Kelly Arndt

572 citations

17 papers · 378 indexed · h-index 10

Co-authors: Marcelo B. Soares Maria de Fátima Bonaldo Veena Rajaram Soma Das Stewart Goldman Min Wang Hehuang Xie Tadanori Tomita
Topics: Genetics and Neurodevelopmental Disorders (4 papers)Epigenetics and DNA Methylation (4 papers)Acute Myeloid Leukemia Research (3 papers)
Cited by: Genetics Hematology Molecular Biology
Journals: Proceedings of the National Academy of Sciences Nucleic Acids Research Blood
Partner nations: United States Canada Brazil

In The Last Decade

Kelly Arndt

17 papers receiving 373 citations

Peers

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

#	Work	Indexed citations
1	A novel telomere biology disease‐associated gastritis identified through a whole exome sequencing‐driven approach 2023 ·The Journal of Pathology Clinical Research ·Namrata Setia,Daniela del Gaudio,(unknown),Kelly Arndt,Melissa Y. Tjota,Peng Wang,Jeremy P. Segal,(unknown),John Hart	1
2	Feasibility and limitations of cultured skin fibroblasts for germline genetic testing in hematologic disorders 2022 ·Human Mutation ·(unknown),(unknown),Kristin Petras,Kelly Arndt,(unknown),Pankhuri Wanjari,(unknown),David M. Montes,James McElherne,(unknown),(unknown),Soma Das,Lucy A. Godley,Jeremy Segal,Daniela del Gaudio,Carrie Fitzpatrick,Jane E. Churpek	17
3	Assessing the Feasibility and Limitations of Cultured Skin Fibroblasts for Germline Genetic Testing in Hematologic Disorders 2020 ·Blood ·(unknown),(unknown),Kristin Petras,Kelly Arndt,(unknown),Pankhuri Wanjari,(unknown),David M. Montes,Soma Das,Lucy A. Godley,Jeremy Segal,Daniela del Gaudio,Carrie Fitzpatrick,Jane E. Churpek	2
4	Further delineation of a recognizable type of syndromic short stature caused by biallelic SEMA3A loss‐of‐function variants 2020 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),Jacqueline Leonard,Louise C. Pyle,(unknown),Kelly Arndt,Colin P. Hawkes,Daniela del Gaudio	3
5	Targeted exome analysis identifies the genetic basis of disease in over 50% of patients with a wide range of ataxia-related phenotypes 2018 ·Genetics in Medicine ·Miao Sun,Amy Knight Johnson,Viswateja Nelakuditi,Lucia Guidugli,David S. Fischer,Kelly Arndt,Lan Ma,Erin Sandford,Vikram G. Shakkottai,Kym M. Boycott,Jodi Warman‐Chardon,Zejuan Li,Daniela del Gaudio,Margit Burmeister,Christopher M. Gómez,Darrel Waggoner,Soma Das	49
6	Clinical utility of gene panel-based testing for hereditary myelodysplastic syndrome/acute leukemia predisposition syndromes 2017 ·Leukemia ·Lucia Guidugli,Amy Knight Johnson,Gorka Alkorta‐Aranburu,Viswateja Nelakuditi,Kelly Arndt,Jane E. Churpek,Lucy A. Godley,(unknown),Neal S. Young,Carrie Fitzpatrick,Daniela del Gaudio,Soma Das,(unknown)	32
7	Pancreatic Histopathology of Human Monogenic Diabetes Due to Causal Variants in KCNJ11, HNF1A, GATA6, and LMNA 2017 ·The Journal of Clinical Endocrinology & Metabolism ·May Sanyoura,Laura M. Jacobsen,David Carmody,Daniela del Gaudio,Gorka Alkorta‐Aranburu,Kelly Arndt,(unknown),(unknown),Irina Kusmartseva,Mark A. Atkinson,Louis H. Philipson,Desmond Schatz,Martha Campbell‐Thompson,Siri Atma W. Greeley	16
8	Identification of Genetic Hereditary Predisposition to Hematologic Malignancies By Clinical Next-Generation Sequencing 2015 ·Blood ·Amy E. Knight Johnson,Lucia Guidugli,Kelly Arndt,Gorka Alkorta‐Aranburu,Viswateja Nelakuditi,Jane E. Churpek,Lucy A. Godley,Daniela del Gaudio,Soma Das,Zejuan Li	1
