Max A. Tischfield

3.2k total citations
27 papers, 1.6k citations indexed

About

Max A. Tischfield is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Max A. Tischfield has authored 27 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 9 papers in Genetics and 8 papers in Cellular and Molecular Neuroscience. Recurrent topics in Max A. Tischfield's work include Cellular transport and secretion (5 papers), Microtubule and mitosis dynamics (4 papers) and Ophthalmology and Eye Disorders (4 papers). Max A. Tischfield is often cited by papers focused on Cellular transport and secretion (5 papers), Microtubule and mitosis dynamics (4 papers) and Ophthalmology and Eye Disorders (4 papers). Max A. Tischfield collaborates with scholars based in United States, United Kingdom and Saudi Arabia. Max A. Tischfield's co-authors include Elizabeth C. Engle, G. Cederquist, Mohan L. Gupta, Masahiro Fukaya, Ethan G. Hughes, Dwight E. Bergles, Amit Agarwal, Pei-Hsun Wu, Abraham J. Langseth and Denis Wirtz and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Neuron.

In The Last Decade

Max A. Tischfield

25 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Max A. Tischfield United States 17 812 454 325 306 304 27 1.6k
Jesper Ryge Sweden 12 971 1.2× 506 1.1× 205 0.6× 212 0.7× 196 0.6× 16 1.5k
Joanna Dzwonek Poland 15 898 1.1× 620 1.4× 253 0.8× 154 0.5× 221 0.7× 21 1.7k
Richard Fairless Germany 23 518 0.6× 597 1.3× 138 0.4× 102 0.3× 231 0.8× 39 1.4k
Zhengmao Hu China 25 1000 1.2× 430 0.9× 207 0.6× 535 1.7× 209 0.7× 127 1.9k
Jason Liauw United States 18 717 0.9× 866 1.9× 108 0.3× 138 0.5× 242 0.8× 29 1.8k
Tanjew Dittgen Germany 10 468 0.6× 387 0.9× 113 0.3× 137 0.4× 166 0.5× 10 1.0k
Jay B. Bikoff United States 14 975 1.2× 909 2.0× 567 1.7× 228 0.7× 112 0.4× 22 1.8k
Fatima Memic Sweden 11 1.3k 1.6× 567 1.2× 225 0.7× 172 0.6× 427 1.4× 15 2.5k
Yongcheol Cho South Korea 18 1.1k 1.3× 890 2.0× 249 0.8× 343 1.1× 74 0.2× 34 1.8k
Chen Gu United States 23 626 0.8× 453 1.0× 232 0.7× 83 0.3× 139 0.5× 37 1.2k

Countries citing papers authored by Max A. Tischfield

Since Specialization
Citations

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

Fields of papers citing papers by Max A. Tischfield

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Max A. Tischfield. 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 Max A. Tischfield. The network helps show where Max A. Tischfield may publish in the future.

