myeloid Leukemia Research (6 papers), Prenatal Screening and Diagnostics (5 papers) and Cancer Genomics and Diagnostics (5 papers). Michael J. Hafez collaborates with scholars based in United States, Taiwan and Canada. Michael J. Hafez's co-authors include James R. Eshleman, Kathleen M. Murphy, Kathleen M. Murphy, Christopher D. Gocke, Karin D. Berg, Alexis Norris-Kirby, Athanasios C. Tsiatis, Tanya Geiger, Russell Vang and Thomas G. McConnell and has published in prestigious journals such as Journal of Clinical Oncology, Cancer Research and British Journal of Cancer.

In The Last Decade

Michael J. Hafez

24 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michael J. Hafez United States 12 393 299 295 278 272 24 1.2k
Caroline M. Bateman Australia 12 359 0.9× 331 1.1× 302 1.0× 67 0.2× 131 0.5× 23 1.0k
Albert N. Békássy Sweden 18 249 0.6× 78 0.3× 244 0.8× 108 0.4× 96 0.4× 36 1.1k
Ester Mejstříková Czechia 25 349 0.9× 87 0.3× 192 0.7× 155 0.6× 188 0.7× 68 1.4k
Robert Wasserman United States 18 545 1.4× 90 0.3× 344 1.2× 177 0.6× 70 0.3× 35 1.8k
Rajive Kumar India 19 351 0.9× 83 0.3× 146 0.5× 147 0.5× 62 0.2× 96 973
Ondřej Hrušák Czechia 23 384 1.0× 84 0.3× 190 0.6× 172 0.6× 265 1.0× 82 1.5k
Lara Mussolin Italy 20 409 1.0× 375 1.3× 337 1.1× 610 2.2× 84 0.3× 73 1.2k
Mark Tein United Kingdom 5 634 1.6× 326 1.1× 112 0.4× 92 0.3× 1.4k 5.0× 5 1.9k
Andreas Willer Germany 18 428 1.1× 156 0.5× 326 1.1× 102 0.4× 32 0.1× 37 1.1k
Barbara Buldini Italy 19 274 0.7× 81 0.3× 196 0.7× 159 0.6× 219 0.8× 56 1.2k

Countries citing papers authored by Michael J. Hafez

Since Specialization
Citations

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

Fields of papers citing papers by Michael J. Hafez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael J. Hafez. 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 Michael J. Hafez. The network helps show where Michael J. Hafez may publish in the future.

