Tara Wenger

2.1k total citations
42 papers, 377 citations indexed

About

Tara Wenger is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Tara Wenger has authored 42 papers receiving a total of 377 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 11 papers in Surgery and 9 papers in Molecular Biology. Recurrent topics in Tara Wenger's work include Craniofacial Disorders and Treatments (12 papers), Cleft Lip and Palate Research (10 papers) and Vascular Malformations and Hemangiomas (5 papers). Tara Wenger is often cited by papers focused on Craniofacial Disorders and Treatments (12 papers), Cleft Lip and Palate Research (10 papers) and Vascular Malformations and Hemangiomas (5 papers). Tara Wenger collaborates with scholars based in United States, Australia and Canada. Tara Wenger's co-authors include Elaine H. Zackai, Donna M. McDonald‐McGinn, Beverly S. Emanuel, Judith S. Miller, Caitlin C. Clements, Ashley de Marchena, Robert T. Schultz, Jeffrey S. Gerdes, Matthew A. Deardorff and Daniel T. Swarr and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Tara Wenger

38 papers receiving 370 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Tara Wenger United States 11 196 144 73 70 50 42 377
E. Robert Wassman United States 13 375 1.9× 223 1.5× 83 1.1× 95 1.4× 136 2.7× 23 603
Karen E. Wain United States 14 378 1.9× 120 0.8× 46 0.6× 48 0.7× 123 2.5× 28 567
Benedicte Paus Norway 13 320 1.6× 67 0.5× 84 1.2× 175 2.5× 22 0.4× 28 531
Srinivasan Muthuswamy India 9 95 0.5× 140 1.0× 42 0.6× 34 0.5× 80 1.6× 29 391
Weiyi Mu United States 10 148 0.8× 141 1.0× 46 0.6× 34 0.5× 35 0.7× 28 346
Sawona Biswas United States 10 374 1.9× 110 0.8× 23 0.3× 35 0.5× 88 1.8× 13 513
Cristina Molinatto Italy 10 296 1.5× 270 1.9× 43 0.6× 27 0.4× 196 3.9× 12 472
Nina B. Gold United States 10 220 1.1× 186 1.3× 34 0.5× 23 0.3× 76 1.5× 37 457
Kei Ohashi Japan 9 93 0.5× 83 0.6× 80 1.1× 26 0.4× 30 0.6× 22 266
Katherine Rose United States 10 73 0.4× 180 1.3× 64 0.9× 19 0.3× 19 0.4× 22 427

Countries citing papers authored by Tara Wenger

Since Specialization
Citations

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

Fields of papers citing papers by Tara Wenger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tara Wenger. 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 Tara Wenger. The network helps show where Tara Wenger may publish in the future.

