Matthew Halvorsen

2.0k total citations
38 papers, 999 citations indexed

About

Matthew Halvorsen is a scholar working on Molecular Biology, Genetics and Clinical Psychology. According to data from OpenAlex, Matthew Halvorsen has authored 38 papers receiving a total of 999 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 13 papers in Genetics and 9 papers in Clinical Psychology. Recurrent topics in Matthew Halvorsen's work include Obsessive-Compulsive Spectrum Disorders (8 papers), Autism Spectrum Disorder Research (7 papers) and Genetic Associations and Epidemiology (6 papers). Matthew Halvorsen is often cited by papers focused on Obsessive-Compulsive Spectrum Disorders (8 papers), Autism Spectrum Disorder Research (7 papers) and Genetic Associations and Epidemiology (6 papers). Matthew Halvorsen collaborates with scholars based in United States, Sweden and Denmark. Matthew Halvorsen's co-authors include Alain Laederach, Joshua S. Martin, David B. Goldstein, Slavé Petrovski, Quanli Wang, Amanda Solem, Orrin Devinsky, Laura Gould, Silvia B. V. Ramos and Andrew S. Allen and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Blood.

In The Last Decade

Matthew Halvorsen

33 papers receiving 992 citations

Peers

Countries citing papers authored by Matthew Halvorsen

Since Specialization

Citations

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

Fields of papers citing papers by Matthew Halvorsen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matthew Halvorsen. 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 Matthew Halvorsen. The network helps show where Matthew Halvorsen may publish in the future.

