M. E. Hodes

5.4k total citations
163 papers, 4.1k citations indexed

About

M. E. Hodes is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, M. E. Hodes has authored 163 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 98 papers in Molecular Biology, 39 papers in Genetics and 23 papers in Cellular and Molecular Neuroscience. Recurrent topics in M. E. Hodes's work include Neurological diseases and metabolism (11 papers), Mitochondrial Function and Pathology (9 papers) and Hereditary Neurological Disorders (9 papers). M. E. Hodes is often cited by papers focused on Neurological diseases and metabolism (11 papers), Mitochondrial Function and Pathology (9 papers) and Hereditary Neurological Disorders (9 papers). M. E. Hodes collaborates with scholars based in United States, France and Canada. M. E. Hodes's co-authors include Erwin Chargaff, Catherine G. Palmer, Stephen R. Dlouhy, Victoria M. Pratt, Margaret Crisp, Christoph Tamm, Bernardino Ghetti, S. R. Dlouhy, P. Michael Conneally and P.M. Conneally and has published in prestigious journals such as Nature, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

M. E. Hodes

157 papers receiving 3.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. E. Hodes United States 33 2.5k 919 856 485 361 163 4.1k
C. J. Epstein United States 29 1.7k 0.7× 539 0.6× 276 0.3× 340 0.7× 279 0.8× 60 3.3k
Reuven Stein Israel 39 2.9k 1.2× 484 0.5× 723 0.8× 214 0.4× 270 0.7× 120 4.8k
Toichiro Kuwabara United States 51 3.4k 1.4× 321 0.3× 640 0.7× 416 0.9× 316 0.9× 182 8.0k
Hitoshi Osaka Japan 37 3.0k 1.2× 1.3k 1.5× 980 1.1× 350 0.7× 465 1.3× 235 5.0k
Johannes Vogel Switzerland 34 1.7k 0.7× 289 0.3× 593 0.7× 727 1.5× 424 1.2× 102 4.6k
Rodrigo Bravo United States 37 3.2k 1.3× 731 0.8× 1.0k 1.2× 237 0.5× 149 0.4× 60 6.5k
David M. Kurnit United States 37 4.7k 1.9× 1.5k 1.6× 769 0.9× 203 0.4× 240 0.7× 116 8.0k
David A. Wenger United States 55 4.1k 1.7× 734 0.8× 333 0.4× 528 1.1× 295 0.8× 221 9.2k
Jerome Schaack United States 46 3.9k 1.6× 1.0k 1.1× 689 0.8× 110 0.2× 277 0.8× 108 6.1k
B. Dastugue France 36 2.2k 0.9× 528 0.6× 614 0.7× 103 0.2× 85 0.2× 157 3.9k

Countries citing papers authored by M. E. Hodes

Since Specialization
Citations

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

Fields of papers citing papers by M. E. Hodes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. E. Hodes

