(Q33794546)

29 July 2017

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders (English)

1 reference

29 July 2017

autism spectrum disorder

0 references

0 references

75

1 reference

29 July 2017

92

1 reference

29 July 2017

106

1 reference

29 July 2017

108

1 reference

29 July 2017

111

1 reference

Margaret A. Pericak-Vance

29 July 2017

87

Margaret Pericak-Vance

1 reference

Bhooma Thiruvahindrapuram

29 July 2017

42

Lonnie Zwaigenbaum

0 references

7

Bhooma Thiruvahindrapuram

1 reference

29 July 2017

46

Herman van Engeland

1 reference

29 July 2017

Kirsty Wing

44

0 references

Susana Mouga

Susana Mouga

53

0 references

Frederico Duque

Frederico Duque

69

0 references

Dalila Pinto

Dalila Pinto

1

0 references

Suma Jacob

Suma Jacob

62

0 references

Sean Ennis

Sean Ennis

100

0 references

Guiomar Oliveira

Guiomar Oliveira

90

0 references

James S. Sutcliffe

James S Sutcliffe

104

0 references

Louise Gallagher

Louise Gallagher

110

0 references

Richard Anney

Richard Anney

38

0 references

Andrew D. Paterson

Andrew D Paterson

88

0 references

Jonathan Green

Jonathan Green

65

0 references

Marion Leboyer

Marion Leboyer

58

0 references

John I. Nurnberger

John I Nurnberger

91

0 references

Richard Delorme

Richard Delorme

70

0 references

Sven Bölte

77

Sven Bölte

1 reference

29 July 2017

52

Fritz Poustka

1 reference

29 July 2017

67

Christopher Gillberg

1 reference

29 July 2017

57

Catherine Lord

1 reference

29 July 2017

71

Geraldine Dawson

1 reference

29 July 2017

103

Peter Szatmari

1 reference

29 July 2017

81

Evdokia Anagnostou

1 reference

29 July 2017

97

Daniel H Geschwind

1 reference

29 July 2017

Hakon Hakonarson

95

1 reference

29 July 2017

107

Edwin H Cook

1 reference

29 July 2017

112

Stephen W Scherer

1 reference

29 July 2017

6

Lambertus Klei

1 reference

29 July 2017

Nadia Bolshakova

36

0 references

Jonathan L Haines

96

Jonathan L Haines

1 reference

29 July 2017

79

Gillian Baird

1 reference

29 July 2017

51

Wendy Roberts

1 reference

29 July 2017

39

Steven Gallinger

1 reference

29 July 2017

Inês C Conceição

31

1 reference

ORCID Public Data File 2021

Michelle Cotterchio

40

Michelle Cotterchio

1 reference

29 July 2017

3

Daniele Merico

1 reference

29 July 2017

84

Veronica J Vieland

1 reference

29 July 2017

Alistair T Pagnamenta

16

Alistair T Pagnamenta

1 reference

29 July 2017

68

Bridget A Fernandez

1 reference

29 July 2017

5

Alison Merikangas

1 reference

29 July 2017

27

Michael Cuccaro

1 reference

29 July 2017

33

Jillian P Casey

1 reference

29 July 2017

83

Ellen M Wijsman

1 reference

29 July 2017

85

Astrid M Vicente

1 reference

29 July 2017

89

Jeremy R Parr

1 reference

29 July 2017

94

Sabine M Klauck

1 reference

29 July 2017

98

Christine M Freitag

1 reference

29 July 2017

93

Elena Maestrini

1 reference

29 July 2017

18

Christian R Marshall

1 reference

29 July 2017

102

Agatino Battaglia

1 reference

29 July 2017

59

Ann S Le Couteur

1 reference

29 July 2017

105

Joachim Hallmayer

1 reference

29 July 2017

73

Cátia Café

1 reference

29 July 2017

10

Zhuozhi Wang

1 reference

29 July 2017

11

Jacob A S Vorstman

1 reference

29 July 2017

13

Regina Regan

1 reference

29 July 2017

15

Giovanna Pellecchia

1 reference

29 July 2017

24

Eftichia Duketis

1 reference

29 July 2017

30

Judith Conroy

1 reference

29 July 2017

Andreas G Chiocchetti

32

Andreas G Chiocchetti

1 reference

29 July 2017

37

Elena Bacchelli

1 reference

29 July 2017

45

Simon Wallace

1 reference

29 July 2017

48

Susanne Thomson

1 reference

29 July 2017

49

Latha Soorya

1 reference

29 July 2017

72

Pauline Chaste

1 reference

29 July 2017

99

Susan E Folstein

1 reference

29 July 2017

101

Hilary Coon

1 reference

29 July 2017

2

Elsa Delaby

1 reference

29 July 2017

Gerard D Schellenberg

86

Gerard D Schellenberg

1 reference

Patricia Jiménez González

29 July 2017

61

Patricia Jiménez González

1 reference

29 July 2017

34

Guiqing Cai

1 reference

29 July 2017

22

Anthony J Griswold

1 reference

29 July 2017

4

Mafalda Barbosa

1 reference

29 July 2017

47

Ana Tryfon

1 reference

29 July 2017

Xiao Xu

8

1 reference

29 July 2017

Robert Ziman

9

1 reference

29 July 2017

Ann Thompson

12

1 reference

29 July 2017

Marion Pilorge

14

1 reference

29 July 2017

Bárbara Oliveira

17

1 reference

29 July 2017

Tiago R Magalhaes

19

1 reference

29 July 2017

Jennifer K Lowe

20

1 reference

29 July 2017

Jennifer L Howe

21

1 reference

29 July 2017

John Gilbert

23

1 reference

29 July 2017

Beth A Dombroski

25

1 reference

29 July 2017

Maretha V De Jonge

26

1 reference

29 July 2017

Emily L Crawford

28

1 reference

29 July 2017

Catarina T Correia

29

1 reference

29 July 2017

Christelle Cabrol

35

1 reference

29 July 2017

Graham Casey

41

1 reference

29 July 2017

Kerstin Wittemeyer

43

1 reference

29 July 2017

Bernadette Rogé

50

1 reference

29 July 2017

Nancy Minshew

54

1 reference

29 July 2017

L Alison McInnes

55

1 reference

29 July 2017

Susan G McGrew

56

1 reference

29 July 2017

Alexander Kolevzon

60

1 reference

29 July 2017

Richard Holt

63

1 reference

29 July 2017

Stephen Guter

64

1 reference

29 July 2017

Andrew Green

66

1 reference

29 July 2017

Sean Brennan

74

1 reference

29 July 2017

Patrick F Bolton

76

1 reference

29 July 2017

Raphael Bernier

78

1 reference

29 July 2017

Anthony J Bailey

80

