Ingrid Tarr

501 total citations
7 papers, 148 citations indexed

About

Ingrid Tarr is a scholar working on Neurology, Genetics and Surgery. According to data from OpenAlex, Ingrid Tarr has authored 7 papers receiving a total of 148 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Neurology, 3 papers in Genetics and 2 papers in Surgery. Recurrent topics in Ingrid Tarr's work include Amyotrophic Lateral Sclerosis Research (4 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Cardiac Structural Anomalies and Repair (2 papers). Ingrid Tarr is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (4 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Cardiac Structural Anomalies and Repair (2 papers). Ingrid Tarr collaborates with scholars based in Australia, United States and South Korea. Ingrid Tarr's co-authors include Kelly L. Williams, Ian P. Blair, Garth A. Nicholson, Dominic B. Rowe, Emily P. McCann, Jennifer A. Fifita, John O’Connor, Denis C. Bauer, Katharine Y. Zhang and Alison Hogan and has published in prestigious journals such as PLoS ONE, Scientific Reports and Human Molecular Genetics.

In The Last Decade

Ingrid Tarr

6 papers receiving 148 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ingrid Tarr Australia	5	110	77	72	27	18	7	148
Summer Gibson United States	7	109 1.0×	56 0.7×	40 0.6×	33 1.2×	19 1.1×	12	148
Annie Levert Canada	5	73 0.7×	50 0.6×	112 1.6×	29 1.1×	53 2.9×	7	179
Sarah Ryan United Kingdom	6	103 0.9×	76 1.0×	75 1.0×	13 0.5×	20 1.1×	8	151
Rick A. A. van der Spek Netherlands	5	91 0.8×	62 0.8×	42 0.6×	19 0.7×	14 0.8×	5	122
Daniela Bernardo Italy	6	68 0.6×	31 0.4×	72 1.0×	22 0.8×	47 2.6×	13	146
Alexander Bampton United Kingdom	4	117 1.1×	81 1.1×	120 1.7×	30 1.1×	19 1.1×	5	197
D. G. Hernandez United Kingdom	3	126 1.1×	57 0.7×	67 0.9×	55 2.0×	45 2.5×	3	216
Florence Esselin France	7	113 1.0×	68 0.9×	34 0.5×	21 0.8×	13 0.7×	13	136
Stefan Putz Germany	5	112 1.0×	76 1.0×	120 1.7×	12 0.4×	29 1.6×	5	206
Saúl Herranz-Martín United Kingdom	8	57 0.5×	51 0.7×	109 1.5×	10 0.4×	36 2.0×	9	167

Countries citing papers authored by Ingrid Tarr

Since Specialization

Citations

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

Fields of papers citing papers by Ingrid Tarr

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ingrid Tarr

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

All Works

Sort: Min cites: Since: Top N: Style:

7 of 7 papers shown

1.

McGrath‐Cadell, Lucy, Stephanie Hesselson, Ingrid Tarr, et al.. (2025). Spontaneous Coronary Artery Dissection and a Family History of Aortic Dissection: A Genetic Association Study. Journal of the American Heart Association. 14(8). e037921–e037921.

2.

McGrath‐Cadell, Lucy, Stephanie Hesselson, Siiri E. Iismaa, et al.. (2024). COL3A1 Variants in Spontaneous Coronary Artery Dissection. JACC Advances. 3(7). 100986–100986. 2 indexed citations

3.

Tarr, Ingrid, Emily P. McCann, Beben Benyamin, et al.. (2019). Monozygotic twins and triplets discordant for amyotrophic lateral sclerosis display differential methylation and gene expression. Scientific Reports. 9(1). 8254–8254. 30 indexed citations

4.

Hogan, Alison, Emily K. Don, Stephanie L. Rayner, et al.. (2017). Expression of ALS/FTD-linked mutant CCNF in zebrafish leads to increased cell death in the spinal cord and an aberrant motor phenotype. Human Molecular Genetics. 26(14). 2616–2626. 35 indexed citations

5.

Fifita, Jennifer A., Katharine Y. Zhang, Jasmin Galper, et al.. (2017). Genetic and Pathological Assessment of hnRNPA1, hnRNPA2/B1, and hnRNPA3 in Familial and Sporadic Amyotrophic Lateral Sclerosis. Neurodegenerative Diseases. 17(6). 304–312. 24 indexed citations

6.

McCann, Emily P., Kelly L. Williams, Jennifer A. Fifita, et al.. (2017). The genotype–phenotype landscape of familial amyotrophic lateral sclerosis in Australia. Clinical Genetics. 92(3). 259–266. 50 indexed citations

7.

Tarr, Ingrid, et al.. (2014). Social Modulation of Stress Reactivity and Learning in Young Worker Honey Bees. PLoS ONE. 9(12). e113630–e113630. 7 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.

Explore authors with similar magnitude of impact