Melissa Raspa

3.2k total citations
67 papers, 2.2k citations indexed

About

Melissa Raspa is a scholar working on Genetics, Cognitive Neuroscience and Clinical Psychology. According to data from OpenAlex, Melissa Raspa has authored 67 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Genetics, 39 papers in Cognitive Neuroscience and 27 papers in Clinical Psychology. Recurrent topics in Melissa Raspa's work include Genetics and Neurodevelopmental Disorders (39 papers), Autism Spectrum Disorder Research (38 papers) and Family and Disability Support Research (25 papers). Melissa Raspa is often cited by papers focused on Genetics and Neurodevelopmental Disorders (39 papers), Autism Spectrum Disorder Research (38 papers) and Family and Disability Support Research (25 papers). Melissa Raspa collaborates with scholars based in United States, Switzerland and Denmark. Melissa Raspa's co-authors include Donald B. Bailey, Ellen Bishop, David B. Holiday, Murrey Olmsted, Anne Wheeler, Elizabeth Berry‐Kravis, Catharine Riley, Rebecca Moultrie, Carla Bann and Amanda Wylie and has published in prestigious journals such as PLoS ONE, PEDIATRICS and Frontiers in Immunology.

In The Last Decade

Melissa Raspa

65 papers receiving 2.1k citations

Peers

Melissa Raspa
Anne Wheeler United States
Joanna Moss United Kingdom
Jeremy Turk United Kingdom
Marc Woodbury‐Smith United Kingdom
Sarah Spence United States
Marsha R. Mailick United States
Kate Lawrence United Kingdom
Caroline Richards United Kingdom
Emma van Daalen Netherlands
Anne Wheeler United States
Melissa Raspa
Citations per year, relative to Melissa Raspa Melissa Raspa (= 1×) peers Anne Wheeler

Countries citing papers authored by Melissa Raspa

Since Specialization
Citations

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

Fields of papers citing papers by Melissa Raspa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Melissa Raspa

This figure shows the co-authorship network connecting the top 25 collaborators of Melissa Raspa. A scholar is included among the top collaborators of Melissa Raspa 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 Melissa Raspa. Melissa Raspa 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
2.
Raspa, Melissa, et al.. (2023). Uncertainties experienced by parents of children diagnosed with severe combined immunodeficiency through newborn screening. European Journal of Human Genetics. 32(4). 392–398. 5 indexed citations
3.
Raspa, Melissa, et al.. (2022). Research Gaps in Fragile X Syndrome: An Updated Literature Review to Inform Clinical and Public Health Practice. Journal of Developmental & Behavioral Pediatrics. 44(1). e56–e65. 2 indexed citations
4.
Paquin, Ryan S., Megan A. Lewis, Rebecca Moultrie, et al.. (2020). Outreach to new mothers through direct mail and email: recruitment in the Early Check research study. Clinical and Translational Science. 14(3). 880–889. 8 indexed citations
5.
Wagner, Laura, Lauren Turner‐Brown, Anne Edwards, et al.. (2020). Preferences for the research use of electronic health records among young adults with fragile X syndrome or autism spectrum disorder. Disability and health journal. 13(4). 100927–100927. 3 indexed citations
6.
Raspa, Melissa, Molly Lynch, Linda Squiers, et al.. (2020). Information and Emotional Support Needs of Families Whose Infant Was Diagnosed With SCID Through Newborn Screening. Frontiers in Immunology. 11. 885–885. 15 indexed citations
7.
McCormack, Lauren, Amanda Wylie, Rebecca Moultrie, et al.. (2019). Supporting informed clinical trial decisions: Results from a randomized controlled trial evaluating a digital decision support tool for those with intellectual disability. PLoS ONE. 14(10). e0223801–e0223801. 9 indexed citations
8.
Wylie, Amanda, Melissa Raspa, Beth Vogel, et al.. (2019). Clinical models of telehealth in genetics: A regional telegenetics landscape. Journal of Genetic Counseling. 28(3). 673–691. 46 indexed citations
9.
Kołacz, Jacek, Melissa Raspa, Keri J. Heilman, & Stephen W. Porges. (2018). Evaluating Sensory Processing in Fragile X Syndrome: Psychometric Analysis of the Brain Body Center Sensory Scales (BBCSS). Journal of Autism and Developmental Disorders. 48(6). 2187–2202. 13 indexed citations
10.
Raspa, Melissa, et al.. (2018). A comparison of functional academic and daily living skills in males with fragile X syndrome with and without autism. Research in Developmental Disabilities. 78. 1–14. 12 indexed citations
11.
Wheeler, Anne, Melissa Raspa, Randi J. Hagerman, Marsha R. Mailick, & Catharine Riley. (2017). Implications of theFMR1Premutation for Children, Adolescents, Adults, and Their Families. PEDIATRICS. 139(Supplement_3). S172–S182. 34 indexed citations
12.
Raspa, Melissa, Anne Wheeler, & Catharine Riley. (2017). Public Health Literature Review of Fragile X Syndrome. PEDIATRICS. 139(Supplement_3). S153–S171. 45 indexed citations
13.
Raspa, Melissa, Denise M. Levis, Julia Kish‐Doto, et al.. (2015). Examining Parents' Experiences and Information Needs Regarding Early Identification of Developmental Delays. Journal of Developmental & Behavioral Pediatrics. 36(8). 575–585. 44 indexed citations
14.
Yang, Jui‐Chen, et al.. (2015). Caregiver Preferences for the Treatment of Males with Fragile X Syndrome. Journal of Developmental & Behavioral Pediatrics. 37(1). 71–79. 15 indexed citations
15.
Ouyang, Lijing, Scott D. Grosse, Catharine Riley, et al.. (2014). A comparison of family financial and employment impacts of fragile X syndrome, autism spectrum disorders, and intellectual disability. Research in Developmental Disabilities. 35(7). 1518–1527. 52 indexed citations
16.
Wheeler, Anne, Ellen Bishop, Melissa Raspa, et al.. (2014). DSM-5 Changes and the Prevalence of Parent-Reported Autism Spectrum Symptoms in Fragile X Syndrome. Journal of Autism and Developmental Disorders. 45(3). 816–829. 31 indexed citations
17.
Bailey, Donald B., Melissa Raspa, & Anne Wheeler. (2013). Parent Ratings of Ability to Consent for Clinical Trials in Fragile X Syndrome. Value in Health. 16(7). A603–A604. 2 indexed citations
18.
Bailey, Donald B., Ellen Bishop, Melissa Raspa, & Debra Skinner. (2012). Caregiver opinions about fragile X population screening. Genetics in Medicine. 14(1). 115–121. 23 indexed citations
19.
Bailey, Donald B., Melissa Raspa, Ellen Bishop, et al.. (2011). Medication Utilization for Targeted Symptoms in Children and Adults With Fragile X Syndrome. Journal of Developmental & Behavioral Pediatrics. 33(1). 62–69. 45 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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