R. Lofthouse

2.9k total citations
29 papers, 1.7k citations indexed

About

R. Lofthouse is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, R. Lofthouse has authored 29 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 9 papers in Cellular and Molecular Neuroscience and 6 papers in Neurology. Recurrent topics in R. Lofthouse's work include Prion Diseases and Protein Misfolding (7 papers), Neurological diseases and metabolism (6 papers) and Neurotransmitter Receptor Influence on Behavior (6 papers). R. Lofthouse is often cited by papers focused on Prion Diseases and Protein Misfolding (7 papers), Neurological diseases and metabolism (6 papers) and Neurotransmitter Receptor Influence on Behavior (6 papers). R. Lofthouse collaborates with scholars based in United Kingdom, United States and Italy. R. Lofthouse's co-authors include F. Owen, Mark Poulter, Timothy J. Crow, John Collinge, T.J. Crow, G.W. Roberts, A.J. Cross, H. F. Baker, J.F.W. Deakin and R.M. Ridley and has published in prestigious journals such as New England Journal of Medicine, The Lancet and Journal of Biological Chemistry.

In The Last Decade

R. Lofthouse

29 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
R. Lofthouse United Kingdom 19 939 508 448 319 290 29 1.7k
N. Suzan Nadi United States 25 660 0.7× 231 0.5× 1.2k 2.7× 162 0.5× 231 0.8× 37 1.9k
D M Chuang United States 26 1.4k 1.5× 183 0.4× 1.3k 2.8× 65 0.2× 247 0.9× 34 2.4k
Shelley J. Russek United States 31 1.5k 1.6× 262 0.5× 1.9k 4.3× 114 0.4× 252 0.9× 58 2.9k
Richard A. Morrisett United States 30 1.2k 1.2× 264 0.5× 2.1k 4.6× 220 0.7× 321 1.1× 57 2.8k
Pavel I. Ortinski United States 26 862 0.9× 343 0.7× 1.4k 3.0× 99 0.3× 307 1.1× 46 2.4k
Susan E. Bergeson United States 25 950 1.0× 488 1.0× 846 1.9× 120 0.4× 52 0.2× 53 2.1k
Halina Baran Austria 26 760 0.8× 274 0.5× 1.0k 2.3× 58 0.2× 473 1.6× 55 2.3k
Marie‐Christine Miquel France 26 1.6k 1.7× 175 0.3× 1.4k 3.2× 119 0.4× 96 0.3× 44 2.8k
Sarah Bailey United Kingdom 24 727 0.8× 117 0.2× 456 1.0× 93 0.3× 100 0.3× 55 1.6k
John Mastropaolo United States 24 787 0.8× 86 0.2× 1.1k 2.4× 60 0.2× 285 1.0× 66 1.8k

