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Pathway-Based Approaches for Analysis of Genomewide Association Studies

American journal of human genetics, 2007-12, Vol.81 (6), p.1278-1283

2007

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Functional significance of rare neuroligin 1 variants found in autism

PLoS genetics, 2017-08, Vol.13 (8), p.e1006940-e1006940

2017

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The Contribution of Mosaic Variants to Autism Spectrum Disorder

PLoS genetics, 2016-09, Vol.12 (9), p.e1006245-e1006245

2016

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PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

Genome Research, 2007-11, Vol.17 (11), p.1665-1674

2007

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Allelic contribution of Nrxn1α to autism-relevant behavioral phenotypes in mice

PLoS genetics, 2023-02, Vol.19 (2), p.e1010659-e1010659

2023

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The Role of Synaptic Cell Adhesion Molecules and Associated Scaffolding Proteins in Social Affiliative Behaviors

Biological psychiatry (1969), 2020-09, Vol.88 (6), p.442-451

2020

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Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms

Nucleic acids research, 2008-11, Vol.36 (19), p.e126

2008

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Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition

PLoS genetics, 2017-07, Vol.13 (7), p.e1006886-e1006886

2017

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Contrasting Views of Autism Spectrum Traits in Adults, Especially in Self-Reports vs. Informant-Reports for Women High in Autism Spectrum Traits

Journal of autism and developmental disorders, 2024-03, Vol.54 (3), p.1088-1100

2024

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Rediscovering the value of families for psychiatric genetics research

Molecular psychiatry, 2019-04, Vol.24 (4), p.523-535

2019

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2022 Benjamin Franklin NextGen Award presented to Kafui Dzirasa, M.D., Ph.D

Journal of the Franklin Institute, 2022-12, Vol.359 (18), p.10288-10293

2022

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Sufficient sleep duration in autistic children and the role of physical activity

Autism, 2022-05, Vol.26 (4), p.814-826

2022

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Polygenic Risk of Psychiatric Disorders Exhibits Cross-trait Associations in Electronic Health Record Data From European Ancestry Individuals

Biological psychiatry (1969), 2021-02, Vol.89 (3), p.236-245

2021

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A Role for AMP-Activated Protein Kinase in Contraction- and Hypoxia-Regulated Glucose Transport in Skeletal Muscle

Molecular cell, 2001-05, Vol.7 (5), p.1085-1094

2001

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Phenotypic and ancestry-related assortative mating in autism

Molecular autism, 2024-06, Vol.15 (1), p.27-14, Article 27

2024

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A population-based study of KCNH7 p.Arg394His and bipolar spectrum disorder

Human molecular genetics, 2014-12, Vol.23 (23), p.6395-6406

2014

Volltextzugriff (PDF)

The relationship between autism spectrum and sleep–wake traits

Autism research, 2022-04, Vol.15 (4), p.641-652

2022

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Genetic pleiotropy between mood disorders, metabolic, and endocrine traits in a multigenerational pedigree

Translational psychiatry, 2018-10, Vol.8 (1), p.218-12, Article 218

2018

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From mouse to human: evolutionary genomics analysis of human orthologs of essential genes

PLoS genetics, 2013-05, Vol.9 (5), p.e1003484-e1003484

2013

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Self-supervised learning of accelerometer data provides new insights for sleep and its association with mortality

NPJ digital medicine, 2024-05, Vol.7 (1), p.86-10, Article 86

2024

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Author Correction: Self-supervised learning of accelerometer data provides new insights for sleep and its association with mortality

NPJ digital medicine, 2024-07, Vol.7 (1), p.175-1, Article 175

2024

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Expanding the phenotype half of the genotype—phenotype space

Proceedings of the National Academy of Sciences - PNAS, 2016-02, Vol.113 (6), p.1477-1479

Bućan, Maja

2016

Volltextzugriff (PDF)

A population-specific reference panel empowers genetic studies of Anabaptist populations

Scientific reports, 2017-07, Vol.7 (1), p.6079-9, Article 6079

2017

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2015 BENJAMIN FRANKLIN MEDAL IN LIFE SCIENCE PRESENTED TO CORNELIA BARGMANN, PH.D

Journal of the Franklin Institute, 2017-01, Vol.354 (1), p.68-73

Bucan, Maja

2017

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Increased burden of deleterious variants in essential genes in autism spectrum disorder

Proceedings of the National Academy of Sciences - PNAS, 2016-12, Vol.113 (52), p.15054-15059

2016

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Pathway-Based Approaches for Analysis of Genomewide Association Studies

Functional significance of rare neuroligin 1 variants found in autism

The Contribution of Mosaic Variants to Autism Spectrum Disorder

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

Allelic contribution of Nrxn1α to autism-relevant behavioral phenotypes in mice

The Role of Synaptic Cell Adhesion Molecules and Associated Scaffolding Proteins in Social Affiliative Behaviors

Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms

Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition

Contrasting Views of Autism Spectrum Traits in Adults, Especially in Self-Reports vs. Informant-Reports for Women High in Autism Spectrum Traits

Rediscovering the value of families for psychiatric genetics research

2022 Benjamin Franklin NextGen Award presented to Kafui Dzirasa, M.D., Ph.D

Sufficient sleep duration in autistic children and the role of physical activity

Polygenic Risk of Psychiatric Disorders Exhibits Cross-trait Associations in Electronic Health Record Data From European Ancestry Individuals

A Role for AMP-Activated Protein Kinase in Contraction- and Hypoxia-Regulated Glucose Transport in Skeletal Muscle

Phenotypic and ancestry-related assortative mating in autism

A population-based study of KCNH7 p.Arg394His and bipolar spectrum disorder

The relationship between autism spectrum and sleep–wake traits

Genetic pleiotropy between mood disorders, metabolic, and endocrine traits in a multigenerational pedigree

From mouse to human: evolutionary genomics analysis of human orthologs of essential genes

Self-supervised learning of accelerometer data provides new insights for sleep and its association with mortality

Author Correction: Self-supervised learning of accelerometer data provides new insights for sleep and its association with mortality

Expanding the phenotype half of the genotype—phenotype space

A population-specific reference panel empowers genetic studies of Anabaptist populations

2015 BENJAMIN FRANKLIN MEDAL IN LIFE SCIENCE PRESENTED TO CORNELIA BARGMANN, PH.D

Increased burden of deleterious variants in essential genes in autism spectrum disorder

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