Martin M. Sachs

7.4k total citations · 2 hit papers
74 papers, 5.9k citations indexed

About

Martin M. Sachs is a scholar working on Plant Science, Molecular Biology and Hepatology. According to data from OpenAlex, Martin M. Sachs has authored 74 papers receiving a total of 5.9k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Plant Science, 37 papers in Molecular Biology and 7 papers in Hepatology. Recurrent topics in Martin M. Sachs's work include Plant responses to water stress (24 papers), Plant Stress Responses and Tolerance (16 papers) and Photosynthetic Processes and Mechanisms (9 papers). Martin M. Sachs is often cited by papers focused on Plant responses to water stress (24 papers), Plant Stress Responses and Tolerance (16 papers) and Photosynthetic Processes and Mechanisms (9 papers). Martin M. Sachs collaborates with scholars based in United States, Germany and Australia. Martin M. Sachs's co-authors include Walter Birchmeier, Chalivendra C. Subbaiah, Michael Freeling, Ronald Okimoto, Jürgen Behrens, Imad N. Saab, K. Michael Weidner, Volker Brinkmann, Douglas Bush and Ute Schaeper and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Martin M. Sachs

72 papers receiving 5.7k citations

Hit Papers

Negative Feedback Loop of Wnt Signaling thro... 1980 2026 1995 2010 2002 1980 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martin M. Sachs United States 39 3.3k 2.6k 607 508 500 74 5.9k
Cuiling Li China 38 4.0k 1.2× 1.2k 0.5× 80 0.1× 407 0.8× 842 1.7× 83 5.4k
Tim Thomas Australia 46 4.4k 1.3× 670 0.3× 92 0.2× 424 0.8× 931 1.9× 138 6.3k
Jenny Xiang United States 28 3.4k 1.0× 1.1k 0.4× 84 0.1× 530 1.0× 406 0.8× 62 5.6k
R. E. K. Fournier United States 34 3.0k 0.9× 375 0.1× 150 0.2× 310 0.6× 1.2k 2.3× 91 3.9k
Motohiro Mihara Japan 17 1.8k 0.5× 427 0.2× 170 0.3× 1.1k 2.2× 207 0.4× 28 2.8k
Zugen Chen United States 32 4.5k 1.3× 1.0k 0.4× 57 0.1× 1.2k 2.3× 853 1.7× 70 6.3k
Jian Huang China 36 3.6k 1.1× 1.3k 0.5× 63 0.1× 463 0.9× 303 0.6× 114 4.7k
Andrew D Sharrocks United Kingdom 48 7.3k 2.2× 620 0.2× 107 0.2× 1.7k 3.3× 866 1.7× 106 9.2k
Jixin Dong United States 36 5.2k 1.6× 1.0k 0.4× 157 0.3× 917 1.8× 191 0.4× 72 8.4k
Shuichi Tsutsumi Japan 43 4.4k 1.3× 323 0.1× 81 0.1× 773 1.5× 606 1.2× 83 5.8k

