Individual common variants exert weak effects on the risk for autism spectrum disorders (Q28943296)

57

Christopher J. McDougle

Christopher J.

McDougle

1 reference

14 March 2017

58

Nadine M. Melhem

Nadine M.

Melhem

1 reference

14 March 2017

59

Alison Merikangas

Alison

Merikangas

1 reference

14 March 2017

61

Ghazala K. Mirza

Ghazala K.

Mirza

1 reference

14 March 2017

62

Jeff Munson

Jeff

Munson

1 reference

14 March 2017

Katerina Papanikolaou

65

Katerina Papanikolaou

Katerina

Papanikolaou

1 reference

14 March 2017

64

Gudrun Nygren

Gudrun

Nygren

1 reference

14 March 2017

Alistair T Pagnamenta

66

Alistair T. Pagnamenta

Alistair T.

Margaret A. Pericak-Vance

Pagnamenta

1 reference

14 March 2017

67

Barbara Parrini

Barbara

Parrini

1 reference

14 March 2017

Andrew Pickles

69

Andrew

Pickles

0 references

71

Fritz Poustka

Fritz

Poustka

1 reference

14 March 2017

68

Tara Paton

Tara

Paton

1 reference

14 March 2017

72

Jiannis Ragoussis

Jiannis

Ragoussis

0 references

73

Regina Regan

Regina

Regan

1 reference

14 March 2017

74

Wendy Roberts

Wendy

Roberts

1 reference

14 March 2017

Kathryn Roeder

75

Kathryn

Roeder

0 references

Michael L. Rutter

77

Michael L.

Rutter

0 references

79

Naisha Shah

Naisha

Shah

1 reference

14 March 2017

80

Val C. Sheffield

Val C.

Sheffield

1 reference

14 March 2017

81

Latha Soorya

Latha

Soorya

1 reference

14 March 2017

83

Vera Stoppioni

Vera

Stoppioni

1 reference

14 March 2017

84

Nuala Sykes

Nuala

Sykes

1 reference

14 March 2017

85

Raffaella Tancredi

Raffaella

Tancredi

1 reference

14 March 2017

87

Susanne Thomson

Susanne

Thomson

1 reference

14 March 2017

88

Ana Tryfon

Ana

Tryfon

1 reference

14 March 2017

89

John Tsiantis

John

Tsiantis

1 reference

14 March 2017

92

Fred Volkmar

Fred

Volkmar

1 reference

14 March 2017

94

Simon Wallace

Simon

Wallace

1 reference

14 March 2017

Kirsty Wing

95

Kirsty

Wing

0 references

98

Danielle Zurawiecki

Danielle

Zurawiecki

1 reference

14 March 2017

99

Lonnie Zwaigenbaum

Lonnie

Zwaigenbaum

0 references

101

Agatino Battaglia

Agatino

Battaglia

1 reference

14 March 2017

102

Rita M. Cantor

Rita M.

Cantor

1 reference

14 March 2017

103

Hilary Coon

Hilary

Coon

1 reference

14 March 2017

104

Michael L. Cuccaro

Michael L.

Cuccaro

1 reference

14 March 2017

105

Geraldine Dawson

Geraldine

Dawson

1 reference

14 March 2017

Sean Ennis

106

Sean

Ennis

0 references

107

Christine M. Freitag

Christine M.

Freitag

1 reference

14 March 2017

108

Daniel H. Geschwind

Daniel H.

Geschwind

1 reference

14 March 2017

109

Jonathan L. Haines

Jonathan L.

Haines

1 reference

14 March 2017

110

Sabine M. Klauck

Sabine M.

Klauck

1 reference

14 March 2017

112

Elena Maestrini

Elena

Maestrini

1 reference

14 March 2017

Anthony P. Monaco

114

Anthony P.

Monaco

0 references

115

Stanley F. Nelson

Stanley F.

Nelson

1 reference

14 March 2017

116

John I. Nurnberger

John I.

Nurnberger

1 reference

14 March 2017

Guiomar Oliveira

117

Guiomar

Oliveira

0 references

118

Jeremy R. Parr

Jeremy R.

Parr

1 reference

14 March 2017

119

Margaret A. Pericak-Vance

Margaret A.

Pericak-Vance

1 reference

14 March 2017

120

Joseph Piven

Joseph

Piven

1 reference

14 March 2017

122

Stephen W. Scherer

Stephen W.

Scherer

1 reference

14 March 2017

Astrid M. Vicente

123

Astrid M.

Vicente

0 references

124

Thomas H. Wassink

Thomas H.

Wassink

1 reference

14 March 2017

Ellen M. Wijsman

125

Ellen M.

Wijsman

0 references

126

Catalina Betancur

Catalina

Betancur

0 references

Joseph D. Buxbaum

127

Joseph D.

Buxbaum

0 references

128

Edwin H. Cook

Edwin H.

Cook

1 reference

14 March 2017

Louise Gallagher

129

Louise

Gallagher

0 references

Michael Gill

130

Michael

Gill

0 references

131

Joachim Hallmayer

Joachim

Hallmayer

1 reference

14 March 2017

Andrew D. Paterson

132

Andrew D.

Paterson

0 references

133

James S. Sutcliffe

James S.

