Articles with public access mandates - David E LarsonLearn more
Available somewhere: 58
Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences
L Ganel, L Chen, R Christ, J Vangipurapu, E Young, I Das, K Kanchi, ...
Human genomics 15 (1), 1-17, 2021
Mandates: US National Institutes of Health, Academy of Finland, UK Medical Research …
Bam-readcount-rapid generation of basepair-resolution sequence metrics
A Khanna, DE Larson, SN Srivatsan, M Mosior, TE Abbott, S Kiwala, ...
ArXiv, 2021
Mandates: US National Institutes of Health
Association of structural variation with cardiometabolic traits in Finns
L Chen, HJ Abel, I Das, DE Larson, L Ganel, KL Kanchi, AA Regier, ...
The American Journal of Human Genetics 108 (4), 583-596, 2021
Mandates: US National Institutes of Health, Academy of Finland
Mitochondrial genome copy number in human blood-derived DNA is strongly associated with insulin levels and related metabolic traits and primarily reflects cell-type composition …
L Ganel, L Chen, R Christ, J Vangipurapu, E Young, I Das, K Kanchi, ...
MedRxiv, 2020.10. 23.20218586, 2020
Mandates: US National Institutes of Health, Academy of Finland
Mapping and characterization of structural variation in 17,795 human genomes
HJ Abel, DE Larson, AA Regier, C Chiang, I Das, KL Kanchi, RM Layer, ...
Nature 583 (7814), 83-89, 2020
Mandates: US National Institutes of Health, Academy of Finland, State of Califonia
The clonal evolution of metastatic colorectal cancer
HX Dang, BA Krasnick, BS White, JG Grossman, MS Strand, J Zhang, ...
Science advances 6 (24), eaay9691, 2020
Mandates: US National Institutes of Health
Exome sequencing of Finnish isolates enhances rare-variant association power
AE Locke, KM Steinberg, CWK Chiang, SK Service, AS Havulinna, L Stell, ...
Nature 572 (7769), 323-328, 2019
Mandates: US National Institutes of Health, National Health and Medical Research …
svtools: population-scale analysis of structural variation
DE Larson, HJ Abel, C Chiang, A Badve, I Das, JM Eldred, RM Layer, ...
Bioinformatics 35 (22), 4782-4787, 2019
Mandates: US National Institutes of Health
A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease
X Zhang, C Zhu, G Beecham, BN Vardarajan, Y Ma, D Lancour, JJ Farrell, ...
Alzheimer's & Dementia 15 (3), 441-452, 2019
Mandates: US National Institutes of Health
Exome sequencing identifies high-impact trait-associated alleles enriched in Finns
AE Locke, K Meltz Steinberg, CWK Chiang, SK Service, AS Havulinna, ...
bioRxiv, 464255, 2018
Mandates: National Health and Medical Research Council, Australia, Academy of Finland …
Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects
AA Regier, Y Farjoun, DE Larson, O Krasheninina, HM Kang, ...
Nature communications 9 (1), 4038, 2018
Mandates: US National Institutes of Health
The prognostic effects of somatic mutations in ER-positive breast cancer
OL Griffith, NC Spies, M Anurag, M Griffith, J Luo, D Tu, B Yeo, J Kunisaki, ...
Nature communications 9 (1), 3476, 2018
Mandates: US Department of Defense, US National Institutes of Health, Canadian Cancer …
Bioconda: Sustainable and comprehensive software distribution for the life sciences
R Dale, B Grüning, A Sjödin, J Rowe, BA Chapman, CH Tomkins-Tinch, ...
Nature Methods 15 (7), 475-476, 2018
Mandates: US National Institutes of Health, German Research Foundation, Netherlands …
Comprehensive discovery of noncoding RNAs in acute myeloid leukemia cell transcriptomes
J Zhang, M Griffith, CA Miller, OL Griffith, DH Spencer, JR Walker, ...
Experimental Hematology 55, 19-33, 2017
Mandates: US National Institutes of Health
The Alzheimer's disease sequencing project: study design and sample selection
GW Beecham, JC Bis, ER Martin, SH Choi, AL DeStefano, CM Van Duijn, ...
Neurology Genetics 3 (5), 2017
Mandates: US Department of Defense, US National Institutes of Health
CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancer
M Griffith, NC Spies, K Krysiak, JF McMichael, AC Coffman, AM Danos, ...
Nature genetics 49 (2), 170-174, 2017
Mandates: US National Institutes of Health, Government of Spain, Federal Ministry of …
Rare Variation in TET2 Is Associated with Clinically Relevant Prostate Carcinoma in African Americans
DC Koboldt, KL Kanchi, B Gui, DE Larson, RS Fulton, WB Isaacs, A Kraja, ...
Cancer Epidemiology, Biomarkers & Prevention 25 (11), 1456-1463, 2016
Mandates: US National Institutes of Health
The role of rare protein‐coding variants to anti‐TNF treatment response in rheumatoid arthritis
J Cui, D Diogo, EA Stahl, H Canhao, X Mariette, JD Greenberg, Y Okada, ...
Arthritis & Rheumatology, 2016
Mandates: US National Institutes of Health, National Institute for Health Research, UK
Truncating Prolactin Receptor Mutations Promote Tumor Growth in Murine Estrogen Receptor-Alpha Mammary Carcinomas
OL Griffith, SR Chan, M Griffith, K Krysiak, ZL Skidmore, J Hundal, ...
Cell Reports 17 (1), 249-260, 2016
Mandates: US National Institutes of Health
Aromatase inhibition remodels the clonal architecture of estrogen-receptor-positive breast cancers
CA Miller, Y Gindin, C Lu, OL Griffith, M Griffith, D Shen, J Hoog, T Li, ...
Nature Communications 7, 2016
Mandates: US National Institutes of Health, Susan G. Komen
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