Lawrence Zukerberg

13.4k total citations · 3 hit papers
155 papers, 9.6k citations indexed

About

Lawrence Zukerberg is a scholar working on Oncology, Pathology and Forensic Medicine and Surgery. According to data from OpenAlex, Lawrence Zukerberg has authored 155 papers receiving a total of 9.6k indexed citations (citations by other indexed papers that have themselves been cited), including 60 papers in Oncology, 55 papers in Pathology and Forensic Medicine and 48 papers in Surgery. Recurrent topics in Lawrence Zukerberg's work include Lymphoma Diagnosis and Treatment (39 papers), Cancer-related Molecular Pathways (20 papers) and Viral-associated cancers and disorders (17 papers). Lawrence Zukerberg is often cited by papers focused on Lymphoma Diagnosis and Treatment (39 papers), Cancer-related Molecular Pathways (20 papers) and Viral-associated cancers and disorders (17 papers). Lawrence Zukerberg collaborates with scholars based in United States, Japan and Canada. Lawrence Zukerberg's co-authors include Nancy L. Harris, Judith A. Ferry, Margareta Nikolić, Gentry N. Patrick, Pieter Dikkes, Suzanne de la Monte, Li‐Huei Tsai, Andrew Arnold, Emmett V. Schmidt and Timothy C. Wang and has published in prestigious journals such as Nature, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

Lawrence Zukerberg

151 papers receiving 9.4k citations

Hit Papers

Conversion of p35 to p25 ... 1994 2026 2004 2015 1999 1994 2012 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lawrence Zukerberg United States 47 3.9k 3.4k 2.4k 1.9k 1.0k 155 9.6k
Yusuke Nakamura Japan 54 2.1k 0.6× 4.6k 1.4× 1.3k 0.5× 1.2k 0.6× 919 0.9× 160 10.4k
Yuzuru Kanakura Japan 58 3.4k 0.9× 4.6k 1.4× 1.1k 0.5× 1.9k 1.0× 761 0.8× 368 16.5k
Catharina Larsson Sweden 62 4.2k 1.1× 6.1k 1.8× 1.3k 0.5× 2.1k 1.1× 574 0.6× 358 14.4k
Robert M.W. Hofstra Netherlands 60 2.7k 0.7× 5.1k 1.5× 2.8k 1.2× 3.4k 1.8× 348 0.3× 251 12.9k
Pierre Dubus France 42 4.0k 1.0× 5.3k 1.6× 1.1k 0.5× 1.3k 0.7× 504 0.5× 163 9.7k
Shigeo Mori Japan 46 3.4k 0.9× 2.4k 0.7× 2.4k 1.0× 663 0.4× 508 0.5× 213 7.9k
Hiroshi Yokozaki Japan 62 4.1k 1.1× 6.1k 1.8× 1.9k 0.8× 2.2k 1.2× 784 0.8× 305 12.0k
Ronald A. DeLellis United States 51 2.6k 0.7× 2.6k 0.8× 1.5k 0.6× 2.3k 1.2× 350 0.3× 204 9.8k
Eiichi Morii Japan 53 2.5k 0.6× 4.3k 1.3× 699 0.3× 1.3k 0.7× 457 0.5× 431 10.4k
Stéphane Dalle France 52 4.0k 1.0× 3.0k 0.9× 1.0k 0.4× 1.2k 0.6× 483 0.5× 325 9.1k

Countries citing papers authored by Lawrence Zukerberg

Since Specialization
Citations

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

Fields of papers citing papers by Lawrence Zukerberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lawrence Zukerberg

