V. Reid Sutton

1.7k total citations
11 papers, 167 citations indexed

About

V. Reid Sutton is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, V. Reid Sutton has authored 11 papers receiving a total of 167 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Clinical Biochemistry and 4 papers in Genetics. Recurrent topics in V. Reid Sutton's work include Metabolism and Genetic Disorders (6 papers), Mitochondrial Function and Pathology (3 papers) and Genomics and Rare Diseases (2 papers). V. Reid Sutton is often cited by papers focused on Metabolism and Genetic Disorders (6 papers), Mitochondrial Function and Pathology (3 papers) and Genomics and Rare Diseases (2 papers). V. Reid Sutton collaborates with scholars based in United States, Italy and United Kingdom. V. Reid Sutton's co-authors include Nicholas Ah Mew, Keiko Ueda, Gregory M. Enns, Andrea Gropman, Eddie Island, Brittany Smith, Tiina K. Urv, Dietrich Matern, Charles P. Venditti and Anupam Chakrapani and has published in prestigious journals such as Genetics in Medicine, Molecular Genetics and Metabolism and Journal of Child Neurology.

In The Last Decade

V. Reid Sutton

8 papers receiving 165 citations

Peers

V. Reid Sutton

MB

CB

GENET

RHEUM

PPCH

Amy Hietala United States

Flávia Piazzon Brazil

Tomoko Tsuruoka Japan

Laura Konczal United States

Tracey Bishop United States

Aisha Al Shamsi United Arab Emirates

Mari‐Anne Vals Estonia

Tatiana Krylova Russia

Doreen Meissner South Africa

Dan Glass United Kingdom

Amy Hietala United States

V. Reid Sutton

113 ×0.9

MB

94 ×0.9

CB

15 ×0.4

GENET

10 ×0.3

RHEUM

15 ×0.5

PPCH

Citations per year, relative to V. Reid Sutton V. Reid Sutton (= 1×) peers Amy Hietala

Countries citing papers authored by V. Reid Sutton

Since Specialization

Citations

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

Fields of papers citing papers by V. Reid Sutton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by V. Reid Sutton. 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 V. Reid Sutton. The network helps show where V. Reid Sutton may publish in the future.

Co-authorship network of co-authors of V. Reid Sutton

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

All Works

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11 of 11 papers shown

1.

Miller, Marcus J., Adam D. Kennedy, Rebecca McClellan, et al.. (2025). The emerging role of metabolomics analysis in genetic and genomic testing: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 27(10). 101493–101493.

2.

Sutton, V. Reid, et al.. (2025). Newborn Screening: Advances, Challenges, and Future Directions. Clinics in Perinatology. 52(3). 449–459.

3.

Glinton, Kevin E., et al.. (2022). Advancements in therapeutics for inborn errors of metabolism. Current Opinion in Pediatrics. 34(6). 559–564. 3 indexed citations

4.

Ward, Scott M., et al.. (2021). Impact of COVID-19 on newborn screening in South Texas. Molecular Genetics and Metabolism. 132. S16–S16. 1 indexed citations

5.

Almannai, Mohammed, Ronit Marom, Fernando Scaglia, et al.. (2017). Milder clinical and biochemical phenotypes associated with the c.482G > A (p.Arg161Gln) pathogenic variant in cobalamin C disease: Implications for management and screening. Molecular Genetics and Metabolism. 122(1-2). 60–66. 16 indexed citations

6.

Cappuccio, Gerarda, Paldeep S. Atwal, Taraka Donti, et al.. (2016). Expansion of the Phenotypic Spectrum of Propionic Acidemia with Isolated Elevated Propionylcarnitine. JIMD Reports. 35. 33–37. 6 indexed citations

7.

Stark, Ryan J., Bindi Naik‐Mathuria, Fong Lam, et al.. (2012). Extracorporeal Membrane Oxygenation Support of a Severe Metabolic Crisis in a Child With Methylmalonic Acidemia. ASAIO Journal. 58(4). 438–439.

8.

Chapman, Kimberly A., Andrea Gropman, Nicholas Ah Mew, et al.. (2011). Natural history of propionic acidemia. Molecular Genetics and Metabolism. 105(1). 5–9. 92 indexed citations

9.

Douglas, Ganka, Marni E. Axelrad, Mary L. Brandt, et al.. (2010). Consensus in Guidelines for Evaluation of DSD by the Texas Children's Hospital Multidisciplinary Gender Medicine Team. International Journal of Pediatric Endocrinology. 2010. 1–17. 30 indexed citations

10.

Swarr, Daniel T. & V. Reid Sutton. (2010). Skeletal Dysplasias in the Newborn: Diagnostic Evaluation and Developmental Genetics. NeoReviews. 11(6). e290–e305. 3 indexed citations

11.

Scaglia, Fernando, V. Reid Sutton, Olaf A. Bodamer, et al.. (2001). Mitochondrial DNA Depletion Associated With Partial Complex II and IV Deficiencies and 3-Methylglutaconic Aciduria. Journal of Child Neurology. 16(2). 136–138. 16 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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