(Q24531526)

9

0 references

Judith L. Rapoport

10

object named as

Judith L Rapoport

0 references

Joseph A Gogos

11

object named as

Joseph A Gogos

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author name string

Hui Liu

1

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Simon C Heath

2

0 references

J Louw Roos

4

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Brandi L Galke

5

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Maude L Blundell

6

0 references

Marge Lenane

7

0 references

Brian Robertson

8

0 references

Maria Karayiorgou

Proceedings of the National Academy of Sciences of the United States of America

12

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language of work or name

English

0 references

publication date

19 March 2002

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published in

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volume

99

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issue

6

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page(s)

3717-22

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cites work

Isolation of a novel gene from the DiGeorge syndrome critical region with homology to Drosophila gdl and to human LAMC1 genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122590

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122590

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122590

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122590

The DNA sequence of human chromosome 22

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122590

A common molecular basis for rearrangement disorders on chromosome 22q11

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122590

Early, non-psychotic deviant behavior in schizophrenia: a possible endophenotypic marker for genetic studies

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122590

Genetics of schizophrenia and the new millennium: progress and pitfalls

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122590

Differential gene expression in p53-mediated apoptosis-resistant vs. apoptosis-sensitive tumor cell lines

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122590

The 22q11 deletion syndromes

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122590

Psychiatric inpatients and chromosome deletions within 22q11.2.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122590

Fluorescence polarization in homogeneous nucleic acid analysis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122590

The mammalian brain high-affinity L-proline transporter is enriched preferentially in synaptic vesicles in a subpopulation of excitatory nerve terminals in rat forebrain.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122590

22q11 deletion syndrome in adults with schizophrenia

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122590

Detection of Numerous Y Chromosome Biallelic Polymorphisms by Denaturing High-Performance Liquid Chromatography

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122590

Diagnostic interview for genetic studies. Rationale, unique features, and training. NIMH Genetics Initiative

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122590

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=122590

A haplotype-based 'haplotype relative risk' approach to detecting allelic associations.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122590

Velo-cardio-facial syndrome: language and psychological profiles.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122590

High rates of schizophrenia in adults with velo-cardio-facial syndrome.

30 May 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.042700699

Velocardiofacial syndrome in childhood-onset schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.042700699

Premorbid speech and language impairments in childhood-onset schizophrenia: association with risk factors

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.042700699

TRAIL-induced apoptosis in human vascular endothelium is regulated by phosphatidylinositol 3-kinase/Akt through the short form of cellular FLIP and Bcl-2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.042700699

Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122590

A de novo pathological point mutation at the 21-hydroxylase locus: implications for gene conversion in the human genome

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11891283

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.042700699

1 reference

release_shhkngncibgz7n2lpu4737cffi

0 references

0 references

2556517

1 reference

1 reference

2556517

PubMed publication ID

11891283

1 reference