Beth Rosner

680 citations
9 papers · 507 · h-index 8

Impact in

    • Williams Syndrome Research
  • Genetics top 10%
    • Genetics and Neurodevelopmental Disorders
    • Genetic Syndromes and Imprinting
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Papers in

    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
    • Genetics and Neurodevelopmental Disorders 2
    • Genetic Syndromes and Imprinting 2
    • Autism Spectrum Disorder Research 1

Beth Rosner

9 papers receiving 474 citations

Peers

Beth Rosner
Comparison fields: 5 of 65
  • Developmental Neuroscience 165
  • Genetics 189
  • Cognitive Neuroscience 119
  • Developmental and Educational Psychology 42
  • Genetics 26
Replace Klaus Sarimski with:
Klaus Sarimski Germany
Montse Fernández‐Prieto Spain
J Turk United Kingdom
Kiyotaka Tomiwa Japan
L.M.G. Curfs Netherlands
Elizabeth Dykens United States
Marilee A. Martens United States
Elena Garayzábal Spain
Natalia Freitas Rossi Brazil
Katy Berg United Kingdom
Beth Rosner relative to Klaus Sarimski Germany Klaus Sarimski's profile →
Citations per field
00.5×1.5×2.4×
Klaus Sarimski · 1×
Citations per year

Countries citing papers authored by Beth Rosner

Since Specialization
Citations

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

Fields of papers citing papers by Beth Rosner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 13 scholars most cited alongside Beth Rosner, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Beth Rosner Line = papers co-authored together Beth Rosner links everyone, so they are left out of the graph.

All Works

9 of 9 papers shown
#Work
1 1999114
2 200491
3 199962
4 200759
5 199857
6 200549
7 200547
8 200423
9 20065

About Beth Rosner

Beth Rosner is a scholar working on Genetics, Cognitive Neuroscience, Developmental Neuroscience, Surgery and Molecular Biology, having authored 9 papers that have together received 507 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Genetic Syndromes and Imprinting (2 papers), Williams Syndrome Research (2 papers), Autism Spectrum Disorder Research (1 paper), Diverse Music Education Insights (1 paper), Family and Disability Support Research (1 paper) and Inclusion and Disability in Education and Sport (1 paper). The work is most often cited by research in Developmental Neuroscience (165 citations), Genetics (189 citations), Cognitive Neuroscience (119 citations), Developmental and Educational Psychology (42 citations) and Genetics (26 citations). Beth Rosner has collaborated with scholars based in United States and Denmark. Frequent co-authors include Elisabeth M. Dykens, Jeannie Visootsak, John M. Graham, Robert M. Hodapp, Deborah J. Fidler, Nicole Tartaglia, Matthew W. State, Tran M. Ly, Andrés Martin and Bryan H. King. Their work appears in journals such as Journal of Applied Research in Intellectual Disabilities, The Journal of Pediatrics, Journal of Investigative Medicine, Journal of the American Academy of Child & Adolescent Psychiatry and Child and Adolescent Psychiatric Clinics of North America.

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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