Bronwyn Glaser

3.8k total citations
56 papers, 2.8k citations indexed

About

Bronwyn Glaser is a scholar working on Molecular Biology, Cognitive Neuroscience and Genetics. According to data from OpenAlex, Bronwyn Glaser has authored 56 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 32 papers in Cognitive Neuroscience and 21 papers in Genetics. Recurrent topics in Bronwyn Glaser's work include Congenital heart defects research (37 papers), Autism Spectrum Disorder Research (31 papers) and Genetics and Neurodevelopmental Disorders (20 papers). Bronwyn Glaser is often cited by papers focused on Congenital heart defects research (37 papers), Autism Spectrum Disorder Research (31 papers) and Genetics and Neurodevelopmental Disorders (20 papers). Bronwyn Glaser collaborates with scholars based in Switzerland, United States and Belgium. Bronwyn Glaser's co-authors include Stéphan Eliez, Martin Debbané, Allan L. Reiss, Marie Schaer, David Hessl, Stéphan Eliez, Jennifer Dyer-Friedman, Christine Blasey, Annette K. Taylor and Martina Franchini and has published in prestigious journals such as PLoS ONE, American Journal of Psychiatry and PEDIATRICS.

In The Last Decade

Bronwyn Glaser

56 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bronwyn Glaser Switzerland 31 1.5k 1.4k 1.2k 543 502 56 2.8k
Stéphan Eliez Switzerland 26 1.4k 0.9× 1.4k 1.0× 983 0.9× 518 1.0× 540 1.1× 78 3.5k
Wendy R. Kates United States 40 2.0k 1.3× 2.1k 1.5× 1.4k 1.2× 925 1.7× 380 0.8× 105 4.3k
Hower Kwon United States 14 1.6k 1.0× 666 0.5× 978 0.8× 180 0.3× 253 0.5× 15 2.4k
Martin Debbané Switzerland 38 1.7k 1.1× 1.3k 1.0× 542 0.5× 601 1.1× 1.3k 2.5× 152 4.3k
Michael T. Abrams United States 24 1.9k 1.3× 869 0.6× 1.5k 1.3× 108 0.2× 368 0.7× 39 3.2k
Maude Schneider Switzerland 26 1.1k 0.7× 961 0.7× 410 0.4× 377 0.7× 348 0.7× 115 2.2k
Christine Wu Nordahl United States 34 3.2k 2.1× 625 0.5× 1.6k 1.4× 80 0.1× 494 1.0× 70 4.2k
Courtney Burnette United States 19 1.1k 0.7× 331 0.2× 300 0.3× 148 0.3× 335 0.7× 24 1.8k
Peder Rasmussen Sweden 20 835 0.6× 397 0.3× 400 0.3× 154 0.3× 551 1.1× 37 2.3k
Jamie O. Edgin United States 25 884 0.6× 148 0.1× 436 0.4× 268 0.5× 301 0.6× 63 2.6k

