UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 36

Sortiert nach

Prevalence of Heart Failure Stages in a Universal Health Care System: The Military Health System Experience

The American journal of medicine, 2023-11, Vol.136 (11), p.1079-1086.e1

2023

Volltextzugriff (PDF)

Computational in silico genetic variant prediction tools in cardiovascular disease

Annals of noninvasive electrocardiology, 2023-09, Vol.28 (5), p.e13079-n/a

2023

Volltextzugriff (PDF)

Eligibility, uptake and response to germline genetic testing in women with DCIS

Frontiers in oncology, 2022-08, Vol.12, p.918757-918757

2022

Volltextzugriff (PDF)

Genetic testing in Non-Hispanic Black women with breast cancer treated within an equal-access healthcare system

Genetics in medicine, 2022-01, Vol.24 (1), p.232-237

2022

Volltextzugriff (PDF)

A Review of the Hereditary Component of Triple Negative Breast Cancer: High- and Moderate-Penetrance Breast Cancer Genes, Low-Penetrance Loci, and the Role of Nontraditional Genetic Elements

Journal of oncology, 2019, Vol.2019, p.4382606-10

2019

Volltextzugriff (PDF)

Influence of germline test results on surgical decision making in women with invasive breast cancer

Cancer genetics, 2022-08, Vol.266-267, p.81-85

2022

Volltextzugriff (PDF)

Applying Pharmacogenomic Guidelines to Combat Medical Care

Military medicine, 2022-01, Vol.187 (Supplement_1), p.18-24

2022

Volltextzugriff (PDF)

Heritability of Low ER Staining/HER2-Breast Tumors: Are We Missing an Opportunity for Germline Testing?

Genes, 2020-12, Vol.11 (12), p.1469

2020

Volltextzugriff (PDF)

Should Genetic Testing for Cancer Predisposition Be Standard-of-Care for Women with Invasive Breast Cancer? The Murtha Cancer Center Experience

Cancers, 2020-01, Vol.12 (1), p.234

2020

Volltextzugriff (PDF)

Using a pilot-centric, qualitative drug risk assessment model to identify opportunities for implementing pharmacogenetics

Future journal of pharmaceutical sciences, 2022-09, Vol.8 (1), p.1-8, Article 37

2022

Volltextzugriff (PDF)

O09: Phenome-wide studies of hereditary transthyretin amyloidosis in the All of Us research program

Genetics in Medicine Open, 2024, Vol.2, p.101013, Article 101013

2024

Volltextzugriff (PDF)

Management of Incidental Findings in the Era of Next-generation Sequencing

Current genomics, 2015-06, Vol.16 (3), p.159-174

2015

Volltextzugriff (PDF)

Abstract P3-14-04: Genetic testing in non-Hispanic Black women with breast cancer treated within an equal-access healthcare system

Cancer research (Chicago, Ill.), 2022-02, Vol.82 (4_Supplement), p.P3-P3-14-04

2022

Volltextzugriff (PDF)

Abstract 4624: Should genetic testing for cancer predisposition be standard-of-care for women with invasive breast cancer: The Murtha Cancer Center experience

Cancer research (Chicago, Ill.), 2020-08, Vol.80 (16_Supplement), p.4624-4624

2020

Volltextzugriff (PDF)

Impact of germline mutations on surgical decision-making in women with DCIS

Journal of clinical oncology, 2022-06, Vol.40 (16_suppl), p.10576-10576

2022

Volltextzugriff (PDF)

Abstract P197: Heart Failure In A Universally Insured Working Age Population: The Military Community Experience

Circulation (New York, N.Y.), 2022-03, Vol.145 (Suppl_1)

2022

Volltextzugriff (PDF)

A health systems assessment of genetic counseling in cardiovascular care in a large health system: Adherence to genetics recommendations in the Military Health System

Journal of genetic counseling, 2024-08, Vol.33 (4), p.888-896

2024

Volltextzugriff (PDF)

Ebstein's Anomaly and Left Ventricular Non-Compaction in Association With A Novel MYH7 Gene Mutation

Pediatrics (Evanston), 2021-03, Vol.147 (3_MeetingAbstract), p.1037-1039

2021

Volltextzugriff (PDF)

Genotype first: Clinical genomics research through a reverse phenotyping approach

American journal of human genetics, 2023-01, Vol.110 (1), p.3-12

2023

Volltextzugriff (PDF)

18. Investigation of pathogenic and truncated variants of RUNX1 and DDX41 in All of Us

Cancer genetics, 2023-11, Vol.278-279, p.6

2023

Volltextzugriff (PDF)

