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Probing the limits of gate-based charge sensing

Nature communications, 2015-01, Vol.6 (1), p.6084-6084, Article 6084

2015

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Nutrition management for head and neck cancer patients improves clinical outcome and survival

Nutrition research (New York, N.Y.), 2017-12, Vol.48, p.1-8

2017

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Nasopharynxkarzinom – ein aktueller Überblick über eine spezielle Tumorentität

Best practice onkologie, 2024-03, Vol.19 (3), p.74-83

2024

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Dimensionality effects on the luminescence properties of hBN

Nanoscale, 2016-04, Vol.8 (13), p.6986-6993

2016

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Dispersively Detected Pauli Spin-Blockade in a Silicon Nanowire Field-Effect Transistor

Nano letters, 2015-07, Vol.15 (7), p.4622-4627

2015

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Mutations in POGLUT1, Encoding Protein O-Glucosyltransferase 1, Cause Autosomal-Dominant Dowling-Degos Disease

American journal of human genetics, 2014-01, Vol.94 (1), p.135-143

2014

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Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis

American journal of human genetics, 2016-08, Vol.99 (2), p.337-351

2016

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Gate-Sensing Coherent Charge Oscillations in a Silicon Field-Effect Transistor

Nano letters, 2016-03, Vol.16 (3), p.1614-1619

2016

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The brain in myotonic dystrophy 1 and 2: evidence for a predominant white matter disease

Brain (London, England : 1878), 2011-12, Vol.134 (12), p.3527-3543

2011

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Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex

American journal of human genetics, 2018-11, Vol.103 (5), p.777-785

2018

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Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness

PloS one, 2021-09, Vol.16 (9), p.e0256846-e0256846

2021

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A path through the reticulate pigmentation disorder jungle

British journal of dermatology (1951), 2017-10, Vol.177 (4), p.893-894

Betz, R.C.

2017

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Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome

American journal of human genetics, 2020-07, Vol.107 (1), p.34-45

2020

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Whole-exome sequencing in eccrine porocarcinoma indicates promising therapeutic strategies

Cancer gene therapy, 2022-06, Vol.29 (6), p.697-708

2022

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Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia

American journal of human genetics, 2012-11, Vol.91 (5), p.906-911

2012

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Loss-of-Function Mutations in the Keratin 5 Gene Lead to Dowling-Degos Disease

American journal of human genetics, 2006-03, Vol.78 (3), p.510-519

2006

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Lysophosphatidic acid receptor LPAR6 supports the tumorigenicity of hepatocellular carcinoma

Cancer research (Chicago, Ill.), 2015-02, Vol.75 (3), p.532-543

2015

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Tracking the brain in myotonic dystrophies: A 5-year longitudinal follow-up study

PloS one, 2019-03, Vol.14 (3), p.e0213381-e0213381

2019

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G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth

Nature genetics, 2008-03, Vol.40 (3), p.329-334

2008

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Clinical significance of copy number variations in the 11p15.5 imprinting control regions: new cases and review of the literature

Journal of Medical Genetics, 2012-09, Vol.49 (9), p.547-553

2012

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New aspects in thyroid cancer treatment : Highlights of the 2019 ASCO Annual Meeting

HNO, 2019-12, Vol.67 (12), p.925

2019

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Acousto-ultrasonic sensing using fiber Bragg gratings

Smart materials and structures, 2003-02, Vol.12 (1), p.122-128

2003

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Multicenter evaluation of an interdisciplinary 52-week weight loss program for obesity with regard to body weight, comorbidities and quality of life-a prospective study

International Journal of Obesity, 2012-04, Vol.36 (4), p.614-624

2012

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Genetic lessons learned from pathogenic variants in KRT1

Journal of the European Academy of Dermatology and Venereology, 2022-10, Vol.36 (10), p.1683-1684

Betz, Regina C.

2022

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A woman with hyperpigmented macules and papules

Journal der Deutschen Dermatologischen Gesellschaft, 2021-11, Vol.19 (11), p.1656-1660

2021

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Probing the limits of gate-based charge sensing

Nutrition management for head and neck cancer patients improves clinical outcome and survival

Nasopharynxkarzinom – ein aktueller Überblick über eine spezielle Tumorentität

Dimensionality effects on the luminescence properties of hBN

Dispersively Detected Pauli Spin-Blockade in a Silicon Nanowire Field-Effect Transistor

Mutations in POGLUT1, Encoding Protein O-Glucosyltransferase 1, Cause Autosomal-Dominant Dowling-Degos Disease

Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis

Gate-Sensing Coherent Charge Oscillations in a Silicon Field-Effect Transistor

The brain in myotonic dystrophy 1 and 2: evidence for a predominant white matter disease

Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex

Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness

A path through the reticulate pigmentation disorder jungle

Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome

Whole-exome sequencing in eccrine porocarcinoma indicates promising therapeutic strategies

Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia

Loss-of-Function Mutations in the Keratin 5 Gene Lead to Dowling-Degos Disease

Lysophosphatidic acid receptor LPAR6 supports the tumorigenicity of hepatocellular carcinoma

Tracking the brain in myotonic dystrophies: A 5-year longitudinal follow-up study

G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth

Clinical significance of copy number variations in the 11p15.5 imprinting control regions: new cases and review of the literature

New aspects in thyroid cancer treatment : Highlights of the 2019 ASCO Annual Meeting

Acousto-ultrasonic sensing using fiber Bragg gratings

Multicenter evaluation of an interdisciplinary 52-week weight loss program for obesity with regard to body weight, comorbidities and quality of life-a prospective study

Genetic lessons learned from pathogenic variants in KRT1

A woman with hyperpigmented macules and papules

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