Thomas P. Slavin

2.9k total citations
44 papers, 917 citations indexed

About

Thomas P. Slavin is a scholar working on Genetics, Cancer Research and Molecular Biology. According to data from OpenAlex, Thomas P. Slavin has authored 44 papers receiving a total of 917 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 18 papers in Cancer Research and 15 papers in Molecular Biology. Recurrent topics in Thomas P. Slavin's work include Cancer Genomics and Diagnostics (16 papers), BRCA gene mutations in cancer (13 papers) and Genetic factors in colorectal cancer (12 papers). Thomas P. Slavin is often cited by papers focused on Cancer Genomics and Diagnostics (16 papers), BRCA gene mutations in cancer (13 papers) and Genetic factors in colorectal cancer (12 papers). Thomas P. Slavin collaborates with scholars based in United States, United Kingdom and Mexico. Thomas P. Slavin's co-authors include Jeffrey N. Weitzel, Stacy W. Gray, Muhammed Murtaza, Ajay Goel, Prativa Sahoo, Russell C. Rockne, Laura H. Goetz, Colin C. Pritchard, Nicholas J. Schork and Robert C. Elston and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Oncology and SHILAP Revista de lepidopterología.

In The Last Decade

Thomas P. Slavin

43 papers receiving 894 citations

Peers

Countries citing papers authored by Thomas P. Slavin

Since Specialization

Citations

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

Fields of papers citing papers by Thomas P. Slavin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thomas P. Slavin. 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 Thomas P. Slavin. The network helps show where Thomas P. Slavin may publish in the future.

Co-authorship network of co-authors of Thomas P. Slavin

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas P. Slavin. A scholar is included among the top collaborators of Thomas P. Slavin 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 Thomas P. Slavin. Thomas P. Slavin 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

#	Title	Journal	Authors	Indexed citations
1	Association of Genomic Instability Score, Tumor Mutational Burden, and Tumor-Infiltrating Lymphocytes as Biomarkers in Uterine Serous Carcinoma	Cancers	Regina S. Whitaker, Shonagh Russell et al.	1
2	Clonal Hematopoiesis and Mosaicism Revealed by a Multi-Tissue Analysis of Constitutional TP53 Status	Cancer Epidemiology Biomarkers & Prevention	Danielle Castillo, Bita Nehoray et al.	7
3	Comprehensive Breast Cancer Risk Assessment for CHEK2 and ATM Pathogenic Variant Carriers Incorporating a Polygenic Risk Score and the Tyrer-Cuzick Model	JCO Precision Oncology	Shannon Gallagher, Elisha Hughes et al.	14
4	Mutation screening of germline TP53 mutations in high-risk Chinese breast cancer patients	BMC Cancer	Ava Kwong, Vivian Y. Shin et al.	8
5	Pathogenic and likely pathogenic variants in PALB2 , CHEK2 , and other known breast cancer susceptibility genes among 1054 BRCA ‐negative Hispanics with breast cancer	Cancer	Jeffrey N. Weitzel, Susan L. Neuhausen et al.	36
6	The Burden of Breast Cancer Predisposition Variants Across The Age Spectrum Among 10 000 Patients	Journal of the American Geriatrics Society	Yanin Chávarri-Guerra, Carolyn B. Hendricks et al.	10
7	Association between Clonal Hematopoiesis and Late Nonrelapse Mortality after Autologous Hematopoietic Cell Transplantation	Biology of Blood and Marrow Transplantation	Thomas P. Slavin, Jennifer Berano Teh et al.	18
8	Personalized circulating tumor DNA analysis to detect residual disease after neoadjuvant therapy in breast cancer	Science Translational Medicine	Bradon R. McDonald, Tania Contente‐Cuomo et al.	201
9	Circulating tumor DNA as an early cancer detection tool	Pharmacology & Therapeutics	Jeffrey N. Weitzel, Prativa Sahoo et al.	156
10	Novel candidates in early-onset familial colorectal cancer	Familial Cancer	Pradipta Ghosh, Tikam Chand Dakal et al.	16
11	Older breast cancer survivors may harbor hereditary cancer predisposition pathogenic variants and are at risk for clonal hematopoiesis	Journal of Geriatric Oncology	Thomas P. Slavin, Can‐Lan Sun et al.	9
12	Prevalence and characteristics of likely-somatic variants in cancer susceptibility genes among individuals who had hereditary pan-cancer panel testing	Cancer Genetics	Thomas P. Slavin, Bradford Coffee et al.	24
13	Experience Gained from the Development and Execution of a Multidisciplinary Multi-syndrome Hereditary Colon Cancer Family Conference	Journal of Cancer Education	Ilana Solomon, Kathleen R. Blazer et al.	1
14	Expanding the BP1-BP2 15q11.2 Microdeletion Phenotype: Tracheoesophageal Fistula and Congenital Cataracts	SHILAP Revista de lepidopterología	David Young, Thomas P. Slavin et al.	15
15	Genetic associations of relaxin: preterm birth and premature rupture of fetal membranes	American Journal of Obstetrics and Gynecology	Thomas P. Slavin, Dongmei Li et al.	18
16	Clinical Presentation and Positive Outcome of Two Siblings with Holocarboxylase Synthetase Deficiency Caused by a Homozygous L216R Mutation	JIMD Reports	Thomas P. Slavin, Charles R. Neal et al.	5
17	Monozygotic twins discordant for trisomy 13	Journal of Perinatology	Thomas P. Slavin, George Graham et al.	17
18	Microarray comparative genomic hybridization and cytogenetic characterization of tissue‐specific mosaicism in three patients	American Journal of Medical Genetics Part A	Elena Repnikova, Caroline Astbury et al.	17
19	Two-marker association tests yield new disease associations for coronary artery disease and hypertension	Human Genetics	Thomas P. Slavin, Tao Feng et al.	61
20	Developmental defects and childhood cancer	Current Opinion in Pediatrics	Thomas P. Slavin, Georgia L. Wiesner	8

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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