Andrew J. Sharp

13.7k total citations · 2 hit papers
103 papers, 6.6k citations indexed

About

Andrew J. Sharp is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Andrew J. Sharp has authored 103 papers receiving a total of 6.6k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Genetics, 57 papers in Molecular Biology and 23 papers in Plant Science. Recurrent topics in Andrew J. Sharp's work include Genomic variations and chromosomal abnormalities (33 papers), Epigenetics and DNA Methylation (21 papers) and Chromosomal and Genetic Variations (21 papers). Andrew J. Sharp is often cited by papers focused on Genomic variations and chromosomal abnormalities (33 papers), Epigenetics and DNA Methylation (21 papers) and Chromosomal and Genetic Variations (21 papers). Andrew J. Sharp collaborates with scholars based in United States, United Kingdom and Switzerland. Andrew J. Sharp's co-authors include Evan E. Eichler, Ze Cheng, Daniel Pinkel, Donna G. Albertson, Paras Garg, David Robinson, Patricia A. Jacobs, L.M. Pertz, Jeffrey A. Bailey and Corey T. Watson and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and Nature Genetics.

In The Last Decade

Andrew J. Sharp

101 papers receiving 6.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Fine-scale structural variation of the human genome

2005 742 citations Andrew J. Sharp, Donna G. Albertson et al. Nature Genetics profile →
Segmental Duplications and Copy-Number Variation in the Human Genome

2005 678 citations Andrew J. Sharp, Ze Cheng et al. The American Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Andrew J. Sharp United States	39	4.1k	3.7k	1.3k	908	440	103	6.6k
Daníel F. Guðbjartsson Iceland	41	3.9k 1.0×	3.2k 0.9×	705 0.5×	592 0.7×	477 1.1×	81	8.1k
Lisenka E.L.M. Vissers Netherlands	39	5.1k 1.2×	3.6k 1.0×	790 0.6×	943 1.0×	586 1.3×	98	7.7k
Lars Feuk Sweden	35	5.5k 1.3×	4.9k 1.3×	1.7k 1.3×	828 0.9×	1.2k 2.8×	85	8.8k
Samantha J.L. Knight United Kingdom	38	4.0k 1.0×	3.0k 0.8×	1.0k 0.8×	657 0.7×	309 0.7×	89	5.8k
Paweł Stankiewicz United States	50	6.2k 1.5×	5.0k 1.4×	2.2k 1.6×	1.4k 1.5×	563 1.3×	198	9.2k
Sau Wai Cheung United States	47	5.6k 1.4×	3.8k 1.0×	1.2k 0.9×	2.2k 2.5×	510 1.2×	181	7.9k
Richard Redon France	27	3.2k 0.8×	2.9k 0.8×	872 0.7×	342 0.4×	549 1.2×	73	5.4k
Richard R. Meehan United Kingdom	49	2.7k 0.6×	6.8k 1.9×	502 0.4×	568 0.6×	610 1.4×	111	8.4k
Rolph Pfundt Netherlands	42	2.9k 0.7×	2.6k 0.7×	520 0.4×	586 0.6×	436 1.0×	136	5.2k
P. Pearson Netherlands	55	4.7k 1.1×	6.3k 1.7×	1.4k 1.1×	901 1.0×	662 1.5×	209	10.7k

Countries citing papers authored by Andrew J. Sharp

Since Specialization

Citations

This map shows the geographic impact of Andrew J. Sharp'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. Sharp 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. Sharp more than expected).

Fields of papers citing papers by Andrew J. Sharp

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

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

All Works

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20 of 20 papers shown

Liu, Clifford Z., Bharati Jadhav, Yu Liu, et al.. (2023). Feeder-free generation and characterization of endocardial and cardiac valve cells from human pluripotent stem cells. iScience. 27(1). 108599–108599. 6 indexed citations

Richter, Felix, et al.. (2023). Small open reading frames: a comparative genetics approach to validation. BMC Genomics. 24(1). 226–226. 3 indexed citations

Sharp, Andrew J., et al.. (2022). Temporal quality degradation in AI models. Scientific Reports. 12(1). 11654–11654. 79 indexed citations

Rushing, Clark S., Andrew J. Sharp, Viviana Ruiz‐Gutiérrez, et al.. (2021). Integrating tracking and resight data enables unbiased inferences about migratory connectivity and winter range survival from archival tags. Ornithological applications. 123(2). 18 indexed citations

