Martin Moorhead

5.2k total citations
31 papers, 1.8k citations indexed

About

Martin Moorhead is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Martin Moorhead has authored 31 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 10 papers in Genetics and 8 papers in Hematology. Recurrent topics in Martin Moorhead's work include Cancer Genomics and Diagnostics (7 papers), Multiple Myeloma Research and Treatments (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Martin Moorhead is often cited by papers focused on Cancer Genomics and Diagnostics (7 papers), Multiple Myeloma Research and Treatments (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Martin Moorhead collaborates with scholars based in United States, Japan and Singapore. Martin Moorhead's co-authors include Malek Faham, Jianbiao Zheng, Victoria Carlton, T. D. Willis, Dario Campana, Patricia Stow, Elaine Coustan‐Smith, Ching‐Hon Pui, François Pépin and Katherine A. Kong and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Journal of Clinical Oncology.

In The Last Decade

Martin Moorhead

31 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martin Moorhead United States 18 577 493 445 389 383 31 1.8k
Todd W. Kelley United States 26 707 1.2× 341 0.7× 119 0.3× 325 0.8× 426 1.1× 68 2.0k
Peter Papenhausen United States 20 872 1.5× 205 0.4× 706 1.6× 234 0.6× 335 0.9× 63 1.8k
Linda B. Baughn United States 18 699 1.2× 163 0.3× 206 0.5× 363 0.9× 617 1.6× 101 1.4k
Shareef Nahas United States 22 1.0k 1.8× 153 0.3× 570 1.3× 238 0.6× 360 0.9× 43 1.8k
Tobias Menne United Kingdom 19 1.3k 2.2× 254 0.5× 539 1.2× 493 1.3× 659 1.7× 69 2.6k
K Michalová Czechia 26 844 1.5× 211 0.4× 262 0.6× 217 0.6× 1.1k 2.8× 171 2.1k
Samuli Eldfors Finland 16 403 0.7× 273 0.6× 114 0.3× 239 0.6× 286 0.7× 41 1.0k
Anne Hinks United Kingdom 28 559 1.0× 224 0.5× 593 1.3× 201 0.5× 517 1.3× 46 2.3k
Douglas Tkachuk United States 14 1.1k 2.0× 189 0.4× 327 0.7× 245 0.6× 734 1.9× 17 2.0k
Gerald Wertheim United States 23 618 1.1× 105 0.2× 170 0.4× 523 1.3× 405 1.1× 83 1.5k

Countries citing papers authored by Martin Moorhead

Since Specialization
Citations

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

Fields of papers citing papers by Martin Moorhead

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martin Moorhead

This figure shows the co-authorship network connecting the top 25 collaborators of Martin Moorhead. A scholar is included among the top collaborators of Martin Moorhead 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 Moorhead. Martin Moorhead 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.
Stowe, T. D., Andrew L. Young, John McLaughlin, et al.. (2022). Cell-Selective Adeno-Associated Virus-Mediated SCN1A Gene Regulation Therapy Rescues Mortality and Seizure Phenotypes in a Dravet Syndrome Mouse Model and Is Well Tolerated in Nonhuman Primates. Human Gene Therapy. 33(11-12). 579–597. 68 indexed citations
2.
Takezako, Naoki, Jianbiao Zheng, Martin Moorhead, et al.. (2017). Prognostic value of sequencing-based minimal residual disease detection in patients with multiple myeloma who underwent autologous stem-cell transplantation. Annals of Oncology. 28(10). 2503–2510. 33 indexed citations
3.
Faham, Malek, Victoria Carlton, Martin Moorhead, et al.. (2016). Discovery of T Cell Receptor β Motifs Specific to HLA–B27–Positive Ankylosing Spondylitis by Deep Repertoire Sequence Analysis. Arthritis & Rheumatology. 69(4). 774–784. 71 indexed citations
4.
Takamatsu, Hiroyuki, Jianbiao Zheng, Martin Moorhead, et al.. (2015). Prognostic Value of Sequencing-Based Minimal Residual Disease Detection in Patients with Multiple Myeloma Who Underwent Autologous Stem Cell Transplantation. Blood. 126(23). 1788–1788. 3 indexed citations
5.
Klinger, Mark, François Pépin, Tobias Wittkop, et al.. (2015). Multiplex Identification of Antigen-Specific T Cell Receptors Using a Combination of Immune Assays and Immune Receptor Sequencing. PLoS ONE. 10(10). e0141561–e0141561. 74 indexed citations
6.
Takamatsu, Hiroyuki, Jianbiao Zheng, Martin Moorhead, et al.. (2015). A Comparison of Minimal Residual Disease Detection Among ASO-PCR, Dd-PCR and Deep-Sequencing in Patients with Multiple Myeloma Who Underwent Autologous Stem Cell Transplantation. Blood. 126(23). 1782–1782. 1 indexed citations
7.
Roschewski, Mark, Kieron Dunleavy, Stefania Pittaluga, et al.. (2015). Circulating tumour DNA and CT monitoring in patients with untreated diffuse large B-cell lymphoma: a correlative biomarker study. The Lancet Oncology. 16(5). 541–549. 307 indexed citations
8.
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
9.
Logan, Aaron C., Malek Faham, Victoria Carlton, et al.. (2014). Immunoglobulin and T Cell Receptor Gene High-Throughput Sequencing Quantifies Minimal Residual Disease in Acute Lymphoblastic Leukemia and Predicts Post-Transplantation Relapse and Survival. Biology of Blood and Marrow Transplantation. 20(9). 1307–1313. 101 indexed citations
10.
Klinger, Mark, Katherine A. Kong, Martin Moorhead, et al.. (2013). Combining Next-Generation Sequencing and Immune Assays: A Novel Method for Identification of Antigen-Specific T Cells. PLoS ONE. 8(9). e74231–e74231. 29 indexed citations
11.
Logan, Aaron C., Bing Zhang, Balasubramanian Narasimhan, et al.. (2013). Minimal residual disease quantification using consensus primers and high-throughput IGH sequencing predicts post-transplant relapse in chronic lymphocytic leukemia. Leukemia. 27(8). 1659–1665. 96 indexed citations
12.
Faham, Malek, Jianbiao Zheng, Martin Moorhead, et al.. (2012). Deep Sequencing Approach for Minimal Residual Disease Detection in Acute Lymphoblastic Leukemia. Blood. 120(21). 1388–1388. 10 indexed citations
13.
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
14.
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
15.
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
16.
Zheng, Jianbiao, Eugeni Namsaraev, Victoria Carlton, et al.. (2008). Rapid identification of somatic mutations in colorectal and breast cancer tissues using mismatch repair detection (MRD). Human Mutation. 29(3). 441–450. 20 indexed citations
17.
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
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.
Clayton, David, Neil Walker, Deborah J. Smyth, et al.. (2005). Population structure, differential bias and genomic control in a large-scale, case-control association study. Nature Genetics. 37(11). 1243–1246. 354 indexed citations
20.
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

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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