Molly Losh

5.7k total citations
75 papers, 3.9k citations indexed

About

Molly Losh is a scholar working on Cognitive Neuroscience, Genetics and Developmental and Educational Psychology. According to data from OpenAlex, Molly Losh has authored 75 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 71 papers in Cognitive Neuroscience, 48 papers in Genetics and 32 papers in Developmental and Educational Psychology. Recurrent topics in Molly Losh's work include Autism Spectrum Disorder Research (69 papers), Genetics and Neurodevelopmental Disorders (46 papers) and Language Development and Disorders (28 papers). Molly Losh is often cited by papers focused on Autism Spectrum Disorder Research (69 papers), Genetics and Neurodevelopmental Disorders (46 papers) and Language Development and Disorders (28 papers). Molly Losh collaborates with scholars based in United States, Hong Kong and Sweden. Molly Losh's co-authors include Joseph Piven, Lisa Capps, Gary E. Martin, Robert S. Hurley, Jessica Klusek, Morgan Parlier, J. Steven Reznick, Christopher A. Thurber, Ralph Adolphs and Shannon M. Couture and has published in prestigious journals such as Psychological Bulletin, PLoS ONE and PEDIATRICS.

In The Last Decade

Molly Losh

69 papers receiving 3.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Molly Losh United States 31 3.2k 1.5k 1.4k 1.2k 643 75 3.9k
Cory Shulman Israel 28 3.2k 1.0× 1.2k 0.8× 1.8k 1.3× 915 0.8× 846 1.3× 51 4.4k
Michelle Dawson Canada 22 2.9k 0.9× 682 0.4× 790 0.6× 1.1k 0.9× 514 0.8× 36 3.4k
Leslie J. Carver United States 33 3.9k 1.2× 885 0.6× 1.5k 1.1× 1.4k 1.1× 951 1.5× 59 4.9k
Isabelle Soulières Canada 24 3.3k 1.0× 820 0.5× 702 0.5× 1.2k 1.0× 549 0.9× 61 3.6k
Jeff Munson United States 19 2.4k 0.8× 957 0.6× 821 0.6× 575 0.5× 436 0.7× 31 2.8k
Stelios Georgiades Canada 38 3.7k 1.2× 1.0k 0.7× 2.5k 1.8× 722 0.6× 936 1.5× 149 4.6k
Emily J. H. Jones United Kingdom 35 4.3k 1.4× 1.0k 0.7× 1.9k 1.3× 929 0.8× 1.2k 1.9× 158 5.6k
Rosa A. Hoekstra United Kingdom 33 3.5k 1.1× 1.0k 0.7× 2.2k 1.6× 564 0.5× 967 1.5× 86 4.6k
Benjamin E. Yerys United States 32 3.4k 1.1× 702 0.5× 1.0k 0.7× 1.0k 0.8× 537 0.8× 84 4.3k
John Sideris United States 34 2.5k 0.8× 1.4k 0.9× 1.2k 0.9× 934 0.8× 749 1.2× 91 3.6k

Countries citing papers authored by Molly Losh

Since Specialization
Citations

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

Fields of papers citing papers by Molly Losh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Molly Losh

