Amie Blanco

2.8k total citations
36 papers, 983 citations indexed

About

Amie Blanco is a scholar working on Oncology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, Amie Blanco has authored 36 papers receiving a total of 983 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Oncology, 19 papers in Pathology and Forensic Medicine and 15 papers in Genetics. Recurrent topics in Amie Blanco's work include Genetic factors in colorectal cancer (19 papers), BRCA gene mutations in cancer (13 papers) and Cancer Genomics and Diagnostics (12 papers). Amie Blanco is often cited by papers focused on Genetic factors in colorectal cancer (19 papers), BRCA gene mutations in cancer (13 papers) and Cancer Genomics and Diagnostics (12 papers). Amie Blanco collaborates with scholars based in United States, Canada and Spain. Amie Blanco's co-authors include Jonathan P. Terdiman, Miriam Kuppermann, Grace Wang, Uri Ladabaum, Kathryn A. Phillips, James M. Ford, C. Richard Boland, Elena B. Elkin, Peggy Conrad and Lee-may Chen and has published in prestigious journals such as Journal of Clinical Oncology, Annals of Internal Medicine and Cancer.

In The Last Decade

Amie Blanco

36 papers receiving 961 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Amie Blanco United States	18	538	470	431	335	127	36	983
Kara Semotiuk Canada	14	351 0.7×	551 1.2×	243 0.6×	383 1.1×	160 1.3×	32	934
Patrice Watson United States	8	549 1.0×	398 0.8×	365 0.8×	241 0.7×	125 1.0×	8	800
Jessica N. Everett United States	16	306 0.6×	312 0.7×	316 0.7×	397 1.2×	149 1.2×	30	985
Lisa R. Susswein United States	15	331 0.6×	192 0.4×	575 1.3×	249 0.7×	236 1.9×	25	913
Leon C. Verhoog Netherlands	8	251 0.5×	337 0.7×	860 2.0×	411 1.2×	209 1.6×	9	1.1k
Katja Aktan–Collan Finland	10	1.2k 2.3×	937 2.0×	528 1.2×	332 1.0×	126 1.0×	19	1.5k
Susan Tinley United States	13	329 0.6×	240 0.5×	490 1.1×	112 0.3×	125 1.0×	35	824
C. Snyder United States	5	670 1.2×	484 1.0×	874 2.0×	502 1.5×	268 2.1×	6	1.4k
Marit Holmqvist Sweden	15	174 0.3×	329 0.7×	277 0.6×	293 0.9×	91 0.7×	19	766
Wendy A.G. van Zelst–Stams Netherlands	12	309 0.6×	227 0.5×	208 0.5×	209 0.6×	93 0.7×	21	524

Countries citing papers authored by Amie Blanco

Since Specialization

Citations

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

Fields of papers citing papers by Amie Blanco

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amie Blanco

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

All Works

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20 of 20 papers shown

Wright, Francis, A. Jo Chien, Jasmine Wong, et al.. (2024). Synchronous or metachronous breast and colorectal cancers in younger-than-average-age patients: a case series. The Oncologist. 29(9). e1159–e1168. 1 indexed citations

Kwon, Daniel H., Hala T. Borno, Rahul Aggarwal, et al.. (2023). Implementation of a Telehealth Genetic Testing Station to Deliver Germline Testing for Men With Prostate Cancer. JCO Oncology Practice. 19(5). e773–e783. 9 indexed citations

Schwartz, Christopher J., et al.. (2023). Clinicopathologic and genetic analysis of invasive breast carcinomas in women with germline CHEK2 variants. Breast Cancer Research and Treatment. 204(1). 171–179. 6 indexed citations

Walker, Evan J., Dena Goldberg, Julia Carnevale, et al.. (2021). Implementation of an Embedded In-Clinic Genetic Testing Station to Optimize Germline Testing for Patients with Pancreatic Adenocarcinoma. The Oncologist. 26(11). e1982–e1991. 23 indexed citations

Weitzel, Jeffrey N., Susan L. Neuhausen, Aaron W. Adamson, et al.. (2019). Pathogenic and likely pathogenic variants in PALB2 , CHEK2 , and other known breast cancer susceptibility genes among 1054 BRCA ‐negative Hispanics with breast cancer. Cancer. 125(16). 2829–2836. 36 indexed citations

