Sandy DeVries

8.7k citations
40 papers · 2.9k · h-index 24

Impact in

Papers in

    • Genomic variations and chromosomal abnormalities 13
    • Gene expression and cancer classification 4
    • Molecular Biology Techniques and Applications 4

Sandy DeVries

40 papers receiving 2.9k citations

Peers

Sandy DeVries
Comparison fields: 5 of 100
  • Cancer Research 929
  • Pathology and Forensic Medicine 626
  • Genetics 704
  • Oncology 632
  • Dermatology 164
Replace Raihanatou Diallo with:
Raihanatou Diallo Germany
Fujio Kasumi Japan
Kirsten M. Timms United States
Jeffrey Swensen United States
Nadine Collins United Kingdom
Gisela Keller Germany
Maryou B. Lambros United Kingdom
Sigurður Ingvarsson Iceland
S Hirohashi Japan
J Kassel United States
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Citations per field
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Citations per year

Countries citing papers authored by Sandy DeVries

Since Specialization
Citations

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

Fields of papers citing papers by Sandy DeVries

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Sandy DeVries, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Sandy DeVries Line = papers co-authored together Sandy DeVries links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 40 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Analysis of changes in DNA sequence copy number by comparative genomic hybridization in archival paraffin-embedded tumor samples.
1994341
2 2005275
3 2006205
4
Array-based comparative genomic hybridization for genome-wide screening of DNA copy number in bladder tumors.
2003203
5 1995183
6
Differentiation of lobular versus ductal breast carcinomas by expression microarray analysis.
2003178
7 1997164
8 2005136
9 2004134
10 1997112
11 1998111
12 2009107
13 200998
14 200496
15 200265
16 201357
17
Genetic alterations in ERBB2-amplified breast carcinomas.
199954
18 200153
19 200952
20 200550

About Sandy DeVries

Sandy DeVries is a scholar working on Genetics, Molecular Biology, Cancer Research, Pathology and Forensic Medicine and Surgery, having authored 40 papers that have together received 2.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Cancer Genomics and Diagnostics (10 papers), Radiomics and Machine Learning in Medical Imaging (5 papers), Bladder and Urothelial Cancer Treatments (5 papers), Genetic factors in colorectal cancer (5 papers), Gene expression and cancer classification (4 papers), Molecular Biology Techniques and Applications (4 papers) and Prostate Cancer Diagnosis and Treatment (3 papers). The work is most often cited by research in Cancer Research (929 citations), Pathology and Forensic Medicine (626 citations), Genetics (704 citations), Oncology (632 citations) and Dermatology (164 citations). Sandy DeVries has collaborated with scholars based in United States, Canada and Finland. Frequent co-authors include Frederic M. Waldman, F. Waldman, James E. Korkola, L.W. Chu, Jorma Isola, Karen Chew, Siavash Ghazvini, Jane Fridlyand, Sunanda Pejavar and Peter R. Carroll. Their work appears in journals such as Journal of Clinical Oncology, Human Pathology, Clinical Cancer Research, Genes Chromosomes and Cancer and BMC Cancer.

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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