Thaddeus Judkins

1.0k total citations
19 papers, 607 citations indexed

About

Thaddeus Judkins is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Thaddeus Judkins has authored 19 papers receiving a total of 607 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 7 papers in Molecular Biology and 5 papers in Pathology and Forensic Medicine. Recurrent topics in Thaddeus Judkins's work include BRCA gene mutations in cancer (15 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetic factors in colorectal cancer (5 papers). Thaddeus Judkins is often cited by papers focused on BRCA gene mutations in cancer (15 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetic factors in colorectal cancer (5 papers). Thaddeus Judkins collaborates with scholars based in United States and Germany. Thaddeus Judkins's co-authors include Benjamin B. Roa, Richard Wenstrup, Brant C. Hendrickson, Karla R. Bowles, Praveen Kaushik, Matthew B. Yurgelun, Brian Allen, Sapna Syngal, Rajesh Kaldate and Anne‐Renee Hartman and has published in prestigious journals such as Journal of Clinical Oncology, Gastroenterology and Cancer.

In The Last Decade

Thaddeus Judkins

19 papers receiving 594 citations

Peers

Thaddeus Judkins

GENET

MB

PFM

CR

ONCOL

F. B. F. Law Hong Kong

Antoine Rousselin France

Mar Infante Spain

Paraskevi Apostolou Greece

Sabine Pagès France

Pedro Pinto Portugal

S. Gayther United Kingdom

Kristen Hanson United States

Barbara Bulman United Kingdom

Elżbieta Marczyk Poland

F. B. F. Law Hong Kong

Thaddeus Judkins

242 ×0.6

GENET

228 ×0.9

MB

91 ×0.4

PFM

127 ×0.7

CR

96 ×0.6

ONCOL

Citations per year, relative to Thaddeus Judkins Thaddeus Judkins (= 1×) peers F. B. F. Law

Countries citing papers authored by Thaddeus Judkins

Since Specialization

Citations

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

Fields of papers citing papers by Thaddeus Judkins

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thaddeus Judkins

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

All Works

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19 of 19 papers shown

1.

Hughes, Elisha, Susanne Wagner, Thaddeus Judkins, et al.. (2021). Integrating Clinical and Polygenic Factors to Predict Breast Cancer Risk in Women Undergoing Genetic Testing. JCO Precision Oncology. 307–316. 19 indexed citations

2.

Hughes, Elisha, Shannon Gallagher, Susanne Wagner, et al.. (2020). Development and Validation of a Clinical Polygenic Risk Score to Predict Breast Cancer Risk. JCO Precision Oncology. 4(4). 585–592. 41 indexed citations

3.

Mancini‐DiNardo, Debora, Thaddeus Judkins, John Kidd, et al.. (2019). Detection of large rearrangements in a hereditary pan-cancer panel using next-generation sequencing. BMC Medical Genomics. 12(1). 138–138. 16 indexed citations

4.

Bowles, Karla R., Debora Mancini‐DiNardo, Bradford Coffee, et al.. (2018). Hereditary Cancer Testing Challenges: Assembling the Analytical Pieces to Solve the Patient Clinical Puzzle. Future Oncology. 15(1). 65–79. 3 indexed citations

5.

Hughes, Elisha, Thaddeus Judkins, Susanne Wagner, et al.. (2018). Abstract PD1-08: Development and validation of a combined residual risk score to predict breast cancer risk in unaffected women negative for mutations on a multi-gene hereditary cancer panel. Cancer Research. 78(4_Supplement). PD1–8. 3 indexed citations

6.

Qian, Yaping, Debora Mancini‐DiNardo, Thaddeus Judkins, et al.. (2017). Identification of pathogenic retrotransposon insertions in cancer predisposition genes. Cancer Genetics. 216-217. 159–169. 29 indexed citations

7.

