Katrin Mannik
Geneve, GE 2030, Switzerland
Last Updated: 09/26/2026
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Found 25 publications
Genetic modifiers and ascertainment drive variable expressivity of complex disorders.
Journal: medRxiv : the preprint server for health sciences
Published: September 10, 2024
Genetic modifiers and ascertainment drive variable expressivity of complex disorders.
Journal: Cell
Published: August 19, 2024
Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts.
Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts.
Journal: NPJ genomic medicine
Published: June 09, 2021
Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.
Journal: Addiction biology
Published: August 21, 2019
The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals.
Journal: American journal of human genetics
Published: June 27, 2019
Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: April 17, 2018
CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits.
Journal: Nature communications
Published: February 28, 2017
Analysis of shared heritability in common disorders of the brain.
Journal: Science (New York, N.Y.)
Published: April 15, 2016
Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities.
Journal: JAMA psychiatry
Published: December 03, 2015
Last Updated: 09/26/2026