Marni J. Falk

10.6k total citations · 1 hit paper
135 papers, 4.6k citations indexed

About

Marni J. Falk is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Marni J. Falk has authored 135 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 103 papers in Molecular Biology, 53 papers in Clinical Biochemistry and 23 papers in Genetics. Recurrent topics in Marni J. Falk's work include Mitochondrial Function and Pathology (86 papers), Metabolism and Genetic Disorders (53 papers) and Genetics, Aging, and Longevity in Model Organisms (18 papers). Marni J. Falk is often cited by papers focused on Mitochondrial Function and Pathology (86 papers), Metabolism and Genetic Disorders (53 papers) and Genetics, Aging, and Longevity in Model Organisms (18 papers). Marni J. Falk collaborates with scholars based in United States, Sweden and United Kingdom. Marni J. Falk's co-authors include Richard Haas, Elizabeth M. McCormick, Bruce H. Cohen, Russell P. Saneto, Sumit Parikh, Zarazuela Zolkipli‐Cunningham, Erzsébet Polyák, Rebecca Ganetzky, Peter Ekblom and Nicole I. Wolf and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and SHILAP Revista de lepidopterología.

In The Last Decade

Marni J. Falk

131 papers receiving 4.5k 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
Marni J. Falk United States	41	3.3k	1.4k	728	411	353	135	4.6k
Jan Törnell Sweden	36	3.6k 1.1×	557 0.4×	964 1.3×	1.3k 3.1×	404 1.1×	81	6.9k
Ann Saada Israel	51	6.2k 1.9×	2.8k 2.0×	695 1.0×	796 1.9×	75 0.2×	170	8.3k
Rudolf J. Wiesner Germany	43	2.9k 0.9×	506 0.4×	312 0.4×	947 2.3×	117 0.3×	107	4.3k
William J. Craigen United States	41	5.1k 1.6×	1.3k 0.9×	851 1.2×	620 1.5×	33 0.1×	104	6.8k
Miguel A. Martı́n Spain	42	3.8k 1.2×	1.4k 1.0×	896 1.2×	985 2.4×	36 0.1×	238	6.4k
Rita Horváth United Kingdom	51	7.1k 2.2×	3.2k 2.2×	823 1.1×	884 2.2×	78 0.2×	280	9.4k
Richard I. Kelley United States	55	7.4k 2.3×	2.3k 1.6×	1.8k 2.5×	809 2.0×	40 0.1×	143	10.1k
Edward Byrne Australia	34	3.1k 1.0×	1.1k 0.7×	805 1.1×	900 2.2×	86 0.2×	130	5.6k
Eduardo Bonilla United States	49	6.9k 2.1×	3.5k 2.4×	486 0.7×	943 2.3×	56 0.2×	127	9.0k
Johannes Loffing Switzerland	57	7.2k 2.2×	339 0.2×	677 0.9×	616 1.5×	33 0.1×	154	9.9k

Countries citing papers authored by Marni J. Falk

Since Specialization

Citations

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

Fields of papers citing papers by Marni J. Falk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marni J. Falk. 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 Marni J. Falk. The network helps show where Marni J. Falk may publish in the future.

Co-authorship network of co-authors of Marni J. Falk

This figure shows the co-authorship network connecting the top 25 collaborators of Marni J. Falk. A scholar is included among the top collaborators of Marni J. Falk 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 Marni J. Falk. Marni J. Falk 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

Bedell, Victoria M., Han Lee, D. Bailey, et al.. (2025). Zebrafishology, study design guidelines for rigorous and reproducible data using zebrafish. Communications Biology. 8(1). 739–739. 4 indexed citations

Chandel, Navdeep S., Marni J. Falk, Janine H. Santos, et al.. (2025). Mitochondria transfer. Nature Metabolism. 7(9). 1716–1719. 1 indexed citations

Boris, Jeffrey R., et al.. (2025). The Long‐Term Postural Orthostatic Tachycardia Syndrome Outcomes Survey‐Gynecologic Findings: A Cross‐Sectional Survey in Young Women. Obstetrics and Gynecology International. 2025(1). 8872884–8872884.

Alves, Cesar, Maria Camilla Rossi‐Espagnet, Francisco A. Perez, et al.. (2025). Single Large-Scale Mitochondrial Deletion Syndromes: Neuroimaging Phenotypes and Longitudinal Progression in Pediatric Patients. American Journal of Neuroradiology. 46(6). 1272–1281. 1 indexed citations

Boris, Jeffrey R., et al.. (2025). Long‐Term Postural Orthostatic Tachycardia Syndrome Outcomes Survey: Educational, Economic, and Social Impact. Journal of the American Heart Association. 14(21). e042365–e042365.

