The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language (Q30515982)

11 August 2017

The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language (English)

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11 August 2017

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10

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23 June 2017

35

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PubMed ID

22426781

23 June 2017

Bertram Müller-Myhsok

18

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Jaana Nopola-Hemmi

22

Jaana Nopola-Hemmi

1 reference

11 August 2017

Myriam Peyrard-Janvid

33

Myriam Peyrard-Janvid

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11 August 2017

15

Gerd Schulte-Körne

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Mikko Taipale

Mikko Taipale

7

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Sari Mäkelä

Sari Mäkelä

31

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Catherine M Stein

Catherine M Stein

8

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Davor Stanic

Davor Stanic

28

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Per Hoffmann

Per Hoffmann

19

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Magnus Nordenskjöld

Magnus Nordenskjöld

26

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Markus M Nöthen

Markus Nöthen

16

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Sudha Iyengar

Sudha Iyengar

34

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Heikki Lyytinen

24

Heikki Lyytinen

1 reference

11 August 2017

Jason M. Hall‐Spencer

27

Jason Spencer

1 reference

11 August 2017

23

Paavo H T Leppanen

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11 August 2017

Lara Sucheston-Campbell

2

Lara E Sucheston

1 reference

11 August 2017

Heidi Anthoni

1

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11 August 2017

Barbara A Lewis

3

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11 August 2017

Isabel Tapia-Páez

4

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11 August 2017

Xiaotang Fan

5

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11 August 2017

Marco Zucchelli

6

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11 August 2017

Marie-Estelle Hokkanen

9

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11 August 2017

Bruce F Pennington

11

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11 August 2017

Shelley D Smith

12

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11 August 2017

Richard K Olson

13

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11 August 2017

J Bruce Tomblin

14

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11 August 2017

Johannes Schumacher

17

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11 August 2017

Jeffrey W Gilger

20

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11 August 2017

George W Hynd

21

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11 August 2017

Jacqueline Schoumans

25

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11 August 2017

Wah Chin Boon

29

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11 August 2017

Evan Simpson

30

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11 August 2017

Jan-Åke Gustafsson

32

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11 August 2017

language of work or name

English

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publication date

17 March 2012

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11 August 2017

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11 August 2017

42

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11 August 2017

509-527

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11 August 2017

4

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describes a project that uses

11 August 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3375077/fullTextXML

inferred from PubMed Central ID database lookup

exact match

https://scigraph.springernature.com/pub.10.1007/s10519-012-9532-3

0 references

cites work

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Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.

20 June 2018

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A theoretical molecular network for dyslexia: integrating available genetic findings

20 June 2018

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The multiple roles of estrogens and the enzyme aromatase

20 June 2018

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Aromatase in the brain of teleost fish: expression, regulation and putative functions.

20 June 2018

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Genetics of developmental dyslexia

20 June 2018

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Alternative 5'-untranslated first exons of the mouse Cyp19A1 (aromatase) gene

20 June 2018

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Neuroprotective actions of brain aromatase

20 June 2018

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Aromatase in the brain: not just for reproduction anymore.

20 June 2018

1 reference

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The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia

20 June 2018

1 reference

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The relationship among receptive and expressive vocabulary, listening comprehension, pre-reading skills, word identification skills, and reading comprehension by children with reading disabilities

20 June 2018

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Recognizing rare disorders: aromatase deficiency.

20 June 2018

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Genes, language development, and language disorders

20 June 2018

1 reference

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A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia

20 June 2018

1 reference

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Genetics of dyslexia: the evolving landscape

20 June 2018

1 reference

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Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1.

20 June 2018

1 reference

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Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations

20 June 2018

1 reference

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DYX1C1 functions in neuronal migration in developing neocortex

20 June 2018

1 reference

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From single to multiple deficit models of developmental disorders

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3375077

Brain aromatase: new lessons from non-mammalian model systems.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3375077

TFII-I down-regulates a subset of estrogen-responsive genes through its interaction with an initiator element and estrogen receptor alpha.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3375077

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3375077

Are specific language impairment and dyslexia distinct disorders?

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3375077

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3375077

Direct and indirect effects of estrogen on rat hippocampus

20 June 2018

1 reference

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DCDC2 is associated with reading disability and modulates neuronal development in the brain

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3375077

The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3375077

Developmental dyslexia and specific language impairment: same or different?