Countries citing papers authored by Martin M. Sachs

Since Specialization
Citations

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

Fields of papers citing papers by Martin M. Sachs

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martin M. Sachs

This figure shows the co-authorship network connecting the top 25 collaborators of Martin M. Sachs. A scholar is included among the top collaborators of Martin M. Sachs 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 Martin M. Sachs. Martin M. Sachs 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.
Sachs, Martin M., et al.. (2024). Endogenous oligomer formation underlies DVL2 condensates and promotes Wnt/β-catenin signaling. eLife. 13. 1 indexed citations
2.
Sachs, Martin M. & Benjamin Ehmke. (2013). Cirugía ósea resectiva en periodoncia: un tipo de tratamiento de eficacia comprobada. Dialnet (Universidad de la Rioja). 23(3). 197–209. 1 indexed citations
3.
Sachs, Martin M., et al.. (2010). Liprin-α4 is a new hypoxia-inducible target gene required for maintenance of cell–cell contacts. Experimental Cell Research. 316(17). 2883–2892. 13 indexed citations
4.
Vartapetian, B. B., Martin M. Sachs, & Kurt Fagerstedt. (2008). Plant Anaerobic Stress II. Strategy of Avoidance of Anaerobiosis and Other Aspects of Plant Life under Hypoxia and Anoxia. 9 indexed citations
5.
Subbaiah, Chalivendra C., et al.. (2006). Mitochondrial Localization and Putative Signaling Function of Sucrose Synthase in Maize. Journal of Biological Chemistry. 281(23). 15625–15635. 70 indexed citations
6.
Subbaiah, Chalivendra C. & Martin M. Sachs. (2003). Calcium-Mediated Responses of Maize to Oxygen Deprivation. Russian Journal of Plant Physiology. 50(6). 752–761. 12 indexed citations
7.
Scholl, Randy, Martin M. Sachs, & Doreen Ware. (2003). Maintaining Collections of Mutants for Plant Functional Genomics. Humana Press eBooks. 236. 311–326. 11 indexed citations
8.
Kurz, Steffen M., Sandra S. Diebold, Thomas Hieronymus, et al.. (2002). The impact of c-met/scatter factor receptor on dendritic cell migration. European Journal of Immunology. 32(7). 1832–1832. 49 indexed citations
9.
Subbaiah, Chalivendra C. & Martin M. Sachs. (2000). Maize cap1 Encodes a Novel SERCA-type Calcium-ATPase with a Calmodulin-binding Domain. Journal of Biological Chemistry. 275(28). 21678–21687. 31 indexed citations
10.
Schaeper, Ute, Niels H. Gehring, Klaus Fuchs, et al.. (2000). Coupling of Gab1 to C-Met, Grb2, and Shp2 Mediates Biological Responses. The Journal of Cell Biology. 149(7). 1419–1432. 287 indexed citations
11.
Maluf, Mirian Perez, Imad N. Saab, Eleanore T. Wurtzel, & Martin M. Sachs. (1997). The Viviparous12 Maize Mutant Is Deficient In Abscisic Acid, Carotenoids, And Chlorophyll Synthesis. Scopus. 1 indexed citations
12.
Schaper, Fred, Elmar Siewert, María José Gómez‐Lechón, et al.. (1997). Hepatocyte growth factor/scatter factor (HGF/SF) signals via the STAT3/APRF transcription factor in human hepatoma cells and hepatocytes. FEBS Letters. 405(1). 99–103. 45 indexed citations
14.
Schwerk, Christian, et al.. (1995). Identification of a Transactivation Function in the Progesterone Receptor That Interacts with the TAFII110 Subunit of the TFIID Complex. Journal of Biological Chemistry. 270(36). 21331–21338. 44 indexed citations
15.
Saab, Imad N. & Martin M. Sachs. (1995). Complete cDNA and Genomic Sequence Encoding a Flooding-Responsive Gene from Maize (Zea mays L.) Homologous to Xyloglucan Endotransglycosylase. PLANT PHYSIOLOGY. 108(1). 439–440. 28 indexed citations
16.
Subbaiah, Chalivendra C., Jianhao Zhang, & Martin M. Sachs. (1994). Involvement of Intracellular Calcium in Anaerobic Gene Expression and Survival of Maize Seedlings. PLANT PHYSIOLOGY. 105(1). 369–376. 142 indexed citations
17.
Sachs, Martin M., et al.. (1989). Genetic variation for seedling tolerance to anaerobic stress in maize germplasm. Maydica. 34(4). 329–337. 26 indexed citations
18.
Sachs, Martin M., Elizabeth S. Dennis, Wayne L. Gerlach, & W. James Peacock. (1986). TWO ALLELES OF MAIZE ALCOHOL DEHYDROGENASE 1 HAVE 3' STRUCTURAL AND POLY(A) ADDITION POLYMORPHISMS. Genetics. 113(2). 449–467. 84 indexed citations
19.
Peacock, W. James, Elizabeth S. Dennis, Wayne L. Gerlach, Martin M. Sachs, & Drew Schwartz. (1984). Insertion and Excision of Ds Controlling Elements in Maize. Cold Spring Harbor Symposia on Quantitative Biology. 49(0). 347–354. 48 indexed citations
20.
Okimoto, Ronald, et al.. (1980). Patterns of polypeptide synthesis in various maize organs under anaerobiosis. Planta. 150(1). 89–94. 61 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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