Allison L. Goetsch

554 total citations
20 papers, 149 citations indexed

About

Allison L. Goetsch is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Genetics. According to data from OpenAlex, Allison L. Goetsch has authored 20 papers receiving a total of 149 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pediatrics, Perinatology and Child Health, 8 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in Allison L. Goetsch's work include Sexual Differentiation and Disorders (8 papers), Prenatal Screening and Diagnostics (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Allison L. Goetsch is often cited by papers focused on Sexual Differentiation and Disorders (8 papers), Prenatal Screening and Diagnostics (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Allison L. Goetsch collaborates with scholars based in United States, Canada and Germany. Allison L. Goetsch's co-authors include Emilie K. Johnson, Courtney Finlayson, Heather B. Radtke, Wendy J. Brickman, Reema L. Habiby, Teresa K. Woodruff, Catherine Wicklund, Elizabeth Dabrowski, Andrea M. Lewis and Amanda L. Bergner and has published in prestigious journals such as The Journal of Urology, Urology and Prenatal Diagnosis.

In The Last Decade

Allison L. Goetsch

15 papers receiving 149 citations

Peers

Allison L. Goetsch

GENET

PPCH

PRM

J. Dor Israel

Bridget O’Connor United States

Masafumi Kon Japan

Josh Skorupski United States

Sagit Arbel-Alon Israel

Roberto Fogliani Italy

Maya Spira Israel

Ahmed Kamal United Kingdom

Amalia Mayo United Kingdom

Alexander Maret United States

J. Dor Israel

Allison L. Goetsch

36 ×0.6

GENET

154 ×2.8

PPCH

44 ×0.9

54 ×2.0

PRM

159 ×6.9

Citations per year, relative to Allison L. Goetsch Allison L. Goetsch (= 1×) peers J. Dor

Countries citing papers authored by Allison L. Goetsch

Since Specialization

Citations

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

Fields of papers citing papers by Allison L. Goetsch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Allison L. Goetsch. 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 Allison L. Goetsch. The network helps show where Allison L. Goetsch may publish in the future.

Co-authorship network of co-authors of Allison L. Goetsch

This figure shows the co-authorship network connecting the top 25 collaborators of Allison L. Goetsch. A scholar is included among the top collaborators of Allison L. Goetsch 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 Allison L. Goetsch. Allison L. Goetsch 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

Finlayson, Courtney, Elizabeth B. Yerkes, Allison L. Goetsch, et al.. (2025). Role of endocrine and genetic evaluation for infants with proximal hypospadias. Journal of Pediatric Urology. 21(5). 1146–1153.

Finlayson, Courtney, et al.. (2025). Finding acceptance: How adolescents and young adults with Klinefelter Syndrome navigate identity, disclosure, and support. Journal of Genetic Counseling. 34(3). e70074–e70074.

Lee, Victoria, Allison L. Goetsch, Ilina Rosoklija, et al.. (2024). Mixed Gonadal Dysgenesis: A Narrative Literature Review and Clinical Primer for the Urologist. The Journal of Urology. 212(5). 660–671. 3 indexed citations

Finlayson, Courtney, et al.. (2024). Turner Syndrome With Y Chromosome and Germ Cells: A Case Report Highlighting the Need to Prioritize Individualized Care. Urology. 192. e100–e103. 2 indexed citations

Aschbacher‐Smith, Lindsey, Allison L. Goetsch, Katherine Kim, et al.. (2024). Expanding the phenotype of neurofibromatosis type 1 microdeletion syndrome. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 196(4). e32095–e32095.

Goetsch, Allison L., et al.. (2023). Clinical utility of early rapid genome sequencing in the evaluation of patients with differences of sex development. American Journal of Medical Genetics Part A. 194(2). 351–357.

Alvarado, Jorge, et al.. (2023). Outcomes and Associated Extracardiac Malformations in Neonates from Colombia with Severe Congenital Heart Disease. Pediatric Cardiology. 45(1). 55–62.

Radtke, Heather B., et al.. (2023). Neurofibromatosis Type 1 (NF1): Addressing the Transition from Pediatric to Adult Care. Pediatric Health Medicine and Therapeutics. Volume 14. 19–32. 8 indexed citations

Goetsch, Allison L., et al.. (2023). Cardiovascular Manifestations of Turner Syndrome: Phenotypic Differences Between Karyotype Subtypes. Pediatric Cardiology. 45(7). 1407–1414. 7 indexed citations

10.

Goetsch, Allison L., et al.. (2023). Neurofibromatosis‐ and schwannomatosis‐associated tumors: Approaches to genetic testing and counseling considerations. American Journal of Medical Genetics Part A. 191(10). 2467–2481. 2 indexed citations

11.

Rosoklija, Ilina, Allison L. Goetsch, J.S. Dungan, et al.. (2022). Prenatal detection and evaluation of differences of sex development: A qualitative interview study of parental perspectives and unmet needs. Prenatal Diagnosis. 42(10). 1332–1342. 7 indexed citations

12.

Huang, Jonathan, et al.. (2022). Ocular findings in pediatric turner syndrome. Ophthalmic Genetics. 43(4). 450–453. 5 indexed citations

13.

Radtke, Heather B., Amanda L. Bergner, Allison L. Goetsch, et al.. (2020). Genetic Counseling for Neurofibromatosis 1, Neurofibromatosis 2, and Schwannomatosis—Practice Resource of the National Society of Genetic Counselors. Journal of Genetic Counseling. 29(5). 692–714. 15 indexed citations

14.

Torres, Raúl, Rotem Ben‐Shachar, Jodi D. Hoffman, et al.. (2020). Evaluation and classification of severity for 176 genes on an expanded carrier screening panel. Prenatal Diagnosis. 40(10). 1246–1257. 28 indexed citations

15.

D’Oro, Anthony, Ilina Rosoklija, Elizabeth A. Leeth, et al.. (2020). Impact of cell‐free DNA screening on parental knowledge of fetal sex and disorders of sex development. Prenatal Diagnosis. 40(11). 1489–1496. 8 indexed citations

16.

Goetsch, Allison L., et al.. (2020). Transition Readiness Assessment in Adolescents and Young Adults with Neurofibromatosis Type 1 (NF1). Comprehensive Child and Adolescent Nursing. 46(3). 223–239. 11 indexed citations

17.

Johnson, Emilie K., Deborah L. Jacobson, Courtney Finlayson, et al.. (2020). Proximal Hypospadias—Isolated Genital Condition or Marker of More?. The Journal of Urology. 204(2). 345–352. 11 indexed citations

18.

Dabrowski, Elizabeth, Emilie K. Johnson, Shanlee Davis, et al.. (2019). Turner Syndrome with Y Chromosome: Spontaneous Thelarche, Menarche, and Risk of Malignancy. Journal of Pediatric and Adolescent Gynecology. 33(1). 10–14. 28 indexed citations

19.

Goetsch, Allison L., et al.. (2017). Fertility Preservation and Restoration for Patients with Complex Medical Conditions. Digital Access to Libraries (Université catholique de Louvain (UCL), l'Université de Namur (UNamur) and the Université Saint-Louis (USL-B)). 4 indexed citations

20.

Goetsch, Allison L., Catherine Wicklund, Marla L. Clayman, & Teresa K. Woodruff. (2015). Reproductive Endocrinologists’ Utilization of Genetic Counselors for Oncofertility and Preimplantation Genetic Diagnosis (PGD) Treatment of BRCA1/2 Mutation Carriers. Journal of Genetic Counseling. 25(3). 561–571. 10 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