Countries citing papers authored by Bronwyn Glaser

Since Specialization
Citations

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

Fields of papers citing papers by Bronwyn Glaser

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bronwyn Glaser

This figure shows the co-authorship network connecting the top 25 collaborators of Bronwyn Glaser. A scholar is included among the top collaborators of Bronwyn Glaser 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 Bronwyn Glaser. Bronwyn Glaser 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.
Kojovic, Nada, et al.. (2021). The impact of social complexity on the visual exploration of others' actions in preschoolers with autism spectrum disorder. BMC Psychology. 9(1). 50–50. 8 indexed citations
2.
Franchini, Martina, et al.. (2021). Emotional vs. Neutral Face Exploration and Habituation: An Eye-Tracking Study of Preschoolers With Autism Spectrum Disorders. Frontiers in Psychiatry. 11. 568997–568997. 7 indexed citations
3.
Badoud, Déborah, et al.. (2017). Understanding others: a pilot investigation of cognitive and affective facets of social cognition in patients with 22q11.2 deletion syndrome (22q11DS). Journal of Neurodevelopmental Disorders. 9(1). 35–35. 13 indexed citations
4.
Franchini, Martina, et al.. (2017). Social orienting and joint attention in preschoolers with autism spectrum disorders. PLoS ONE. 12(6). e0178859–e0178859. 45 indexed citations
5.
6.
Schneider, Maude, Marie Schaer, Ayhan Mutlu, et al.. (2013). Clinical and cognitive risk factors for psychotic symptoms in 22q11.2 deletion syndrome: a transversal and longitudinal approach. European Child & Adolescent Psychiatry. 23(6). 425–436. 53 indexed citations
7.
Schneider, Maude, Martial Van der Linden, Bronwyn Glaser, et al.. (2012). Preliminary structure and predictive value of attenuated negative symptoms in 22q11.2 deletion syndrome. Psychiatry Research. 196(2-3). 277–284. 55 indexed citations
8.
Peelen, Marius V., Bronwyn Glaser, Patrik Vuilleumier, & Stéphan Eliez. (2009). Differential development of selectivity for faces and bodies in the fusiform gyrus. Developmental Science. 12(6). F16–25. 112 indexed citations
9.
Green, Tamar, Doron Gothelf, Bronwyn Glaser, et al.. (2009). Psychiatric Disorders and Intellectual Functioning Throughout Development in Velocardiofacial (22q11.2 Deletion) Syndrome. Journal of the American Academy of Child & Adolescent Psychiatry. 48(11). 1060–1068. 222 indexed citations
10.
Debbané, Martin, et al.. (2006). Hippocampal volume reduction in 22q11.2 deletion syndrome. Neuropsychologia. 44(12). 2360–2365. 57 indexed citations
11.
Debbané, Martin, et al.. (2006). Psychotic symptoms in children and adolescents with 22q11.2 deletion syndrome: Neuropsychological and behavioral implications. Schizophrenia Research. 84(2-3). 187–193. 108 indexed citations
12.
Glaser, Bronwyn, Martin Debbané, Christine Hinard, et al.. (2006). No Evidence for an Effect of COMT Val158Met Genotype on Executive Function in Patients With 22q11 Deletion Syndrome. American Journal of Psychiatry. 163(3). 537–539. 37 indexed citations
13.
Schaer, Marie, J. Eric Schmitt, Bronwyn Glaser, et al.. (2006). Abnormal patterns of cortical gyrification in velo-cardio-facial syndrome (deletion 22q11.2): An MRI study. Psychiatry Research Neuroimaging. 146(1). 1–11. 61 indexed citations
14.
Hessl, David, et al.. (2005). Social behavior and cortisol reactivity in children with fragile X syndrome. Journal of Child Psychology and Psychiatry. 47(6). 602–610. 103 indexed citations
15.
Johnston, Cindy, David Hessl, Christine Blasey, et al.. (2003). Factors Associated with Parenting Stress in Mothers of Children with Fragile X Syndrome. Journal of Developmental & Behavioral Pediatrics. 24(4). 267–275. 123 indexed citations
16.
Hessl, David, Bronwyn Glaser, Jennifer Dyer-Friedman, et al.. (2002). Cortisol and behavior in fragile X syndrome. Psychoneuroendocrinology. 27(7). 855–872. 99 indexed citations
17.
Rivera, Susan M., Vinod Menon, Christopher D. White, Bronwyn Glaser, & Allan L. Reiss. (2002). Functional brain activation during arithmetic processing in females with fragile X syndrome is related to FMR1 protein expression. Human Brain Mapping. 16(4). 206–218. 100 indexed citations
18.
Dyer-Friedman, Jennifer, Bronwyn Glaser, David Hessl, et al.. (2002). Genetic and Environmental Influences on the Cognitive Outcomes of Children With Fragile X Syndrome. Journal of the American Academy of Child & Adolescent Psychiatry. 41(3). 237–244. 68 indexed citations
19.
Glaser, Bronwyn, David Hessl, Cindy Johnston, et al.. (2002). Biological and environmental contributions to adaptive behavior in fragile X syndrome. American Journal of Medical Genetics Part A. 117A(1). 21–29. 48 indexed citations
20.
Johnston, Cindy, Stéphan Eliez, Jennifer Dyer-Friedman, et al.. (2001). Neurobehavioral phenotype in carriers of the fragile X premutation. American Journal of Medical Genetics. 103(4). 314–319. 96 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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