(Q28744110)

Kirsty Wing

5

0 references

Dalila Pinto

Dalila Pinto

4

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Emanuela V Volpi

Emanuela V Volpi

8

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Anthony Monaco

Anthony P Monaco

9

0 references

Stephen W. Scherer

7

Stephen W Scherer

0 references

Alistair T Pagnamenta

1

Alistair T Pagnamenta

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author name string

Richard Holt

2

0 references

Mohammed Yusuf

Journal of Neurodevelopmental Disorders

3

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language of work or name

English

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publication date

June 2011

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published in

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volume

3

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issue

2

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page(s)

124-31

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cites work

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Functional impact of global rare copy number variation in autism spectrum disorders

16 March 2017

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Epidemiology of Pervasive Developmental Disorders

16 March 2017

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Copy-number variations associated with neuropsychiatric conditions

16 March 2017

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

16 March 2017

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Structural variation of chromosomes in autism spectrum disorder

16 March 2017

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Mapping autism risk loci using genetic linkage and chromosomal rearrangements

16 March 2017

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Detection of large-scale variation in the human genome

16 March 2017

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A new mathematical model for relative quantification in real-time RT-PCR

16 March 2017

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Comparing family members' motivations and attitudes towards genetic testing for hereditary breast and ovarian cancer: a qualitative analysis

16 March 2017

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Pregnenolone sulphate- and cholesterol-regulated TRPM3 channels coupled to vascular smooth muscle secretion and contraction

3 June 2018

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Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia

3 June 2018

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What is a meaningful result? Disclosing the results of genomic research in autism to research participants

3 June 2018

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A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

3 June 2018

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Dystrophin gene mutation location and the risk of cognitive impairment in Duchenne muscular dystrophy

3 June 2018

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Role of mental retardation-associated dystrophin-gene product Dp71 in excitatory synapse organization, synaptic plasticity and behavioral functions

3 June 2018

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Predictive diagnosis of the cancer prone Li-Fraumeni syndrome by accident: new challenges through whole genome array testing.

3 June 2018

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Is heart rate variability a valid parameter to predict sudden death in patients with Becker's muscular dystrophy?

3 June 2018

1 reference

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A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

3 June 2018

1 reference

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Population data on benign and severe forms of X-linked muscular dystrophy

3 June 2018

1 reference

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Neuropsychiatric disorders in males with duchenne muscular dystrophy: frequency rate of attention-deficit hyperactivity disorder (ADHD), autism spectrum disorder, and obsessive--compulsive disorder.

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Association of autistic spectrum disorders with dystrophinopathies.

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TRPM3 is expressed in sphingosine-responsive myelinating oligodendrocytes

21 January 2018

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Molecular karyotyping in 17 patients and mutation screening in 41 patients with Kabuki syndrome.

21 January 2018

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A TRP channel-steroid marriage

21 January 2018

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Strategy for comprehensive molecular testing for Duchenne and Becker muscular dystrophies.

21 January 2018

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Cognitive and psychological profile of males with Becker muscular dystrophy

21 January 2018

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Duplications in the DMD gene

21 January 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/21484199