David Zagzag

32.6k total citations · 5 hit papers
258 papers, 19.3k citations indexed

About

David Zagzag is a scholar working on Genetics, Molecular Biology and Neurology. According to data from OpenAlex, David Zagzag has authored 258 papers receiving a total of 19.3k indexed citations (citations by other indexed papers that have themselves been cited), including 105 papers in Genetics, 63 papers in Molecular Biology and 62 papers in Neurology. Recurrent topics in David Zagzag's work include Glioma Diagnosis and Treatment (105 papers), Cancer, Hypoxia, and Metabolism (43 papers) and MRI in cancer diagnosis (24 papers). David Zagzag is often cited by papers focused on Glioma Diagnosis and Treatment (105 papers), Cancer, Hypoxia, and Metabolism (43 papers) and MRI in cancer diagnosis (24 papers). David Zagzag collaborates with scholars based in United States, Canada and Germany. David Zagzag's co-authors include Glyn Johnson, Meng Law, Edmond A. Knopp, Gregg L. Semenza, Jonathan W. Simons, Soonmee Cha, Elizabeth W. Newcomb, James S. Babb, Erik Laughner and George D. Yancopoulos and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

David Zagzag

257 papers receiving 18.9k citations

Hit Papers

Overexpression of hypoxia... 1999 2026 2008 2017 1999 1999 2003 1999 2000 500 1000 1.5k

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
David Zagzag 7.8k 5.9k 5.3k 4.2k 3.4k 258 19.3k
Gregory N. Fuller 8.0k 1.0× 7.1k 1.2× 4.6k 0.9× 1.9k 0.4× 5.0k 1.5× 416 20.2k
Manfred Westphal 5.9k 0.8× 8.0k 1.3× 3.6k 0.7× 2.1k 0.5× 3.1k 0.9× 434 18.6k
Paul S. Mischel 10.5k 1.3× 6.0k 1.0× 5.9k 1.1× 1.8k 0.4× 4.5k 1.3× 218 19.5k
C. David James 10.4k 1.3× 7.8k 1.3× 4.8k 0.9× 1.4k 0.3× 4.7k 1.4× 237 19.5k
Samuel K. Ludwin 7.0k 0.9× 11.0k 1.9× 3.9k 0.7× 2.7k 0.6× 3.1k 0.9× 78 20.4k
Nicolas de Tribolet 6.2k 0.8× 7.0k 1.2× 3.1k 0.6× 1.7k 0.4× 3.9k 1.2× 189 16.4k
Howard A. Fine 9.1k 1.2× 9.6k 1.6× 4.9k 0.9× 1.7k 0.4× 5.2k 1.5× 235 21.3k
Barbara Fisher 5.5k 0.7× 12.0k 2.0× 3.6k 0.7× 2.8k 0.7× 3.5k 1.0× 47 18.3k
Karl Bélanger 6.0k 0.8× 11.3k 1.9× 3.8k 0.7× 2.7k 0.6× 3.4k 1.0× 39 17.6k
Johannes A. Hainfellner 6.0k 0.8× 7.5k 1.3× 3.1k 0.6× 1.6k 0.4× 2.4k 0.7× 297 14.9k