Co-authorship network of co-authors of Max A. Tischfield

This figure shows the co-authorship network connecting the top 25 collaborators of Max A. Tischfield. A scholar is included among the top collaborators of Max A. Tischfield 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 Max A. Tischfield. Max A. Tischfield 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.
Tischfield, Max A., et al.. (2025). Genetic advances and translational phenotypes in rodent models for Tourette disorder. Current Opinion in Neurobiology. 90. 102967–102967. 1 indexed citations
2.
Suh, Joonho, et al.. (2025). PRDX5 Regulates Mitochondrial Function and Nuclear Spreading in Myogenesis and Acts With PRDX3 to Delay Muscle Aging. Journal of Cachexia Sarcopenia and Muscle. 16(6). e70098–e70098.
3.
Nasello, Cara, Junbing Wu, Joshua K. Thackray, et al.. (2024). Human mutations in high-confidence Tourette disorder genes affect sensorimotor behavior, reward learning, and striatal dopamine in mice. Proceedings of the National Academy of Sciences. 121(19). e2307156121–e2307156121. 8 indexed citations
4.
Tischfield, Max A., et al.. (2023). Loss of Twist1 and balanced retinoic acid signaling from the meninges causes cortical folding in mice. Development. 150(18). 3 indexed citations
5.
Pattison, Luke A., Heather L. Rossi, Joshua K. Thackray, et al.. (2023). Mapping the neuroethological signatures of pain, analgesia, and recovery in mice. Neuron. 111(18). 2811–2830.e8. 26 indexed citations
6.
Wu, Junbing, et al.. (2023). Piezo1 agonist restores meningeal lymphatic vessels, drainage, and brain-CSF perfusion in craniosynostosis and aged mice. Journal of Clinical Investigation. 134(4). 31 indexed citations
7.
Tischfield, Max A., et al.. (2023). Understanding the development, pathogenesis, and injury response of meningeal lymphatic networks through the use of animal models. Cellular and Molecular Life Sciences. 80(11). 332–332. 6 indexed citations
8.
Wu, Junbing, et al.. (2022). Planar cell polarity and the pathogenesis of Tourette Disorder: New hypotheses and perspectives. Developmental Biology. 489. 14–20. 3 indexed citations
9.
Whitman, Mary C., et al.. (2022). TWIST1, a gene associated with Saethre-Chotzen syndrome, regulates extraocular muscle organization in mouse. Developmental Biology. 490. 126–133. 5 indexed citations
10.
Reid, Russell R., et al.. (2022). Cranium growth, patterning and homeostasis. Development. 149(22). 4 indexed citations
11.
Tischfield, Max A., et al.. (2021). The growth and expansion of meningeal lymphatic networks are affected in craniosynostosis. Development. 149(1). 12 indexed citations
12.
13.
Tischfield, Max A., Caroline D. Robson, Shek Man Chim, et al.. (2017). Cerebral Vein Malformations Result from Loss of Twist1 Expression and BMP Signaling from Skull Progenitor Cells and Dura. Developmental Cell. 42(5). 445–461.e5. 35 indexed citations
14.
Park, Jong G., Max A. Tischfield, Alicia Nugent, et al.. (2016). Loss of MAFB Function in Humans and Mice Causes Duane Syndrome, Aberrant Extraocular Muscle Innervation, and Inner-Ear Defects. The American Journal of Human Genetics. 98(6). 1220–1227. 54 indexed citations
15.
Whitman, Mary C., Caroline Andrews, Wai‐Man Chan, et al.. (2015). Two unique TUBB3 mutations cause both CFEOM3 and malformations of cortical development. American Journal of Medical Genetics Part A. 170(2). 297–305. 47 indexed citations
16.
Zhou, Yulian, Yanshu Wang, Max A. Tischfield, et al.. (2014). Canonical WNT signaling components in vascular development and barrier formation. Journal of Clinical Investigation. 124(9). 3825–3846. 252 indexed citations
17.
Cederquist, G., Anna Łuchniak, Max A. Tischfield, et al.. (2012). An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation. Human Molecular Genetics. 21(26). 5484–5499. 95 indexed citations
18.
Tischfield, Max A., G. Cederquist, Mohan L. Gupta, & Elizabeth C. Engle. (2011). Phenotypic spectrum of the tubulin-related disorders and functional implications of disease-causing mutations. Current Opinion in Genetics & Development. 21(3). 286–294. 166 indexed citations
19.
Bosley, Thomas M., Ibrahim A. Alorainy, Mustafa A. Salih, et al.. (2008). The clinical spectrum of homozygous HOXA1 mutations. American Journal of Medical Genetics Part A. 146A(10). 1235–1240. 75 indexed citations
20.
Tischfield, Max A., Thomas M. Bosley, Mustafa A. Salih, et al.. (2005). Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development. Nature Genetics. 37(10). 1035–1037. 206 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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