Patrick R. Blackburn

3.3k total citations · 1 hit paper
74 papers, 1.7k citations indexed

About

Patrick R. Blackburn is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Patrick R. Blackburn has authored 74 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 22 papers in Genetics and 11 papers in Genetics. Recurrent topics in Patrick R. Blackburn's work include Genomics and Rare Diseases (8 papers), Epigenetics and DNA Methylation (8 papers) and Acute Myeloid Leukemia Research (6 papers). Patrick R. Blackburn is often cited by papers focused on Genomics and Rare Diseases (8 papers), Epigenetics and DNA Methylation (8 papers) and Acute Myeloid Leukemia Research (6 papers). Patrick R. Blackburn collaborates with scholars based in United States, Netherlands and Germany. Patrick R. Blackburn's co-authors include Laurence S. Freedman, David J. Spiegelhalter, Paldeep S. Atwal, Stephen C. Ekker, Eric W. Klee, Jan B. Egan, Victoria M. Garbitt, Marta Chesi, Rafaël Fonseca and A. Keith Stewart and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Patrick R. Blackburn

67 papers receiving 1.6k 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.

Clonal competition with alternating dominance in multiple myeloma

2012 456 citations Jonathan J. Keats, Marta Chesi et al. Blood profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Patrick R. Blackburn United States	19	923	369	328	250	235	74	1.7k
Sung Choe United States	20	1.1k 1.2×	113 0.3×	140 0.4×	243 1.0×	345 1.5×	48	1.8k
Milton W. Datta United States	24	1.4k 1.5×	81 0.2×	253 0.8×	468 1.9×	349 1.5×	61	2.3k
Ming Lin China	20	778 0.8×	33 0.1×	137 0.4×	235 0.9×	217 0.9×	51	1.3k
Luke Hughes‐Davies United Kingdom	21	1.5k 1.6×	52 0.1×	468 1.4×	540 2.2×	505 2.1×	52	2.2k
Philip D. Cotter United States	26	1.3k 1.4×	146 0.4×	994 3.0×	200 0.8×	298 1.3×	95	2.4k
Henrik Edgren Finland	24	1.9k 2.1×	129 0.3×	233 0.7×	546 2.2×	979 4.2×	53	2.7k
Yunyu Zhang United States	17	1.7k 1.8×	303 0.8×	331 1.0×	488 2.0×	615 2.6×	28	2.2k
Thomas Zwingers Germany	16	386 0.4×	156 0.4×	54 0.2×	1.2k 4.7×	446 1.9×	30	2.2k
Chirayu Goswami United States	25	1.1k 1.2×	52 0.1×	154 0.5×	443 1.8×	572 2.4×	44	1.8k
Julie B. Sneddon United States	17	1.7k 1.8×	34 0.1×	402 1.2×	1.0k 4.1×	859 3.7×	26	3.2k

Countries citing papers authored by Patrick R. Blackburn

Since Specialization

Citations

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

Fields of papers citing papers by Patrick R. Blackburn

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Patrick R. Blackburn. 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 Patrick R. Blackburn. The network helps show where Patrick R. Blackburn may publish in the future.

Co-authorship network of co-authors of Patrick R. Blackburn

This figure shows the co-authorship network connecting the top 25 collaborators of Patrick R. Blackburn. A scholar is included among the top collaborators of Patrick R. Blackburn 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 Patrick R. Blackburn. Patrick R. Blackburn 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

Blackburn, Patrick R., et al.. (2025). EWSR1::CREM Fusion in a Pediatric Patient With Testicular Leydig Cell Tumor. Genes Chromosomes and Cancer. 64(3). e70038–e70038. 1 indexed citations

Ma, Jing, Jennifer Neary, Selene C. Koo, et al.. (2024). Pediatric Erythroid Sarcoma Diagnostically Confirmed by Identification of a Recurrent NFIA::CBFA2T3 Fusion. Genes Chromosomes and Cancer. 63(6). e23251–e23251. 1 indexed citations

Chiang, Jason, Daniel C. Moreira, Yen‐Chun Liu, et al.. (2022). A CTNNB1 ‐altered medulloblastoma shows the immunophenotypic, DNA methylation and transcriptomic profiles of SHH‐activated, and not WNT‐activated, medulloblastoma. Neuropathology and Applied Neurobiology. 48(5). e12815–e12815. 3 indexed citations

