Bryce A. Heese

1.0k total citations
16 papers, 258 citations indexed

About

Bryce A. Heese is a scholar working on Molecular Biology, Physiology and Clinical Biochemistry. According to data from OpenAlex, Bryce A. Heese has authored 16 papers receiving a total of 258 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Physiology and 6 papers in Clinical Biochemistry. Recurrent topics in Bryce A. Heese's work include Metabolism and Genetic Disorders (6 papers), Lysosomal Storage Disorders Research (5 papers) and Mitochondrial Function and Pathology (4 papers). Bryce A. Heese is often cited by papers focused on Metabolism and Genetic Disorders (6 papers), Lysosomal Storage Disorders Research (5 papers) and Mitochondrial Function and Pathology (4 papers). Bryce A. Heese collaborates with scholars based in United States, Canada and Sweden. Bryce A. Heese's co-authors include Uttam Garg, Richard J. Schroer, Susan A. Berry, Timothy C. Wood, Lisa A. Schimmenti, Piero Rinaldo, Stephen Cederbaum, Kyriakie Sarafoglou, Nicola Longo and Marzia Pasquali and has published in prestigious journals such as Clinical Pharmacology & Therapeutics, Journal of Medical Genetics and Molecular Genetics and Metabolism.

In The Last Decade

Bryce A. Heese

16 papers receiving 246 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bryce A. Heese United States	7	141	122	57	53	47	16	258
Ana Pop Netherlands	10	77 0.5×	154 1.3×	14 0.2×	31 0.6×	34 0.7×	16	270
P Bührdel Germany	6	222 1.6×	161 1.3×	61 1.1×	37 0.7×	30 0.6×	29	320
Bijina Balakrishnan United States	8	119 0.8×	108 0.9×	46 0.8×	30 0.6×	52 1.1×	15	224
Carla Valongo Portugal	7	107 0.8×	59 0.5×	5 0.1×	47 0.9×	10 0.2×	8	219
Andrea Schlune Germany	11	218 1.5×	157 1.3×	55 1.0×	50 0.9×	89 1.9×	24	319
Izelle Smuts South Africa	12	192 1.4×	273 2.2×	17 0.3×	12 0.2×	13 0.3×	25	354
Elisenda Cortès‐Saladelafont Spain	9	111 0.8×	99 0.8×	37 0.6×	15 0.3×	36 0.8×	21	231
Wen J. Chen United States	3	44 0.3×	102 0.8×	14 0.2×	7 0.1×	32 0.7×	5	191
Ramona Salvarinova Canada	8	80 0.6×	109 0.9×	13 0.2×	24 0.5×	16 0.3×	18	202
J Vaquerizo Spain	5	108 0.8×	121 1.0×	12 0.2×	13 0.2×	28 0.6×	12	152

Countries citing papers authored by Bryce A. Heese

Since Specialization

Citations

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

Fields of papers citing papers by Bryce A. Heese

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bryce A. Heese. 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 Bryce A. Heese. The network helps show where Bryce A. Heese may publish in the future.

Co-authorship network of co-authors of Bryce A. Heese

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

All Works

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16 of 16 papers shown

Frazee, C. Clinton, et al.. (2022). Tandem Mass Spectrometry for the Analysis of Plasma/Serum Acylcarnitines for the Diagnosis of Certain Organic Acidurias and Fatty Acid Oxidation Disorders. Methods in molecular biology. 2546. 27–34. 2 indexed citations

Cadieux‐Dion, Maxime, Jennifer Gannon, Brandon Newell, et al.. (2021). Delayed diagnosis of holocarboxylase synthetase deficiency in three patients with prominent skin findings. Pediatric Dermatology. 38(3). 655–658. 4 indexed citations

White, Amy, Dawn Peck, Jennifer Gannon, et al.. (2021). The role of biomarkers for the follow up of infants with positive newborn screening results for Fabry disease. Molecular Genetics and Metabolism. 132. S20–S20. 2 indexed citations

Thiffault, Isabelle, Andrea M. Atherton, Bryce A. Heese, et al.. (2020). Pathogenic variants in KPTN gene identified by clinical whole-genome sequencing. Molecular Case Studies. 6(3). a003970–a003970. 4 indexed citations

Larson, Austin, Shanti Balasubramaniam, John Christodoulou, et al.. (2018). Biochemical signatures mimicking multiple carboxylase deficiency in children with mutations in MT-ATP6. Mitochondrion. 44. 58–64. 17 indexed citations

Heese, Bryce A., et al.. (2018). Early childhood onset of high-grade atrioventricular block in Hunter syndrome. Cardiology in the Young. 28(5). 786–787. 2 indexed citations

Atherton, Andrea M., Dana Doheny, Dawn Peck, et al.. (2015). Newborn screening for Fabry disease: Is the A143T allele a pathogenic mutation or a pseudodeficiency allele?. Molecular Genetics and Metabolism. 114(2). S14–S15. 1 indexed citations

Heese, Bryce A., et al.. (2015). Quantification of Free Carnitine and Acylcarnitines in Plasma or Serum Using HPLC/MS/MS. Methods in molecular biology. 1378. 11–19. 10 indexed citations

Atherton, Andrea M., Dawn Peck, Katherine Christensen, et al.. (2015). The first two years of full population pilot newborn screening for lysosomal disorders: The Missouri experience. Molecular Genetics and Metabolism. 114(2). S15–S15. 1 indexed citations

10.

Price, Kristin E., Robin E. Pearce, Uttam Garg, et al.. (2011). Effects of Valproic Acid on Organic Acid Metabolism in Children: A Metabolic Profiling Study. Clinical Pharmacology & Therapeutics. 89(6). 867–874. 29 indexed citations

11.

Heese, Bryce A.. (2008). Current Strategies in the Management of Lysosomal Storage Diseases. Seminars in Pediatric Neurology. 15(3). 119–126. 26 indexed citations

12.

Mineri, Rossana, M. Rimoldi, Alberto Burlina, et al.. (2008). Identification of new mutations in the ETHE1 gene in a cohort of 14 patients presenting with ethylmalonic encephalopathy. Journal of Medical Genetics. 45(7). 473–478. 54 indexed citations

13.

Dagli, Aditi I, Roberto T. Zori, & Bryce A. Heese. (2008). Testing Strategy for Inborn Errors of Metabolism in the Neonate. NeoReviews. 9(7). e291–e298. 1 indexed citations

14.

Schimmenti, Lisa A., Eric Crombez, Bernd Schwahn, et al.. (2006). Expanded newborn screening identifies maternal primary carnitine deficiency. Molecular Genetics and Metabolism. 90(4). 441–445. 72 indexed citations

15.

Heese, Bryce A., et al.. (2006). A boy with fever and whorl keratopathy.. PubMed. 33(6). 1210–1. 4 indexed citations

16.

Heese, Bryce A., et al.. (1995). CARCASS SELECTION IN A HIGH ALTITUDE POPULATION OF THE BURYING BEETLE, NICROPHOR US INVESTIGATOR (SILPHIDAE). 29 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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