Arthur S. Aylsworth

9.4k total citations
93 papers, 3.8k citations indexed

About

Arthur S. Aylsworth is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Arthur S. Aylsworth has authored 93 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Genetics, 34 papers in Molecular Biology and 18 papers in Surgery. Recurrent topics in Arthur S. Aylsworth's work include Genomic variations and chromosomal abnormalities (18 papers), Cleft Lip and Palate Research (15 papers) and Craniofacial Disorders and Treatments (15 papers). Arthur S. Aylsworth is often cited by papers focused on Genomic variations and chromosomal abnormalities (18 papers), Cleft Lip and Palate Research (15 papers) and Craniofacial Disorders and Treatments (15 papers). Arthur S. Aylsworth collaborates with scholars based in United States, Canada and Germany. Arthur S. Aylsworth's co-authors include Robert E. Meyer, Cynthia M. Powell, Stephanie Watkins, Ronald P. Strauss, Kathleen W. Rao, Iain McIntosh, Gary A. Bellus, Clair A. Francomano, Ilkka Kaitila and Lisa G. Shaffer and has published in prestigious journals such as Nature Genetics, PLoS ONE and Brain.

In The Last Decade

Arthur S. Aylsworth

91 papers receiving 3.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Arthur S. Aylsworth United States 32 1.9k 1.8k 596 575 369 93 3.8k
Joël Zlotogora Israel 35 2.0k 1.1× 1.9k 1.1× 690 1.2× 381 0.7× 443 1.2× 170 5.0k
Yukihiro Hasegawa Japan 31 1.5k 0.8× 2.1k 1.2× 396 0.7× 608 1.1× 229 0.6× 258 5.0k
Michael A. Morris Switzerland 37 1.7k 0.9× 2.1k 1.2× 427 0.7× 306 0.5× 352 1.0× 118 4.8k
Frits A. Beemer Netherlands 31 1.7k 0.9× 2.0k 1.2× 280 0.5× 392 0.7× 511 1.4× 71 3.6k
Hope Northrup United States 38 1.5k 0.8× 2.0k 1.1× 875 1.5× 628 1.1× 206 0.6× 156 6.1k
Howard M. Saal United States 33 2.4k 1.3× 1.3k 0.7× 765 1.3× 470 0.8× 425 1.2× 114 4.2k
Kenjiro Kosaki Japan 35 1.8k 1.0× 2.7k 1.5× 591 1.0× 623 1.1× 317 0.9× 363 5.2k
Patrick MacLeod Canada 29 910 0.5× 1.3k 0.8× 403 0.7× 469 0.8× 147 0.4× 74 3.1k
John Dean United Kingdom 30 1.4k 0.7× 1.3k 0.7× 575 1.0× 246 0.4× 146 0.4× 103 3.5k
Carlos A. Bacino United States 38 3.1k 1.7× 2.4k 1.4× 934 1.6× 405 0.7× 230 0.6× 134 5.0k

Countries citing papers authored by Arthur S. Aylsworth

Since Specialization
Citations

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

Fields of papers citing papers by Arthur S. Aylsworth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Arthur S. Aylsworth. 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 Arthur S. Aylsworth. The network helps show where Arthur S. Aylsworth may publish in the future.

