Patrick R. Blackburn

Author

Also Known As

Blackburn, Patrick R., P R Blackburn, P.R. Blackburn, Patrick Blackburn, Patrick R Blackburn, Patrick R. Blackburn, Patrick R. Blackburn, Tim Niehues

128

Publications

3.2K

Citations

H-Index

105

Concepts

All Affiliations

Mayo Clinic Mayo Clinic in Florida Mayo Clinic in Arizona WinnMed Inserm

About

Patrick R. Blackburn is an author at Mayo Clinic specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	20	22	1.4K
2	Engineering	4	4	153
3	Health Sciences	2	2	312
4	Natural Sciences	1	1	20
5	Public Health	1	1	22

Patrick R. Blackburn

Publications

2.9K

Citations

H-Index

Page 1

	Year	Citations
Clonal competition with alternating dominance in multiple myeloma Jonathan J. Keats, Marta Chesi, Jan B. Egan, Blood	2012	630
Monitoring clinical trials: Conditional or predictive power? David J. Spiegelhalter, Laurence S. Freedman, Patrick R. Blackburn Controlled Clinical Trials Clinical Trial ManagementClinical TrialsOutcomes ResearchRandomized Controlled TrialMedicine	1986	302
Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during Fetal Cortical Development Ashley L. Lennox, Mariah L. Hoye, Ruiji Jiang, Neuron Developmental BiologyBrain DevelopmentDevelopmental GeneticsGeneticsRna Biology	2020	205
Bi-allelic Alterations in AEBP1 Lead to Defective Collagen Assembly and Connective Tissue Structure Resulting in a Variant of Ehlers-Danlos Syndrome Patrick R. Blackburn, Xu Zhi, Kathleen E. Tumelty, The American Journal of Human Genetics Ehlers-danlos SyndromeDefective Collagen AssemblyFibrosisAutoimmune DiseaseGenetic Disorder	2018	167
Activation of P-TEFb by Androgen Receptor-Regulated Enhancer RNAs in Castration-Resistant Prostate Cancer Yu Zhao, Liguo Wang, Shancheng Ren, Cell Reports	2016	130
KAT6A Syndrome: genotype–phenotype correlation in 76 patients with pathogenic KAT6A variants Joanna Kennedy, David Goudie, Edward Blair, Genetics in Medicine Pathogenic Kat6a VariantsKat6a SyndromeGeneticsPathogenesisGenetic Epidemiology	2018	105
tp53 deficiency causes a wide tumor spectrum and increases embryonal rhabdomyosarcoma metastasis in zebrafish Myron S. Ignatius, Madeline N. Hayes, Finola E. Moore, eLife	2018	77
CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum Enrico D.H. Konrad, Niels Nardini, Almuth Caliebe, Genetics in Medicine	2019	67
Impact of integrated translational research on clinical exome sequencing Eric W. Klee, Margot A. Cousin, Filippo Pinto e Vairo, Genetics in Medicine	2020	57
FusX: A Rapid One-Step Transcription Activator-Like Effector Assembly System for Genome Science C. H. Alvin, Melissa S. McNulty, Tanya L. Poshusta, Human Gene Therapy Assemble TalesEngineeringGeneticsMolecular BiologyGene Regulatory Network	2016	52

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