NHGRI logo

Accomplishments in Genomic Medicine

The NHGRI Genomic Medicine Working Group (GMWG) compiles a list of interesting advances and helpful educational resources in genomic medicine. To submit notable accomplishments for consideration to the GMWG, please email: GMWG@nih.gov.

Search for specific publications by title, author, category and/or by date range.  For an explanation about the selection criteria and categories, see the list of categories and their definitions.


2020

January 14, 2020 - Comprehensive genetic diagnosis of Japanese patients with severe proteinuria

First Author: Nagano C

Category: Systematic Implementation , Sequencing

2019

December 20, 2019 - Assessing relatives’ readiness for hereditary cancer cascade genetic testing

First Author: Bednar E

Category: Pilot Implementation , Oncology

December 05, 2019 - TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands

First Author: van der Meij K

Category: Systematic Implementation

November 29, 2019 - Prospective, Phenotype-Driven Selection of Critically Ill Neonates for Rapid Exome Sequencing Is Associated With High Diagnostic Yield

First Author: Gubbels, C

Category: Sequencing , Systematic Implementation

November 25, 2019 - Returning incidental findings in African genomics research

First Author: Wonkam A

Category: Resource

November 11, 2019 - Rare Genetic Variants Associated With Sudden Cardiac Death in Adults

First Author: Khera, A

Category: Gene-Disease Validation

October 31, 2019 - Elexacaftor-Tezacaftor-Ivacaftor fo Cystic Fibrosis with a Single Phe508del Allele

First Author: Middleton, P

Category: Gene-Disease Validation

October 31, 2019 - Genome Sequencing Explore Complexity of Chromosomal Abnormalities in Recurrent Miscarriage

First Author: Dong, Z

Category: Sequencing

October 24, 2019 - A Genotype-Guided Strategy for Oral P2Y12 Inhibitors in Primary PCI

First Author: Claassens, D

Category: Pharmacogenomics

October 09, 2019 - Patient-customized oligonucleotide therapy for a rare genetic disease

First Author: Kim J

Category: Pilot Implementation

October 02, 2019 - Assessment of Diagnostic Outcomes of RNA Genetic Testing for Hereditary Cancer 

First Author: Karam R

Category: Oncology , Risk Assessment/Prediction , Variant Classification

August 22, 2019 - Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network

First Author: eMERGE Consortium

Category: Sequencing , Systematic Implementation

August 17, 2019 - A Decision-Theoretic Approach to Panel-Based, Preemptive Genotyping.

First Author: Shi, Y

Category: Pharmacogenomics , Systematic Implementation

August 05, 2019 - Opportunities, resources, and techniques for implementing genomics in clinical care

First Author: Manolio T

Category: Resource

August 05, 2019 - Building evidence and measuring clinical outcomes for genomic medicine

First Author: Peterson J

Category: Resource

August 05, 2019 - Genomic medicine for undiagnosed diseases

First Author: Wise A

Category: Resource

August 05, 2019 - Pharmacogenomics

First Author: Roden D

Category: Resource

August 05, 2019 - Family health history: underused for actionable risk assessment

First Author: Ginsburg G

Category: Resource

Last updated: September 11, 2024