Angela E. Scheuerle

5.3k total citations
118 papers, 2.6k citations indexed

About

Angela E. Scheuerle is a scholar working on Pediatrics, Perinatology and Child Health, Surgery and Genetics. According to data from OpenAlex, Angela E. Scheuerle has authored 118 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Pediatrics, Perinatology and Child Health, 39 papers in Surgery and 33 papers in Genetics. Recurrent topics in Angela E. Scheuerle's work include Prenatal Screening and Diagnostics (24 papers), Pregnancy and Medication Impact (21 papers) and Congenital Anomalies and Fetal Surgery (18 papers). Angela E. Scheuerle is often cited by papers focused on Prenatal Screening and Diagnostics (24 papers), Pregnancy and Medication Impact (21 papers) and Congenital Anomalies and Fetal Surgery (18 papers). Angela E. Scheuerle collaborates with scholars based in United States, Germany and France. Angela E. Scheuerle's co-authors include Mark A. Canfield, Peter H. Langlois, Tunu Ramadhani, Paul A. Romitti, Mary K. Ethen, Charlotte M. Druschel, Diego F. Wyszynski, John M. Thorp, Hugh H. Tilson and D. Kim Waller and has published in prestigious journals such as Gastroenterology, Brain and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Angela E. Scheuerle

112 papers receiving 2.5k citations

Peers

Angela E. Scheuerle
Angela E. Scheuerle
Citations per year, relative to Angela E. Scheuerle Angela E. Scheuerle (= 1×) peers Maurizio Clementi

Countries citing papers authored by Angela E. Scheuerle

Since Specialization
Citations

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

Fields of papers citing papers by Angela E. Scheuerle

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Angela E. Scheuerle. 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 Angela E. Scheuerle. The network helps show where Angela E. Scheuerle may publish in the future.

Co-authorship network of co-authors of Angela E. Scheuerle

This figure shows the co-authorship network connecting the top 25 collaborators of Angela E. Scheuerle. A scholar is included among the top collaborators of Angela E. Scheuerle 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 Angela E. Scheuerle. Angela E. Scheuerle 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.
Benjamin, Renata H., Joanne Nguyen, Margaret Drummond‐Borg, et al.. (2024). Classification of isolated versus multiple birth defects: An automated process for population‐based registries. American Journal of Medical Genetics Part A. 194(10). e63714–e63714.
2.
Albano, Jessica D., Angela E. Scheuerle, D. Heather Watts, et al.. (2024). The Antiretroviral Pregnancy Registry: Three decades of prospective monitoring for birth defects. Pharmacoepidemiology and Drug Safety. 33(6). e5801–e5801. 2 indexed citations
4.
Benjamin, Renata H., Scott McLean, Hope Northrup, et al.. (2020). Patterns of co-occurring birth defects among infants with hypospadias. Journal of Pediatric Urology. 17(1). 64.e1–64.e8. 2 indexed citations
5.
Morris, Colleen A., Stephen R. Braddock, Emily Chen, et al.. (2020). Health Care Supervision for Children With Williams Syndrome. PEDIATRICS. 145(2). 55 indexed citations
6.
Miller, David T., Debra Freedenberg, Elizabeth K. Schorry, et al.. (2019). Health Supervision for Children With Neurofibromatosis Type 1. PEDIATRICS. 143(5). 117 indexed citations
7.
Namazy, Jennifer A., Lucie Blais, Elizabeth Andrews, et al.. (2019). Pregnancy outcomes in the omalizumab pregnancy registry and a disease-matched comparator cohort. Journal of Allergy and Clinical Immunology. 145(2). 528–536.e1. 97 indexed citations
8.
Ryan, Marisa A., Andrew F. Olshan, Mark A. Canfield, et al.. (2019). Sociodemographic, health behavioral, and clinical risk factors for anotia/microtia in a population-based case-control study. International Journal of Pediatric Otorhinolaryngology. 122. 18–26. 24 indexed citations
9.
Ng, Bobby G., Kimiyo Raymond, Martin Kircher, et al.. (2015). Expanding the Molecular and Clinical Phenotype of SSR4-CDG. Human Mutation. 36(11). 1048–1051. 25 indexed citations
11.
Scheuerle, Angela E.. (2011). Clinical differentiation of patent foramen ovale and secundum atrial septal defect: a survey of pediatric cardiologists in Dallas, Texas, USA.. PubMed. 38(1). 4–8. 7 indexed citations
12.
Ramadhani, Tunu, Mark A. Canfield, Noha H. Farag, et al.. (2011). Do foreign‐ and U.S.‐born mothers across racial/ethnic groups have a similar risk profile for selected sociodemographic and periconceptional factors?. Birth Defects Research Part A Clinical and Molecular Teratology. 91(9). 823–830. 7 indexed citations
13.
Watts, D. Heather, Sharon Huang, Mary Culnane, et al.. (2010). Birth defects among a cohort of infants born to HIV-infected women on antiretroviral medication. Journal of Perinatal Medicine. 39(2). 163–70. 28 indexed citations
14.
Scheuerle, Angela E., Vani Vannappagari, & Mary K. Miller. (2009). Measurements of birth defect prevalence: Which is most useful as a comparator group for pharmaceutical pregnancy registries?. Birth Defects Research Part A Clinical and Molecular Teratology. 85(7). 611–620. 5 indexed citations
15.
Ramadhani, Tunu, Vanessa L. Short, Mark A. Canfield, et al.. (2009). Are birth defects among Hispanics related to maternal nativity or number of years lived in the United States?. Birth Defects Research Part A Clinical and Molecular Teratology. 85(9). 755–763. 22 indexed citations
16.
Langlois, Peter H., Angela E. Scheuerle, Scott Horel, & Susan E. Carozza. (2009). Urban versus rural residence and occurrence of septal heart defects in Texas. Birth Defects Research Part A Clinical and Molecular Teratology. 85(9). 764–772. 23 indexed citations
17.
Langlois, Peter H., Jean D. Brender, Lucina Suarez, et al.. (2009). Maternal residential proximity to waste sites and industrial facilities and conotruncal heart defects in offspring. Paediatric and Perinatal Epidemiology. 23(4). 321–331. 29 indexed citations
18.
Simpson, Michael A., et al.. (2009). Mutations in FAM20C also identified in non‐lethal osteosclerotic bone dysplasia. Clinical Genetics. 75(3). 271–276. 88 indexed citations
19.
Tomson, Torbjörn, Dina Battino, Jacqueline A. French, et al.. (2007). Antiepileptic drug exposure and major congenital malformations: The role of pregnancy registries. Epilepsy & Behavior. 11(3). 277–282. 38 indexed citations
20.
Scheuerle, Angela E. & Deborah L. Covington. (2004). Clinical review procedures for the Antiretroviral Pregnancy Registry. Pharmacoepidemiology and Drug Safety. 13(8). 529–536. 14 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

Rankless by CCL
2026