Kelli Sumner

467 total citations
15 papers, 292 citations indexed

About

Kelli Sumner is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Kelli Sumner has authored 15 papers receiving a total of 292 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 4 papers in Genetics and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Kelli Sumner's work include Pulmonary Hypertension Research and Treatments (4 papers), RNA and protein synthesis mechanisms (3 papers) and Molecular Biology Techniques and Applications (2 papers). Kelli Sumner is often cited by papers focused on Pulmonary Hypertension Research and Treatments (4 papers), RNA and protein synthesis mechanisms (3 papers) and Molecular Biology Techniques and Applications (2 papers). Kelli Sumner collaborates with scholars based in United States, Ireland and Germany. Kelli Sumner's co-authors include D. Hunter Best, C. Gregory Elliott, Pınar Bayrak‐Toydemir, Lynette Brown, Elaine Lyon, Rong Mao, Geneviève Pont-Kingdon, Kevin O. Leslie, Ivan M. Robbins and Wendy K. Chung and has published in prestigious journals such as CHEST Journal, Clinical Chemistry and Human Mutation.

In The Last Decade

Kelli Sumner

15 papers receiving 288 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kelli Sumner United States	7	173	73	70	68	58	15	292
Alan T. Nurden France	7	73 0.4×	47 0.6×	28 0.4×	98 1.4×	29 0.5×	7	312
Ferrin C. Wheeler United States	7	65 0.4×	82 1.1×	29 0.4×	178 2.6×	63 1.1×	16	314
Takashi Aurues Japan	14	120 0.7×	47 0.6×	9 0.1×	99 1.5×	156 2.7×	17	372
Cassandra P. Loren United States	7	36 0.2×	68 0.9×	96 1.4×	111 1.6×	31 0.5×	8	342
A Hornkohl United States	9	86 0.5×	59 0.8×	122 1.7×	25 0.4×	16 0.3×	10	419
Aimin Dang China	11	200 1.2×	49 0.7×	19 0.3×	60 0.9×	62 1.1×	23	295
Adeline Blandinières France	11	73 0.4×	16 0.2×	45 0.6×	113 1.7×	49 0.8×	20	261
Alexandra N. Modiri United States	4	196 1.1×	119 1.6×	13 0.2×	73 1.1×	81 1.4×	11	410
Émilie Groyer France	9	59 0.3×	23 0.3×	22 0.3×	67 1.0×	54 0.9×	12	329
AB Kelly United States	8	124 0.7×	130 1.8×	78 1.1×	27 0.4×	80 1.4×	9	497

Countries citing papers authored by Kelli Sumner

Since Specialization

Citations

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

Fields of papers citing papers by Kelli Sumner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kelli Sumner

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

All Works

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15 of 15 papers shown

Tian, Wei, et al.. (2018). An investigation of PIK3CA mutations in isolated macrodactyly. Journal of Hand Surgery (European Volume). 43(7). 756–760. 19 indexed citations

Day, Ronald W., et al.. (2016). Pulmonary veno-occlusive disease: Two children with gradual disease progression. Respiratory Medicine Case Reports. 20. 82–86. 2 indexed citations

Best, D. Hunter, Kelli Sumner, Benjamin P. Smith, et al.. (2016). EIF2AK4 Mutations in Patients Diagnosed With Pulmonary Arterial Hypertension. CHEST Journal. 151(4). 821–828. 51 indexed citations

McGovern, Eiméar, Paul McNally, Maureen J. O’Sullivan, et al.. (2015). Infantile pulmonary capillary haemangiomatosis: a lethal form of pulmonary hypertension. Cardiology in the Young. 26(4). 663–668. 1 indexed citations

Sumner, Kelli, Jeffrey Swensen, Melinda Procter, et al.. (2014). Noncontinuously Binding Loop-Out Primers for Avoiding Problematic DNA Sequences in PCR and Sanger Sequencing. Journal of Molecular Diagnostics. 16(5). 477–480. 3 indexed citations

Best, D. Hunter, Kelli Sumner, Eric D. Austin, et al.. (2013). EIF2AK4 Mutations in Pulmonary Capillary Hemangiomatosis. CHEST Journal. 145(2). 231–236. 135 indexed citations

Sumner, Kelli, Geneviève Pont-Kingdon, Andrew Wilson, et al.. (2012). Validation of an Unlabeled Probe Melting Analysis Assay Combined with High-Throughput Extractions for Genotyping of the Most Common Variants in HFE -Associated Hereditary Hemochromatosis, C282Y, H63D, and S65C. Genetic Testing and Molecular Biomarkers. 16(7). 656–660. 2 indexed citations

Wooderchak‐Donahue, Whitney, Cecily P. Vaughn, Lan‐Szu Chou, et al.. (2011). Verification of Multiplex Ligation-Dependent Probe Amplification Probes in the Absence of Positive Samples. Genetic Testing and Molecular Biomarkers. 15(11). 793–799. 1 indexed citations

Svensson, Annika, Lan‐Szu Chou, Cindy Meadows, et al.. (2011). Implementation of a Cost-Effective Unlabeled Probe High-Resolution Melt Assay for Genotyping of Factor V Leiden. Genetic Testing and Molecular Biomarkers. 15(4). 207–213. 2 indexed citations

10.

Sumner, Kelli, et al.. (2011). The SPRED1 Variants Repository for Legius Syndrome. G3 Genes Genomes Genetics. 1(6). 451–456. 11 indexed citations

11.

Crockett, David K., et al.. (2010). The Alport syndrome COL4A5 variant database. Human Mutation. 31(8). E1652–E1657. 35 indexed citations

12.

Pont-Kingdon, Geneviève, Kelli Sumner, Friederike Gedge, et al.. (2009). Molecular testing for adult type Alport syndrome. BMC Nephrology. 10(1). 38–38. 11 indexed citations

13.

Bohnsack, John F., Kelli Sumner, April Whiting, et al.. (2009). Lack of association between beta 2‐adrenergic receptor polymorphisms and juvenile idiopathic arthritis. Scandinavian Journal of Rheumatology. 38(2). 91–95. 4 indexed citations

14.

Pont-Kingdon, Geneviève, Rebecca L. Margraf, Kelli Sumner, et al.. (2008). Design and Application of Noncontinuously Binding Probes Used for Haplotyping and Genotyping. Clinical Chemistry. 54(6). 990–999. 6 indexed citations

15.

Pont-Kingdon, Geneviève, Lan‐Szu Chou, Kristy Damjanovich, et al.. (2007). Multiplex Genotyping by Melting Analysis of Loci-Spanning Probes: β-globin as an Example. BioTechniques. 42(2). 193–197. 9 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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