Fran Annese

1.7k total citations
22 papers, 1.2k citations indexed

About

Fran Annese is a scholar working on Genetics, Cognitive Neuroscience and Clinical Psychology. According to data from OpenAlex, Fran Annese has authored 22 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 12 papers in Cognitive Neuroscience and 9 papers in Clinical Psychology. Recurrent topics in Fran Annese's work include Genetics and Neurodevelopmental Disorders (19 papers), Autism Spectrum Disorder Research (12 papers) and Family and Disability Support Research (9 papers). Fran Annese is often cited by papers focused on Genetics and Neurodevelopmental Disorders (19 papers), Autism Spectrum Disorder Research (12 papers) and Family and Disability Support Research (9 papers). Fran Annese collaborates with scholars based in United States, Canada and France. Fran Annese's co-authors include Jane B. Lane, Alan K. Percy, Daniel G. Glaze, Judy O. Barrish, Steven A. Skinner, Jeffrey L. Neul, Kathleen J. Motil, Suzanne Geerts, Lauren McNair and Hye‐Seung Lee and has published in prestigious journals such as Nature Immunology, Neurology and Annals of Neurology.

In The Last Decade

Fran Annese

22 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fran Annese United States 17 1.1k 759 436 385 97 22 1.2k
Judy O. Barrish United States 16 1.1k 1.0× 780 1.0× 473 1.1× 313 0.8× 129 1.3× 20 1.2k
Walter E. Kaufmann United States 15 867 0.8× 661 0.9× 325 0.7× 313 0.8× 97 1.0× 24 1.0k
Suzanne Geerts United States 9 697 0.7× 508 0.7× 325 0.7× 189 0.5× 97 1.0× 10 744
S. Naidu United States 11 462 0.4× 385 0.5× 121 0.3× 374 1.0× 73 0.8× 15 734
Lauren McNair United States 8 639 0.6× 460 0.6× 286 0.7× 185 0.5× 79 0.8× 8 683
Christopher J. Smith United States 11 682 0.6× 790 1.0× 163 0.4× 317 0.8× 114 1.2× 12 1.0k
Barbara Manzi Italy 13 516 0.5× 633 0.8× 67 0.2× 284 0.7× 197 2.0× 17 979
Susan Harris United States 9 1.1k 1.1× 821 1.1× 101 0.2× 595 1.5× 50 0.5× 13 1.2k
Hayley Archer United Kingdom 14 1.0k 1.0× 407 0.5× 104 0.2× 558 1.4× 133 1.4× 17 1.1k
Linda S. Weaving Australia 9 619 0.6× 262 0.3× 65 0.1× 428 1.1× 78 0.8× 10 771

