P. L. Murphy

1.2k total citations
18 papers, 922 citations indexed

About

P. L. Murphy is a scholar working on Neurology, Genetics and Genetics. According to data from OpenAlex, P. L. Murphy has authored 18 papers receiving a total of 922 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Neurology, 5 papers in Genetics and 4 papers in Genetics. Recurrent topics in P. L. Murphy's work include Amyotrophic Lateral Sclerosis Research (8 papers), Neurogenetic and Muscular Disorders Research (4 papers) and Genetic Associations and Epidemiology (3 papers). P. L. Murphy is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (8 papers), Neurogenetic and Muscular Disorders Research (4 papers) and Genetic Associations and Epidemiology (3 papers). P. L. Murphy collaborates with scholars based in United States, United Kingdom and Iceland. P. L. Murphy's co-authors include Lewis P. Rowland, Hannes Pétursson, David Curtis, M. L. Del Bene, Steven M. Albert, Robin Sherrington, Gursharan Kalsi, Baljinder S. Mankoo, Thordur Sigmundsson and Timothy D. Read and has published in prestigious journals such as American Journal of Psychiatry, Neurology and Annals of Neurology.

In The Last Decade

P. L. Murphy

18 papers receiving 898 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
P. L. Murphy United States 13 308 296 274 134 115 18 922
Irene Pichler Italy 21 401 1.3× 386 1.3× 273 1.0× 145 1.1× 39 0.3× 45 1.2k
Emilio Di Maria Italy 22 565 1.8× 461 1.6× 243 0.9× 500 3.7× 37 0.3× 66 1.4k
Laurence Mignon United States 12 368 1.2× 138 0.5× 54 0.2× 214 1.6× 191 1.7× 28 860
Michael A. Nalls United States 14 940 3.1× 206 0.7× 268 1.0× 100 0.7× 40 0.3× 19 1.5k
Elisa De Grandis Italy 15 153 0.5× 173 0.6× 106 0.4× 69 0.5× 49 0.4× 46 578
Kristel R. van Eijk Netherlands 15 381 1.2× 88 0.3× 272 1.0× 46 0.3× 61 0.5× 23 783
Lucy J. Treiman United States 11 445 1.4× 130 0.4× 373 1.4× 454 3.4× 27 0.2× 14 1.1k
Vadlamudi Raghavendra Rao India 15 190 0.6× 144 0.5× 223 0.8× 99 0.7× 12 0.1× 60 812
Javier Ruiz‐Martínez Spain 22 260 0.8× 726 2.5× 82 0.3× 267 2.0× 25 0.2× 46 1.2k
Marcelo Kauffman Argentina 16 244 0.8× 270 0.9× 244 0.9× 287 2.1× 21 0.2× 67 898

Countries citing papers authored by P. L. Murphy

Since Specialization
Citations

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

Fields of papers citing papers by P. L. Murphy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P. L. Murphy

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

All Works

18 of 18 papers shown
1.
Redmond, T. Michael, et al.. (2007). Plasmablastic lymphoma presenting as a paravertebral mass in a patient with Crohn’s disease after immunosuppressive therapy. Journal of Clinical Pathology. 60(1). 80–81. 33 indexed citations
2.
Clarke, Tara, et al.. (2006). SPEECH AND LANGUAGE DISORDERS AGGREGATE IN ROLANDIC EPILEPSY FAMILIES. Neuropediatrics. 37(S 1). 2 indexed citations
3.
4.
Haugabook, Sharie J., Debra Yager, Elizabeth A. Eckman, et al.. (2000). Reduction of Aβ accumulation in the Tg2576 animal model of Alzheimer's disease after oral administration of the phosphatidylinositol kinase inhibitor wortmannin. The FASEB Journal. 15(1). 16–18. 49 indexed citations
5.
Murphy, P. L., Steven M. Albert, Christian Weber, M. L. Del Bene, & Lewis P. Rowland. (2000). Impact of spirituality and religiousness on outcomes in patients with ALS. Neurology. 55(10). 1581–1584. 66 indexed citations
6.
Albert, Steven M., P. L. Murphy, M. L. Del Bene, & Lewis P. Rowland. (1999). A prospective study of preferences and actual treatment choices in ALS. Neurology. 53(2). 278–278. 77 indexed citations
7.
Rowland, Lewis P., Gordon Gilbert, David S. Younger, et al.. (1998). Lymphoproliferative disorders and motor neuron disease. Neurology. 50(2). 576–576. 2 indexed citations
8.
Curtis, David, Jon Brynjolfsson, Jane O’Neill, et al.. (1997). Two-Locus Admixture Linkage Analysis of Bipolar and Unipolar Affective Disorder Supports the Presence of Susceptibility Loci on Chromosomes 11p15 and 21q22. Genomics. 39(3). 271–278. 70 indexed citations
9.
Gilbert, Gordon, Lewis P. Rowland, David S. Younger, et al.. (1997). Lymphoproliferative disorders and motor neuron disease. Neurology. 48(6). 1671–1678. 88 indexed citations
10.
Przedborski, Serge, David M. Donaldson, P. L. Murphy, et al.. (1996). Blood Superoxide Dismutase, Catalase and Glutathione Peroxidase Activities in Familial and Sporadic Amyotrophic Lateral Sclerosis. PubMed. 5(1). 57–64. 44 indexed citations
11.
Wilhelmsen, Kirk C., Timothy Lynch, Mildred Vera, et al.. (1996). Chromosome 12‐linked autosomal dominant scapuloperoneal muscular dystrophy. Annals of Neurology. 39(4). 507–520. 63 indexed citations
12.
Przedborski, Serge, Vijay Dhawan, David M. Donaldson, et al.. (1996). Nigrostriatal dopaminergic function in familial amyotrophic lateral sclerosis patients with and without copper/zinc superoxide dismutase mutations. Neurology. 47(6). 1546–1551. 30 indexed citations
13.
14.
Kalsi, Gursharan, Robin Sherrington, Jon Brynjolfsson, et al.. (1996). Linkage study of the D5 dopamine receptor gene (DRD5) in multiplex Icelandic and English schizophrenia pedigrees. American Journal of Psychiatry. 153(1). 107–109. 11 indexed citations
15.
Kalsi, Gursharan, Baljinder S. Mankoo, Jon Brynjolfsson, et al.. (1994). The Marfan syndrome gene locus as a favoured locus for susceptibility to schizophrenia. Psychiatric Genetics. 4(4). 219–228. 12 indexed citations
16.
Lange, Dale J., et al.. (1994). Management of Patients with Amyotrophic Lateral Sclerosis. Neurorehabilitation and neural repair. 8(2). 75–82. 3 indexed citations
17.
Sanders, Katherine, Lewis P. Rowland, P. L. Murphy, et al.. (1993). Motor neuron diseases and amyotrophic lateral Sclerosis. Neurology. 43(2). 418–418. 31 indexed citations
18.
Rowland, Lewis P., William H. Sherman, Norman Latov, et al.. (1992). Amyotrophic lateral sclerosis and lymphoma. Neurology. 42(5). 1101–1101. 25 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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