Arthur S. Aylsworth

9.4k citations

93 papers · 3.8k indexed · h-index 32

Genetics top 0.5%
- Genomic variations and chromosomal abnormalities 18
- Cleft Lip and Palate Research 15
- Craniofacial Disorders and Treatments 15
- Genetics and Neurodevelopmental Disorders 10
- Neurogenetic and Muscular Disorders Research 6
- Connective tissue disorders research 5
Pediatrics, Perinatology and Child Health top 2%
Molecular Biology top 5%
Developmental Biology top 5%
Genetics top 5%
- Genomic variations and chromosomal abnormalities 18
- Cleft Lip and Palate Research 15
- Craniofacial Disorders and Treatments 15
- Genetics and Neurodevelopmental Disorders 10
- Neurogenetic and Muscular Disorders Research 6
- Connective tissue disorders research 5
Surgery
- Congenital Anomalies and Fetal Surgery 7
Pulmonary and Respiratory Medicine
- Tracheal and airway disorders 6

Co-authors: Robert E. Meyer Cynthia M. Powell Ronald P. Strauss Stephanie Watkins Kathleen W. Rao Clair A. Francomano Iain McIntosh Ilkka Kaitila
Cited by: Genetics Pediatrics, Perinatology and Child Health Molecular Biology
Journals: Nature Genetics (2 papers)PLoS ONE (1 paper)Brain (1 paper)
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

