Renee Temme

795 total citations
8 papers, 258 citations indexed

About

Renee Temme is a scholar working on Epidemiology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, Renee Temme has authored 8 papers receiving a total of 258 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Epidemiology, 4 papers in Pulmonary and Respiratory Medicine and 3 papers in Genetics. Recurrent topics in Renee Temme's work include Cystic Fibrosis Research Advances (3 papers), Neonatal Respiratory Health Research (3 papers) and Respiratory viral infections research (2 papers). Renee Temme is often cited by papers focused on Cystic Fibrosis Research Advances (3 papers), Neonatal Respiratory Health Research (3 papers) and Respiratory viral infections research (2 papers). Renee Temme collaborates with scholars based in United States, Canada and India. Renee Temme's co-authors include Nancy J. Mendelsohn, Shawna M. Pyott, Ezzat Elsobky, Thao Tran, Melanie Pepin, I. C. Verma, Peter H. Byers, Emily H. Turner, Solaf M. Elsayed and Dru F. Leistritz and has published in prestigious journals such as The American Journal of Human Genetics, The Journal of Pediatrics and American Journal of Respiratory Cell and Molecular Biology.

In The Last Decade

Renee Temme

7 papers receiving 252 citations

Peers

Renee Temme

GENET

MB

RHEUM

ONCOL

EPIDE

Denise L. Lind United States

F Skovby Denmark

María Gabriela Obregón Argentina

Ali Awaji Saudi Arabia

Janet M. Legare United States

Bijal Kikani United States

Ana Medeira Portugal

Carole Brewer United Kingdom

Antonio González‐Meneses Spain

M. Elizabeth McCready Canada

Denise L. Lind United States

Renee Temme

107 ×0.6

GENET

57 ×0.6

MB

50 ×0.7

RHEUM

21 ×0.6

ONCOL

19 ×0.7

EPIDE

Citations per year, relative to Renee Temme Renee Temme (= 1×) peers Denise L. Lind

Countries citing papers authored by Renee Temme

Since Specialization

Citations

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

Fields of papers citing papers by Renee Temme

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Renee Temme

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

All Works

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8 of 8 papers shown

1.

Joynt, Anya T., Karen S. Raraigh, Lori L. Vanscoy, et al.. (2024). Investigation of CFTR Function in Human Nasal Epithelial Cells Informs Personalized Medicine. American Journal of Respiratory Cell and Molecular Biology. 71(5). 577–588. 2 indexed citations

2.

Griffiths, Anne, et al.. (2023). Deletions in DNAL1 Cause Primary Ciliary Dyskinesia Across North American Indigenous Populations. The Journal of Pediatrics. 261. 113362–113362. 4 indexed citations

3.

Roggenbuck, Jennifer, et al.. (2014). The Long and Short of Genetic Counseling Summary Letters: A Case–control Study. Journal of Genetic Counseling. 24(4). 645–653. 16 indexed citations

4.

Temme, Renee, et al.. (2014). Assessment of Parental Understanding of Positive Newborn Screening Results and Carrier Status for Cystic Fibrosis with the use of a Short Educational Video. Journal of Genetic Counseling. 24(3). 473–481. 14 indexed citations

5.

Pyott, Shawna M., Thao Tran, Dru F. Leistritz, et al.. (2013). WNT1 Mutations in Families Affected by Moderately Severe and Progressive Recessive Osteogenesis Imperfecta. The American Journal of Human Genetics. 92(4). 590–597. 170 indexed citations

6.

Mendelsohn, Nancy J., Timothy C. Wood, Rebecca Olson, et al.. (2013). Spondyloepiphyseal Dysplasias and Bilateral Legg-Calvé-Perthes Disease: Diagnostic Considerations for Mucopolysaccharidoses. JIMD Reports. 11. 125–132. 16 indexed citations

7.

Gandomi, Stephanie, Kelly Gonzalez, Layla Shahmirzadi, et al.. (2013). Diagnostic Exome Sequencing Identifies Two Novel IQSEC2 Mutations Associated with X‐Linked Intellectual Disability with Seizures: Implications for Genetic Counseling and Clinical Diagnosis. Journal of Genetic Counseling. 23(3). 289–298. 35 indexed citations

8.

Temme, Renee, Jennifer Roggenbuck, & John McNamara. (2012). CF versus CRMS: diagnostic challenges in cystic fibrosis.. PubMed. 95(10). 42–4. 1 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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