Miho Ishida

1.7k total citations
28 papers, 703 citations indexed

About

Miho Ishida is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Miho Ishida has authored 28 papers receiving a total of 703 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 19 papers in Genetics and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Miho Ishida's work include Genetic Syndromes and Imprinting (13 papers), Epigenetics and DNA Methylation (10 papers) and Prenatal Screening and Diagnostics (10 papers). Miho Ishida is often cited by papers focused on Genetic Syndromes and Imprinting (13 papers), Epigenetics and DNA Methylation (10 papers) and Prenatal Screening and Diagnostics (10 papers). Miho Ishida collaborates with scholars based in United Kingdom, Japan and India. Miho Ishida's co-authors include Gudrun E. Moore, Hiroshi Kitagawa, Philip Stanier, Satomi Nadanaka, Sayeda Abu‐Amero, Anna Thomas, Veronica A. Kinsler, Sam Loughlin, Jane Chalker and Rodger Palmer and has published in prestigious journals such as The Lancet, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Miho Ishida

27 papers receiving 698 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Miho Ishida United Kingdom 11 415 315 183 167 127 28 703
Neil McCarthy United States 12 378 0.9× 235 0.7× 102 0.6× 125 0.7× 243 1.9× 14 703
Clare V. Logan United Kingdom 17 690 1.7× 446 1.4× 163 0.9× 191 1.1× 43 0.3× 21 1.0k
Saghira Malik Sharif United Kingdom 10 343 0.8× 339 1.1× 96 0.5× 79 0.5× 38 0.3× 12 672
Jiang Fu United States 14 622 1.5× 203 0.6× 124 0.7× 30 0.2× 81 0.6× 21 824
Seido Takae Japan 13 522 1.3× 113 0.4× 136 0.7× 121 0.7× 45 0.4× 46 1.5k
Isabelle De Bie Canada 9 628 1.5× 70 0.2× 115 0.6× 144 0.9× 37 0.3× 27 918
Mark A. Edson United States 12 474 1.1× 203 0.6× 53 0.3× 60 0.4× 81 0.6× 17 1.1k
Nicole L. Hoppman United States 14 279 0.7× 279 0.9× 32 0.2× 115 0.7× 55 0.4× 62 704
Silvana Guerneri Italy 17 357 0.9× 406 1.3× 36 0.2× 344 2.1× 71 0.6× 50 902
Alexander N. Yatsenko United States 18 787 1.9× 527 1.7× 76 0.4× 126 0.8× 35 0.3× 35 1.4k