Hughes, Elisha, Thaddeus Judkins, Susanne Wagner, et al.. (2017). Development and validation of a residual risk score to predict breast cancer risk in unaffected women negative for mutations on a multi-gene hereditary cancer panel.. Journal of Clinical Oncology. 35(15_suppl). 1579–1579. 7 indexed citations

8.

Yurgelun, Matthew B., Brian Allen, Rajesh Kaldate, et al.. (2015). Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome. Gastroenterology. 149(3). 604–613.e20. 184 indexed citations

9.

Mancini‐DiNardo, Debora, Thaddeus Judkins, Natalia Gutin, et al.. (2014). Design and validation of an oligonucleotide microarray for the detection of genomic rearrangements associated with common hereditary cancer syndromes. Journal of Experimental & Clinical Cancer Research. 33(1). 74–74. 5 indexed citations

10.

Mancini‐DiNardo, Debora, Thaddeus Judkins, Natalia Gutin, et al.. (2014). Design and validation of an oligonucleotide microarray for the detection of genomic rearrangements associated with common hereditary cancer syndromes. Journal of Experimental & Clinical Cancer Research. 33(1). 74–74. 1 indexed citations

11.

Judkins, Thaddeus, Eric T. Rosenthal, Christopher Arnell, et al.. (2012). Clinical significance of large rearrangements in BRCA1 and BRCA2. Cancer. 118(21). 5210–5216. 96 indexed citations

12.

Weitzel, Jeffrey N., Veronica I. Lagos, Josef Herzog, et al.. (2007). Evidence for Common Ancestral Origin of a Recurring BRCA1 Genomic Rearrangement Identified in High-Risk Hispanic Families. Cancer Epidemiology Biomarkers & Prevention. 16(8). 1615–1620. 72 indexed citations

13.

Wenstrup, Richard, Thaddeus Judkins, Kristilyn Eliason, et al.. (2007). Molecular genetic testing for large genomic deletion and duplication mutations in the BRCA1 and BRCA2 genes for hereditary breast and ovarian cancer. Journal of Clinical Oncology. 25(18_suppl). 10513–10513. 2 indexed citations

14.

Judkins, Thaddeus, Brant C. Hendrickson, Amie M. Deffenbaugh, & Thomas Scholl. (2005). Single nucleotide polymorphisms in clinical genetic testing: the characterization of the clinical significance of genetic variants and their application in clinical research for BRCA1. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 573(1-2). 168–179. 17 indexed citations

15.

Ward, Benjamin D., Brant C. Hendrickson, Thaddeus Judkins, et al.. (2005). A Multi-Exonic BRCA1 Deletion Identified in Multiple Families through Single Nucleotide Polymorphism Haplotype Pair Analysis and Gene Amplification with Widely Dispersed Primer Sets. Journal of Molecular Diagnostics. 7(1). 139–142. 8 indexed citations

16.

Hendrickson, Brant C., Thaddeus Judkins, Benjamin D. Ward, et al.. (2005). Prevalence of five previously reported and recurrent BRCA1 genetic rearrangement mutations in 20,000 patients from hereditary breast/ovarian cancer families. Genes Chromosomes and Cancer. 43(3). 309–313. 43 indexed citations

17.

Judkins, Thaddeus, Brant C. Hendrickson, Amie M. Deffenbaugh, et al.. (2005). Application of Embryonic Lethal or Other Obvious Phenotypes to Characterize the Clinical Significance of Genetic Variants Found in Trans with Known Deleterious Mutations. Cancer Research. 65(21). 10096–10103. 51 indexed citations

18.

Hendrickson, Brant C., et al.. (2004). Two rare novel polymorphisms in the D8S1179 and D13S317 markers and method to mitigate their impact on human identification.. PubMed. 45(4). 457–60. 9 indexed citations

19.

Hendrickson, Brant C., et al.. (2004). Recurrent intragenic rearrangement mutations in the tumor suppressor gene BRCA1: Prevalence results from 12,272 patients at high risk for breast and/or ovarian cancers and methods of biochemical analysis. Journal of Clinical Oncology. 22(14_suppl). 9533–9533. 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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