Robert M. Gemmill

7.7k total citations · 1 hit paper
116 papers, 6.2k citations indexed

About

Robert M. Gemmill is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Robert M. Gemmill has authored 116 papers receiving a total of 6.2k indexed citations (citations by other indexed papers that have themselves been cited), including 88 papers in Molecular Biology, 38 papers in Genetics and 21 papers in Oncology. Recurrent topics in Robert M. Gemmill's work include Genomic variations and chromosomal abnormalities (16 papers), Cancer-related gene regulation (14 papers) and RNA modifications and cancer (13 papers). Robert M. Gemmill is often cited by papers focused on Genomic variations and chromosomal abnormalities (16 papers), Cancer-related gene regulation (14 papers) and RNA modifications and cancer (13 papers). Robert M. Gemmill collaborates with scholars based in United States, France and Japan. Robert M. Gemmill's co-authors include Harry A. Drabkin, Wilbur A. Franklin, Joëlle Roche, Anna E. Barón, Patrick Nasarre, James West, Joseph M. Calvo, Ferenc Boldog, Claude Turc‐Carel and A.A. Sandberg and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Genetics.

In The Last Decade

Robert M. Gemmill

116 papers receiving 6.1k citations

Hit Papers

Cloning of the SCA7 gene reveals a highly unstable CAG re... 1997 2026 2006 2016 1997 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert M. Gemmill United States 45 4.5k 1.4k 1.1k 1.0k 1.0k 116 6.2k
Kentaro Semba Japan 42 4.6k 1.0× 3.0k 2.1× 723 0.6× 501 0.5× 1.0k 1.0× 143 7.8k
Waldemar Debinski United States 45 2.5k 0.5× 1.6k 1.1× 565 0.5× 955 0.9× 706 0.7× 174 6.6k
David F. Barker United States 33 2.7k 0.6× 1.3k 0.9× 1.4k 1.3× 1.5k 1.5× 703 0.7× 77 6.5k
Barbara J. Graves United States 41 6.0k 1.3× 1.0k 0.7× 1.1k 0.9× 269 0.3× 780 0.8× 72 7.8k
Ji‐Ying Song Netherlands 41 3.0k 0.7× 2.5k 1.7× 528 0.5× 473 0.5× 841 0.8× 120 6.0k
Astar Winoto United States 45 4.7k 1.0× 1.7k 1.2× 721 0.6× 1.2k 1.1× 873 0.9× 83 8.3k
Sebastian Nijman Austria 26 5.7k 1.3× 1.7k 1.2× 710 0.6× 426 0.4× 1.4k 1.4× 40 7.3k
Keith C. Robbins United States 48 5.1k 1.1× 1.8k 1.3× 1.5k 1.3× 276 0.3× 797 0.8× 94 8.1k
Kurt Ballmer‐Hofer Switzerland 40 3.7k 0.8× 1.5k 1.1× 437 0.4× 544 0.5× 663 0.7× 96 5.4k
Ruth H. Palmer Sweden 41 3.1k 0.7× 1.3k 0.9× 312 0.3× 623 0.6× 728 0.7× 121 5.4k

Countries citing papers authored by Robert M. Gemmill

Since Specialization
Citations

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

Fields of papers citing papers by Robert M. Gemmill

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert M. Gemmill. 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 Robert M. Gemmill. The network helps show where Robert M. Gemmill may publish in the future.

