Deborah L. Chapman

4.9k total citations · 2 hit papers
32 papers, 3.8k citations indexed

About

Deborah L. Chapman is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Deborah L. Chapman has authored 32 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 10 papers in Genetics and 3 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Deborah L. Chapman's work include Developmental Biology and Gene Regulation (16 papers), Congenital heart defects research (15 papers) and Genomics and Chromatin Dynamics (7 papers). Deborah L. Chapman is often cited by papers focused on Developmental Biology and Gene Regulation (16 papers), Congenital heart defects research (15 papers) and Genomics and Chromatin Dynamics (7 papers). Deborah L. Chapman collaborates with scholars based in United States, Australia and Latvia. Deborah L. Chapman's co-authors include Virginia E. Papaioannou, Argiris Efstratiadis, Jeh-Ping Liu, Scott Zeitlin, Lee M. Silver, Sarah Hancock, Thomas Ludwig, Sergei I. Agulnik, Nancy Garvey and Maria Alexiou and has published in prestigious journals such as Nature, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Deborah L. Chapman

32 papers receiving 3.8k citations

Hit Papers

Increased apoptosis and e... 1995 2026 2005 2015 1995 1996 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Deborah L. Chapman United States 23 3.3k 950 635 377 274 32 3.8k
Michel Cohen‐Tannoudji France 32 2.6k 0.8× 756 0.8× 391 0.6× 338 0.9× 243 0.9× 73 3.5k
William C. Skarnes United Kingdom 28 3.5k 1.0× 1.1k 1.2× 657 1.0× 756 2.0× 325 1.2× 39 4.3k
Lauren Snider United States 23 4.1k 1.2× 762 0.8× 730 1.1× 368 1.0× 160 0.6× 33 4.7k
Ronald A. Conlon United States 31 4.9k 1.5× 1.0k 1.1× 710 1.1× 857 2.3× 282 1.0× 45 6.1k
Mākoto Ishibashi Japan 20 3.1k 0.9× 971 1.0× 537 0.8× 380 1.0× 379 1.4× 56 4.2k
Siew‐Lan Ang United States 37 4.4k 1.3× 988 1.0× 640 1.0× 462 1.2× 452 1.6× 48 6.2k
C.E. Lindsell United States 16 2.9k 0.9× 705 0.7× 266 0.4× 382 1.0× 186 0.7× 23 4.0k
Tiffany Cook United States 32 2.5k 0.7× 681 0.7× 941 1.5× 599 1.6× 180 0.7× 75 3.7k
François Coulier France 24 3.4k 1.0× 789 0.8× 569 0.9× 949 2.5× 348 1.3× 46 4.2k
Alar Karis Estonia 24 2.0k 0.6× 461 0.5× 479 0.8× 255 0.7× 267 1.0× 33 3.3k

Countries citing papers authored by Deborah L. Chapman

Since Specialization
Citations

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

Fields of papers citing papers by Deborah L. Chapman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Deborah L. Chapman. 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 Deborah L. Chapman. The network helps show where Deborah L. Chapman may publish in the future.

