Ericka Okenfuss

542 total citations
9 papers, 275 citations indexed

About

Ericka Okenfuss is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ericka Okenfuss has authored 9 papers receiving a total of 275 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ericka Okenfuss's work include Connective tissue disorders research (4 papers), Birth, Development, and Health (2 papers) and Tuberous Sclerosis Complex Research (1 paper). Ericka Okenfuss is often cited by papers focused on Connective tissue disorders research (4 papers), Birth, Development, and Health (2 papers) and Tuberous Sclerosis Complex Research (1 paper). Ericka Okenfuss collaborates with scholars based in United States, Australia and Argentina. Ericka Okenfuss's co-authors include Billur Moghaddam, Andrew L. Avins, Deborah Krakow, David L. Rimoin, Daniel H. Cohn, Phi Luong, Tara Funari, Laurie S. Sadler, Joris Vriens and Natalia Camacho and has published in prestigious journals such as The American Journal of Human Genetics, Bone and American Journal of Medical Genetics Part A.

In The Last Decade

Ericka Okenfuss

9 papers receiving 270 citations

Peers

Ericka Okenfuss

GENET

SS

MB

SURGE

PRM

Nadia Cerutti Italy

Brian G. Jorgensen United States

Mariko Isshiki Japan

Nikita Ved United Kingdom

Huanzheng Li China

Kathleen A. McNulty United States

Kyung Jin Roh South Korea

Xixiang Ma China

Rolando Carrisoza‐Gaytan United States

Paola Malatesta Italy

Nadia Cerutti Italy

Ericka Okenfuss

38 ×0.3

GENET

137 ×1.5

SS

118 ×1.4

MB

39 ×1.0

SURGE

36 ×0.9

PRM

Citations per year, relative to Ericka Okenfuss Ericka Okenfuss (= 1×) peers Nadia Cerutti

Countries citing papers authored by Ericka Okenfuss

Since Specialization

Citations

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

Fields of papers citing papers by Ericka Okenfuss

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ericka Okenfuss

This figure shows the co-authorship network connecting the top 25 collaborators of Ericka Okenfuss. A scholar is included among the top collaborators of Ericka Okenfuss 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 Ericka Okenfuss. Ericka Okenfuss is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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9 of 9 papers shown

1.

Sohn, Young Bae, N. Matthew Ellinwood, Ericka Okenfuss, et al.. (2022). Timing is everything: Clinical courses of Hunter syndrome associated with age at initiation of therapy in a sibling pair. Molecular Genetics and Metabolism Reports. 30. 100845–100845. 9 indexed citations

2.

Hoover‐Fong, Julie, Moira Cheung, Virginia Fano, et al.. (2021). Lifetime impact of achondroplasia: Current evidence and perspectives on the natural history. Bone. 146. 115872–115872. 53 indexed citations

3.

Okenfuss, Ericka, Ravi Savarirayan, Klane K. White, et al.. (2021). Multidisciplinary Care of Neurosurgical Patients with Genetic Syndromes. Neurosurgery Clinics of North America. 33(1). 7–15. 1 indexed citations

4.

Okenfuss, Ericka, Billur Moghaddam, & Andrew L. Avins. (2020). Natural history of achondroplasia: A retrospective review of longitudinal clinical data. American Journal of Medical Genetics Part A. 182(11). 2540–2551. 35 indexed citations

5.

Hoover‐Fong, Julie, Michael C. Ain, Ivor Berkowitz, et al.. (2019). Blood pressure in adults with short stature skeletal dysplasias. American Journal of Medical Genetics Part A. 182(1). 150–161. 14 indexed citations

6.

Thacker, Mihir M., Ericka Okenfuss, Angela L. Duker, et al.. (2017). Aneurysmal bone cysts and pathologic fracture associated with supernumerary ring chromosome 6 in two unrelated patients. American Journal of Medical Genetics Part A. 173(12). 3205–3210. 4 indexed citations

7.

Reinstein, Eyal, Ericka Okenfuss, Yael Wilnai, et al.. (2013). Axial spondylometaphyseal dysplasia with retinitis pigmentosa—a clinical report and diagnostic clues. Journal of Applied Genetics. 54(2). 231–234. 1 indexed citations

8.

Baratela, Wagner Antonio da Rosa, Michael B. Bober, George E. Tiller, et al.. (2012). A newly recognized syndrome with characteristic facial features, skeletal dysplasia, and developmental delay. American Journal of Medical Genetics Part A. 158A(8). 1815–1822. 10 indexed citations

9.

Krakow, Deborah, Joris Vriens, Natalia Camacho, et al.. (2009). Mutations in the Gene Encoding the Calcium-Permeable Ion Channel TRPV4 Produce Spondylometaphyseal Dysplasia, Kozlowski Type and Metatropic Dysplasia. The American Journal of Human Genetics. 84(3). 307–315. 148 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.

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