Anu Chittenden

1.1k total citations
32 papers, 599 citations indexed

About

Anu Chittenden is a scholar working on Pathology and Forensic Medicine, Cancer Research and Genetics. According to data from OpenAlex, Anu Chittenden has authored 32 papers receiving a total of 599 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Pathology and Forensic Medicine, 17 papers in Cancer Research and 15 papers in Genetics. Recurrent topics in Anu Chittenden's work include Genetic factors in colorectal cancer (18 papers), Cancer Genomics and Diagnostics (16 papers) and BRCA gene mutations in cancer (13 papers). Anu Chittenden is often cited by papers focused on Genetic factors in colorectal cancer (18 papers), Cancer Genomics and Diagnostics (16 papers) and BRCA gene mutations in cancer (13 papers). Anu Chittenden collaborates with scholars based in United States, Italy and Germany. Anu Chittenden's co-authors include Judy E. Garber, Andrea Farkas Patenaude, Katherine A. Schneider, Michel Dorval, Sapna Syngal, Elena M. Stoffel, Matthew B. Yurgelun, Kristen M. Shannon, Jennifer R. Klemp and Laura J. Esserman and has published in prestigious journals such as Journal of Clinical Oncology, Gastroenterology and Neurology.

In The Last Decade

Anu Chittenden

31 papers receiving 590 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anu Chittenden United States 12 328 231 212 174 120 32 599
Lisa R. Susswein United States 15 575 1.8× 331 1.4× 249 1.2× 192 1.1× 236 2.0× 25 913
Jessica N. Everett United States 16 316 1.0× 306 1.3× 397 1.9× 312 1.8× 149 1.2× 30 985
Wendy A.G. van Zelst–Stams Netherlands 12 208 0.6× 309 1.3× 209 1.0× 227 1.3× 93 0.8× 21 524
Shanna Gustafson United States 12 290 0.9× 109 0.5× 173 0.8× 79 0.5× 95 0.8× 16 636
Johanna Lee United Kingdom 4 432 1.3× 318 1.4× 221 1.0× 260 1.5× 93 0.8× 5 712
Cheryl L. Soderberg United States 8 568 1.7× 187 0.8× 348 1.6× 196 1.1× 262 2.2× 9 873
Heidi Rothenmund Canada 12 220 0.7× 279 1.2× 288 1.4× 491 2.8× 141 1.2× 21 732
Dorothea Gadzicki Germany 14 494 1.5× 161 0.7× 294 1.4× 192 1.1× 292 2.4× 30 913
Kaylene Ready United States 15 486 1.5× 112 0.5× 268 1.3× 180 1.0× 163 1.4× 27 705
Katrina Lowstuter United States 12 537 1.6× 216 0.9× 291 1.4× 339 1.9× 306 2.5× 18 919

