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Patient‐individual phenotypes of glioblastoma stem cells are conserved in culture and associate with radioresistance, brain infiltration and patient prognosis

International journal of cancer, 2022-05, Vol.150 (10), p.1722-1733

2022

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The functional neuroanatomy of spontaneous retrieval and strategic monitoring of delayed intentions

Neuropsychologia, 2014-01, Vol.52, p.37-50

2014

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Angiokeratoma corporis diffusum with severe acroparesthesia, an endothelial abnormality, and inconspicuous genetic findings

Journal of cutaneous pathology, 2022-03, Vol.49 (3), p.293-298

2022

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Primary and secondary rewards differentially modulate neural activity dynamics during working memory

PloS one, 2010-02, Vol.5 (2), p.e9251-e9251

2010

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Dissociable Neural Routes to Successful Prospective Memory

Psychological science, 2013-09, Vol.24 (9), p.1791-1800

2013

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Natural history of Krabbe disease – a nationwide study in Germany using clinical and MRI data

Orphanet journal of rare diseases, 2020-09, Vol.15 (1), p.1-243, Article 243

2020

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Novel homozygous LAMB1 in-frame deletion in a pediatric patient with brain anomalies and cerebrovascular event

American journal of medical genetics. Part A, 2023-10, Vol.191 (10), p.2656-2663

2023

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Phenotypic variation between siblings with Metachromatic Leukodystrophy

Orphanet journal of rare diseases, 2019-06, Vol.14 (1), p.136-136, Article 136

2019

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FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum

Journal of medical genetics, 2017-01, Vol.54 (1), p.64

2017

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Further evidence for de novo variants in SYNCRIP as the cause of a neurodevelopmental disorder

Human mutation, 2021-09, Vol.42 (9), p.1094-1100

2021

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Iodine images in dual energy CT: A monocentric study benchmarking quantitative iodine concentration values of the healthy liver

PloS one, 2022-07, Vol.17 (7), p.e0270805-e0270805

2022

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Novel Variants of SOX4 in Patients with Intellectual Disability

International journal of molecular sciences, 2023-02, Vol.24 (4), p.3519

2023

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Homozygous TBC1 domain-containing kinase (TBCK) mutation causes a novel lysosomal storage disease - a new type of neuronal ceroid lipofuscinosis (CLN15)?

Acta neuropathologica communications, 2018-12, Vol.6 (1), p.145-145, Article 145

2018

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A Taxonomy of Path-Related Goodness-of-Fit Indices and Recommended Criterion Values

Psychological methods, 2016-09, Vol.21 (3), p.388-404

2016

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Skewed X‐inactivation in a family with DLG3‐associated X‐linked intellectual disability

American journal of medical genetics. Part A, 2017-09, Vol.173 (9), p.2545-2550

2017

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Effects of Ginkgo biloba extract EGb 761® on cognitive control functions, mental activity of the prefrontal cortex and stress reactivity in elderly adults with subjective memory impairment - a randomized double-blind placebo-controlled trial

Human psychopharmacology, 2016-05, Vol.31 (3), p.227-242

2016

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Implementation of Basic Life Support training in schools: a randomised controlled trial evaluating self-regulated learning as alternative training concept

BMC public health, 2020-01, Vol.20 (1), p.50-50, Article 50

2020

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The adult phenotype of Schaaf-Yang syndrome

Orphanet journal of rare diseases, 2020-10, Vol.15 (1), p.1-294, Article 294

2020

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Health-related quality of life and self-reported cognitive function in patients with delayed neurocognitive recovery after radical prostatectomy: a prospective follow-up study

Health and quality of life outcomes, 2021-02, Vol.19 (1), p.64-64, Article 64

2021

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Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H/SPG35 in 4 families

Neurology, 2016-07, Vol.87 (2), p.186

2016

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Protonated Ethylene Carbonate: A Highly Resonance‐Stabilized Cation

ChemistryOpen (Weinheim), 2021-12, Vol.10 (12), p.1160-1165

2021

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Protonated Ethylene Carbonate: A Highly Resonance‐Stabilized Cation

ChemistryOpen (Weinheim), 2021-12, Vol.10 (12), p.1159-1159

2021

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Enhancement of cognitive control by approach and avoidance motivational states

Cognition and emotion, 2010-02, Vol.24 (2), p.338-356

2010

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SOPH syndrome in three affected individuals showing similarities with progeroid cutis laxa conditions in early infancy

Journal of human genetics, 2019-07, Vol.64 (7), p.609-616

2019

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Patient‐individual phenotypes of glioblastoma stem cells are conserved in culture and associate with radioresistance, brain infiltration and patient prognosis

The functional neuroanatomy of spontaneous retrieval and strategic monitoring of delayed intentions

Angiokeratoma corporis diffusum with severe acroparesthesia, an endothelial abnormality, and inconspicuous genetic findings

Primary and secondary rewards differentially modulate neural activity dynamics during working memory

Dissociable Neural Routes to Successful Prospective Memory

Natural history of Krabbe disease – a nationwide study in Germany using clinical and MRI data

Novel homozygous LAMB1 in-frame deletion in a pediatric patient with brain anomalies and cerebrovascular event

Phenotypic variation between siblings with Metachromatic Leukodystrophy

A single center experience of prenatal parent‐fetus trio exome sequencing for pregnancies with congenital anomalies

FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum

Further evidence for de novo variants in SYNCRIP as the cause of a neurodevelopmental disorder

Iodine images in dual energy CT: A monocentric study benchmarking quantitative iodine concentration values of the healthy liver

Novel Variants of SOX4 in Patients with Intellectual Disability

Homozygous TBC1 domain-containing kinase (TBCK) mutation causes a novel lysosomal storage disease - a new type of neuronal ceroid lipofuscinosis (CLN15)?

A Taxonomy of Path-Related Goodness-of-Fit Indices and Recommended Criterion Values

Skewed X‐inactivation in a family with DLG3‐associated X‐linked intellectual disability

Effects of Ginkgo biloba extract EGb 761® on cognitive control functions, mental activity of the prefrontal cortex and stress reactivity in elderly adults with subjective memory impairment - a randomized double-blind placebo-controlled trial

Implementation of Basic Life Support training in schools: a randomised controlled trial evaluating self-regulated learning as alternative training concept

The adult phenotype of Schaaf-Yang syndrome

Health-related quality of life and self-reported cognitive function in patients with delayed neurocognitive recovery after radical prostatectomy: a prospective follow-up study

Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H/SPG35 in 4 families

Protonated Ethylene Carbonate: A Highly Resonance‐Stabilized Cation

Protonated Ethylene Carbonate: A Highly Resonance‐Stabilized Cation

Enhancement of cognitive control by approach and avoidance motivational states

SOPH syndrome in three affected individuals showing similarities with progeroid cutis laxa conditions in early infancy

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