Spring Holter

4.4k total citations
41 papers, 1.8k citations indexed

About

Spring Holter is a scholar working on Oncology, Cancer Research and Pathology and Forensic Medicine. According to data from OpenAlex, Spring Holter has authored 41 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Oncology, 25 papers in Cancer Research and 19 papers in Pathology and Forensic Medicine. Recurrent topics in Spring Holter's work include Cancer Genomics and Diagnostics (24 papers), Genetic factors in colorectal cancer (19 papers) and Pancreatic and Hepatic Oncology Research (15 papers). Spring Holter is often cited by papers focused on Cancer Genomics and Diagnostics (24 papers), Genetic factors in colorectal cancer (19 papers) and Pancreatic and Hepatic Oncology Research (15 papers). Spring Holter collaborates with scholars based in Canada, United States and Australia. Spring Holter's co-authors include Steven Gallinger, Kara Semotiuk, Malcolm J. Moore, Ayelet Borgida, David W. Hedley, Robert C. Grant, Steven A. Narod, Talia Golan, Eitan Friedman and Dan Aderka and has published in prestigious journals such as Journal of Clinical Oncology, Gastroenterology and JNCI Journal of the National Cancer Institute.

In The Last Decade

Spring Holter

40 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Spring Holter Canada 19 1.2k 793 689 340 327 41 1.8k
Brandie Heald United States 24 753 0.6× 417 0.5× 1.0k 1.5× 392 1.2× 402 1.2× 97 1.8k
Melyssa Aronson Canada 24 1.5k 1.2× 776 1.0× 2.1k 3.0× 522 1.5× 460 1.4× 73 2.8k
Leigha Senter United States 23 904 0.7× 688 0.9× 925 1.3× 474 1.4× 217 0.7× 74 2.2k
Tadashi Nomizu Japan 17 656 0.5× 319 0.4× 657 1.0× 433 1.3× 157 0.5× 100 1.3k
Michael C. Luce United States 18 949 0.8× 336 0.4× 1.3k 1.9× 653 1.9× 262 0.8× 27 2.3k
Ayelet Borgida Canada 18 846 0.7× 529 0.7× 192 0.3× 350 1.0× 201 0.6× 34 1.2k
JT Wijnen Netherlands 16 653 0.5× 291 0.4× 877 1.3× 223 0.7× 175 0.5× 27 1.4k
C. Marleen Kets Netherlands 18 413 0.3× 407 0.5× 438 0.6× 334 1.0× 153 0.5× 32 1.2k
Marion Gauthier‐Villars France 25 838 0.7× 413 0.5× 204 0.3× 1.0k 3.0× 206 0.6× 67 2.3k
Anita Ringberg Sweden 25 674 0.6× 1.2k 1.5× 654 0.9× 169 0.5× 657 2.0× 55 1.8k

Countries citing papers authored by Spring Holter

Since Specialization
Citations

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

Fields of papers citing papers by Spring Holter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Spring Holter