Countries citing papers authored by Anu Chittenden

Since Specialization
Citations

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

Fields of papers citing papers by Anu Chittenden

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anu Chittenden

This figure shows the co-authorship network connecting the top 25 collaborators of Anu Chittenden. A scholar is included among the top collaborators of Anu Chittenden 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 Anu Chittenden. Anu Chittenden 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.
Rana, Huma Q., Anu Chittenden, Raymond A. Isidro, et al.. (2024). Advancing Precision Oncology in Hereditary Paraganglioma-Pheochromocytoma Syndromes: Integrated Interpretation and Data Sharing of the Germline and Tumor Genomes. Cancers. 16(5). 947–947. 1 indexed citations
2.
Isidro, Raymond A., Anu Chittenden, Alison Schwartz, et al.. (2024). Development and evaluation of INT2GRATE: a platform for comprehensive assessment of the role of germline variants informed by tumor signature profile in Lynch syndrome. Frontiers in Oncology. 13. 1284690–1284690. 1 indexed citations
3.
Uno, Hajime, Chinedu Ukaegbu, Anu Chittenden, et al.. (2023). Clinical factors associated with skin neoplasms in individuals with Lynch syndrome in a longitudinal observational cohort. Journal of the American Academy of Dermatology. 88(6). 1282–1290. 2 indexed citations
4.
5.
Schwartz, Alison, Danielle K. Manning, Anu Chittenden, et al.. (2022). An integrated somatic and germline approach to aid interpretation of germline variants of uncertain significance in cancer susceptibility genes. Frontiers in Oncology. 12. 942741–942741. 6 indexed citations
6.
7.
Yurgelun, Matthew B., Hajime Uno, C. Sloane Furniss, et al.. (2022). Development and Validation of the PREMMplus Model for Multigene Hereditary Cancer Risk Assessment. Journal of Clinical Oncology. 40(35). 4083–4094. 7 indexed citations
8.
Ukaegbu, Chinedu, Zohar Levi, Hajime Uno, et al.. (2020). Characterizing germline APC and MUTYH variants in Ashkenazi Jews compared to other individuals. Familial Cancer. 20(2). 111–116. 6 indexed citations
9.
Underhill‐Blazey, Meghan, Jill E. Stopfer, Anu Chittenden, et al.. (2019). Development and testing of the KnowGene scale to assess general cancer genetic knowledge related to multigene panel testing. Patient Education and Counseling. 102(8). 1558–1564. 17 indexed citations
10.
Yurgelun, Matthew B., Anu Chittenden, Chinedu Ukaegbu, et al.. (2018). Implementing universal genetic counseling (GC) and multigene germline testing (MGT) for pancreatic cancer (PC) patients (pts).. Journal of Clinical Oncology. 36(15_suppl). 1512–1512. 3 indexed citations
11.
Watkins, Jaclyn C., Eric Yang, Michael G. Muto, et al.. (2016). Universal Screening for Mismatch-Repair Deficiency in Endometrial Cancers to Identify Patients With Lynch Syndrome and Lynch-like Syndrome. International Journal of Gynecological Pathology. 36(2). 115–127. 67 indexed citations
12.
Yurgelun, Matthew B., Jason L. Hornick, Chinedu Ukaegbu, et al.. (2013). Therapy-Associated Polyposis as a Late Sequela of Cancer Treatment. Clinical Gastroenterology and Hepatology. 12(6). 1046–1050. 7 indexed citations
13.
Shannon, Kristen M. & Anu Chittenden. (2012). Genetic Testing by Cancer Site. The Cancer Journal. 18(4). 310–319. 19 indexed citations
14.
Tomšič, Jerneja, Sandya Liyanarachchi, Heather Hampel, et al.. (2011). An American founder mutation in MLH1. International Journal of Cancer. 130(9). 2088–2095. 12 indexed citations
15.
Dewanwala, Akriti, Anu Chittenden, Margery Rosenblatt, et al.. (2011). Attitudes toward childbearing and prenatal testing in individuals undergoing genetic testing for Lynch Syndrome. Familial Cancer. 10(3). 549–556. 19 indexed citations
16.
Dandapani, Monica, et al.. (2011). Sebaceous neoplasms in Lynch syndrome. Hereditary Cancer in Clinical Practice. 9(Suppl 1). P7–P7. 1 indexed citations
17.
Stoffel, Elena M. & Anu Chittenden. (2010). Genetic Testing for Hereditary Colorectal Cancer: Challenges in Identifying, Counseling, and Managing High-Risk Patients. Gastroenterology. 139(5). 1436–1441.e1. 21 indexed citations
18.
Schneider, Katherine A., Anu Chittenden, Steven Joffe, et al.. (2006). Ethical Issues in Cancer Genetics: 1) Whose Information Is It?. Journal of Genetic Counseling. 15(6). 491–503. 11 indexed citations
19.
Euhus, David, Linda Robinson, Olufunmilayo I. Olopade, et al.. (2002). Pretest Prediction of BRCA1 or BRCA2 Mutation by Risk Counselors and the Computer Model BRCAPRO. JNCI Journal of the National Cancer Institute. 94(11). 844–851. 119 indexed citations
20.
Stephan, Dietrich, Neil R.M. Buist, Anu Chittenden, et al.. (1994). A rippling muscle disease gene is localized to 1q41. Neurology. 44(10). 1915–1915. 32 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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