Morgan Parlier

1.5k total citations
16 papers, 1.1k citations indexed

About

Morgan Parlier is a scholar working on Cognitive Neuroscience, Genetics and Clinical Psychology. According to data from OpenAlex, Morgan Parlier has authored 16 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Cognitive Neuroscience, 9 papers in Genetics and 5 papers in Clinical Psychology. Recurrent topics in Morgan Parlier's work include Autism Spectrum Disorder Research (16 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Virology and Viral Diseases (5 papers). Morgan Parlier is often cited by papers focused on Autism Spectrum Disorder Research (16 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Virology and Viral Diseases (5 papers). Morgan Parlier collaborates with scholars based in United States, Canada and United Kingdom. Morgan Parlier's co-authors include Joseph Piven, Molly Losh, J. Steven Reznick, Robert S. Hurley, Julie L. Daniels, Noah J. Sasson, Kristen S. L. Lam, Ralph Adolphs, Michael Spezio and Sergio Starkstein and has published in prestigious journals such as Current Biology, Cerebral Cortex and Journal of Autism and Developmental Disorders.

In The Last Decade

Morgan Parlier

14 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Morgan Parlier United States 12 945 497 371 202 184 16 1.1k
Nicola Gillan United Kingdom 15 892 0.9× 408 0.8× 323 0.9× 317 1.6× 146 0.8× 17 1.0k
Rebecca Chilvers United Kingdom 7 798 0.8× 400 0.8× 217 0.6× 151 0.7× 260 1.4× 8 889
Marko Kielinen Finland 10 1.0k 1.1× 412 0.8× 331 0.9× 357 1.8× 274 1.5× 18 1.1k
William P. L. Mandy United Kingdom 10 667 0.7× 337 0.7× 232 0.6× 203 1.0× 233 1.3× 12 809
Lindsey Sterling United States 8 865 0.9× 385 0.8× 211 0.6× 213 1.1× 129 0.7× 10 938
Uttom Chowdhury United Kingdom 10 735 0.8× 558 1.1× 227 0.6× 256 1.3× 270 1.5× 32 1.0k
Patricia Rios Canada 6 1.1k 1.2× 455 0.9× 389 1.0× 269 1.3× 250 1.4× 8 1.2k
Cees Ketelaars Netherlands 12 727 0.8× 290 0.6× 273 0.7× 333 1.6× 176 1.0× 13 891
Leslie Speer United States 8 699 0.7× 285 0.6× 194 0.5× 151 0.7× 208 1.1× 9 760
Bernadette Rogé France 12 751 0.8× 298 0.6× 195 0.5× 150 0.7× 206 1.1× 32 917

Countries citing papers authored by Morgan Parlier

Since Specialization
Citations

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

Fields of papers citing papers by Morgan Parlier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Morgan Parlier

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

All Works

16 of 16 papers shown
1.
Daniels, Julie L., et al.. (2020). The Broad Autism Phenotype Questionnaire: Prevalence and Diagnostic Classification. UNC Libraries. 2 indexed citations
2.
Woodbury‐Smith, Marc, Mehdi Zarrei, John Wei, et al.. (2020). Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 183(5). 268–276. 8 indexed citations
3.
4.
Woodbury‐Smith, Marc, Andrew D. Paterson, Mehdi Zarrei, et al.. (2018). A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees. Journal of Neurodevelopmental Disorders. 10(1). 20–20. 15 indexed citations
5.
Girimaji, Satish Chandra, et al.. (2015). Translation of the Broad Autism Phenotype Questionnaire to an Indian language: A description of the process. Asian Journal of Psychiatry. 15. 62–67. 11 indexed citations
6.
Starkstein, Sergio, et al.. (2015). High rates of parkinsonism in adults with autism. Journal of Neurodevelopmental Disorders. 7(1). 29–29. 70 indexed citations
7.
Belger, Ayşenil, et al.. (2014). Abnormal Neural Activation to Faces in the Parents of Children with Autism. Cerebral Cortex. 25(12). 4653–4666. 39 indexed citations
8.
Sasson, Noah J., Daniel J. Faso, Morgan Parlier, Julie L. Daniels, & Joseph Piven. (2014). When Father Doesn't Know Best: Selective Disagreement Between Self‐Report and Informant Report of the Broad Autism Phenotype in Parents of a Child with Autism. Autism Research. 7(6). 731–739. 18 indexed citations
9.
Piven, Joseph, Veronica J. Vieland, Morgan Parlier, et al.. (2013). A molecular genetic study of autism and related phenotypes in extended pedigrees. Journal of Neurodevelopmental Disorders. 5(1). 30–30. 14 indexed citations
10.
Kats, Dmitry, et al.. (2013). Prevalence of selected clinical problems in older adults with autism and intellectual disability. Journal of Neurodevelopmental Disorders. 5(1). 27–27. 43 indexed citations
11.
Sasson, Noah J., Kristen S. L. Lam, Morgan Parlier, Julie L. Daniels, & Joseph Piven. (2013). Autism and the broad autism phenotype: familial patterns and intergenerational transmission. Journal of Neurodevelopmental Disorders. 5(1). 11–11. 82 indexed citations
12.
Sasson, Noah J., et al.. (2013). The Broad Autism Phenotype Questionnaire: Prevalence and Diagnostic Classification. Autism Research. 6(2). 134–143. 127 indexed citations
13.
Losh, Molly, Jessica Klusek, Gary E. Martin, et al.. (2012). Defining genetically meaningful language and personality traits in relatives of individuals with fragile X syndrome and relatives of individuals with autism. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 159B(6). 660–668. 61 indexed citations
14.
Adolphs, Ralph, Michael Spezio, Morgan Parlier, & Joseph Piven. (2008). Distinct Face-Processing Strategies in Parents of Autistic Children. Current Biology. 18(14). 1090–1093. 94 indexed citations
15.
Piven, Joseph, Robert S. Hurley, Molly Losh, Morgan Parlier, & J. Steven Reznick. (2008). Response to: Genichi Sugihara, Kenji J. Tsuchiya, Nori Takei, Letter to the Editor: Broad Autism Phenotype from Schizophrenia-Spectrum Disorders. Journal of Autism and Developmental Disorders. 38(10). 2000–2001.
16.
Hurley, Robert S., Molly Losh, Morgan Parlier, J. Steven Reznick, & Joseph Piven. (2006). The Broad Autism Phenotype Questionnaire. Journal of Autism and Developmental Disorders. 37(9). 1679–1690. 466 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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