K. Männik

Discipline

Anthropologie biologique (1)

Type de document

Articles (15)

Co-auteur

Date

Source

Mot-clé

Deletion (12) Number (10) association (9) adulte (9) Phenotype (9) Social groups (9) Human beings (9) Carriers (9) adulte (9) Chromosomes (7) Body mass index (7) risque (6) ADN (6) Cases (6) Genes (6) Risk (6) Obesity (6) DNA (6) Autism (6) Cases (6) adolescent (6) cohorte (6) puits (5) analyse (5) effet (5) maladie (5) enfant (5) jeune (5) Variation (5) Control (5)

Documents écrit par K. Männik (15) | parle de K. Männik (0)

Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts.
G. Giannuzzi et al. (17 juin 2022)
Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants.
L. Pizzo et al.
Analysis of shared heritability in common disorders of the brain.
V. Anttila et al. (22 juin 2018)
CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits.
A. Macé et al. (29 sept. 2017)
Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes.
M.N. Loviglio et al. (2017)
The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition.
L. Hippolyte et al. (15 juil. 2016)
Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities.
D'Angelo D. et al. (2016)
The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesity.
A.M. Maillard et al.
Copy number variations and cognitive phenotypes in unselected populations
K. Männik et al. (2015)
A genome-wide association study of anorexia nervosa.
V. Boraska et al. (2014)
16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy.
E.M. Reinthaler et al. (2014)
Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity.
R.G. Walters et al. (2013)
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.
F. Zufferey et al. (2012)
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.
S. Jacquemont et al. (2011)
A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.
R.G. Walters et al. (4 févr. 2010)