Lemuel J. Pelentsov

826 total citations
21 papers, 518 citations indexed

About

Lemuel J. Pelentsov is a scholar working on General Health Professions, Genetics and Speech and Hearing. According to data from OpenAlex, Lemuel J. Pelentsov has authored 21 papers receiving a total of 518 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in General Health Professions, 6 papers in Genetics and 4 papers in Speech and Hearing. Recurrent topics in Lemuel J. Pelentsov's work include Genomics and Rare Diseases (5 papers), Mental Health and Patient Involvement (5 papers) and Adolescent and Pediatric Healthcare (4 papers). Lemuel J. Pelentsov is often cited by papers focused on Genomics and Rare Diseases (5 papers), Mental Health and Patient Involvement (5 papers) and Adolescent and Pediatric Healthcare (4 papers). Lemuel J. Pelentsov collaborates with scholars based in Australia, United Kingdom and Ireland. Lemuel J. Pelentsov's co-authors include Adrian Esterman, Thomas A. Laws, Andrea Fielder, Kate Khair, A. L. Gordon, Ellen Davies, Zlatko Kopecki, Fleur O’Hare, Lauren N. Ayton and Karyn L. Galvin and has published in prestigious journals such as Journal of Clinical Nursing, Orphanet Journal of Rare Diseases and BMC Family Practice.

In The Last Decade

Lemuel J. Pelentsov

18 papers receiving 507 citations

Peers

Lemuel J. Pelentsov
Comparison fields: 5 of 83
  • Genetics 158
  • Clinical Psychology 140
  • Pediatrics, Perinatology and Child Health 131
  • General Health Professions 79
  • Sociology and Political Science 78
Replace Thomas A. Laws with:
Thomas A. Laws Australia
Jeffrey P. Brosco United States
Lauren Mednick United States
Penny Titman United Kingdom
Kate Tsiplova Canada
Lindsay M. Anderson United States
Stephanie Luca Canada
Margaret Sahhar Australia
Catherine A. Perz United States
Christina Grant Canada
Thomas A. Laws Australia View profile →
Citations per field, relative to Lemuel J. Pelentsov
Lemuel J. Pelentsov · 1×
Citations per year, relative to Lemuel J. Pelentsov
Lemuel J. Pelentsov · 1×

Countries citing papers authored by Lemuel J. Pelentsov

Since Specialization
Citations

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

Fields of papers citing papers by Lemuel J. Pelentsov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lemuel J. Pelentsov. 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 Lemuel J. Pelentsov. The network helps show where Lemuel J. Pelentsov may publish in the future.

Co-authorship network of co-authors of Lemuel J. Pelentsov

This figure shows the co-authorship network connecting the top 25 collaborators of Lemuel J. Pelentsov. A scholar is included among the top collaborators of Lemuel J. Pelentsov 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 Lemuel J. Pelentsov. Lemuel J. Pelentsov 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
# Work Indexed citations
1 2
2 0
3 4
4 0
5 1
6 0
7 9
8 6
9 3
10 3
11 18
12 7
13 12
14 19
15 113
16
Informing the midwife on rare genetic disorders and their effects on mothers breastfeeding – a mixed methods study
3
17 196
18 77
19
What are the supportive care needs of parents caring for a child diagnosed with Ectodermal Dysplasia : a rare genetic disorder?
9
20 35

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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