Countries citing papers authored by R. Lofthouse

Since Specialization
Citations

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

Fields of papers citing papers by R. Lofthouse

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R. Lofthouse

This figure shows the co-authorship network connecting the top 25 collaborators of R. Lofthouse. A scholar is included among the top collaborators of R. Lofthouse 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 R. Lofthouse. R. Lofthouse 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.
DeLisi, Lynn E., R. Lofthouse, Thomas Lehner, et al.. (1995). Failure to find a chromosome 18 pericentric linkage in families with schizophrenia. American Journal of Medical Genetics. 60(6). 532–534. 14 indexed citations
2.
Polymeropoulos, Mihael H., Hilary Coon, William Byerley, et al.. (1994). Search for a schizophrenia susceptibility locus on human chromosome 22. American Journal of Medical Genetics. 54(2). 93–99. 63 indexed citations
3.
Rubinsztein, David C., Jayne Leggo, S. Goodburn, et al.. (1994). Study of the Huntington's disease (HD) gene CAG repeats in schizophrenic patients shows overlap of the normal and HD affected ranges but absence of correlation with schizophrenia.. Journal of Medical Genetics. 31(9). 690–693. 19 indexed citations
4.
Crow, T.J., Mark Poulter, R. Lofthouse, et al.. (1993). Male siblings with schizophrenia share alleles at the androgen receptor above chance expectation. American Journal of Medical Genetics. 48(3). 159–160. 17 indexed citations
5.
DeLisi, Lynn E., Thomas Lehner, Nicholas Bass, et al.. (1993). Evidence for a sex chromosome locus for schizophrenia. Schizophrenia Research. 9(2-3). 117–117. 1 indexed citations
6.
Owen, F., Mark Poulter, John Collinge, et al.. (1992). A dementing illness associated with a novel insertion in the prion protein gene. Molecular Brain Research. 13(1-2). 155–157. 71 indexed citations
7.
Collinge, John, Jeremy M. Brown, John Hardy, et al.. (1992). INHERITED PRION DISEASE WITH 144 BASE PAIR GENE INSERTION: 2. CLINICAL AND PATHOLOGICAL FEATURES. Brain. 115(3). 687–710. 139 indexed citations
8.
Poulter, Mark, H. F. Baker, Chris Frith, et al.. (1992). INHERITED PRION DISEASE WITH 144 BASE PAIR GENE INSERTION: 1. GENEALOGICAL AND MOLECULAR STUDIES. Brain. 115(3). 675–685. 136 indexed citations
9.
Lehner, Thomas, Jürg Ott, R. Lofthouse, et al.. (1992). Linkage analysis and sib pair test for linkage of schizophrenia with D11S35. Schizophrenia Research. 6(2). 92–92. 2 indexed citations
10.
Collinge, Janelle E., Lynn E. DeLisi, A. Boccio, et al.. (1991). Evidence for a Pseudo-autosomal Locus for Schizophrenia Using the Method of Affected Sibling Pairs. The British Journal of Psychiatry. 158(5). 624–629. 49 indexed citations
11.
Polymeropoulos, Mihael H., et al.. (1991). Genetic linkage studies in schizophrenia using (CA)n repeat polymorphisms. Schizophrenia Research. 4(3). 283–283. 1 indexed citations
12.
Deakin, J.F.W., et al.. (1990). A neuroendocrine study of 5HT function in depression: evidence for biological mechanisms of endogenous and psychosocial causation. Psychopharmacology. 101(1). 85–92. 115 indexed citations
13.
Owen, F., Mark Poulter, John Collinge, et al.. (1990). An in-frame insertion in the prion protein gene in familial Creutzfeldt-Jakob disease. Molecular Brain Research. 7(3). 273–276. 108 indexed citations
14.
Collinge, John, F. Owen, R. Lofthouse, et al.. (1989). DIAGNOSIS OF GERSTMANN-STRÄUSSLER SYNDROME IN FAMILIAL DEMENTIA WITH PRION PROTEIN GENE ANALYSIS. The Lancet. 334(8653). 15–17. 114 indexed citations
15.
Roberts, G.W., R. Lofthouse, David Allsop, et al.. (1988). CNS amyloid proteins in neurodegenerative diseases. Neurology. 38(10). 1534–1534. 65 indexed citations
16.
Owen, F., Timothy J. Crow, Chris Frith, et al.. (1987). Selective Decreases in MAO-B Activity in Post-Mortem Brains from Schizophrenic Patients with Type II Syndrome. The British Journal of Psychiatry. 151(4). 514–519. 17 indexed citations
17.
Owen, F., A.J. Cross, Timothy J. Crow, R. Lofthouse, & Mark Poulter. (1981). Neurotransmitter receptors in brain in schizophrenia. Acta Psychiatrica Scandinavica. 63(S291). 20–28. 50 indexed citations
18.
Cross, A.J., J.F.W. Deakin, R. Lofthouse, et al.. (1979). On the mechanism of action of electroconvulsive therapy: some behavioural and biochemical consequences of repeated electrically induced seizures in rats [proceedings].. PubMed. 66(1). 111P–111P. 6 indexed citations
19.
Owen, F., R. Lofthouse, & Rachel C. Bourne. (1979). A radioreceptor assay for diazepam and its metabolites in serum. Clinica Chimica Acta. 93(3). 305–310. 20 indexed citations
20.
Cross, A.J., et al.. (1978). Some observations on human brain monoamine oxidase [proceedings].. PubMed. 62(3). 408P–408P. 1 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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