This figure shows the co-authorship network connecting the top 25 collaborators of M. E. Hodes. A scholar is included among the top collaborators of M. E. Hodes 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 M. E. Hodes. M. E. Hodes 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.
Inoue, Ken, Hitoshi Osaka, Virginia C. Thurston, et al.. (2002). Genomic Rearrangements Resulting in PLP1 Deletion Occur by Nonhomologous End Joining and Cause Different Dysmyelinating Phenotypes in Males and Females. The American Journal of Human Genetics. 71(4). 838–853. 125 indexed citations
2.
Kirkwood, Sandra C., Eric Siemers, Richard J. Viken, et al.. (2002). Evaluation of psychological symptoms among presymptomatic HD gene carriers as measured by selected MMPI scales. Journal of Psychiatric Research. 36(6). 377–382. 16 indexed citations
3.
Kirkwood, Sandra C., Eric Siemers, Julie C. Stout, et al.. (1999). Longitudinal Cognitive and Motor Changes Among Presymptomatic Huntington Disease Gene Carriers. Archives of Neurology. 56(5). 563–563. 83 indexed citations
4.
Hodes, M. E., et al.. (1998). X-linked spastic paraplegia due to a mutation (C506T; Ser169Phe) in exon 4 of the proteolipid protein gene (PLP). American Journal of Medical Genetics. 75(5). 516–517. 9 indexed citations
5.
Wei, Jian‐Jun, M. E. Hodes, Roberto Piva, et al.. (1998). Characterization of MurineGirk2Transcript Isoforms: Structure and Differential Expression. Genomics. 51(3). 379–390. 45 indexed citations
6.
7.
Wei, Jian‐Jun, M. E. Hodes, Yu Wang, et al.. (1996). Direct cDNA selection with DNA microdissected from mouse chromosome 16: isolation of novel clones and construction of a partial transcription map of the C3-C4 region.. Genome Research. 6(8). 678–687. 6 indexed citations
8.
Yang, Min, et al.. (1996). Improved procedure for eluting DNA from dried blood spots. Clinical Chemistry. 42(7). 1115–1116. 19 indexed citations
9.
Hodes, M. E., William DeMyer, Victoria M. Pratt, Mary K. Edwards, & Stephen R. Dlouhy. (1995). Girl with signs of Pelizaeus‐Merzbacher disease heterozygous for a mutation in exon 2 of the proteolipid protein gene. American Journal of Medical Genetics. 55(4). 397–401. 29 indexed citations
10.
Wei, Jian‐Jun, Stephen R. Dlouhy, Jianguo Zhu, Bernardino Ghetti, & M. E. Hodes. (1994). Analysis of region-specific library constructed by sequence-independent amplification of microdissected fragments surrounding weaver (wv) gene on mouse chromosome 16. Somatic Cell and Molecular Genetics. 20(5). 401–408. 5 indexed citations
11.
Beiraghi, Soraya, et al.. (1994). Possible localization of a major gene for cleft lip and palate to 4q. Clinical Genetics. 46(3). 255–256. 44 indexed citations
12.
Hodes, M. E., et al.. (1993). Genetics of Pelizaeus-Merzbacher Disease. Developmental Neuroscience. 15(6). 383–394. 107 indexed citations
13.
Mocharla, Hanna, et al.. (1990). α-Amylase gene transcription in tissues of normal dog. Nucleic Acids Research. 18(4). 1031–1036. 19 indexed citations
14.
Hodes, M. E., et al.. (1985). An Amylase-Producing Serous Cystadenocarcinoma of the Ovary. Oncology. 42(4). 242–247. 18 indexed citations
15.
Butler, Merlin G., et al.. (1984). Linkage analysis in a large kindred with autosomal dominant transmission of polyglandular autoimmune disease type II (Schmidt syndrome). American Journal of Medical Genetics. 18(1). 61–65. 13 indexed citations
16.
Palmer, Catherine G., et al.. (1983). Juvenile chronic granulocytic leukemia in a patient with trisomy 8, neurofibromatosis, and prolonged Epstein-Barr virus infection. The Journal of Pediatrics. 102(6). 888–892. 30 indexed citations
17.
Hansen, Deborah K. & M. E. Hodes. (1983). Metabolism of phenytoin in teratogenesis-susceptible and -resistant strains of mice.. Drug Metabolism and Disposition. 11(1). 21–24. 14 indexed citations
18.
Merritt, A.D., et al.. (1976). Chromosome 6: linkage of the eighth component of complement (C8) to the histocompatibility region (HLA). Cytogenetic and Genome Research. 16(1-5). 331–334. 13 indexed citations
19.
Hodes, M. E., et al.. (1962). Bile Acid Excretion in Man Following Administration of L3:5:3′ Triiodothyronine. American Journal of Clinical Nutrition. 11(1). 4–11. 4 indexed citations
20.
Chargaff, Erwin, Rakoma Lipshitz, Charlotte Green, & M. E. Hodes. (1951). THE COMPOSITION OF THE DESOXYRIBONUCLEIC ACID OF SALMON SPERM. Journal of Biological Chemistry. 192(1). 223–230. 97 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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