Arthur S. Aylsworth

9.4k citations

93 papers · 3.8k indexed · h-index 32

Genetics top 0.5%
Molecular Biology top 5%
Pediatrics, Perinatology and Child Health top 2%
Surgery top 5%
Epidemiology top 10%

Co-authors: Robert E. Meyer Cynthia M. Powell Ronald P. Strauss Stephanie Watkins Kathleen W. Rao Clair A. Francomano Iain McIntosh Ilkka Kaitila
Topics: Genomic variations and chromosomal abnormalities (18 papers)Cleft Lip and Palate Research (15 papers)Craniofacial Disorders and Treatments (15 papers)
Cited by: Genetics Pediatrics, Perinatology and Child Health Molecular Biology
Journals: Nature Genetics PLoS ONE Brain
Partner nations: United States Canada Germany

In The Last Decade

Arthur S. Aylsworth

91 papers receiving 3.6k citations

Peers

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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Variants in ACTC1 underlie distal arthrogryposis accompanied by congenital heart defects 2023 ·Human Genetics and Genomics Advances ·Jessica X. Chong,Matthew C. Childers,Colby T. Marvin,(unknown),Hernán Gonorazky,Lili‐Naz Hazrati,James J. Dowling,(unknown),Yasemin Alanay,Yolanda Ber,Miguel Ángel Marín Gabriel,Arthur S. Aylsworth,Kati J. Buckingham,Kathryn M. Shively,(unknown),(unknown),Michael Regnier,Michael J. Bamshad	9
2	De Novo Missense Variants in WDR37 Cause a Severe Multisystemic Syndrome 2019 ·The American Journal of Human Genetics ·Linda M. Reis,Елена А. Сорокина,(unknown),Sanaa Muheisen,Milen Velinov,Carlos Zamora,Arthur S. Aylsworth,Elena V. Semina	25
3	An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening 2019 ·The Journal of Pediatrics ·Laura V. Milko,Julianne O’Daniel,(unknown),Stephanie B. Crowley,Ann Katherine M. Foreman,Kathleen Wallace,(unknown),Natasha T. Strande,(unknown),(unknown),Arthur S. Aylsworth,Müge Güçsavaş‐Çalıkoğlu,Dianne M. Frazier,Neeta L. Vora,Myra I. Roche,Bradford C. Powell,Cynthia M. Powell,Jonathan S. Berg	44
4	Prenatal Alcohol Exposure in Relation to Autism Spectrum Disorder: Findings from the Study to Explore Early Development (SEED) 2017 ·Paediatric and Perinatal Epidemiology ·Alison B. Singer,Arthur S. Aylsworth,(unknown),Lisa Croen,Carolyn DiGuiseppi,M. Daniele Fallin,Amy H. Herring,Stephen R. Hooper,(unknown),Laura A. Schieve,Gayle C. Windham,Julie L. Daniels	14
5	Aortopathy in the 7q11.23 microduplication syndrome 2014 ·American Journal of Medical Genetics Part A ·(unknown),Jeanne James,Paula Goldenberg,Robert B. Hinton,Erin Miller,Amy Shikany,Arthur S. Aylsworth,Kathleen Kaiser‐Rogers,(unknown),Seema R. Lalani,Stephanie M. Ware	25
6	Classification, Epidemiology, and Genetics of Orofacial Clefts 2014 ·Clinics in Plastic Surgery ·Stephanie Watkins,Robert E. Meyer,Ronald P. Strauss,Arthur S. Aylsworth	169
7	Maternal Exposure to Criteria Air Pollutants and Congenital Heart Defects in Offspring: Results from the National Birth Defects Prevention Study 2014 ·Environmental Health Perspectives ·Jeanette A. Stingone,Thomas J. Luben,Julie L. Daniels,Montserrat Fuentes,David B. Richardson,Arthur S. Aylsworth,Amy H. Herring,Marlene Anderka,Lorenzo D. Botto,Adolfo Correa,Suzanne M. Gilboa,Peter H. Langlois,Bridget Mosley,Gary M. Shaw,Csaba Siffel,Andrew F. Olshan,(unknown)	82
8	Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes 2012 ·European Journal of Human Genetics ·(unknown),Jill A. Rosenfeld,Ryan N. Traylor,G. Bradley Schaefer,Elizabeth McPherson,Blake C. Ballif,Eva Klopocki,Stefan Mundlos,Lisa G. Shaffer,Arthur S. Aylsworth	82
9	Deletion of Hepatocyte Nuclear Factor-1-Beta in an Infant with Prune Belly Syndrome 2010 ·American Journal of Perinatology ·Sina Haeri,Patricia Devers,Kathleen Kaiser‐Rogers,(unknown),Beth A. Torchia,Amanda Horton,Honor M. Wolfe,Arthur S. Aylsworth	40