The 25 scholars most cited alongside Arthur S. Aylsworth, 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 Arthur S. Aylsworth Line = papers co-authored together Arthur S. Aylsworth links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Variants in ACTC1 underlie distal arthrogryposis accompanied by congenital heart defects Human Genetics and Genomics Advances ·Jessica X. Chong,Matthew C. Childers,Colby T. Marvin,Anthony J. Marcello,Hernán Gonorazky,Lili‐Naz Hazrati,James J. Dowling,Fatema Al Amrani,Yasemin Alanay,Yolanda Ber,Miguel Ángel Marín Gabriel,Arthur S. Aylsworth,Kati J. Buckingham,Kathryn M. Shively,Olivia Sommers,Kailyn Anderson,Michael Regnier,Michael J. Bamshad	2023	9
2	De Novo Missense Variants in WDR37 Cause a Severe Multisystemic Syndrome The American Journal of Human Genetics ·Linda M. Reis,Елена А. Сорокина,Samuel Thompson,Sanaa Muheisen,Milen Velinov,Carlos Zamora,Arthur S. Aylsworth,Elena V. Semina	2019	25
3	An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening The Journal of Pediatrics ·Laura V. Milko,Julianne O’Daniel,Daniela M. DeCristo,Stephanie B. Crowley,Ann Katherine M. Foreman,Kathleen Wallace,Lonna Mollison,Natasha T. Strande,Zahra S. Girnary,Lacey Boshe,Arthur S. Aylsworth,Müge Güçsavaş‐Çalıkoğlu,Dianne M. Frazier,Neeta L. Vora,Myra I. Roche,Bradford C. Powell,Cynthia M. Powell,Jonathan S. Berg	2019	44
4	Prenatal Alcohol Exposure in Relation to Autism Spectrum Disorder: Findings from the Study to Explore Early Development (SEED) Paediatric and Perinatal Epidemiology ·Alison B. Singer,Arthur S. Aylsworth,Christina Cordero,Lisa Croen,Carolyn DiGuiseppi,M. Daniele Fallin,Amy H. Herring,Stephen R. Hooper,Rebecca Edmondson Pretzel,Laura A. Schieve,Gayle C. Windham,Julie L. Daniels	2017	14
5	Aortopathy in the 7q11.23 microduplication syndrome American Journal of Medical Genetics Part A ·Ashley Parrott,Jeanne James,Paula Goldenberg,Robert B. Hinton,Erin Miller,Amy Shikany,Arthur S. Aylsworth,Kathleen Kaiser‐Rogers,Sunita J. Ferns,Seema R. Lalani,Stephanie M. Ware	2014	25
6	Classification, Epidemiology, and Genetics of Orofacial Clefts Clinics in Plastic Surgery ·Stephanie Watkins,Robert E. Meyer,Ronald P. Strauss,Arthur S. Aylsworth	2014	169
7	Maternal Exposure to Criteria Air Pollutants and Congenital Heart Defects in Offspring: Results from the National Birth Defects Prevention Study 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)	2014	82
8	Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes 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	2012	82
9	Deletion of Hepatocyte Nuclear Factor-1-Beta in an Infant with Prune Belly Syndrome American Journal of Perinatology ·Sina Haeri,Patricia Devers,Kathleen Kaiser‐Rogers,Vincent Moylan,Beth A. Torchia,Amanda Horton,Honor M. Wolfe,Arthur S. Aylsworth	2010	40
10	Small Deletions of SATB2 Cause Some of the Clinical Features of the 2q33.1 Microdeletion Syndrome PLoS ONE ·Jill A. Rosenfeld,Blake C. Ballif,Ann Lucas,Edward J. Spence,Cynthia M. Powell,Arthur S. Aylsworth,Beth A. Torchia,Lisa G. Shaffer	2009	93
11	Maternal Body Mass Index and Lifestyle Exposures and the Risk of Bilateral Renal Agenesis or Hypoplasia: The National Birth Defects Prevention Study American Journal of Epidemiology ·Jennifer E. Slickers,Andrew F. Olshan,A. M. Siega-Riz,Margaret A. Honein,Arthur S. Aylsworth,(unknown)	2008	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 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	2007	65
13	Submicroscopic deletion 9(q34.4) and duplication 19(p13.3): Identified by subtelomere specific FISH probes American Journal of Medical Genetics Part A ·Denise I. Quigley,Kathleen Kaiser‐Rogers,Arthur S. Aylsworth,Kathleen W. Rao	2003	8
14	Type I diabetes mellitus in a patient with chromosome 22q11.2 deletion syndrome American Journal of Medical Genetics ·Deborah A. Elder,Kathleen Kaiser‐Rogers,Arthur S. Aylsworth,Ali S. Çalıkoğlu	2001	18
15	The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2 American Journal of Ophthalmology ·Arthur S. Aylsworth,J. C Carey,BR Korf,Joan H. Marks,RE Pyeritz,Allan E. Rubenstein,David Viskochil,David H. Gutmann	1997	49
16	Hypochondroplasia: Molecular Analysis of the Fibroblast Growth Factor Receptor 3 Gene Annals of the New York Academy of Sciences ·Gary A. Bellus,Iain McIntosh,Jinny Szabo,Arthur S. Aylsworth,Ilkka Kaitila,Clair A. Francomano	1996	20
17	Distribution of 13 truncating mutations in the neurofibromatosis 1 gene Human Molecular Genetics ·Ruth A. Heim,Lauren Kam-Morgan,Cameron G. Binnie,David D. Corns,Matthew C. Cayouette,Rosann A. Farber,Arthur S. Aylsworth,Lawrence M. Silverman,Michael C. Luce	1995	144
18	An Extensive de novo deletion removing FMR1 in a patient with mental retardation and the fragile X syndrome phenotype Human Molecular Genetics ·Jack Tarleton,Renee Richle,Charles Schwarsz,Kathleen Rao,Arthur S. Aylsworth,Ave Lachlewicz	1993	58
19	Neurological aspects of del(1q) syndrome American Journal of Medical Genetics ·Keiko Murayama,Robert Greenwood,Kathleen W. Rao,Arthur S. Aylsworth	1991	23
20	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 ·Arthur S. Aylsworth,Harold A. Taylor,Carole M. Stuart,George H. Thomas	1976	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), Craniofacial Disorders and Treatments (15 papers), Genetics and Neurodevelopmental Disorders (10 papers), Congenital Anomalies and Fetal Surgery (7 papers), Tracheal and airway disorders (6 papers), Neurogenetic and Muscular Disorders Research (6 papers) and Connective tissue disorders research (5 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.

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