Sandra Bedrosian‐Sermone

506 total citations
5 papers, 151 citations indexed

About

Sandra Bedrosian‐Sermone is a scholar working on Molecular Biology, Cognitive Neuroscience and Genetics. According to data from OpenAlex, Sandra Bedrosian‐Sermone has authored 5 papers receiving a total of 151 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Cognitive Neuroscience and 3 papers in Genetics. Recurrent topics in Sandra Bedrosian‐Sermone's work include Genetics and Neurodevelopmental Disorders (3 papers), Autism Spectrum Disorder Research (3 papers) and Congenital heart defects research (2 papers). Sandra Bedrosian‐Sermone is often cited by papers focused on Genetics and Neurodevelopmental Disorders (3 papers), Autism Spectrum Disorder Research (3 papers) and Congenital heart defects research (2 papers). Sandra Bedrosian‐Sermone collaborates with scholars based in United States, Israel and Belgium. Sandra Bedrosian‐Sermone's co-authors include R. Frank Kooy, Illana Gozes, Anke Van Dijck, Orly Elpeleg, Elisa Cappuyns, Anne B. Arnett, E. Giladi, Jennifer Gerdts, Evan E. Eichler and Raphael Bernier and has published in prestigious journals such as Frontiers in Endocrinology, Translational Psychiatry and Autism Research.

In The Last Decade

Sandra Bedrosian‐Sermone

5 papers receiving 148 citations

Peers

Sandra Bedrosian‐Sermone
Emily Hansen‐Kiss United States
Simona Carone Italy
Marisela Dy-Hollins United States
Alberto Parras Switzerland
M-R Rautiainen Finland
Sonia Amabile Italy
Crina M. Floruta United States
Ahm M. Huq United States
Ryan A. Szeto United States
Rosa Pasquariello Italy
Emily Hansen‐Kiss United States
Sandra Bedrosian‐Sermone
Citations per year, relative to Sandra Bedrosian‐Sermone Sandra Bedrosian‐Sermone (= 1×) peers Emily Hansen‐Kiss

Countries citing papers authored by Sandra Bedrosian‐Sermone

Since Specialization
Citations

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

Fields of papers citing papers by Sandra Bedrosian‐Sermone

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sandra Bedrosian‐Sermone. 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 Sandra Bedrosian‐Sermone. The network helps show where Sandra Bedrosian‐Sermone may publish in the future.

Co-authorship network of co-authors of Sandra Bedrosian‐Sermone

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

All Works

5 of 5 papers shown
1.
Frazier, Thomas, Robyn M. Busch, Patricia Klaas, et al.. (2023). Development of informant‐report neurobehavioral survey scales for PTEN hamartoma tumor syndrome and related neurodevelopmental genetic syndromes. American Journal of Medical Genetics Part A. 191(7). 1741–1757. 7 indexed citations
2.
Kolevzon, A lexander, Tess Levy, Sandra Bedrosian‐Sermone, et al.. (2022). An open-label study evaluating the safety, behavioral, and electrophysiological outcomes of low-dose ketamine in children with ADNP syndrome. Human Genetics and Genomics Advances. 3(4). 100138–100138. 11 indexed citations
3.
Arnett, Anne B., Kendra Hoekzema, Tychele N. Turner, et al.. (2018). The autism spectrum phenotype in ADNP syndrome. Autism Research. 11(9). 1300–1310. 43 indexed citations
4.
Gozes, Illana, Anke Van Dijck, Gal Hacohen-Kleiman, et al.. (2017). Premature primary tooth eruption in cognitive/motor-delayed ADNP-mutated children. Translational Psychiatry. 7(2). e1043–e1043. 59 indexed citations
5.
Gozes, Illana, Marc C. Patterson, Anke Van Dijck, et al.. (2017). The Eight and a Half Year Journey of Undiagnosed AD: Gene Sequencing and Funding of Advanced Genetic Testing Has Led to Hope and New Beginnings. Frontiers in Endocrinology. 8. 107–107. 31 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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2026