Patrick R. Blackburn

3.3k citations

74 papers · 1.7k indexed · 1 hit paper · h-index 19

Molecular Biology top 10%
Hematology top 2%
Genetics top 10%
Oncology top 10%
Cancer Research top 10%

Co-authors: Laurence S. Freedman David J. Spiegelhalter Paldeep S. Atwal Stephen C. Ekker Eric W. Klee Jan B. Egan Victoria M. Garbitt Marta Chesi
Topics: Genomics and Rare Diseases (8 papers)Epigenetics and DNA Methylation (8 papers)Acute Myeloid Leukemia Research (6 papers)
Cited by: Hematology Statistics and Probability Cancer Research
Journals: Journal of Biological ChemistrySHILAP Revista de lepidopterologíaBlood
Partner nations: United States Netherlands Germany

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

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

#	Work	Indexed citations
1	EWSR1::CREM Fusion in a Pediatric Patient With Testicular Leydig Cell Tumor 2025 ·Genes Chromosomes and Cancer ·(unknown),Patrick R. Blackburn,Larissa V. Furtado,Alberto S. Pappo,Selene C. Koo	1
2	Pediatric Erythroid Sarcoma Diagnostically Confirmed by Identification of a Recurrent NFIA::CBFA2T3 Fusion 2024 ·Genes Chromosomes and Cancer ·(unknown),Jing Ma,Jennifer Neary,Selene C. Koo,Hiroto Inaba,(unknown),(unknown),(unknown),Lan N. Bui,Jeffery M. Klco,(unknown),Patrick R. Blackburn	1
3	A CTNNB1 ‐altered medulloblastoma shows the immunophenotypic, DNA methylation and transcriptomic profiles of SHH‐activated, and not WNT‐activated, medulloblastoma 2022 ·Neuropathology and Applied Neurobiology ·Jason Chiang,Daniel C. Moreira,(unknown),Yen‐Chun Liu,Patrick R. Blackburn,Zonggao Shi,Maria Cardenas,David A. Wheeler,Larissa V. Furtado	3
4	SeekFusion - A Clinically Validated Fusion Transcript Detection Pipeline for PCR-Based Next-Generation Sequencing of RNA 2021 ·Frontiers in Genetics ·(unknown),Garrett Jenkinson,Asha Nair,(unknown),(unknown),Jesse S. Voss,(unknown),Emily G. Barr Fritcher,Christian Roß,Caterina Giannini,Aditya Raghunathan,Benjamin R. Kipp,Robert B. Jenkins,(unknown),Kevin C. Halling,Patrick R. Blackburn,Surendra Dasari,Gavin R. Oliver,Eric W. Klee	11
5	Structural Models for the Dynamic Effects of Loss-of-Function Variants in the Human SIM1 Protein Transcriptional Activation Domain 2020 ·Biomolecules ·(unknown),Patrick R. Blackburn,Murray L. Whitelaw,Mieke M. van Haelst,Paldeep S. Atwal,Thomas R. Caulfield	42
6	Expanding the clinical and phenotypic heterogeneity associated with biallelic variants in ACO2 2020 ·Annals of Clinical and Translational Neurology ·Patrick R. Blackburn,Matthew Schultz,(unknown),Dong Li,Elizabeth Bhoj,(unknown),Deborah L. Renaud,(unknown),Niema Ibrahim,Mais Hashem,Mohammed Zain Seidahmed,Linda Hasadsri,Samantha A. Schrier Vergano,Fowzan S. Alkuraya,Brendan C. Lanpher	5
7	PIK3CA mutations in lipomatosis of nerve with or without nerve territory overgrowth 2019 ·Modern Pathology ·Patrick R. Blackburn,Dragana Milosevic,Tomáš Marek,Andrew L. Folpe,B. Matthew Howe,Robert J. Spinner,Jodi M. Carter	25
8	Protein modeling and clinical description of a novel in‐frame GLB1 deletion causing GM1 gangliosidosis type II 2018 ·Molecular Genetics & Genomic Medicine ·(unknown),Michael T. Zimmermann,Patrick R. Blackburn,(unknown),Eric W. Klee,Laura Pollard,Colleen Macmurdo,Paldeep S. Atwal,Thomas R. Caulfield	4
9	tp53 deficiency causes a wide tumor spectrum and increases embryonal rhabdomyosarcoma metastasis in zebrafish 2018 ·eLife ·Myron S. Ignatius,Madeline N. Hayes,Finola E. Moore,Qin Tang,Sara P. Garcia,Patrick R. Blackburn,(unknown),Long Wang,(unknown),Ashwin Ramakrishnan,Sophia M. Reeder,Yidong Chen,G. Petur Nielsen,Eleanor Y. Chen,Robert P. Hasserjian,Franck Tirode,Stephen C. Ekker,David M. Langenau	44
