(Q28291465)

19

0 references

Rodney Cotterill

20

0 references

Elena Bonora

Elena Bonora

1

0 references

Janine A Lamb

Janine A Lamb

2

0 references

Michael Rutter

Michael Rutter

26

0 references

Anthony Monaco

Anthony P Monaco

31

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Chantal Kemner

23

Chantal Kemner

0 references

Annemarie Poustka

29

Annemarie Poustka

0 references

author name string

Gabrielle Barnby

3

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Nuala Sykes

4

0 references

Thomas Moberly

5

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Kim S Beyer

6

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Sabine M Klauck

7

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Firtz Poustka

8

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Elena Bacchelli

9

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Francesca Blasi

10

0 references

Elena Maestrini

11

0 references

Agatino Battaglia

12

0 references

Demetrios Haracopos

13

0 references

Lennart Pedersen

14

0 references

Torben Isager

15

0 references

Gunna Eriksen

16

0 references

Birgitte Viskum

17

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Ester-Ulsted Sorensen

18

0 references

Herman von Engeland

21

0 references

Maretha de Jonge

22

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Karlijn Steggehuis

24

0 references

Margret Scherpenisse

25

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Patrick F Bolton

27

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Jeremy R Parr

28

0 references

Anthony J Bailey

European Journal of Human Genetics

30

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language of work or name

English

0 references

publication date

February 2005

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published in

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volume

13

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issue

2

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page(s)

198-207

0 references

cites work

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Autism and genetics. A decade of research

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The epidemiology of autism: a review.

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Pervasive Developmental Disorders in Preschool Children

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Autism and megalencephaly.

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Association between idiopathic infantile macrocephaly and autism spectrum disorders.

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Brief report: neuroanatomic observations of the brain in pervasive developmental disorders

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A clinicopathological study of autism.

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Infantile autism: a genetic study of 21 twin pairs

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Autism as a strongly genetic disorder: evidence from a British twin study

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A case-control family history study of autism

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Genetics of austim: complex aetiology for a heterogeneous disorder

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The protein CDP, but not CP1, footprints on the CCAAT region of the γ-globin gene in unfractionated B-cell extracts

21 January 2018

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CASP, the alternatively spliced product of the gene encoding the CCAAT-displacement protein transcription factor, is a Golgi membrane protein related to giantin

21 January 2018

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SRPK2: a differentially expressed SR protein-specific kinase involved in mediating the interaction and localization of pre-mRNA splicing factors in mammalian cells

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The Vineland Adaptive Behavior Scales: supplementary norms for individuals with autism.

21 January 2018

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The synaptic vesicle protein synaptophysin: purification and characterization of its channel activity

21 January 2018

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Neuronal laminins and their cellular receptors

21 January 2018

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Nr-CAM: a cell adhesion molecule with ligand and receptor functions

21 January 2018

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The relationship between adhesion molecules and neuronal plasticity

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

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

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Serotonin transporter (5-HTT) gene variants associated with autism?

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Exon/intron structure and alternative transcripts of the CUTL1 gene

21 January 2018

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Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region

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Human non-synonymous SNPs: server and survey

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Analysis of reelin as a candidate gene for autism

21 January 2018

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PedCheck: a program for identification of genotype incompatibilities in linkage analysis

21 January 2018

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A multipoint method for detecting genotyping errors and mutations in sibling-pair linkage data

21 January 2018

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Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

21 January 2018

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Autism: the phenotype in relatives.

21 January 2018

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Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes

21 January 2018

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Many amino acid substitution variants identified in DNA repair genes during human population screenings are predicted to impact protein function.

21 January 2018

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Candidate-gene approaches for studying complex genetic traits: practical considerations

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Are rare variants responsible for susceptibility to complex diseases?

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Human genome sequence variation and the influence of gene history, mutation and recombination

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Replication of linkage studies of complex traits: an examination of variation in location estimates

21 January 2018

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Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

21 January 2018

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Transmission disequilibrium, family controls, and great expectations

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Transmission/disequilibrium tests for extended marker haplotypes

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

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7 January 2021

2-year-old boy who has been diagnosed with autism

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7 January 2021

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

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Affected-sib-pair interval mapping and exclusion for complex genetic traits: sampling considerations

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7 January 2021

Single nucleotide polymorphism and linkage disequilibrium within the TCR alpha/delta locus

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7 January 2021