(Q24634151)

51

0 references

Terho Lehtimäki

35

0 references

George Kirov

3

0 references

Mary-Claire King

72

Mary-Claire King

0 references

Diane E. Dickel

Diane E Dickel

8

0 references

Vladimir Vacic

Vladimir Vacic

28

0 references

Anjene M. Addington

Anjene M Addington

4

0 references

Lilia M. Iakoucheva

Lilia M Iakoucheva

30

0 references

Detelina Grozeva

Detelina Grozeva

13

0 references

Jonathan Sebat

Jonathan Sebat

73

0 references

Louise Gallagher

Louise Gallagher

59

0 references

Tom Walsh

Tom Walsh

15

0 references

James S. Sutcliffe

James S Sutcliffe

56

0 references

Francis J. McMahon

Francis J McMahon

46

0 references

Michael Gill

Michael Gill

58

0 references

Michael C O'Donovan

Michael C O'Donovan

64

0 references

Markus M Nöthen

Markus M Nöthen

50

0 references

Virginia L Willour

Virginia L Willour

40

0 references

Patrick F. Sullivan

68

Patrick F Sullivan

0 references

Judith L. Rapoport

70

Judith Rapoport

0 references

Jeffrey Lieberman

33

Jeffrey A Lieberman

0 references

Thomas G. Schulze

49

Thomas G Schulze

0 references

T. Scott Stroup

34

T Scott Stroup

0 references

James B Potash

48

James B Potash

0 references

Clara M. Lajonchere

55

Clara M Lajonchere

0 references

Deborah M Levy

71

Deborah L Levy

0 references

Nick Craddock

62

Nick Craddock

0 references

Dheeraj Malhotra

14

Dheeraj Malhotra

0 references

Shane McCarthy

1

Shane E McCarthy

0 references

Jon Mcclellan

5

Jon McClellan

0 references

Olga Krastoshevsky

10

Olga Krastoshevsky

0 references

Verena Krause

11

Verena Krause

0 references

Sydney Gary

29

Sydney Gary

0 references

Layla Kassem

43

Layla Kassem

0 references

Paige Kaplan

17

Paige Kaplan

0 references

author name string

Vladimir Makarov

2

0 references

Seungtai Yoon

6

0 references

Diana O Perkins

7

0 references

Mary Kusenda

9

0 references

Ravinesh A Kumar

12

0 references

Elaine H Zackai

16

0 references

Jaya Ganesh

18

0 references

Ian D Krantz

19

0 references

Nancy B Spinner

20

0 references

Patricia Roccanova

21

0 references

Abhishek Bhandari

22

0 references

Kevin Pavon

23

0 references

B Lakshmi

24

0 references

Anthony Leotta

25

0 references

Jude Kendall

26

0 references

Yoon-Ha Lee

27

0 references

Timothy J Crow

31

0 references

Susan L Christian

32

0 references

Kaija Puura

36

0 references

Chad Haldeman-Englert

37

0 references

Justin Pearl

38

0 references

Meredith Goodell

39

0 references

Pamela Derosse

41

0 references

Jo Steele

42

0 references

Jessica Wolff

44

0 references

Nisha Chitkara

45

0 references

Anil K Malhotra

47

0 references

Ellen Leibenluft

53

0 references

Vlad Kustanovich

54

0 references

David Skuse

57

0 references

Nancy R Mendell

60

0 references

Michael J Owen

63

0 references

Tamim H Shaikh

65

0 references

Ezra Susser

66

0 references

Lynn E Delisi

67

0 references

Curtis K Deutsch

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities

69

0 references

language of work or name

English

0 references

publication date

November 2009

0 references

published in

Nature Genetics

0 references

volume

41

0 references

issue

11

0 references

page(s)

1223-7

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2951180

Disruption of the neurexin 1 gene is associated with schizophrenia

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2951180

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2951180

Large recurrent microdeletions associated with schizophrenia

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2951180

Rare chromosomal deletions and duplications increase risk of schizophrenia

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2951180

Structural variation of chromosomes 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=2951180

Disruption of neurexin 1 associated with 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=2951180

Strong association of de novo copy number mutations 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=2951180

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2951180

Mapping Early Brain Development in 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=2951180

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2951180

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2951180

Association between microdeletion and microduplication at 16p11.2 and 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=2951180

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2951180

Disturbance of cerebellar synaptic maturation in mutant mice lacking BSRPs, a novel brain-specific receptor-like protein family

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2951180

Large-scale copy number polymorphism in the human genome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2951180

Disruption of two novel genes by a translocation co-segregating with schizophrenia

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2951180

Integrated detection and population-genetic analysis of SNPs and copy number variation

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2951180

New models of collaboration in genome-wide association studies: the Genetic Association Information Network

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2951180

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2951180

Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2951180

Systematic assessment of copy number variant detection via genome-wide SNP genotyping

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2951180

Recurrent 16p11.2 microdeletions in autism

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2951180

A review of neurocognitive and behavioral profiles associated with 22q11 deletion syndrome: implications for clinical evaluation and treatment

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2951180

Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2951180

When is the brain enlarged in autism? A meta-analysis of all brain size reports

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2951180

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2951180

Head circumference in autism and other pervasive developmental disorders

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2951180

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.

30 May 2018

1 reference

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Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG.474

Macrocephaly in autism and other pervasive developmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG.474

Evidence of brain overgrowth in the first year of life in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG.474

Accelerated head growth in early development of individuals with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG.474

Head circumference and height in autism: a study by the Collaborative Program of Excellence in Autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG.474

Growth of head circumference in autistic infants during the first year of life

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG.474

Knockout of ERK1 MAP kinase enhances synaptic plasticity in the striatum and facilitates striatal-mediated learning and memory

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG.474

Doc2alpha is an activity-dependent modulator of excitatory synaptic transmission.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG.474

A novel microdeletion at 16p11.2 harbors candidate genes for aortic valve development, seizure disorder, and mild mental retardation

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19855392

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Novel genomic alterations and clonal evolution in chronic lymphocytic leukemia revealed by representational oligonucleotide microarray analysis (ROMA)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19855392

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NG.474

1 reference

Dimensions Publication ID

1011794963

0 references

1 reference

1 reference

PubMed publication ID

19855392

1 reference