10	Whole Exome Sequencing and Molecular Modeling of a Missense Variant in TNFAIP3 That Segregates with Disease in a Family with Chronic Urticaria and Angioedema 2018 ·SHILAP Revista de lepidopterología ·(unknown),Patrick R. Blackburn,(unknown),Jennifer Gass,Thomas R. Caulfield,(unknown),Paldeep S. Atwal	6
11	Characterization of three ciliopathy pedigrees expands the phenotype associated with biallelic C2CD3 variants 2018 ·European Journal of Human Genetics ·Nicole J. Boczek,Katharina Hopp,(unknown),Daniel Kraft,Margot A. Cousin,Patrick R. Blackburn,Charles D. Madsen,Gavin R. Oliver,Asha Nair,Jie Na,Diana W. Bianchi,(unknown),Peter C. Harris,Pavel N. Pichurin,Eric W. Klee	17
12	Co‐occurrence of a novel PDGFRB variant and likely pathogenic variant in CASR in an individual with extensive intracranial calcifications and hypocalcaemia 2017 ·Clinical Case Reports ·(unknown),Jeremy D. Burgess,Patrick R. Blackburn,Jennifer Gass,(unknown),(unknown),Jay A. van Gerpen,Paldeep S. Atwal	7
13	BARD1 nonsense variant c.1921C>T in a patient with recurrent breast cancer 2017 ·Clinical Case Reports ·Jennifer Gass,(unknown),Patrick R. Blackburn,Stephanie L. Hines,Paldeep S. Atwal	4
14	Whole exome sequencing of a patient with suspected mitochondrial myopathy reveals novel compound heterozygous variants in RYR1 2017 ·Molecular Genetics & Genomic Medicine ·Patrick R. Blackburn,Duygu Selcen,Jennifer Gass,(unknown),Sarah Macklin,Margot A. Cousin,Nicole J. Boczek,Eric W. Klee,Elliot L. Dimberg,Kathleen D. Kennelly,Paldeep S. Atwal	4
15	Expanded phenotype in a patient with spastic paraplegia 7 2017 ·Clinical Case Reports ·Jennifer Gass,Patrick R. Blackburn,(unknown),Sarah Macklin,Jay Van Gerpen,Paldeep S. Atwal	8
16	Novel Pathogenic Variant in TGFBR2 Confirmed by Molecular Modeling Is a Rare Cause of Loeys-Dietz Syndrome 2017 ·SHILAP Revista de lepidopterología ·Michael T. Zimmermann,Raúl Urrutia,Patrick R. Blackburn,Margot A. Cousin,Nicole J. Boczek,Eric W. Klee,Colleen Macmurdo,Paldeep S. Atwal	3
17	A novel splice site variant in CYP11A1 in trans with the p.E314K variant in a male patient with congenital adrenal insufficiency 2017 ·Molecular Genetics & Genomic Medicine ·Montserrat Lara‐Velazquez,Alexander Perdomo‐Pantoja,Patrick R. Blackburn,Jennifer Gass,Thomas R. Caulfield,Paldeep S. Atwal	10
18	The clinical heterogeneity of late-onset MELAS 2017 ·Molecular Genetics and Metabolism Reports ·(unknown),Jennifer Gass,Patrick R. Blackburn,Paldeep S. Atwal	3
19	The CRISPR System—Keeping Zebrafish Gene Targeting Fresh 2013 ·Zebrafish ·Patrick R. Blackburn,Jarryd M. Campbell,Karl J. Clark,Stephen C. Ekker	75
20	Clonal competition with alternating dominance in multiple myelomabreakdown → 2012 ·Blood ·Jonathan J. Keats,Marta Chesi,Jan B. Egan,Victoria M. Garbitt,Stephen Palmer,Esteban Braggio,Scott Van Wier,Patrick R. Blackburn,Angela Baker,Angela Dispenzieri,Shaji Kumar,S. Vincent Rajkumar,John D. Carpten,Michael T. Barrett,Rafaël Fonseca,A. Keith Stewart,P. Leif Bergsagel	456

About Patrick R. Blackburn

Patrick R. Blackburn is a scholar working on Genetics, Hematology and Genetics, having authored 74 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (8 papers), Epigenetics and DNA Methylation (8 papers) and Acute Myeloid Leukemia Research (6 papers). The work is most often cited by research in Hematology (369 citations), Statistics and Probability (177 citations) and Cancer Research (235 citations). Patrick R. Blackburn has collaborated with scholars based in United States, Netherlands and Germany. Frequent 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. Their work appears in journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Blood.

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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