M. Oetjens

发表

Predicting warfarin dosage in European-Americans and African-Americans using DNA samples linked to an electronic health record.

Melissa A. Basford, Raquel M. Zink, D. Roden, 2012, Pharmacogenomics.

Evidence for extensive pleiotropy among pharmacogenes.

W. Bush, J. Denny, M. Ritchie, 2016, Pharmacogenomics.

Unravelling the human genome–phenome relationship using phenome-wide association studies

Dana C. Crawford, William S. Bush, W. Bush, 2016, Nature Reviews Genetics.

Predicting Clopidogrel Response Using DNA Samples Linked to an Electronic Health Record

D. Roden, J. Schildcrout, M. Ritchie, 2012, Clinical pharmacology and therapeutics.

An Evolutionary Genomic Approach to Identify Genes Involved in Human Birth Timing

Leena Peltonen, Edward Kuczynski, Scott Doniger, 2011, PLoS genetics.

Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders

D. Ledbetter, M. Oetjens, A. Sturm, 2019, Nature Communications.

Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study

Yusuke Nakamura, Dan M Roden, Matthew Oetjens, 2013, The Lancet.

Inferring chimpanzee Y chromosome history and amplicon diversity from whole genome sequencing

J. Kidd, F. Shen, M. Oetjens, 2015 .

Identification of Neuropsychiatric Copy Number Variants in a Health Care System Population

D. Ledbetter, C. Martin, L. Habegger, 2020, JAMA psychiatry.

Frequency of truncating FLCN variants and Birt-Hogg-Dubé-associated phenotypes in a health care system population.

D. Ledbetter, C. Martin, M. Oetjens, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Molecular Diagnostic Yield of Exome Sequencing in Patients With Cerebral Palsy.

Vladimir G. Gainullin, D. Ledbetter, C. Martin, 2021, JAMA.

Distal chromosome 16p11.2 duplications containing SH2B1 in patients with scoliosis

Nephi A. Walton, Yared H. Kidane, T. Druley, 2019, Journal of Medical Genetics.

Whole genome sequencing reveals host factors underlying critical Covid-19 Accelerated Article Preview

G. Abecasis, C. Ponting, K. Rawlik, 2022 .

Y-Chromosome Structural Diversity in the Bonobo and Chimpanzee Lineages

J. Kidd, Sarah B. Emery, F. Shen, 2016, bioRxiv.

ANGPTL7, a therapeutic target for increased intraocular pressure and glaucoma

Alexander E. Lopez, Tanya M. Teslovich, Gaurang C. Patel, 2022, Communications Biology.

Prevalence and Penetrance of Rare Pathogenic Variants in Neurodevelopmental Psychiatric Genes in a Health Care System Population.

D. Ledbetter, C. Martin, M. Oetjens, 2022, The American journal of psychiatry.

Medical manifestations and healthcare utilization among adult MyCode participants with neurodevelopmental psychiatric copy number variants

D. Ledbetter, L. Habegger, H. Kirchner, 2021, Genetics in Medicine.

Whole-genome sequencing reveals host factors underlying critical COVID-19

Eurie L. Hong, Mohammed A. Eid, Daniel J. Wilson, 2022, Nature.

GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms

Alexander E. Lopez, Dustin N. Hartzel, Andrew L Blumenfeld, 2021, Nature Communications.

Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank

Alexander E. Lopez, David P. vanMaanen, K. Lunetta, 2022, Nature Genetics.

Ancient European dog genomes reveal continuity since the Early Neolithic

Matthew Oetjens, Joachim Burger, Amelie Scheu, 2016, Nature Communications.

Gene-level analysis of rare variants in 379,066 whole exome sequences identifies an association of GIGYF1 loss of function with type 2 diabetes

Alexander E. Lopez, Dustin N. Hartzel, Andrew L Blumenfeld, 2021, Scientific Reports.

Population Genomic Screening for Genetic Etiologies of Neurodevelopmental/Psychiatric Disorders Demonstrates Personal Utility and Positive Participant Responses

D. Ledbetter, C. Martin, M. Oetjens, 2021, Journal of personalized medicine.

Developing and Optimizing Innovative Tools to Address Familial Hypercholesterolemia Underdiagnosis

Laney K. Jones, Ilene G. Ladd, Nephi A. Walton, 2021, Circulation. Genomic and precision medicine.