Co-authorship network of co-authors of Arthur S. Aylsworth

This figure shows the co-authorship network connecting the top 25 collaborators of Arthur S. Aylsworth. A scholar is included among the top collaborators of Arthur S. Aylsworth 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 Arthur S. Aylsworth. Arthur S. Aylsworth 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.
Chong, Jessica X., Matthew C. Childers, Colby T. Marvin, et al.. (2023). Variants in ACTC1 underlie distal arthrogryposis accompanied by congenital heart defects. Human Genetics and Genomics Advances. 4(3). 100213–100213. 9 indexed citations
2.
Aylsworth, Arthur S., Lisa Croen, Julie L. Daniels, et al.. (2023). Prenatal Alcohol Exposure in Relation to Autism Spectrum Disorder: Findings from the Study to Explore Early Development (SEED). UNC Libraries.
3.
Shapira, Stuart K., Lin H. Tian, Arthur S. Aylsworth, et al.. (2019). A Novel Approach to Dysmorphology to Enhance the Phenotypic Classification of Autism Spectrum Disorder in the Study to Explore Early Development. Journal of Autism and Developmental Disorders. 49(5). 2184–2202. 7 indexed citations
4.
Reis, Linda M., Елена А. Сорокина, Sanaa Muheisen, et al.. (2019). De Novo Missense Variants in WDR37 Cause a Severe Multisystemic Syndrome. The American Journal of Human Genetics. 105(2). 425–433. 25 indexed citations
5.
Singer, Alison B., Arthur S. Aylsworth, Lisa Croen, et al.. (2017). Prenatal Alcohol Exposure in Relation to Autism Spectrum Disorder: Findings from the Study to Explore Early Development (SEED). Paediatric and Perinatal Epidemiology. 31(6). 573–582. 14 indexed citations
6.
Allori, Alexander C., Anna R. Carlson, Stephanie Watkins, et al.. (2016). Nasal Airway Dysfunction in Children with Cleft Lip and Cleft Palate: Results of a Cross-Sectional Population-Based Study, with Anatomical and Surgical Considerations. Plastic & Reconstructive Surgery. 138(6). 1275–1285. 24 indexed citations
7.
James, Jeanne, Paula Goldenberg, Robert B. Hinton, et al.. (2014). Aortopathy in the 7q11.23 microduplication syndrome. American Journal of Medical Genetics Part A. 167(2). 363–370. 25 indexed citations
8.
Vatta, Matteo, et al.. (2012). A Novel STXBP1 Mutation Causes Focal Seizures With Neonatal Onset. Journal of Child Neurology. 27(6). 811–814. 33 indexed citations
9.
Stamm, Demetra S., Cynthia M. Powell, Jeffrey M. Stajich, et al.. (2008). Novel congenital myopathy locus identified in Native American Indians at 12q13.13-14.1. Neurology. 71(22). 1764–1769. 23 indexed citations
10.
Stamm, Demetra S., Arthur S. Aylsworth, Jeffrey M. Stajich, et al.. (2008). Native American myopathy: Congenital myopathy with cleft palate, skeletal anomalies, and susceptibility to malignant hyperthermia. American Journal of Medical Genetics Part A. 146A(14). 1832–1841. 50 indexed citations
11.
Quigley, Denise I., Kathleen Kaiser‐Rogers, Arthur S. Aylsworth, & Kathleen W. Rao. (2003). Submicroscopic deletion 9(q34.4) and duplication 19(p13.3): Identified by subtelomere specific FISH probes. American Journal of Medical Genetics Part A. 125A(1). 67–72. 8 indexed citations
12.
Elder, Deborah A., Kathleen Kaiser‐Rogers, Arthur S. Aylsworth, & Ali S. Çalıkoğlu. (2001). Type I diabetes mellitus in a patient with chromosome 22q11.2 deletion syndrome. American Journal of Medical Genetics. 101(1). 17–19. 18 indexed citations
13.
Aylsworth, Arthur S., et al.. (1997). The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2. American Journal of Ophthalmology. 124(5). 718–719. 49 indexed citations
14.
Hansen, Wendy, L.E. Bernard, Sylvie Langlois, et al.. (1997). MATERNAL UNIPARENTAL DISOMY OF CHROMOSOME 2 AND CONFINED PLACENTAL MOSAICISM FOR TRISOMY 2 IN A FETUS WITH INTRAUTERINE GROWTH RESTRICTION, HYPOSPADIAS, AND OLIGOHYDRAMNIOS. Prenatal Diagnosis. 17(5). 443–450. 50 indexed citations
15.
Reitnauer, Pamela J., Nancy P. Callanan, Rosann A. Farber, & Arthur S. Aylsworth. (1997). Prenatal exposure to disulfiram implicated in the cause of malformations in discordant monozygotic twins. Teratology. 56(6). 358–362. 14 indexed citations
16.
Bellus, Gary A., et al.. (1996). Hypochondroplasia: Molecular Analysis of the Fibroblast Growth Factor Receptor 3 Gene. Annals of the New York Academy of Sciences. 785(1). 182–187. 20 indexed citations
17.
Estabrooks, Laurel L., Kathleen W. Rao, Deborah A. Driscoll, et al.. (1995). Preliminary phenotypic map of chromosome 4p16 based on 4p deletions. American Journal of Medical Genetics. 57(4). 581–586. 158 indexed citations
18.
Greenwood, Robert, et al.. (1991). Neurological aspects of del(1q) syndrome. American Journal of Medical Genetics. 40(4). 488–492. 23 indexed citations
19.
Vance, Jeffery M., Larry H. Yamaoka, Jeffery M. Vance, et al.. (1987). Linkage studies in peripheral neurofibromatosis.. Journal of Medical Genetics. 24(9). 530–532. 3 indexed citations
20.
Aylsworth, Arthur S., et al.. (1976). Mannosidosis: Phenotype of a severely affected child and characterization of α-mannosidase activity in cultured fibroblasts from the patient and his parents. The Journal of Pediatrics. 88(5). 814–818. 20 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Joël Zlotogora Breakdown of academic impact, for papers by Yukihiro Hasegawa Breakdown of academic impact, for papers by Michael A. Morris Breakdown of academic impact, for papers by Frits A. Beemer Breakdown of academic impact, for papers by Hope Northrup Breakdown of academic impact, for papers by Howard M. Saal Breakdown of academic impact, for papers by Kenjiro Kosaki Breakdown of academic impact, for papers by Patrick MacLeod Breakdown of academic impact, for papers by John Dean Breakdown of academic impact, for papers by Carlos A. Bacino
Rankless by CCL
2026