Mari Mori

1.1k total citations
54 papers, 585 citations indexed

About

Mari Mori is a scholar working on Molecular Biology, Rheumatology and Physiology. According to data from OpenAlex, Mari Mori has authored 54 papers receiving a total of 585 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 9 papers in Rheumatology and 9 papers in Physiology. Recurrent topics in Mari Mori's work include Metabolism and Genetic Disorders (6 papers), Glycogen Storage Diseases and Myoclonus (4 papers) and Biochemical and Molecular Research (3 papers). Mari Mori is often cited by papers focused on Metabolism and Genetic Disorders (6 papers), Glycogen Storage Diseases and Myoclonus (4 papers) and Biochemical and Molecular Research (3 papers). Mari Mori collaborates with scholars based in United States, Japan and Poland. Mari Mori's co-authors include Priya S. Kishnani, Masashi Mori, Stephanie DeArmey, Thomas J. Weber, Hiroshi Hasegawa, Yukio Yamori, Toshinori Tanaka, M. Otani, Emily Qian and Rita L. McGill and has published in prestigious journals such as SHILAP Revista de lepidopterología, Kidney International and Journal of the American Society of Nephrology.

In The Last Decade

Mari Mori

50 papers receiving 570 citations

Peers

Mari Mori

PHYSI

RHEUM

GENET

Katarzyna Winsz‐Szczotka Poland

Georgios Loudianos Italy

M.J. Foglietti France

Rasha H. Mohamed Egypt

Fei Xiong China

R. Tenaglia Italy

Wenjun Lin China

Leonardo Gómez Rosso Argentina

Christian Freise Germany

Hassen Kamoun Tunisia

Katarzyna Winsz‐Szczotka Poland

Mari Mori

176 ×0.9

28 ×0.3

79 ×1.0

PHYSI

70 ×1.0

RHEUM

60 ×0.9

GENET

Citations per year, relative to Mari Mori Mari Mori (= 1×) peers Katarzyna Winsz‐Szczotka

Countries citing papers authored by Mari Mori

Since Specialization

Citations

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

Fields of papers citing papers by Mari Mori

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mari Mori

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Mori, Mari, Steven Estes, Swetha Ramadesikan, et al.. (2025). Novel Intragenic Duplication of GATAD2B in a Patient With GAND. American Journal of Medical Genetics Part A. 197(12). e64205–e64205.

Bajerska, Joanna, Mari Mori, Toshiya Toda, et al.. (2024). Equol-producing ability of Polish postmenopausal women and the dietary determinants of S-(-) equol formation [pdf]. Acta Scientiarum Polonorum Technologia Alimentaria. 77–86. 1 indexed citations

Mori, Mari, Jirair K. Bedoyan, Miriam Conces, et al.. (2023). ECHS1 DEFICIENCY PRESENTING AS LETHAL NEONATAL LACTIC ACIDOSIS COMPLICATED BY INTRAUTERINE GROWTH RESTRICTION AND HYPOXIC-ISCHEMIC ENCEPHALOPATHY. Molecular Genetics and Metabolism. 138(3). 107463–107463.

Madden, Jill A., Christy L. Cummings, Melissa J. Rose, et al.. (2023). Perinatal-lethal nonimmune fetal hydrops attributed toMECOM-associated bone marrow failure. Molecular Case Studies. 9(3). a006289–a006289. 1 indexed citations

Reddi, Honey V., Hannah Wand, Nancy C. Rose, et al.. (2023). The clinical application of polygenic risk scores: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 25(5). 100803–100803. 37 indexed citations

Taylor, Anne, et al.. (2022). eP035: Genotype-phenotype correlation of glycogen storage disease type IV. Genetics in Medicine. 24(3). S23–S23. 1 indexed citations

Bajerska, Joanna, Karolina Łagowska, Mari Mori, et al.. (2021). A Meta-Analysis of Randomized Controlled Trials of the Effects of Soy Intake on Inflammatory Markers in Postmenopausal Women. Journal of Nutrition. 152(1). 5–15. 14 indexed citations

Zhang, Yuzhou, C. John Sperati, Kammi Henriksen, et al.. (2020). A Mutation in Complement Factor B Causing Massive Fluid-Phase Dysregulation of the Alternative Complement Pathway Can Result in Atypical Hemolytic Uremic Syndrome. Journal of the American Society of Nephrology. 31(10S). 682–682.

Witters, Peter, Rita Barone, Katrin Õunap, et al.. (2020). Clinical and biochemical improvement with galactose supplementation in SLC35A2-CDG. Genetics in Medicine. 22(6). 1102–1107. 56 indexed citations

10.

Zhang, Yuzhou, C. John Sperati, Kammi Henriksen, et al.. (2020). Mutation of complement factor B causing massive fluid-phase dysregulation of the alternative complement pathway can result in atypical hemolytic uremic syndrome. Kidney International. 98(5). 1265–1274. 8 indexed citations

11.

Uzun, Alper, et al.. (2019). Effect of prematurity on genome wide methylation in the placenta. BMC Medical Genetics. 20(1). 116–116. 19 indexed citations

12.

Haskell, Gloria, Mari Mori, Cynthia M. Powell, et al.. (2018). Combination of exome sequencing and immune testing confirms Aicardi–Goutières syndrome type 5 in a challenging pediatric neurology case. Molecular Case Studies. 4(5). a002758–a002758. 4 indexed citations

13.

Mori, Mari, Gloria Haskell, Zoheb B. Kazi, et al.. (2017). Sensitivity of whole exome sequencing in detecting infantile- and late-onset Pompe disease. Molecular Genetics and Metabolism. 122(4). 189–197. 19 indexed citations

14.

Mori, Mari, Stephanie DeArmey, Thomas J. Weber, & Priya S. Kishnani. (2016). Case series: Odontohypophosphatasia or missed diagnosis of childhood/adult-onset hypophosphatasia? – Call for a long-term follow-up of premature loss of primary teeth. Bone Reports. 5. 228–232. 44 indexed citations

15.

Shoji, Hiromichi, Akira Watanabe, Mari Mori, et al.. (2016). Influence of gestational age on serum incretin levels in preterm infants. Journal of Developmental Origins of Health and Disease. 7(6). 685–688. 4 indexed citations

16.

Mori, Mari, John R. Mytinger, Lisa Martin, Dennis Bartholomew, & Scott E. Hickey. (2014). m.8993T>G-Associated Leigh Syndrome with Hypocitrullinemia on Newborn Screening. JIMD Reports. 17. 47–51. 13 indexed citations

17.

Muhihi, Alfa, Marina Njelekela, Rose Mpembeni, et al.. (2012). Physical activity and cardiovascular disease risk factors among young and middle-aged men in urban Mwanza, Tanzania. SHILAP Revista de lepidopterología. 8 indexed citations

18.

Tanaka, Eiji, et al.. (2011). Auxin Production by the Rice Blast Fungus and its Localization in Host Tissue. Journal of Phytopathology. 159(7-8). 522–530. 19 indexed citations

19.

Mori, Mari, et al.. (2007). Long serial analysis of gene expression for transcriptome profiling during the initiation of ligninolytic enzymes production in Phanerochaete chrysosporium. Applied Microbiology and Biotechnology. 75(3). 609–618. 13 indexed citations

20.

Minelli, Liliana, et al.. (1990). [Knowledge and attitudes regarding family clinics on the part of women who use or do not use them].. PubMed. 1(6). 1633–45. 1 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.

Explore authors with similar magnitude of impact