Timothy Fee

403 total citations
9 papers, 78 citations indexed

About

Timothy Fee is a scholar working on Genetics, Surgery and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Timothy Fee has authored 9 papers receiving a total of 78 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Surgery and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Timothy Fee's work include Genomic variations and chromosomal abnormalities (4 papers), Prenatal Screening and Diagnostics (2 papers) and Genetic Mapping and Diversity in Plants and Animals (1 paper). Timothy Fee is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Prenatal Screening and Diagnostics (2 papers) and Genetic Mapping and Diversity in Plants and Animals (1 paper). Timothy Fee collaborates with scholars based in United States. Timothy Fee's co-authors include Larry Martin, Mark McKenney, Barbara R. DuPont, Benjamin Hilton, Alka Chaubey, Ashis K. Mondal, Ravindra Kolhe, Alex Hastie, Nikhil Sahajpal and Lawrence C. Layman and has published in prestigious journals such as Genome Research, The American Journal of Surgery and Annals of Plastic Surgery.

In The Last Decade

Timothy Fee

8 papers receiving 75 citations

Peers

Timothy Fee

SURGE

GENET

PPCH

MB

PRM

Marc Popelier France

Timothy Morgan New Zealand

Alfonso Pezzella Italy

Marine Legendre France

Heike Weigand Germany

Jade Harris United Kingdom

Madelena Martin United States

Beate Kuppers Italy

J. Barnes United States

H. Melanie Bedford Canada

Marc Popelier France

Timothy Fee

32 ×0.7

SURGE

25 ×0.8

GENET

13 ×0.8

PPCH

16 ×1.3

MB

2 ×0.2

PRM

Citations per year, relative to Timothy Fee Timothy Fee (= 1×) peers Marc Popelier

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-authorship network of co-authors of Timothy Fee

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

All Works

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9 of 9 papers shown

1.

Sahajpal, Nikhil, Jane H. Dean, Benjamin Hilton, et al.. (2025). Optical genome mapping identifies rare structural variants in neural tube defects. Genome Research. 35(4). 798–809.

2.

Sahajpal, Nikhil, Ashis K. Mondal, Timothy Fee, et al.. (2023). Clinical Validation and Diagnostic Utility of Optical Genome Mapping in Prenatal Diagnostic Testing. Journal of Molecular Diagnostics. 25(4). 234–246. 19 indexed citations

3.

Fang, Xiaolan, et al.. (2023). Clinical case report: mosaicANK3pathogenic variant in a patient with autism spectrum disorder and neurodevelopmental delay. Molecular Case Studies. 9(3). a006233–a006233. 3 indexed citations

4.

Butler, Kameryn M., Timothy Fee, Barbara R. DuPont, et al.. (2022). A SOX3 duplication and lumbosacral spina bifida in three generations. American Journal of Medical Genetics Part A. 188(5). 1572–1577. 5 indexed citations

5.

Fee, Timothy, Renee Bend, Raymond J. Louie, et al.. (2022). Mosaicism of common pathogenic MECP2 variants identified in two males with a clinical diagnosis of Rett syndrome. American Journal of Medical Genetics Part A. 188(10). 2988–2998. 5 indexed citations

6.

Sahajpal, Nikhil, Ashis K. Mondal, Sudha Ananth, et al.. (2022). Optical Genome Mapping and Single Nucleotide Polymorphism Microarray: An Integrated Approach for Investigating Products of Conception. Genes. 13(4). 643–643. 2 indexed citations

7.

Chaubey, Alka, et al.. (2018). 47. Serendipitous identification of meiotic crossover events in struma ovarii tumors by whole genome SNP microarray analysis. Cancer Genetics. 226-227. 53–54. 1 indexed citations

8.

Fee, Timothy & H. Hollis Caffee. (1997). Predictors of Postoperative Aesthetics Following Explantation of the Augmented Breast. Annals of Plastic Surgery. 38(3). 217–222. 2 indexed citations

9.

McKenney, Mark, et al.. (1996). A simple device for closure of fasciotomy wounds. The American Journal of Surgery. 172(3). 275–277. 41 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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