Robert O. Heuckeroth

9.9k total citations · 1 hit paper
91 papers, 6.8k citations indexed

About

Robert O. Heuckeroth is a scholar working on Surgery, Molecular Biology and Gastroenterology. According to data from OpenAlex, Robert O. Heuckeroth has authored 91 papers receiving a total of 6.8k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Surgery, 32 papers in Molecular Biology and 18 papers in Gastroenterology. Recurrent topics in Robert O. Heuckeroth's work include Congenital gastrointestinal and neural anomalies (45 papers), Gastrointestinal motility and disorders (18 papers) and Intestinal Malrotation and Obstruction Disorders (17 papers). Robert O. Heuckeroth is often cited by papers focused on Congenital gastrointestinal and neural anomalies (45 papers), Gastrointestinal motility and disorders (18 papers) and Intestinal Malrotation and Obstruction Disorders (17 papers). Robert O. Heuckeroth collaborates with scholars based in United States, Italy and France. Robert O. Heuckeroth's co-authors include Jeffrey Milbrandt, Jeffrey I. Gordon, Eugene M. Johnson, Hideki Enomoto, Judith P. Golden, Patricia A. Lampe, Jonathan I. Lake, Eugene M. Johnson, Douglas J. Creedon and Toshiyuki Araki and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Robert O. Heuckeroth

89 papers receiving 6.6k citations

Hit Papers

Neurturin, a relative of glial-cell-line-derived neurotro... 1996 2026 2006 2016 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
Robert O. Heuckeroth United States 43 2.9k 2.3k 1.7k 943 941 91 6.8k
Patrick B. Allen United States 45 4.0k 1.4× 1.0k 0.5× 2.8k 1.7× 356 0.4× 248 0.3× 102 9.3k
Norman Latov United States 53 1.9k 0.6× 407 0.2× 4.0k 2.4× 302 0.3× 468 0.5× 192 9.2k
Sadakazu Aiso Japan 46 2.3k 0.8× 1.4k 0.6× 976 0.6× 237 0.3× 92 0.1× 225 7.3k
Lesley Probert Greece 44 2.2k 0.7× 472 0.2× 1.1k 0.7× 474 0.5× 167 0.2× 101 7.4k
P. Kay Lund United States 52 3.1k 1.0× 1.7k 0.7× 916 0.5× 134 0.1× 263 0.3× 132 7.8k
Vivaldo Moura‐Neto Brazil 47 2.6k 0.9× 274 0.1× 768 0.5× 436 0.5× 106 0.1× 162 5.7k
T. Kendall Harden United States 61 6.6k 2.2× 653 0.3× 1.7k 1.0× 69 0.1× 206 0.2× 214 11.5k
Brian P. Eliceiri United States 43 4.4k 1.5× 439 0.2× 562 0.3× 114 0.1× 168 0.2× 147 7.5k
Luca Battistini Italy 60 3.4k 1.2× 748 0.3× 853 0.5× 379 0.4× 60 0.1× 157 11.4k
Lu Zhou China 25 2.2k 0.7× 326 0.1× 1.1k 0.7× 836 0.9× 55 0.1× 68 6.4k

Countries citing papers authored by Robert O. Heuckeroth

Since Specialization
Citations

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

Fields of papers citing papers by Robert O. Heuckeroth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert O. Heuckeroth. 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 Robert O. Heuckeroth. The network helps show where Robert O. Heuckeroth may publish in the future.

