Martin P. Powers

1.3k total citations · 1 hit paper
18 papers, 805 citations indexed

About

Martin P. Powers is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Martin P. Powers has authored 18 papers receiving a total of 805 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Cancer Research and 5 papers in Genetics. Recurrent topics in Martin P. Powers's work include Sarcoma Diagnosis and Treatment (4 papers), Cancer Genomics and Diagnostics (4 papers) and Glioma Diagnosis and Treatment (3 papers). Martin P. Powers is often cited by papers focused on Sarcoma Diagnosis and Treatment (4 papers), Cancer Genomics and Diagnostics (4 papers) and Glioma Diagnosis and Treatment (3 papers). Martin P. Powers collaborates with scholars based in United States, United Kingdom and Israel. Martin P. Powers's co-authors include Scott Topper, Keith Nykamp, Nila Patil, Michael J. Anderson, John Garcia, Yuya Kobayashi, Janita Thusberg, Blanca Herrera, M. Jody Westbrook and Yuan-Yuan Ho and has published in prestigious journals such as Journal of Clinical Oncology, Human Molecular Genetics and Journal of neurosurgery.

In The Last Decade

Martin P. Powers

18 papers receiving 792 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Sherloc: a comprehensive refinement of the ACMG–AMP variant classification criteria

2017 465 citations Keith Nykamp, Michael J. Anderson et al. Genetics in Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Martin P. Powers United States	11	349	292	137	133	97	18	805
Marios Kambouris United States	18	436 1.2×	430 1.5×	169 1.2×	286 2.2×	77 0.8×	50	1.3k
Minjie Luo United States	18	460 1.3×	306 1.0×	207 1.5×	158 1.2×	47 0.5×	65	1.0k
Isabelle Thiffault United States	23	822 2.4×	482 1.7×	96 0.7×	75 0.6×	73 0.8×	65	1.4k
Enrico Grosso Italy	18	436 1.2×	271 0.9×	85 0.6×	96 0.7×	223 2.3×	49	936
José‐Mario Capo‐Chichi Canada	14	515 1.5×	414 1.4×	120 0.9×	54 0.4×	40 0.4×	38	974
Prodipto Pal Canada	17	306 0.9×	213 0.7×	166 1.2×	388 2.9×	79 0.8×	49	956
Kristiina Avela Finland	17	633 1.8×	402 1.4×	132 1.0×	40 0.3×	68 0.7×	34	1.1k
Irene Bottillo Italy	18	531 1.5×	253 0.9×	74 0.5×	179 1.3×	29 0.3×	65	1.1k
Delphine Bacq France	10	522 1.5×	304 1.0×	151 1.1×	64 0.5×	32 0.3×	12	888
Caroline Michot France	16	395 1.1×	436 1.5×	42 0.3×	142 1.1×	58 0.6×	43	823

Countries citing papers authored by Martin P. Powers

Since Specialization

Citations

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

Fields of papers citing papers by Martin P. Powers

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Martin P. Powers. 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 Martin P. Powers. The network helps show where Martin P. Powers may publish in the future.

Co-authorship network of co-authors of Martin P. Powers

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

All Works

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18 of 18 papers shown

Rennert, Robert C., Martin P. Powers, Jeffrey A. Steinberg, et al.. (2019). Histology of the vertebral artery–dural junction: relevance to posterolateral approaches to the skull base. Journal of neurosurgery. 134(1). 131–136. 2 indexed citations

Troll, Christopher J., Nicholas H. Putnam, Paul D. Hartley, et al.. (2018). Structural Variation Detection by Proximity Ligation from Formalin-Fixed, Paraffin-Embedded Tumor Tissue. Journal of Molecular Diagnostics. 21(3). 375–383. 8 indexed citations

Nykamp, Keith, Michael J. Anderson, Martin P. Powers, et al.. (2017). Sherloc: a comprehensive refinement of the ACMG–AMP variant classification criteria. Genetics in Medicine. 19(10). 1105–1117. 465 indexed citations breakdown →