1 reference

29 July 2017

Joana Almeida

82

1 reference

29 July 2017

Bernie Devlin

109

1 reference

29 July 2017

language of work or name

English

0 references

publication date

24 April 2014

1 reference

American Journal of Human Genetics

29 July 2017

1 reference

29 July 2017

94

1 reference

29 July 2017

5

1 reference

29 July 2017

677-694

1 reference

Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing

29 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Interpretation of genomic variants using a unified biological network approach

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

The interstitial duplication 15q11.2-q13 syndrome includes autism, mild facial anomalies and a characteristic EEG signature

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Examining and interpreting the female protective effect against autistic behavior

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Using whole-exome sequencing to identify inherited causes of autism

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

FMRP targets distinct mRNA sequence elements to regulate protein expression

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Individual common variants exert weak effects on the risk for autism spectrum disorders

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

De Novo Gene Disruptions in Children on the Autistic Spectrum

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

SHANK1 Deletions in Males with Autism Spectrum Disorder

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Genetic architecture in autism spectrum disorder

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

High frequencies of de novo CNVs in bipolar disorder and schizophrenia

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Chromosome 1p21.3 microdeletions comprising DPYD and MIR137 are associated with intellectual disability

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Genome-wide association study identifies five new schizophrenia loci

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Defects in translational regulation contributing to human cognitive and behavioral disease

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Epigenetic mechanisms in cognition

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Rare structural variation of synapse and neurotransmission genes in autism

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Genotype-environment interactions in microsatellite stable/microsatellite instability-low colorectal cancer: results from a genome-wide association study

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Characterization of the proteome, diseases and evolution of the human postsynaptic density.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Characterising and predicting haploinsufficiency in the human genome.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

A genome-wide scan for common alleles affecting risk for autism

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

A genome-wide association study of alcohol dependence

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Dysregulation of mTOR signaling in fragile X syndrome

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Dosage-dependent severity of the phenotype in patients with mental retardation due to a recurrent copy-number gain at Xq28 mediated by an unusual recombination.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary disease

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Structural variation of chromosomes in autism spectrum disorder

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Germline rates of de novo meiotic deletions and duplications causing several genomic disorders

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

The Mammalian Phenotype Ontology as a tool for annotating, analyzing and comparing phenotypic information

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

RIM1alpha forms a protein scaffold for regulating neurotransmitter release at the active zone

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Overexpression of a neural-specific rho family GTPase, cRac1B, selectively induces enhanced neuritogenesis and neurite branching in primary neurons.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Autism diagnostic observation schedule: a standardized observation of communicative and social behavior

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Mutations in SYNGAP1 cause intellectual disability, autism, and a specific form of epilepsy by inducing haploinsufficiency.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Diagnostic exome sequencing in persons with severe intellectual disability

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Autism recurrence in half siblings: strong support for genetic mechanisms of transmission in ASD.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorder.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Excess phosphoinositide 3-kinase subunit synthesis and activity as a novel therapeutic target in fragile X syndrome

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Colon Cancer Family Registry: an international resource for studies of the genetic epidemiology of colon cancer.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

Combining information from multiple sources in the diagnosis of autism spectrum disorders.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067558

10.1016/J.AJHG.2014.03.018

30 October 2018

Identifiers

DOI

1 reference

29 July 2017

1 reference

29 July 2017

1 reference