Kathryn Singh

783 total citations
16 papers, 350 citations indexed

About

Kathryn Singh is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Kathryn Singh has authored 16 papers receiving a total of 350 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Surgery. Recurrent topics in Kathryn Singh's work include Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic factors in colorectal cancer (2 papers). Kathryn Singh is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic factors in colorectal cancer (2 papers). Kathryn Singh collaborates with scholars based in United States and United Kingdom. Kathryn Singh's co-authors include Virginia Kimonis, Nandini Kundu, Angelika Brekman, Alla Polotskaia, Jill Bargonetti, Jason A. Zell, Michael J. Stamos, Thomas H. Taylor, Ruth Dworsky and Laurence N. Kolonel and has published in prestigious journals such as Breast Cancer Research, Genetics in Medicine and Pediatric Pulmonology.

In The Last Decade

Kathryn Singh

16 papers receiving 338 citations

Peers

Kathryn Singh

ONCOL

GENET

PFM

SURGE

J. Hunn United States

Geriolda Topi Sweden

M. Navarro Spain

Shi Yang China

Jonathan Evans United Kingdom

Chieko Tamura Japan

Liang Zhuang China

Junqi Wang China

Luciano Mariani Italy

J. Hunn United States

Kathryn Singh

130 ×0.9

86 ×0.7

ONCOL

54 ×0.7

GENET

36 ×0.5

PFM

29 ×0.7

SURGE

Citations per year, relative to Kathryn Singh Kathryn Singh (= 1×) peers J. Hunn

Countries citing papers authored by Kathryn Singh

Since Specialization

Citations

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

Fields of papers citing papers by Kathryn Singh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kathryn Singh

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

All Works

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16 of 16 papers shown

Platt, Julia, et al.. (2024). Analysis of financial barriers experienced by prospective genetic counseling students. Genetics in Medicine. 26(11). 101175–101175. 1 indexed citations

Culver, Julie O., Yuxi Liu, Charité Ricker, et al.. (2023). Clinical implications of conflicting variant interpretations in the cancer genetics clinic. Genetics in Medicine. 25(7). 100837–100837. 3 indexed citations

Singh, Kathryn, et al.. (2023). Non-mosaic trisomy 22 and congenital heart surgery using the shared decision making model: a case report. BMC Pediatrics. 23(1). 122–122. 1 indexed citations

Haanpää, Maria K., Bobby G. Ng, Natalie M. Gallant, et al.. (2019). ALG11‐CDG syndrome: Expanding the phenotype. American Journal of Medical Genetics Part A. 179(3). 498–502. 12 indexed citations

Powis, Zöe, Kelly D. Farwell Hagman, Kirsten Blanco, et al.. (2019). When moments matter: Finding answers with rapid exome sequencing. Molecular Genetics & Genomic Medicine. 8(2). e1027–e1027. 9 indexed citations

Singh, Kathryn, et al.. (2018). Orbital infections: a complete cycle 7-year audit and a management guideline. European Archives of Oto-Rhino-Laryngology. 275(8). 2079–2088. 2 indexed citations

Freeman, Rebecca, et al.. (2017). Two cases of Legg–Perthes and intellectual disability in Tricho–Rhino–Phalangeal syndrome type 1 associated with novel TRPS1 mutations. American Journal of Medical Genetics Part A. 173(6). 1663–1667. 8 indexed citations

Mullegama, Sureni V., Steven D. Klein, T. Niroshini Senaratne, et al.. (2017). De novo loss‐of‐function variants in STAG2 are associated with developmental delay, microcephaly, and congenital anomalies. American Journal of Medical Genetics Part A. 173(5). 1319–1327. 36 indexed citations

Singh, Kathryn, et al.. (2014). Colorectal Cancer Incidence Among Young Adults in California. Journal of Adolescent and Young Adult Oncology. 3(4). 176–184. 62 indexed citations

10.

Singh, Kathryn, et al.. (2014). Amelioration of the typical cognitive phenotype in a patient with the 5pter deletion associated with Cri‐du‐chat syndrome in addition to a partial duplication of CTNND2. American Journal of Medical Genetics Part A. 164(7). 1761–1764. 20 indexed citations

11.

Nussbaum, Eliezer, et al.. (2013). Diagnosis of cystic fibrosis in the kindred of an infant with CFTR‐related metabolic syndrome: Importance of follow‐up that includes monitoring sweat chloride concentrations over time. Pediatric Pulmonology. 49(3). E103–8. 8 indexed citations

12.

Kimonis, Virginia, et al.. (2012). Clinical and radiological features in young individuals with nevoid basal cell carcinoma syndrome. Genetics in Medicine. 15(1). 79–83. 32 indexed citations

13.

Lin, Angela E., et al.. (2011). An additional patient with mycophenolate mofetil embryopathy: Cardiac and facial analyses. American Journal of Medical Genetics Part A. 155(4). 748–756. 32 indexed citations

14.

Brekman, Angelika, Kathryn Singh, Alla Polotskaia, Nandini Kundu, & Jill Bargonetti. (2011). A p53-independent role of Mdm2 in estrogen-mediated activation of breast cancer cell proliferation. Breast Cancer Research. 13(1). R3–R3. 69 indexed citations

15.

Henderson, B. E., et al.. (1985). Cancer incidence in the islands of the Pacific.. PubMed. 69. 73–81. 47 indexed citations

16.

Hp, Lee, C Cuello, & Kathryn Singh. (1982). Review of the epidemiology of cervical cancer in the Pacific Basin.. PubMed. 62. 197–9. 8 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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