J.F. Gusella

6.1k total citations · 1 hit paper
22 papers, 2.3k citations indexed

About

J.F. Gusella is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, J.F. Gusella has authored 22 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Physiology. Recurrent topics in J.F. Gusella's work include DNA Repair Mechanisms (4 papers), Genetic Neurodegenerative Diseases (4 papers) and Genomics and Chromatin Dynamics (4 papers). J.F. Gusella is often cited by papers focused on DNA Repair Mechanisms (4 papers), Genetic Neurodegenerative Diseases (4 papers) and Genomics and Chromatin Dynamics (4 papers). J.F. Gusella collaborates with scholars based in United States, Germany and United Kingdom. J.F. Gusella's co-authors include Rudolph E. Tanzi, Marc d. Paradis, Ashley I. Bush, Jean Paul Vonsattel, Warren H. Pettingell, K Beyreuther, Colin L. Masters, Gerd Multhaup, F Solomon and Wilma Wasco and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

J.F. Gusella

22 papers receiving 2.3k citations

Hit Papers

Rapid induction of Alzheimer A beta amyloid formation by ... 1994 2026 2004 2015 1994 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J.F. Gusella United States 14 1.2k 1.1k 566 325 272 22 2.3k
Marc d. Paradis United States 8 1.4k 1.2× 722 0.7× 735 1.3× 204 0.6× 311 1.1× 10 2.1k
Dirk Beher United Kingdom 32 2.4k 2.0× 2.0k 1.8× 473 0.8× 444 1.4× 242 0.9× 58 4.1k
Dean L. Pountney Australia 33 663 0.6× 900 0.8× 475 0.8× 625 1.9× 67 0.2× 64 2.7k
Andrea Schlicksupp Germany 15 645 0.6× 592 0.5× 421 0.7× 218 0.7× 198 0.7× 20 1.4k
Robert A. Colvin United States 23 314 0.3× 997 0.9× 831 1.5× 479 1.5× 131 0.5× 54 2.3k
Deborah J. Tew Australia 26 1.8k 1.6× 1.0k 1.0× 517 0.9× 223 0.7× 120 0.4× 35 2.6k
Lawrence J. Hayward United States 36 733 0.6× 2.4k 2.2× 271 0.5× 777 2.4× 121 0.4× 52 4.5k
Christa J. Maynard Australia 11 622 0.5× 568 0.5× 389 0.7× 218 0.7× 37 0.1× 11 1.3k
Denise Drago Italy 19 661 0.6× 653 0.6× 399 0.7× 179 0.6× 75 0.3× 28 1.8k
Subramanian Rajagopalan United States 22 647 0.6× 936 0.9× 333 0.6× 576 1.8× 44 0.2× 27 2.5k

