Christopher Dravis

1.4k total citations
21 papers, 984 citations indexed

About

Christopher Dravis is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Oncology. According to data from OpenAlex, Christopher Dravis has authored 21 papers receiving a total of 984 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Cellular and Molecular Neuroscience and 8 papers in Oncology. Recurrent topics in Christopher Dravis's work include Axon Guidance and Neuronal Signaling (9 papers), Cancer Cells and Metastasis (8 papers) and Epigenetics and DNA Methylation (3 papers). Christopher Dravis is often cited by papers focused on Axon Guidance and Neuronal Signaling (9 papers), Cancer Cells and Metastasis (8 papers) and Epigenetics and DNA Methylation (3 papers). Christopher Dravis collaborates with scholars based in United States, Russia and Germany. Christopher Dravis's co-authors include Mark Henkemeyer, Geoffrey M. Wahl, Christy L. Trejo, Linda A. Baker, Benjamin T. Spike, Michael J. Chumley, Nobuhiko Yokoyama, Chad A. Cowan, Robert Silvany and Elizabeth A. Vallen and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Cell Biology and Cancer Cell.

In The Last Decade

Christopher Dravis

20 papers receiving 977 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christopher Dravis United States 17 654 307 237 212 149 21 984
Maria Genander Sweden 11 594 0.9× 187 0.6× 390 1.6× 247 1.2× 94 0.6× 22 993
Mikhail V. Semënov United States 11 979 1.5× 153 0.5× 130 0.5× 139 0.7× 47 0.3× 13 1.2k
Nahyun Choi South Korea 12 386 0.6× 134 0.4× 131 0.6× 132 0.6× 132 0.9× 22 886
Claudio Cantù Sweden 22 946 1.4× 274 0.9× 74 0.3× 79 0.4× 145 1.0× 47 1.2k
Mònica Suelves Spain 16 906 1.4× 90 0.3× 64 0.3× 99 0.5× 157 1.1× 26 1.1k
Raksha Mudbhary United States 8 831 1.3× 99 0.3× 65 0.3× 226 1.1× 91 0.6× 8 1.0k
Francesca Truzzi Italy 16 376 0.6× 169 0.6× 146 0.6× 128 0.6× 59 0.4× 26 791
Yaroslava Ruzankina United States 7 653 1.0× 224 0.7× 34 0.1× 116 0.5× 113 0.8× 8 911
Matthew Swift United States 14 672 1.0× 119 0.4× 84 0.4× 255 1.2× 100 0.7× 19 1.0k
Ronit Lahav United States 8 390 0.6× 126 0.4× 81 0.3× 212 1.0× 87 0.6× 8 740

Countries citing papers authored by Christopher Dravis

Since Specialization
Citations

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

Fields of papers citing papers by Christopher Dravis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christopher Dravis

