Nancy Hanson

934 total citations
11 papers, 503 citations indexed

About

Nancy Hanson is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Nancy Hanson has authored 11 papers receiving a total of 503 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 3 papers in Pediatrics, Perinatology and Child Health and 2 papers in Molecular Biology. Recurrent topics in Nancy Hanson's work include BRCA gene mutations in cancer (5 papers), Genomics and Rare Diseases (2 papers) and Cancer Genomics and Diagnostics (2 papers). Nancy Hanson is often cited by papers focused on BRCA gene mutations in cancer (5 papers), Genomics and Rare Diseases (2 papers) and Cancer Genomics and Diagnostics (2 papers). Nancy Hanson collaborates with scholars based in United States, Austria and Germany. Nancy Hanson's co-authors include Junko Oshima, Lishan Chen, Yousef Shafeghati, Olav Sletvold, Abhimanyu Garg, Shahzad I. Mian, Lin Lee, Brian K. Kennedy, Eleanor G. Botha and Heloísa G. dos Santos and has published in prestigious journals such as The Lancet, SHILAP Revista de lepidopterología and PEDIATRICS.

In The Last Decade

Nancy Hanson

10 papers receiving 495 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nancy Hanson United States	6	360	82	58	58	44	11	503
Hiroshi Kumimoto Japan	11	245 0.7×	55 0.7×	48 0.8×	82 1.4×	20 0.5×	17	423
Helen Snowden United Kingdom	8	184 0.5×	74 0.9×	38 0.7×	53 0.9×	71 1.6×	10	420
Hólmfríður Hilmarsdóttir Iceland	11	451 1.3×	165 2.0×	30 0.5×	162 2.8×	18 0.4×	12	635
Estela G. Toraño Spain	9	292 0.8×	82 1.0×	29 0.5×	61 1.1×	19 0.4×	9	431
Sonia Nanda Canada	7	190 0.5×	234 2.9×	53 0.9×	108 1.9×	20 0.5×	8	426
Karolina Pesz Poland	10	247 0.7×	78 1.0×	56 1.0×	87 1.5×	29 0.7×	31	376
Roxane Hervé France	12	189 0.5×	57 0.7×	8 0.1×	23 0.4×	75 1.7×	17	449
Richard Herrscher United States	4	213 0.6×	39 0.5×	29 0.5×	16 0.3×	10 0.2×	8	322
Johanna M. Schuetz Canada	11	179 0.5×	66 0.8×	119 2.1×	58 1.0×	74 1.7×	20	431
J. Seidel Germany	7	168 0.5×	90 1.1×	11 0.2×	51 0.9×	47 1.1×	18	304

Countries citing papers authored by Nancy Hanson

Since Specialization

Citations

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

Fields of papers citing papers by Nancy Hanson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nancy Hanson

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

All Works

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11 of 11 papers shown

Drescher, Charles W., J. David Beatty, Robert G. Resta, et al.. (2016). The effect of referral for genetic counseling on genetic testing and surgical prevention in women at high risk for ovarian cancer: Results from a randomized controlled trial. Cancer. 122(22). 3509–3518. 5 indexed citations

Roberts, Maegan E., Douglas L. Riegert‐Johnson, Brittany C. Thomas, et al.. (2014). A clinical scoring system to identify patients with sebaceous neoplasms at risk for the Muir–Torre variant of Lynch syndrome. Genetics in Medicine. 16(9). 711–716. 81 indexed citations

Weaver, Nancy L., et al.. (2014). Assessing community-based injury prevention services in U.S. Children’s Hospitals. SHILAP Revista de lepidopterología. 1(4). 199–210.

Andersen, M. Robyn, Jason D. Thorpe, Diana S.M. Buist, et al.. (2014). Cancer Risk Awareness and Concern among Women with a Family History of Breast or Ovarian Cancer. Behavioral Medicine. 42(1). 18–28. 12 indexed citations

Pocobelli, Gaia, Jessica Chubak, Nancy Hanson, et al.. (2012). Prophylactic oophorectomy rates in relation to a guideline update on referral to genetic counseling. Gynecologic Oncology. 126(2). 229–235. 5 indexed citations

Giardino, Angelo P., et al.. (2011). Child Abuse Pediatrics: New Specialty, Renewed Mission. PEDIATRICS. 128(1). 156–159. 12 indexed citations

Wollina, Uwe, et al.. (2004). Topical PDGF-BB results in limited healing in a patient with Werner’s syndrome and chronic leg ulcers. Journal of Wound Care. 13(10). 415–416. 8 indexed citations

Chen, Lishan, Lin Lee, Brian A. Kudlow, et al.. (2003). LMNA mutations in atypical Werner's syndrome. The Lancet. 362(9382). 440–445. 321 indexed citations

Kudlow, Brian A., Olav Sletvold, Yousef Shafeghati, et al.. (2003). LMNA mutations identify a new genetic subset of subjects with progeroid features of werner syndrome. 1 indexed citations

10.

Pagon, Roberta A, Peter Tarczy‐Hornoch, Thomas D. Bird, et al.. (2002). GeneTests-GeneClinics: Genetic testing information for a growing audience. Human Mutation. 19(5). 501–509. 57 indexed citations

11.

Pagon, Roberta A, Peter Tarczy‐Hornoch, & Nancy Hanson. (2001). Internet Resources in Medical Genetics. Current Protocols in Human Genetics. 29(1). 1 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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