Ronald E. Majocha

979 total citations
40 papers, 861 citations indexed

About

Ronald E. Majocha is a scholar working on Molecular Biology, Physiology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ronald E. Majocha has authored 40 papers receiving a total of 861 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 26 papers in Physiology and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ronald E. Majocha's work include Alzheimer's disease research and treatments (25 papers), Prion Diseases and Protein Misfolding (12 papers) and Computational Drug Discovery Methods (5 papers). Ronald E. Majocha is often cited by papers focused on Alzheimer's disease research and treatments (25 papers), Prion Diseases and Protein Misfolding (12 papers) and Computational Drug Discovery Methods (5 papers). Ronald E. Majocha collaborates with scholars based in United States and Ireland. Ronald E. Majocha's co-authors include Charles A. Marotta, Barbara Tate, Ross J. Baldessarini, Francine M. Beneš, Sayeeda B. Zain, Julie Newton, Beverly A. Brown, Donna M. Staton, Firoze B. Jungalwala and Robert P. Friedland and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Brain Research and Annals of the New York Academy of Sciences.

In The Last Decade

Ronald E. Majocha

40 papers receiving 844 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ronald E. Majocha United States	20	497	462	197	131	102	40	861
Henrike Hartmann Germany	14	616 1.2×	592 1.3×	330 1.7×	143 1.1×	107 1.0×	17	970
Gerda Huber Switzerland	16	609 1.2×	618 1.3×	342 1.7×	174 1.3×	132 1.3×	25	1.3k
Janelle Nunan Australia	8	510 1.0×	373 0.8×	205 1.0×	164 1.3×	72 0.7×	9	783
N.K. Robakis United States	8	392 0.8×	316 0.7×	193 1.0×	115 0.9×	62 0.6×	9	580
Asha Naidu United States	7	668 1.3×	286 0.6×	281 1.4×	172 1.3×	181 1.8×	8	794
Jianyi Ma United States	7	839 1.7×	569 1.2×	220 1.1×	174 1.3×	162 1.6×	7	1.1k
Jason J. Fritz United States	12	575 1.2×	441 1.0×	241 1.2×	122 0.9×	149 1.5×	14	883
Mark Rapoport United States	8	657 1.3×	349 0.8×	340 1.7×	212 1.6×	136 1.3×	8	973
Bruno Bonici France	8	671 1.4×	305 0.7×	369 1.9×	178 1.4×	143 1.4×	9	824
Yunn-Chyn Tung United States	8	530 1.1×	395 0.9×	280 1.4×	135 1.0×	158 1.5×	9	835

Countries citing papers authored by Ronald E. Majocha

Since Specialization

Citations

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

Fields of papers citing papers by Ronald E. Majocha

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ronald E. Majocha. 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 Ronald E. Majocha. The network helps show where Ronald E. Majocha may publish in the future.

Co-authorship network of co-authors of Ronald E. Majocha

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

All Works

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20 of 20 papers shown

Newton, Julie, et al.. (1998). Indomethacin Reverses the Microglial Response to Amyloid β-Protein. Neurobiology of Aging. 19(3). 201–204. 82 indexed citations

Majocha, Ronald E., Sudhir Agrawal, Jinyan Tang, Eric W. Humke, & Charles A. Marotta. (1994). Modulation of the PC12 cell response to nerve growth factor by antisense oligonucleotide to amyloid precursor protein. Cellular and Molecular Neurobiology. 14(5). 425–437. 23 indexed citations

Friedland, Robert P., et al.. (1994). Development of an anti-Aβ monoclonal antibody for in vivo imaging of amyloid angiopathy in Alzheimer's disease. Molecular Neurobiology. 9(1-3). 107–113. 21 indexed citations

Majocha, Ronald E., Barbara Tate, & Charles A. Marotta. (1993). PC12 cells release stimulatory factors after transfection with β/A4-C-terminal DNA of the Alzheimer amyloid precursor protein. Molecular and Chemical Neuropathology. 18(1-2). 99–113. 3 indexed citations

Maestre, Gladys E., Barbara Tate, Ronald E. Majocha, & Charles A. Marotta. (1993). Membrane surface ruffling in cells that over-express Alzheimer amyloid β/A4 C-terminal peptide. Brain Research. 621(1). 145–149. 13 indexed citations

