Michele Ono

1.5k total citations
12 papers, 1.0k citations indexed

About

Michele Ono is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Michele Ono has authored 12 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 8 papers in Cognitive Neuroscience and 7 papers in Molecular Biology. Recurrent topics in Michele Ono's work include Genetics and Neurodevelopmental Disorders (10 papers), Autism Spectrum Disorder Research (8 papers) and Genomic variations and chromosomal abnormalities (3 papers). Michele Ono is often cited by papers focused on Genetics and Neurodevelopmental Disorders (10 papers), Autism Spectrum Disorder Research (8 papers) and Genomic variations and chromosomal abnormalities (3 papers). Michele Ono collaborates with scholars based in United States, Australia and Spain. Michele Ono's co-authors include Randi J. Hagerman, Beth L. Goodlin‐Jones, Marjorie Solomon, Susan G. Timmer, Nicole Tartaglia, David Hessl, Louise W. Gane, Flora Tassone, Jonathan Picker and Walter E. Kaufmann and has published in prestigious journals such as PEDIATRICS, Clinical Chemistry and Journal of Autism and Developmental Disorders.

In The Last Decade

Michele Ono

12 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Michele Ono United States	10	808	691	461	215	116	12	1.0k
Christopher J. Smith United States	11	682 0.8×	790 1.1×	317 0.7×	163 0.8×	114 1.0×	12	1.0k
Susan Harris United States	9	1.1k 1.4×	821 1.2×	595 1.3×	101 0.5×	50 0.4×	13	1.2k
Karin Ziliotto Dias Brazil	10	1.1k 1.4×	854 1.2×	649 1.4×	283 1.3×	92 0.8×	19	1.4k
Dejan B. Budimirovic United States	19	1.1k 1.4×	980 1.4×	553 1.2×	148 0.7×	100 0.9×	43	1.3k
Ave M. Lachiewicz United States	23	1.6k 1.9×	1.2k 1.7×	784 1.7×	242 1.1×	153 1.3×	38	1.9k
Sarah A. Ravan United States	9	834 1.0×	928 1.3×	329 0.7×	157 0.7×	147 1.3×	9	1.2k
Yujun Shao United States	9	736 0.9×	739 1.1×	313 0.7×	81 0.4×	92 0.8×	18	1.0k
Irena Bukelis United States	9	754 0.9×	726 1.1×	291 0.6×	148 0.7×	89 0.8×	12	975
Danielle Halpern United States	15	618 0.8×	617 0.9×	350 0.8×	173 0.8×	143 1.2×	30	1.2k
Jennifer Gerdts United States	15	424 0.5×	608 0.9×	260 0.6×	189 0.9×	136 1.2×	27	901

Countries citing papers authored by Michele Ono

Since Specialization

Citations

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

Fields of papers citing papers by Michele Ono

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michele Ono

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

All Works

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12 of 12 papers shown

Brick, David J., Hubert E. Nethercott, Maria G. Bañuelos, et al.. (2014). The Autism Spectrum Disorders Stem Cell Resource at Children's Hospital of Orange County: Implications for Disease Modeling and Drug Discovery. Stem Cells Translational Medicine. 3(11). 1275–1286. 25 indexed citations

Godler, David E., Howard R. Slater, Minh Bui, et al.. (2012). Fragile X Mental Retardation 1 (FMR1) Intron 1 Methylation in Blood Predicts Verbal Cognitive Impairment in Female Carriers of Expanded FMR1 Alleles: Evidence from a Pilot Study. Clinical Chemistry. 58(3). 590–598. 31 indexed citations

Godler, David E., Howard R. Slater, Minh Bui, et al.. (2011). FMR1 Intron 1 Methylation Predicts FMRP Expression in Blood of Female Carriers of Expanded FMR1 Alleles. Journal of Molecular Diagnostics. 13(5). 528–536. 37 indexed citations

Pessah, Isaac N., Louise W. Gane, Michele Ono, et al.. (2010). Early onset of neurological symptoms in fragile X premutation carriers exposed to neurotoxins. NeuroToxicology. 31(4). 399–402. 32 indexed citations

Harris, Susan, David Hessl, Michele Ono, et al.. (2008). Secondary medical diagnosis in fragile X syndrome with and without autism spectrum disorder. American Journal of Medical Genetics Part A. 146A(15). 1911–1916. 69 indexed citations

Solomon, Marjorie, Michele Ono, Susan G. Timmer, & Beth L. Goodlin‐Jones. (2008). The Effectiveness of Parent–Child Interaction Therapy for Families of Children on the Autism Spectrum. Journal of Autism and Developmental Disorders. 38(9). 1767–1776. 162 indexed citations

Hagerman, Randi J., Elizabeth Berry‐Kravis, Walter E. Kaufmann, et al.. (2008). Advances in the Treatment of Fragile X Syndrome. PEDIATRICS. 123(1). 378–390. 425 indexed citations

Tassone, Flora, et al.. (2007). The Prader-Willi Phenotype of Fragile X Syndrome. Journal of Developmental & Behavioral Pediatrics. 28(2). 133–138. 104 indexed citations

Bourgeois, James A., Jennifer B. Cogswell, David Hessl, et al.. (2007). Cognitive, anxiety and mood disorders in the fragile X-associated tremor/ataxia syndrome. General Hospital Psychiatry. 29(4). 349–356. 70 indexed citations

10.

Tartaglia, Nicole, Susan Bacalman, Robin Hansen, et al.. (2007). Autism Spectrum Disorders in XXY, XYY, and XXYY Syndromes. Journal of Developmental & Behavioral Pediatrics. 28(4). S8–S8. 2 indexed citations

11.

Tassone, Flora, et al.. (2006). 69 THE PRADER-WILLI CLINICAL SUBPHENOTYPE OF FRAGILE X SYNDROME.. Journal of Investigative Medicine. 54(1). S91.4–S91. 1 indexed citations

12.

Hagerman, Randi J., Michele Ono, & Paul J. Hagerman. (2005). Recent advances in fragile X: a model for autism and neurodegeneration. Current Opinion in Psychiatry. 18(5). 490–496. 87 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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