Katrin Männik
University of Tartu(EE)University of Lausanne(CH)
Publications by Year
Research Areas
Genetic Associations and Epidemiology, Eating Disorders and Behaviors, Genomics and Rare Diseases, Obesity, Physical Activity, Diet, Genomic variations and chromosomal abnormalities
Most-Cited Works
- → A genome-wide association study of anorexia nervosa(2014)332 cited
- → Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome(2009)218 cited
- → Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index(2016)75 cited
- → Increased Dosage of RAB39B Affects Neuronal Development and Could Explain the Cognitive Impairment in Male Patients with Distal Xq28 Copy Number Gains(2013)64 cited
- → The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals(2019)52 cited
- → Maternally and paternally inherited deletion of 7q31 involving the FOXP2 gene in two families(2011)36 cited
- → A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling(2017)35 cited
- → 5.9 Mb microdeletion in chromosome band 17q22–q23.2 associated with tracheo-esophageal fistula and conductive hearing loss(2008)30 cited
- → Genetic modifiers and ascertainment drive variable expressivity of complex disorders(2025)6 cited
- → Leveraging biobank-scale rare and common variant analyses to identify ASPHD1 as the main driver of reproductive traits in the 16p11.2 locus(2019)5 cited