Tara Newcomb

1.3k total citations
12 papers, 454 citations indexed

About

Tara Newcomb is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Tara Newcomb has authored 12 papers receiving a total of 454 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Genetics. Recurrent topics in Tara Newcomb's work include Neurogenetic and Muscular Disorders Research (4 papers), RNA modifications and cancer (3 papers) and Mitochondrial Function and Pathology (3 papers). Tara Newcomb is often cited by papers focused on Neurogenetic and Muscular Disorders Research (4 papers), RNA modifications and cancer (3 papers) and Mitochondrial Function and Pathology (3 papers). Tara Newcomb collaborates with scholars based in United States and Italy. Tara Newcomb's co-authors include Kathryn J. Swoboda, Matthew Sweney, Russell J. Butterfield, Diane M. Dunn, Marcia L. Feldkamp, Robert B. Weiss, Katie Mayne, Nicholas E. Johnson, Brett Duval and Aga Lewelt and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Neurology.

In The Last Decade

Tara Newcomb

12 papers receiving 445 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tara Newcomb United States	10	263	119	116	101	63	12	454
Claudia Castiglioni Chile	15	320 1.2×	111 0.9×	125 1.1×	125 1.2×	61 1.0×	47	566
C. Ortez Spain	15	422 1.6×	146 1.2×	118 1.0×	121 1.2×	92 1.5×	76	691
Soledad Monges Argentina	12	360 1.4×	110 0.9×	52 0.4×	109 1.1×	39 0.6×	28	509
Hernán Gonorazky Canada	12	532 2.0×	76 0.6×	182 1.6×	208 2.1×	33 0.5×	43	710
Adnan Manzur United Kingdom	13	453 1.7×	74 0.6×	55 0.5×	126 1.2×	39 0.6×	37	588
Monica Traverso Italy	13	348 1.3×	66 0.6×	122 1.1×	30 0.3×	16 0.3×	32	488
Sandra Whalen France	13	268 1.0×	59 0.5×	157 1.4×	41 0.4×	20 0.3×	28	417
Krzysztof Szczałuba Poland	15	328 1.2×	63 0.5×	369 3.2×	37 0.4×	26 0.4×	57	638
Laurence E. Walsh United States	11	214 0.8×	114 1.0×	191 1.6×	21 0.2×	159 2.5×	32	598
Gabriele Gillessen‐Kaesbach Germany	15	337 1.3×	84 0.7×	471 4.1×	80 0.8×	63 1.0×	23	753

Countries citing papers authored by Tara Newcomb

Since Specialization

Citations

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

Fields of papers citing papers by Tara Newcomb

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tara Newcomb

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

All Works

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12 of 12 papers shown

Johnson, Nicholas E., Russell J. Butterfield, Katie Mayne, et al.. (2021). Population-Based Prevalence of Myotonic Dystrophy Type 1 Using Genetic Analysis of Statewide Blood Screening Program. Neurology. 96(7). e1045–e1053. 85 indexed citations

Butterfield, Russell J., Katie Mayne, Tara Newcomb, et al.. (2021). High throughput screening for expanded CTG repeats in myotonic dystrophy type 1 using melt curve analysis. Molecular Genetics & Genomic Medicine. 9(4). e1619–e1619. 3 indexed citations

Ho, Karen S., Lenora M. Olson, Xiaoming Sheng, et al.. (2018). A survey of antiepileptic drug responses identifies drugs with potential efficacy for seizure control in Wolf–Hirschhorn syndrome. Epilepsy & Behavior. 81. 55–61. 10 indexed citations

Ostrander, Betsy, Russell J. Butterfield, Brent S. Pedersen, et al.. (2018). Whole-genome analysis for effective clinical diagnosis and gene discovery in early infantile epileptic encephalopathy. npj Genomic Medicine. 3(1). 22–22. 54 indexed citations

Margraf, Rebecca L., Jacob Durtschi, Bryan L. Krock, et al.. (2018). Novel PLP1 Mutations Identified With Next-Generation Sequencing Expand the Spectrum of PLP1-Associated Leukodystrophy Clinical Phenotypes. SHILAP Revista de lepidopterología. 5. 2329048X18789282–2329048X18789282. 2 indexed citations

Zaworski, Phillip G., Katharine M. von Herrmann, Sara Sunshine, et al.. (2016). SMN Protein Can Be Reliably Measured in Whole Blood with an Electrochemiluminescence (ECL) Immunoassay: Implications for Clinical Trials. PLoS ONE. 11(3). e0150640–e0150640. 33 indexed citations

Bend, Eric G., Yue Si, David A. Stevenson, et al.. (2016). NALCN channelopathies. Neurology. 87(11). 1131–1139. 29 indexed citations

Rothwell, Erin, et al.. (2014). Perceptions of Equine-Assisted Activities and Therapies by Parents and Children With Spinal Muscular Atrophy. Pediatric Physical Therapy. 26(2). 237–244. 22 indexed citations

Butterfield, Russell J., Tamara J. Stevenson, Lingyan Xing, et al.. (2014). Congenital lethal motor neuron disease with a novel defect in ribosome biogenesis. Neurology. 82(15). 1322–1330. 43 indexed citations

10.

Sweney, Matthew, Tara Newcomb, & Kathryn J. Swoboda. (2014). The Expanding Spectrum of Neurological Phenotypes in Children With ATP1A3 Mutations, Alternating Hemiplegia of Childhood, Rapid-onset Dystonia-Parkinsonism, CAPOS and Beyond. Pediatric Neurology. 52(1). 56–64. 96 indexed citations

11.

Swoboda, Kathryn J., Rebecca L. Margraf, John C. Carey, et al.. (2013). A novel germline PIGA mutation in Ferro‐Cerebro‐Cutaneous syndrome: A neurodegenerative X‐linked epileptic encephalopathy with systemic iron‐overload. American Journal of Medical Genetics Part A. 164(1). 17–28. 51 indexed citations

12.

Lewelt, Aga, Tara Newcomb, & Kathryn J. Swoboda. (2011). New Therapeutic Approaches to Spinal Muscular Atrophy. Current Neurology and Neuroscience Reports. 12(1). 42–53. 26 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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