UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Return of individual genomic research results: what do consent forms tell participants?

European journal of human genetics : EJHG, 2016-11, Vol.24 (11), p.1524-1529

2016

Volltextzugriff (PDF)

Researchers' Ethical Concerns About Using Adaptive Deep Brain Stimulation for Enhancement

Frontiers in human neuroscience, 2022-04, Vol.16, p.813922

2022

Volltextzugriff (PDF)

Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study

Frontiers in genetics, 2022-04, Vol.13, p.867371-867371

2022

Volltextzugriff (PDF)

Do privacy and security regulations need a status update? Perspectives from an intergenerational survey

PloS one, 2017-09, Vol.12 (9), p.e0184525-e0184525

2017

Volltextzugriff (PDF)

Ask me later: deciding to have clinical exome trio sequencing for my critically ill child

Genetics in medicine, 2021-10, Vol.23 (10), p.1836-1837

Robinson, Jill Oliver

2021

Volltextzugriff (PDF)

Challenges to Building a Gene Variant Commons to Assess Hereditary Cancer Risk: Results of a Modified Policy Delphi Panel Deliberation

Journal of personalized medicine, 2021-07, Vol.11 (7), p.646

2021

Volltextzugriff (PDF)

Participants’ recall and understanding of genomic research and large-scale data sharing

Journal of empirical research on human research ethics, 2013-10, Vol.8 (4), p.42-52

2013

Volltextzugriff (PDF)

“The truth should not be hidden”: Experiences and recommendations of individuals making NPE discoveries through genetic genealogy databases

Genetics in medicine, 2024-10, Vol.26 (10), p.101210, Article 101210

2024

Volltextzugriff (PDF)

Perceived Benefits, Risks, and Utility of Newborn Genomic Sequencing in the BabySeq Project

Pediatrics (Evanston), 2019-01, Vol.143 (Suppl 1), p.S6-S13

2019

Volltextzugriff (PDF)

Psychosocial Effect of Newborn Genomic Sequencing on Families in the BabySeq Project: A Randomized Clinical Trial

JAMA pediatrics, 2021-11, Vol.175 (11), p.1132

2021

Volltextzugriff (PDF)

Measuring perceived utility of genomic sequencing: Development and validation of the GENEtic Utility (GENE-U) scale for adult screening

Genetics in medicine, 2024-11, Vol.26 (11), p.101240, Article 101240

2024

Volltextzugriff (PDF)

Measuring perceived utility of genomic sequencing: Development and validation of the GENEtic Utility (GENE-U) scale for pediatric diagnostic testing

Genetics in medicine, 2024-08, Vol.26 (8), p.101146, Article 101146

2024

Volltextzugriff (PDF)

Parents’ decision-making regarding whether to receive adult-onset only genetic findings for their children: Findings from the BabySeq Project

Genetics in medicine, 2023-03, Vol.25 (3), p.100002-100002, Article 100002

2023

Volltextzugriff (PDF)

Pediatric data sharing in genomic research: attitudes and preferences of parents

Pediatrics (Evanston), 2014-04, Vol.133 (4), p.690-697

2014

Volltextzugriff (PDF)

Comprehensive red blood cell and platelet antigen prediction from whole genome sequencing: proof of principle

Transfusion (Philadelphia, Pa.), 2016-03, Vol.56 (3), p.743-754

2016

Volltextzugriff (PDF)

The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine

Trials, 2014-03, Vol.15 (1), p.85-85, Article 85

2014

Volltextzugriff (PDF)

Airmen and health-care providers' attitudes toward the use of genomic sequencing in the US Air Force: findings from the MilSeq Project

Genetics in medicine, 2020-12, Vol.22 (12), p.2003-2010

2020

Volltextzugriff (PDF)

Perceived Utility of Genomic Sequencing: Qualitative Analysis and Synthesis of a Conceptual Model to Inform Patient-Centered Instrument Development

The patient : patient-centered outcomes research, 2022-05, Vol.15 (3), p.317-328

2022

Volltextzugriff (PDF)

A systematic approach to the reporting of medically relevant findings from whole genome sequencing

BMC medical genetics, 2014-12, Vol.15 (1), p.134-134, Article 134

2014

Volltextzugriff (PDF)

Airmen and Healthcare Providers’ attitudes toward the use of genomic sequencing in the US Air Force: Findings from the MilSeq Project

Genetics in medicine, 2020-08, Vol.22 (12), p.2003-2010

2020

Volltextzugriff (PDF)

Summarizing polygenic risks for complex diseases in a clinical whole-genome report

