The search for allelic variants that cause monogenic disorders or predispose to common, complex polygenic phenotypes.

Authors:
Antonarakis SE.

Journal:
Dialogues Clin Neurosci

Publication Year: 2001

PMCID:
PMC3181641

PMID:
22034389

Journal Information

Journal Title: Dialogues Clin Neurosci

Detailed journal information not available.

Publication Details

Subject Category: Neurosciences

Available in Europe PMC: Yes

Available in PMC: Yes

PDF Available: No

Transparency Score
1/6
0.0% Transparent
Transparency Indicators
Click on green indicators to view evidence text
Core Indicators
Data Sharing
Code Sharing
COI Disclosure
Evidence found in paper:

"I thank Dr Robert Lyle for critical reading of this manuscript; I also thank all the members of our laboratory, past and present, for ideas, debates, curiosity, experiments, enthusiasm, and hard work. The research in our laboratory has been supported over the last 20 years by numerous funding agencies, mainly the NIH, the Swiss National Science Foundation, and the European Union,"

Protocol Registration
Open Access
Additional Indicators
Replication
Novelty Statement
Assessment Info

Tool: rtransparent

OST Version: N/A

Last Updated: Aug 05, 2025