Dimitar Gavrilov

1.7k total citations
35 papers, 901 citations indexed

About

Dimitar Gavrilov is a scholar working on Clinical Biochemistry, Physiology and Molecular Biology. According to data from OpenAlex, Dimitar Gavrilov has authored 35 papers receiving a total of 901 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Clinical Biochemistry, 15 papers in Physiology and 12 papers in Molecular Biology. Recurrent topics in Dimitar Gavrilov's work include Metabolism and Genetic Disorders (16 papers), Lysosomal Storage Disorders Research (9 papers) and Mitochondrial Function and Pathology (8 papers). Dimitar Gavrilov is often cited by papers focused on Metabolism and Genetic Disorders (16 papers), Lysosomal Storage Disorders Research (9 papers) and Mitochondrial Function and Pathology (8 papers). Dimitar Gavrilov collaborates with scholars based in United States, Canada and Australia. Dimitar Gavrilov's co-authors include Devin Oglesbee, Silvia Tortorelli, Dietrich Matern, Piero Rinaldo, Kimiyo Raymond, Coleman Turgeon, Mark J Magera, Pierre Allard, Dawn Peck and Jean M. Lacey and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gastroenterology and Human Molecular Genetics.

In The Last Decade

Dimitar Gavrilov

31 papers receiving 881 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dimitar Gavrilov United States 15 437 403 345 200 152 35 901
Coleman Turgeon United States 13 404 0.9× 380 0.9× 307 0.9× 147 0.7× 132 0.9× 26 821
Anupam Chakrapani United Kingdom 19 628 1.4× 546 1.4× 466 1.4× 132 0.7× 175 1.2× 57 1.2k
Ali Dursun Türkiye 17 438 1.0× 434 1.1× 215 0.6× 110 0.6× 165 1.1× 97 995
Shawn E. McCandless United States 17 604 1.4× 495 1.2× 372 1.1× 299 1.5× 239 1.6× 34 1.2k
Jim McGill Australia 15 376 0.9× 306 0.8× 243 0.7× 155 0.8× 198 1.3× 34 829
Ayşegül Tokatlı Türkiye 17 575 1.3× 610 1.5× 249 0.7× 157 0.8× 184 1.2× 101 1.3k
Go Tajima Japan 15 301 0.7× 285 0.7× 190 0.6× 157 0.8× 89 0.6× 56 663
Wenjuan Qiu China 22 606 1.4× 730 1.8× 378 1.1× 283 1.4× 373 2.5× 146 1.5k
Hélène Ogier France 13 415 0.9× 443 1.1× 292 0.8× 76 0.4× 113 0.7× 16 877
Ksenija Fumić Croatia 15 329 0.8× 498 1.2× 248 0.7× 78 0.4× 286 1.9× 62 868

Countries citing papers authored by Dimitar Gavrilov

Since Specialization
Citations

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

Fields of papers citing papers by Dimitar Gavrilov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dimitar Gavrilov

