T. Prior

685 total citations
11 papers, 502 citations indexed

About

T. Prior is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, T. Prior has authored 11 papers receiving a total of 502 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Pathology and Forensic Medicine and 2 papers in Genetics. Recurrent topics in T. Prior's work include Genetics and Neurodevelopmental Disorders (2 papers), Mast cells and histamine (1 paper) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (1 paper). T. Prior is often cited by papers focused on Genetics and Neurodevelopmental Disorders (2 papers), Mast cells and histamine (1 paper) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (1 paper). T. Prior collaborates with scholars based in United States and United Kingdom. T. Prior's co-authors include Jerry R. Mendell, Patricia McAndrew, Arthur H.M. Burghes, ST Iannaccone, D. Williams Parsons, Ryan Noss, James L. Fisher, Julie Stephens, Robert Pilarski and Pamela J. Snyder and has published in prestigious journals such as Neurology, The American Journal of Human Genetics and Journal of Medical Genetics.

In The Last Decade

T. Prior

11 papers receiving 495 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
T. Prior United States	8	301	173	94	82	77	11	502
P.F. Jacobsen Australia	11	316 1.0×	186 1.1×	52 0.6×	113 1.4×	48 0.6×	25	631
T. Schweitzer Germany	10	179 0.6×	74 0.4×	147 1.6×	100 1.2×	50 0.6×	15	504
Kunyu Harada Japan	12	146 0.5×	89 0.5×	38 0.4×	84 1.0×	74 1.0×	25	459
D. W. Ellison United Kingdom	10	170 0.6×	174 1.0×	49 0.5×	127 1.5×	26 0.3×	16	488
Debbie K. Song United States	11	116 0.4×	96 0.6×	61 0.6×	103 1.3×	71 0.9×	16	345
Yosuke Iwata Japan	10	269 0.9×	36 0.2×	59 0.6×	59 0.7×	107 1.4×	14	484
Krzysztof Zakrzewski Poland	13	193 0.6×	196 1.1×	28 0.3×	79 1.0×	109 1.4×	66	514
Jean-François Vanbellinghen Belgium	10	149 0.5×	154 0.9×	74 0.8×	65 0.8×	53 0.7×	18	542
Melissa M. Fraser United States	7	272 0.9×	169 1.0×	50 0.5×	107 1.3×	28 0.4×	7	464
Ruth A. Heim United States	13	155 0.5×	80 0.5×	117 1.2×	111 1.4×	17 0.2×	21	643

Countries citing papers authored by T. Prior

Since Specialization

Citations

This map shows the geographic impact of T. Prior'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 T. Prior with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. Prior more than expected).

Fields of papers citing papers by T. Prior

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of T. Prior

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

All Works

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11 of 11 papers shown

Shell, Richard, W. David Arnold, T. Prior, et al.. (2018). SMA THERAPIES I. Neuromuscular Disorders. 28. S82–S82. 2 indexed citations

Pilarski, Robert, Julie Stephens, Ryan Noss, James L. Fisher, & T. Prior. (2011). Predicting PTEN mutations: an evaluation of Cowden syndrome and Bannayan–Riley–Ruvalcaba syndrome clinical features. Journal of Medical Genetics. 48(8). 505–512. 99 indexed citations

Hegde, Madhuri, et al.. (2005). Assay Validation for Identification of Hereditary Nonpolyposis Colon Cancer-Causing Mutations in Mismatch Repair Genes MLH1, MSH2, and MSH6. Journal of Molecular Diagnostics. 7(4). 525–534. 27 indexed citations

Prior, T., et al.. (2004). Duration of action of antispasmodic agents: novel use of a mouse model as an in vivo pharmacological assay. European Journal of Cardio-Thoracic Surgery. 26(5). 988–994. 6 indexed citations

Parsons, D. Williams, Patricia McAndrew, ST Iannaccone, et al.. (1998). Intragenic telSMN Mutations: Frequency, Distribution, Evidence of a Founder Effect, and Modification of the Spinal Muscular Atrophy Phenotype by cenSMN Copy Number. The American Journal of Human Genetics. 63(6). 1712–1723. 142 indexed citations

Das, Soma, Takeo Kubota, Min‐Ae Song, et al.. (1997). Methylation Analysis of the Fragile X Syndrome by PCR. Genetic Testing. 1(3). 151–155. 36 indexed citations

Lee, Hakho, T. Prior, B. C. Casto, et al.. (1997). Ineffectiveness of the presence of H-ras/p53 combination of mutations in squamous cell carcinoma cells to induce a conversion of a nontumorigenic to a tumorigenic phenotype. Cell Biology and Toxicology. 13(6). 419–434. 9 indexed citations

Welling, D. Bradley, Marco Guida, Dennis K. Pearl, et al.. (1996). Mutational spectrum in the neurofibromatosis type 2 gene in sporadic and familial schwannomas. Human Genetics. 98(2). 189–193. 53 indexed citations

Snyder, Peter J., et al.. (1996). Strategies for amplification of trinucleotide repeats: Optimization of fragile X and androgen receptor PCR. Molecular Diagnosis. 1(1). 59–64. 7 indexed citations

10.

Brainard, Jennifer, Joel K. Greenson, Raymond J. Tesi, et al.. (1994). Detection of cytomegalovirus in liver transplant biopsies. A comparison of light microscopy, immunohistochemistry, duplex PCR and nested PCR.. PubMed. 57(12). 1753–7. 25 indexed citations

11.

Amato, A., et al.. (1993). Kennedy's disease. Neurology. 43(4). 791–791. 96 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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