Cristopher Van Hout
6PUBLICATIONS
54CO-AUTHORS
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Publications (6)
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|Apr 14, 2025
A rare variant in <i>GPR156</i> associated with depression in a Mennonite pedigree causes habenula hyperactivity and stress sensitivity in mice.Bradley R Miller, Claudia Gonzaga-Jauregui, Karlla W Brigatti
|Aug 28, 2024
Identification and functional validation of rare coding variants in genes linked to monogenic obesity.Çiğdem Köroğlu, Michael Traurig, Yunhua L Muller
|Mar 17, 2023
Clinical case study meets population cohort: identification of a BRCA1 pathogenic founder variant in Orcadians.Shona M Kerr, Emma Cowan, Lucija Klaric
|Dec 02, 2021
Genetic and functional evidence links a missense variant in <i>B4GALT1</i> to lower LDL and fibrinogen.May E Montasser, Cristopher V Van Hout, Lawrence Miloscio
|Oct 22, 2020
Exome sequencing and characterization of 49,960 individuals in the UK Biobank.Cristopher V Van Hout, Ioanna Tachmazidou, Joshua D Backman
|Sep 07, 2014
Using Mendelian inheritance to improve high-throughput SNP discovery.Nancy Chen, Cristopher V Van Hout, Srikanth Gottipati
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Frequent Collaborators
3 joint publications
Aris N Economides
2 joint publications
Alan R Shuldiner
1 joint publications
Nancy Chen
1 joint publications
Cristen J Willer
1 joint publications
Joseph B Leader
1 joint publications
David H Ledbetter
1 joint publications
Jeffrey G Reid
1 joint publications
Robert A Scott
1 joint publications
Laura Yerges-Armstrong
1 joint publications
Aris Baras