Assessment of a pharmacogenomic marker panel in a polypharmacy population identified from electronic medical records.

Nicole A. Restrepo, Melissa A. Basford, Niloufar B. Gillani, 2013, Pharmacogenomics.

Comprehensive identification of somatic nucleotide variants in human brain tissue

Peter J. Park, Jonathan Pevsner, Eduardo Soriano, 2020, bioRxiv.

Electronic health record analysis identifies kidney disease as the leading risk factor for hospitalization in confirmed COVID-19 patients

Dustin N. Hartzel, D. Ledbetter, H. Kirchner, 2020, PloS one.

Population Stratification in the Context of Diverse Epidemiologic Surveys Sans Genome-Wide Data

Dana C. Crawford, Holli H. Dilks, Robert J. Goodloe, 2016, Front. Genet..

Peer Review File Manuscript Title: Whole genome sequencing identifies multiple loci for critical illness caused by COVID-19 Reviewer Comments & Author Rebuttals

Mohammed A. Eid, Daniel J. Wilson, Nathan D. Berkowitz, 2022 .

Leveraging population‐based exome screening to impact clinical care: The evolution of variant assessment in the Geisinger MyCode research project

D. Ledbetter, C. Martin, M. Oetjens, 2021, American journal of medical genetics. Part C, Seminars in medical genetics.

Analysis of the canid Y-chromosome phylogeny using short-read sequencing data reveals the presence of distinct haplogroups among Neolithic European dogs

K. Veeramah, J. Kidd, M. Oetjens, 2018, BMC Genomics.

Frequency of FLCN Loss of Function Variants and Birt-Hogg-Dube-Associated Phenotypes in a Healthcare System Population

D. Ledbetter, M. Oetjens, A. Moreno-De-Luca, 2022, medRxiv.

Association of the FTO obesity risk variant rs8050136 with percentage of energy intake from fat in multiple racial/ethnic populations: the PAGE study.

Robert J. Goodloe, B. Henderson, C. Haiman, 2013, American journal of epidemiology.

Comprehensive identification of somatic nucleotide variants in human brain tissue

J. V. Moran, Lovelace J. Luquette, Laurel L. Ball, 2021, Genome Biology.

Analysis of the canid Y-chromosome phylogeny using short-read sequencing data reveals the presence of distinct haplogroups among Neolithic European dogs

K. Veeramah, J. Kidd, M. Oetjens, 2018, BMC Genomics.

Facilitating pharmacogenetic studies using electronic health records and natural-language processing: a case study of warfarin

Hua Xu, Marylyn D. Ritchie, Joshua C. Denny, 2011, J. Am. Medical Informatics Assoc..

Helitrons: Enigmatic abductors and mobilizers of host genome sequences

M. Oetjens, L. C. Hannah, S. Lal, 2009 .

Yield of Familial Hypercholesterolemia Genetic and Phenotypic Diagnoses After Electronic Health Record and Genomic Data Screening

H. Kirchner, M. Oetjens, A. Sturm, 2023, Journal of the American Heart Association.

Association of Supernumerary Sex Chromosome Aneuploidies With Venous Thromboembolism.

D. Ledbetter, C. Martin, H. Kirchner, 2023, JAMA.

Subtyping Severe Hypercholesterolemia by Genetic Determinant to Stratify Risk of Coronary Artery Disease

E. Sijbrands, S. Gidding, M. Oetjens, 2023, Arteriosclerosis, Thrombosis and Vascular Biology.

Common and Rare Variant Contributions to Bradyarrhythmias from Multi-Ancestry Meta-Analyses

K. Lunetta, H. May, P. Ellinor, 2023, medRxiv.

Abstract 19509: Identifying Genotype-Phenotype Relations in Electronic Medical Record Systems: Application to Warfarin Pharmacogenomics.

Marylyn D. Ritchie, Joshua C. Denny, Dana C. Crawford, 2010 .

Genetic Effects on the Correlation Structure of CVD Risk Factors: Exome-Wide Data From a Ghanaian Population.

Rafal S. Sobota, Scott M. Williams, M. Aldrich, 2017, Global heart.

Predicting Clopidogrel Response Using DNA Samples Linked to an Electronic Health Record

Melissa A. Basford, Raquel M. Zink, D. Roden, 2012, Clinical pharmacology and therapeutics.