Co-authorship network of co-authors of Deborah L. Chapman

This figure shows the co-authorship network connecting the top 25 collaborators of Deborah L. Chapman. A scholar is included among the top collaborators of Deborah L. Chapman 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 Deborah L. Chapman. Deborah L. Chapman 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.
Chapman, Deborah L., et al.. (2022). Ectopic expression of T in the paraxial mesoderm disrupts somite maturation in the mouse. Developmental Biology. 485. 37–49. 1 indexed citations
2.
Chapman, Deborah L., et al.. (2020). Functionally distinct roles for T and Tbx6 during mouse development. Biology Open. 9(8). 5 indexed citations
3.
Chapman, Deborah L.. (2018). Impaired intermediate formation in mouse embryos expressing reduced levels of Tbx6. genesis. 57(3). e23270–e23270. 3 indexed citations
4.
Dai, Hai‐Qiang, Lu Yang, Jiajia Chen, et al.. (2016). TET-mediated DNA demethylation controls gastrulation by regulating Lefty–Nodal signalling. Nature. 538(7626). 528–532. 145 indexed citations
5.
Sparrow, Duncan B., Aideen McInerney‐Leo, Zoran Gucev, et al.. (2013). Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6. Human Molecular Genetics. 22(8). 1625–1631. 56 indexed citations
6.
Chalamalasetty, Ravindra B., William C. Dunty, Kristin K. Biris, et al.. (2011). The Wnt3a/β-catenin target gene Mesogenin1 controls the segmentation clock by activating a Notch signalling program. Nature Communications. 2(1). 390–390. 52 indexed citations
7.
Chapman, Deborah L., et al.. (2010). Tbx18 and Tbx15 null-like phenotypes in mouse embryos expressing Tbx6 in somitic and lateral plate mesoderm. Developmental Biology. 347(2). 404–413. 10 indexed citations
8.
Chapman, Deborah L., et al.. (2009). Kinked tail mutation results in notochord defects in heterozygotes and distal visceral endoderm defects in homozygotes. Developmental Dynamics. 238(12). 3237–3247. 8 indexed citations
9.
Gallo, Phillip H., et al.. (2009). Generation of transgenic mice expressing Cre recombinase under the control of the Dll1 mesoderm enhancer element. genesis. 47(5). 309–313. 9 indexed citations
10.
Oginuma, Masayuki, Yasutaka Niwa, Deborah L. Chapman, & Yumiko Saga. (2008). Mesp2 and Tbx6 cooperatively create periodic patterns coupled with the clock machinery during mouse somitogenesis. Development. 135(15). 2555–2562. 85 indexed citations
11.
Chapman, Deborah L., et al.. (2005). Dll1 is a downstream target of Tbx6 in the paraxial mesoderm. genesis. 42(3). 193–202. 49 indexed citations
12.
Hogan, Kelly A., Carrie A. Ambler, Deborah L. Chapman, & Victoria L. Bautch. (2004). The neural tube patterns vessels developmentally using the VEGF signaling pathway. Development. 131(7). 1503–1513. 124 indexed citations
13.
Agulnik, Sergei I., Nancy Garvey, Sarah Hancock, et al.. (1996). Evolution of Mouse T-box Genes by Tandem Duplication and Cluster Dispersion. Genetics. 144(1). 249–254. 165 indexed citations
14.
Chapman, Deborah L., et al.. (1996). Tbx6,a Mouse T-Box Gene Implicated in Paraxial Mesoderm Formation at Gastrulation. Developmental Biology. 180(2). 534–542. 224 indexed citations
15.
Zeitlin, Scott, Jeh-Ping Liu, Deborah L. Chapman, Virginia E. Papaioannou, & Argiris Efstratiadis. (1995). Increased apoptosis and early embryonic lethality in mice nullizygous for the Huntington's disease gene homologue. Nature Genetics. 11(2). 155–163. 597 indexed citations breakdown →
16.
Chapman, Deborah L., et al.. (1994). Expression of proliferating cell nuclear antigen in the mouse germ line and surrounding somatic cells suggests both proliferation-dependent and -independent modes of function. The International Journal of Developmental Biology. 38(3). 491–497. 64 indexed citations
17.
Chapman, Deborah L., et al.. (1994). Regulation of M-Phase Promoting Factor Activity during Development of Mouse Male Germ Cells. Developmental Biology. 165(2). 500–506. 46 indexed citations
19.
Chapman, Deborah L. & Debra J. Wolgemuth. (1992). Identification of a mouse B‐type cyclin which exhibits developmentally regulated expression in the germ line. Molecular Reproduction and Development. 33(3). 259–269. 86 indexed citations
20.
Piepkorn, Michael W. & Deborah L. Chapman. (1985). Glycosaminoglycans and the substrate attachment of murine myeloma, 3T3, and cutaneous fibrosarcoma cells.. PubMed. 53(1). 22–9. 8 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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