This figure shows the co-authorship network connecting the top 25 collaborators of Molly Losh. A scholar is included among the top collaborators of Molly Losh 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 Molly Losh. Molly Losh 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.
Nayar, Kritika, et al.. (2024). Narrative Ability in Autism and First-Degree Relatives. Journal of Autism and Developmental Disorders. 55(11). 3822–3837. 2 indexed citations
2.
3.
Martin, Gary E., et al.. (2023). A longitudinal investigation of pragmatic language across contexts in autism and related neurodevelopmental conditions. Frontiers in Neurology. 14. 1155691–1155691. 2 indexed citations
4.
Martin, Gary E., et al.. (2023). A profile of prosodic speech differences in individuals with autism spectrum disorder and first-degree relatives. Journal of Communication Disorders. 102. 106313–106313. 4 indexed citations
5.
Hogan, Abigail L., et al.. (2022). Slower Peak Pupillary Response to Emotional Faces in Parents of Autistic Individuals. Frontiers in Psychology. 13. 836719–836719.
6.
Nayar, Kritika, et al.. (2021). A cross-cultural study showing deficits in gaze-language coordination during rapid automatized naming among individuals with ASD. Scientific Reports. 11(1). 13401–13401. 6 indexed citations
7.
Nayar, Kritika, Abigail L. Hogan, Gary E. Martin, et al.. (2019). Language processing skills linked to FMR1 variation: A study of gaze-language coordination during rapid automatized naming among women with the FMR1 premutation. PLoS ONE. 14(7). e0219924–e0219924. 9 indexed citations
8.
Nayar, Kritika, et al.. (2019). Understanding Social Communication Differences in Autism Spectrum Disorder and First-Degree Relatives: A Study of Looking and Speaking. Journal of Autism and Developmental Disorders. 50(6). 2128–2141. 20 indexed citations
9.
Crowley, James J., Jin Szatkiewicz, Anna K. Kähler, et al.. (2018). Common-variant associations with fragile X syndrome. Molecular Psychiatry. 24(3). 338–344. 6 indexed citations
10.
Martin, Gary E., et al.. (2017). Signaling of noncomprehension in communication breakdowns in fragile X syndrome, Down syndrome, and autism spectrum disorder. Journal of Communication Disorders. 65. 22–34. 27 indexed citations
11.
Lee, Michelle, Gary E. Martin, Elizabeth Berry‐Kravis, & Molly Losh. (2016). A developmental, longitudinal investigation of autism phenotypic profiles in fragile X syndrome. Journal of Neurodevelopmental Disorders. 8(1). 47–47. 44 indexed citations
12.
Smith, Matthew J., Michael F. Fleming, Michael Wright, et al.. (2015). Brief Report: Vocational Outcomes for Young Adults with Autism Spectrum Disorders at Six Months After Virtual Reality Job Interview Training. Journal of Autism and Developmental Disorders. 45(10). 3364–3369. 103 indexed citations
13.
Hogan, Abigail L., et al.. (2014). Eye-voice span during rapid automatized naming: evidence of reduced automaticity in individuals with autism spectrum disorder and their siblings. Journal of Neurodevelopmental Disorders. 6(1). 33–33. 21 indexed citations
14.
Klusek, Jessica, Jane E. Roberts, & Molly Losh. (2014). Cardiac autonomic regulation in autism and Fragile X syndrome: A review.. Psychological Bulletin. 141(1). 141–175. 78 indexed citations
15.
Losh, Molly, et al.. (2011). Lower birth weight indicates higher risk of autistic traits in discordant twin pairs. Psychological Medicine. 42(5). 1091–1102. 50 indexed citations
16.
Konneker, Thomas, et al.. (2008). A searchable database of genetic evidence for psychiatric disorders. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(6). 671–675. 25 indexed citations
17.
Losh, Molly, et al.. (2007). Defining key features of the broad autism phenotype: A comparison across parents of multiple‐ and single‐incidence autism families. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(4). 424–433. 228 indexed citations
18.
Wassink, Thomas H., Molly Losh, Joseph Piven, et al.. (2006). Systematic Screening for Subtelomeric Anomalies in a Clinical Sample of Autism. Journal of Autism and Developmental Disorders. 37(4). 703–708. 4 indexed citations
19.
Losh, Molly & Joseph Piven. (2006). Social‐cognition and the broad autism phenotype: identifying genetically meaningful phenotypes. Journal of Child Psychology and Psychiatry. 48(1). 105–112. 157 indexed citations
20.
Wassink, Thomas H., Molly Losh, Veronica J. Vieland, et al.. (2005). A case of autism and uniparental disomy of chromosome 1. Human Genetics. 117(2-3). 200–206. 12 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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