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher Dravis. A scholar is included among the top collaborators of Christopher Dravis 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 Christopher Dravis. Christopher Dravis 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.
Christin, John R., Chunhui Wang, Chi-Yeh Chung, et al.. (2020). Stem Cell Determinant SOX9 Promotes Lineage Plasticity and Progression in Basal-like Breast Cancer. Cell Reports. 31(10). 107742–107742. 40 indexed citations
2.
Chung, Chi‐Yeh, Zhibo Ma, Christopher Dravis, et al.. (2019). Single-Cell Chromatin Analysis of Mammary Gland Development Reveals Cell-State Transcriptional Regulators and Lineage Relationships. Cell Reports. 29(2). 495–510.e6. 63 indexed citations
3.
Dravis, Christopher, Chi‐Yeh Chung, Nikki K. Lytle, et al.. (2018). Epigenetic and Transcriptomic Profiling of Mammary Gland Development and Tumor Models Disclose Regulators of Cell State Plasticity. Cancer Cell. 34(3). 466–482.e6. 88 indexed citations
4.
Giraddi, Rajshekhar R., Chi-Yeh Chung, Richard E. Heinz, et al.. (2018). Single-Cell Transcriptomes Distinguish Stem Cell State Changes and Lineage Specification Programs in Early Mammary Gland Development. Cell Reports. 24(6). 1653–1666.e7. 105 indexed citations
5.
Dravis, Christopher, Chi‐Yeh Chung, Nikki K. Lytle, et al.. (2018). Epigenetic and Transcriptomic Profiling of Mammary Gland Development and Tumor Models Disclose Regulators of Cell State Plasticity. SSRN Electronic Journal. 2 indexed citations
6.
Trejo, Christy L., et al.. (2017). Lgr5 is a marker for fetal mammary stem cells, but is not essential for stem cell activity or tumorigenesis. npj Breast Cancer. 3(1). 16–16. 28 indexed citations
7.
Dravis, Christopher, Benjamin T. Spike, J. Chuck Harrell, et al.. (2015). Sox10 Regulates Stem/Progenitor and Mesenchymal Cell States in Mammary Epithelial Cells. Cell Reports. 12(12). 2035–2048. 86 indexed citations
8.
Robichaux, Michael A., George Chenaux, Hsin‐Yi Henry Ho, et al.. (2014). EphB receptor forward signaling regulates area-specific reciprocal thalamic and cortical axon pathfinding. Proceedings of the National Academy of Sciences. 111(6). 2188–2193. 31 indexed citations
9.
Lal, Charitharth Vivek, Haiming Xu, George Chenaux, et al.. (2013). Ephrin-B2 Reverse Signaling Increases α5β1 Integrin–Mediated Fibronectin Deposition and Reduces Distal Lung Compliance. American Journal of Respiratory Cell and Molecular Biology. 49(4). 680–687. 16 indexed citations
10.
Makarem, Maisam, Benjamin T. Spike, Christopher Dravis, et al.. (2013). Stem Cells and the Developing Mammary Gland. Journal of Mammary Gland Biology and Neoplasia. 18(2). 209–219. 31 indexed citations
11.
Lee, Kenneth, et al.. (2013). Asymmetry in semicircular canal diameters may account for circling behavior in EphB‐deficient mice. The Laryngoscope. 124(7). E278–82.
12.
Dravis, Christopher, et al.. (2012). Characterization of the Larynx in Ephrin-B2 Knockout Mice. Archives of Otolaryngology - Head and Neck Surgery. 138(10). 969–969. 3 indexed citations
13.
Villasenor, Alethia, et al.. (2012). EphB3 marks delaminating endocrine progenitor cells in the developing pancreas. Developmental Dynamics. 241(5). 1008–1019. 23 indexed citations
14.
Dravis, Christopher & Mark Henkemeyer. (2011). Ephrin-B reverse signaling controls septation events at the embryonic midline through separate tyrosine phosphorylation-independent signaling avenues. Developmental Biology. 355(1). 138–151. 53 indexed citations
15.
Fang, Xiao‐Dong, Jianying Luo, Ryuichi Nishihama, et al.. (2010). Biphasic targeting and cleavage furrow ingression directed by the tail of a myosin II. The Journal of Cell Biology. 191(7). 1333–1350. 89 indexed citations
16.
Yücel, Selçuk, Christopher Dravis, Nilda M. García, Mark Henkemeyer, & Linda A. Baker. (2007). Hypospadias and anorectal malformations mediated by defective Eph/ephrin signaling. Journal of Pediatric Urology. 3(5). 354–363. 25 indexed citations
17.
Dravis, Christopher, Tao Wu, Michael J. Chumley, et al.. (2006). EphB2 and ephrin-B2 regulate the ionic homeostasis of vestibular endolymph. Hearing Research. 223(1-2). 93–104. 34 indexed citations
18.
García, Nilda M., Jacqueline R. Batanian, Christopher Dravis, et al.. (2006). Deletion mapping of critical region for hypospadias, penoscrotal transposition and imperforate anus on human chromosome 13. Journal of Pediatric Urology. 2(4). 233–242. 26 indexed citations
19.
Altick, Amy L., et al.. (2004). EphB receptor tyrosine kinases control morphological development of the ventral midbrain. Mechanisms of Development. 122(4). 501–512. 3 indexed citations
20.
Dravis, Christopher, Nobuhiko Yokoyama, Michael J. Chumley, et al.. (2004). Bidirectional signaling mediated by ephrin-B2 and EphB2 controls urorectal development. Developmental Biology. 271(2). 272–290. 186 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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