Co-authorship network of co-authors of Matthew Halvorsen

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew Halvorsen. A scholar is included among the top collaborators of Matthew Halvorsen 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 Matthew Halvorsen. Matthew Halvorsen 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	Optimizing genetic ancestry adjustment in DNA methylation studies: a comparative analysis of approaches 2025 ·Epigenetics & Chromatin ·(unknown), Şeyma Katrinli, Matthew Halvorsen, Anne-Kristin Stavrum, Kevin S. O’Connell, Alexey Shadrin, Srdjan Djurovic, Ole A. Andreassen, James J. Crowley, Jan Haavik, Kristen Hagen, Gerd Kvale, (unknown), Bjarne Hansen, Jair C. Soares, Gabriel R. Fries, Alicia K. Smith, Stéphanie Le Hellard	0
2	Polygenic scores and symptom severity change after internet-delivered cognitive behaviour therapy for depression and anxiety 2025 ·Discover Mental Health ·Julia Boberg, John Wallert, Matthew Halvorsen, James J. Crowley, David Mataix‐Cols, Christian Rück	1
3	ARFID Genes and Environment (ARFID-GEN): study protocol 2023 ·BMC Psychiatry ·Cynthia M. Bulik, Nadia Micali, Casey M. MacDermod, (unknown), Melissa A. Munn‐Chernoff, Laura M. Thornton, (unknown), Lisa Dinkler, Emily M. Pisetsky, Jessica Johnson, (unknown), Shelby N. Ortiz, (unknown), (unknown), (unknown), Jerry Guintivano, Matthew Halvorsen, James J. Crowley	7
4	Exome sequencing in obsessive–compulsive disorder reveals a burden of rare damaging coding variants 2021 ·Nature Neuroscience ·Matthew Halvorsen, Jack Samuels, Ying Wang, Benjamin D. Greenberg, Abby J. Fyer, James T. McCracken, Daniel Geller, James A. Knowles, Anthony W. Zoghbi, Tess D. Pottinger, (unknown), Mark A. Riddle, O. Joseph Bienvenu, Paul S. Nestadt, Janice Krasnow, Fernando S. Goes, Brion S. Maher, Gerald Nestadt, David B. Goldstein	36
5	Genetic architecture of Tourette syndrome: our current understanding 2021 ·Psychological Medicine ·(unknown), Carolina Cappi, Matthew Halvorsen	9
6	Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease 2020 ·Blood ·Karl C. Desch, Ayse Bilge Ozel, Matthew Halvorsen, Paula M. Jacobi, Krista Golden, Mary Underwood, Marine Germain, David‐Alexandre Trégouët, Pieter H. Reitsma, Clive Kearon, Lauren E. Mokry, J. Brent Richards, Frances M. K. Williams, Jun Z. Li, David B. Goldstein, David Ginsburg	31
7	Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia 2020 ·Nature Communications ·Matthew Halvorsen, Ruth Huh, Nikolay Oskolkov, Jia Wen, Sergiu Netotea, Paola Giusti‐Rodríguez, Robert Karlsson, Julien Bryois, Björn Nystedt, Adam Ameur, Anna K. Kähler, (unknown), Martilias S. Farrell, James J. Crowley, Yun Li, Patrik K. E. Magnusson, Ulf Gyllensten, Christina M. Hultman, Patrick F. Sullivan, Jin Szatkiewicz	42
8	Sudden unexpected death in asymptomatic infants due to PPA2 variants 2019 ·Molecular Genetics & Genomic Medicine ·Colin K. L. Phoon, Matthew Halvorsen, David B. Goldstein, Rachel Rabin, Frank Cecchin, Laura Gould, Orrin Devinsky	20
9	Nordic OCD & Related Disorders Consortium: Rationale, design, and methods 2019 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·David Mataix‐Cols, Bjarne Hansen, Manuel Mattheisen, Elinor K. Karlsson, Anjené Addington, Julia Boberg, Diana R. Djurfeldt, Matthew Halvorsen, Paul Lichtenstein, Stian Solem, Kerstin Lindblad‐Toh, Jan Haavik, Gerd Kvale, Christian Rück, James J. Crowley	11
10	meaRtools: An R package for the analysis of neuronal networks recorded on microelectrode arrays 2018 ·PLoS Computational Biology ·Sahar Gelfman, Quanli Wang, Yifan Lu, (unknown), Christopher D. Bostick, Ryan S. Dhindsa, Matthew Halvorsen, K. Melodi McSweeney, (unknown), (unknown), Michael Beaumont, Wayne N. Frankel, Slavé Petrovski, Andrew S. Allen, Michael J. Boland, David B. Goldstein, Stephen J. Eglen	19
11	Annotating pathogenic non-coding variants in genic regions 2017 ·Nature Communications ·Sahar Gelfman, Quanli Wang, K. Melodi McSweeney, Zhong Ren, Francesca La Carpia, Matthew Halvorsen, Kelly Schoch, (unknown), Erin L. Heinzen, Michael J. Boland, Slavé Petrovski, David B. Goldstein	99
12	Exome Sequencing Studies Identify Mutations in STAB2 As a Genetic Risk for Venous Thromboembolic Disease 2017 ·Blood ·Karl C. Desch, Ayse Bilge Ozel, Matthew Halvorsen, Alison Michels, Laura L. Swystun, Lauren E. Mokry, Brent Richards, Marine Germain, David‐Alexandre Trégouët, Pieter H. Reitsma, Clive Kearon, Jun Z. Li, David B. Goldstein, David Lillicrap, David Ginsburg	4
13	Whole Exome Sequencing Reveals Severe Thrombophilia in Acute Unprovoked Idiopathic Fatal Pulmonary Embolism 2017 ·EBioMedicine ·Matthew Halvorsen, Ying Lin, Barbara A. Sampson, Dawei Wang, Bo Zhou, (unknown), Sung Yon Um, Orrin Devinsky, David B. Goldstein, Yingying Tang	11
14	A unified analytic framework for prioritization of non-coding variants of uncertain significance in heritable breast and ovarian cancer 2016 ·BMC Medical Genomics ·Eliseos J. Mucaki, Natasha Caminsky, Ami M. Perri, (unknown), Alain Laederach, Matthew Halvorsen, Joan H.M. Knoll, Peter K. Rogan	14
15	Short- and long-term effects of exercise on neck muscle function in cervical radiculopathy: A randomized clinical trial 2016 ·Journal of Rehabilitation Medicine ·Matthew Halvorsen, Deborah Falla, Leonardo Gizzi, Karin Harms‐Ringdahl, Anneli Peolsson, Åsa Dedering	21
16	Mosaic mutations in early-onset genetic diseases 2015 ·Genetics in Medicine ·Matthew Halvorsen, Slavé Petrovski, Renée A. Shellhaas, Yingying Tang, Laura Gould, David B. Goldstein, Orrin Devinsky	47
17	Multiple conformations are a conserved and regulatory feature of the RB1 5′ UTR 2015 ·RNA ·Katrina M. Kutchko, Wes Sanders, (unknown), Gabriela Phillips, Amanda Solem, Matthew Halvorsen, Kevin M. Weeks, Nathaniel J. Moorman, Alain Laederach	51
18	Structural effects of linkage disequilibrium on the transcriptome 2011 ·RNA ·Joshua S. Martin, Matthew Halvorsen, (unknown), Justin Ritz, (unknown), Arthur Beauregard, Alain Laederach	34
19	A novel application of pattern recognition for accurate SNP and indel discovery from high-throughput data: Targeted resequencing of the glucocorticoid receptor co-chaperone FKBP5 in a Caucasian population 2011 ·Molecular Genetics and Metabolism ·Linda L. Pelleymounter, Irene Moon, Julie A. Johnson, Alain Laederach, Matthew Halvorsen, Bruce W. Eckloff, Ryan Abo, Sandro Rossetti	16
20	Sharing and archiving nucleic acid structure mapping data 2011 ·RNA ·Philippe Rocca‐Serra, Stanislav Bellaousov, Amanda Birmingham, Chunxia Chen, Pablo Cordero, Rhiju Das, (unknown), Caia D. S. Duncan, Matthew Halvorsen, Rob Knight, Neocles B. Leontis, David H. Mathews, Justin Ritz, Jesse Stombaugh, Kevin M. Weeks, Craig L. Zirbel, Alain Laederach	24

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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