Timothy Fee

441 citations
11 papers · 298 · h-index 6

Impact in

    • Genomics and Rare Diseases
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
    • Genetic Syndromes and Imprinting
    • Epigenetics and DNA Methylation

Papers in

    • Genomic variations and chromosomal abnormalities 3
    • Genomics and Rare Diseases 3
    • Genetic Syndromes and Imprinting 2
    • Genetics and Neurodevelopmental Disorders 2
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
    • Congenital limb and hand anomalies 1

Timothy Fee

11 papers receiving 295 citations

Peers

Timothy Fee
Comparison fields: 5 of 35
  • Genetics 176
  • Molecular Biology 137
  • Developmental Biology 3
  • Cancer Research 18
  • Pediatrics, Perinatology and Child Health 22
Replace Mindy H. Li with:
Mindy H. Li United States
Ataf Hussain Sabir United Kingdom
Ellen Markljung Sweden
Stefano Petrocchi Italy
Milena Simioni Brazil
Houda Karmous‐Benailly France
Fiorenza Soli Italy
Janet M. Legare United States
Marleen Kets Netherlands
Lindsey Campbell United States
Timothy Fee relative to Mindy H. Li United States Mindy H. Li's profile →
Citations per field
00.5×2×3.0×
Mindy H. Li · 1×
Citations per year

Countries citing papers authored by Timothy Fee

Since Specialization
Citations

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

Fields of papers citing papers by Timothy Fee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

11 of 11 papers shown
#Work
1 2021116
2 202255
3 202444
4 199643
5 202322
6 20226
7 20226
8 20222
9 19972
10 20221
11 20181

About Timothy Fee

Timothy Fee is a scholar working on Genetics, Developmental Biology, Surgery, Orthopedics and Sports Medicine and Molecular Biology, having authored 11 papers that have together received 298 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (3 papers), Genetic Syndromes and Imprinting (2 papers), Epigenetics and DNA Methylation (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper), Cancer Genomics and Diagnostics (1 paper) and Congenital limb and hand anomalies (1 paper). The work is most often cited by research in Genetics (176 citations), Molecular Biology (137 citations), Developmental Biology (3 citations), Cancer Research (18 citations) and Pediatrics, Perinatology and Child Health (22 citations). Timothy Fee has collaborated with scholars based in United States, Netherlands and Canada. Frequent co-authors include Mark George McKenney, Kimberley A. Lentz, Larry Martin, Barbara R. DuPont, Lawrence Clarke Layman, Alex R. Hastie, Ravindra B Kolhe, Alka Chaubey, Nikhil Sahajpal and Ashis Kumar Mondal. Their work appears in journals such as Genetics in Medicine, Annals of Plastic Surgery, The American Journal of Surgery, Human Genetics and Genomics Advances and Genes.

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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