The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population (Q30847370)

16 October 2017

The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population (English)

1 reference

16 October 2017

1 reference

Andres Moreno-De-Luca

13

object named as

Andres Moreno-De-Luca

0 references

Christa Lese Martin

22

object named as

Christa L Martin

1 reference

16 October 2017

23

David H Ledbetter

1 reference

16 October 2017

Ellen Hanson

1

1 reference

16 October 2017

Raphael Bernier

2

1 reference

16 October 2017

Ken Porche

3

1 reference

16 October 2017

Frank I Jackson

4

1 reference

16 October 2017

Robin P Goin-Kochel

5

1 reference

16 October 2017

LeeAnne Green Snyder

6

1 reference

16 October 2017

Anne V Snow

7

1 reference

16 October 2017

Arianne Stevens Wallace

8

1 reference

16 October 2017

Katherine L Campe

9

1 reference

16 October 2017

Yuan Zhang

10

1 reference

16 October 2017

Qixuan Chen

11

1 reference

16 October 2017

Debra D'Angelo

12

1 reference

16 October 2017

Andres Moreno-De-Luca

13

1 reference

16 October 2017

Patrick T Orr

14

1 reference

16 October 2017

K B Boomer

15

1 reference

16 October 2017

David W Evans

16

1 reference

16 October 2017

Stephen Kanne

17

1 reference

16 October 2017

Leandra Berry

18

1 reference

16 October 2017

Fiona K Miller

19

1 reference

16 October 2017

Jennifer Olson

20

1 reference

16 October 2017

Elliot Sherr

21

1 reference

16 October 2017

John E Spiro

24

1 reference

16 October 2017

Wendy K Chung

25

1 reference

16 October 2017

Simons Variation in Individuals Project Consortium

26

1 reference

16 October 2017

language of work or name

English

0 references

publication date

16 June 2014

1 reference

16 October 2017

Biological Psychiatry

1 reference

16 October 2017

77

1 reference

16 October 2017

785-793

1 reference

16 October 2017

9

1 reference

CNVs conferring risk of autism or schizophrenia affect cognition in controls

16 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Simons Variation in Individuals Project (Simons VIP): a genetics-first approach to studying autism spectrum and related neurodevelopmental disorders

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Research review: structural language in autistic spectrum disorder - characteristics and causes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Common neurological co-morbidities in autism spectrum disorders.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

The potential value of sibling controls compared with population controls for association studies of lifestyle-related risk factors: an example from the Breast Cancer Family Registry

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Speech delays and behavioral problems are the predominant features in individuals with developmental delays and 16p11.2 microdeletions and microduplications

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Commentary: Advent of sibling designs

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Cognitive and behavioral characterization of 16p11.2 deletion syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Preschool depression: homotypic continuity and course over 24 months

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Standardizing ADOS scores for a measure of severity in autism spectrum disorders

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Copy-number variations associated with neuropsychiatric conditions

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Five systems of psychiatric classification for preschool children: do differences in validity, usefulness and reliability make for competitive or complimentary constellations?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Advances in autism genetics: on the threshold of a new neurobiology

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Association between microdeletion and microduplication at 16p11.2 and autism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Prevalence of motor impairment in autism spectrum disorders.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

An Investigation of Language Impairment in Autism: Implications for Genetic Subgroups

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Efficient study designs for test of genetic association using sibship data and unrelated cases and controls

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Identifying neurocognitive phenotypes in autism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Choosing a retrospective design to assess joint genetic and environmental contributions to risk

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

The Child Behavior Checklist and related forms for assessing behavioral/emotional problems and competencies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Family-based association studies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

NIMH Diagnostic Interview Schedule for Children Version IV (NIMH DISC-IV): description, differences from previous versions, and reliability of some common diagnoses

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

The assessment and analysis of handedness: The Edinburgh inventory

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Genetic influence on general mental ability increases between infancy and middle childhood.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Stability of assessment results of autistic and non-autistic language-impaired children from preschool years to early school age.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

The role of age at assessment, developmental level, and test in the stability of intelligence scores in young autistic children.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Psychological predictors of adjustment by siblings of developmentally disabled children.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Instability of performance on cognitive tests in infants and young children with Down's syndrome.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Convergent validity of the Mullen Scales of Early Learning and the differential ability scales in children with autism spectrum disorders

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Intragenic rearrangements in NRXN1 in three families with autism spectrum disorder, developmental delay, and speech delay

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Speech and prosody characteristics of adolescents and adults with high-functioning autism and Asperger syndrome.

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Advances in empirically based assessment: revised cross-informant syndromes and new DSM-oriented scales for the CBCL, YSR, and TRF: comment on Lengua, Sadowksi, Friedrich, and Fischer (2001).

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5410712

Enhanced detection of clinically relevant genomic imbalances using a targeted plus whole genome oligonucleotide microarray

25 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25064419

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Relation between depressive symptoms and stressful life events in a sample of disadvantaged mothers

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25064419

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.BIOPSYCH.2014.04.021

1 reference

release_euupjy6lgfhipaeiz2eq7peubu

16 October 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/euupjy6lgfhipaeiz2eq7peubu

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

16 October 2017

1 reference