Amy Goldstein

2.6k total citations · 1 hit paper
29 papers, 1.1k citations indexed

About

Amy Goldstein is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Amy Goldstein has authored 29 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 18 papers in Clinical Biochemistry and 5 papers in Genetics. Recurrent topics in Amy Goldstein's work include Mitochondrial Function and Pathology (19 papers), Metabolism and Genetic Disorders (18 papers) and Genomics and Rare Diseases (5 papers). Amy Goldstein is often cited by papers focused on Mitochondrial Function and Pathology (19 papers), Metabolism and Genetic Disorders (18 papers) and Genomics and Rare Diseases (5 papers). Amy Goldstein collaborates with scholars based in United States, Canada and Belgium. Amy Goldstein's co-authors include Amel Karaa, Richard Haas, Bruce H. Cohen, Jerry Vockley, Mary Kay Koenig, Sumit Parikh, Fernando Scaglia, Lynne A. Wolfe, Mark A. Tarnopolsky and Russell P. Saneto and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Human Molecular Genetics.

In The Last Decade

Amy Goldstein

26 papers receiving 1.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society

2014 372 citations Sumit Parikh, Amy Goldstein et al. Genetics in Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Amy Goldstein United States	15	779	532	144	144	89	29	1.1k
Concetta Meli Italy	15	460 0.6×	573 1.1×	181 1.3×	140 1.0×	106 1.2×	45	874
François Feillet France	15	248 0.3×	251 0.5×	212 1.5×	152 1.1×	98 1.1×	45	685
Ann Bowron United Kingdom	13	424 0.5×	303 0.6×	100 0.7×	79 0.5×	107 1.2×	29	997
Cheryl Garganta United States	15	249 0.3×	212 0.4×	158 1.1×	90 0.6×	62 0.7×	28	745
Lance H. Rodan United States	17	285 0.4×	144 0.3×	64 0.4×	118 0.8×	79 0.9×	48	763
Yoshinobu Ohtani Japan	12	339 0.4×	275 0.5×	94 0.7×	111 0.8×	291 3.3×	25	726
Juan Darío Ortigoza‐Escobar Spain	14	243 0.3×	199 0.4×	63 0.4×	60 0.4×	109 1.2×	49	712
Areeg El‐Gharbawy United States	17	299 0.4×	248 0.5×	341 2.4×	249 1.7×	43 0.5×	31	1.1k
Claire Douillard France	18	412 0.5×	140 0.3×	212 1.5×	202 1.4×	74 0.8×	59	968
Parvaneh Karimzadeh Iran	14	141 0.2×	141 0.3×	230 1.6×	48 0.3×	122 1.4×	95	579

Countries citing papers authored by Amy Goldstein

Since Specialization

Citations

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

Fields of papers citing papers by Amy Goldstein

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amy Goldstein

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

All Works

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20 of 20 papers shown

Ganetzky, Rebecca, et al.. (2025). Improving acute care for Primary Mitochondrial Disease: Development of a publicly available clinical care pathway. Molecular Genetics and Metabolism. 144(4). 109058–109058.

Finn, Laury, Amy Goldstein, & Holly L. Hedrick. (2025). Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE) Phenotype Associated With Unique Compound Heterozygous POLG Variants: Case Presentation and Review of the Literature. Pediatric and Developmental Pathology. 28(4). 288–299.

Kandemirli, Sedat Giray, et al.. (2025). Overview of neuroimaging in primary mitochondrial disorders. Pediatric Radiology. 55(4). 765–791.

Karaa, Amel, Michelangelo Mancuso, Bruce M. Cohen, et al.. (2022). Genetic subgroup learnings from MMPOWER-3 trial: Elamipretide improved six-minute walk test in individuals with mtDNA replisome disorders. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1863. 148868–148868. 1 indexed citations

Toro, Camilo, Roderick Hori, May Christine V. Malicdan, et al.. (2017). A recurrent de novo missense mutation in UBTF causes developmental neuroregression. Human Molecular Genetics. 27(4). 691–705. 29 indexed citations

Obeid, Rawad, et al.. (2017). A Newborn With Hyperlactatemia and Epileptic Encephalopathy. Seminars in Pediatric Neurology. 26. 104–107. 2 indexed citations

Parikh, Sumit, Amel Karaa, Amy Goldstein, et al.. (2016). Solid organ transplantation in primary mitochondrial disease: Proceed with caution. Molecular Genetics and Metabolism. 118(3). 178–184. 46 indexed citations

Ghaloul‐Gonzalez, Lina, Amy Goldstein, Catherine Walsh Vockley, et al.. (2016). Mitochondrial respiratory chain disorders in the Old Order Amish population. Molecular Genetics and Metabolism. 118(4). 296–303. 3 indexed citations

Koenig, Mary Kay, Lisa Emrick, Amel Karaa, et al.. (2016). Recommendations for the Management of Strokelike Episodes in Patients With Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes. JAMA Neurology. 73(5). 591–591. 72 indexed citations

10.

Zuccoli, Giulio, et al.. (2015). Bilateral symmetrical basal ganglia and thalamic lesions in children: an update (2015). Neuroradiology. 57(10). 973–989. 20 indexed citations

11.

Goldstein, Amy, Riyad El‐Khoury, Malgorzata Rak, et al.. (2015). ANT2-defective fibroblasts exhibit normal mitochondrial bioenergetics. SHILAP Revista de lepidopterología. 3. 43–46. 4 indexed citations

12.

Hu, Jie, Malini Sathanoori, Meron Azage, et al.. (2015). A novel maternally inherited 8q24.3 and a rare paternally inherited 14q23.3 CNVs in a family with neurodevelopmental disorders. American Journal of Medical Genetics Part A. 167(8). 1921–1926. 16 indexed citations

13.

El‐Gharbawy, Areeg, Jessica Sebastian, Lina Ghaloul‐Gonzalez, et al.. (2015). LARS mutations in non-Irish travelers: An under-recognized multi-system disorder characterized by infantile hepatopathy during physiological stress. Mitochondrion. 24. S40–S41. 3 indexed citations

14.

Parikh, Sumit, Amy Goldstein, Mary Kay Koenig, et al.. (2014). Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society. Genetics in Medicine. 17(9). 689–701. 372 indexed citations breakdown →

15.

Kazmerski, Traci M., Ingrid Libman, Amy Goldstein, et al.. (2013). Infantile Hypophosphatasia Secondary to a Novel Compound Heterozygous Mutation Presenting with Pyridoxine-Responsive Seizures. JIMD Reports. 11. 17–24. 29 indexed citations

16.

Goldstein, Amy & Lynne A. Wolfe. (2013). The Elusive Magic Pill: Finding Effective Therapies for Mitochondrial Disorders. Neurotherapeutics. 10(2). 320–328. 11 indexed citations

17.

Goldstein, Amy, et al.. (2013). Mitochondrial Disease in Childhood: Nuclear Encoded. Neurotherapeutics. 10(2). 212–226. 28 indexed citations

18.

Vandewalle, Joke, Marijke Bauters, Hilde Van Esch, et al.. (2013). The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability. Human Genetics. 132(10). 1177–1185. 22 indexed citations

19.

Goldstein, Amy, et al.. (2012). Update on Nuclear Mitochondrial Genes and Neurologic Disorders. Seminars in Pediatric Neurology. 19(4). 181–193. 4 indexed citations

20.

Abuelo, Dianne, et al.. (1991). Anxiety in women with low maternal serum alpha‐fetoprotein screening results. Prenatal Diagnosis. 11(6). 381–385. 53 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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