Maestre, Gladys E., Barbara Tate, Ronald E. Majocha, & Charles A. Marotta. (1992). Cell surface extensions associated with overexpression of Alzheimer ß/A4 amyloid. Brain Research. 599(1). 64–72. 13 indexed citations

Marotta, Charles A., Ronald E. Majocha, & Barbara Tate. (1992). Molecular and cellular biology of Alzheimer amyloid. Journal of Molecular Neuroscience. 3(3). 111–125. 31 indexed citations

Beneš, Francine M., et al.. (1991). Evidence for axonal loss in regions occupied by senile plaques in Alzheimer cortex. Neuroscience. 42(3). 651–660. 35 indexed citations

Zain, Sayeeda B., et al.. (1990). Alzheimer cortical neurons containing abundant amyloid mRNA. Relationship to amyloid deposition and senile plaques. Journal of Psychiatric Research. 24(1). 37–50. 8 indexed citations

10.

Majocha, Ronald E., et al.. (1990). of Amino Terminal and A4 (β-Amyloid) Antigens in Alzheimer Plaques: Evidence for Coordinated Processing of the Amyloid Precursor Protein. Journal of Geriatric Psychiatry and Neurology. 3(3). 139–145. 2 indexed citations

11.

Beneš, Francine M., et al.. (1989). Evidence for a diffusional model of Alzheimer amyloid A4 (β-amyloid) deposition during neuritic plaque formation. Neuroscience. 33(3). 483–488. 19 indexed citations

12.

Majocha, Ronald E., et al.. (1989). Monoclonal Antibody to Embryonic CNS Antigen A2B5 Provides Evidence for the Involvement of Membrane Components at Sites of Alzheimer Degeneration and Detects Sulfatides as Well as Gangliosides. Journal of Neurochemistry. 53(3). 953–961. 49 indexed citations

13.

Zhu, Wenliang, et al.. (1989). Extracytoplasmic and A4 domains of the amyloid precursor protein: molecular cloning, genetically engineered cell lines and immunocytochemical investigations.. PubMed. 317. 991–9. 1 indexed citations

14.

Marotta, Charles A., et al.. (1989). Overexpression of amyloid precursor protein A4 (beta-amyloid) immunoreactivity in genetically transformed cells: implications for a cellular model of Alzheimer amyloidosis.. Proceedings of the National Academy of Sciences. 86(1). 337–341. 18 indexed citations

15.

Shea, Thomas, Ronald E. Majocha, Charles A. Marotta, & Ralph A. Nixon. (1988). Soluble, phosphorylated forms of the high molecular weight neurofilament protein in perikarya of cultured neuronal cells. Neuroscience Letters. 92(3). 291–297. 30 indexed citations

16.

Sajdel-Sulkowska, Elizabeth M., Sayeed Ur Rehman, Ronald E. Majocha, et al.. (1988). Genetic Expression of Amyloid and Glial-specific Protein in the Alzheimer Brain. Journal of the American Geriatrics Society. 36(6). 558–564. 7 indexed citations

17.

Salim, Mohammad, Sayeed Ur Rehman, Elizabeth M. Sajdel-Sulkowska, et al.. (1988). Preparation of a recombinant cDNA library from poly(A+) RNA of the Alzheimer brain. Identification and characterization of a cDNA copy encoding a glial-specific protein. Neurobiology of Aging. 9(2). 163–171. 9 indexed citations

18.

Sajdel-Sulkowska, Elizabeth M., et al.. (1988). The postmortem Alzheimer brain is a source of structurally and functionally intact astrocytic messenger RNA. Journal of Neuroscience Methods. 23(2). 173–179. 20 indexed citations

19.

Zain, Sayeeda B., et al.. (1988). Molecular cloning of amyloid cDNA derived from mRNA of the Alzheimer disease brain: coding and noncoding regions of the fetal precursor mRNA are expressed in the cortex.. Proceedings of the National Academy of Sciences. 85(3). 929–933. 51 indexed citations

20.

Zain, Sayeeda B., et al.. (1987). Molecular cloning of complementary dna transcribed from messenger rna of the alzheimer brain identification of complementary dna for amyloid and glial fibrillary acidic protein. The Society for Neuroscience Abstracts. 13(1). 558. 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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