Countries citing papers authored by J.F. Gusella

Since Specialization
Citations

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

Fields of papers citing papers by J.F. Gusella

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J.F. Gusella

This figure shows the co-authorship network connecting the top 25 collaborators of J.F. Gusella. A scholar is included among the top collaborators of J.F. Gusella 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 J.F. Gusella. J.F. Gusella 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.
Jones, Lesley, J.F. Gusella, Marcy E. MacDonald, et al.. (2014). A03 Genetic Modifiers Affecting The Age At Motor Onset In Huntington's Disease. Journal of Neurology Neurosurgery & Psychiatry. 85(Suppl 1). A1–A2. 1 indexed citations
2.
Handley, Renée R., Stefano Patassini, Skye R. Rudiger, et al.. (2011). Characterisation of a transgenic ovine model of Huntington’s disease. Clinical Genetics. 1 indexed citations
3.
Kluwe, Lan, Victor Mautner, Dilys M. Parry, et al.. (2000). The parental origin of new mutations in neurofibromatosis 2. Neurogenetics. 3(1). 17–24. 23 indexed citations
4.
McNeil, Sandra, Andrea Novelletto, Jayalakshmi Srinidhi, et al.. (1997). Reduced Penetrance of the Huntington's Disease Mutation. Human Molecular Genetics. 6(5). 775–779. 99 indexed citations
5.
MacDonald, Marcy E., Mabel P. Duyao, Anna B. Auerbach, et al.. (1996). . Cold Spring Harbor Symposia on Quantitative Biology. 61(1). 627–638. 8 indexed citations
6.
Trofatter, James A., Keren Long, Jill R. Murrell, et al.. (1995). An expression-independent catalog of genes from human chromosome 22.. Genome Research. 5(3). 214–224. 22 indexed citations
7.
Haines, Jonathan L., et al.. (1994). Genomic screening for dissection of a complex disease: The multiple sclerosis phenotype. The American Journal of Human Genetics. 55. 1 indexed citations
8.
Bush, Ashley I., Warren H. Pettingell, Gerd Multhaup, et al.. (1994). Rapid induction of Alzheimer A beta amyloid formation by zinc. Science. 265(5177). 1464–1467. 1308 indexed citations breakdown →
9.
Lerner, Terry J., et al.. (1994). Linkage disequilibrium between the juvenile neuronal ceroid lipofuscinosis gene and marker loci on chromosome 16p 12.1.. PubMed. 54(1). 88–94. 33 indexed citations
10.
Kwiatkowski, David J., Colette Dib, Susan A. Slaugenhaupt, et al.. (1993). An index marker map of chromosome 9 provides strong evidence for positive interference.. PubMed. 53(6). 1279–88. 33 indexed citations
11.
Bates, Gillian P., John Valdes, Holger Hummerich, et al.. (1992). Characterization of a yeast artificial chromosome contig spanning the Huntington's disease gene candidate region. Nature Genetics. 1(3). 180–187. 50 indexed citations
12.
Wasco, Wilma, et al.. (1992). Identification of a mouse brain cDNA that encodes a protein related to the Alzheimer disease-associated amyloid beta protein precursor.. Proceedings of the National Academy of Sciences. 89(22). 10758–10762. 308 indexed citations
13.
Phelan, Mary C., Cynthia C. Morton, Roger E. Stevenson, et al.. (1988). Molecular and cytogenetic characterization of a de novo t(5p;21q) in a patient previously diagnosed as monosomy 21.. PubMed. 43(4). 511–9. 25 indexed citations
14.
Minden, MD, J.F. Gusella, & David E. Housman. (1984). Chromosome-mediated transfer of the malignant phenotype by human acute myelogenous leukemic cells. Blood. 64(4). 842–846. 3 indexed citations
15.
Gusella, J.F., Carol Jones, Fa‐Ten Kao, David Housman, & Theodore T. Puck. (1982). Genetic fine-structure mapping in human chromosome 11 by use of repetitive DNA sequences.. Proceedings of the National Academy of Sciences. 79(24). 7804–7808. 49 indexed citations
16.
Wong, Wing C., et al.. (1982). Commitment of murine erythroleukemia (MEL) cells to terminal differentiation is associated with coordinated expression of globin and ribosomal genes.. PubMed. 102 pt A. 69–79. 8 indexed citations
17.
Housman, D & J.F. Gusella. (1982). Molecular genetic approaches to neural degenerative disorders. 415–422. 5 indexed citations
18.
Gusella, J.F., et al.. (1980). Hemin does not cause commitment of murine erythroleukemia (MEL) cells to terminal differentiation. Blood. 56(3). 481–487. 80 indexed citations
19.
Gusella, J.F., et al.. (1980). Hemin does not cause commitment of murine erythroleukemia (MEL) cells to terminal differentiation. Blood. 56(3). 481–487. 7 indexed citations
20.
Gusella, J.F., Fa‐Ten Kao, C. Jones, et al.. (1979). Precise localization of human beta-globin gene complex on chromosome 11.. Proceedings of the National Academy of Sciences. 76(10). 5239–5242. 157 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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