(Q37203703)

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14 December 2019

title

A highly significant association between a COMT haplotype and schizophrenia (English)

1 reference

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14 December 2019

0 references

1

1 reference

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14 December 2019

Abraham Weizman

6

1 reference

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14 December 2019

Jacques S Beckmann

17

1 reference

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14 December 2019

18

Benjamin Yakir

1 reference

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14 December 2019

author name string

Michal Bronstein

2

1 reference

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14 December 2019

Meira Sternfeld

3

1 reference

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14 December 2019

Anne Pisanté-Shalom

4

1 reference

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14 December 2019

Efrat Lev-Lehman

5

1 reference

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14 December 2019

Ilya Reznik

7

1 reference

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14 December 2019

Baruch Spivak

8

1 reference

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14 December 2019

Nimrod Grisaru

9

1 reference

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14 December 2019

Leon Karp

10

1 reference

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14 December 2019

Richard Schiffer

11

1 reference

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14 December 2019

Moshe Kotler

12

1 reference

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14 December 2019

Rael D Strous

13

1 reference

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14 December 2019

Marnina Swartz-Vanetik

14

1 reference

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14 December 2019

Haim Y Knobler

15

1 reference

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14 December 2019

Eilat Shinar

16

1 reference

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14 December 2019

Neil Risch

19

1 reference

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14 December 2019

Naomi B Zak

20

1 reference

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14 December 2019

Ariel Darvasi

21

1 reference

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14 December 2019

language of work or name

English

0 references

publication date

25 October 2002

1 reference

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American Journal of Human Genetics

14 December 2019

published in

1 reference

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14 December 2019

volume

71

1 reference

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14 December 2019

issue

6

1 reference

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14 December 2019

page(s)

1296-1302

1 reference

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Enzymatic O-methylation of epinephrine and other catechols.

14 December 2019

cites work

1 reference

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Population isolates: their special value for locating genes for bipolar disorder

6 September 2017

1 reference

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Prefrontal neurons and the genetics of schizophrenia

6 September 2017

1 reference

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Population-based gene discovery in the post-genomic era.

6 September 2017

1 reference

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Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia

6 September 2017

1 reference

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Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease

6 September 2017

1 reference

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Search for schizophrenia susceptibility genes

6 September 2017

1 reference

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A protein kinase encoded by the t complex responder gene causes non-mendelian inheritance

6 September 2017

1 reference

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Male-offspring-specific, haplotype-dependent, nonrandom cosegregation of alleles at loci on two mouse chromosomes

6 September 2017

1 reference

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Sex-of-offspring-specific transmission ratio distortion on mouse chromosome X.

6 September 2017

1 reference

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Catechol-O-methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior

6 September 2017

1 reference

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Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome.

6 September 2017

1 reference

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Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder

6 September 2017

1 reference

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The future of genetic studies of complex human diseases

6 September 2017

1 reference

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A comparison of linkage disequilibrium measures for fine-scale mapping

6 September 2017

1 reference

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Testing for linkage disequilibrium in genotypic data using the Expectation-Maximization algorithm

6 September 2017

1 reference

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The genetics of retinoblastoma, revisited

6 September 2017

1 reference

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Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

6 September 2017

1 reference

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Antiandrogenic treatment of obsessive-compulsive neurosis

6 September 2017

1 reference

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The role of gender differences in the reduction of etiologic heterogeneity in schizophrenia

6 September 2017

1 reference

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Human liver catechol-O-methyltransferase pharmacogenetics

28 September 2017

1 reference

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The genetic epidemiology of schizophrenia in a Finnish twin cohort. A population-based modeling study

28 September 2017

1 reference

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Onset of obsessive-compulsive disorder in pregnancy

26 June 2018

1 reference

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A genetic profile of contemporary Jewish populations

26 June 2018

1 reference

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Model-free analysis and permutation tests for allelic associations.

3 September 2018

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Velocardiofacial syndrome in childhood-onset schizophrenia.

3 September 2018

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

3 September 2018

1 reference

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Global variation in the frequencies of functionally different catechol-O-methyltransferase alleles.

3 September 2018

1 reference

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Characterization and implications of estrogenic down-regulation of human catechol-O-methyltransferase gene transcription

3 September 2018

1 reference

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Sex-restricted non-Mendelian inheritance of mouse chromosome 11 in the offspring of crosses between C57BL/6J and (C57BL/6J x DBA/2J)F1 mice

3 September 2018

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Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders.

3 September 2018

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Genetic basis of schizophrenia

3 September 2018

1 reference

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Activity of catechol-O-methyltransferase in brain regions and adrenal gland during the oestrus cycle

3 September 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/12402217

12 December 2020

Techniques for estimating genetic admixture and applications to the problem of the origin of the Icelanders and the Ashkenazi Jews

1 reference

https://pubmed.ncbi.nlm.nih.gov/12402217

12 December 2020

Assessing allele frequencies of single nucleotide polymorphisms in DNA pools by pyrosequencing technology

1 reference

https://pubmed.ncbi.nlm.nih.gov/12402217

12 December 2020

The value of isolated populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/12402217

12 December 2020

Segregation analysis of tetra- and pentanucleotide short tandem repeat polymorphisms: Deviation from Mendelian expectations

1 reference

https://pubmed.ncbi.nlm.nih.gov/12402217

12 December 2020

Jewish diseases and origins

1 reference

https://pubmed.ncbi.nlm.nih.gov/12402217

12 December 2020

Identifiers

DOI

10.1086/344514

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12402217%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12402217%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

PubMed publication ID

12402217

1 reference