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

All Works

20 of 20 papers shown
1.
Hall, Patricia, Amy White, Dawn Peck, et al.. (2025). Two-tiered newborn screening for infantile Krabbe disease allows timely treatment initiation and avoids false-positive results. Genetics in Medicine. 101572–101572.
2.
Turgeon, Coleman, Kari Casas, Ryan Flanagan, et al.. (2024). Pre-analytic decrease of phenylalanine in plasma of patients with phenylketonuria treated with pegvaliase. Molecular Genetics and Metabolism Reports. 40. 101110–101110. 1 indexed citations
3.
White, Amy, Tiffany Grider, Josef Alawneh, et al.. (2024). P004: Urine polyols for diagnosis of sorbitol dehydrogenase (SORD) deficiency-related peripheral neuropathy*. SHILAP Revista de lepidopterología. 2. 100881–100881.
4.
White, Amy, Dawn Peck, Dimitar Gavrilov, et al.. (2024). Sensitivity of transferrin isoform analysis for PMM2-CDG. Molecular Genetics and Metabolism. 143(1-2). 108564–108564. 1 indexed citations
5.
Peck, Dawn, Jean M. Lacey, Amy White, et al.. (2020). Incorporation of Second-Tier Biomarker Testing Improves the Specificity of Newborn Screening for Mucopolysaccharidosis Type I. International Journal of Neonatal Screening. 6(1). 10–10. 28 indexed citations
6.
Gavrilov, Dimitar, et al.. (2019). Clinical, biochemical and molecular characteristics of malonyl-CoA decarboxylase deficiency and long-term follow-up of nine patients. Molecular Genetics and Metabolism. 128(1-2). 113–121. 6 indexed citations
7.
Газатова, Н. Д., et al.. (2019). Features of cellular immunity and regeneration for alcoholic fibrosis of the liver. SHILAP Revista de lepidopterología. 18(1). 175–189.
8.
Conboy, Erin, Silvia Tortorelli, Kim K. Nickander, et al.. (2019). Multiplex testing for the screening of lysosomal storage disease in urine: Sulfatides and glycosaminoglycan profiles in 40 cases of sulfatiduria. Molecular Genetics and Metabolism. 129(2). 106–110. 10 indexed citations
9.
Netzel, Brian C., Dimitar Gavrilov, Dietrich Matern, et al.. (2018). Expanded analysis of Lyso-GB3 analogues and correlation with total Lyso-GB3 and Fabry status in 59 clinical patients. Molecular Genetics and Metabolism. 123(2). S105–S105. 1 indexed citations
10.
Milosevic, Dragana, Ramanath Majumdar, Dimitar Gavrilov, et al.. (2017). A Droplet Digital PCR Method for Severe Combined Immunodeficiency Newborn Screening. Journal of Molecular Diagnostics. 19(5). 755–765. 16 indexed citations
11.
Tortorelli, Silvia, Joseph J. Orsini, Colleen F. Stevens, et al.. (2017). Moonlighting newborn screening markers: the incidental discovery of a second-tier test for Pompe disease. Genetics in Medicine. 20(8). 840–846. 44 indexed citations
12.
Peck, Dawn, Jean M. Lacey, Coleman Turgeon, et al.. (2017). Precision newborn screening for lysosomal disorders. Genetics in Medicine. 20(8). 847–854. 95 indexed citations
13.
Conboy, Erin, Filippo Pinto e Vairo, Matthew Schultz, et al.. (2017). Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency: Unique Presenting Laboratory Values and a Review of Biochemical and Clinical Features. JIMD Reports. 40. 63–69. 29 indexed citations
14.
Wong, Derek A., Silvia Tortorelli, L.A. Bishop, et al.. (2015). Outcomes of four patients with homocysteine remethylation disorders detected by newborn screening. Genetics in Medicine. 18(2). 162–167. 21 indexed citations
15.
Hall, Patricia, Virginia V. Michels, Dimitar Gavrilov, et al.. (2013). Aripiprazole and trazodone cause elevations of 7-dehydrocholesterol in the absence of Smith–Lemli–Opitz Syndrome. Molecular Genetics and Metabolism. 110(1-2). 176–178. 34 indexed citations
16.
Magera, Mark J, Wendy J. Introne, Silvia Tortorelli, et al.. (2010). Homogentisic acid interference in routine urine creatinine determination. Molecular Genetics and Metabolism. 100(1). 103–104. 12 indexed citations
17.
McHugh, David, Dimitar Gavrilov, Kimiyo Raymond, et al.. (2010). Allelic diversity in MCAD deficiency: The biochemical classification of 54 variants identified during 5years of ACADM sequencing. Molecular Genetics and Metabolism. 100(3). 241–250. 44 indexed citations
18.
Rinaldo, Piero, et al.. (2008). Newborn Screening of Metabolic Disorders: Recent Progress and Future Developments. PubMed. 62. 81–96. 11 indexed citations
19.
Salomons, Gajja S., C. Jakobs, Lorna Pope, et al.. (2006). Clinical, enzymatic and molecular characterization of nine new patients with malonyl‐coenzyme A decarboxylase deficiency. Journal of Inherited Metabolic Disease. 30(1). 23–28. 34 indexed citations
20.
Savov, Alexey, Albena Jordanova, Dimitar Gavrilov, Dora Angelicheva, & Luba Kalaydjieva. (1994). G1244V: a novel missense mutation in exon 20 of the CFTR gene in a Bulgarian cystic fibrosis patient. Human Molecular Genetics. 3(3). 513–514. 2 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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