This figure shows the co-authorship network connecting the top 25 collaborators of Spring Holter. A scholar is included among the top collaborators of Spring Holter 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 Spring Holter. Spring Holter 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.
Holter, Spring, Ayelet Borgida, Anna Dodd, et al.. (2022). Germline BRCA2 variants in advanced pancreatic acinar cell carcinoma: A case report and review of literature. World Journal of Gastroenterology. 28(45). 6421–6432. 6 indexed citations
2.
Oldfield, Leslie E., Tiantian Li, Alicia Tone, et al.. (2020). An Integrative DNA Sequencing and Methylation Panel to Assess Mismatch Repair Deficiency. Journal of Molecular Diagnostics. 23(2). 242–252. 11 indexed citations
3.
Holter, Spring, et al.. (2019). Examining intrafamilial communication of colorectal cancer risk status to family members and kin responses to colonoscopy: a qualitative study. Hereditary Cancer in Clinical Practice. 17(1). 16–16. 21 indexed citations
4.
Aronson, Melyssa, Kara Semotiuk, Spring Holter, et al.. (2019). Patient-physician relationships, health self-efficacy, and gynecologic cancer screening among women with Lynch syndrome. Hereditary Cancer in Clinical Practice. 17(1). 24–24. 12 indexed citations
5.
Stjepanovic, Neda, Tracy Stockley, Philippe L. Bédard, et al.. (2018). Additional germline findings from a tumor profiling program. BMC Medical Genomics. 11(1). 65–65. 13 indexed citations
6.
Aronson, Melyssa, et al.. (2016). Physician trust moderates the relationship between intolerance of uncertainty and cancer worry interference among women with Lynch syndrome. Journal of Behavioral Medicine. 39(3). 420–428. 8 indexed citations
7.
AlDubayan, Saud H., Ashton A. Connor, Beatrix Wong, et al.. (2016). Genetic testing for Lynch syndrome in the province of Ontario. Cancer. 122(11). 1672–1679. 9 indexed citations
8.
Aronson, Melyssa, Spring Holter, Kara Semotiuk, et al.. (2015). DNA Mismatch Repair Status Predicts Need for Future Colorectal Surgery for Metachronous Neoplasms in Young Individuals Undergoing Colorectal Cancer Resection. Diseases of the Colon & Rectum. 58(7). 645–652. 17 indexed citations
9.
Golan, Talia, Zaheer Kanji, Ron Epelbaum, et al.. (2014). Overall survival and clinical characteristics of pancreatic cancer in BRCA mutation carriers. British Journal of Cancer. 111(6). 1132–1138. 311 indexed citations
10.
Keogh, Louise, Sherri Sheinfeld Gorin, Sheri D. Schully, et al.. (2013). How do researchers manage genetic results in practice? The experience of the multinational Colon Cancer Family Registry. Journal of Community Genetics. 5(2). 99–108. 15 indexed citations
11.
Skeldon, Sean, Kara Semotiuk, Melyssa Aronson, et al.. (2012). Patients with Lynch Syndrome Mismatch Repair Gene Mutations Are at Higher Risk for Not Only Upper Tract Urothelial Cancer but Also Bladder Cancer. European Urology. 63(2). 379–385. 76 indexed citations
12.
Al-Sukhni, Wigdan, Anath C. Lionel, Nora Zwingerman, et al.. (2012). Identification of germline genomic copy number variation in familial pancreatic cancer. Human Genetics. 131(9). 1481–1494. 22 indexed citations
13.
Rumilla, Kandelaria M., Noralane M. Lindor, Brittany C. Thomas, et al.. (2011). Frequency of Deletions of EPCAM (TACSTD1) in MSH2-Associated Lynch Syndrome Cases. Journal of Molecular Diagnostics. 13(1). 93–99. 58 indexed citations
14.
Al-Sukhni, Wigdan, Ayelet Borgida, Heidi Rothenmund, et al.. (2011). Screening for Pancreatic Cancer in a High-Risk Cohort: An Eight-Year Experience. Journal of Gastrointestinal Surgery. 16(4). 771–783. 110 indexed citations
15.
Kastrinos, Fay, Ewout W. Steyerberg, Rowena Mercado, et al.. (2010). The PREMM1,2,6 Model Predicts Risk of MLH1, MSH2, and MSH6 Germline Mutations Based on Cancer History. Gastroenterology. 140(1). 73–81.e5. 141 indexed citations
16.
Maheu, Christine, Heidi Rothenmund, Steve Gallinger, et al.. (2010). Pancreatic cancer risk counselling and screening: impact on perceived risk and psychological functioning. Familial Cancer. 9(4). 617–624. 47 indexed citations
17.
Durno, Carol, Spring Holter, Philip M. Sherman, & Steven Gallinger. (2010). The Gastrointestinal Phenotype of Germline Biallelic Mismatch Repair Gene Mutations. The American Journal of Gastroenterology. 105(11). 2449–2456. 45 indexed citations
18.
Holter, Spring, Aaron Pollett, Mark Clendenning, et al.. (2008). Café‐au‐lait macules and pediatric malignancy caused by biallelic mutations in the DNA mismatch repair (MMR) gene PMS2. Pediatric Blood & Cancer. 50(6). 1268–1270. 19 indexed citations
19.
Ghorpade, Anuja, Susan Swindells, Kathleen Borgmann, et al.. (2005). Neuroinflammatory responses from microglia recovered from HIV-1-infected and seronegative subjects. Journal of Neuroimmunology. 163(1-2). 145–156. 25 indexed citations
20.
Holter, Spring, Kathleen Borgmann, Raisa Persidsky, et al.. (2003). Regulation of tissue inhibitor of metalloproteinase‐1 by astrocytes: Links to HIV‐1 dementia. Glia. 44(1). 47–56. 83 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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