Co-authorship network of co-authors of Michael J. Hafez

This figure shows the co-authorship network connecting the top 25 collaborators of Michael J. Hafez. A scholar is included among the top collaborators of Michael J. Hafez 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 Michael J. Hafez. Michael J. Hafez 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.
Shackelford, Rodney E., et al.. (2013). Liquid Bead Array Technology in the Detection of Common Translocations in Acute and Chronic Leukemias. Methods in molecular biology. 999. 93–103. 3 indexed citations
2.
Yoon, Harry H., Paul J. Catalano, Kathleen M. Murphy, et al.. (2011). Genetic variation in DNA-repair pathways and response to radiochemotherapy in esophageal adenocarcinoma: a retrospective cohort study of the Eastern Cooperative Oncology Group. BMC Cancer. 11(1). 176–176. 20 indexed citations
3.
Lin, Ming‐Tseh, Li‐Hui Tseng, Michael J. Hafez, et al.. (2011). Δ-PCR, A Simple Method to Detect Translocations and Insertion/Deletion Mutations. Journal of Molecular Diagnostics. 13(1). 85–92. 19 indexed citations
4.
5.
Lin, Ming‐Tseh, Li‐Hui Tseng, Katie Beierl, et al.. (2011). Analysis of Hematopoietic Stem Cell Transplant Engraftment. Diagnostic Molecular Pathology. 20(4). 194–202. 3 indexed citations
6.
Tsiatis, Athanasios C., Alexis Norris-Kirby, Michael J. Hafez, et al.. (2010). Comparison of Sanger Sequencing, Pyrosequencing, and Melting Curve Analysis for the Detection of KRAS Mutations. Journal of Molecular Diagnostics. 12(4). 425–432. 368 indexed citations
7.
Hafez, Michael J., et al.. (2010). Performance and Clinical Evaluation of a Sensitive Multiplex Assay for the Rapid Detection of Common NPM1 Mutations. Journal of Molecular Diagnostics. 12(5). 629–635. 14 indexed citations
8.
Tsiatis, Athanasios C., Michael J. Hafez, Anne Jedlicka, et al.. (2010). Abstract 1781: Use of SNP arrays to assess loss of heterozygosity in gliomas. Cancer Research. 70(8_Supplement). 1781–1781. 1 indexed citations
9.
Murphy, Kathleen M., Thomas G. McConnell, Michael J. Hafez, Russell Vang, & Brigitte M. Ronnett. (2009). Molecular Genotyping of Hydatidiform Moles. Journal of Molecular Diagnostics. 11(6). 598–605. 64 indexed citations
10.
McConnell, Thomas G., Kathleen M. Murphy, Michael J. Hafez, Russell Vang, & Brigitte M. Ronnett. (2009). Diagnosis and Subclassification of Hydatidiform Moles Using p57 Immunohistochemistry and Molecular Genotyping: Validation and Prospective Analysis in Routine and Consultation Practice Settings With Development of an Algorithmic Approach. The American Journal of Surgical Pathology. 33(6). 805–817. 87 indexed citations
11.
12.
Hafez, Michael J., et al.. (2008). Application of Traditional Clinical Pathology Quality Control Techniques to Molecular Pathology. Journal of Molecular Diagnostics. 10(2). 142–146. 9 indexed citations
13.
Lin, Ming‐Tseh, Michael J. Hafez, Li‐Hui Tseng, et al.. (2007). A Molecular Fraction Collecting Tool for the ABI 310 Automated Sequencer. Journal of Molecular Diagnostics. 9(5). 598–603. 9 indexed citations
14.
Murphy, Kathleen M., Shengle Zhang, Tanya Geiger, et al.. (2006). Comparison of the Microsatellite Instability Analysis System and the Bethesda Panel for the Determination of Microsatellite Instability in Colorectal Cancers. Journal of Molecular Diagnostics. 8(3). 305–311. 199 indexed citations
15.
Swierczynski, Sharon L., et al.. (2005). Bone Marrow Engraftment Analysis after Granulocyte Transfusion. Journal of Molecular Diagnostics. 7(3). 422–426. 6 indexed citations
16.
Murphy, Kathleen M., et al.. (2005). Capillary Electrophoresis Artifact Due to Eosin. Journal of Molecular Diagnostics. 7(1). 143–148. 11 indexed citations
17.
Murphy, Kathleen M., Tanya Geiger, Michael J. Hafez, et al.. (2003). A Single Nucleotide Primer Extension Assay to Detect the APC I1307K Gene Variant. Journal of Molecular Diagnostics. 5(4). 222–226. 13 indexed citations
18.
Murphy, Kathleen M., et al.. (2003). Evaluation of Temperature Gradient Capillary Electrophoresis for Detection of the Factor V Leiden Mutation. Molecular Diagnosis. 7(1). 35–40. 13 indexed citations
19.
Murphy, Kathleen M., Mark J. Levis, Michael J. Hafez, et al.. (2003). Detection of FLT3 Internal Tandem Duplication and D835 Mutations by a Multiplex Polymerase Chain Reaction and Capillary Electrophoresis Assay. Journal of Molecular Diagnostics. 5(2). 96–102. 147 indexed citations
20.
Antonarakis, Stylianos E., Michael B. Petersen, Melvin G. McInnis, et al.. (1992). The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms. PubMed. 50(3). 544–50. 150 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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