Alexandra Lebensohn

689 total citations
10 papers, 323 citations indexed

About

Alexandra Lebensohn is a scholar working on Oncology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, Alexandra Lebensohn has authored 10 papers receiving a total of 323 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Oncology, 3 papers in Pulmonary and Respiratory Medicine and 3 papers in Genetics. Recurrent topics in Alexandra Lebensohn's work include BRCA gene mutations in cancer (3 papers), Cancer Genomics and Diagnostics (2 papers) and Genetic factors in colorectal cancer (2 papers). Alexandra Lebensohn is often cited by papers focused on BRCA gene mutations in cancer (3 papers), Cancer Genomics and Diagnostics (2 papers) and Genetic factors in colorectal cancer (2 papers). Alexandra Lebensohn collaborates with scholars based in United States, South Korea and Spain. Alexandra Lebensohn's co-authors include James M. Ford, Melinda L. Telli, Allison W. Kurian, Tanya Gupta, Meredith Mills, Jennifer L. Caswell‐Jin, Evan Hall, Iva Petrovchich, Nicolette M. Chun and Kerry Kingham and has published in prestigious journals such as The American Journal of Gastroenterology, The Oncologist and Breast Cancer Research and Treatment.

In The Last Decade

Alexandra Lebensohn

9 papers receiving 321 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alexandra Lebensohn United States 6 192 115 111 96 59 10 323
Judith Balmaña Gelpí Spain 4 150 0.8× 98 0.9× 126 1.1× 94 1.0× 36 0.6× 9 256
Sonia Nanda Canada 7 234 1.2× 108 0.9× 141 1.3× 190 2.0× 53 0.9× 8 426
Elisabetta Razzaboni Italy 8 182 0.9× 64 0.6× 103 0.9× 93 1.0× 67 1.1× 16 307
Kristen J. Vogel Postula United States 8 219 1.1× 112 1.0× 84 0.8× 95 1.0× 118 2.0× 13 313
Nicolette M. Chun United States 9 262 1.4× 119 1.0× 58 0.5× 142 1.5× 87 1.5× 24 382
Paraskevi Apostolou Greece 10 300 1.6× 130 1.1× 91 0.8× 211 2.2× 95 1.6× 22 449
Astrid Bechtold Germany 5 197 1.0× 142 1.2× 76 0.7× 93 1.0× 46 0.8× 5 308
Barbara Bulman United Kingdom 5 158 0.8× 187 1.6× 120 1.1× 183 1.9× 44 0.7× 5 344
Amal Yussuf United States 11 178 0.9× 125 1.1× 95 0.9× 92 1.0× 90 1.5× 29 322
Ann Strydom United Kingdom 5 282 1.5× 102 0.9× 131 1.2× 90 0.9× 38 0.6× 6 348

Countries citing papers authored by Alexandra Lebensohn

Since Specialization
Citations

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

Fields of papers citing papers by Alexandra Lebensohn

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexandra Lebensohn

This figure shows the co-authorship network connecting the top 25 collaborators of Alexandra Lebensohn. A scholar is included among the top collaborators of Alexandra Lebensohn 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 Alexandra Lebensohn. Alexandra Lebensohn is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

10 of 10 papers shown
1.
Vocke, Cathy D., C. Ricketts, Alexandra Lebensohn, et al.. (2025). Multigenerational VHL family characterized by pathogenic germline ELOC variant: Response to belzutifan. Urologic Oncology Seminars and Original Investigations. 44(2). 120.e21–120.e27.
2.
Lebensohn, Alexandra, Azam Ghafoor, Leslie Castelo‐Soccio, et al.. (2024). Multiple Onychopapillomas and BAP1 Tumor Predisposition Syndrome. JAMA Dermatology. 160(8). 838–838. 2 indexed citations
3.
Nair, Nishanth Ulhas, Qun Jiang, Jun S. Wei, et al.. (2023). Genomic and transcriptomic analyses identify a prognostic gene signature and predict response to therapy in pleural and peritoneal mesothelioma. Cell Reports Medicine. 4(2). 100938–100938. 11 indexed citations
4.
Hu, Zishuo I., Markku Miettinen, Martha Quezado, et al.. (2021). Meningiomas in Patients With Malignant Pleural Mesothelioma Harboring Germline BAP1 Mutations. Journal of Thoracic Oncology. 17(3). 461–466. 3 indexed citations
5.
Patel, Shyam A., Teri A. Longacre, Uri Ladabaum, et al.. (2018). Tumor Molecular Testing Guides Anti-PD-1 Therapy and Provides Evidence for Pathogenicity of Mismatch Repair Variants. The Oncologist. 23(12). 1395–1400. 7 indexed citations
6.
Caswell‐Jin, Jennifer L., Tanya Gupta, Evan Hall, et al.. (2017). Racial/ethnic differences in multiple-gene sequencing results for hereditary cancer risk. Genetics in Medicine. 20(2). 234–239. 126 indexed citations
7.
Jacobs, Aryana, Marc D. Schwartz, Heiðdís Valdimarsdóttir, et al.. (2016). Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancer. Familial Cancer. 15(4). 529–539. 25 indexed citations
8.
Idos, Gregory, Allison W. Kurian, Kevin McDonnell, et al.. (2015). “The GI Gap” in Genetic Testing for Inherited Susceptibility to Cancer. The American Journal of Gastroenterology. 110. S606–S607. 1 indexed citations
9.
Villalobos, Víctor M., Lynn Million, Kristin C. Jensen, et al.. (2012). Chest Wall Leiomyosarcoma After Breast-Conservative Therapy for Early-Stage Breast Cancer in a Young Woman With Li-Fraumeni Syndrome. Journal of the National Comprehensive Cancer Network. 10(8). 939–942. 27 indexed citations
10.
Masciari, Serena, Deborah Dillon, M Rath, et al.. (2012). Breast cancer phenotype in women with TP53 germline mutations: a Li-Fraumeni syndrome consortium effort. Breast Cancer Research and Treatment. 133(3). 1125–1130. 121 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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