Co-authorship network of co-authors of Tara Wenger

This figure shows the co-authorship network connecting the top 25 collaborators of Tara Wenger. A scholar is included among the top collaborators of Tara Wenger 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 Tara Wenger. Tara Wenger 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.
2.
Wenger, Tara & Margaret P Adam. (2025). Commentary: Interventional Genetics. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 199(3). 151–153.
3.
Burns, Karen, et al.. (2025). Treatment of PDGFRB ‐Related Penttinen Syndrome With Imatinib in a Young Child. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 199(3). 176–182.
4.
Strong, Alanna, Michael March, Christopher J. Cardinale, et al.. (2024). Novel insights into the phenotypic spectrum and pathogenesis of Hardikar syndrome. Genetics in Medicine. 26(10). 101222–101222. 2 indexed citations
5.
Mallory, Benjamin J., Tara Wenger, Irene J. Chang, et al.. (2024). 3-hour genome sequencing and targeted analysis to rapidly assess genetic risk. SHILAP Revista de lepidopterología. 2. 101833–101833. 7 indexed citations
6.
Wenger, Tara, et al.. (2023). P352: Expanding the neurodevelopmental phenotype of HIVEP2-related disorder. SHILAP Revista de lepidopterología. 1(1). 100380–100380. 1 indexed citations
7.
Timberlake, Andrew T., Garrett Allington, Emre Kiziltug, et al.. (2023). De novo variants implicate chromatin modification, transcriptional regulation, and retinoic acid signaling in syndromic craniosynostosis. The American Journal of Human Genetics. 110(5). 846–862. 11 indexed citations
8.
Richardson, Clare, Jonathan N. Perkins, Dana M. Jensen, et al.. (2022). Primary targeted medical therapy for management of bilateral head and neck lymphatic malformations in infants. International Journal of Pediatric Otorhinolaryngology. 164. 111371–111371. 3 indexed citations
9.
Wenger, Tara, John P. Dahl, Randall A. Bly, et al.. (2022). Avoidance of surgery for head and neck infantile myofibromatosis using imatinib monotherapy. SHILAP Revista de lepidopterología. 10(2). e05382–e05382. 3 indexed citations
10.
Wenger, Tara, Sheila Ganti, James T. Bennett, et al.. (2022). Alpelisib for the treatment of PIK3CA-related head and neck lymphatic malformations and overgrowth. Genetics in Medicine. 24(11). 2318–2328. 27 indexed citations
11.
Chen, Maida Lynn, et al.. (2021). Risk Factors and Inadequacy of Screening for Sleep-Disordered Breathing in Children with Marfan Syndrome. Pediatric Cardiology. 42(3). 510–516. 2 indexed citations
12.
Forster, Catherine S., Weston T. Powell, Daniel J. Moore, et al.. (2021). Perspectives from the Society for Pediatric Research: advice on sustaining science and mentoring during COVID-19. Pediatric Research. 90(4). 738–743. 5 indexed citations
13.
14.
Wenger, Tara, Emily R. Gallagher, & Elizabeth Bhoj. (2018). An Algorithm for the Assessment of Facial Asymmetry in Children With Focus on Etiology and Treatment. The Cleft Palate-Craniofacial Journal. 56(3). 419–424. 1 indexed citations
15.
Clements, Caitlin C., Tara Wenger, Alisa R. Zoltowski, et al.. (2017). Critical region within 22q11.2 linked to higher rate of autism spectrum disorder. Molecular Autism. 8(1). 58–58. 31 indexed citations
16.
Tully, Hannah M., Tara Wenger, Walter A. Kukull, Dan Doherty, & William B. Dobyns. (2016). Anatomical configurations associated with posthemorrhagic hydrocephalus among premature infants with intraventricular hemorrhage. Neurosurgical FOCUS. 41(5). E5–E5. 5 indexed citations
17.
Wenger, Tara, Charlly Kao, Donna M. McDonald‐McGinn, et al.. (2016). The Role of mGluR Copy Number Variation in Genetic and Environmental Forms of Syndromic Autism Spectrum Disorder. Scientific Reports. 6(1). 19372–19372. 24 indexed citations
18.
Wenger, Tara, John P. Dahl, Elizabeth Bhoj, et al.. (2016). Tracheal cartilaginous sleeves in children with syndromic craniosynostosis. Genetics in Medicine. 19(1). 62–68. 22 indexed citations
19.
Wenger, Tara, Judith S. Miller, Ashley de Marchena, et al.. (2016). 22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening. Molecular Autism. 7(1). 27–27. 61 indexed citations
20.
North, Michael, et al.. (2002). LICENSING THE USE OF SPECIAL COLLECTIONS MATERIALS. 3(2). 124–143. 4 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

Breakdown of academic impact, for papers by E. Robert Wassman Breakdown of academic impact, for papers by Karen E. Wain Breakdown of academic impact, for papers by Benedicte Paus Breakdown of academic impact, for papers by Srinivasan Muthuswamy Breakdown of academic impact, for papers by Weiyi Mu Breakdown of academic impact, for papers by Sawona Biswas Breakdown of academic impact, for papers by Cristina Molinatto Breakdown of academic impact, for papers by Nina B. Gold Breakdown of academic impact, for papers by Kei Ohashi Breakdown of academic impact, for papers by Katherine Rose
Rankless by CCL
2026