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Structural Variations Contribute to the Genetic Etiology of Autism Spectrum Disorder and Language Impairments

International journal of molecular sciences, 2023-09, Vol.24 (17), p.13248

2023

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Improvement of automated analysis of coronary Doppler echocardiograms

Scientific reports, 2022-05, Vol.12 (1), p.7490-7490, Article 7490

2022

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Defining the genetic architecture of human developmental language impairment

Life sciences (1973), 2012-04, Vol.90 (13-14), p.469-475

2012

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MicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders

Genes, 2022-07, Vol.13 (8), p.1329

2022

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The Rosetta Phenotype Harmonization Method Facilitates Finding a Relationship Quantitative Trait Locus for a Complex Cognitive Trait

Genes, 2023-08, Vol.14 (9), p.1748

2023

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An integrative analysis of regional gene expression profiles in the human brain

Methods (San Diego, Calif.), 2015-02, Vol.73, p.54-70

2015

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Understanding developmental language disorder - the Helsinki longitudinal SLI study (HelSLI): a study protocol

BMC Psychology, 2018-05, Vol.6 (1), p.24-24, Article 24

2018

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Forming Big Datasets through Latent Class Concatenation of Imperfectly Matched Databases Features

Genes, 2019-09, Vol.10 (9), p.727

2019

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Collection and extraction of saliva DNA for next generation sequencing

Journal of visualized experiments, 2014-08 (90)

2014

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Gene × smoking interactions on human brain gene expression: finding common mechanisms in adolescents and adults

Journal of child psychology and psychiatry, 2013-10, Vol.54 (10), p.1109-1119

2013

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Gene × Gene Interaction in Shared Etiology of Autism and Specific Language Impairment

Biological psychiatry (1969), 2012-10, Vol.72 (8), p.692-699

2012

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Who is afraid of math? Two sources of genetic variance for mathematical anxiety

Journal of child psychology and psychiatry, 2014-09, Vol.55 (9), p.1056-1064

2014

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A Review on Genomics APIs

Computational and structural biotechnology journal, 2016-01, Vol.14 (C), p.8-15

2016

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Validation of a cost-efficient multi-purpose SNP panel for disease based research

PloS one, 2011-05, Vol.6 (5), p.e19699-e19699

2011

Volltextzugriff (PDF)

Early considerations of genetics in aphasia rehabilitation: a narrative review

Aphasiology, 2023-06, Vol.37 (6), p.835-853

2023

Volltextzugriff (PDF)

Common genetic risk factors in ASD and ADHD co-occurring families

Human genetics, 2023-02, Vol.142 (2), p.217-230

2023

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MiR-29b is associated with perinatal inflammation in extremely preterm infants

Pediatric research, 2021-03, Vol.89 (4), p.889-893

2021

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Outcomes following a comprehensive versus a selective approach for infants born at 22 weeks of gestation

Journal of perinatology, 2019-01, Vol.39 (1), p.39-47

2019

Volltextzugriff (PDF)

The MPRINT Hub Data, Model, Knowledge and Research Coordination Center: Bridging the gap in maternal–pediatric therapeutics research through data integration and pharmacometrics

Pharmacotherapy, 2023-05, Vol.43 (5), p.391-402

2023

Volltextzugriff (PDF)

Effects of Updating Linkage Evidence across Subsets of Data: Reanalysis of the Autism Genetic Resource Exchange Data Set

American journal of human genetics, 2005-04, Vol.76 (4), p.688-695

2005

Volltextzugriff (PDF)

A Genome Scan for Loci Shared by Autism Spectrum Disorder and Language Impairment

The American journal of psychiatry, 2014-01, Vol.171 (1), p.72-81

2014

Volltextzugriff (PDF)

Invasive or More Direct Measurements Can Provide an Objective Early-Stopping Ceiling for Training Deep Neural Networks on Non-invasive or Less-Direct Biomedical Data

SN computer science, 2023-01, Vol.4 (2), p.161-161, Article 161

2023

Volltextzugriff (PDF)

Gene x Gene Interaction in Shared Etiology of Autism and Specific Language Impairment

Biological psychiatry (1969), 2012-10, Vol.72 (8), p.692-699

2012

Volltextzugriff (PDF)

A Major Susceptibility Locus for Specific Language Impairment Is Located on 13q21

American journal of human genetics, 2002-07, Vol.71 (1), p.45-55

2002

Volltextzugriff (PDF)

Behavioral and Molecular Genetics of Reading-Related AM and FM Detection Thresholds

Behavior genetics, 2017-03, Vol.47 (2), p.193-201

2017

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Structural Variations Contribute to the Genetic Etiology of Autism Spectrum Disorder and Language Impairments

Improvement of automated analysis of coronary Doppler echocardiograms

Defining the genetic architecture of human developmental language impairment

MicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders

The Rosetta Phenotype Harmonization Method Facilitates Finding a Relationship Quantitative Trait Locus for a Complex Cognitive Trait

An integrative analysis of regional gene expression profiles in the human brain

Understanding developmental language disorder - the Helsinki longitudinal SLI study (HelSLI): a study protocol

Forming Big Datasets through Latent Class Concatenation of Imperfectly Matched Databases Features

Collection and extraction of saliva DNA for next generation sequencing

Gene × smoking interactions on human brain gene expression: finding common mechanisms in adolescents and adults

Gene × Gene Interaction in Shared Etiology of Autism and Specific Language Impairment

Who is afraid of math? Two sources of genetic variance for mathematical anxiety

A Review on Genomics APIs

Validation of a cost-efficient multi-purpose SNP panel for disease based research

Early considerations of genetics in aphasia rehabilitation: a narrative review

Common genetic risk factors in ASD and ADHD co-occurring families

MiR-29b is associated with perinatal inflammation in extremely preterm infants

Outcomes following a comprehensive versus a selective approach for infants born at 22 weeks of gestation

The MPRINT Hub Data, Model, Knowledge and Research Coordination Center: Bridging the gap in maternal–pediatric therapeutics research through data integration and pharmacometrics

Effects of Updating Linkage Evidence across Subsets of Data: Reanalysis of the Autism Genetic Resource Exchange Data Set

A Genome Scan for Loci Shared by Autism Spectrum Disorder and Language Impairment

Invasive or More Direct Measurements Can Provide an Objective Early-Stopping Ceiling for Training Deep Neural Networks on Non-invasive or Less-Direct Biomedical Data

Gene x Gene Interaction in Shared Etiology of Autism and Specific Language Impairment

A Major Susceptibility Locus for Specific Language Impairment Is Located on 13q21

Behavioral and Molecular Genetics of Reading-Related AM and FM Detection Thresholds

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