Rachel Pearlman

4.6k total citations · 1 hit paper
33 papers, 1.3k citations indexed

About

Rachel Pearlman is a scholar working on Pathology and Forensic Medicine, Oncology and Cancer Research. According to data from OpenAlex, Rachel Pearlman has authored 33 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Pathology and Forensic Medicine, 23 papers in Oncology and 17 papers in Cancer Research. Recurrent topics in Rachel Pearlman's work include Genetic factors in colorectal cancer (29 papers), Colorectal Cancer Screening and Detection (17 papers) and Cancer Genomics and Diagnostics (16 papers). Rachel Pearlman is often cited by papers focused on Genetic factors in colorectal cancer (29 papers), Colorectal Cancer Screening and Detection (17 papers) and Cancer Genomics and Diagnostics (16 papers). Rachel Pearlman collaborates with scholars based in United States, Australia and Spain. Rachel Pearlman's co-authors include Heather Hampel, Georgia L. Wiesner, Adam H. Buchanan, Robin L. Bennett, Wendy L. Frankel, Colin C. Pritchard, Albert de la Chapelle, Sigurdís Haraldsdóttir, Jerneja Tomšič and Peter P. Stanich and has published in prestigious journals such as Journal of Clinical Oncology, Gastroenterology and PLoS ONE.

In The Last Decade

Rachel Pearlman

32 papers receiving 1.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment

2014 373 citations Heather Hampel, Robin L. Bennett et al. Genetics in Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rachel Pearlman United States	17	873	624	623	307	220	33	1.3k
Laura Renkonen‐Sinisalo Finland	22	858 1.0×	643 1.0×	346 0.6×	219 0.7×	314 1.4×	48	1.3k
Michelle Landon United States	4	1.1k 1.3×	840 1.3×	542 0.9×	238 0.8×	239 1.1×	4	1.4k
Christopher Arnell United States	7	866 1.0×	659 1.1×	530 0.9×	528 1.7×	326 1.5×	14	1.4k
Peggy Conrad United States	18	1.3k 1.5×	884 1.4×	504 0.8×	416 1.4×	168 0.8×	26	1.7k
Astrid Stormorken Norway	12	643 0.7×	428 0.7×	326 0.5×	234 0.8×	111 0.5×	24	811
Jai Min Ryu South Korea	18	257 0.3×	365 0.6×	584 0.9×	149 0.5×	111 0.5×	114	1.0k
Brian Allen United States	17	1.4k 1.6×	1.2k 1.9×	946 1.5×	996 3.2×	675 3.1×	39	2.4k
Annette Bröcker‐Vriends Netherlands	13	538 0.6×	399 0.6×	365 0.6×	207 0.7×	222 1.0×	14	1.2k
H. T. Lynch United States	9	911 1.0×	885 1.4×	572 0.9×	545 1.8×	281 1.3×	11	1.5k
Kari L. Ring United States	20	377 0.4×	500 0.8×	302 0.5×	150 0.5×	269 1.2×	74	1.3k

Countries citing papers authored by Rachel Pearlman

Since Specialization

Citations

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

Fields of papers citing papers by Rachel Pearlman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rachel Pearlman

This figure shows the co-authorship network connecting the top 25 collaborators of Rachel Pearlman. A scholar is included among the top collaborators of Rachel Pearlman 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 Rachel Pearlman. Rachel Pearlman 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

Prizment, Anna E., Conghui Qu, Shuo Wang, et al.. (2025). Functional variants in the cystic fibrosis transmembrane conductance regulator (CFTR) gene are associated with increased risk of colorectal cancer. Human Molecular Genetics. 34(7). 617–625. 1 indexed citations

Gallon, Richard, Christine Hayes, Gillian M. Borthwick, et al.. (2024). Detection of Mismatch Repair Deficiency in Endometrial Cancer: Assessment of IHC, Fragment Length Analysis, and Amplicon Sequencing Based MSI Testing. Cancers. 16(23). 3970–3970. 1 indexed citations

Ramsey, Mitchell L., Brandie Heald, Yevgeniya Gokun, et al.. (2024). Germline multigene panel testing in acute and chronic pancreatitis. PLoS ONE. 19(8). e0307076–e0307076. 3 indexed citations

Chen, Wei, Rachel Pearlman, Heather Hampel, et al.. (2023). Mismatch repair protein status of non-neoplastic uterine and intestinal mucosa in patients with Lynch syndrome and double somatic mismatch repair protein mutations. Human Pathology. 137. 1–9.