Co-authorship network of co-authors of Robert M. Gemmill

This figure shows the co-authorship network connecting the top 25 collaborators of Robert M. Gemmill. A scholar is included among the top collaborators of Robert M. Gemmill 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 Robert M. Gemmill. Robert M. Gemmill 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.
Drabkin, Harry, Patrick Nasarre, & Robert M. Gemmill. (2014). The emerging role of class-3 semaphorins and their neuropilin receptors in oncology. OncoTargets and Therapy. 7. 1663–1663. 69 indexed citations
2.
Nasarre, Patrick, Robert M. Gemmill, Vincent Potiron, et al.. (2013). Neuropilin-2 Is Upregulated in Lung Cancer Cells during TGF-β1–Induced Epithelial–Mesenchymal Transition. Cancer Research. 73(23). 7111–7121. 55 indexed citations
3.
Chakravarty, Swapnajit, Wei-Cheng Lai, Yi Zou, et al.. (2012). Multiplexed specific label-free detection of NCI-H358 lung cancer cell line lysates with silicon based photonic crystal microcavity biosensors. Biosensors and Bioelectronics. 43. 50–55. 74 indexed citations
4.
Brauweiler, Anne, et al.. (2010). The TRC8 Ubiquitin Ligase Is Sterol Regulated and Interacts with Lipid and Protein Biosynthetic Pathways. Molecular Cancer Research. 8(1). 93–106. 61 indexed citations
5.
Sheridan, Molly B., Takema Kato, Chad Haldeman‐Englert, et al.. (2010). A Palindrome-Mediated Recurrent Translocation with 3:1 Meiotic Nondisjunction: The t(8;22)(q24.13;q11.21). The American Journal of Human Genetics. 87(2). 209–218. 48 indexed citations
6.
Stagg, Helen R., Mair Thomas, Emmanuel J. H. J. Wiertz, et al.. (2009). The TRC8 E3 ligase ubiquitinates MHC class I molecules before dislocation from the ER. The Journal of Cell Biology. 186(5). 685–692. 123 indexed citations
7.
Potiron, Vincent, Girish Sharma, Patrick Nasarre, et al.. (2007). Semaphorin SEMA3F Affects Multiple Signaling Pathways in Lung Cancer Cells. Cancer Research. 67(18). 8708–8715. 67 indexed citations
8.
Sugita, Michio, Jerry Haney, Robert M. Gemmill, & Wilbur A. Franklin. (2001). One-Step Duplex Reverse Transcription–Polymerase Chain Reaction for Quantitative Assessment of RNA Degradation. Analytical Biochemistry. 295(1). 113–116. 9 indexed citations
9.
Varella-Garcia, M., et al.. (1998). Chromosomal duplication accompanies allelic loss in non-small cell lung carcinoma.. PubMed. 58(20). 4701–7. 42 indexed citations
10.
Beau, Michelle M. Le, Harry A. Drabkin, Thomas W. Glover, et al.. (1998). AnFHIT tumor suppressor gene?. Genes Chromosomes and Cancer. 21(4). 281–289. 67 indexed citations
11.
Boldog, Ferenc, Robert M. Gemmill, James West, et al.. (1997). Chromosome 3p14 Homozygous Deletions and Sequence Analysis of FRA3B. Human Molecular Genetics. 6(2). 193–203. 117 indexed citations
12.
David, Gilles, Paola Giunti, N. Abbas, et al.. (1996). The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locus.. PubMed. 59(6). 1328–36. 52 indexed citations
13.
Todd, S., et al.. (1995). YAC contigs covering an 8-megabase region of 3p deleted in the small-cell lung cancer cell line U2020. Genomics. 25(1). 19–28. 13 indexed citations
14.
Klauck, Sabine M., Jeanne B. Lawrence, John A. McNeil, et al.. (1994). Cytogenetic and fluorescence in situ hybridization studies on sporadic and hereditary tumors associated with von Hippel-Lindau syndrome (VHL). Cancer Genetics and Cytogenetics. 77(1). 1–13. 13 indexed citations
15.
Wilke, Charles M., Bryan K. Hall, Ferenc Boldog, et al.. (1994). Multicolor FISH Mapping of YAC Clones in 3p14 and Identification of a YAC Spanning both FRA3B and the t(3;8) Associated with Hereditary Renal Cell Carcinoma. Genomics. 22(2). 319–326. 59 indexed citations
16.
Longfield, Jenice N., John F. Brundage, Gary J. Badger, et al.. (1994). Look-Back Investigation after Human Immunodeficiency Virus Seroconversion in a Pediatric Dentist. The Journal of Infectious Diseases. 169(1). 1–8. 8 indexed citations
17.
Gemmill, Robert M., et al.. (1989). A 1.5-Megabase restriction map surrounding MYC does not include the translocation breakpoint in familial renal cell carcinoma. Genomics. 4(1). 28–35. 16 indexed citations
18.
Gemmill, Robert M., et al.. (1989). Loss of heterozygosity on 3p in a renal cell carcinoma in von Hippel-Lindau syndrome. Cancer Genetics and Cytogenetics. 39(2). 289–293. 21 indexed citations
19.
Tajara, Eloíza H., Carol Berger, Barbara K. Hecht, et al.. (1988). Loss of common 3p14 fragile site expression in renal cell carcinoma with deletion breakpoint at 3p14. Cancer Genetics and Cytogenetics. 31(1). 75–82. 12 indexed citations
20.
Gemmill, Robert M., et al.. (1987). Construction of long-range restriction maps in human DNA using pulsed field gel electrophoresis. PubMed. 4(6). 119–131. 36 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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