Kendra Engleman

540 total citations
6 papers, 26 citations indexed

About

Kendra Engleman is a scholar working on Oncology, Molecular Biology and Genetics. According to data from OpenAlex, Kendra Engleman has authored 6 papers receiving a total of 26 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Oncology, 2 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Kendra Engleman's work include Genomics and Rare Diseases (2 papers), Peptidase Inhibition and Analysis (2 papers) and Barrier Structure and Function Studies (1 paper). Kendra Engleman is often cited by papers focused on Genomics and Rare Diseases (2 papers), Peptidase Inhibition and Analysis (2 papers) and Barrier Structure and Function Studies (1 paper). Kendra Engleman collaborates with scholars based in United States and France. Kendra Engleman's co-authors include Carol Saunders, Maxime Cadieux‐Dion, Isabelle Thiffault, Lee Zellmer, Emily Farrow, Elena Repnikova, Shivarajan Amudhavalli, Pierre‐Emmanuel Gleizes, Marie-Françoise O’Donohue and Nikita Raje and has published in prestigious journals such as Human Mutation, Clinical Genetics and American Journal of Medical Genetics Part A.

In The Last Decade

Kendra Engleman

6 papers receiving 26 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kendra Engleman United States	4	16	12	5	5	4	6	26
Anand Vasudevan Australia	3	14 0.9×	9 0.8×	5 1.0×	5 1.0×		5	36
Deirdre Donnelly United Kingdom	3	27 1.7×	7 0.6×	2 0.4×	2 0.4×	4 1.0×	4	38
Longquan Quan China	4	23 1.4×	8 0.7×	3 0.6×	6 1.2×		5	36
Hannah J. Perrin United States	2	18 1.1×	8 0.7×	2 0.4×	3 0.6×	2 0.5×	3	27
Giselle Kerry United Kingdom	2	10 0.6×	14 1.2×	3 0.6×	4 0.8×		3	24
Sadegheh Haghshenas Canada	4	33 2.1×	16 1.3×	3 0.6×	2 0.4×	2 0.5×	9	45
Cecilia Rivas United States	3	31 1.9×	6 0.5×	5 1.0×	2 0.4×	2 0.5×	3	40
Kerri McGreal United States	3	19 1.2×	20 1.7×	3 0.6×	2 0.4×	6 1.5×	4	32
Edward J. Higginbotham Canada	4	19 1.2×	28 2.3×	4 0.8×	2 0.4×	5 1.3×	6	44
Randa Bassiouni Egypt	4	19 1.2×	15 1.3×	2 0.4×	4 0.8×	2 0.5×	7	36

Countries citing papers authored by Kendra Engleman

Since Specialization

Citations

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

Fields of papers citing papers by Kendra Engleman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kendra Engleman

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

All Works

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6 of 6 papers shown

1.

Cadieux‐Dion, Maxime, Emily Farrow, Isabelle Thiffault, et al.. (2022). Phenotypic expansion and variable expressivity in individuals with JARID2 ‐related intellectual disability: A case series. Clinical Genetics. 102(2). 136–141. 2 indexed citations

2.

Lebaron, Simon, Marie-Françoise O’Donohue, Kendra Engleman, et al.. (2021). Functionally impaired RPL8 variants associated with Diamond–Blackfan anemia and a Diamond–Blackfan anemia‐like phenotype. Human Mutation. 43(3). 389–402. 5 indexed citations

3.

Chen, Dong, Eric T. Rush, Kendra Engleman, et al.. (2021). A novel likely pathogenic variant in a patient with Hermansky–Pudlak syndrome. Molecular Case Studies. 7(5). a006110–a006110. 1 indexed citations

4.

Cadieux‐Dion, Maxime, Susan Hughes, Kendra Engleman, Eric T. Rush, & Carol Saunders. (2021). Nager syndrome in patient lacking acrofacial dysostosis: Expanding the phenotypic spectrum of SF3B4‐related disease. American Journal of Medical Genetics Part A. 185(5). 1515–1518. 6 indexed citations

5.

Cadieux‐Dion, Maxime, Nicole P. Safina, Kendra Engleman, et al.. (2018). Novel heterozygous pathogenic variants in CHUK in a patient with AEC-like phenotype, immune deficiencies and 1q21.1 microdeletion syndrome: a case report. BMC Medical Genetics. 19(1). 41–41. 6 indexed citations

6.

Grote, Lauren, Isabelle Thiffault, Emily Farrow, et al.. (2018). Incidental diagnosis of tuberous sclerosis complex by exome sequencing in three families with subclinical findings. Neurogenetics. 19(3). 205–213. 6 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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