Juliane Winkelmann

Michael Zech 10 collaborations

Barbara Schormair 8 collaborations

Robert Jech 5 collaborations

Chen Zhao 5 collaborations

Konrad Oexle 5 collaborations

Matias Wagner 4 collaborations

Klaus Berger 4 collaborations

Claudia Trenkwalder 4 collaborations

Christian Gieger 4 collaborations

Annette Peters 4 collaborations

None None 3 collaborations

Eric W Klee 3 collaborations

Franziska Hopfner 3 collaborations

Theresa Brunet 3 collaborations

Tahir N Khan 2 collaborations

Daniel D Lam 2 collaborations

Nicholas Katsanis 2 collaborations

Susan Redline 2 collaborations

Rhonda E Schnur 2 collaborations

Ralitza H Gavrilova 2 collaborations

G Bradley Schaefer 2 collaborations

Katja Lohmann 2 collaborations

Wolfgang Lieb 2 collaborations

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Daniela Berg 2 collaborations

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Christine Klein 2 collaborations

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Philip Harrer 2 collaborations

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Birgit Högl 2 collaborations

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Walter Paulus 2 collaborations

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Andre Franke 2 collaborations

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Kamal Khan 1 collaboration

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Affiliations

Publications (23)

Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia.

Biological and clinical insights from genetics of insomnia symptoms.

De novo variants of NR4A2 are associated with neurodevelopmental disorder and epilepsy.

Rare Variants in Specific Lysosomal Genes Are Associated With Parkinson's Disease.

Therapeutic effectiveness of thalidomide in a patient with treatment-resistant restless legs syndrome.

Defining the genotypic and phenotypic spectrum of X-linked MSL3-related disorder.

Blood DNA methylation provides an accurate biomarker of KMT2B-related dystonia and predicts onset.

The role of patient navigators in ambulatory care: overview of systematic reviews.

Variant recurrence confirms the existence of a FBXO31-related spastic-dystonic cerebral palsy syndrome.

Candidate variants in TUB are associated with familial tremor.

Phenotypic and genome-wide studies on dicarbonyls: major associations to glomerular filtration rate and gamma-glutamyltransferase activity.

Oral health care in Europe: Financing, access and provision.

Variants in ATP5F1B are associated with dominantly inherited dystonia.

The genetic etiology of periodic limb movement in sleep.

Identification of Autophagy as a Functional Target Suitable for the Pharmacological Treatment of Mitochondrial Membrane Protein-Associated Neurodegeneration (MPAN) In Vitro.

Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction.

Loss-of-Function Variants in CUL3 Cause a Syndromic Neurodevelopmental Disorder.

Genetic Risk Factors in Isolated Dystonia Escape Genome-Wide Association Studies.

Tremor-Dominant Movement Disorder in

Patient Engagement in a Technology-Enhanced, Stepped-Care Intervention to Address the Mental Health Needs of Trauma Center Patients.

Opioid Misuse: An Organizational Response While Managing Cancer-Related Pain.

Update on KMT2B-Related Dystonia.

Identification of Restless Legs Syndrome Genes by Mutational Load Analysis.

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