Co-authorship network of co-authors of Robert O. Heuckeroth

This figure shows the co-authorship network connecting the top 25 collaborators of Robert O. Heuckeroth. A scholar is included among the top collaborators of Robert O. Heuckeroth 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 Robert O. Heuckeroth. Robert O. Heuckeroth 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.
Lou, Meng, Robert O. Heuckeroth, & Naomi E. Butler Tjaden. (2024). Neuroimmune Crossroads: The Interplay of the Enteric Nervous System and Intestinal Macrophages in Gut Homeostasis and Disease. Biomolecules. 14(9). 1103–1103. 1 indexed citations
2.
Palmer, Nicholas J., Peter J. Carman, Małgorzata Boczkowska, et al.. (2024). Molecular mechanisms linking missense ACTG2 mutations to visceral myopathy. Science Advances. 10(22). eadn6615–eadn6615. 3 indexed citations
3.
Schneider, Sabine, Christina M. Wright, Guang Hai Yan, et al.. (2024). BAP1 is required prenatally for differentiation and maintenance of postnatal murine enteric nervous system. Journal of Clinical Investigation. 134(9).
4.
Carman, Peter J., et al.. (2022). A solution to the long-standing problem of actin expression and purification. Proceedings of the National Academy of Sciences. 119(41). e2209150119–e2209150119. 12 indexed citations
5.
Schneider, Kai Markus, Jihee Kim, Klaas Bahnsen, Robert O. Heuckeroth, & Christoph A. Thaiss. (2022). Environmental perception and control of gastrointestinal immunity by the enteric nervous system. Trends in Molecular Medicine. 28(11). 989–1005. 18 indexed citations
6.
White, James P., Shanshan Xiong, Nicole P. Malvin, et al.. (2018). Intestinal Dysmotility Syndromes following Systemic Infection by Flaviviruses. Cell. 175(5). 1198–1212.e12. 51 indexed citations
7.
Avetisyan, Marina, Christina M. Wright, Karim Mesbah, et al.. (2018). Loss of Tbx3 in murine neural crest reduces enteric glia and causes cleft palate, but does not influence heart development or bowel transit. Developmental Biology. 444. S337–S351. 11 indexed citations
8.
Avetisyan, Marina, Hongtao Wang, John R. Grider, et al.. (2015). Hepatocyte Growth Factor and MET Support Mouse Enteric Nervous System Development, the Peristaltic Response, and Intestinal Epithelial Proliferation in Response to Injury. Journal of Neuroscience. 35(33). 11543–11558. 32 indexed citations
9.
Jain, Sanjay, Amanda Knoten, Masato Hoshi, et al.. (2010). Organotypic specificity of key RET adaptor-docking sites in the pathogenesis of neurocristopathies and renal malformations in mice. Journal of Clinical Investigation. 120(3). 778–790. 43 indexed citations
10.
Zhang, Bin, Jufang Chang, M.W. Fu, et al.. (2009). Correction: Dosage Effects of Cohesin Regulatory Factor PDS5 on Mammalian Development: Implications for Cohesinopathies. PLoS ONE. 4(5). 18 indexed citations
11.
Zhang, Bin, Jufang Chang, Ming Fu, et al.. (2009). Dosage Effects of Cohesin Regulatory Factor PDS5 on Mammalian Development: Implications for Cohesinopathies. PLoS ONE. 4(5). e5232–e5232. 68 indexed citations
12.
Sato, Yoshiharu & Robert O. Heuckeroth. (2008). Retinoic acid regulates murine enteric nervous system precursor proliferation, enhances neuronal precursor differentiation, and reduces neurite growth in vitro. Developmental Biology. 320(1). 185–198. 50 indexed citations
13.
Wang, Hongtao, Yan Zhang, & Robert O. Heuckeroth. (2007). Tissue-type plasminogen activator deficiency exacerbates cholestatic liver injury in mice. Hepatology. 45(6). 1527–1537. 22 indexed citations
17.
Heuckeroth, Robert O.. (2003). Finding Your Way to the End. Neuron. 40(5). 871–873. 9 indexed citations
18.
Mazziotti, Mark V., Lauren K. Willis, Robert O. Heuckeroth, et al.. (1999). Anomalous development of the hepatobiliary system in the inv mouse. Hepatology. 30(2). 372–378. 94 indexed citations
19.
Enomoto, Hideki, Toshiyuki Araki, Alana Jackman, et al.. (1998). GFRα1-Deficient Mice Have Deficits in the Enteric Nervous System and Kidneys. Neuron. 21(2). 317–324. 373 indexed citations
20.
Baloh, Robert H., Malú G. Tansey, Judith P. Golden, et al.. (1997). TrnR2, a Novel Receptor That Mediates Neurturin and GDNF Signaling through Ret. Neuron. 18(5). 793–802. 300 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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