Anne Naumer

967 total citations
16 papers, 447 citations indexed

About

Anne Naumer is a scholar working on Surgery, Endocrinology, Diabetes and Metabolism and Molecular Biology. According to data from OpenAlex, Anne Naumer has authored 16 papers receiving a total of 447 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Surgery, 7 papers in Endocrinology, Diabetes and Metabolism and 6 papers in Molecular Biology. Recurrent topics in Anne Naumer's work include Pituitary Gland Disorders and Treatments (7 papers), Adrenal and Paraganglionic Tumors (7 papers) and Cancer-related Molecular Pathways (5 papers). Anne Naumer is often cited by papers focused on Pituitary Gland Disorders and Treatments (7 papers), Adrenal and Paraganglionic Tumors (7 papers) and Cancer-related Molecular Pathways (5 papers). Anne Naumer collaborates with scholars based in United States, Canada and Israel. Anne Naumer's co-authors include Wendy Kohlmann, Joshua D. Schiffman, Bailey Gallinger, Jonathan D. Wasserman, Derek Stephens, Anita Villani, Harriet Druker, Jonathan L. Finlay, David Malkin and Uri Tabori and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Oncology and SHILAP Revista de lepidopterología.

In The Last Decade

Anne Naumer

13 papers receiving 441 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anne Naumer United States	7	171	155	127	109	77	16	447
Stacy Mosier United States	9	275 1.6×	196 1.3×	95 0.7×	258 2.4×	46 0.6×	9	747
Capucine Delnatte France	9	219 1.3×	100 0.6×	144 1.1×	78 0.7×	56 0.7×	15	426
Shari Baldinger United States	11	244 1.4×	49 0.3×	266 2.1×	60 0.6×	226 2.9×	16	642
Boo Messahel United Kingdom	14	409 2.4×	100 0.6×	54 0.4×	56 0.5×	36 0.5×	24	582
Isabel Spier Germany	13	293 1.7×	183 1.2×	221 1.7×	145 1.3×	103 1.3×	36	662
Viorel Vasiliu France	12	229 1.3×	84 0.5×	71 0.6×	68 0.6×	86 1.1×	23	414
Jonas Carlsson Almlöf Sweden	12	329 1.9×	82 0.5×	150 1.2×	120 1.1×	42 0.5×	16	681
Jennifer L. Geurts United States	9	245 1.4×	136 0.9×	290 2.3×	102 0.9×	43 0.6×	27	505
David L. Tait United States	16	239 1.4×	158 1.0×	162 1.3×	75 0.7×	86 1.1×	40	531

Countries citing papers authored by Anne Naumer

Since Specialization

Citations

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

Fields of papers citing papers by Anne Naumer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne Naumer

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

All Works

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16 of 16 papers shown

White, Michelle J., Shi Liang, Mana Espahbodi, et al.. (2025). Implementation of point-of-care genetic testing for head and neck paragangliomas: early experience and future directions. Oral Oncology. 168. 107600–107600.

Naumer, Anne, et al.. (2025). Characterization of hereditary tumor risk in individuals with SDHA germline variants.. Journal of Clinical Oncology. 43(16_suppl). 10610–10610.

Naumer, Anne, Luke Maese, Joshua D. Schiffman, et al.. (2025). Hematologic Malignancy Frequency, Phenotypes, and Outcomes in Li-Fraumeni Syndrome. JCO Precision Oncology. 9(9). e2400860–e2400860.

Naumer, Anne, Luke Buchmann, Wendy Kohlmann, et al.. (2024). Management of bilateral head and neck paragangliomas at a single‐institution across four decades. Head & Neck. 47(1). 386–393. 3 indexed citations

Le, Anh N., Greg Kelly, Ryan Hausler, et al.. (2024). Increased risk for thyroid carcinoma in patients with Li-Fraumeni syndrome.. Journal of Clinical Oncology. 42(16_suppl). 10612–10612. 1 indexed citations

Kohlmann, Wendy, et al.. (2023). P083: Incidental findings in FH and SDHA genes: Navigating cancer risk assessment and follow-up recommendations. SHILAP Revista de lepidopterología. 1(1). 100102–100102. 1 indexed citations

Wiggins, Richard H., Mana Espahbodi, Anne Naumer, et al.. (2023). The Natural History of Observed SDHx-Related Head and Neck Paragangliomas Using Three-Dimensional Volumetric Tumor Analysis. Otology & Neurotology. 44(9). 931–940. 3 indexed citations

Kohlmann, Wendy, et al.. (2021). Lung Cancer in Li-Fraumeni Syndrome. JCO Precision Oncology. 5(5). 552–556. 6 indexed citations

Greenberg, Samantha, et al.. (2021). Paraganglioma and other tumour detection rates in individuals with SDHx pathogenic variants by age of diagnosis and after the age of 50. Clinical Endocrinology. 95(3). 447–452. 3 indexed citations

10.

Greenberg, Samantha, Michelle F. Jacobs, Heather Wachtel, et al.. (2020). Tumor detection rates in screening of individuals with SDHx-related hereditary paraganglioma–pheochromocytoma syndrome. Genetics in Medicine. 22(12). 2101–2107. 18 indexed citations

11.

Greenberg, Samantha, Michelle F. Jacobs, Heather Wachtel, et al.. (2020). Tumor detection rates in screening carriers with SDHx-related hereditary paraganglioma-pheochromocytoma syndrome based on prior tumor history.. Journal of Clinical Oncology. 38(15_suppl). 1545–1545. 1 indexed citations

12.

McCrary, Hilary C., Anne Naumer, Samantha Greenberg, et al.. (2019). Characterization of Malignant Head and Neck Paragangliomas at a Single Institution Across Multiple Decades. JAMA Otolaryngology–Head & Neck Surgery. 145(7). 641–641. 31 indexed citations

13.

Michaeli, Orli, Uri Tabori, Joshua D. Schiffman, et al.. (2019). Gliomas in the context of Li-Fraumeni syndrome: An international cohort.. Journal of Clinical Oncology. 37(15_suppl). 1517–1517. 6 indexed citations

14.

Villani, Anita, Jonathan D. Wasserman, Derek Stephens, et al.. (2016). Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: 11 year follow-up of a prospective observational study. The Lancet Oncology. 17(9). 1295–1305. 322 indexed citations

15.

Martin, Sandra L., et al.. (2001). Mutation frequency and type during ageing in mouse seminiferous tubules. Mechanisms of Ageing and Development. 122(12). 1321–1331. 14 indexed citations

16.

Tecklenburg, Marianne, et al.. (1995). The dif resolvase locus of the Escherichia coli chromosome can be replaced by a 33-bp sequence, but function depends on location.. Proceedings of the National Academy of Sciences. 92(5). 1352–1356. 38 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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