Search details
1.
Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing.
Am J Hum Genet
; 110(11): 1950-1958, 2023 11 02.
Article
in English
| MEDLINE | ID: mdl-37883979
2.
Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study.
Circulation
; 145(12): 877-891, 2022 03 22.
Article
in English
| MEDLINE | ID: mdl-34930020
3.
Returning integrated genomic risk and clinical recommendations: The eMERGE study.
Genet Med
; 25(4): 100006, 2023 04.
Article
in English
| MEDLINE | ID: mdl-36621880
4.
Rates of Actionable Genetic Findings in Individuals with Colorectal Cancer or Polyps Ascertained from a Community Medical Setting.
Am J Hum Genet
; 105(3): 526-533, 2019 09 05.
Article
in English
| MEDLINE | ID: mdl-31422818
5.
Pleiotropy of systemic lupus erythematosus risk alleles and cardiometabolic disorders: A phenome-wide association study and inverse-variance weighted meta-analysis.
Lupus
; 30(8): 1264-1272, 2021 Jul.
Article
in English
| MEDLINE | ID: mdl-33977795
6.
The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype.
Genet Epidemiol
; 43(1): 63-81, 2019 02.
Article
in English
| MEDLINE | ID: mdl-30298529
7.
Association of Genetic Risk of Obesity with Postoperative Complications Using Mendelian Randomization.
World J Surg
; 44(1): 84-94, 2020 01.
Article
in English
| MEDLINE | ID: mdl-31605180
8.
Probing the Virtual Proteome to Identify Novel Disease Biomarkers.
Circulation
; 138(22): 2469-2481, 2018 11 27.
Article
in English
| MEDLINE | ID: mdl-30571344
9.
Consideration of disease penetrance in the selection of secondary findings gene-disease pairs: A policy statement of the American College of Medical Genetics and Genomics (ACMG).
Genet Med
; : 101142, 2024 May 30.
Article
in English
| MEDLINE | ID: mdl-38819344
10.
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
11.
Pathogenic variants for Mendelian and complex traits in exomes of 6,517 European and African Americans: implications for the return of incidental results.
Am J Hum Genet
; 95(2): 183-93, 2014 Aug 07.
Article
in English
| MEDLINE | ID: mdl-25087612
12.
Response to McGurk et al.
Genet Med
; 24(3): 747-748, 2022 03.
Article
in English
| MEDLINE | ID: mdl-34906521
13.
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
14.
Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset.
Hum Mol Genet
; 23(8): 1957-63, 2014 Apr 15.
Article
in English
| MEDLINE | ID: mdl-24282029
15.
PGRNseq: a targeted capture sequencing panel for pharmacogenetic research and implementation.
Pharmacogenet Genomics
; 26(4): 161-168, 2016 Apr.
Article
in English
| MEDLINE | ID: mdl-26736087
16.
ACMG SF v3.0 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
; 23(8): 1381-1390, 2021 08.
Article
in English
| MEDLINE | ID: mdl-34012068
17.
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG).
Genet Med
; 23(8): 1391-1398, 2021 08.
Article
in English
| MEDLINE | ID: mdl-34012069
18.
Correction to: ACMG SF v3.0 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
; 23(8): 1582-1584, 2021 Aug.
Article
in English
| MEDLINE | ID: mdl-34345026
19.
Rare coding variation in paraoxonase-1 is associated with ischemic stroke in the NHLBI Exome Sequencing Project.
J Lipid Res
; 55(6): 1173-8, 2014 06.
Article
in English
| MEDLINE | ID: mdl-24711634
20.
Refining the structure and content of clinical genomic reports.
Am J Med Genet C Semin Med Genet
; 166C(1): 85-92, 2014 Mar.
Article
in English
| MEDLINE | ID: mdl-24616401