M. Goodman

3.2k total citations
57 papers, 2.5k citations indexed

About

M. Goodman is a scholar working on Molecular Biology, Genetics and Paleontology. According to data from OpenAlex, M. Goodman has authored 57 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 12 papers in Genetics and 10 papers in Paleontology. Recurrent topics in M. Goodman's work include Genomics and Phylogenetic Studies (11 papers), Evolution and Paleontology Studies (10 papers) and Genomics and Chromatin Dynamics (9 papers). M. Goodman is often cited by papers focused on Genomics and Phylogenetic Studies (11 papers), Evolution and Paleontology Studies (10 papers) and Genomics and Chromatin Dynamics (9 papers). M. Goodman collaborates with scholars based in United States, Brazil and Germany. M. Goodman's co-authors include J L Slightom, John Czelusniak, Danilo A. Tagle, Ben F. Koop, Michael M. Miyamoto, Horácio Schneider, Iracilda Sampaio, Maria Paula Cruz Schneider, Maria Lúcia Harada and Wendy J. Bailey and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Blood.

In The Last Decade

M. Goodman

57 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Goodman United States 28 1.4k 661 521 444 379 57 2.5k
John Czelusniak United States 30 2.2k 1.5× 1.2k 1.8× 790 1.5× 657 1.5× 665 1.8× 46 3.7k
Lutz Walter Germany 37 1.4k 1.0× 452 0.7× 405 0.8× 139 0.3× 191 0.5× 140 4.3k
Maryellen Ruvolo United States 22 992 0.7× 878 1.3× 756 1.5× 407 0.9× 251 0.7× 29 2.4k
Hans Zischler Germany 34 2.0k 1.4× 1.1k 1.7× 612 1.2× 239 0.5× 894 2.4× 95 3.7k
Calvin A. Porter United States 20 795 0.6× 593 0.9× 334 0.6× 379 0.9× 424 1.1× 35 1.8k
Juan C. Opazo Chile 31 918 0.6× 634 1.0× 205 0.4× 395 0.9× 181 0.5× 87 2.5k
Satoshi Horai Japan 39 4.9k 3.4× 2.5k 3.8× 297 0.6× 254 0.6× 159 0.4× 93 7.4k
Joan Pontius United States 10 889 0.6× 385 0.6× 429 0.8× 183 0.4× 237 0.6× 14 2.0k
A. E. Friday United Kingdom 12 632 0.4× 305 0.5× 113 0.2× 704 1.6× 198 0.5× 16 2.0k
Kenji Hayasaka Japan 18 818 0.6× 837 1.3× 361 0.7× 192 0.4× 108 0.3× 22 1.8k

Countries citing papers authored by M. Goodman

Since Specialization
Citations

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

Fields of papers citing papers by M. Goodman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Goodman

