Kate Mowrey

806 total citations
13 papers, 37 citations indexed

About

Kate Mowrey is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Kate Mowrey has authored 13 papers receiving a total of 37 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Oncology and 6 papers in Genetics. Recurrent topics in Kate Mowrey's work include Tuberous Sclerosis Complex Research (4 papers), Polyomavirus and related diseases (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Kate Mowrey is often cited by papers focused on Tuberous Sclerosis Complex Research (4 papers), Polyomavirus and related diseases (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Kate Mowrey collaborates with scholars based in United States and Germany. Kate Mowrey's co-authors include Hope Northrup, Laura S. Farach, David Rodriguez‐Buritica, Mary Kay Koenig, S. Shahrukh Hashmi, Deborah A. Pearson, Pedro Mancías, Steven L. Roberds, Alexander J. Towbin and Jamie K. Capal and has published in prestigious journals such as SHILAP Revista de lepidopterología, Genetics in Medicine and Frontiers in Genetics.

In The Last Decade

Kate Mowrey

8 papers receiving 37 citations

Peers

Kate Mowrey

PHYSI

ONCOL

GENET

EPIDE

Abolfazl Heidari Iran

E. Steve Roach United States

Fatemeh Afrashteh Iran

Tanguy Demaret Belgium

C. Luci Italy

Christine N. Goldfarb United States

Aaina Kochhar United States

Oana Moldovan Portugal

Carolin Sachs United States

Rajendra V. E. Chilukuri United States

Abolfazl Heidari Iran

Kate Mowrey

8 ×0.5

PHYSI

4 ×0.3

ONCOL

17 ×1.5

13 ×1.4

GENET

6 ×0.8

EPIDE

Citations per year, relative to Kate Mowrey Kate Mowrey (= 1×) peers Abolfazl Heidari

Countries citing papers authored by Kate Mowrey

Since Specialization

Citations

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

Fields of papers citing papers by Kate Mowrey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kate Mowrey

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

All Works

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13 of 13 papers shown

Turner, Kelly, et al.. (2023). Malignant Melanoma within a Giant Congenital Melanocytic Nevus in a Pediatric Patient. SKIN The Journal of Cutaneous Medicine. 7(1). 608–611.

Shields, Kathleen, et al.. (2023). Genetics in the NICU: Nurses' Perceived Knowledge and Desired Education. The Journal of Continuing Education in Nursing. 54(1). 16–24. 3 indexed citations

Langley, Elizabeth, Laura S. Farach, Mary Kay Koenig, et al.. (2022). NEXMIF pathogenic variants in individuals of Korean, Vietnamese, and Mexican descent. American Journal of Medical Genetics Part A. 188(6). 1688–1692. 3 indexed citations

Northrup, Hope, et al.. (2022). Identification of a novel microdeletion causative of Nance‐Horan syndrome. Molecular Genetics & Genomic Medicine. 10(3). e1879–e1879. 4 indexed citations

Langley, Elizabeth, Laura S. Farach, & Kate Mowrey. (2022). Case Report: Novel pathogenic variant in NFIX in two sisters with Malan syndrome due to germline mosaicism. Frontiers in Genetics. 13. 1044660–1044660.

Mowrey, Kate, Hope Northrup, S. Shahrukh Hashmi, & David Rodriguez‐Buritica. (2022). Expanding Our Knowledge of Menstrual Irregularities Reported by Females With Tuberous Sclerosis Complex. SHILAP Revista de lepidopterología. 4. 798983–798983.

Mowrey, Kate, et al.. (2022). Metaphyseal Dysplasia, Spahr Type; A Case Report of Variable Expressivity in Non-Consanguineous Filipino Siblings. Journal of Orthopaedic Case Reports. 12(9). 20–25.

Shields, Kathleen, et al.. (2022). eP246: Novel EFTUD2 variant adds to understanding of phenotypic spectrum of mandibulofacial dysostosis with microcephaly. Genetics in Medicine. 24(3). S156–S157.

Koenig, Mary Kay, et al.. (2021). A De Novo case of autosomal dominant mitochondrial membrane protein‐associated neurodegeneration. Molecular Genetics & Genomic Medicine. 9(7). e1706–e1706. 3 indexed citations

10.

Mowrey, Kate, et al.. (2021). Two new reported cases of 16q22.3q23.3 duplication syndrome highlight intrafamilial variability and potential sex expression differences within a rare duplication syndrome. SHILAP Revista de lepidopterología. 9(3). 1629–1633. 3 indexed citations

11.

Mowrey, Kate, Hope Northrup, S. Shahrukh Hashmi, et al.. (2021). Frequency, Progression, and Current Management: Report of 16 New Cases of Nonfunctional Pancreatic Neuroendocrine Tumors in Tuberous Sclerosis Complex and Comparison With Previous Reports. Frontiers in Neurology. 12. 627672–627672. 11 indexed citations

12.

Mowrey, Kate, Mary Kay Koenig, C. Ákos Szabó, et al.. (2020). Two different genetic etiologies for tuberous sclerosis complex (TSC) in a single family. Molecular Genetics & Genomic Medicine. 8(7). e1296–e1296. 4 indexed citations

13.

Mowrey, Kate, Deborah A. Pearson, S. Shahrukh Hashmi, et al.. (2018). The Impact of Psychiatric Symptoms on Tuberous Sclerosis Complex and Utilization of Mental Health Treatment. Pediatric Neurology. 91. 41–49. 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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