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Use of genetic data to guide therapy in arterial disease

Journal of thrombosis and haemostasis, 2015-06, Vol.13 (S1), p.S281-S289

2015

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Placing children and adolescents at the centre of the Sustainable Development Goals will deliver for current and future generations

Global health action, 2019-01, Vol.12 (1), p.1670015-1670015

2019

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Tight Junction in the Intestinal Epithelium: Its Association with Diseases and Regulation by Phytochemicals

Journal of Immunology Research, 2018-01, Vol.2018, p.2645465-11

2018

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The importance of variant reinterpretation in inherited cardiovascular diseases: Establishing the optimal timeframe

PloS one, 2024-05, Vol.19 (5), p.e0297914-e0297914

2024

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De novo copy number variations in candidate genomic regions in patients of severe autism spectrum disorder in Vietnam

PloS one, 2024-03, Vol.19 (3), p.e0290936-e0290936

2024

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4-aminopyridine improves evoked potentials and ambulation in the taiep rat: A model of hypomyelination with atrophy of basal ganglia and cerebellum

PloS one, 2024-03, Vol.19 (3), p.e0298208-e0298208

2024

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Comparative exploration of mammalian deafness gene homologues in the Drosophila auditory organ shows genetic correlation between insect and vertebrate hearing

PloS one, 2024-02, Vol.19 (2), p.e0297846-e0297846

2024

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Exome sequencing in 16 patients with pituitary stalk interruption syndrome: A monocentric study

PloS one, 2023-12, Vol.18 (12), p.e0292664-e0292664

2023

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The TTN p. Tyr4418Ter mutation causes cardiomyopathy in human and mice

PloS one, 2024-02, Vol.19 (2), p.e0296802-e0296802

2024

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Type 2 diabetes linked FTO gene variant rs8050136 is significantly associated with gravidity in gestational diabetes in a sample of Bangladeshi women: Meta-analysis and case-control study

PloS one, 2023-11, Vol.18 (11), p.e0288318-e0288318

2023

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Whole exome data prioritization unveils the hidden weight of Mendelian causes of male infertility. A report from the first Italian cohort

PloS one, 2023-08, Vol.18 (8), p.e0288336-e0288336

2023

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A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans-A cohort study

PloS one, 2023-12, Vol.18 (12), p.e0294969-e0294969

2023

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A genome-wide and candidate gene association study of preterm birth in Korean pregnant women

PloS one, 2023-11, Vol.18 (11), p.e0294948-e0294948

2023

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Identification of the genetic basis of pediatric neurogenetic disorders at a tertiary referral hospital in Indonesia: Contribution of whole exome sequencing

PloS one, 2023-10, Vol.18 (10), p.e0293113-e0293113

2023

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Study of the parent-of-origin effect in monogenic diseases with variable age of onset. Application on ATTRv

PloS one, 2023-08, Vol.18 (8), p.e0288958-e0288958

2023

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Gene mutations as a non-invasive measure of adult cochlear implant performance: Variable outcomes in patients with select TMPRSS3 mutations

PloS one, 2023-09, Vol.18 (9), p.e0291600-e0291600

2023

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Identification of candidate genes for developmental colour agnosia in a single unique family

PloS one, 2023-09, Vol.18 (9), p.e0290013-e0290013

2023

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Programmed Death Ligand 2 in Cancer-Induced Immune Suppression

Clinical & developmental immunology, 2012-01, Vol.2012, p.656340-8

2012

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The Interplay between MicroRNAs and Cellular Components of Tumour Microenvironment (TME) on Non-Small-Cell Lung Cancer (NSCLC) Progression

Journal of Immunology Research, 2019-01, Vol.2019, p.3046379-12

2019

Volltextzugriff (PDF)

Immunoinformatics Approach for Epitope-Based Peptide Vaccine Design and Active Site Prediction against Polyprotein of Emerging Oropouche Virus

Journal of Immunology Research, 2018-01, Vol.2018, p.6718083-22

2018

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Impact of body mass index versus physical activity and calorie intake on assisted reproduction outcomes

European journal of obstetrics & gynecology and reproductive biology, 2012-07, Vol.163 (1), p.52-56

2012

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Clinical Features and Genetic Background of the Periodic Fever Syndrome with Aphthous Stomatitis, Pharyngitis, and Adenitis: A Single Center Longitudinal Study of 81 Patients

Mediators of Inflammation, 2015-01, Vol.2015 (1), p.293417-293417

2015

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Functional Stability of Plasminogen Activator Inhibitor-1

TheScientificWorld, 2014, Vol.2014, p.858293-11

2014

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The Dark Side of Organizational Behavior: Examining Undesirable Aspects of Organizational Life

1, 2023

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Dark Sides of Organizational Life: Hostility, Rivalry, Gossip, Envy and other Difficult Behaviors

1, 2023

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Use of genetic data to guide therapy in arterial disease

Placing children and adolescents at the centre of the Sustainable Development Goals will deliver for current and future generations

Tight Junction in the Intestinal Epithelium: Its Association with Diseases and Regulation by Phytochemicals

The importance of variant reinterpretation in inherited cardiovascular diseases: Establishing the optimal timeframe

De novo copy number variations in candidate genomic regions in patients of severe autism spectrum disorder in Vietnam

4-aminopyridine improves evoked potentials and ambulation in the taiep rat: A model of hypomyelination with atrophy of basal ganglia and cerebellum

Comparative exploration of mammalian deafness gene homologues in the Drosophila auditory organ shows genetic correlation between insect and vertebrate hearing

Exome sequencing in 16 patients with pituitary stalk interruption syndrome: A monocentric study

The TTN p. Tyr4418Ter mutation causes cardiomyopathy in human and mice

Type 2 diabetes linked FTO gene variant rs8050136 is significantly associated with gravidity in gestational diabetes in a sample of Bangladeshi women: Meta-analysis and case-control study

Whole exome data prioritization unveils the hidden weight of Mendelian causes of male infertility. A report from the first Italian cohort

A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans-A cohort study

A genome-wide and candidate gene association study of preterm birth in Korean pregnant women

Identification of the genetic basis of pediatric neurogenetic disorders at a tertiary referral hospital in Indonesia: Contribution of whole exome sequencing

Study of the parent-of-origin effect in monogenic diseases with variable age of onset. Application on ATTRv

Gene mutations as a non-invasive measure of adult cochlear implant performance: Variable outcomes in patients with select TMPRSS3 mutations

Identification of candidate genes for developmental colour agnosia in a single unique family

Programmed Death Ligand 2 in Cancer-Induced Immune Suppression

The Interplay between MicroRNAs and Cellular Components of Tumour Microenvironment (TME) on Non-Small-Cell Lung Cancer (NSCLC) Progression

Immunoinformatics Approach for Epitope-Based Peptide Vaccine Design and Active Site Prediction against Polyprotein of Emerging Oropouche Virus

Impact of body mass index versus physical activity and calorie intake on assisted reproduction outcomes

Clinical Features and Genetic Background of the Periodic Fever Syndrome with Aphthous Stomatitis, Pharyngitis, and Adenitis: A Single Center Longitudinal Study of 81 Patients

Functional Stability of Plasminogen Activator Inhibitor-1

The Dark Side of Organizational Behavior: Examining Undesirable Aspects of Organizational Life

Dark Sides of Organizational Life: Hostility, Rivalry, Gossip, Envy and other Difficult Behaviors

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