Behavioural genetics articles within European Journal of Human Genetics

Featured

• Review Article
  09 February 2023 | Open Access

  Johann Gregor Mendel: the victory of statistics over human imagination

  • Martina Raudenska
  • , Tomas Vicar
  •  & Michal Masarik

• Article | 04 January 2023

  CDK13-related disorder: a deep characterization of speech and language abilities and addition of 33 novel cases

  • Lottie D. Morison
  • , Olivia van Reyk
  •  & Angela T. Morgan

• Article
  23 December 2021 | Open Access

  A summary-statistics-based approach to examine the role of serotonin transporter promoter tandem repeat polymorphism in psychiatric phenotypes

  • Arunabha Majumdar
  • , Preksha Patel
  •  & Roel A. Ophoff

• Article | 27 April 2021

  Speech and language deficits are central to SETBP1 haploinsufficiency disorder

  • Angela Morgan
  • , Ruth Braden
  •  & Bregje W. van Bon

• Article
  29 August 2020 | Open Access

  Genetic modifiers in rare disorders: the case of fragile X syndrome

  • Hayley Crawford
  • , Gaia Scerif
  •  & Joseph McCleery

• Article | 26 May 2020

  Judging in the genomic era: judges’ genetic knowledge, confidence and need for training

  • Fatos Selita
  • , Vanessa Smereczynska
  •  & Yulia Kovas

• Article | 28 October 2019

  Knowledge and views about genetics: a public-based cross-sectional study

  • Basima A. Almomani
  • , Maha S. Al-Keilani
  •  & Nour A. Al-Sawalha

• Article | 11 April 2019

  A genome-wide analysis in consanguineous families reveals new chromosomal loci in specific language impairment (SLI)

  • Erin M. Andres
  • , Huma Hafeez
  •  & Muhammad Hashim Raza

• Article | 27 April 2018

  Effects of autozygosity and schizophrenia polygenic risk on cognitive and brain developmental trajectories

  • Aldo Córdova-Palomera
  • , Tobias Kaufmann
  •  & Lars T. Westlye

• Article
  05 July 2017 | Open Access

  Sexual dimorphism in the genetic influence on human childlessness

  • Renske M Verweij
  • , Melinda C Mills
  •  & Harold Snieder

• Article | 11 January 2017

  Association analysis of dyslexia candidate genes in a Dutch longitudinal sample

  • Amaia Carrion-Castillo
  • , Ben Maassen
  •  & Simon E Fisher

• Short Report | 23 November 2016

  A method to customize population-specific arrays for genome-wide association testing

  • Erik A Ehli
  • , Abdel Abdellaoui
  •  & Jouke J Hottenga

• Short Report | 09 November 2016

  Klüver–Bucy syndrome associated with a recessive variant in HGSNAT in two siblings with Mucopolysaccharidosis type IIIC (Sanfilippo C)

  • Hao Hu
  • , Christoph Hübner
  •  & Markus Schuelke

• Article | 20 July 2016

  Detection of gene–environment interaction in pedigree data using genome-wide genotypes

  • Michel G Nivard
  • , Christel M Middeldorp
  •  & Conor V Dolan

• Article
  23 September 2015 | Open Access

  Differential effects of the APOE e4 allele on different domains of cognitive ability across the life-course

  • Riccardo E Marioni
  • , Archie Campbell
  •  & Ian J Deary

• Article | 25 February 2015

  Intelligence: shared genetic basis between Mendelian disorders and a polygenic trait

  • Sanja Franić
  • , Maria M Groen-Blokhuis
  •  & Dorret I Boomsma

• Short Report | 23 March 2011

  Intermediate FMR1 alleles and cognitive and/or behavioural phenotypes

  • Irene Madrigal
  • , Mar Xunclà
  •  & Montserrat Milà

• Article | 21 July 2010

  Genotype–phenotype relationship in three cases with overlapping 19p13.12 microdeletions

  • Maria C Bonaglia
  • , Susan Marelli
  •  & Orsetta Zuffardi

• Policy | 10 March 2010

  Italian appeal court: a genetic predisposition to commit murder?

  • Francesca Forzano
  • , Pascal Borry
  •  & Martina Cornel