Sutcliffe

1 reference

14 March 2017

134

Peter Szatmari

Peter

Szatmari

1 reference

14 March 2017

135

Veronica J. Vieland

Veronica J.

Vieland

1 reference

14 March 2017

136

Hakon Hakonarson

Hakon

Hakonarson

0 references

137

Bernie Devlin

Bernie

Devlin

1 reference

14 March 2017

111

William M. McMahon

1 reference

14 March 2017

91

John B. Vincent

1 reference

14 March 2017

Gerard D Schellenberg

121

Gerard D. Schellenberg

1 reference

14 March 2017

82

Inês Sousa

1 reference

14 March 2017

70

David J. Posey

1 reference

14 March 2017

18

Maretha de Jonge

1 reference

14 March 2017

78

Sabine Schlitt

1 reference

14 March 2017

Joana Almeida

4

1 reference

14 March 2017

Patrick F. Bolton

9

1 reference

14 March 2017

Sean Brennan

11

1 reference

14 March 2017

Emily L. Crawford

17

1 reference

14 March 2017

John Gilbert

27

1 reference

14 March 2017

Stephen J. Guter

32

1 reference

14 March 2017

Richard Holt

34

1 reference

14 March 2017

Jennifer L. Howe

35

1 reference

14 March 2017

Gillian Hughes

36

1 reference

14 March 2017

Graham P. Kenny

40

1 reference

14 March 2017

Cecilia Kim

41

1 reference

14 March 2017

Alexander Kolevzon

42

1 reference

14 March 2017

Miriam Law-Smith

46

1 reference

14 March 2017

Frances Lombard

51

1 reference

14 March 2017

Tiago R. Magalhaes

55

1 reference

14 March 2017

Nancy J. Minshew

60

1 reference

14 March 2017

Carolyn Noakes

63

1 reference

14 March 2017

Bernadette Roge

76

1 reference

14 March 2017

Ann P. Thompson

86

1 reference

14 March 2017

Herman Van Engeland

90

1 reference

14 March 2017

J. a. S. Vorstman

93

1 reference

14 March 2017

Kerstin Wittemeyer

96

1 reference

14 March 2017

Shawn Wood

97

1 reference

14 March 2017

Anthony J. Bailey

100

1 reference

14 March 2017

Judith Miller

Loci nominally associated with autism from genome-wide analysis show enrichment of brain expression quantitative trait loci but not lymphoblastoid cell line expression quantitative trait loci

113

1 reference

14 March 2017

1 November 2012

1 reference

14 March 2017

Human Molecular Genetics

1 reference

14 March 2017

21

1 reference

14 March 2017

4781–4792

1 reference

14 March 2017

21

1 reference

14 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

SHANK1 Deletions in Males with Autism Spectrum Disorder

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Rare deletions at the neurexin 3 locus in autism spectrum disorder

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Using ancestry matching to combine family-based and unrelated samples for genome-wide association studies

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

A genome-wide association study of autism reveals a common novel risk locus at 5p14.1

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Common genetic variants on 5p14.1 associate with autism spectrum disorders

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

A functional genetic link between distinct developmental language disorders

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Copy-number variations associated with neuropsychiatric conditions

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Genome-wide linkage analyses of quantitative and categorical autism subphenotypes

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Structural variation of chromosomes in autism spectrum disorder

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Association between microdeletion and microduplication at 16p11.2 and autism

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

PLINK: a tool set for whole-genome association and population-based linkage analyses

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Strong association of de novo copy number mutations with autism

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Single-nucleotide polymorphisms in NAGNAG acceptors are highly predictive for variations of alternative splicing

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

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

23 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

De Novo Gene Disruptions in Children on the Autistic Spectrum

6 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Genetic architecture in autism spectrum disorder

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorder

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Identification of genetic loci underlying the phenotypic constructs of autism spectrum disorders

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Uncoupling antisense-mediated silencing and DNA methylation in the imprinted Gnas cluster.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Genetic analysis of biological pathway data through genomic randomization

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Do common variants play a role in risk for autism? Evidence and theoretical musings

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

A double hit implicates DIAPH3 as an autism risk gene.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

A genome-wide linkage and association scan reveals novel loci for autism

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Gene associated with seizures, autism, and hepatomegaly in an Amish girl

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

On the use of general control samples for genome-wide association studies: genetic matching highlights causal variants

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Recurrent 16p11.2 microdeletions in autism

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

A genomewide screen for autism susceptibility loci

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Implementing a unified approach to family-based tests of association.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

3 June 2018

Don't give up on GWAS.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Intragenic rearrangements in NRXN1 in three families with autism spectrum disorder, developmental delay, and speech delay

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Discovering genetic ancestry using spectral graph theory

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Ascertainment Through Family History of Disease Often Decreases the Power of Family-based Association Studies

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Case/pseudocontrol analysis in genetic association studies: A unified framework for detection of genotype and haplotype associations, gene-gene and gene-environment interactions, and parent-of-origin effects.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Implications of multilocus inheritance for gene-disease association studies

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3471395

Deletion of 7q34-q36.2 in two siblings with mental retardation, language delay, primary amenorrhea, and dysmorphic features

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22843504

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22843504

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/HMG/DDS301

1 reference

5027800

5027800

1 reference

1 reference

1 reference