Countries citing papers authored by David Zagzag

Since Specialization
Citations

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

Fields of papers citing papers by David Zagzag

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Zagzag

This figure shows the co-authorship network connecting the top 25 collaborators of David Zagzag. A scholar is included among the top collaborators of David Zagzag 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 David Zagzag. David Zagzag 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.
Mehta, Sonal, Richard A. Feelders, Fadime Dogan, et al.. (2025). Somatostatin 5 receptor expression in prolactinomas: Is there a role for Pasireotide in the management of prolactinomas?. Pituitary. 28(6). 123–123.
2.
Lee, Matthew, Rajan Jain, Kristyn Galbraith, et al.. (2024). T2-FLAIR Mismatch Sign Predicts DNA Methylation Subclass and CDKN2A/B Status in IDH -Mutant Astrocytomas. Clinical Cancer Research. 30(16). 3512–3519. 2 indexed citations
3.
Lechpammer, Mirna, Austin Todd, Alexander D. Borowsky, et al.. (2024). Neuropathological Applications of Microscopy with Ultraviolet Surface Excitation (MUSE): A Concordance Study of Human Primary and Metastatic Brain Tumors. Brain Sciences. 14(1). 108–108. 1 indexed citations
4.
Kurz, Sylvia C., Elçin Zan, Andrea B. Troxel, et al.. (2023). Evaluation of the SSTR2-targeted Radiopharmaceutical 177Lu-DOTATATE and SSTR2-specific 68Ga-DOTATATE PET as Imaging Biomarker in Patients with Intracranial Meningioma. Clinical Cancer Research. 30(4). 680–686. 23 indexed citations
5.
Agarwal, Shashank, Vinh Nguyen, Siddhant Dogra, et al.. (2020). Serial Imaging of Virus-Associated Necrotizing Disseminated Acute Leukoencephalopathy (VANDAL) in COVID-19. American Journal of Neuroradiology. 42(2). 279–284. 11 indexed citations
6.
Dogra, Siddhant, Rajan Jain, Meng Cao, et al.. (2020). Hemorrhagic stroke and anticoagulation in COVID-19. Journal of Stroke and Cerebrovascular Diseases. 29(8). 104984–104984. 127 indexed citations
7.
Golub, Danielle, et al.. (2020). Pediatric midline H3K27M-mutant tumor with disseminated leptomeningeal disease and glioneuronal features: case report and literature review. Child s Nervous System. 37(7). 2347–2356. 10 indexed citations
8.
Snuderl, Matija, Guoan Zhang, Pamela Wu, et al.. (2017). Endothelium-Independent Primitive Myxoid Vascularization Creates Invertebrate-Like Channels to Maintain Blood Supply in Optic Gliomas. American Journal Of Pathology. 187(8). 1867–1878. 4 indexed citations
9.
Takano, Naoharu, Yasmeen Sarfraz, Daniele M. Gilkes, et al.. (2014). Decreased Expression of Cystathionine β-Synthase Promotes Glioma Tumorigenesis. Molecular Cancer Research. 12(10). 1398–1406. 53 indexed citations
10.
Najjar, Souhel, Daniel M. Pearlman, Orrin Devinsky, Amanda Najjar, & David Zagzag. (2013). Neurovascular unit dysfunction with blood-brain barrier hyperpermeability contributes to major depressive disorder: a review of clinical and experimental evidence. Journal of Neuroinflammation. 10(1). 142–142. 190 indexed citations
11.
Hardee, Matthew E. & David Zagzag. (2012). Mechanisms of Glioma-Associated Neovascularization. American Journal Of Pathology. 181(4). 1126–1141. 346 indexed citations
12.
Lee, Seung‐Jae, Velasco Cimica, Nandini Ramachandra, David Zagzag, & Ganjam V. Kalpana. (2011). Aurora A Is a Repressed Effector Target of the Chromatin Remodeling Protein INI1/hSNF5 Required for Rhabdoid Tumor Cell Survival. Cancer Research. 71(9). 3225–3235. 70 indexed citations
13.
Lee, Seung Jae, et al.. (2007). INI1 Induces Interferon Signaling and Spindle Checkpoint in Rhabdoid Tumors. Clinical Cancer Research. 13(16). 4721–4730. 32 indexed citations
14.
Lui, Yvonne W., Meng Law, James S. Babb, et al.. (2007). BRAINSTEM CORTICOSPINAL TRACT DIFFUSION TENSOR IMAGING IN PATIENTS WITH PRIMARY POSTERIOR FOSSA NEOPLASMS STRATIFIED BY TUMOR TYPE. Neurosurgery. 61(6). 1199–1208. 18 indexed citations
15.
Krishnamachary, Balaji, David Zagzag, Hideko Nagasawa, et al.. (2006). Hypoxia-Inducible Factor-1-Dependent Repression of E-cadherin in von Hippel-Lindau Tumor Suppressor–Null Renal Cell Carcinoma Mediated by TCF3, ZFHX1A, and ZFHX1B. Cancer Research. 66(5). 2725–2731. 333 indexed citations
16.
Wensky, Allen, Gláucia C. Furtado, Maria Cecília Garibaldi Marcondes, et al.. (2005). IFN-γ Determines Distinct Clinical Outcomes in Autoimmune Encephalomyelitis. The Journal of Immunology. 174(3). 1416–1423. 85 indexed citations
17.
Law, Meng, Stanley Yang, Hao Wang, et al.. (2003). Glioma grading: sensitivity, specificity, and predictive values of perfusion MR imaging and proton MR spectroscopic imaging compared with conventional MR imaging. American Journal of Neuroradiology. 24(10). 1989–1998. 803 indexed citations breakdown →
18.
Cangül, Hakan, Konstantin Salnikow, Herman Yee, et al.. (2002). Enhanced overexpression of an HIF-1/hypoxia-related protein in cancer cells.. Environmental Health Perspectives. 110(suppl 5). 783–788. 44 indexed citations
19.
Zonenshayn, Martin, Suash Sharma, Kenneth B. Hymes, et al.. (1998). Mycosis Fungoides Metastasizing to the Brain Parenchyma: Case Report. Neurosurgery. 42(4). 933–937. 17 indexed citations
20.
Zagzag, David, Marvin M. Goldenberg, & Steven Brem. (1989). Angiogenesis and Blood-Brain Barrier Breakdown Modulate CT Contrast Enhancement: An Experimental Study in a Rabbit Brain-Tumor Model. American Journal of Neuroradiology. 10(3). 529–534. 5 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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