Kelly Arndt

572 total citations
17 papers, 378 citations indexed

About

Kelly Arndt is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Kelly Arndt has authored 17 papers receiving a total of 378 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Hematology. Recurrent topics in Kelly Arndt's work include Genetics and Neurodevelopmental Disorders (4 papers), Epigenetics and DNA Methylation (4 papers) and Acute Myeloid Leukemia Research (3 papers). Kelly Arndt is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Epigenetics and DNA Methylation (4 papers) and Acute Myeloid Leukemia Research (3 papers). Kelly Arndt collaborates with scholars based in United States, Canada and Brazil. Kelly Arndt's co-authors include Maria de Fátima Bonaldo, Marcelo B. Soares, Veena Rajaram, Tadanori Tomita, Hehuang Xie, Soma Das, Min Wang, Stewart Goldman, Daniela del Gaudio and Alexandre Lima de Andrade and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Blood.

In The Last Decade

Kelly Arndt

17 papers receiving 373 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kelly Arndt United States	10	255	120	45	45	43	17	378
Ji Yoo Kim Japan	9	321 1.3×	62 0.5×	74 1.6×	34 0.8×	37 0.9×	13	446
Fatima Amor France	9	430 1.7×	75 0.6×	24 0.5×	30 0.7×	24 0.6×	10	474
Bin Mao China	12	143 0.6×	55 0.5×	47 1.0×	34 0.8×	14 0.3×	24	262
Borko Tanasijevic Canada	14	500 2.0×	67 0.6×	113 2.5×	21 0.5×	65 1.5×	17	599
Annouck Luyten United States	9	361 1.4×	149 1.2×	24 0.5×	112 2.5×	112 2.6×	9	470
Bert Eussen Netherlands	11	317 1.2×	92 0.8×	11 0.2×	28 0.6×	109 2.5×	18	569
Jessica Herbst Germany	8	201 0.8×	93 0.8×	35 0.8×	33 0.7×	92 2.1×	10	353
Irène Aksoy France	11	571 2.2×	88 0.7×	19 0.4×	51 1.1×	85 2.0×	17	671
Dave P. Witte United States	8	233 0.9×	45 0.4×	51 1.1×	29 0.6×	51 1.2×	10	390
Dongmin Gu United States	12	356 1.4×	44 0.4×	37 0.8×	85 1.9×	48 1.1×	16	419

Countries citing papers authored by Kelly Arndt

Since Specialization

Citations

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

Fields of papers citing papers by Kelly Arndt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kelly Arndt

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

All Works

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17 of 17 papers shown

Setia, Namrata, Daniela del Gaudio, Kelly Arndt, et al.. (2023). A novel telomere biology disease‐associated gastritis identified through a whole exome sequencing‐driven approach. The Journal of Pathology Clinical Research. 10(1). e349–e349. 1 indexed citations

Petras, Kristin, Kelly Arndt, Pankhuri Wanjari, et al.. (2022). Feasibility and limitations of cultured skin fibroblasts for germline genetic testing in hematologic disorders. Human Mutation. 43(7). 950–962. 17 indexed citations

Petras, Kristin, Kelly Arndt, Pankhuri Wanjari, et al.. (2020). Assessing the Feasibility and Limitations of Cultured Skin Fibroblasts for Germline Genetic Testing in Hematologic Disorders. Blood. 136(Supplement 1). 35–36. 2 indexed citations

Leonard, Jacqueline, et al.. (2020). Further delineation of a recognizable type of syndromic short stature caused by biallelic SEMA3A loss‐of‐function variants. American Journal of Medical Genetics Part A. 185(3). 889–893. 3 indexed citations

Sun, Miao, Amy Knight Johnson, Viswateja Nelakuditi, et al.. (2018). Targeted exome analysis identifies the genetic basis of disease in over 50% of patients with a wide range of ataxia-related phenotypes. Genetics in Medicine. 21(1). 195–206. 49 indexed citations

Guidugli, Lucia, Amy Knight Johnson, Gorka Alkorta‐Aranburu, et al.. (2017). Clinical utility of gene panel-based testing for hereditary myelodysplastic syndrome/acute leukemia predisposition syndromes. Leukemia. 31(5). 1226–1229. 32 indexed citations

Sanyoura, May, Laura M. Jacobsen, David Carmody, et al.. (2017). Pancreatic Histopathology of Human Monogenic Diabetes Due to Causal Variants in KCNJ11, HNF1A, GATA6, and LMNA. The Journal of Clinical Endocrinology & Metabolism. 103(1). 35–45. 16 indexed citations

Johnson, Amy E. Knight, Lucia Guidugli, Kelly Arndt, et al.. (2015). Identification of Genetic Hereditary Predisposition to Hematologic Malignancies By Clinical Next-Generation Sequencing. Blood. 126(23). 3854–3854. 1 indexed citations

Arndt, Kelly, Soma Das, Elliott Mark Weiss, et al.. (2015). Compound heterozygote CDK5RAP2 mutations in a Guatemalan/Honduran child with autosomal recessive primary microcephaly, failure to thrive and speech delay. American Journal of Medical Genetics Part A. 167(6). 1414–1417. 4 indexed citations

10.

Tan, Christopher, Scott Topper, Daniela del Gaudio, et al.. (2015). Characterization of patients referred for non‐specific intellectual disability testing: the importance of autosomal genes for diagnosis. Clinical Genetics. 89(4). 478–483. 11 indexed citations

11.

Tan, Christopher, et al.. (2013). The first case of CDK5RAP2-related primary microcephaly in a non-consanguineous patient identified by next generation sequencing. Brain and Development. 36(4). 351–355. 25 indexed citations

12.

Tan, Christopher, Kelly Arndt, Dorothy K. Grange, et al.. (2013). Copy number analysis of NIPBL in a cohort of 510 patients reveals rare copy number variants and a mosaic deletion. Molecular Genetics & Genomic Medicine. 2(2). 115–123. 7 indexed citations

13.

Xie, Hong, Alexandre Lima de Andrade, Vasiliy Galat, et al.. (2013). Genome-wide quantitative assessment of variation in DNA methylation patterns. Nucleic Acids Research. 41(14). 7184–7184. 8 indexed citations

14.

Gaudio, Daniela del, et al.. (2013). Analysis of ASPM in an ethnically diverse cohort of 400 patient samples: perspectives of the molecular diagnostic laboratory. Clinical Genetics. 85(4). 353–358. 9 indexed citations

15.

Xie, Hehuang, Min Wang, Alexandre Lima de Andrade, et al.. (2011). Genome-wide quantitative assessment of variation in DNA methylation patterns. Nucleic Acids Research. 39(10). 4099–4108. 78 indexed citations

16.

Xie, Hehuang, Min Wang, Maria de Fátima Bonaldo, et al.. (2010). Epigenomic analysis of Alu repeats in human ependymomas. Proceedings of the National Academy of Sciences. 107(15). 6952–6957. 51 indexed citations

17.

Costa, Fabrício F., Elisabeth A. Seftor, Jared M. Bischof, et al.. (2009). Epigenetically Reprogramming Metastatic Tumor Cells With An Embryonic Microenvironment. Epigenomics. 1(2). 387–398. 64 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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