Julie M. Cunningham

33.3k total citations · 2 hit papers
215 papers, 10.9k citations indexed

About

Julie M. Cunningham is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Julie M. Cunningham has authored 215 papers receiving a total of 10.9k indexed citations (citations by other indexed papers that have themselves been cited), including 89 papers in Molecular Biology, 64 papers in Cancer Research and 50 papers in Genetics. Recurrent topics in Julie M. Cunningham's work include Cancer Genomics and Diagnostics (32 papers), Epigenetics and DNA Methylation (28 papers) and Genetic factors in colorectal cancer (27 papers). Julie M. Cunningham is often cited by papers focused on Cancer Genomics and Diagnostics (32 papers), Epigenetics and DNA Methylation (28 papers) and Genetic factors in colorectal cancer (27 papers). Julie M. Cunningham collaborates with scholars based in United States, Canada and Belarus. Julie M. Cunningham's co-authors include Stephen N. Thibodeau, Daniel J. Schaid, Lawrence J. Burgart, Shannon K. McDonnell, David J. Tester, Patrick C. Roche, Amy J. French, Eric R. Christensen, Ellen L. Goode and Scott J. Hebbring and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Journal of Clinical Investigation.

In The Last Decade

Julie M. Cunningham

212 papers receiving 10.7k 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.

Hypermethylation of the hMLH1 promoter in colon cancer with microsatellite instability.

1998 698 citations Julie M. Cunningham, Lawrence J. Burgart et al. PubMed profile →
The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein

2002 525 citations Christopher J. Ward, Sandro Rossetti et al. profile →

Peers

Countries citing papers authored by Julie M. Cunningham

Since Specialization

Citations

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

Fields of papers citing papers by Julie M. Cunningham

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Julie M. Cunningham. 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 Julie M. Cunningham. The network helps show where Julie M. Cunningham may publish in the future.

Co-authorship network of co-authors of Julie M. Cunningham

This figure shows the co-authorship network connecting the top 25 collaborators of Julie M. Cunningham. A scholar is included among the top collaborators of Julie M. Cunningham 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 Julie M. Cunningham. Julie M. Cunningham 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	Risk Factors for Ovarian Cancer by BRCA Status: A Collaborative Case-Only Analysis	Cancer Epidemiology Biomarkers & Prevention	Renhua Na, Kathryn Alsop et al.	2
2	Evaluating cell type deconvolution in FFPE breast tissue: application to benign breast disease	NAR Genomics and Bioinformatics	Yuanhang Liu, Robert A. Vierkant et al.	1
3	Use of FFPE-derived DNA in next generation sequencing: DNA extraction methods	PLoS ONE	Samantha J. McDonough, Aditya Bhagwate et al.	62
4	Mapping of the IRF8 Gene Identifies a 3′UTR Variant Associated with Risk of Chronic Lymphocytic Leukemia but not Other Common Non-Hodgkin Lymphoma Subtypes	Cancer Epidemiology Biomarkers & Prevention	Susan L. Slager, Sara J. Achenbach et al.	12
5	Genetic association with overall survival of taxane-treated lung cancer patients - a genome-wide association study in human lymphoblastoid cell lines followed by a clinical association study	SHILAP Revista de lepidopterología	Nifang Niu, Daniel J. Schaid et al.	28
6	The Minnesota Center for Twin and Family Research Genome-Wide Association Study	Twin Research and Human Genetics	Michael B. Miller, Saonli Basu et al.	53
7	Genetic Variants Associated with the Risk of Chronic Obstructive Pulmonary Disease with and without Lung Cancer	Cancer Prevention Research	Mariza de Andrade, Yan Li et al.	19
8	Genetic Variation Predicting Cisplatin Cytotoxicity Associated with Overall Survival in Lung Cancer Patients Receiving Platinum-Based Chemotherapy	Clinical Cancer Research	Xiang-Lin Tan, Ann M. Moyer et al.	82
9	Genetic Variations in Multiple Drug Action Pathways and Survival in Advanced Stage Non–Small Cell Lung Cancer Treated with Chemotherapy	Clinical Cancer Research	Yafei Li, Zhifu Sun et al.	22
10	A Rigorous and Comprehensive Validation: Common Genetic Variations and Lung Cancer	Cancer Epidemiology Biomarkers & Prevention	Ping Yang, Yafei Li et al.	30
11	Expression profiling of formalin-fixed paraffin-embedded primary breast tumors using cancer-specific and whole genome gene panels on the DASL®platform	BMC Medical Genomics	Monica M. Reinholz, Jeanette E. Eckel‐Passow et al.	11
12	Childhood Exposure to Secondhand Smoke and Functional Mannose Binding Lectin Polymorphisms Are Associated with Increased Lung Cancer Risk	Cancer Epidemiology Biomarkers & Prevention	Susan Olivo‐Marston, Ping Yang et al.	46
13	Gene Networks and microRNAs Implicated in Aggressive Prostate Cancer	Cancer Research	Liang Wang, Hui Tang et al.	125
14	Polymorphic Variants in Hereditary Pancreatic Cancer Genes Are Not Associated with Pancreatic Cancer Risk	Cancer Epidemiology Biomarkers & Prevention	Robert R. McWilliams, William R. Bamlet et al.	5
15	Genetic Variation in the One-Carbon Transfer Pathway and Ovarian Cancer Risk	Cancer Research	Linda E. Kelemen, Thomas A. Sellers et al.	50
16	Strong Evidence of a Genetic Determinant for Mammographic Density, a Major Risk Factor for Breast Cancer	Cancer Research	Celine M. Vachon, Thomas A. Sellers et al.	58
17	Haplotype analysis improves molecular diagnostics of autosomal recessive polycystic kidney disease	American Journal of Kidney Diseases	Mark Consugar, Sarah Anderson et al.	24
18	Immunohistochemistry Versus Microsatellite Instability Testing in Phenotyping Colorectal Tumors	Journal of Clinical Oncology	Noralane M. Lindor, Lawrence J. Burgart et al.	455
19	Analysis of the RNASEL Gene in Familial and Sporadic Prostate Cancer	The American Journal of Human Genetics	Liang Wang, Shannon K. McDonnell et al.	92
20	Immune complexes in systemic sclerosis; detection by C1q binding, K-cell inhibition and Raji cell radioimmunoassays.	PubMed	Pamela Hughes, Julie M. Cunningham et al.	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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