Malek Faham

8.9k total citations
92 papers, 4.2k citations indexed

About

Malek Faham is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Cancer Research. According to data from OpenAlex, Malek Faham has authored 92 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 31 papers in Pathology and Forensic Medicine and 27 papers in Cancer Research. Recurrent topics in Malek Faham's work include Cancer Genomics and Diagnostics (27 papers), Lymphoma Diagnosis and Treatment (24 papers) and Chronic Lymphocytic Leukemia Research (15 papers). Malek Faham is often cited by papers focused on Cancer Genomics and Diagnostics (27 papers), Lymphoma Diagnosis and Treatment (24 papers) and Chronic Lymphocytic Leukemia Research (15 papers). Malek Faham collaborates with scholars based in United States, France and Japan. Malek Faham's co-authors include Martin Moorhead, Jianbiao Zheng, Victoria Carlton, Mark Klinger, David R. Cox, R Myers, Deepti Bhat, Nila Patil, Andrew S. Peterson and Lawrence Fong and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Malek Faham

90 papers receiving 4.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Malek Faham United States 27 1.5k 1.2k 943 826 748 92 4.2k
Finbarr E. Cotter United Kingdom 38 2.6k 1.8× 1.3k 1.1× 1.2k 1.2× 505 0.6× 331 0.4× 111 5.0k
Takuro Nakamura Japan 42 3.9k 2.6× 1.9k 1.6× 438 0.5× 606 0.7× 555 0.7× 214 7.1k
Ruth Rimokh France 39 3.1k 2.1× 1.3k 1.1× 1.1k 1.1× 282 0.3× 849 1.1× 105 5.1k
José I. Martı́n-Subero Spain 43 2.9k 2.0× 1.3k 1.1× 2.0k 2.1× 654 0.8× 1.3k 1.7× 147 5.7k
Svetlana Pack United States 47 3.1k 2.1× 1.5k 1.3× 690 0.7× 1.1k 1.3× 1.1k 1.4× 130 6.5k
Jamison L. Nourse United States 24 2.9k 1.9× 1.3k 1.1× 354 0.4× 323 0.4× 315 0.4× 36 4.5k
Bill H. Chang United States 28 1.9k 1.3× 645 0.5× 243 0.3× 332 0.4× 424 0.6× 76 3.2k
Jos Domen United States 33 3.6k 2.4× 1.8k 1.6× 1.3k 1.4× 515 0.6× 330 0.4× 51 6.3k
Cristina Montagna United States 36 3.0k 2.0× 1.4k 1.2× 413 0.4× 811 1.0× 756 1.0× 124 4.8k
Rafael Espinosa United States 35 2.7k 1.8× 559 0.5× 286 0.3× 777 0.9× 329 0.4× 67 4.9k

