Logan C. Walker

3.1k citations
87 papers · 2.1k · 1 hit paper · h-index 27

Impact in

  • Genetics top 5%
    • BRCA gene mutations in cancer
    • Genomics and Rare Diseases
    • Cancer Genomics and Diagnostics

Papers in

    • BRCA gene mutations in cancer 30
    • Genomic variations and chromosomal abnormalities 12
    • Genomics and Rare Diseases 12
    • Cancer Genomics and Diagnostics 15

Logan C. Walker

86 papers receiving 2.1k citations

Logan C. Walker's Hit Papers

Using the ACMG/AMP framework to capture evidence related to predicted and observed impact on splicing: Recommendations from the ClinGen SVI Splicing Subgroup 2023 · 177 citations
1770+1+2Years since publication50100150

Peers

Logan C. Walker
Comparison fields: 5 of 108
  • Genetics 827
  • Cancer Research 320
  • Molecular Biology 1.0k
  • Pathology and Forensic Medicine 230
  • Oncology 275
Replace Chela T. James with:
Chela T. James United Kingdom
Susanne Nicole Weber Germany
Jean McGowan‐Jordan Canada
Jelena Kostic Serbia
Brian E. Ward United States
Emma Tham Sweden
Eladio A. Velasco Spain
María Dolores García-Prats Spain
Naofumi Ishikawa Japan
Lise Bjerre Husted Denmark
Logan C. Walker relative to Chela T. James United Kingdom Chela T. James's profile →
Citations per field
00.5×2×2.8×
Chela T. James · 1×
Citations per year

Countries citing papers authored by Logan C. Walker

Since Specialization
Citations

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

Fields of papers citing papers by Logan C. Walker

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Logan C. Walker. 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 Logan C. Walker. The network helps show where Logan C. Walker may publish in the future.

Co-authors

The 25 scholars most cited alongside Logan C. Walker, 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 Logan C. Walker Line = papers co-authored together Logan C. Walker links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 87 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Using the ACMG/AMP framework to capture evidence related to predicted and observed impact on splicing: Recommendations from the ClinGen SVI Splicing Subgroup
Hit paper breakdown →
2023177
2 2011129
3 201887
4 201586
5 201679
6 201476
7 201771
8 202166
9 200364
10 201359
11 200252
12 201049
13 202448
14 201946
15 201644
16 201742
17 202042
18 201841
19 201141
20 201940

About Logan C. Walker

Logan C. Walker is a scholar working on Genetics, Cancer Research, Pathology and Forensic Medicine, Molecular Biology and Oncology, having authored 87 papers that have together received 2.1k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (30 papers), Cancer Genomics and Diagnostics (15 papers), Genomic variations and chromosomal abnormalities (12 papers), Genomics and Rare Diseases (12 papers), Genetic factors in colorectal cancer (12 papers), CRISPR and Genetic Engineering (12 papers), RNA Research and Splicing (7 papers) and Gene expression and cancer classification (6 papers). The work is most often cited by research in Genetics (827 citations), Cancer Research (320 citations), Molecular Biology (1.0k citations), Pathology and Forensic Medicine (230 citations) and Oncology (275 citations). Logan C. Walker has collaborated with scholars based in Australia, New Zealand and United Kingdom. Frequent co-authors include Christine M. Morris, Bridget Anne Robinson, Peter S. Ganly, Amanda B. Spurdle, John C. Pearson, Margaret J. Currie, Helen R. Morrin, George A. R. Wiggins, John D. Potter and Ann K. Richardson. Their work appears in journals such as The American Journal of Human Genetics, Breast Cancer Research and Treatment, Human Mutation, Journal of Medical Genetics and PLoS ONE.

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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