Countries citing papers authored by Fran Annese

Since Specialization
Citations

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

Fields of papers citing papers by Fran Annese

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fran Annese

This figure shows the co-authorship network connecting the top 25 collaborators of Fran Annese. A scholar is included among the top collaborators of Fran Annese 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 Fran Annese. Fran Annese 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.
Li, Joey H., Luke Riggan, Ajit S. Divakaruni, et al.. (2024). MEF2C regulates NK cell effector functions through control of lipid metabolism. Nature Immunology. 25(5). 778–789. 18 indexed citations
2.
Fu, Cary, Jeffrey L. Neul, Tim A. Benke, et al.. (2024). MECP2 Variants in Males: More Common than Previously Appreciated. Pediatric Neurology. 161. 263–267. 3 indexed citations
3.
Fang, Xiaolan, Alan K. Percy, Jeffrey L. Neul, et al.. (2023). Parental age effects and Rett syndrome. American Journal of Medical Genetics Part A. 194(2). 160–173. 2 indexed citations
4.
Motil, Kathleen J., Suzanne Geerts, Fran Annese, et al.. (2022). Anthropometric Measures Correspond with Functional Motor Outcomes in Females with Rett Syndrome. The Journal of Pediatrics. 244. 169–177.e3. 7 indexed citations
5.
Fee, Timothy, Renee Bend, Raymond J. Louie, et al.. (2022). Mosaicism of common pathogenic MECP2 variants identified in two males with a clinical diagnosis of Rett syndrome. American Journal of Medical Genetics Part A. 188(10). 2988–2998. 5 indexed citations
6.
Neul, Jeffrey L., Steven A. Skinner, Fran Annese, et al.. (2020). Metabolic Signatures Differentiate Rett Syndrome From Unaffected Siblings. Frontiers in Integrative Neuroscience. 14. 7–7. 27 indexed citations
7.
Yu, Seok‐Ho, et al.. (2020). Functional analysis of a novel mutation in the TIMM8A gene that causes deafness‐dystonia‐optic neuronopathy syndrome. Molecular Genetics & Genomic Medicine. 8(3). e1121–e1121. 18 indexed citations
8.
Motil, Kathleen J., Jane B. Lane, Judy O. Barrish, et al.. (2019). Biliary Tract Disease in Girls and Young Women With Rett Syndrome. Journal of Pediatric Gastroenterology and Nutrition. 68(6). 799–805. 14 indexed citations
9.
Percy, Alan K., et al.. (2018). When Rett syndrome is due to genes other than MECP2. PubMed. 3(1). 49–53. 22 indexed citations
10.
Sajan, Samin A., Shalini N. Jhangiani, Donna M. Muzny, et al.. (2016). Enrichment of mutations in chromatin regulators in people with Rett syndrome lacking mutations in MECP2. Genetics in Medicine. 19(1). 13–19. 53 indexed citations
11.
Knaus, Alexej, Tomonari Awaya, Ingo Helbig, et al.. (2016). Rare Noncoding Mutations Extend the Mutational Spectrum in the PGAP3 Subtype of Hyperphosphatasia with Mental Retardation Syndrome. Human Mutation. 37(8). 737–744. 35 indexed citations
12.
Tarquinio, Daniel, Wei Hou, Jeffrey L. Neul, et al.. (2015). Age of Diagnosis in Rett Syndrome: Patterns of Recognition Among Diagnosticians and Risk Factors for Late Diagnosis. Pediatric Neurology. 52(6). 585–591.e2. 49 indexed citations
13.
Neul, Jeffrey L., Jane B. Lane, Hye Seung Lee, et al.. (2014). Developmental delay in Rett syndrome: data from the natural history study. Journal of Neurodevelopmental Disorders. 6(1). 20–20. 120 indexed citations
14.
Motil, Kathleen J., Judy O. Barrish, Suzanne Geerts, et al.. (2012). Gastrointestinal and Nutritional Problems Occur Frequently Throughout Life in Girls and Women With Rett Syndrome. Journal of Pediatric Gastroenterology and Nutrition. 55(3). 292–298. 160 indexed citations
15.
Motil, Kathleen J., Judy O. Barrish, Jane B. Lane, et al.. (2011). Vitamin D Deficiency Is Prevalent in Girls and Women With Rett Syndrome. Journal of Pediatric Gastroenterology and Nutrition. 53(5). 569–574. 34 indexed citations
16.
Percy, Alan K., Hye‐Seung Lee, Jeffrey L. Neul, et al.. (2010). Profiling Scoliosis in Rett Syndrome. Pediatric Research. 67(4). 435–439. 52 indexed citations
17.
Percy, Alan K., Jeffrey L. Neul, Daniel G. Glaze, et al.. (2010). Rett syndrome diagnostic criteria: Lessons from the Natural History Study. Annals of Neurology. 68(6). 951–955. 99 indexed citations
18.
Glaze, Daniel G., Alan K. Percy, Steven A. Skinner, et al.. (2010). Epilepsy and the natural history of Rett syndrome. Neurology. 74(11). 909–912. 165 indexed citations
19.
Kirby, Russell S., Jane B. Lane, Steve A. Skinner, et al.. (2009). Longevity in Rett Syndrome: Analysis of the North American Database. The Journal of Pediatrics. 156(1). 135–138.e1. 73 indexed citations
20.
Percy, Alan K., Jane B. Lane, Steve A. Skinner, et al.. (2007). Rett Syndrome: North American Database. Journal of Child Neurology. 22(12). 1338–1341. 71 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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