Countries citing papers authored by Malek Faham

Since Specialization
Citations

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

Fields of papers citing papers by Malek Faham

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Malek Faham

This figure shows the co-authorship network connecting the top 25 collaborators of Malek Faham. A scholar is included among the top collaborators of Malek Faham 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 Malek Faham. Malek Faham 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.
Liu, Tao, Antonella Bacchiocchi, Mengxing Li, et al.. (2024). Ultra-sensitive molecular residual disease detection through whole genome sequencing with single-read error correction. EMBO Molecular Medicine. 16(9). 2188–2209. 4 indexed citations
2.
Oh, David Y., Jason Cham, Li Zhang, et al.. (2016). Immune Toxicities Elicted by CTLA-4 Blockade in Cancer Patients Are Associated with Early Diversification of the T-cell Repertoire. Cancer Research. 77(6). 1322–1330. 173 indexed citations
3.
Munshi, Nikhil C., Joaquín Martínez‐López, Victoria Carlton, et al.. (2016). A Novel Evolutionary Pattern Revealed Using Deep Sequencing of Immunoglobulin Loci at Diagnosis and over the Course of Treatment in Multiple Myeloma Patients. Blood. 128(22). 238–238. 2 indexed citations
4.
Oh, David Y., Jason Cham, Li Zhang, et al.. (2016). Association between T cell repertoire diversification and both clinical response as well as toxicity following immune checkpoint blockade in metastatic cancer patients.. Journal of Clinical Oncology. 34(15_suppl). 3029–3029. 3 indexed citations
5.
Klinger, Mark, Jianbiao Zheng, Kojo S.J. Elenitoba‐Johnson, et al.. (2015). Next-generation IgVH sequencing CLL-like monoclonal B-cell lymphocytosis reveals frequent oligoclonality and ongoing hypermutation. Leukemia. 30(5). 1055–1061. 15 indexed citations
6.
Takamatsu, Hiroyuki, Jianbiao Zheng, Martin Moorhead, et al.. (2014). Prognostic Value of Sequencing-Based Minimal Residual Disease Detection in Multiple Myeloma. Blood. 124(21). 2003–2003. 2 indexed citations
7.
Green, Michael R., Scott V. Bratman, Chih Long Liu, et al.. (2013). Utility Of Non-Invasive Monitoring Of Circulating Tumor DNA At Diagnosis, Interim Therapy, and Relapse Of DLBCL Using High-Throughput Sequencing Of Immunoglobulin Genes. Blood. 122(21). 4264–4264. 2 indexed citations
8.
Roschewski, Mark, Stefania Pittaluga, Kieron Dunleavy, et al.. (2013). DNA Sequencing-Based Monitoring Of Serum Predicts Clinical Relapse Before CT Imaging in Diffuse Large B-Cell Lymphoma. Blood. 122(21). 1767–1767. 3 indexed citations
9.
Rezvani, Katayoun, Joshua Brody, Holbrook E. Kohrt, et al.. (2012). Cancer Vaccines and T Cell Therapy. Biology of Blood and Marrow Transplantation. 19(1). S97–S101. 8 indexed citations
10.
Faham, Malek, Joshua Brody, Holbrook E. Kohrt, et al.. (2012). Deep B and T Cell Repertoire Sequencing to Evaluate Minimal Residual Disease and T Cell Responses in a Therapeutic Vaccine Trial for Mantle Cell Lymphoma. Blood. 120(21). 582–582. 3 indexed citations
11.
Sadanandam, Anguraj, Steffen Durinck, Shivani Nautiyal, et al.. (2010). Prediction of epigenetically regulated genes in breast cancer cell lines. BMC Bioinformatics. 11(1). 305–305. 31 indexed citations
12.
Zhang, Li, Martin Moorhead, Zhigang C. Wang, et al.. (2009). High quality copy number and genotype data from FFPE samples using Molecular Inversion Probe (MIP) microarrays. SHILAP Revista de lepidopterología. 79 indexed citations
13.
Schiffman, Joshua D., Yuker Wang, Lisa McPherson, et al.. (2009). Molecular inversion probes reveal patterns of 9p21 deletion and copy number aberrations in childhood leukemia. Cancer Genetics and Cytogenetics. 193(1). 9–18. 31 indexed citations
14.
Wang, Yuker, Martin Moorhead, George Karlin‐Neumann, et al.. (2008). Performance of Molecular Inversion Probes (MIP) in Allele Copy Number Determination. eScholarship (California Digital Library). 1 indexed citations
15.
Press, Joshua Z., Alessandro De Luca, Niki Boyd, et al.. (2008). Ovarian carcinomas with genetic and epigenetic BRCA1 loss have distinct molecular abnormalities. BMC Cancer. 8(1). 17–17. 210 indexed citations
16.
Wang, Yuker, Martin Moorhead, George Karlin‐Neumann, et al.. (2007). Analysis of molecular inversion probe performance for allele copy number determination. Genome biology. 8(11). R246–R246. 55 indexed citations
17.
Ji, Hanlee P., Jochen Kumm, Michael Zhang, et al.. (2006). Molecular Inversion Probe Analysis of Gene Copy Alterations Reveals Distinct Categories of Colorectal Carcinoma. Cancer Research. 66(16). 7910–7919. 21 indexed citations
18.
Wang, Yuker, et al.. (2006). Copy number analysis and allele quantitation by Molecular Inversion Probe (MIP) on GeneChip arrays. Cancer Research. 66. 990–990. 1 indexed citations
19.
Fakhrai-Rad, Hossein, Jianbiao Zheng, T. D. Willis, et al.. (2004). SNP Discovery in Pooled Samples With Mismatch Repair Detection. Genome Research. 14(7). 1404–1412. 22 indexed citations
20.
Patil, Nila, David R. Cox, Deepti Bhat, et al.. (1995). A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation. Nature Genetics. 11(2). 126–129. 437 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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