10	Small Deletions of SATB2 Cause Some of the Clinical Features of the 2q33.1 Microdeletion Syndrome 2009 ·PLoS ONE ·Jill A. Rosenfeld,Blake C. Ballif,Ann Lucas,(unknown),Cynthia M. Powell,Arthur S. Aylsworth,Beth A. Torchia,Lisa G. Shaffer	93
11	Maternal Body Mass Index and Lifestyle Exposures and the Risk of Bilateral Renal Agenesis or Hypoplasia: The National Birth Defects Prevention Study 2008 ·American Journal of Epidemiology ·(unknown),Andrew F. Olshan,A. M. Siega-Riz,Margaret A. Honein,Arthur S. Aylsworth,(unknown)	41
12	Expanding spectrum of congenital disorder of glycosylation Ig (CDG‐Ig): Sibs with a unique skeletal dysplasia, hypogammaglobulinemia, cardiomyopathy, genital malformations, and early lethality 2007 ·American Journal of Medical Genetics Part A ·Christian Kranz,Alice Basinger,Müge Güçsavaş‐Çalıkoğlu,Liangwu Sun,Cynthia M. Powell,Frederick W. Henderson,Arthur S. Aylsworth,Hudson H. Freeze	65
13	Submicroscopic deletion 9(q34.4) and duplication 19(p13.3): Identified by subtelomere specific FISH probes 2003 ·American Journal of Medical Genetics Part A ·Denise I. Quigley,Kathleen Kaiser‐Rogers,Arthur S. Aylsworth,Kathleen W. Rao	8
14	Type I diabetes mellitus in a patient with chromosome 22q11.2 deletion syndrome 2001 ·American Journal of Medical Genetics ·Deborah A. Elder,Kathleen Kaiser‐Rogers,Arthur S. Aylsworth,Ali S. Çalıkoğlu	18
15	The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2 1997 ·American Journal of Ophthalmology ·Arthur S. Aylsworth,(unknown),(unknown),Joan H. Marks,(unknown),Allan E. Rubenstein,David Viskochil,David H. Gutmann	49
16	Hypochondroplasia: Molecular Analysis of the Fibroblast Growth Factor Receptor 3 Gene 1996 ·Annals of the New York Academy of Sciences ·Gary A. Bellus,Iain McIntosh,(unknown),Arthur S. Aylsworth,Ilkka Kaitila,Clair A. Francomano	20
17	Distribution of 13 truncating mutations in the neurofibromatosis 1 gene 1995 ·Human Molecular Genetics ·Ruth A. Heim,Lauren Kam-Morgan,Cameron G. Binnie,(unknown),Matthew C. Cayouette,Rosann A. Farber,Arthur S. Aylsworth,Lawrence M. Silverman,Michael C. Luce	144
18	An Extensive de novo deletion removing FMR1 in a patient with mental retardation and the fragile X syndrome phenotype 1993 ·Human Molecular Genetics ·Jack Tarleton,(unknown),(unknown),Kathleen Rao,Arthur S. Aylsworth,(unknown)	58
19	Neurological aspects of del(1q) syndrome 1991 ·American Journal of Medical Genetics ·(unknown),Robert Greenwood,Kathleen W. Rao,Arthur S. Aylsworth	23
20	Mannosidosis: Phenotype of a severely affected child and characterization of α-mannosidase activity in cultured fibroblasts from the patient and his parents 1976 ·The Journal of Pediatrics ·Arthur S. Aylsworth,Harold A. Taylor,(unknown),George H. Thomas	20

About Arthur S. Aylsworth

Arthur S. Aylsworth is a scholar working on Developmental Biology, Genetics and Pediatrics, Perinatology and Child Health, having authored 93 papers that have together received 3.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (18 papers), Cleft Lip and Palate Research (15 papers) and Craniofacial Disorders and Treatments (15 papers). The work is most often cited by research in Genetics (1.9k citations), Pediatrics, Perinatology and Child Health (596 citations) and Molecular Biology (1.8k citations). Arthur S. Aylsworth has collaborated with scholars based in United States, Canada and Germany. Frequent co-authors include Robert E. Meyer, Cynthia M. Powell, Ronald P. Strauss, Stephanie Watkins, Kathleen W. Rao, Clair A. Francomano, Iain McIntosh, Ilkka Kaitila, Gary A. Bellus and Lisa G. Shaffer. Their work appears in journals such as Nature Genetics, PLoS ONE and Brain.

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