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Correction: Pleiotropy between language impairment and broader behavioral disorders—an investigation of both common and rare genetic variants

Journal of neurodevelopmental disorders, 2023-09, Vol.15 (1), p.1-31, Article 31

2023

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Pleiotropy between language impairment and broader behavioral disorders-an investigation of both common and rare genetic variants

Journal of neurodevelopmental disorders, 2021-12, Vol.13 (1), p.54-54, Article 54

2021

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Rational confederation of genes and diseases: NGS interpretation via GeneCards, MalaCards and VarElect

Biomedical engineering online, 2017-08, Vol.16 (Suppl 1), p.72-72, Article 72

2017

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A large population-based investigation into the genetics of susceptibility to gastrointestinal infections and the link between gastrointestinal infections and mental illness

Human genetics, 2020-05, Vol.139 (5), p.593-604

2020

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Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth

PLoS genetics, 2020-11, Vol.16 (11), p.e1009163-e1009163

2020

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Maternal pregnancy-related infections and autism spectrum disorder—the genetic perspective

Translational psychiatry, 2022-08, Vol.12 (1), p.334-334, Article 334

2022

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A large-scale investigation into the role of classical HLA loci in multiple types of severe infections, with a focus on overlaps with autoimmune and mental disorders

Journal of translational medicine, 2021-05, Vol.19 (1), p.1-230, Article 230

2021

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Correction: Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorder

European journal of human genetics : EJHG, 2021-08, Vol.29 (8), p.1316-1316

2021

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Circulating S100B levels at birth and risk of six major neuropsychiatric or neurological disorders: a two-sample Mendelian Randomization Study

Translational psychiatry, 2023-05, Vol.13 (1), p.174-174, Article 174

2023

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Genetic assortative mating for schizophrenia and bipolar disorder

European psychiatry, 2022-08, Vol.65 (1), p.1-24

2022

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A family-based study of genetic and epigenetic effects across multiple neurocognitive, motor, social-cognitive and social-behavioral functions

Behavioral and brain functions, 2022-12, Vol.18 (1), p.14-14, Article 14

2022

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Quantitative genome-wide association analyses of receptive language in the Danish High Risk and Resilience Study

BMC neuroscience, 2020-07, Vol.21 (1), p.1-30, Article 30

2020

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The Danish High-Risk and Resilience Study-VIA 15 - A Study Protocol for the Third Clinical Assessment of a Cohort of 522 Children Born to Parents Diagnosed With Schizophrenia or Bipolar Disorder and Population-Based Controls

Frontiers in psychiatry, 2022-04, Vol.13, p.809807-809807

2022

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Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes

Journal of neurodevelopmental disorders, 2016-06, Vol.8 (1), p.24-24, Article 24

2016

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An investigation of NFXL1, a gene implicated in a study of specific language impairment

Journal of neurodevelopmental disorders, 2016-04, Vol.8 (13), p.13-13, Article 13

Nudel, Ron

2016

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MalaCards: an amalgamated human disease compendium with diverse clinical and genetic annotation and structured search

Nucleic acids research, 2017-01, Vol.45 (D1), p.D877-D887

2017

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Correction: Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment

PLoS genetics, 2015-06, Vol.11 (6), p.e1005336-e1005336

2015

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GeneHancer: genome-wide integration of enhancers and target genes in GeneCards

Database : the journal of biological databases and curation, 2017, Vol.2017

2017

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The GeneCards Suite: From Gene Data Mining to Disease Genome Sequence Analyses

Current Protocols in Bioinformatics, 2016-06, Vol.54 (1), p.1.30.1-1.30.33

2016

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Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study

Molecular psychiatry, 2020-10, Vol.25 (10), p.2410-2421

2020

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Genetic and epidemiological analyses of infection load and its relationship with psychiatric disorders

Epidemiology and infection, 2023-05, Vol.151, p.e93-e93, Article e93

2023

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VarElect: the phenotype-based variation prioritizer of the GeneCards Suite

BMC genomics, 2016-06, Vol.17 Suppl 2 (Suppl 2), p.444-444, Article 444

2016

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An immunogenetic investigation of 30 autoimmune and autoinflammatory diseases and their links to psychiatric disorders in a nationwide sample

Immunology, 2023-04, Vol.168 (4), p.622-639

2023

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A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment

Correction: Pleiotropy between language impairment and broader behavioral disorders—an investigation of both common and rare genetic variants

Pleiotropy between language impairment and broader behavioral disorders-an investigation of both common and rare genetic variants

Rational confederation of genes and diseases: NGS interpretation via GeneCards, MalaCards and VarElect

A large population-based investigation into the genetics of susceptibility to gastrointestinal infections and the link between gastrointestinal infections and mental illness

Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth

Maternal pregnancy-related infections and autism spectrum disorder—the genetic perspective

A large-scale investigation into the role of classical HLA loci in multiple types of severe infections, with a focus on overlaps with autoimmune and mental disorders

Correction: Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorder

Circulating S100B levels at birth and risk of six major neuropsychiatric or neurological disorders: a two-sample Mendelian Randomization Study

Genetic assortative mating for schizophrenia and bipolar disorder

A family-based study of genetic and epigenetic effects across multiple neurocognitive, motor, social-cognitive and social-behavioral functions

Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment

Quantitative genome-wide association analyses of receptive language in the Danish High Risk and Resilience Study

The Danish High-Risk and Resilience Study-VIA 15 - A Study Protocol for the Third Clinical Assessment of a Cohort of 522 Children Born to Parents Diagnosed With Schizophrenia or Bipolar Disorder and Population-Based Controls

Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes

An investigation of NFXL1, a gene implicated in a study of specific language impairment

MalaCards: an amalgamated human disease compendium with diverse clinical and genetic annotation and structured search

Correction: Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment

GeneHancer: genome-wide integration of enhancers and target genes in GeneCards

The GeneCards Suite: From Gene Data Mining to Disease Genome Sequence Analyses

Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study

Genetic and epidemiological analyses of infection load and its relationship with psychiatric disorders

VarElect: the phenotype-based variation prioritizer of the GeneCards Suite

An immunogenetic investigation of 30 autoimmune and autoinflammatory diseases and their links to psychiatric disorders in a nationwide sample

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