20 June 2018

1 reference

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Haploview: analysis and visualization of LD and haplotype maps

20 June 2018

1 reference

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Organization of the human aromatase p450 (CYP19) gene

20 June 2018

1 reference

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A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain

20 June 2018

1 reference

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A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32

20 June 2018

1 reference

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A longitudinal investigation of reading outcomes in children with language impairments

20 June 2018

1 reference

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A dominant gene for developmental dyslexia on chromosome 3

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3375077

Estrogen synthetase (aromatase) immunohistochemistry reveals concordance between avian and rodent limbic systems and hypothalami.

20 June 2018

1 reference

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Two translocations of chromosome 15q associated with dyslexia

20 June 2018

1 reference

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A test for linkage and association in general pedigrees: the pedigree disequilibrium test

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3375077

Estrogen and the developing mammalian brain

20 June 2018

1 reference

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Nonword repetition and child language impairment.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3375077

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3375077

Characterization of mice deficient in aromatase (ArKO) because of targeted disruption of the cyp19 gene

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3375077

TFII-I enhances activation of the c-fos promoter through interactions with upstream elements

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3375077

Prevalence of specific language impairment in kindergarten children.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3375077

PAML: a program package for phylogenetic analysis by maximum likelihood

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3375077

Familial aggregation of spelling disability.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3375077

Developmental dyslexia: four consecutive patients with cortical anomalies

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3375077

Steroid hormones as mediators of neural plasticity

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3375077

The binding site of a steroid hormone receptor-like protein within the Drosophila Adh adult enhancer is required for high levels of tissue-specific alcohol dehydrogenase expression

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3375077

A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3375077

Robo1 regulates the development of major axon tracts and interneuron migration in the forebrain.

20 June 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

Relationships between aromatase activity in the brain and gonads and behavioural deficits in homozygous and heterozygous aromatase knockout mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

A 5.6-Mb deletion in 15q14 in a boy with speech and language disorder, cleft palate, epilepsy, a ventricular septal defect, mental retardation and developmental delay.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

Risk markers for SLI: a study of young language-learning children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

Pedigree disequilibrium tests for multilocus haplotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

The study of candidate genes in drug trials: sample size considerations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

Phenylketonuria screening registry as a resource for population genetic studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

Estrogen alters spine number and morphology in prefrontal cortex of aged female rhesus monkeys.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

Developmental expression and regulation of aromatase- and 5alpha-reductase type I mRNA in the male and female mouse hypothalamus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

A novel mutation in the human aromatase gene: insights on the relationship among serum estradiol, longitudinal growth and bone mineral density in an adult man under estrogen replacement treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

Newborn brain event-related potentials revealing atypical processing of sound frequency and the subsequent association with later literacy skills in children with familial dyslexia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

Estradiol stimulates progenitor cell division in the ventricular and subventricular zones of the embryonic neocortex

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

The SCL +40 enhancer targets the midbrain together with primitive and definitive hematopoiesis and is regulated by SCL and GATA proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

Zebra finch aromatase gene expression is regulated in the brain through an alternate promoter

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

[Diagnosis of reading and spelling disorder]

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

Interrelationship and familiality of dyslexia related quantitative measures.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

Prevalence of speech delay in 6-year-old children and comorbidity with language impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

Speech sound disorder influenced by a locus in 15q14 region.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

Language development, literacy skills, and predictive connections to reading in Finnish children with and without familial risk for dyslexia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

A robust, efficient and flexible method for staining myelinated axons in blocks of brain tissue

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

Collection of genomic DNA by buccal swabs for polymerase chain reaction-based biomarker assays

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

Developmental dyslexia--recurrence risk estimates from a german bi-center study using the single proband sib pair design.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-012-9532-3

Learning-associated activation of nuclear MAPK, CREB and Elk-1, along with Fos production, in the rat hippocampus after a one-trial avoidance learning: abolition by NMDA receptor blockade

21 January 2018

1 reference

12 December 2020

The association of reading disability, behavioral disorders, and language impairment among second-grade children

1 reference

12 December 2020

The replication requirement

1 reference

12 December 2020

Pre-literacy skills of subgroups of children with speech sound disorders

1 reference

12 December 2020

Survival and growth of hippocampal neurons in defined medium at low density: advantages of a sandwich culture technique or low oxygen

1 reference

12 December 2020

10.1007/S10519-012-9532-3

Identifiers

DOI

1 reference

Dimensions Publication ID

11 August 2017

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1 reference

11 August 2017

1 reference