UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 37

Sortiert nach

Using Image Recognition to Process Unbalanced Data in Genetic Diseases From Biobanks

Frontiers in genetics, 2022-02, Vol.13, p.822117-822117

2022

Volltextzugriff (PDF)

Genetic risk score constructed from common genetic variants is associated with cardiovascular disease risk in type 2 diabetes mellitus

The journal of gene medicine, 2021-02, Vol.23 (2), p.e3305-n/a

2021

Volltextzugriff (PDF)

GBA1 as a risk gene for osteoporosis in the specific populations and its role in the development of Gaucher disease

Orphanet journal of rare diseases, 2024-04, Vol.19 (1), p.144-144, Article 144

2024

Volltextzugriff (PDF)

Genetic Architecture Associated With Familial Short Stature

The journal of clinical endocrinology and metabolism, 2020-06, Vol.105 (6), p.1801-1813

2020

Volltextzugriff (PDF)

A genome-wide association study on chronic HBV infection and its clinical progression in male Han-Taiwanese

PloS one, 2014-06, Vol.9 (6), p.e99724-e99724

2014

Volltextzugriff (PDF)

Constructing endophenotypes of complex diseases using non-negative matrix factorization and adjusted rand index

PloS one, 2012-07, Vol.7 (7), p.e40996-e40996

2012

Volltextzugriff (PDF)

A non-threshold region-specific method for detecting rare variants in complex diseases

PloS one, 2017-11, Vol.12 (11), p.e0188566-e0188566

2017

Volltextzugriff (PDF)

Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes

Communications biology, 2022-11, Vol.5 (1), p.1175-1175, Article 1175

2022

Volltextzugriff (PDF)

Incidence and Nature of Short-Term Adverse Events following COVID-19 Second Boosters: Insights from Taiwan's Universal Vaccination Strategy

Vaccines (Basel), 2024-01, Vol.12 (2), p.149

2024

Volltextzugriff (PDF)

Maximal Segmental Score Method for Localizing Recessive Disease Variants Based on Sequence Data

Frontiers in genetics, 2020-06, Vol.11, p.555-555

2020

Volltextzugriff (PDF)

Association of human height-related genetic variants with familial short stature in Han Chinese in Taiwan

Scientific reports, 2017-07, Vol.7 (1), p.6372-7, Article 6372

2017

Volltextzugriff (PDF)

Biomedical literature mining: graph kernel-based learning for gene–gene interaction extraction

European journal of medical research, 2024-08, Vol.29 (1), p.404-11, Article 404

2024

Volltextzugriff (PDF)

Effects of sex and generation on hepatitis B viral load in families with hepatocellular carcinoma

World journal of gastroenterology : WJG, 2017-02, Vol.23 (5), p.876-884

2017

Volltextzugriff (PDF)

Effect of genetic variants in cell adhesion pathways on the biochemical recurrence in prostate cancer patients with radical prostatectomy

Cancer medicine (Malden, MA), 2019-06, Vol.8 (6), p.2777-2783

2019

Volltextzugriff (PDF)

Polygenic Risk Score Improves Cataract Prediction in East Asian Population

Biomedicines, 2022-08, Vol.10 (8), p.1920

2022

Volltextzugriff (PDF)

Genome-Wide Polygenic Risk Score for Predicting High Risk Glaucoma Individuals of Han Chinese Ancestry

Journal of personalized medicine, 2021-11, Vol.11 (11), p.1169

2021

Volltextzugriff (PDF)

Lack of association of genetic variants for diabetic retinopathy in Taiwanese patients with diabetic nephropathy

BMJ open diabetes research & care, 2020-01, Vol.8 (1), p.e000727

2020

Volltextzugriff (PDF)

A novel method for identification and quantification of consistently differentially methylated regions

PloS one, 2014-05, Vol.9 (5), p.e97513-e97513

2014

Volltextzugriff (PDF)

Hepatitis B virus persistent infection-related single nucleotide polymorphisms in HLA regions are associated with viral load in hepatoma families

