Matthew Oetjens
Matthew Oetjens
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Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study
MA Perera, LH Cavallari, NA Limdi, ER Gamazon, A Konkashbaev, ...
The Lancet 382 (9894), 790-796, 2013
Unravelling the human genome–phenome relationship using phenome-wide association studies
WS Bush, MT Oetjens, DC Crawford
Nature Reviews Genetics 17 (3), 129, 2016
Ancient European dog genomes reveal continuity since the Early Neolithic
LR Botigué, S Song, A Scheu, S Gopalan, AL Pendleton, M Oetjens, ...
Nature communications 8 (1), 1-11, 2017
Predicting clopidogrel response using DNA samples linked to an electronic health record
JT Delaney, AH Ramirez, E Bowton, JM Pulley, MA Basford, ...
Clinical Pharmacology & Therapeutics 91 (2), 257-263, 2012
An evolutionary genomic approach to identify genes involved in human birth timing
J Plunkett, S Doniger, G Orabona, T Morgan, R Haataja, M Hallman, ...
PLoS Genet 7 (4), e1001365, 2011
Predicting warfarin dosage in European–Americans and African–Americans using DNA samples linked to an electronic health record
AH Ramirez, Y Shi, JS Schildcrout, JT Delaney, H Xu, MT Oetjens, ...
Pharmacogenomics 13 (4), 407-418, 2012
Facilitating pharmacogenetic studies using electronic health records and natural-language processing: a case study of warfarin
H Xu, M Jiang, M Oetjens, EA Bowton, AH Ramirez, JM Jeff, MA Basford, ...
Journal of the American Medical Informatics Association 18 (4), 387-391, 2011
Association of the FTO Obesity Risk Variant rs8050136 With Percentage of Energy Intake From Fat in Multiple Racial/Ethnic Populations: The PAGE Study
SL Park, I Cheng, SA Pendergrass, AM Kucharska-Newton, U Lim, ...
American journal of epidemiology 178 (5), 780-790, 2013
Assessment of a pharmacogenomic marker panel in a polypharmacy population identified from electronic medical records
MT Oetjens, JC Denny, MD Ritchie, NB Gillani, DM Richardson, ...
Pharmacogenomics 14 (7), 735-744, 2013
Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders
MT Oetjens, MA Kelly, AC Sturm, CL Martin, DH Ledbetter
Nature communications 10 (1), 1-10, 2019
Helitrons: Enigmatic abductors and mobilizers of host genome sequences
S Lal, M Oetjens, LC Hannah
Plant Science 176 (2), 181-186, 2009
Y-chromosome structural diversity in the bonobo and chimpanzee lineages
MT Oetjens, F Shen, SB Emery, Z Zou, JM Kidd
Genome biology and evolution 8 (7), 2231-2240, 2016
Utilization of an EMR-biorepository to identify the genetic predictors of calcineurin-inhibitor toxicity in heart transplant recipients
M Oetjens, WS Bush, KA Birdwell, HH Dilks, EA Bowton, JC Denny, ...
Biocomputing 2014, 253-264, 2014
Analysis of the canid Y-chromosome phylogeny using short-read sequencing data reveals the presence of distinct haplogroups among Neolithic European dogs
MT Oetjens, A Martin, KR Veeramah, JM Kidd
BMC genomics 19 (1), 1-9, 2018
Population stratification in the context of diverse epidemiologic surveys sans genome-wide data
MT Oetjens, K Brown-Gentry, R Goodloe, HH Dilks, DC Crawford
Frontiers in genetics 7, 76, 2016
Evidence for extensive pleiotropy among pharmacogenes
MT Oetjens, WS Bush, JC Denny, K Birdwell, N Kodaman, A Verma, ...
Pharmacogenomics 17 (8), 853-866, 2016
Identification of neuropsychiatric copy number variants in a health care system population
CL Martin, KE Wain, MT Oetjens, K Tolwinski, E Palen, A Hare-Harris, ...
JAMA psychiatry 77 (12), 1276-1285, 2020
Distal chromosome 16p11. 2 duplications containing SH2B1 in patients with scoliosis
B Sadler, G Haller, L Antunes, X Bledsoe, J Morcuende, P Giampietro, ...
Journal of medical genetics 56 (7), 427-433, 2019
Genetic effects on the correlation structure of CVD risk factors: exome-wide data from a Ghanaian population
N Kodaman, RS Sobota, FW Asselbergs, MT Oetjens, JH Moore, ...
Global heart 12 (2), 133-140, 2017
Comprehensive identification of somatic nucleotide variants in human brain tissue
Y Wang, T Bae, J Thorpe, MA Sherman, AG Jones, S Cho, K Daily, Y Dou, ...
bioRxiv, 2020
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