Genetics in medicine, 2015-07, Vol.17 (7), p.536-544

2015

Volltextzugriff (PDF)

MEDICAL INFORMATION COMMONS: CONCEPTUAL, LEGAL AND ETHICAL CONSIDERATIONS FOR STAKEHOLDERS

Bioinformatics, Medical Informatics and the Law, 2022

2022

Volltextzugriff (PDF)

Participants and Study Decliners’ Perspectives About the Risks of Participating in a Clinical Trial of Whole Genome Sequencing

Journal of empirical research on human research ethics, 2016-02, Vol.11 (1), p.21-30

2016

Volltextzugriff (PDF)

'Someday it will be the norm': physician perspectives on the utility of genome sequencing for patient care in the MedSeqProject

Personalized medicine, 2015-01, Vol.12 (1), p.23-32

2015

Volltextzugriff (PDF)

'Someday it will be the norm': physician perspectives on the utility of genome sequencing for patient care in the MedSeq Project

Personalized medicine, 2015, Vol.12 (1), p.23-32

2015

Volltextzugriff (PDF)

1 – 25 von 64

Suche als RSS-Feed

Aktive Filter

Nur zeigenMit Volltextzugriff

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(61)

Publikationsform

Artikel
(62)
Buchkapitel
(2)

Sprache

Englisch
(64)
Japanisch
(4)

Erscheinungsjahr

n.n

Thema

Science & Technology
(49)
Life Sciences & Biomedicine
(47)
Humans
(42)
Child
(27)
Pediatrics
(26)
Critical Illness
(17)
Children
(16)
Critically Ill Children
(15)
Diagnosis
(15)
Genomics
(15)
Multiple Organ Failure - Diagnosis
(15)
Risk Factors
(13)
Demographic Aspects
(12)
Evaluation
(11)
Genetics & Heredity
(11)
Organ Dysfunction Scores
(11)
Adult
(10)
Female
(10)
Male
(10)
Multiple Organ Failure - Physiopathology
(10)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Return of individual genomic research results: what do consent forms tell participants?

Researchers' Ethical Concerns About Using Adaptive Deep Brain Stimulation for Enhancement

Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study

Do privacy and security regulations need a status update? Perspectives from an intergenerational survey

Ask me later: deciding to have clinical exome trio sequencing for my critically ill child

Challenges to Building a Gene Variant Commons to Assess Hereditary Cancer Risk: Results of a Modified Policy Delphi Panel Deliberation

Participants’ recall and understanding of genomic research and large-scale data sharing

“The truth should not be hidden”: Experiences and recommendations of individuals making NPE discoveries through genetic genealogy databases

Perceived Benefits, Risks, and Utility of Newborn Genomic Sequencing in the BabySeq Project

Psychosocial Effect of Newborn Genomic Sequencing on Families in the BabySeq Project: A Randomized Clinical Trial

Measuring perceived utility of genomic sequencing: Development and validation of the GENEtic Utility (GENE-U) scale for adult screening

Measuring perceived utility of genomic sequencing: Development and validation of the GENEtic Utility (GENE-U) scale for pediatric diagnostic testing

Parents’ decision-making regarding whether to receive adult-onset only genetic findings for their children: Findings from the BabySeq Project

Pediatric data sharing in genomic research: attitudes and preferences of parents

Comprehensive red blood cell and platelet antigen prediction from whole genome sequencing: proof of principle

The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine

Airmen and health-care providers' attitudes toward the use of genomic sequencing in the US Air Force: findings from the MilSeq Project

Perceived Utility of Genomic Sequencing: Qualitative Analysis and Synthesis of a Conceptual Model to Inform Patient-Centered Instrument Development

A systematic approach to the reporting of medically relevant findings from whole genome sequencing

Airmen and Healthcare Providers’ attitudes toward the use of genomic sequencing in the US Air Force: Findings from the MilSeq Project

Summarizing polygenic risks for complex diseases in a clinical whole-genome report

MEDICAL INFORMATION COMMONS: CONCEPTUAL, LEGAL AND ETHICAL CONSIDERATIONS FOR STAKEHOLDERS

Participants and Study Decliners’ Perspectives About the Risks of Participating in a Clinical Trial of Whole Genome Sequencing

'Someday it will be the norm': physician perspectives on the utility of genome sequencing for patient care in the MedSeqProject

'Someday it will be the norm': physician perspectives on the utility of genome sequencing for patient care in the MedSeq Project

Aktive Filter

Suchergebnisse filtern