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Inference runtime of a neural network to detect atrial fibrillation on customized RISC-V-based hardware

Current directions in biomedical engineering, 2022-09, Vol.8 (2), p.703-706

2022

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A New Configurable Wireless Sensor System for Biomedical Applications with ISO 18000-3 Interface in 0.35 µm CMOS

Sensors (Basel, Switzerland), 2019-09, Vol.19 (19), p.4110

2019

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Design of an Artificial Neural Network Circuit for detecting Atrial Fibrillation in ECG Signals

2021 IEEE Sensors, 2021, p.1-4

2021

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Design of Hardware Accelerators for Optimized and Quantized Neural Networks to Detect Atrial Fibrillation in Patch ECG Device with RISC-V

Sensors (Basel, Switzerland), 2023-03, Vol.23 (5), p.2703

2023

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The ARTEMIS project: Mixed-Signal IC for Edge-AI-based Classification of ECG Signals

Current directions in biomedical engineering, 2023-09, Vol.9 (1), p.327-330

2023

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Detection of atrial fibrillation with an optimized neural network on a RISC-V-based microcontroller for efficient integration into ECG patches

2022 IEEE International Symposium on Medical Measurements and Applications (MeMeA), 2022, p.1-6

2022

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A low-power wireless nano-potentiostat for biomedical applications with ISO 18000-3 interface in 0.35 μm CMOS

2018 12th International Conference on Sensing Technology (ICST), 2018, p.382-387

2018

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Schaltungssimulation mit FE-Modellen für mikroelektromechanische Systeme: Circuit Simulation with FInIte Element Models for MIcroelectromechanical Systems

Information technology (Munich, Germany), 1999-04, Vol.41 (4), p.33-38

1999

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Schaltungssimulation mit FE-Modellen für mikroelektromechanische Systeme

Information technology (Munich, Germany), 1999-04, Vol.41 (4), p.33-38

1999

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Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I

Nature genetics, 2000-01, Vol.24 (1), p.71-74

2000

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A new face of Borjeson–Forssman–Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype

Journal of medical genetics, 2013-12, Vol.50 (12), p.838-847

2013

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Oto-facial syndrome and esophageal atresia, intellectual disability and zygomatic anomalies - expanding the phenotypes associated with EFTUD2 mutations

Orphanet journal of rare diseases, 2013-07, Vol.8 (1), p.110-110, Article 110

2013

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The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype

Journal of molecular medicine (Berlin, Germany), 2021-12, Vol.99 (12), p.1755-1768

2021

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Mutations in the BAF-Complex Subunit DPF2 Are Associated with Coffin-Siris Syndrome

American journal of human genetics, 2018-03, Vol.102 (3), p.468-479

2018

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Delineation of the adult phenotype of Coffin–Siris syndrome in 35 individuals

Human genetics, 2024-01, Vol.143 (1), p.71-84

2024

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Correction to: The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype

Journal of molecular medicine (Berlin, Germany), 2021-12, Vol.99 (12), p.1769-1770

2021

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Bainbridge-Ropers syndrome caused by loss-of-function variants in ASXL3: a recognizable condition

European journal of human genetics : EJHG, 2017-02, Vol.25 (2), p.183-191

2017

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German Environmental Survey for Children (GerES IV) – First results

International journal of hygiene and environmental health, 2007-10, Vol.210 (5), p.535-540

2007

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Mit Sicherheit gesund bauen: Fakten, Argumente und Strategien für das gesunde Bauen, Modernisieren und Wohnen

Second Edition., 2013

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De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum

Human genetics, 2015-01, Vol.134 (1), p.97-109

2015

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Genetic variants in components of the NALCN–UNC80–UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies)

Human genetics, 2018-09, Vol.137 (9), p.753-768

2018

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Inference runtime of a neural network to detect atrial fibrillation on customized RISC-V-based hardware

A New Configurable Wireless Sensor System for Biomedical Applications with ISO 18000-3 Interface in 0.35 µm CMOS

Design of an Artificial Neural Network Circuit for detecting Atrial Fibrillation in ECG Signals

Design of Hardware Accelerators for Optimized and Quantized Neural Networks to Detect Atrial Fibrillation in Patch ECG Device with RISC-V

The ARTEMIS project: Mixed-Signal IC for Edge-AI-based Classification of ECG Signals

Detection of atrial fibrillation with an optimized neural network on a RISC-V-based microcontroller for efficient integration into ECG patches

A low-power wireless nano-potentiostat for biomedical applications with ISO 18000-3 interface in 0.35 μm CMOS

Schaltungssimulation mit FE-Modellen für mikroelektromechanische Systeme: Circuit Simulation with FInIte Element Models for MIcroelectromechanical Systems

Schaltungssimulation mit FE-Modellen für mikroelektromechanische Systeme

Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I

A new face of Borjeson–Forssman–Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype

Oto-facial syndrome and esophageal atresia, intellectual disability and zygomatic anomalies - expanding the phenotypes associated with EFTUD2 mutations

The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype

Mutations in the BAF-Complex Subunit DPF2 Are Associated with Coffin-Siris Syndrome

Delineation of the adult phenotype of Coffin–Siris syndrome in 35 individuals

Correction to: The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype

Bainbridge-Ropers syndrome caused by loss-of-function variants in ASXL3: a recognizable condition

German Environmental Survey for Children (GerES IV) – First results

Mit Sicherheit gesund bauen: Fakten, Argumente und Strategien für das gesunde Bauen, Modernisieren und Wohnen

De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum

Genetic variants in components of the NALCN–UNC80–UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies)

Mit Sicherheit gesund bauen: Fakten, Argumente, Strategien fur das gesunde Bauen und Wohnen

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