Kelly Watkins

994 total citations
4 papers, 99 citations indexed

About

Kelly Watkins is a scholar working on Genetics, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Kelly Watkins has authored 4 papers receiving a total of 99 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 1 paper in Molecular Biology and 1 paper in Clinical Biochemistry. Recurrent topics in Kelly Watkins's work include Genomics and Rare Diseases (2 papers), Cancer Genomics and Diagnostics (1 paper) and Wnt/β-catenin signaling in development and cancer (1 paper). Kelly Watkins is often cited by papers focused on Genomics and Rare Diseases (2 papers), Cancer Genomics and Diagnostics (1 paper) and Wnt/β-catenin signaling in development and cancer (1 paper). Kelly Watkins collaborates with scholars based in United States. Kelly Watkins's co-authors include Stephen F. Kingsmore, Matthew N. Bainbridge, Nathaly M. Sweeney, Matthew R. Williams, James C. Perry, Jeffrey J. Gold, Erica Sanford Kobayashi, Lauge Farnaes, Michelle M. Clark and Nicole G. Coufal and has published in prestigious journals such as Genetics in Medicine, Pediatric Critical Care Medicine and Molecular Case Studies.

In The Last Decade

Kelly Watkins

4 papers receiving 99 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Kelly Watkins United States	3	83	27	19	18	14	4	99
Katharina Löhner Netherlands	4	87 1.0×	59 2.2×	19 1.0×	11 0.6×	28 2.0×	5	137
Sara Caylor United States	4	109 1.3×	44 1.6×	22 1.2×	14 0.8×	34 2.4×	4	139
Helen Dolling United Kingdom	2	130 1.6×	52 1.9×	28 1.5×	22 1.2×	32 2.3×	3	159
Paulette Barahona Australia	6	88 1.1×	36 1.3×	12 0.6×	7 0.4×	74 5.3×	14	148
Stephanie B. Crowley United States	3	75 0.9×	20 0.7×	5 0.3×	19 1.1×	14 1.0×	4	89
Michelle Steinraths Canada	8	104 1.3×	60 2.2×	23 1.2×	5 0.3×	60 4.3×	12	168
Joanna Lazier Canada	8	67 0.8×	46 1.7×	10 0.5×	5 0.3×	55 3.9×	19	126
Giordano B. Soares‐Souza Brazil	7	65 0.8×	25 0.9×	6 0.3×	5 0.3×	4 0.3×	12	103
Lindsey Byrne United States	5	57 0.7×	9 0.3×	7 0.4×	10 0.6×	14 1.0×	11	82
Nicoleta Voian United States	4	77 0.9×	22 0.8×	6 0.3×	21 1.2×	3 0.2×	6	93

Countries citing papers authored by Kelly Watkins

Since Specialization

Citations

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

Fields of papers citing papers by Kelly Watkins

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kelly Watkins

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

All Works

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4 of 4 papers shown

1.

James, Kiely N., Shimul Chowdhury, Yan Ding, et al.. (2023). Genome sequencing detects a wide range of clinically relevant copy-number variants and other genomic alterations. Genetics in Medicine. 26(1). 101006–101006. 1 indexed citations

2.

Mark, Paul R., Stephen A. Murray, Tao Yang, et al.. (2022). Autosomal recessive LRP1-related syndrome featuring cardiopulmonary dysfunction, bone dysmorphology, and corneal clouding.. PubMed. 8(6). 5 indexed citations

3.

Kobayashi, Erica Sanford, Michelle M. Clark, Lauge Farnaes, et al.. (2019). Rapid Whole Genome Sequencing Has Clinical Utility in Children in the PICU*. Pediatric Critical Care Medicine. 20(11). 1007–1020. 88 indexed citations

4.

Kobayashi, Erica Sanford, Kelly Watkins, Shareef Nahas, et al.. (2018). Rapid whole-genome sequencing identifies a novel AIRE variant associated with autoimmune polyendocrine syndrome type 1. Molecular Case Studies. 4(3). a002485–a002485. 5 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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