Mary E. Hatten

16.6k total citations · 4 hit papers
92 papers, 12.7k citations indexed

About

Mary E. Hatten is a scholar working on Molecular Biology, Developmental Neuroscience and Cellular and Molecular Neuroscience. According to data from OpenAlex, Mary E. Hatten has authored 92 papers receiving a total of 12.7k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Molecular Biology, 42 papers in Developmental Neuroscience and 27 papers in Cellular and Molecular Neuroscience. Recurrent topics in Mary E. Hatten's work include Neurogenesis and neuroplasticity mechanisms (42 papers), Developmental Biology and Gene Regulation (15 papers) and Axon Guidance and Neuronal Signaling (14 papers). Mary E. Hatten is often cited by papers focused on Neurogenesis and neuroplasticity mechanisms (42 papers), Developmental Biology and Gene Regulation (15 papers) and Axon Guidance and Neuronal Signaling (14 papers). Mary E. Hatten collaborates with scholars based in United States, Japan and Switzerland. Mary E. Hatten's co-authors include Nathaniel Heintz, Shiaoching Gong, Martin L. Doughty, Ronald K.H. Liem, Carol A. Mason, Wei‐Qiang Gao, Lei Feng, Toshifumi Tomoda, Martine F. Roussel and Zheng Chen and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Mary E. Hatten

92 papers receiving 12.4k citations

Hit Papers

A gene expression atlas of the central nervous s... 1985 2026 1998 2012 2003 2007 1999 1985 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mary E. Hatten United States 54 7.4k 5.3k 4.1k 1.9k 1.4k 92 12.7k
André M. Goffinet Belgium 53 4.6k 0.6× 4.5k 0.8× 4.5k 1.1× 1.7k 0.9× 1.5k 1.1× 141 9.8k
Kazunori Nakajima Japan 57 5.9k 0.8× 5.5k 1.0× 5.7k 1.4× 1.6k 0.9× 1.9k 1.4× 249 13.3k
Ronald W. Oppenheim United States 65 7.5k 1.0× 8.3k 1.6× 4.7k 1.2× 2.0k 1.1× 809 0.6× 196 15.8k
Jeffrey D. Macklis United States 51 6.0k 0.8× 5.0k 0.9× 5.1k 1.3× 971 0.5× 1.5k 1.1× 123 12.0k
Gabriella D’Arcangelo United States 44 4.6k 0.6× 4.2k 0.8× 4.4k 1.1× 1.2k 0.7× 1.4k 1.0× 70 9.2k
Isabel Fariñas Spain 49 6.2k 0.8× 5.5k 1.0× 3.2k 0.8× 1.1k 0.6× 1.2k 0.9× 110 13.3k
Martin Berry United Kingdom 62 4.8k 0.7× 6.5k 1.2× 4.7k 1.2× 971 0.5× 687 0.5× 214 12.3k
Geneviève Rougon France 65 5.4k 0.7× 6.0k 1.1× 4.1k 1.0× 2.4k 1.3× 550 0.4× 192 12.3k
Masaharu Ogawa Japan 41 5.6k 0.8× 3.6k 0.7× 4.2k 1.0× 1.4k 0.8× 986 0.7× 93 9.6k
Melitta Schachner Germany 66 5.9k 0.8× 7.8k 1.5× 3.9k 1.0× 2.8k 1.5× 805 0.6× 221 13.8k