This figure shows the co-authorship network connecting the top 25 collaborators of Lawrence Zukerberg. A scholar is included among the top collaborators of Lawrence Zukerberg 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 Lawrence Zukerberg. Lawrence Zukerberg 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.
Eng, George, Rachid Zagani, Martin S. Taylor, et al.. (2023). Germline Determinants of Esophageal Adenocarcinoma. Gastroenterology. 165(5). 1276–1279.e7. 3 indexed citations
2.
Li, Darrick K., Snehal N. Chaudhari, Yoojin Lee, et al.. (2022). Inhibition of microbial deconjugation of micellar bile acids protects against intestinal permeability and liver injury. Science Advances. 8(34). eabo2794–eabo2794. 31 indexed citations
3.
Feldman, Dan, et al.. (2022). Incidence and natural history of gastric high-grade dysplasia in patients with familial adenomatous polyposis syndrome. Gastrointestinal Endoscopy. 97(1). 25–34.e6. 8 indexed citations
4.
Rickelt, Steffen, Miyeko Mana, Charles A. Whittaker, et al.. (2019). Agrin in the Muscularis Mucosa Serves as a Biomarker Distinguishing Hyperplastic Polyps from Sessile Serrated Lesions. Clinical Cancer Research. 26(6). 1277–1287. 11 indexed citations
5.
Fidias, Panos, Aidan A. Long, Florian J. Fintelmann, & Lawrence Zukerberg. (2015). Case 31-2015. New England Journal of Medicine. 373(15). 1458–1467. 3 indexed citations
6.
Thiagarajah, Jay R., Hasan Yıldız, Taylor L. Carlson, et al.. (2014). Altered Goblet Cell Differentiation and Surface Mucus Properties in Hirschsprung Disease. PLoS ONE. 9(6). e99944–e99944. 45 indexed citations
7.
Clark, Rachel M., et al.. (2014). The N-methyl-D-aspartate Receptor, a Precursor to N-methyl-D-aspartate Receptor Encephalitis, is Found in the Squamous Tissue of Ovarian Teratomas. International Journal of Gynecological Pathology. 33(6). 598–606. 10 indexed citations
8.
Linskey, Katy, et al.. (2013). BerEp4, Cytokeratin 14, and Cytokeratin 17 Immunohistochemical Staining Aid in Differentiation of Basaloid Squamous Cell Carcinoma From Basal Cell Carcinoma With Squamous Metaplasia. Archives of Pathology & Laboratory Medicine. 137(11). 1591–1598. 31 indexed citations
9.
Louissaint, Abner, Adam Ackerman, Dora Dias‐Santagata, et al.. (2012). Pediatric-type nodal follicular lymphoma: an indolent clonal proliferation in children and adults with high proliferation index and no BCL2 rearrangement. Blood. 120(12). 2395–2404. 89 indexed citations
10.
Yılmaz, Ömer, Pekka Katajisto, Dudley W. Lamming, et al.. (2012). mTORC1 in the Paneth cell niche couples intestinal stem-cell function to calorie intake. Nature. 486(7404). 490–495. 547 indexed citations breakdown →
11.
Friel, Anne M., Lingling Zhang, Michael D. Curley, et al.. (2010). Epigenetic regulation of CD133 and tumorigenicity of CD133 positive and negative endometrial cancer cells. Reproductive Biology and Endocrinology. 8(1). 147–147. 47 indexed citations
12.
Geyer, Julia T., Judith A. Ferry, Janina A. Longtine, et al.. (2009). Characteristics of Cutaneous Marginal Zone Lymphomas With Marked Plasmacytic Differentiation and a T Cell–Rich Background. American Journal of Clinical Pathology. 133(1). 59–69. 28 indexed citations
13.
Park, Do Youn, Amitabh Srivastava, Gwang Ha Kim, et al.. (2008). Adenomatous and Foveolar Gastric Dysplasia: Distinct Patterns of Mucin Expression and Background Intestinal Metaplasia. The American Journal of Surgical Pathology. 32(4). 524–533. 69 indexed citations
14.
Wang, Sa A., Neal Olson, Lawrence Zukerberg, & Nancy L. Harris. (2006). Splenic Marginal Zone Lymphoma With Micronodular T-Cell Rich B-Cell Lymphoma. The American Journal of Surgical Pathology. 30(1). 128–132. 8 indexed citations
15.
Zhang, Hui, et al.. (2005). Aberrant splicing of cables gene, a CDK regulator, in human cancers. Cancer Biology & Therapy. 4(11). 1211–1215. 13 indexed citations
16.
Debernardo, Robert, Ramey D. Littell, Huaxiu Luo, et al.. (2005). Defining the extent of cables loss in endometrial cancer subtypes and its effectiveness as an inhibitor of cell proliferation in malignant endometrial cells in vitro and in vivo. Cancer Biology & Therapy. 4(1). 110–114. 16 indexed citations
17.
Deshpande, Vikram, Carlos Fernández‐del Castillo, Alona Muzikansky, et al.. (2004). Cytokeratin 19 Is a Powerful Predictor of Survival in Pancreatic Endocrine Tumors. The American Journal of Surgical Pathology. 28(9). 1145–1153. 85 indexed citations
18.
Wu, Chin‐Lee, et al.. (1995). In Vivo Association of E2F and DP Family Proteins. Molecular and Cellular Biology. 15(5). 2536–2546. 210 indexed citations
19.
Zukerberg, Lawrence, Nancy L. Harris, & Robert H. Young. (1991). Carcinomas of the Urinary Bladder Simulating Malignant Lymphoma. The American Journal of Surgical Pathology. 15(6). 569–576. 136 indexed citations
20.
Zukerberg, Lawrence, Andrew E. Rosenberg, Gregory W. Randolph, Ben Z. Pilch, & Max L. Goodman. (1991). Solitary Fibrous Tumor of the Nasal Cavity and Paranasal Sinuses. The American Journal of Surgical Pathology. 15(2). 126–130. 157 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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