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Author Guide for Addressing Animal Methods Bias in Publishing

Advanced science, 2023-10, Vol.10 (30), p.e2303226-e2303226

2023

Volltextzugriff (PDF)

Systematic Organization of COVID-19 Data Supported by the Adverse Outcome Pathway Framework

Frontiers in public health, 2021-05, Vol.9, p.638605

2021

Volltextzugriff (PDF)

GIGYF2 mutation in late-onset Parkinson's disease with cognitive impairment

Journal of human genetics, 2015-10, Vol.60 (10), p.637-640

2015

Volltextzugriff (PDF)

A survey to assess animal methods bias in scientific publishing

ALTEX, alternatives to animal experimentation, 2023-01, Vol.40 (4), p.665

2023

Volltextzugriff (PDF)

The Sac1 Domain of SYNJ1 Identified Mutated in a Family with Early-Onset Progressive Parkinsonism with Generalized Seizures

Human mutation, 2013-09, Vol.34 (9), p.1200-1207

2013

Volltextzugriff (PDF)

Confronting the bias towards animal experimentation (animal methods bias)

Frontiers in drug discovery, 2024-04, Vol.4

2024

Volltextzugriff (PDF)

Whole blood transcriptome analysis in bipolar disorder reveals strong lithium effect

Psychological medicine, 2020-11, Vol.50 (15), p.2575-2586

2020

Volltextzugriff (PDF)

Proceedings of a workshop to address animal methods bias in scientific publishing

ALTEX, alternatives to animal experimentation, 2023-01, Vol.40 (4), p.677

2023

Volltextzugriff (PDF)

The use of next-generation sequencing in movement disorders

Frontiers in genetics, 2012, Vol.3, p.75-75

2012

Volltextzugriff (PDF)

SCN4A pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsy

Human molecular genetics, 2015-12, Vol.24 (24), p.7111-7120

2015

Volltextzugriff (PDF)

SORT1 Mutation Resulting in Sortilin Deficiency and p75(NTR) Upregulation in a Family With Essential Tremor

ASN neuro, 2015-07, Vol.7 (4)

2015

Volltextzugriff (PDF)

Identification of COL6A2 mutations in progressive myoclonus epilepsy syndrome

Human genetics, 2013-03, Vol.132 (3), p.275-283

2013

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Variable phenotypic expression in families with early-onset Parkinsonism due to PRKN mutations

Journal of neurology, 2014-06, Vol.261 (6), p.1223-1226

2014

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SORT1 Mutation Resulting in Sortilin Deficiency and p75NTR Upregulation in a Family With Essential Tremor

ASN neuro, 2015-08, Vol.7 (4)

2015

Volltextzugriff (PDF)

COVID-19 through Adverse Outcome Pathways: Building networks to better understand the disease - 3rd CIAO AOP Design Workshop

ALTEX, 2022, Vol.39 (2), p.322–335-322–335

2022

Volltextzugriff (PDF)

SCN4A Pore Mutation Pathogenetically Contributes to Autosomal Dominant Essential Tremor and May Increase Susceptibility to Epilepsy

Biophysical journal, 2016-02, Vol.110 (3), p.112a-112a

2016

Volltextzugriff (PDF)

SORT1 Mutation Resulting in Sortilin Deficiency and p75 NTR Upregulation in a Family With Essential Tremor

ASN neuro, 2015-07, Vol.7 (4), p.175909141559829

2015

Volltextzugriff (PDF)

Mutation Resulting in Sortilin Deficiency and p75 Upregulation in a Family With Essential Tremor

ASN neuro, 2015-08, Vol.7

2015

Volltextzugriff (PDF)

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Author Guide for Addressing Animal Methods Bias in Publishing

Systematic Organization of COVID-19 Data Supported by the Adverse Outcome Pathway Framework

GIGYF2 mutation in late-onset Parkinson's disease with cognitive impairment

A survey to assess animal methods bias in scientific publishing

The Sac1 Domain of SYNJ1 Identified Mutated in a Family with Early-Onset Progressive Parkinsonism with Generalized Seizures

Confronting the bias towards animal experimentation (animal methods bias)

Whole blood transcriptome analysis in bipolar disorder reveals strong lithium effect

Proceedings of a workshop to address animal methods bias in scientific publishing

The use of next-generation sequencing in movement disorders

SCN4A pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsy

SORT1 Mutation Resulting in Sortilin Deficiency and p75(NTR) Upregulation in a Family With Essential Tremor

Identification of COL6A2 mutations in progressive myoclonus epilepsy syndrome

Variable phenotypic expression in families with early-onset Parkinsonism due to PRKN mutations

SORT1 Mutation Resulting in Sortilin Deficiency and p75NTR Upregulation in a Family With Essential Tremor

COVID-19 through Adverse Outcome Pathways: Building networks to better understand the disease - 3rd CIAO AOP Design Workshop

SCN4A Pore Mutation Pathogenetically Contributes to Autosomal Dominant Essential Tremor and May Increase Susceptibility to Epilepsy

SORT1 Mutation Resulting in Sortilin Deficiency and p75 NTR Upregulation in a Family With Essential Tremor

Mutation Resulting in Sortilin Deficiency and p75 Upregulation in a Family With Essential Tremor

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