(Q28275978)

disability affecting intellectual abilities

inferred from title

1 reference

21

0 references

Christa Meisinger

28

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Harald Grallert

29

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Heinrich Sticht

30

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Sabine Endele

5

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Juliane Hoyer

15

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André Reis

38

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Anita Rauch

1

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Dagmar Wieczorek

2

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Thomas Meitinger

37

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Christian T Thiel

Christian T Thiel

20

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Andreas Rump

Andreas Rump

27

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Annette Schenck

Annette Schenck

31

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Christiane Zweier

Christiane Zweier

24

0 references

Arif B. Ekici

25

Arif B Ekici

0 references

Olaf Riess

36

Olaf Riess

0 references

Denise Horn

14

Denise Horn

0 references

author name string

Elisabeth Graf

3

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Thomas Wieland

4

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Thomas Schwarzmayr

6

0 references

Beate Albrecht

7

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Deborah Bartholdi

8

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Jasmin Beygo

9

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Nataliya Di Donato

10

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Andreas Dufke

11

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Kirsten Cremer

12

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Maja Hempel

13

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Pascal Joset

16

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Albrecht Röpke

17

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Ute Moog

18

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Angelika Riess

19

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Antje Wiesener

22

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Eva Wohlleber

23

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Alexander M Zink

26

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Hartmut Engels

32

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Gudrun Rappold

33

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Evelin Schröck

34

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Peter Wieacker

35

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Tim M Strom

The epidemiology of mental retardation: challenges and opportunities in the new millennium

39

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language of work or name

English

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publication date

10 November 2012

0 references

published in

The Lancet

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volume

380

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page(s)

1674-82

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issue

9854

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cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Genetics of early onset cognitive impairment

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Deep sequencing reveals 50 novel genes for recessive cognitive disorders.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

A copy number variation morbidity map of developmental delay

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

A de novo paradigm for mental retardation.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Variation in genome-wide mutation rates within and between human families

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Direct measure of the de novo mutation rate in autism and schizophrenia cohorts

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Characterising and predicting haploinsufficiency in the human genome.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Patterns and rates of exonic de novo mutations in autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Analysis of genetic inheritance in a family quartet by whole-genome sequencing

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Detection of nonneutral substitution rates on mammalian phylogenies

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

A WW domain binding region in methyl-CpG-binding protein MeCP2: impact on Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

A systematic survey of loss-of-function variants in human protein-coding genes

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

A population-based study of the recurrence of developmental disabilities--Metropolitan Atlanta Developmental Disabilities Surveillance Program, 1991-94.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

De Novo Gene Disruptions in Children on the Autistic Spectrum

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

A nonsense mutation of the sodium channel gene SCN2A in a patient with intractable epilepsy and mental decline

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Delineation of a critical region on chromosome 18 for the del(18)(q12.2q21.1) syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

De novo mutations of SETBP1 cause Schinzel-Giedion syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Heterozygous nonsense mutation SATB2 associated with cleft palate, osteoporosis, and cognitive defects.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Further delineation of Pitt-Hopkins syndrome: phenotypic and genotypic description of 16 novel patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Heterozygosity for a protein truncation mutation of sodium channel SCN8A in a patient with cerebellar atrophy, ataxia, and mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Neutral Substitutions Occur at a Faster Rate in Exons Than in Noncoding DNA in Primate Genomes

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Dicer and eIF2c are enriched at postsynaptic densities in adult mouse brain and are modified by neuronal activity in a calpain-dependent manner

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Most rare missense alleles are deleterious in humans: implications for complex disease and association studies

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

SYNCRIP, a component of dendritically localized mRNPs, binds to the translation regulator BC200 RNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Isoform-specific regulation of a steroid hormone nuclear receptor by an E3 ubiquitin ligase in Drosophila melanogaster

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Disruption of an EHMT1-associated chromatin-modification module causes intellectual disability

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Activation of somatostatin receptor II expression by transcription factors MIBP1 and SEF-2 in the murine brain

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

Cux1 and Cux2 regulate dendritic branching, spine morphology, and synapses of the upper layer neurons of the cortex

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2812%2961480-9

7 January 2021

10.1016/S0140-6736(12)61480-9

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

release_66p3fxjbkrcudg7yjazsfrwvgy

304957

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/66p3fxjbkrcudg7yjazsfrwvgy

24 November 2022

mapped directly with Wikidata item

304957

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference