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...

Social Outcomes in Mid- to Later Adulthood Among Individuals Diagnosed With Autism and Average Nonverbal IQ as Children

Journal of the American Academy of Child and Adolescent Psychiatry, 2013-06, Vol.52 (6), p.572-581.e1

2013

Volltextzugriff (PDF)

Disclosing pathogenic genetic variants to research participants: quantifying an emerging ethical responsibility

Genome research, 2012-03, Vol.22 (3), p.421-428

2012

Volltextzugriff (PDF)

Short report: Twins with 20p13 duplication. Case report and comprehensive literature review

Molecular genetics & genomic medicine, 2024-05, Vol.12 (5), p.e2436-n/a

2024

Volltextzugriff (PDF)

Using a chat-based informed consent tool in large-scale genomic research

Journal of the American Medical Informatics Association : JAMIA, 2024-01, Vol.31 (2), p.472-478

2024

Volltextzugriff (PDF)

Guidelines for return of research results from pediatric genomic studies: deliberations of the Boston Children's Hospital Gene Partnership Informed Cohort Oversight Board

Genetics in medicine, 2014-07, Vol.16 (7), p.547-552

2014

Volltextzugriff (PDF)

Risk Factors and Modifiers for Cardiovascular Disease Assessment of Patients with Heterozygous Familial Hypercholesterolaemia

Journal of clinical medicine, 2024-04, Vol.13 (8), p.2270

2024

Volltextzugriff (PDF)

Facilitating family communication of familial hypercholesterolemia genetic risk: Assessing engagement with innovative chatbot technology from the IMPACT-FH study

PEC innovation, 2023-12, Vol.2, p.100134-100134, Article 100134

2023

Volltextzugriff (PDF)

Development of a culturally targeted chatbot to inform living kidney donor candidates of African ancestry about APOL1 genetic testing: a mixed methods study

Journal of community genetics, 2024-04, Vol.15 (2), p.205-216

2024

Volltextzugriff (PDF)

P471: Uptake of a chatbot for disclosure of germline genetic test results through a universal genetic testing program

Genetics in Medicine Open, 2024, Vol.2, p.101370, Article 101370

2024

Volltextzugriff (PDF)

Family health history reporting is sensitive to small changes in wording

Genetics in medicine, 2016-12, Vol.18 (12), p.1308-1311

2016

Volltextzugriff (PDF)

The beliefs, motivations, and expectations of parents who have enrolled their children in a genetic biorepository

Genetics in medicine, 2012-03, Vol.14 (3), p.330-337

2012

Volltextzugriff (PDF)

Increased LIS1 expression affects human and mouse brain development

Nature Genetics, 2009-02, Vol.41 (2), p.168-177

2009

Volltextzugriff (PDF)

Cognitive and language skills in adults with autism: a 40-year follow-up

Journal of child psychology and psychiatry, 2014-01, Vol.55 (1), p.49-58

2014

Volltextzugriff (PDF)

Neglectful Behavior by Parents in the Life History of University Students in 17 Countries and Its Relation to Violence Against Dating Partners

Child maltreatment, 2005-05, Vol.10 (2), p.124-135

2005

Volltextzugriff (PDF)

Preferences for the Return of Individual Results From Research on Pediatric Biobank Samples

Journal of empirical research on human research ethics, 2017-04, Vol.12 (2), p.97-106

2017

Volltextzugriff (PDF)

Tyrosinase gene mutations in oculocutaneous albinism 1 (OCA1): definition of the phenotype

Human genetics, 2003-11, Vol.113 (6), p.502-513

2003

Volltextzugriff (PDF)

P gene mutations associated with oculocutaneous albinism type II (OCA2)

Human mutation, 2005-03, Vol.25 (3), p.323-323

2005

Volltextzugriff (PDF)

Enhancing Autonomy in Biobank Decisions: Too Much of a Good Thing?

Journal of empirical research on human research ethics, 2018-04, Vol.13 (2), p.125-138

2018

Volltextzugriff (PDF)

Participant Satisfaction With a Preference-Setting Tool for the Return of Individual Research Results in Pediatric Genomic Research

Journal of empirical research on human research ethics, 2015-10, Vol.10 (4), p.414-426

2015

Volltextzugriff (PDF)

The Development of a Preference-Setting Model for the Return of Individual Genomic Research Results

Journal of empirical research on human research ethics, 2015-04, Vol.10 (2), p.107-120

2015

Volltextzugriff (PDF)

Self and informant reports of mental health difficulties among adults with autism findings from a long-term follow-up study

Autism : the international journal of research and practice, 2015-10, Vol.19 (7), p.832-841

2015

Volltextzugriff (PDF)

eP256: Intrafamilial variability in chromosome 2q13 microdeletion: Case report and review of the literature

