Matthew Halvorsen - Concepedia

Author

Matthew Halvorsen

University of North Carolina at Chapel Hill ORCID

Also Known As

Cobite, Journa, Daniel G Guttfreund, Daniel G. Guttfreund, Gyllensten U, Hagen, Kristen, Halvorsen, Matt, Halvorsen, Matthew, Hentati Isacsson, Nils, Johnson, Jessica, Johnson, Julie A.

116

Publications

1.9K

Citations

H-Index

Concepts

All Affiliations

University of North Carolina at Chapel Hill Karolinska Institutet Columbia University Irving Medical Center Aarhus University Columbia University

About

Matthew Halvorsen is an author at University of North Carolina at Chapel Hill specializing in medicine, social sciences, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	461
2	Social Sciences	6	6	210
3	Engineering	2	2	54
4	Natural Sciences	1	1	37
5	Public Health	1	1	149

Matthew Halvorsen

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Disease-Associated Mutations That Alter the RNA Structural Ensemble Matthew Halvorsen, Joshua S. Martin, Sam Broadaway, PLoS Genetics	2010	336
The Intolerance of Regulatory Sequence to Genetic Variation Predicts Gene Dosage Sensitivity Slavé Petrovski, Ayal B. Gussow, Quanli Wang, PLoS Genetics GeneticsGene CharacterizationDisease Gene IdentificationGenomicsGene Expression Profiling	2015	149
Annotating pathogenic non-coding variants in genic regions Sahar Gelfman, Quanli Wang, K. Melodi McSweeney, Nature Communications	2017	149
Exome sequencing in obsessive–compulsive disorder reveals a burden of rare damaging coding variants Matthew Halvorsen, Jack Samuels, Ying Wang, Nature Neuroscience PsychiatryObsessive–compulsive DisorderExome SequencingObsessive-compulsive DisorderPsychiatric Genetics	2021	88
Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia Matthew Halvorsen, Ruth Huh, Nikolay Oskolkov, Nature Communications	2020	87
Mosaic mutations in early-onset genetic diseases Matthew Halvorsen, Slavé Petrovski, Renée A. Shellhaas, Genetics in Medicine Genetic DiseasesMendelian DisorderMosaic MutationsGenetic DisorderGenetics	2015	65
Multiple conformations are a conserved and regulatory feature of the <i>RB1</i> 5′ UTR Katrina M. Kutchko, Wes Sanders, Ben Ziehr, RNA	2015	61
Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease Karl C. Desch, Ayse Bilge Ozel, Matthew Halvorsen, Blood	2020	55
Structural effects of linkage disequilibrium on the transcriptome Joshua S. Martin, Matthew Halvorsen, Lauren Davis-Neulander, RNA	2011	47
Sharing and archiving nucleic acid structure mapping data Philippe Rocca‐Serra, Stanislav Bellaousov, Amanda Birmingham, RNA Molecular BiologyGenomicsBioinformatics DatabaseData IntegrationMedical Ontology	2011	37

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