Howard D. Rees

5.7k total citations
61 papers, 4.4k citations indexed

About

Howard D. Rees is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Physiology. According to data from OpenAlex, Howard D. Rees has authored 61 papers receiving a total of 4.4k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 21 papers in Cellular and Molecular Neuroscience and 18 papers in Physiology. Recurrent topics in Howard D. Rees's work include Neuroendocrine regulation and behavior (15 papers), Neuroscience and Neuropharmacology Research (14 papers) and Alzheimer's disease research and treatments (14 papers). Howard D. Rees is often cited by papers focused on Neuroendocrine regulation and behavior (15 papers), Neuroscience and Neuropharmacology Research (14 papers) and Alzheimer's disease research and treatments (14 papers). Howard D. Rees collaborates with scholars based in United States, Netherlands and Italy. Howard D. Rees's co-authors include Allan I. Levey, Marla Gearing, Lih‐Shen Chin, Lian Li, Joungil Choi, Susan T. Weintraub, Richard P. Michael, James J. Lah, Robert W. Bonsall and James A. Olzmann and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Neuroscience.

In The Last Decade

Howard D. Rees

61 papers receiving 4.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Howard D. Rees United States 30 2.2k 1.6k 1.2k 870 511 61 4.4k
Tong H. Joh United States 41 1.7k 0.8× 2.1k 1.3× 568 0.5× 523 0.6× 265 0.5× 82 4.4k
Kalpana Merchant United States 39 1.8k 0.8× 2.1k 1.3× 1.0k 0.8× 1.1k 1.3× 283 0.6× 79 4.2k
G. Toffano Italy 40 2.9k 1.4× 3.4k 2.1× 863 0.7× 651 0.7× 398 0.8× 170 6.0k
Joël Prémont France 36 2.6k 1.2× 2.4k 1.5× 759 0.6× 311 0.4× 309 0.6× 78 4.5k
Philippe Marin France 48 3.4k 1.6× 2.8k 1.8× 1.3k 1.0× 452 0.5× 559 1.1× 145 6.2k
Natale Belluardo Italy 44 3.9k 1.8× 3.4k 2.2× 837 0.7× 466 0.5× 452 0.9× 123 6.9k
Ratan V. Bhat United States 32 3.1k 1.4× 2.0k 1.2× 1.3k 1.1× 318 0.4× 498 1.0× 47 5.4k
Jenna C. Carroll United States 23 1.2k 0.5× 1.5k 0.9× 1.8k 1.5× 1.6k 1.9× 352 0.7× 25 4.8k
Cristina Missale Italy 34 3.0k 1.4× 3.6k 2.3× 526 0.4× 701 0.8× 261 0.5× 97 6.0k
Jeffrey D. Erickson United States 38 3.0k 1.4× 3.7k 2.3× 587 0.5× 495 0.6× 809 1.6× 66 6.1k

Countries citing papers authored by Howard D. Rees

Since Specialization
Citations

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

Fields of papers citing papers by Howard D. Rees

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Howard D. Rees. 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 Howard D. Rees. The network helps show where Howard D. Rees may publish in the future.