This figure shows the co-authorship network connecting the top 25 collaborators of M. Goodman. A scholar is included among the top collaborators of M. Goodman 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. Goodman. M. Goodman 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.
Page, Scott L. & M. Goodman. (2001). Catarrhine Phylogeny: Noncoding DNA Evidence for a Diphyletic Origin of the Mangabeys and for a Human–Chimpanzee Clade. Molecular Phylogenetics and Evolution. 18(1). 14–25. 107 indexed citations
2.
3.
Johnson, Robert M., Steven Buck, Horácio Schneider, et al.. (1997). Identification of PRE-γ-GLOBIN. Hemoglobin. 21(2). 143–153. 3 indexed citations
4.
Schmidt, Timothy R., Saied A. Jaradat, M. Goodman, Margaret I. Lomax, & Lawrence I. Grossman. (1997). Molecular evolution of cytochrome c oxidase: rate variation among subunit VIa isoforms. Molecular Biology and Evolution. 14(6). 595–601. 29 indexed citations
5.
Schneider, Horácio, Iracilda Sampaio, Maria Lúcia Harada, et al.. (1996). Molecular phylogeny of the New World monkeys (Platyrrhini, primates) based on two unlinked nuclear genes: IRBP intron 1 and ε-globin sequences. American Journal of Physical Anthropology. 100(2). 153–179. 112 indexed citations
6.
Harada, Maria Lúcia, Horácio Schneider, Maria Paula Cruz Schneider, et al.. (1995). DNA Evidence on the Phylogenetic Systematics of New World Monkeys: Support for the Sister-Grouping of Cebus and Saimiri from Two Unlinked Nuclear Genes. Molecular Phylogenetics and Evolution. 4(3). 331–349. 96 indexed citations
7.
Stanhope, Michael J., Danilo A. Tagle, Mahmood S. Shivji, et al.. (1993). Multiple L1 progenitors in prosimian primates: Phylogenetic evidence from ORF1 sequences. Journal of Molecular Evolution. 37(2). 179–189. 5 indexed citations
8.
Bailey, Wendy J., David Fitch, Danilo A. Tagle, et al.. (1991). Molecular evolution of the psi eta-globin gene locus: gibbon phylogeny and the hominoid slowdown.. Molecular Biology and Evolution. 8(2). 155–84. 123 indexed citations
9.
Fitch, David, et al.. (1990). Molecular history of gene conversions in the primate fetal gamma-globin genes. Nucleotide sequences from the common gibbon, Hylobates lar.. Journal of Biological Chemistry. 265(2). 781–793. 51 indexed citations
10.
Williams, Sarah & M. Goodman. (1989). A statistical test that supports a human/chimpanzee clade based on noncoding DNA sequence data.. Molecular Biology and Evolution. 6(4). 325–30. 24 indexed citations
11.
Koop, Ben F., D. R. Siemieniak, J L Slightom, et al.. (1989). Tarsius δ- and β-globin genes: conversions, evolution, and systematic implications. Journal of Biological Chemistry. 264(1). 68–79. 63 indexed citations
12.
Holmquist, Richard, Michael M. Miyamoto, & M. Goodman. (1988). Higher-primate phylogeny--why can't we decide?. Molecular Biology and Evolution. 5(3). 201–16. 36 indexed citations
13.
Goodman, M., John Czelusniak, Ben F. Koop, Danilo A. Tagle, & J L Slightom. (1987). Globins: A Case Study in Molecular Phylogeny. Cold Spring Harbor Symposia on Quantitative Biology. 52(0). 875–890. 112 indexed citations
14.
Kleinschmidt, T, John Czelusniak, M. Goodman, & G Braunitzer. (1986). Paenungulata: a comparison of the hemoglobin sequences from elephant, hyrax, and manatee.. Molecular Biology and Evolution. 3(5). 427–35. 18 indexed citations
15.
Jong, Wilfried W. de, et al.. (1985). alpha-Crystallin A sequences of Alligator mississippiensis and the lizard Tupinambis teguixin: molecular evolution and reptilian phylogeny.. Molecular Biology and Evolution. 2(6). 484–93. 20 indexed citations
16.
Smith, Temple F., et al.. (1985). Codon usage in the vertebrate hemoglobins and its implications.. Molecular Biology and Evolution. 2(5). 390–8. 15 indexed citations
17.
Baba, Marietta L., et al.. (1984). The early adaptive evolution of calmodulin.. Molecular Biology and Evolution. 1(6). 442–55. 86 indexed citations
18.
Scott, Alan F., Peter Heath, Stephen P. Trusko, et al.. (1984). The sequence of the gorilla fetal globin genes: evidence for multiple gene conversions in human evolution.. Molecular Biology and Evolution. 1(5). 371–89. 56 indexed citations
19.
Goodman, M., et al.. (1964). Salt Requirement for Precipitation of Chicken Antisera in Agar Immunoelectrophoresis. The Journal of Immunology. 93(2). 228–231. 3 indexed citations
20.
Goodman, M.. (1963). A Record of Man's Evolution in the Soluble Proteins of Blood. Vox Sanguinis. 8(4). 505–505. 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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