Protocol for identifying genetic modifiers of phenotypes in individuals with disease-associated variants

Authors

Institutions

Publication Details

Journal
STAR Protocols
Published
2026-05-12
DOI
https://doi.org/10.1016/j.xpro.2026.104546
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Protocol for identifying genetic modifiers of phenotypes in individuals with disease-associated variants

Matthew Jensen, Santhosh Girirajan, Corrine Smolen
STAR Protocols
Genomics and Rare Diseases
article

Protocol for identifying genetic modifiers of phenotypes in individuals with disease-associated variants

Matthew Jensen, Santhosh Girirajan, Corrine Smolen
article en

Abstract

No abstract available for this paper.
STAR ProtocolsVol. 7(2)
Pennsylvania State University (US)
National Institute of General Medical Sciences, National Institute of Neurological Disorders and Stroke
Openalex Percentile: Top 7%
Genomics and Rare Diseases
DOIOpen Access PDFOpenAlex
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Protocol for identifying genetic modifiers of phenotypes in individuals with disease-associated variants — Matthew Jensen, Santhosh Girirajan, et al. · STAR Protocols (2026) | TGRS Research Map | TGRS