Nicolosi, Piper, Scott T. Michalski, Erin O’Leary, et al.. (2017). Need for re-evaluation of current guidelines based on results from germline genetic testing in prostate cancer.. Journal of Clinical Oncology. 35(15_suppl). 5009–5009. 4 indexed citations

Friedman, Eitan, Noa Efrat, Lior Soussan‐Gutman, et al.. (2015). Low-level constitutional mosaicism of a de novoBRCA1 gene mutation. British Journal of Cancer. 112(4). 765–768. 21 indexed citations

Shulman, Joshua M., Selina Imboywa, Νικόλαος Γιαγτζόγλου, et al.. (2013). Functional screening in Drosophila identifies Alzheimer's disease susceptibility genes and implicates Tau-mediated mechanisms. Human Molecular Genetics. 23(4). 870–877. 118 indexed citations

Pua, Heather H., Jessica Farrell, Marta Margeta, et al.. (2013). Novel interstitial 2.6 Mb deletion on 9q21 associated with multiple congenital anomalies. American Journal of Medical Genetics Part A. 164(1). 237–242. 10 indexed citations

Felicella, Michelle M., Jill Hagenkord, Shera Kash, et al.. (2012). A common 8q (MYC) amplification detected in a multifocal anaplastic astrocytoma by SNP array karyotyping. Clinical Neuropathology. 31(7). 210–215. 4 indexed citations

Hiniker, Annie, Jill Hagenkord, Martin P. Powers, et al.. (2012). Gliosarcoma arising from an oligodendroglioma (oligosarcoma). Clinical Neuropathology. 32(5). 165–170. 18 indexed citations

10.

French, Deborah, Andrew J. Smith, Martin P. Powers, & Alan H.B. Wu. (2011). KRAS mutation detection in colorectal cancer by a commercially available gene chip array compares well with Sanger sequencing. Clinica Chimica Acta. 412(17-18). 1578–1581. 12 indexed citations

11.

Powers, Martin P., Karla Alvarez, Hyun‐Jung Kim, & Federico A. Monzon. (2011). Molecular Classification of Adult Renal Epithelial Neoplasms Using MicroRNA Expression and Virtual Karyotyping. Diagnostic Molecular Pathology. 20(2). 63–70. 22 indexed citations

12.

Powers, Martin P., et al.. (2011). Sarcoma arising as a distinct nodule within glioblastoma: a morphological and molecular perspective on gliosarcoma. Journal of Neuro-Oncology. 105(2). 317–323. 5 indexed citations

13.

Powers, Martin P., Wei Zhang, Dolores López‐Terrada, Bogdan Czerniak, & Alexander J. Lazar. (2011). The molecular pathology of sarcomas. Cancer Biomarkers. 9(1-6). 475–491. 14 indexed citations

14.

Olar, Adriana, et al.. (2010). Myxoid liposarcoma: A case report of a sentinel metastasis to the parotid gland with molecular confirmation. Diagnostic Cytopathology. 39(10). 780–783. 1 indexed citations

15.

Powers, Martin P., et al.. (2010). Detection of myxoid liposarcoma-associated FUS–DDIT3 rearrangement variants including a newly identified breakpoint using an optimized RT-PCR assay. Modern Pathology. 23(10). 1307–1315. 61 indexed citations

16.

Ahmed, Arsalan, Martin P. Powers, Keith A. Youker, et al.. (2009). Mast cell burden and reticulin fibrosis in the myeloproliferative neoplasms: A computer-assisted image analysis study. Pathology - Research and Practice. 205(9). 634–638. 10 indexed citations

17.

Powers, Martin P., et al.. (2007). Polymorphisms in TGFbeta and TNFalpha are associated with the myelodysplastic syndrome phenotype.. Archives of Pathology & Laboratory Medicine. 131(12). 1789–93. 15 indexed citations

18.

Powers, Martin P., et al.. (2007). Polymorphisms in TGFβ and TNFα Are Associated With the Myelodysplastic Syndrome Phenotype. Archives of Pathology & Laboratory Medicine. 131(12). 1789–1793. 15 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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