Jenny Thies

971 total citations
14 papers, 171 citations indexed

About

Jenny Thies is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Jenny Thies has authored 14 papers receiving a total of 171 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 5 papers in Clinical Biochemistry and 5 papers in Genetics. Recurrent topics in Jenny Thies's work include Metabolism and Genetic Disorders (5 papers), Genomics and Rare Diseases (4 papers) and Amino Acid Enzymes and Metabolism (2 papers). Jenny Thies is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Genomics and Rare Diseases (4 papers) and Amino Acid Enzymes and Metabolism (2 papers). Jenny Thies collaborates with scholars based in United States, Netherlands and Canada. Jenny Thies's co-authors include James T. Bennett, Christina Lam, Amanda S. Freed, Heather C. Mefford, J. Lawrence Merritt, Jennifer N. Dines, Angela Sun, Irene J. Chang, Ghayda Mirzaa and Kimberly Foss and has published in prestigious journals such as Clinical Chemistry, The Journal of Pediatrics and Journal of Parenteral and Enteral Nutrition.

In The Last Decade

Jenny Thies

14 papers receiving 171 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jenny Thies United States	9	78	69	29	22	18	14	171
Sandra Yang United States	8	91 1.2×	85 1.2×	37 1.3×	39 1.8×	11 0.6×	13	245
Jennifer Arroyo United States	6	59 0.8×	75 1.1×	10 0.3×	14 0.6×	26 1.4×	9	129
Mauricio De Castro United States	9	78 1.0×	51 0.7×	16 0.6×	32 1.5×	6 0.3×	20	230
Nasim Monfared Canada	9	178 2.3×	63 0.9×	14 0.5×	61 2.8×	21 1.2×	9	265
Fatma Tuba Eminoğlu Türkiye	8	28 0.4×	85 1.2×	58 2.0×	40 1.8×	26 1.4×	58	244
Marian Girgis Egypt	10	50 0.6×	95 1.4×	84 2.9×	45 2.0×	16 0.9×	27	246
Graciela Moya Argentina	9	85 1.1×	82 1.2×	7 0.2×	55 2.5×	23 1.3×	18	276
Germaine Pierre United Kingdom	8	37 0.5×	108 1.6×	52 1.8×	10 0.5×	5 0.3×	16	187
M. V. Kranthi Kumar India	6	131 1.7×	119 1.7×	11 0.4×	6 0.3×	7 0.4×	9	257
Chaya N. Murali United States	8	47 0.6×	114 1.7×	11 0.4×	9 0.4×	6 0.3×	31	222

Countries citing papers authored by Jenny Thies

Since Specialization

Citations

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

Fields of papers citing papers by Jenny Thies

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jenny Thies

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

All Works

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14 of 14 papers shown

Marquez, Jonathan, et al.. (2025). Polyamine metabolism is dysregulated in COXFA4-related mitochondrial disease. Human Genetics and Genomics Advances. 6(2). 100418–100418. 1 indexed citations

Zhang, Tong, Christopher J. Collins, Jenny Thies, et al.. (2022). A rapid and non-invasive proteomic analysis using DBS and buccal swab for multiplexed second-tier screening of Pompe disease and Mucopolysaccharidosis type I. Molecular Genetics and Metabolism. 136(4). 296–305. 8 indexed citations

Guenzel, Adam J., Patricia Hall, Anna I. Scott, et al.. (2021). The low excretor phenotype of glutaric acidemia type I is a source of false negative newborn screening results and challenging diagnoses. JIMD Reports. 60(1). 67–74. 5 indexed citations

Scott, Anna I., S.M. Sullivan, Irene J. Chang, et al.. (2020). Tutorial: Triheptanoin and Nutrition Management for Treatment of Long‐Chain Fatty Acid Oxidation Disorders. Journal of Parenteral and Enteral Nutrition. 45(2). 230–238. 14 indexed citations

Yi, Fan, Candace T. Myers, Jenny Thies, et al.. (2020). p.P1379S, a benign variant with reduced ATP7B protein level in Wilson Disease. JIMD Reports. 54(1). 32–36. 2 indexed citations

Freed, Amanda S., Jenny Thies, Heather M. Byers, et al.. (2020). The Impact of Rapid Exome Sequencing on Medical Management of Critically Ill Children. The Journal of Pediatrics. 226. 202–212.e1. 38 indexed citations

Schultz, Matthew, Coleman Turgeon, Devin Oglesbee, et al.. (2020). Immune dysfunction in MGAT2‐CDG: A clinical report and review of the literature. American Journal of Medical Genetics Part A. 185(1). 213–218. 9 indexed citations

Thies, Jenny, Christopher J. Collins, Candace T. Myers, et al.. (2020). The co‐occurrence of Wilson disease and X‐linked agammaglobulinemia in one family highlights the promising diagnostic potential of proteolytic analysis. Molecular Genetics & Genomic Medicine. 8(4). e1172–e1172. 4 indexed citations

Freed, Amanda S., Jenny Thies, Jean K. Mah, et al.. (2020). CHRNB1‐associated congenital myasthenia syndrome: Expanding the clinical spectrum. American Journal of Medical Genetics Part A. 185(3). 827–835. 8 indexed citations

10.

Gotway, Garrett, Julia Kozlitina, Chao Xing, et al.. (2019). Clinical Exome Studies Have Inconsistent Coverage. Clinical Chemistry. 66(1). 199–206. 8 indexed citations

11.

Thies, Jenny, et al.. (2019). Expansion of the Primrose syndrome phenotype through the comparative analysis of two new case reports with ZBTB20 variants. American Journal of Medical Genetics Part A. 179(11). 2228–2232. 2 indexed citations

12.

Thies, Jenny, et al.. (2019). Rapid clinical exome sequencing in a pediatric ICU: Genetic counselor impacts and challenges. Journal of Genetic Counseling. 28(2). 283–291. 16 indexed citations

13.

Starr, Michelle C., Irene J. Chang, Laura S. Finn, et al.. (2018). COQ2 nephropathy: a treatable cause of nephrotic syndrome in children. Pediatric Nephrology. 33(7). 1257–1261. 26 indexed citations

14.

Dines, Jennifer N., Qian Cong, Ghayda Mirzaa, et al.. (2018). Expanding clinical phenotype in CACNA1C related disorders: From neonatal onset severe epileptic encephalopathy to late‐onset epilepsy. American Journal of Medical Genetics Part A. 176(12). 2733–2739. 30 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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