Search details
1.
Personal omics profiling reveals dynamic molecular and medical phenotypes.
Cell
; 148(6): 1293-307, 2012 Mar 16.
Article
in English
| MEDLINE | ID: mdl-22424236
2.
Frequencies of pharmacogenomic alleles across biogeographic groups in a large-scale biobank.
Am J Hum Genet
; 110(10): 1628-1647, 2023 10 05.
Article
in English
| MEDLINE | ID: mdl-37757824
3.
Evaluating the frequency and the impact of pharmacogenetic alleles in an ancestrally diverse Biobank population.
J Transl Med
; 20(1): 550, 2022 11 28.
Article
in English
| MEDLINE | ID: mdl-36443877
4.
Clinical pharmacogenomic testing and reporting: A technical standard of the American College of Medical Genetics and Genomics (ACMG).
Genet Med
; 24(4): 759-768, 2022 04.
Article
in English
| MEDLINE | ID: mdl-35177334
5.
Verifying nomenclature of DNA variants in submitted manuscripts: Guidance for journals.
Hum Mutat
; 42(1): 3-7, 2021 01.
Article
in English
| MEDLINE | ID: mdl-33252176
6.
Review and Consensus on Pharmacogenomic Testing in Psychiatry.
Pharmacopsychiatry
; 54(1): 5-17, 2021 Jan.
Article
in English
| MEDLINE | ID: mdl-33147643
7.
Pharmacogenomics and big genomic data: from lab to clinic and back again.
Hum Mol Genet
; 27(R1): R72-R78, 2018 05 01.
Article
in English
| MEDLINE | ID: mdl-29635477
8.
The association of obesity and coronary artery disease genes with response to SSRIs treatment in major depression.
J Neural Transm (Vienna)
; 126(1): 35-45, 2019 01.
Article
in English
| MEDLINE | ID: mdl-30610379
9.
Preemptive clinical pharmacogenetics implementation: current programs in five US medical centers.
Annu Rev Pharmacol Toxicol
; 55: 89-106, 2015.
Article
in English
| MEDLINE | ID: mdl-25292429
10.
PharmGKB summary: disulfiram pathway.
Pharmacogenet Genomics
; 33(9): 207-216, 2023 12 01.
Article
in English
| MEDLINE | ID: mdl-37728645
11.
Genome-wide and candidate gene approaches of clopidogrel efficacy using pharmacodynamic and clinical end points-Rationale and design of the International Clopidogrel Pharmacogenomics Consortium (ICPC).
Am Heart J
; 198: 152-159, 2018 04.
Article
in English
| MEDLINE | ID: mdl-29653637
12.
ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG).
Genet Med
; 25(8): 100866, 2023 08.
Article
in English
| MEDLINE | ID: mdl-37347242
13.
Sequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence Data.
PLoS Genet
; 11(10): e1005496, 2015 Oct.
Article
in English
| MEDLINE | ID: mdl-26448358
14.
Working toward precision medicine: Predicting phenotypes from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges.
Hum Mutat
; 38(9): 1182-1192, 2017 09.
Article
in English
| MEDLINE | ID: mdl-28634997
15.
PharmGKB summary: acyclovir/ganciclovir pathway.
Pharmacogenet Genomics
; 32(5): 201-208, 2022 07 01.
Article
in English
| MEDLINE | ID: mdl-35665708
16.
PharmGKB summary: heparin-induced thrombocytopenia pathway, adverse drug reaction.
Pharmacogenet Genomics
; 32(3): 117-124, 2022 04 01.
Article
in English
| MEDLINE | ID: mdl-35102073
17.
Standardizing terms for clinical pharmacogenetic test results: consensus terms from the Clinical Pharmacogenetics Implementation Consortium (CPIC).
Genet Med
; 19(2): 215-223, 2017 02.
Article
in English
| MEDLINE | ID: mdl-27441996
18.
ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG).
Genet Med
; 24(7): 1407-1414, 2022 07.
Article
in English
| MEDLINE | ID: mdl-35802134
19.
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Genet Med
; 19(2): 249-255, 2017 02.
Article
in English
| MEDLINE | ID: mdl-27854360
20.
Expanding evidence leads to new pharmacogenomics payer coverage.
Genet Med
; 23(5): 830-832, 2021 05.
Article
in English
| MEDLINE | ID: mdl-33627827