Co-authorship network of co-authors of Howard D. Rees

This figure shows the co-authorship network connecting the top 25 collaborators of Howard D. Rees. A scholar is included among the top collaborators of Howard D. Rees 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 Howard D. Rees. Howard D. Rees 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.
Gozal, Yair M., Eric B. Dammer, Duc M. Duong, et al.. (2011). Proteomic Analysis of Hippocampal Dentate Granule Cells in Frontotemporal Lobar Degeneration: Application of Laser Capture Technology. Frontiers in Neurology. 2. 24–24. 17 indexed citations
2.
Dammer, Eric B., Chan Hyun Na, Ping Xu, et al.. (2011). Polyubiquitin Linkage Profiles in Three Models of Proteolytic Stress Suggest the Etiology of Alzheimer Disease. Journal of Biological Chemistry. 286(12). 10457–10465. 146 indexed citations
3.
Gozal, Yair M., Nicholas T. Seyfried, Marla Gearing, et al.. (2011). Aberrant septin 11 is associated with sporadic frontotemporal lobar degeneration. Molecular Neurodegeneration. 6(1). 82–82. 19 indexed citations
4.
Jang, Sung‐Wuk, Xia Liu, Haian Fu, et al.. (2009). Interaction of Akt-phosphorylated SRPK2 with 14-3-3 Mediates Cell Cycle and Cell Death in Neurons. Journal of Biological Chemistry. 284(36). 24512–24525. 100 indexed citations
5.
Shrivastava-Ranjan, Punya, Victor Faúndez, Guofu Fang, et al.. (2007). Mint3/X11γ Is an ADP-Ribosylation Factor-dependent Adaptor that Regulates the Traffic of the Alzheimer's Precursor Protein from theTrans-Golgi Network. Molecular Biology of the Cell. 19(1). 51–64. 47 indexed citations
6.
Wuu, Joanne, Howard D. Rees, Marla Gearing, et al.. (2007). Neuronal LR11/sorLA expression is reduced in mild cognitive impairment. Annals of Neurology. 62(6). 640–647. 80 indexed citations
7.
Loreti, Simona, M. Teresa Vilaró, Sergio Visentin, et al.. (2006). Rat Schwann cells express M1–M4 muscarinic receptor subtypes. Journal of Neuroscience Research. 84(1). 97–105. 46 indexed citations
8.
Choi, Joungil, Howard D. Rees, Susan T. Weintraub, et al.. (2005). Oxidative Modifications and Aggregation of Cu,Zn-Superoxide Dismutase Associated with Alzheimer and Parkinson Diseases. Journal of Biological Chemistry. 280(12). 11648–11655. 244 indexed citations
9.
Olzmann, James A., Keith D. Wilkinson, Howard D. Rees, et al.. (2004). Familial Parkinson's Disease-associated L166P Mutation Disrupts DJ-1 Protein Folding and Function. Journal of Biological Chemistry. 279(9). 8506–8515. 231 indexed citations
10.
Liao, Lujian, Dongmei Cheng, Jian Wang, et al.. (2004). Proteomic Characterization of Postmortem Amyloid Plaques Isolated by Laser Capture Microdissection. Journal of Biological Chemistry. 279(35). 37061–37068. 245 indexed citations
11.
Wigston, DJ, et al.. (2000). LIM kinase 1 accumulates in presynaptic terminals during synapse maturation. The Journal of Comparative Neurology. 416(3). 319–334. 28 indexed citations
12.
Kottaridis, PD, Howard D. Rees, Graham A. Smith, et al.. (1999). A fatal case of autoimmune thrombocytopenia with an IgM anti-GPIb/IX following one antigen mismatched unrelated donor bone marrow transplantation. Bone Marrow Transplantation. 23(7). 739–741. 17 indexed citations
13.
Manning, Karen, et al.. (1999). Muscarinic receptor subtypes in the lateral geniculate nucleus: A light and electron microscopic analysis. The Journal of Comparative Neurology. 404(3). 408–425. 40 indexed citations
14.
Levey, Allan I., James J. Lah, Norman Nash, et al.. (1997). Presenilin‐1 protein expression in familial and sporadic Alzheimer's disease. Annals of Neurology. 41(6). 742–753. 34 indexed citations
15.
Bonsall, Robert W., et al.. (1988). Metabolism and nuclear uptake of tritiated testosterone in the brain of the fetal macaque. The Society for Neuroscience Abstracts. 14(1). 707. 1 indexed citations
16.
Rees, Howard D., et al.. (1986). Sites of action of testosterone in the brain of the female primate. Experimental Brain Research. 63(1). 67–75. 11 indexed citations
17.
Rees, Howard D., J. Verhoef, A. Witter, Willem Hendrik Gispen, & D. de Wied. (1980). Autoradiographic studies with a behaviorally potent 3H-ACTH4–9 analog in the brain after intraventricular injection in rats. Brain Research Bulletin. 5(5). 509–514. 18 indexed citations
18.
Rees, Howard D., et al.. (1977). Stimulation increases incorporation of [3H]lysine into rat brain and liver proteins. Brain Research Bulletin. 2(4). 243–245. 5 indexed citations
19.
Rees, Howard D., Adrian J. Dunn, & P. Michael Iuvone. (1976). Behavioral and biochemical responses of mice to the intraventricular administration of ACTH analogs and lysine vasopressin. Life Sciences. 18(11). 1333–1339. 55 indexed citations
20.
Soloff, Melvyn S., Howard D. Rees, Madhabananda Sar, & Walter E. Stumpf. (1975). Autoradiographic Localization of Radioactivity from [3H]Oxytocin in the Rat Mammary Gland and Oviduct1. Endocrinology. 96(6). 1475–1477. 27 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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