Ramsey, Mitchell L., Rachel Pearlman, Laith Abushahin, et al.. (2022). Mainstreaming germline genetic testing for patients with pancreatic cancer increases uptake. Familial Cancer. 22(1). 91–97. 23 indexed citations

Hampel, Heather, Matthew F. Kalady, Rachel Pearlman, & Peter P. Stanich. (2022). Hereditary Colorectal Cancer. Hematology/Oncology Clinics of North America. 36(3). 429–447. 22 indexed citations

Stanich, Peter P., Rachel Pearlman, Matthew F. Kalady, et al.. (2022). Universal tumor screening for lynch syndrome on colorectal cancer biopsies impacts surgical treatment decisions. Familial Cancer. 22(1). 71–76. 3 indexed citations

Stanich, Peter P., et al.. (2020). A High Percentage of Early-age Onset Colorectal Cancer Is Potentially Preventable. Gastroenterology. 160(5). 1850–1852. 30 indexed citations

Hampel, Heather, Rachel Pearlman, Dan Jones, et al.. (2020). Unexpected expression of mismatch repair protein is more commonly seen with pathogenic missense than with other mutations in Lynch syndrome. Human Pathology. 103. 34–41. 19 indexed citations

10.

Hampel, Heather, Rachel Pearlman, Albert de la Chapelle, et al.. (2020). Double somatic mismatch repair gene pathogenic variants as common as Lynch syndrome among endometrial cancer patients. Gynecologic Oncology. 160(1). 161–168. 26 indexed citations

11.

Jeter, Joanne, Heather Hampel, Peter P. Stanich, et al.. (2019). A phase II study of PD-1 inhibition for the prevention of colon adenomas in patients with Lynch syndrome and a history of partial colectomy.. Journal of Clinical Oncology. 37(15_suppl). TPS1587–TPS1587. 2 indexed citations

12.

Chen, Wei, Rachel Pearlman, Heather Hampel, et al.. (2019). MSH6 immunohistochemical heterogeneity in colorectal cancer: comparative sequencing from different tumor areas. Human Pathology. 96. 104–111. 16 indexed citations

13.

Stanich, Peter P. & Rachel Pearlman. (2019). Hereditary or Not? Understanding Serrated Polyposis Syndrome. Current Treatment Options in Gastroenterology. 17(4). 692–701. 7 indexed citations

14.

Rañola, John Michael O., Rachel Pearlman, Heather Hampel, & Brian H. Shirts. (2018). Modified capture–recapture estimates of the number of families with Lynch syndrome in Central Ohio. Familial Cancer. 18(1). 67–73. 2 indexed citations

15.

Pearlman, Rachel, Michael J. Markow, Deborah A. Knight, et al.. (2018). Two-stain immunohistochemical screening for Lynch syndrome in colorectal cancer may fail to detect mismatch repair deficiency. Modern Pathology. 31(12). 1891–1900. 46 indexed citations

16.

Stanich, Peter P., Rachel Pearlman, Alice Hinton, et al.. (2018). Prevalence of Germline Mutations in Polyposis and Colorectal Cancer–Associated Genes in Patients With Multiple Colorectal Polyps. Clinical Gastroenterology and Hepatology. 17(10). 2008–2015.e3. 45 indexed citations

17.

Hemminger, Jessica, Rachel Pearlman, Sigurdís Haraldsdóttir, et al.. (2018). Histology of colorectal adenocarcinoma with double somatic mismatch-repair mutations is indistinguishable from those caused by Lynch syndrome. Human Pathology. 78. 125–130. 19 indexed citations

18.

Haraldsdóttir, Sigurdís, Rachel Roth, Rachel Pearlman, et al.. (2015). Mismatch repair deficiency concordance between primary colorectal cancer and corresponding metastasis. Familial Cancer. 15(2). 253–260. 32 indexed citations

19.

Hampel, Heather, Robin L. Bennett, Adam H. Buchanan, Rachel Pearlman, & Georgia L. Wiesner. (2014). A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment. Genetics in Medicine. 17(1). 70–87. 373 indexed citations breakdown →

20.

Haraldsdóttir, Sigurdís, Heather Hampel, Jerneja Tomšič, et al.. (2014). Colon and Endometrial Cancers With Mismatch Repair Deficiency Can Arise From Somatic, Rather Than Germline, Mutations. Gastroenterology. 147(6). 1308–1316.e1. 256 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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