Li, Dong, Armelle Magot, Yann Péréon, et al.. (2024). Expanding the Spectrum of Congenital Myopathy Linked to Variants in the MYBPC1 Gene. Neurology Clinical Practice. 14(3). e200228–e200228. 1 indexed citations

Sharma, Sonal, Sergey Magnitsky, Mitchell S. Schwartz, et al.. (2023). Novel Development of Magnetic Resonance Imaging to Quantify the Structural Anatomic Growth of Diverse Organs in Adult and Mutant Zebrafish. Zebrafish. 21(1). 28–38. 1 indexed citations

McCormick, Elizabeth M., Julie P. Taylor, Alison J. Coffey, et al.. (2023). Expert Panel Curation of 113 Primary Mitochondrial Disease Genes for the Leigh Syndrome Spectrum. Annals of Neurology. 94(4). 696–712. 23 indexed citations

Haroon, Suraiya, Heeyong Yoon, Christoph Seiler, et al.. (2023). N-acetylcysteine and cysteamine bitartrate prevent azide-induced neuromuscular decompensation by restoring glutathione balance in two novel surf1 −/− zebrafish deletion models of Leigh syndrome. Human Molecular Genetics. 32(12). 1988–2004. 8 indexed citations

10.

Alves, Cesar, Alireza Zandifar, Rebecca Ganetzky, et al.. (2023). MELAS: Phenotype Classification into Classic-versus-Atypical Presentations. American Journal of Neuroradiology. 44(5). 602–610. 17 indexed citations

11.

Cuddapah, Vishnu Anand, Holly Dubbs, Laura Adang, et al.. (2021). Understanding the phenotypic spectrum of ASXL‐related disease: Ten cases and a review of the literature. American Journal of Medical Genetics Part A. 185(6). 1700–1711. 18 indexed citations

12.

Wang, Jing, Jorune Balciuniene, Maria Alejandra Diaz‐Miranda, et al.. (2021). Advanced approach for comprehensive mtDNA genome testing in mitochondrial disease. Molecular Genetics and Metabolism. 135(1). 93–101. 9 indexed citations

13.

Alves, Cesar, Amy Goldstein, Sara Reis Teixeira, et al.. (2020). Involvement of the Spinal Cord in Primary Mitochondrial Disorders: A Neuroimaging Mimicker of Inflammation and Ischemia in Children. American Journal of Neuroradiology. 42(2). 389–396. 8 indexed citations

14.

Gonçalves, Fabrício Guimarães, Colleen Muraresku, Elizabeth M. McCormick, et al.. (2020). The Perirolandic Sign: A Unique Imaging Finding Observed in Association with Polymerase γ-Related Disorders. American Journal of Neuroradiology. 41(5). 917–922. 8 indexed citations

15.

Tříska, Petr, Kristiyana Kaneva, Daria Merkurjev, et al.. (2019). Landscape of Germline and Somatic Mitochondrial DNA Mutations in Pediatric Malignancies. Cancer Research. 79(7). 1318–1330. 29 indexed citations

16.

McCormick, Elizabeth M., L. Perera, Matthew J. Longley, et al.. (2019). Mitochondrial single-stranded DNA binding protein novel de novo SSBP1 mutation in a child with single large-scale mtDNA deletion (SLSMD) clinically manifesting as Pearson, Kearns-Sayre, and Leigh syndromes. PLoS ONE. 14(9). e0221829–e0221829. 31 indexed citations

17.

Byrnes, James R., Rebecca Ganetzky, Richard Lightfoot, et al.. (2017). Pharmacologic modeling of primary mitochondrial respiratory chain dysfunction in zebrafish. Neurochemistry International. 117. 23–34. 45 indexed citations

18.

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 →

19.

Rea, Shane L., Brett H. Graham, Eiko Nakamaru‐Ogiso, Adwitiya Kar, & Marni J. Falk. (2010). Bacteria, yeast, worms, and flies: Exploiting simple model organisms to investigate human mitochondrial diseases. PubMed. 16(2). 200–218. 47 indexed citations

20.

Haas, Richard, Sumit Parikh, & Marni J. Falk. (2007). Enfermedad mitocondrial: abordaje práctico para los médicos de atención primaria. PEDIATRICS. 64(6). 321–328.

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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