Fingerprint Fingerprint is based on mining the text of the person's scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.

  • 4 Similar Profiles
Genes Medicine & Life Sciences
Mutation Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Neural Tube Defects Medicine & Life Sciences
Intellectual Disability Medicine & Life Sciences
Mothers Medicine & Life Sciences
Chromosomes Medicine & Life Sciences
Pregnancy Medicine & Life Sciences

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Projects 1999 2018

Research Output 1970 2017

Camptodactyly and the 22q11.2 deletion syndrome

Couser, N. L., Pande, C. K., Walsh, J. M., Tepperberg, J. & Aylsworth, A. S. Feb 1 2017 In : American Journal of Medical Genetics, Part A. 173, 2, p. 515-518 4 p.

Research output: Research - peer-reviewArticle

DiGeorge Syndrome
Laryngomalacia
Microarray Analysis
Single Nucleotide Polymorphism
Joints
2 Citations

Bayesian multinomial probit modeling of daily windows of susceptibility for maternal PM2.5 exposure and congenital heart defects

Warren, J. L., Stingone, J. A., Herring, A. H., Luben, T. J., Fuentes, M., Aylsworth, A. S., Langlois, P. H., Botto, L. D., Correa, A., Olshan, A. F. & National Birth Defects Prevention Study Jul 20 2016 In : Statistics in Medicine. 35, 16, p. 2786-2801 16 p.

Research output: Research - peer-reviewArticle

Probit
Susceptibility
Defects
Modeling
Heart
Teratogens
Registries
Morbidity
First Pregnancy Trimester
Embryonic Development
19 Citations

Survival of children with trisomy 13 and trisomy 18: A multi-state population-based study

Meyer, R. E., Liu, G., Gilboa, S. M., Ethen, M. K., Aylsworth, A. S., Powell, C. M., Flood, T. J., Mai, C. T., Wang, Y., Canfield, M. A. & for the National Birth Defects Prevention Network Apr 1 2016 In : American Journal of Medical Genetics, Part A. 170, 4, p. 825-837 13 p.

Research output: Research - peer-reviewArticle

Population
Trisomy 13 syndrome
Trisomy 18
Mortality
Trisomy
11 Citations

Aortopathy in the 7q11.23 microduplication syndrome

Parrott, A., James, J., Goldenberg, P., Hinton, R. B., Miller, E., Shikany, A., Aylsworth, A. S., Kaiser-Rogers, K., Ferns, S. J., Lalani, S. R. & Ware, S. M. Feb 1 2015 In : American Journal of Medical Genetics, Part A. 167, 2, p. 363-370 8 p.

Research output: Research - peer-reviewArticle

Supravalvular Aortic Stenosis
Williams Syndrome
Dilatation
Phenotype
Language Development Disorders