(Q36116735)

12 August 2017

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

1 reference

12 August 2017

21

Jouke-Jan Hottenga

0 references

Dorret Boomsma

Dorret I Boomsma

22

0 references

René Pool

René Pool

5

0 references

Narelle Hansell

Narelle K Hansell

12

0 references

Nick Martin

Nicholas G Martin

13

0 references

Hilleke Hulshoff Pol

Hilleke E Hulshoff Pol

17

0 references

Meike Bartels

19

Meike Bartels

1 reference

12 August 2017

10

Sophie van der Sluis

1 reference

12 August 2017

18

Eco J C de Geus

1 reference

12 August 2017

Catharina E M van Beijsterveldt

15

Catherina E M van Beijsterveldt

1 reference

12 August 2017

3

Conor V Dolan

1 reference

12 August 2017

11

Abdel Abdellaoui

1 reference

12 August 2017

8

Erik A Ehli

1 reference

12 August 2017

Maria M Groen-Blokhuis

2

Maria M Groen-Blokhuis

1 reference

12 August 2017

14

James J Hudziak

1 reference

12 August 2017

6

Xiangjun Xiao

1 reference

12 August 2017

1

Sanja Franić

1 reference

12 August 2017

16

Suzanne C Swagerman

1 reference

12 August 2017

4

Mathijs V Kattenberg

1 reference

12 August 2017

Paul A Scheet

7

1 reference

12 August 2017

Gareth E Davies

9

1 reference

12 August 2017

H Hilger Ropers

20

1 reference

12 August 2017

25 February 2015

1 reference

European Journal of Human Genetics

12 August 2017

1 reference

12 August 2017

23

1 reference

12 August 2017

10

1 reference

12 August 2017

1378-1383

1 reference

Population structure, migration, and diversifying selection in the Netherlands

12 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Childhood intelligence is heritable, highly polygenic and associated with FNBP1L

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Twins, tissue, and time: an assessment of SNPs and CNVs

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Most reported genetic associations with general intelligence are probably false positives

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Genome-wide association studies establish that human intelligence is highly heritable and polygenic

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Genomic inflation factors under polygenic inheritance

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

GATES: a rapid and powerful gene-based association test using extended Simes procedure

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Revisiting Mendelian disorders through exome sequencing

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Genome-wide association studies: results from the first few years and potential implications for clinical medicine

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Stressed-induced TMEM135 protein is part of a conserved genetic network involved in fat storage and longevity regulation in Caenorhabditis elegans

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Hundreds of variants clustered in genomic loci and biological pathways affect human height

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

A versatile gene-based test for genome-wide association studies

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

TbPRMT6 is a type I protein arginine methyltransferase that contributes to cytokinesis in Trypanosoma brucei

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Single gene disorders come into focus--again

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

A three-stage genome-wide association study of general cognitive ability: hunting the small effects.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

The heritability of general cognitive ability increases linearly from childhood to young adulthood

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Parkinson's disease: from monogenic forms to genetic susceptibility factors

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Genetic foundations of human intelligence

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Mendelian forms of Parkinson's disease

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Common variants near MC4R are associated with fat mass, weight and risk of obesity

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Genome-wide quantitative trait locus association scan of general cognitive ability using pooled DNA and 500K single nucleotide polymorphism microarrays.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

PLINK: a tool set for whole-genome association and population-based linkage analyses

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Mendelian disorders deserve more attention

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Genetic variation in ABC transporter A1 contributes to HDL cholesterol in the general population

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Molecular and comparative genetics of mental retardation

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Cognitive change and the APOE epsilon 4 allele

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Snapin: a SNARE-associated protein implicated in synaptic transmission

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Common variants in WFS1 confer risk of type 2 diabetes

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

The Young Netherlands Twin Register (YNTR): longitudinal twin and family studies in over 70,000 children.

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Deep sequencing reveals 50 novel genes for recessive cognitive disorders.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Netherlands Twin Register: from twins to twin families

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4592100

Evaluation of Common Variants in the Six Known Maturity-Onset Diabetes of the Young (MODY) Genes for Association With Type 2 Diabetes

23 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2015.3

The Elp2 Subunit of Elongator and Elongating RNA Polymerase II Holoenzyme Is a WD40 Repeat Protein

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2015.3

The Use of Imputed Sibling Genotypes in Sibship-Based Association Analysis: On Modeling Alternatives, Power and Model Misspecification

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25712083

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/EJHG.2015.3

1 reference

12 August 2017

1 reference

12 August 2017

PubMed publication ID

25712083

1 reference