UB Paderborn / Katalog / Suche / in CDI

Risk factors and disease profile of post-vaccination SARS-CoV-2 infection in UK users of the COVID Symptom Study app: a prospective, community-based, nested, case-control study

The Lancet infectious diseases, 2022-01, Vol.22 (1), p.43-55

2022

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Illness duration and symptom profile in symptomatic UK school-aged children tested for SARS-CoV-2

The lancet child & adolescent health, 2021-10, Vol.5 (10), p.708-718

2021

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The Genetic Architecture of High Bone Mass

Frontiers in endocrinology (Lausanne), 2020-10, Vol.11, p.595653

2020

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The Musculoskeletal Knowledge Portal: Making Omics Data Useful to the Broader Scientific Community

Journal of bone and mineral research, 2020-09, Vol.35 (9), p.1626-1633

2020

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Genome-wide association study of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes

Bone (New York, N.Y.), 2018-09, Vol.114, p.62-71

2018

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Massively Parallel Sequencing for Rare Genetic Disorders: Potential and Pitfalls

Frontiers in endocrinology (Lausanne), 2021-02, Vol.11, p.628946-628946

2021

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LRP5 Regulates Human Body Fat Distribution by Modulating Adipose Progenitor Biology in a Dose- and Depot-Specific Fashion

Cell metabolism, 2015-02, Vol.21 (2), p.262-273

2015

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National surveillance data analysis of COVID-19 vaccine uptake in England by women of reproductive age

Nature communications, 2023-02, Vol.14 (1), p.956-956, Article 956

2023

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Multicentric Carpotarsal Osteolysis Is Caused by Mutations Clustering in the Amino-Terminal Transcriptional Activation Domain of MAFB

American journal of human genetics, 2012-03, Vol.90 (3), p.494-501

2012

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A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data

Circulation. Genomic and precision medicine, 2018-03, Vol.11 (3), p.e001978-e001978

2018

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Short-Rib Polydactyly and Jeune Syndromes Are Caused by Mutations in WDR60

American journal of human genetics, 2013-09, Vol.93 (3), p.515-523

2013

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Marked increase in proton pump inhibitors use in Australia

Pharmacoepidemiology and drug safety, 2010-10, Vol.19 (10), p.1019-1024

2010

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Author Correction: National surveillance data analysis of COVID-19 vaccine uptake in England by women of reproductive age

Nature communications, 2023-09, Vol.14 (1), p.5655-5655, Article 5655

2023

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The ATM Ser49Cys Variant Effects ATM Function as a Regulator of Oncogene-Induced Senescence

International journal of molecular sciences, 2024-02, Vol.25 (3), p.1664

2024

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Whole-exome re-sequencing in a family quartet identifies POP1 mutations as the cause of a novel skeletal dysplasia

PLoS genetics, 2011-03, Vol.7 (3), p.e1002027-e1002027

2011

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Loss of wild-type ATRX expression in somatic cell hybrids segregates with activation of Alternative Lengthening of Telomeres

PloS one, 2012-11, Vol.7 (11), p.e50062-e50062

2012

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A novel serogenetic approach determines the community prevalence of celiac disease and informs improved diagnostic pathways

BMC medicine, 2013-08, Vol.11 (1), p.188-188, Article 188

2013

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Metabolomic and gut microbiome profiles across the spectrum of community-based COVID and non-COVID disease

Scientific reports, 2023-06, Vol.13 (1), p.10407-10407, Article 10407

2023

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Is Secretory Activation Delayed in Women with Type Two Diabetes? A Pilot Study

Nutrients, 2022-03, Vol.14 (7), p.1323

2022

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Pheo-Type: A Diagnostic Gene-expression Assay for the Classification of Pheochromocytoma and Paraganglioma

The journal of clinical endocrinology and metabolism, 2016-03, Vol.101 (3), p.1034-1043

2016

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Mutations in Known Monogenic High Bone Mass Loci Only Explain a Small Proportion of High Bone Mass Cases

Journal of bone and mineral research, 2016-03, Vol.31 (3), p.640-649

2016

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Profiling post-COVID-19 condition across different variants of SARS-CoV-2: a prospective longitudinal study in unvaccinated wild-type, unvaccinated alpha-variant, and vaccinated delta-variant populations

The Lancet. Digital health, 2023-07, Vol.5 (7), p.e421-e434

2023

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Atypical Femoral Fracture: A Fascinating Story in Evolution

Journal of bone and mineral research, 2018-12, Vol.33 (12), p.2089-2090

Duncan, Emma L

2018

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Illness Characteristics of COVID-19 in Children Infected with the SARS-CoV-2 Delta Variant

Children (Basel), 2022-05, Vol.9 (5), p.652

2022

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Attributes and predictors of long COVID

Nature Medicine, 2021-04, Vol.27 (4), p.626-631

2021

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Risk factors and disease profile of post-vaccination SARS-CoV-2 infection in UK users of the COVID Symptom Study app: a prospective, community-based, nested, case-control study

Illness duration and symptom profile in symptomatic UK school-aged children tested for SARS-CoV-2

The Genetic Architecture of High Bone Mass

The Musculoskeletal Knowledge Portal: Making Omics Data Useful to the Broader Scientific Community

Genome-wide association study of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes

Massively Parallel Sequencing for Rare Genetic Disorders: Potential and Pitfalls

LRP5 Regulates Human Body Fat Distribution by Modulating Adipose Progenitor Biology in a Dose- and Depot-Specific Fashion

National surveillance data analysis of COVID-19 vaccine uptake in England by women of reproductive age

Multicentric Carpotarsal Osteolysis Is Caused by Mutations Clustering in the Amino-Terminal Transcriptional Activation Domain of MAFB

A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data

Short-Rib Polydactyly and Jeune Syndromes Are Caused by Mutations in WDR60

Marked increase in proton pump inhibitors use in Australia

Author Correction: National surveillance data analysis of COVID-19 vaccine uptake in England by women of reproductive age

The ATM Ser49Cys Variant Effects ATM Function as a Regulator of Oncogene-Induced Senescence

Whole-exome re-sequencing in a family quartet identifies POP1 mutations as the cause of a novel skeletal dysplasia

Loss of wild-type ATRX expression in somatic cell hybrids segregates with activation of Alternative Lengthening of Telomeres

A novel serogenetic approach determines the community prevalence of celiac disease and informs improved diagnostic pathways

Metabolomic and gut microbiome profiles across the spectrum of community-based COVID and non-COVID disease

Is Secretory Activation Delayed in Women with Type Two Diabetes? A Pilot Study

Pheo-Type: A Diagnostic Gene-expression Assay for the Classification of Pheochromocytoma and Paraganglioma

Mutations in Known Monogenic High Bone Mass Loci Only Explain a Small Proportion of High Bone Mass Cases

Profiling post-COVID-19 condition across different variants of SARS-CoV-2: a prospective longitudinal study in unvaccinated wild-type, unvaccinated alpha-variant, and vaccinated delta-variant populations

Atypical Femoral Fracture: A Fascinating Story in Evolution

Illness Characteristics of COVID-19 in Children Infected with the SARS-CoV-2 Delta Variant

Attributes and predictors of long COVID

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