Sharib, Jeremy, Amie Blanco, Dena Goldberg, et al.. (2019). Abdominal Imaging of Pancreatic Cysts and Cyst-Associated Pancreatic Cancer in BRCA1/2 Mutation Carriers: A Retrospective Cross-Sectional Study. Journal of the American College of Surgeons. 230(1). 53–63e1. 3 indexed citations

Kidambi, Trilokesh D., Dena Goldberg, Robert L. Nussbaum, et al.. (2018). Novel variant of unknown significance in MUTYH in a patient with MUTYH-associated polyposis: a case to reclassify. Clinical Journal of Gastroenterology. 11(6). 457–460. 2 indexed citations

Chapman, Jocelyn, et al.. (2018). Disparities in genetics assessment for women with ovarian cancer: Can we do better?. Gynecologic Oncology. 149(1). 84–88. 55 indexed citations

Walker, Evan J., Julia Carnevale, Amie Blanco, et al.. (2018). Referral frequency, attrition rate, and outcomes of germline testing in patients with pancreatic adenocarcinoma. Familial Cancer. 18(2). 241–251. 22 indexed citations

10.

Walker, Evan J., Julia Carnevale, Amie Blanco, et al.. (2018). Referral patterns and attrition rate for germline testing in pancreatic cancer (PC) patients.. Journal of Clinical Oncology. 36(15_suppl). 1591–1591. 1 indexed citations

11.

Kidambi, Trilokesh D., et al.. (2017). Lower gastrointestinal neuroendocrine neoplasms associated with hereditary cancer syndromes: a case series. Familial Cancer. 16(4). 537–543. 12 indexed citations

12.

Kidambi, Trilokesh D., Amie Blanco, Jessica Van Ziffle, & Jonathan P. Terdiman. (2016). Constitutional MLH1 methylation presenting with colonic polyposis syndrome and not Lynch syndrome. Familial Cancer. 15(2). 275–280. 12 indexed citations

13.

Kidambi, Trilokesh D., Rita J. Jeremy, Peggy Conrad, et al.. (2016). Differences in neuropsychological and behavioral parameters and brain structure in patients with familial adenomatous polyposis: a sibling-paired study. Hereditary Cancer in Clinical Practice. 14(1). 20–20. 6 indexed citations

14.

Rabban, Joseph T., et al.. (2014). Association of Tumor Morphology With Mismatch-repair Protein Status in Older Endometrial Cancer Patients. The American Journal of Surgical Pathology. 38(6). 793–800. 43 indexed citations

15.

Yurgelun, Matthew B., Rowena Mercado, Margery Rosenblatt, et al.. (2012). Impact of genetic testing on endometrial cancer risk-reducing practices in women at risk for Lynch syndrome. Gynecologic Oncology. 127(3). 544–551. 20 indexed citations

16.

Khan, Omar, Amie Blanco, Peggy Conrad, et al.. (2011). Performance of Lynch Syndrome Predictive Models in a Multi-Center US Referral Population. The American Journal of Gastroenterology. 106(10). 1822–1827. 23 indexed citations

17.

Truta, Brindusa, Yunn-Yi Chen, Amie Blanco, et al.. (2008). Tumor histology helps to identify Lynch syndrome among colorectal cancer patients. Familial Cancer. 7(3). 267–274. 10 indexed citations

18.

Peterson, Susan K., Rebecca D. Pentz, Salma K. Marani, et al.. (2008). Psychological functioning in persons considering genetic counseling and testing for Li–Fraumeni syndrome. Psycho-Oncology. 17(8). 783–789. 31 indexed citations

19.

Peterson, Susan K., Rebecca D. Pentz, Amie Blanco, et al.. (2006). Evaluation of a decision aid for families considering p53 genetic counseling and testing. Genetics in Medicine. 8(4). 226–233. 21 indexed citations

20.

Wedell, J, et al.. (1980). [Local recurrence following anterior resection of rectal cancer. CEA-titer (author's transl)].. PubMed. 105(13). 833–41. 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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