9	Compound heterozygote CDK5RAP2 mutations in a Guatemalan/Honduran child with autosomal recessive primary microcephaly, failure to thrive and speech delay 2015 ·American Journal of Medical Genetics Part A ·(unknown),Kelly Arndt,Soma Das,Elliott Mark Weiss,Yaning Wu,(unknown),Karuna Shekdar,Elaine H. Zackai	4
10	Characterization of patients referred for non‐specific intellectual disability testing: the importance of autosomal genes for diagnosis 2015 ·Clinical Genetics ·Christopher Tan,Scott Topper,Daniela del Gaudio,Viswateja Nelakuditi,(unknown),Małgorzata J.M. Nowaczyk,Susan Zeesman,Lauren Brady,Laura Russell,Naomi Meeks,(unknown),Kelly Arndt,(unknown),(unknown),Soma Das	11
11	The first case of CDK5RAP2-related primary microcephaly in a non-consanguineous patient identified by next generation sequencing 2013 ·Brain and Development ·Christopher Tan,Scott Topper,(unknown),Jennifer Stein,(unknown),Kelly Arndt,Soma Das	25
12	Genome-wide quantitative assessment of variation in DNA methylation patterns 2013 ·Nucleic Acids Research ·Hong Xie,(unknown),Alexandre Lima de Andrade,(unknown),Vasiliy Galat,Kelly Arndt,Veena Rajaram,Stephen L. Goldman,Taketeru Tomita,MA Soares	8
13	Copy number analysis of NIPBL in a cohort of 510 patients reveals rare copy number variants and a mosaic deletion 2013 ·Molecular Genetics & Genomic Medicine ·(unknown),Christopher Tan,(unknown),Kelly Arndt,(unknown),Dorothy K. Grange,Beth A. Kozel,Nathaniel H. Robin,Darrel Waggoner,Carrie Fitzpatrick,Soma Das,Daniela del Gaudio	7
14	Analysis of ASPM in an ethnically diverse cohort of 400 patient samples: perspectives of the molecular diagnostic laboratory 2013 ·Clinical Genetics ·(unknown),Daniela del Gaudio,Melissa A Dempsey,Kelly Arndt,(unknown),(unknown),Soma Das	9
15	Genome-wide quantitative assessment of variation in DNA methylation patterns 2011 ·Nucleic Acids Research ·Hehuang Xie,Min Wang,Alexandre Lima de Andrade,Maria de Fátima Bonaldo,Vasiliy Galat,Kelly Arndt,Veena Rajaram,Stewart Goldman,Tadanori Tomita,Marcelo B. Soares	78
16	Epigenomic analysis of Alu repeats in human ependymomas 2010 ·Proceedings of the National Academy of Sciences ·Hehuang Xie,Min Wang,Maria de Fátima Bonaldo,Veena Rajaram,(unknown),Christina Smith,Kelly Arndt,Stewart Goldman,Tadanori Tomita,Marcelo B. Soares	51
17	Epigenetically Reprogramming Metastatic Tumor Cells With An Embryonic Microenvironment 2009 ·Epigenomics ·Fabrício F. Costa,Elisabeth A. Seftor,Jared M. Bischof,Dawn A. Kirschmann,Luigi Strizzi,Kelly Arndt,Maria de Fátima Bonaldo,Marcelo B. Soares,Mary J.C. Hendrix	64

About Kelly Arndt

Kelly Arndt is a scholar working on Hematology, Genetics and Cancer Research, having authored 17 papers that have together received 378 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (4 papers), Epigenetics and DNA Methylation (4 papers) and Acute Myeloid Leukemia Research (3 papers). The work is most often cited by research in Genetics (120 citations), Hematology (45 citations) and Molecular Biology (255 citations). Kelly Arndt has collaborated with scholars based in United States, Canada and Brazil. Frequent co-authors include Marcelo B. Soares, Maria de Fátima Bonaldo, Veena Rajaram, Soma Das, Stewart Goldman, Min Wang, Hehuang Xie, Tadanori Tomita, Daniela del Gaudio and Alexandre Lima de Andrade. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Blood.

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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