Countries citing papers authored by Mary E. Hatten

Since Specialization
Citations

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

Fields of papers citing papers by Mary E. Hatten

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mary E. Hatten

This figure shows the co-authorship network connecting the top 25 collaborators of Mary E. Hatten. A scholar is included among the top collaborators of Mary E. Hatten 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 Mary E. Hatten. Mary E. Hatten 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.
Mätlik, Kärt, Eve‐Ellen Govek, & Mary E. Hatten. (2025). Histone bivalency in CNS development. Genes & Development. 39(7-8). 428–444. 3 indexed citations
2.
Maloney, Susan E., Shiaoching Gong, Kärt Mätlik, et al.. (2024). Mice lacking Astn2 have ASD-like behaviors and altered cerebellar circuit properties. Proceedings of the National Academy of Sciences. 121(34). e2405901121–e2405901121. 3 indexed citations
3.
Mätlik, Kärt, Eve‐Ellen Govek, Matthew R. Paul, C. David Allis, & Mary E. Hatten. (2023). Histone bivalency regulates the timing of cerebellar granule cell development. Genes & Development. 37(13-14). 570–589. 15 indexed citations
4.
Behesti, Hourinaz, Arif Kocabas, David E. Buchholz, Thomas S. Carroll, & Mary E. Hatten. (2021). Altered temporal sequence of transcriptional regulators in the generation of human cerebellar granule cells. eLife. 10. 11 indexed citations
5.
Buchholz, David E., Thomas S. Carroll, Arif Kocabas, et al.. (2020). Novel genetic features of human and mouse Purkinje cell differentiation defined by comparative transcriptomics. Proceedings of the National Academy of Sciences. 117(26). 15085–15095. 23 indexed citations
6.
Minis, Adi, José Antonio Rodríguez, Avi Levin, et al.. (2019). The proteasome regulator PI31 is required for protein homeostasis, synapse maintenance, and neuronal survival in mice. Proceedings of the National Academy of Sciences. 116(49). 24639–24650. 27 indexed citations
7.
Penas, Clara, Vasileios Stathias, Jun Long, et al.. (2019). Time series modeling of cell cycle exit identifies Brd4 dependent regulation of cerebellar neurogenesis. Nature Communications. 10(1). 3028–3028. 22 indexed citations
8.
Hwang, Hun‐Way, Eric Van Otterloo, Eve‐Ellen Govek, et al.. (2018). Differential 3’ processing of specific transcripts expands regulatory and protein diversity across neuronal cell types. eLife. 7. 19 indexed citations
9.
Behesti, Hourinaz, et al.. (2018). N-cadherin provides a cis and trans ligand for astrotactin that functions in glial-guided neuronal migration. Proceedings of the National Academy of Sciences. 115(42). 10556–10563. 31 indexed citations
10.
Behesti, Hourinaz, et al.. (2018). ASTN2 modulates synaptic strength by trafficking and degradation of surface proteins. Proceedings of the National Academy of Sciences. 115(41). E9717–E9726. 34 indexed citations
11.
Zhu, Xiaodong, Eve‐Ellen Govek, Marian Mellén, et al.. (2015). Role of Tet1/3 Genes and Chromatin Remodeling Genes in Cerebellar Circuit Formation. Neuron. 89(1). 100–112. 54 indexed citations
12.
Roussel, Martine F. & Mary E. Hatten. (2011). Cerebellum. Current topics in developmental biology. 94. 235–282. 154 indexed citations
13.
Salero, Enrique & Mary E. Hatten. (2007). Differentiation of ES cells into cerebellar neurons. Proceedings of the National Academy of Sciences. 104(8). 2997–3002. 102 indexed citations
14.
Tomoda, Toshifumi, et al.. (2004). Role of Unc51.1 and its binding partners in CNS axon outgrowth. Genes & Development. 18(5). 541–558. 144 indexed citations
15.
Hatten, Mary E., Janet Alder, Kathryn A. Zimmerman, & Nathaniel Heintz. (1997). Genes involved in cerebellar cell specification and differentiation. Current Opinion in Neurobiology. 7(1). 40–47. 175 indexed citations
16.
Fink, James M., Betsy Hirsch, Zheng Chen, et al.. (1997). Astrotactin (ASTN), a Gene for Glial-Guided Neuronal Migration, Maps to Human Chromosome 1q25.2. Genomics. 40(1). 202–205. 20 indexed citations
17.
Kofuji, Paulo, Magdalena Hofer, Kathleen J. Millen, et al.. (1996). Functional Analysis of the weaver Mutant GIRK2 K+ Channel and Rescue of weaver Granule Cells. Neuron. 16(5). 941–952. 170 indexed citations
18.
Alder, Janet, et al.. (1996). Embryonic Precursor Cells from the Rhombic Lip Are Specified to a Cerebellar Granule Neuron Identity. Neuron. 17(3). 389–399. 187 indexed citations
19.
Gao, Wei‐Qiang, Nathaniel Heintz, & Mary E. Hatten. (1991). Cerebellar granule cell neurogenesis is regulated by cell-cell interactions in vitro. Neuron. 6(5). 705–715. 227 indexed citations
20.
Hatten, Mary E., et al.. (1984). Neuron–Astroglial Interactions In Vitro and Their Implications for Repair of CNS Injury. PubMed. 1(1). 15–27. 22 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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