World journal of gastroenterology : WJG, 2021-10, Vol.27 (37), p.6262-6276

2021

Volltextzugriff (PDF)

TMEM132D and VIPR2 Polymorphisms as Genetic Risk Loci for Retinal Detachment: A Genome-Wide Association Study and Polygenic Risk Score Analysis

Investigative ophthalmology & visual science, 2023-09, Vol.64 (12), p.17-17

2023

Volltextzugriff (PDF)

Comparative analysis of genetic risk scores for predicting biochemical recurrence in prostate cancer patients after radical prostatectomy

BMC urology, 2024-07, Vol.24 (1), p.1-12, Article 136

2024

Volltextzugriff (PDF)

Genome-Wide and Candidate Gene Association Analyses Identify a 14-SNP Combination for Hypertension in Patients With Type 2 Diabetes

American journal of hypertension, 2021-06, Vol.34 (6), p.651-661

2021

Volltextzugriff (PDF)

Genetic factors of idiopathic central precocious puberty and their polygenic risk in early puberty

European journal of endocrinology, 2021-10, Vol.185 (4), p.441

2021

Volltextzugriff (PDF)

Using Maximal Segmental Score in Genome-Wide Association Studies

Genetic epidemiology, 2012-09, Vol.36 (6), p.594-601

2012

Volltextzugriff (PDF)

Body constitutions of traditional Chinese medicine caused a significant effect on irritable bowel syndrome

Journal of the Chinese Medical Association, 2024-05, Vol.87 (5), p.558-566

2024

Volltextzugriff (PDF)

1 – 25 von 37

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(33)
Mit Volltextzugriff
(35)

Publikationsform

Artikel
(37)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

Using Image Recognition to Process Unbalanced Data in Genetic Diseases From Biobanks

Genetic risk score constructed from common genetic variants is associated with cardiovascular disease risk in type 2 diabetes mellitus

GBA1 as a risk gene for osteoporosis in the specific populations and its role in the development of Gaucher disease

Genetic Architecture Associated With Familial Short Stature

A genome-wide association study on chronic HBV infection and its clinical progression in male Han-Taiwanese

Constructing endophenotypes of complex diseases using non-negative matrix factorization and adjusted rand index

A non-threshold region-specific method for detecting rare variants in complex diseases

Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes

Incidence and Nature of Short-Term Adverse Events following COVID-19 Second Boosters: Insights from Taiwan's Universal Vaccination Strategy

Maximal Segmental Score Method for Localizing Recessive Disease Variants Based on Sequence Data

Association of human height-related genetic variants with familial short stature in Han Chinese in Taiwan

Biomedical literature mining: graph kernel-based learning for gene–gene interaction extraction

Effects of sex and generation on hepatitis B viral load in families with hepatocellular carcinoma

Effect of genetic variants in cell adhesion pathways on the biochemical recurrence in prostate cancer patients with radical prostatectomy

Polygenic Risk Score Improves Cataract Prediction in East Asian Population

Genome-Wide Polygenic Risk Score for Predicting High Risk Glaucoma Individuals of Han Chinese Ancestry

Lack of association of genetic variants for diabetic retinopathy in Taiwanese patients with diabetic nephropathy

A novel method for identification and quantification of consistently differentially methylated regions

Hepatitis B virus persistent infection-related single nucleotide polymorphisms in HLA regions are associated with viral load in hepatoma families

TMEM132D and VIPR2 Polymorphisms as Genetic Risk Loci for Retinal Detachment: A Genome-Wide Association Study and Polygenic Risk Score Analysis

Comparative analysis of genetic risk scores for predicting biochemical recurrence in prostate cancer patients after radical prostatectomy

Genome-Wide and Candidate Gene Association Analyses Identify a 14-SNP Combination for Hypertension in Patients With Type 2 Diabetes

Genetic factors of idiopathic central precocious puberty and their polygenic risk in early puberty

Using Maximal Segmental Score in Genome-Wide Association Studies

Body constitutions of traditional Chinese medicine caused a significant effect on irritable bowel syndrome

Suchergebnisse filtern