Garg, Paras, Alejandro Martin-Trujillo, Oscar L. Rodriguez, et al.. (2021). Pervasive cis effects of variation in copy number of large tandem repeats on local DNA methylation and gene expression. The American Journal of Human Genetics. 108(5). 809–824. 21 indexed citations

N., Anh, Corey T. Watson, Ariella Cohain, et al.. (2019). Dual transcriptomic and epigenomic study of reaction severity in peanut-allergic children. Journal of Allergy and Clinical Immunology. 145(4). 1219–1230. 49 indexed citations

Jadhav, Bharati, Ramin Monajemi, Kristina Gagalova, et al.. (2019). RNA-Seq in 296 phased trios provides a high-resolution map of genomic imprinting. BMC Biology. 17(1). 50–50. 22 indexed citations

Richter, Felix, Gabriel E. Hoffman, Kathryn B. Manheimer, et al.. (2019). ORE identifies extreme expression effects enriched for rare variants. Bioinformatics. 35(20). 3906–3912. 5 indexed citations

Peter, Cyril, Laura Fischer, Marija Kundaković, et al.. (2016). DNA Methylation Signatures of Early Childhood Malnutrition Associated With Impairments in Attention and Cognition. Biological Psychiatry. 80(10). 765–774. 101 indexed citations

10.

Brault, Véronique, Arnaud Duchon, Caroline Romestaing, et al.. (2015). Opposite Phenotypes of Muscle Strength and Locomotor Function in Mouse Models of Partial Trisomy and Monosomy 21 for the Proximal Hspa13-App Region. PLoS Genetics. 11(3). e1005062–e1005062. 32 indexed citations

11.

Gymrek, Melissa, Thomas Willems, Audrey Guilmatre, et al.. (2015). Abundant contribution of short tandem repeats to gene expression variation in humans. Nature Genetics. 48(1). 22–29. 245 indexed citations

12.

Forni, Diego, et al.. (2015). Determining multiallelic complex copy number and sequence variation from high coverage exome sequencing data. BMC Genomics. 16(1). 34–36. 2 indexed citations

13.

Watson, Corey T., Tomàs Marquès‐Bonet, Andrew J. Sharp, & Heather C. Mefford. (2014). The Genetics of Microdeletion and Microduplication Syndromes: An Update. Annual Review of Genomics and Human Genetics. 15(1). 215–244. 125 indexed citations

14.

Duchon, Arnaud, Stéphanie Pothion, Véronique Brault, et al.. (2010). The telomeric part of the human chromosome 21 from Cstb to Prmt2 is not necessary for the locomotor and short-term memory deficits observed in the Tc1 mouse model of Down syndrome. Behavioural Brain Research. 217(2). 271–281. 25 indexed citations

15.

Sharp, Andrew J., Eugenia Migliavacca, Elisavet Stathaki, et al.. (2010). Methylation profiling in individuals with uniparental disomy identifies novel differentially methylated regions on chromosome 15. Genome Research. 20(9). 1271–1278. 28 indexed citations

16.

Mefford, Heather C., Séverine Clauin, Andrew J. Sharp, et al.. (2007). Recurrent Reciprocal Genomic Rearrangements of 17q12 Are Associated with Renal Disease, Diabetes, and Epilepsy. The American Journal of Human Genetics. 81(5). 1057–1069. 185 indexed citations

17.

Sharp, Andrew J., Rebecca R. Selzer, Ze Cheng, et al.. (2006). Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome. Nature Genetics. 38(9). 1038–1042. 429 indexed citations

18.

Sharp, Andrew J. & Robert J. Slater. (2003). Mung-Bean Nuclease 1 (EC 3.1.30.1). Humana Press eBooks. 16. 253–262. 1 indexed citations

19.

Sharp, Andrew J., William Tapper, Peter Strike, D Robinson, & P. A. Jacobs. (2002). LINE repeats are associated with the spread of X inactivation. ePrints Soton (University of Southampton). 2 indexed citations

20.

Mergenthaler, Susanne, Andrew J. Sharp, Michael B. Ranke, et al.. (2001). Gene Dosage Analysis in Silver-Russell Syndrome: Use of Quantitative Competitive PCR and Dual-Color FISH to Estimate the Frequency of Duplications in 7p11.2–p13. Genetic Testing. 5(3). 261–266. 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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