Heterogeneity and hypothesis testing in neuropsychiatric illness.

about

Non-Mendelian etiologic factors in neuropsychiatric illness: pleiotropy, epigenetics, and convergence Attention deficits, Attention-Deficit Hyperactivity Disorder, and intellectual disabilities

P2860

Q36584692-B07FEB55-07FE-419A-A247-032789A22B5E Q36646041-FA7CC746-D586-48CE-8A93-7ED951E00B5B

P2860

Heterogeneity and hypothesis testing in neuropsychiatric illness.

Item

http://www.wikidata.org/entity/Q42585906

description

2008 nî lūn-bûn

@nan

2008年の論文

@ja

2008年論文

@yue

2008年論文

@zh-hant

2008年論文

@zh-hk

2008年論文

@zh-mo

2008年論文

@zh-tw

2008年论文

@wuu

2008年论文

@zh

2008年论文

@zh-cn

name

Heterogeneity and hypothesis testing in neuropsychiatric illness.

@en

Heterogeneity and hypothesis testing in neuropsychiatric illness.

@nl

type

Item

label

Heterogeneity and hypothesis testing in neuropsychiatric illness.

@en

Heterogeneity and hypothesis testing in neuropsychiatric illness.

@nl

prefLabel

Heterogeneity and hypothesis testing in neuropsychiatric illness.

@en

Heterogeneity and hypothesis testing in neuropsychiatric illness.

@nl

P1476

Heterogeneity and hypothesis testing in neuropsychiatric illness.

@en

P2093

Curtis K Deutsch

http://www.w3.org/2001/XMLSchema#string

Wesley W Ludwig

http://www.w3.org/2001/XMLSchema#string

William J McIlvane

http://www.w3.org/2001/XMLSchema#string

P2860

Strong association of de novo copy number mutations with autism

Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations

Detection of large-scale variation in the human genome

Large-scale copy number polymorphism in the human genome

Disordered connectivity in the autistic brain: Challenges for the ‘new psychophysiology’

Model of autism: increased ratio of excitation/inhibition in key neural systems

Autism spectrum disorders: developmental disconnection syndromes

Cortical activation and synchronization during sentence comprehension in high-functioning autism: evidence of underconnectivity

Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).

Behavior phenotype in the RSH/Smith-Lemli-Opitz syndrome.

P304

266-267

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1017/S0140525X08004275

http://www.w3.org/2001/XMLSchema#string

P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2008-06-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

24013907

http://www.w3.org/2001/XMLSchema#string

P932

3763735

http://www.w3.org/2001/XMLSchema#string

Heterogeneity and hypothesis testing in neuropsychiatric illness.

about

P2860

P2860

Heterogeneity and hypothesis testing in neuropsychiatric illness.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P932