Genetics in medicine, 2022-03, Vol.24 (3), p.S162-S163

2022

Volltextzugriff (PDF)

MC1R Mutations Modify the Classic Phenotype of Oculocutaneous Albinism Type 2 (OCA2)

American journal of human genetics, 2003-09, Vol.73 (3), p.638-645

2003

Volltextzugriff (PDF)

Modeling and comparison of costs and high-risk variant detection between a genetic counseling chatbot and a traditional genetic counseling pathway (169)

Gynecologic oncology, 2023-09, Vol.176, p.S64-S64

2023

Volltextzugriff (PDF)

Growing older with autism – The experiences of adult siblings of individuals with autism

Research in autism spectrum disorders, 2019-07, Vol.63, p.42-51

2019

Volltextzugriff (PDF)

1 – 25 von 529

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(460)
Mit Volltextzugriff
(429)

Publikationsform

3 weitere anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(346)
Life Sciences & Biomedicine
(263)
Humans
(210)
Female
(108)
Male
(98)
Adult
(70)
Physical Sciences
(63)
Middle Aged
(53)
Chemistry
(48)
Genetics & Heredity
(43)
Biological And Medical Sciences
(42)
Animals
(41)
Child
(39)
Technology
(36)
Medical Sciences
(35)
Adolescent
(34)
Social Sciences
(34)
Genomes
(31)
Science & Technology - Other Topics
(30)
Genomics
(28)

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

MEDLINE
(233)
EZB Electronic Journals Library
(225)
Journals@Ovid Ovid Full Text
(154)
Ingenta
(153)
Publisher or Other Site
(110)
IngentaConnect Journals
(71)
ScienceDirect
(58)
Wiley Online Library
(47)
JSTOR
(44)
SpringerLink_现刊
(43)
Springer Nature - Connect here FIRST to enable access
(39)
Elsevier Journal Backfiles on ScienceDirect (DFG Nationallizenzen)
(38)
Wiley Online Library
(32)
Oxford Journals
(26)
BMJ_英国医学会期刊
(23)
SAGE Journals
(23)
Oxford Journals 2020 Medicine
(21)
Ebook Central Perpetual and DDA
(19)
eBooks on EBSCOhost
(18)
Nexis Uni
(18)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

Social Outcomes in Mid- to Later Adulthood Among Individuals Diagnosed With Autism and Average Nonverbal IQ as Children

Disclosing pathogenic genetic variants to research participants: quantifying an emerging ethical responsibility

Short report: Twins with 20p13 duplication. Case report and comprehensive literature review

Using a chat-based informed consent tool in large-scale genomic research

Guidelines for return of research results from pediatric genomic studies: deliberations of the Boston Children's Hospital Gene Partnership Informed Cohort Oversight Board

Risk Factors and Modifiers for Cardiovascular Disease Assessment of Patients with Heterozygous Familial Hypercholesterolaemia

Facilitating family communication of familial hypercholesterolemia genetic risk: Assessing engagement with innovative chatbot technology from the IMPACT-FH study

Development of a culturally targeted chatbot to inform living kidney donor candidates of African ancestry about APOL1 genetic testing: a mixed methods study

P471: Uptake of a chatbot for disclosure of germline genetic test results through a universal genetic testing program

Family health history reporting is sensitive to small changes in wording

The beliefs, motivations, and expectations of parents who have enrolled their children in a genetic biorepository

Increased LIS1 expression affects human and mouse brain development

Cognitive and language skills in adults with autism: a 40-year follow-up

Neglectful Behavior by Parents in the Life History of University Students in 17 Countries and Its Relation to Violence Against Dating Partners

Preferences for the Return of Individual Results From Research on Pediatric Biobank Samples

Tyrosinase gene mutations in oculocutaneous albinism 1 (OCA1): definition of the phenotype

P gene mutations associated with oculocutaneous albinism type II (OCA2)

Enhancing Autonomy in Biobank Decisions: Too Much of a Good Thing?

Participant Satisfaction With a Preference-Setting Tool for the Return of Individual Research Results in Pediatric Genomic Research

The Development of a Preference-Setting Model for the Return of Individual Genomic Research Results

Self and informant reports of mental health difficulties among adults with autism findings from a long-term follow-up study

eP256: Intrafamilial variability in chromosome 2q13 microdeletion: Case report and review of the literature

MC1R Mutations Modify the Classic Phenotype of Oculocutaneous Albinism Type 2 (OCA2)

Modeling and comparison of costs and high-risk variant detection between a genetic counseling chatbot and a traditional genetic counseling pathway (169)

Growing older with autism – The experiences of adult siblings of individuals with autism

Suchergebnisse filtern