Diagnosis of Bardet-Biedl Syndrome in Consecutive Pregnancies Affected with Echogenic Kidneys and Polydactyly in a Consanguineous Couple

Case reports in genetics, 2013-01, Vol.2013, p.159143-3

2013

Volltextzugriff (PDF)

Practical recommendations for the transition to adulthood for the adolescent with a genetic diagnosis. Special emphasis on inborn errors of metabolism

Translational science of rare diseases, 2020-04, Vol.4 (3-4), p.159-168

2020

Volltextzugriff (PDF)

Uncommon Protein-Coding Variants Associated With Suicide Attempt in a Diverse Sample of U.S. Army Soldiers

Biological psychiatry (1969), 2024-07, Vol.96 (1), p.15-25

2024

Volltextzugriff (PDF)

TU50. RARE VARIANT ANALYSIS OF SUICIDE ATTEMPT IN THE ARMY STARRS COHORT

European neuropsychopharmacology, 2021-10, Vol.51, p.e122-e122

2021

Volltextzugriff (PDF)

PD65-12 GERMLINE MUTATION LANDSCAPE OF DNA REPAIR GENES IN AFRICAN AMERICAN PROSTATE CANCER PATIENTS HIGHLIGHT POTENTIALLY TARGETABLE RAD GENES

The Journal of urology, 2021-09, Vol.206 (Supplement 3)

2021

Volltextzugriff (PDF)

1 – 25 von 36

Suche als RSS-Feed

Aktive Filter

ThemaHumans

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

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

Publikationsform

Artikel
(33)
Berichte
(3)

Sprache

Englisch
(36)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Prevalence of Heart Failure Stages in a Universal Health Care System: The Military Health System Experience

Computational in silico genetic variant prediction tools in cardiovascular disease

Eligibility, uptake and response to germline genetic testing in women with DCIS

Genetic testing in Non-Hispanic Black women with breast cancer treated within an equal-access healthcare system

A Review of the Hereditary Component of Triple Negative Breast Cancer: High- and Moderate-Penetrance Breast Cancer Genes, Low-Penetrance Loci, and the Role of Nontraditional Genetic Elements

Influence of germline test results on surgical decision making in women with invasive breast cancer

Applying Pharmacogenomic Guidelines to Combat Medical Care

Heritability of Low ER Staining/HER2-Breast Tumors: Are We Missing an Opportunity for Germline Testing?

Should Genetic Testing for Cancer Predisposition Be Standard-of-Care for Women with Invasive Breast Cancer? The Murtha Cancer Center Experience

Using a pilot-centric, qualitative drug risk assessment model to identify opportunities for implementing pharmacogenetics

O09: Phenome-wide studies of hereditary transthyretin amyloidosis in the All of Us research program

Management of Incidental Findings in the Era of Next-generation Sequencing

Abstract P3-14-04: Genetic testing in non-Hispanic Black women with breast cancer treated within an equal-access healthcare system

Abstract 4624: Should genetic testing for cancer predisposition be standard-of-care for women with invasive breast cancer: The Murtha Cancer Center experience

Impact of germline mutations on surgical decision-making in women with DCIS

Abstract P197: Heart Failure In A Universally Insured Working Age Population: The Military Community Experience

A health systems assessment of genetic counseling in cardiovascular care in a large health system: Adherence to genetics recommendations in the Military Health System

Ebstein's Anomaly and Left Ventricular Non-Compaction in Association With A Novel MYH7 Gene Mutation

Genotype first: Clinical genomics research through a reverse phenotyping approach

18. Investigation of pathogenic and truncated variants of RUNX1 and DDX41 in All of Us

Diagnosis of Bardet-Biedl Syndrome in Consecutive Pregnancies Affected with Echogenic Kidneys and Polydactyly in a Consanguineous Couple

Practical recommendations for the transition to adulthood for the adolescent with a genetic diagnosis. Special emphasis on inborn errors of metabolism

Uncommon Protein-Coding Variants Associated With Suicide Attempt in a Diverse Sample of U.S. Army Soldiers

TU50. RARE VARIANT ANALYSIS OF SUICIDE ATTEMPT IN THE ARMY STARRS COHORT

PD65-12 GERMLINE MUTATION LANDSCAPE OF DNA REPAIR GENES IN AFRICAN AMERICAN PROSTATE CANCER PATIENTS HIGHLIGHT POTENTIALLY TARGETABLE RAD GENES

Aktive Filter

Suchergebnisse filtern