Jenkinson, Garrett, Asha Nair, Jesse S. Voss, et al.. (2021). SeekFusion - A Clinically Validated Fusion Transcript Detection Pipeline for PCR-Based Next-Generation Sequencing of RNA. Frontiers in Genetics. 12. 739054–739054. 11 indexed citations

Blackburn, Patrick R., et al.. (2020). Structural Models for the Dynamic Effects of Loss-of-Function Variants in the Human SIM1 Protein Transcriptional Activation Domain. Biomolecules. 10(9). 1314–1314. 42 indexed citations

Blackburn, Patrick R., Matthew Schultz, Dong Li, et al.. (2020). Expanding the clinical and phenotypic heterogeneity associated with biallelic variants in ACO2. Annals of Clinical and Translational Neurology. 7(6). 1013–1028. 5 indexed citations

Blackburn, Patrick R., Dragana Milosevic, Tomáš Marek, et al.. (2019). PIK3CA mutations in lipomatosis of nerve with or without nerve territory overgrowth. Modern Pathology. 33(3). 420–430. 25 indexed citations

Zimmermann, Michael T., Patrick R. Blackburn, Eric W. Klee, et al.. (2018). Protein modeling and clinical description of a novel in‐frame GLB1 deletion causing GM1 gangliosidosis type II. Molecular Genetics & Genomic Medicine. 6(6). 1229–1235. 4 indexed citations

Ignatius, Myron S., Madeline N. Hayes, Finola E. Moore, et al.. (2018). tp53 deficiency causes a wide tumor spectrum and increases embryonal rhabdomyosarcoma metastasis in zebrafish. eLife. 7. 44 indexed citations

10.

Blackburn, Patrick R., et al.. (2018). Whole Exome Sequencing and Molecular Modeling of a Missense Variant in TNFAIP3 That Segregates with Disease in a Family with Chronic Urticaria and Angioedema. SHILAP Revista de lepidopterología. 2018. 1–6. 6 indexed citations

11.

Boczek, Nicole J., Katharina Hopp, Daniel Kraft, et al.. (2018). Characterization of three ciliopathy pedigrees expands the phenotype associated with biallelic C2CD3 variants. European Journal of Human Genetics. 26(12). 1797–1809. 17 indexed citations

12.

Burgess, Jeremy D., et al.. (2017). Co‐occurrence of a novel PDGFRB variant and likely pathogenic variant in CASR in an individual with extensive intracranial calcifications and hypocalcaemia. Clinical Case Reports. 6(1). 8–13. 7 indexed citations

13.

Gass, Jennifer, et al.. (2017). BARD1 nonsense variant c.1921C>T in a patient with recurrent breast cancer. Clinical Case Reports. 5(2). 104–107. 4 indexed citations

14.

Blackburn, Patrick R., Duygu Selcen, Jennifer Gass, et al.. (2017). Whole exome sequencing of a patient with suspected mitochondrial myopathy reveals novel compound heterozygous variants in RYR1. Molecular Genetics & Genomic Medicine. 5(3). 295–302. 4 indexed citations

15.

Gass, Jennifer, et al.. (2017). Expanded phenotype in a patient with spastic paraplegia 7. Clinical Case Reports. 5(10). 1620–1622. 8 indexed citations

16.

Zimmermann, Michael T., Raúl Urrutia, Patrick R. Blackburn, et al.. (2017). Novel Pathogenic Variant in TGFBR2 Confirmed by Molecular Modeling Is a Rare Cause of Loeys-Dietz Syndrome. SHILAP Revista de lepidopterología. 2017. 1–4. 3 indexed citations

17.

Lara‐Velazquez, Montserrat, Alexander Perdomo‐Pantoja, Patrick R. Blackburn, et al.. (2017). A novel splice site variant in CYP11A1 in trans with the p.E314K variant in a male patient with congenital adrenal insufficiency. Molecular Genetics & Genomic Medicine. 5(6). 781–787. 10 indexed citations

18.

Gass, Jennifer, et al.. (2017). The clinical heterogeneity of late-onset MELAS. Molecular Genetics and Metabolism Reports. 11. 30–30. 3 indexed citations

19.

Blackburn, Patrick R., Jarryd M. Campbell, Karl J. Clark, & Stephen C. Ekker. (2013). The CRISPR System—Keeping Zebrafish Gene Targeting Fresh. Zebrafish. 10(1). 116–118. 75 indexed citations

20.

Keats, Jonathan J., Marta Chesi, Jan B. Egan, et al.. (2012). Clonal competition with alternating dominance in multiple myeloma. Blood. 120(5). 1067–1076. 456 indexed citations breakdown →

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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