UB Paderborn / Katalog / Suche / in CDI

2007 Joint Meeting of the 6th International Symposium on Noninvasive Functional Source Imaging of the Brain and Heart and the International Conference on Functional Biomedical Imaging, 2007, p.8-13

2007

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IEEE_Xplore

Uptake and accumulation of emerging contaminants in processing tomato irrigated with tertiary treated wastewater effluent: a pilot-scale study

Frontiers in plant science, 2023-08, Vol.14, p.1238163-1238163

2023

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PD-L1 Expression Heterogeneity in Non–Small Cell Lung Cancer: Defining Criteria for Harmonization between Biopsy Specimens and Whole Sections

Journal of thoracic oncology, 2018-08, Vol.13 (8), p.1113-1120

2018

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Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes

Brain (London, England : 1878), 2022-09, Vol.145 (9), p.3308-3327

2022

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Blepharophimosis with intellectual disability and Helsmoortel‐Van Der Aa Syndrome share episignature and phenotype

American journal of medical genetics. Part C, Seminars in medical genetics, 2024-06, p.e32089-e32089

2024

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CHAMP1-related disorders: pathomechanisms triggered by different genomic alterations define distinct nosological categories

European journal of human genetics : EJHG, 2023-06, Vol.31 (6), p.648-653

2023

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De novo SMARCA2 variants clustered outside the helicase domain cause a new recognizable syndrome with intellectual disability and blepharophimosis distinct from Nicolaides-Baraitser syndrome

Genetics in medicine, 2020-11, Vol.22 (11), p.1838-1850

2020

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Resilience and cross-network connectivity: A neural model for post-trauma survival

Working memory of somatosensory stimuli: An fMRI study

Sensory-Motor Modulations of EEG Event-Related Potentials Reflect Walking-Related Macro-Affordances

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Uptake and accumulation of emerging contaminants in processing tomato irrigated with tertiary treated wastewater effluent: a pilot-scale study

PD-L1 Expression Heterogeneity in Non–Small Cell Lung Cancer: Defining Criteria for Harmonization between Biopsy Specimens and Whole Sections

Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis

Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes

Blepharophimosis with intellectual disability and Helsmoortel‐Van Der Aa Syndrome share episignature and phenotype

CHAMP1-related disorders: pathomechanisms triggered by different genomic alterations define distinct nosological categories

De novo SMARCA2 variants clustered outside the helicase domain cause a new recognizable syndrome with intellectual disability and blepharophimosis distinct from Nicolaides-Baraitser syndrome

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