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Katrin Männik
Katrin Männik
Center for Integrative Genomics, University of Lausanne; Estonian Genome Center, University of Tartu
Verified email at unil.ch
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Cited by
Cited by
Year
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
13702018
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa
HJ Watson, Z Yilmaz, LM Thornton, C Hübel, JRI Coleman, HA Gaspar, ...
Nature genetics 51 (8), 1207-1214, 2019
7942019
Investigating neural primacy in Major Depressive Disorder: multivariate Granger causality analysis of resting-state fMRI time-series data
JP Hamilton, G Chen, ME Thomason, ME Schwartz, IH Gotlib
Molecular psychiatry 16 (7), 763-772, 2011
696*2011
A new highly penetrant form of obesity due to deletions on chromosome 16p11. 2
RG Walters, S Jacquemont, A Valsesia, AJ de Smith, D Martinet, ...
Nature 463 (7281), 671-675, 2010
5912010
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11. 2 locus
S Jacquemont, A Reymond, F Zufferey, L Harewood, RG Walters, ...
Nature 478 (7367), 97-102, 2011
5302011
A 600 kb deletion syndrome at 16p11. 2 leads to energy imbalance and neuropsychiatric disorders
F Zufferey, EH Sherr, ND Beckmann, E Hanson, AM Maillard, L Hippolyte, ...
Journal of medical genetics 49 (10), 660-668, 2012
3082012
Defining the effect of the 16p11. 2 duplication on cognition, behavior, and medical comorbidities
D D’Angelo, S Lebon, Q Chen, S Martin-Brevet, LAG Snyder, L Hippolyte, ...
JAMA psychiatry 73 (1), 20-30, 2016
2262016
Fourteen new cases contribute to the characterization of the 7q11. 23 microduplication syndrome
N Van der Aa, L Rooms, G Vandeweyer, J van den Ende, E Reyniers, ...
European journal of medical genetics 52 (2-3), 94-100, 2009
2262009
The 16p11. 2 locus modulates brain structures common to autism, schizophrenia and obesity
AM Maillard, A Ruef, F Pizzagalli, E Migliavacca, L Hippolyte, ...
Molecular psychiatry 20 (1), 140-147, 2015
1972015
Copy number variations and cognitive phenotypes in unselected populations
K Männik, R Mägi, A Macé, B Cole, AL Guyatt, HA Shihab, AM Maillard, ...
Jama 313 (20), 2044-2054, 2015
1722015
Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants
L Pizzo, M Jensen, A Polyak, JA Rosenfeld, K Mannik, A Krishnan, ...
Genetics in Medicine 21 (4), 816-825, 2019
1492019
Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders, and known risk factors
N Mullins, JE Kang, AI Campos, JRI Coleman, AC Edwards, H Galfalvy, ...
Biological psychiatry 91 (3), 313-327, 2022
1362022
The number of genomic copies at the 16p11. 2 locus modulates language, verbal memory, and inhibition
L Hippolyte, AM Maillard, B Rodriguez-Herreros, A Pain, S Martin-Brevet, ...
Biological psychiatry 80 (2), 129-139, 2016
962016
Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes
MN Loviglio, M Leleu, K Männik, M Passeggeri, G Giannuzzi, ...
Molecular Psychiatry 22 (6), 836-849, 2017
892017
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index
A Hinney, M Kesselmeier, S Jall, AL Volckmar, M Föcker, J Antel, IM Heid, ...
Molecular psychiatry 22 (2), 192-201, 2017
842017
16p11. 2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy
EM Reinthaler, D Lal, S Lebon, MS Hildebrand, HHM Dahl, BM Regan, ...
Human molecular genetics 23 (22), 6069-6080, 2014
782014
A potential contributory role for ciliary dysfunction in the 16p11. 2 600 kb BP4-BP5 pathology
E Migliavacca, C Golzio, K Männik, I Blumenthal, EC Oh, L Harewood, ...
The American Journal of Human Genetics 96 (5), 784-796, 2015
672015
Increased Dosage of RAB 39 B Affects Neuronal Development and Could Explain the Cognitive Impairment in Male Patients with Distal X q28 Copy Number Gains
L Vanmarsenille, M Giannandrea, N Fieremans, J Verbeeck, S Belet, ...
Human mutation 35 (3), 377-383, 2014
662014
Shared genetic risk between eating disorder‐and substance‐use‐related phenotypes: Evidence from genome‐wide association studies
MA Munn‐Chernoff, EC Johnson, YL Chou, JRI Coleman, LM Thornton, ...
Addiction biology 26 (1), e12880, 2021
552021
Associations between attention-deficit/hyperactivity disorder and various eating disorders: a Swedish nationwide population study using multiple genetically informative approaches
S Yao, R Kuja-Halkola, J Martin, Y Lu, P Lichtenstein, C Norring, ...
Biological psychiatry 86 (8), 577-586, 2019
532019
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