Andrew J. Rimmer

1.4k total citations
6 papers, 370 citations indexed

About

Andrew J. Rimmer is a scholar working on Molecular Biology, Nephrology and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Andrew J. Rimmer has authored 6 papers receiving a total of 370 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 2 papers in Nephrology and 2 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Andrew J. Rimmer's work include Pituitary Gland Disorders and Treatments (2 papers), Genetic Syndromes and Imprinting (1 paper) and Genomics and Rare Diseases (1 paper). Andrew J. Rimmer is often cited by papers focused on Pituitary Gland Disorders and Treatments (2 papers), Genetic Syndromes and Imprinting (1 paper) and Genomics and Rare Diseases (1 paper). Andrew J. Rimmer collaborates with scholars based in United Kingdom, Australia and United States. Andrew J. Rimmer's co-authors include Lorna Gregory, Gil McVean, David Buck, M. Andrew Nesbit, Rajesh V. Thakker, Caroline M. Gorvin, Moustafa Attar, Fadil Hannan, Sarah Howles and Paul Newey and has published in prestigious journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and PLoS Genetics.

In The Last Decade

Andrew J. Rimmer

6 papers receiving 364 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Andrew J. Rimmer United Kingdom	5	176	150	98	94	72	6	370
Maki Uraoka Japan	6	123 0.7×	168 1.1×	24 0.2×	78 0.8×	33 0.5×	6	407
Yah-Huei Chou United States	5	178 1.0×	194 1.3×	74 0.8×	65 0.7×	33 0.5×	6	420
Simon Wöhrle Austria	9	152 0.9×	501 3.3×	114 1.2×	177 1.9×	27 0.4×	10	690
Kamran Hamidi Asl United States	10	107 0.6×	467 3.1×	78 0.8×	118 1.3×	41 0.6×	12	504
Takuo Fujita Japan	11	125 0.7×	135 0.9×	170 1.7×	49 0.5×	19 0.3×	16	351
Jitka Štekrová Czechia	14	147 0.8×	287 1.9×	54 0.6×	230 2.4×	12 0.2×	47	504
J T Pang United Kingdom	8	79 0.4×	207 1.4×	290 3.0×	55 0.6×	386 5.4×	15	648
María Jesús Lloret Spain	11	151 0.9×	175 1.2×	67 0.7×	38 0.4×	9 0.1×	27	478
Jingcheng Liu China	10	76 0.4×	145 1.0×	115 1.2×	16 0.2×	24 0.3×	30	346

Countries citing papers authored by Andrew J. Rimmer

Since Specialization

Citations

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

Fields of papers citing papers by Andrew J. Rimmer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrew J. Rimmer. 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 Andrew J. Rimmer. The network helps show where Andrew J. Rimmer may publish in the future.

Co-authorship network of co-authors of Andrew J. Rimmer

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

All Works

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6 of 6 papers shown

1.

Bull, Katherine R., Andrew J. Rimmer, Owen M. Siggs, et al.. (2013). Unlocking the Bottleneck in Forward Genetics Using Whole-Genome Sequencing and Identity by Descent to Isolate Causative Mutations. PLoS Genetics. 9(1). e1003219–e1003219. 30 indexed citations

2.

Newey, Paul, M. Andrew Nesbit, Andrew J. Rimmer, et al.. (2013). Whole-exome sequencing studies of non-functioning pituitary adenomas. Endocrine Abstracts. 1–1. 2 indexed citations

3.

Bull, Katherine R., Andrew J. Rimmer, Tanya L. Crockford, et al.. (2013). Next‐generation sequencing to dissect hereditary nephrotic syndrome in mice identifies a hypomorphic mutation in Lamb2 and models Pierson's syndrome. The Journal of Pathology. 233(1). 18–26. 5 indexed citations

4.

Newey, Paul, M. Andrew Nesbit, Andrew J. Rimmer, et al.. (2013). Whole-Exome Sequencing Studies of Nonfunctioning Pituitary Adenomas. The Journal of Clinical Endocrinology & Metabolism. 98(4). E796–E800. 61 indexed citations

5.

Newey, Paul, M. Andrew Nesbit, Andrew J. Rimmer, et al.. (2012). Whole-Exome Sequencing Studies of Nonhereditary (Sporadic) Parathyroid Adenomas. The Journal of Clinical Endocrinology & Metabolism. 97(10). E1995–E2005. 95 indexed citations

6.

Nesbit, M. Andrew, Fadil Hannan, Sarah Howles, et al.. (2012). Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3. Nature Genetics. 45(1). 93–97. 177 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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