Countries citing papers authored by Miho Ishida

Since Specialization
Citations

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

Fields of papers citing papers by Miho Ishida

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Miho Ishida

This figure shows the co-authorship network connecting the top 25 collaborators of Miho Ishida. A scholar is included among the top collaborators of Miho Ishida 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 Miho Ishida. Miho Ishida 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.
McGlacken‐Byrne, Sinead, Jenifer P. Suntharalingham, Miho Ishida, et al.. (2025). A Tiered Approach to Exome Sequencing Analysis in Early-Onset Primary Ovarian Insufficiency. The Journal of Clinical Endocrinology & Metabolism. 110(11). 3142–3154.
2.
Suntharalingham, Jenifer P., Ignacio del Valle, Federica Buonocore, et al.. (2025). The transcriptomic landscape of monosomy X (45,X) during early human fetal and placental development. Communications Biology. 8(1). 249–249. 1 indexed citations
3.
Maharaj, Avinaash, Miho Ishida, Anna Rybak, et al.. (2024). QSOX2 Deficiency-induced short stature, gastrointestinal dysmotility and immune dysfunction. Nature Communications. 15(1). 8420–8420. 2 indexed citations
4.
Suntharalingham, Jenifer P., Miho Ishida, Sinead McGlacken‐Byrne, et al.. (2023). Analysis of genetic variability in Turner syndrome linked to long-term clinical features. Frontiers in Endocrinology. 14. 1227164–1227164. 4 indexed citations
5.
Kessler, Noah J., Miho Ishida, Charalambos Demetriou, et al.. (2022). Tissue- and ethnicity-independent hypervariable DNA methylation states show evidence of establishment in the early human embryo. Nucleic Acids Research. 50(12). 6735–6752. 7 indexed citations
6.
Suntharalingham, Jenifer P., Miho Ishida, Ignacio del Valle, et al.. (2022). Emerging phenotypes linked to variants in SAMD9 and MIRAGE syndrome. Frontiers in Endocrinology. 13. 953707–953707. 7 indexed citations
7.
Monteagudo, Ana, Marta Sánchez-Delgado, José V. Medrano, et al.. (2018). Epigenetic Symmetry of DLGAP2: Pre-Implantation Maternal Methylation Switches to a Random Monoallelic Profile in Somatic Tissues. 2(3). 1–27. 6 indexed citations
8.
Ishida, Miho, Thomas Cullup, C. R. Boustred, et al.. (2017). A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly. Clinical Genetics. 93(4). 870–879. 22 indexed citations
9.
Ishida, Miho, Stefanie Böhm, Jennifer M. Frost, et al.. (2015). Genome-wide methylation analysis in Silver–Russell syndrome patients. Human Genetics. 134(3). 317–332. 17 indexed citations
10.
Demetriou, Charalambos, Sayeda Abu‐Amero, Anna Thomas, et al.. (2014). Paternally Expressed, Imprinted Insulin-Like Growth Factor-2 in Chorionic Villi Correlates Significantly with Birth Weight. PLoS ONE. 9(1). e85454–e85454. 40 indexed citations
11.
Kinsler, Veronica A., Anna Thomas, Miho Ishida, et al.. (2013). Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS. Journal of Investigative Dermatology. 133(9). 2229–2236. 196 indexed citations
12.
Ishida, Miho, David Monk, Andrew Duncan, et al.. (2012). Maternal Inheritance of a Promoter Variant in the Imprinted PHLDA2 Gene Significantly Increases Birth Weight. The American Journal of Human Genetics. 90(4). 715–719. 35 indexed citations
13.
Ishida, Miho & Gudrun E. Moore. (2012). The role of imprinted genes in humans. Molecular Aspects of Medicine. 34(4). 826–840. 121 indexed citations
14.
Thomas, Anna, Jennifer M. Frost, Miho Ishida, et al.. (2012). The speech gene FOXP2 is not imprinted. Journal of Medical Genetics. 49(11). 669–670. 6 indexed citations
15.
Ishida, Miho, David Monk, Sayeda Abu‐Amero, et al.. (2011). Inheritance of a copy number variant in the imprinted PHLDA2 gene promoter significantly increases fetal birth weight. UCL Discovery (University College London). 1 indexed citations
16.
Nadanaka, Satomi, et al.. (2008). Chondroitin 4-O-Sulfotransferase-1 Modulates Wnt-3a Signaling through Control of E Disaccharide Expression of Chondroitin Sulfate. Journal of Biological Chemistry. 283(40). 27333–27343. 80 indexed citations
17.
Uyama, Toru, Miho Ishida, Tomomi Izumikawa, et al.. (2006). Chondroitin 4-O-Sulfotransferase-1 Regulates E Disaccharide Expression of Chondroitin Sulfate Required for Herpes Simplex Virus Infectivity. Journal of Biological Chemistry. 281(50). 38668–38674. 82 indexed citations
18.
Sunada, Satoshi, et al.. (2006). Electrochemical Characteristics of Fe-Cu-C Sintered Steels. Journal of the Japan Society of Powder and Powder Metallurgy. 53(8). 661–666. 5 indexed citations
19.
Ishida, Miho, et al.. (1997). Effect of Hypotaurine in Fertilization Medium on Fertilization of In Vitro Matured Bovine Oocytes and Their Subsequent Development. Journal of Reproduction and Development. 43(6). j33–j40. 1 indexed citations
20.
GOTO, Kazufumi, et al.. (1994). Activation of unaged bovine oocytes by various parthenogenetic stimuli. Theriogenology. 41(1). 207–207. 3 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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