UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 131

Sortiert nach

College of American Pathologists' laboratory standards for next-generation sequencing clinical tests

Archives of pathology & laboratory medicine (1976), 2015-04, Vol.139 (4), p.481-493

2015

Volltextzugriff (PDF)

Frequency and clinical outcomes of CYP2C19 genotype-guided escalation and de-escalation of antiplatelet therapy in a real-world clinical setting

Genetics in medicine, 2020-01, Vol.22 (1), p.160-169

2020

Volltextzugriff (PDF)

Genotype-Guided Tamoxifen Dosing Increases Active Metabolite Exposure in Women With Reduced CYP2D6 Metabolism: A Multicenter Study

Journal of clinical oncology, 2011-08, Vol.29 (24), p.3232-3239

2011

Volltextzugriff (PDF)

Public Interest in Population Genetic Screening for Cancer Risk

Frontiers in genetics, 2022-07, Vol.13, p.886640-886640

2022

Volltextzugriff (PDF)

Verifying nomenclature of DNA variants in submitted manuscripts: Guidance for journals

Human mutation, 2021-01, Vol.42 (1), p.3-7

2021

Volltextzugriff (PDF)

Interpretation of genomic sequencing: variants should be considered uncertain until proven guilty

Genetics in medicine, 2018-03, Vol.20 (3), p.291-293

Weck, Karen E

2018

Volltextzugriff (PDF)

FNA smears as a potential source of DNA for targeted next‐generation sequencing of lung adenocarcinomas

Cancer cytopathology, 2016-06, Vol.124 (6), p.406-414

2016

Volltextzugriff (PDF)

Recommendations for Clinical CYP2C19 Genotyping Allele Selection: A Report of the Association for Molecular Pathology

The Journal of molecular diagnostics : JMD, 2018-05, Vol.20 (3), p.269-276

2018

Volltextzugriff (PDF)

Hepatitis C Virus Genotyping: Interrogation of the 5′ Untranslated Region Cannot Accurately Distinguish Genotypes 1a and 1b

Journal of Clinical Microbiology, 2002-09, Vol.40 (9), p.3127-3134

2002

Volltextzugriff (PDF)

Next generation massively parallel sequencing of targeted exomes to identify genetic mutations in primary ciliary dyskinesia: implications for application to clinical testing

Genetics in medicine, 2011-03, Vol.13 (3), p.218-229

2011

Volltextzugriff (PDF)

The phenotype of multiple congenital anomalies-hypotonia-seizures syndrome 1: Report and review

American journal of medical genetics. Part A, 2015-09, Vol.167A (9), p.2176-2181

2015

Volltextzugriff (PDF)

Recommendations for Clinical CYP2D6 Genotyping Allele Selection: A Joint Consensus Recommendation of the Association for Molecular Pathology, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, and the European Society for Pharmacogenomics and Personalized Therapy

The Journal of molecular diagnostics : JMD, 2021-09, Vol.23 (9), p.1047-1064

2021

Volltextzugriff (PDF)

Murine Gammaherpesvirus 68 Infection Is Associated with Lymphoproliferative Disease and Lymphoma in BALB β2 Microglobulin-Deficient Mice

Journal of Virology, 2005-12, Vol.79 (23), p.14668-14679

2005

Volltextzugriff (PDF)

Recommendations for Clinical CYP2C9 Genotyping Allele Selection: A Joint Recommendation of the Association for Molecular Pathology and College of American Pathologists

The Journal of molecular diagnostics : JMD, 2019-09, Vol.21 (5), p.746-755

2019

Volltextzugriff (PDF)

Acute Myeloid Leukemia with Co‐mutated ASXL1 and SRSF2 Exhibits Monocytic Differentiation and has a Mutational Profile Overlapping with Chronic Myelomonocytic Leukemia

HemaSphere, 2019-10, Vol.3 (5), p.1-4

2019

Volltextzugriff (PDF)

Cri du Chat Syndrome and Primary Ciliary Dyskinesia: A Common Genetic Cause on Chromosome 5p

The Journal of pediatrics, 2014-10, Vol.165 (4), p.858-861

2014

Volltextzugriff (PDF)

An approach to integrating exome sequencing for fetal structural anomalies into clinical practice

Genetics in medicine, 2020-05, Vol.22 (5), p.954-961

2020

Volltextzugriff (PDF)

Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project

American journal of human genetics, 2020-10, Vol.107 (4), p.596-611

2020

Volltextzugriff (PDF)

Development and Validation of Clinical Whole-Exome and Whole-Genome Sequencing for Detection of Germline Variants in Inherited Disease

Archives of pathology & laboratory medicine (1976), 2017-06, Vol.141 (6), p.798-805

2017

Volltextzugriff (PDF)

The Next Generation of Molecular Pathology is Here: Validation of Next-Generation Sequencing Technology for Clinical Molecular Testing Across Multiple Different Disciplines

Archives of pathology & laboratory medicine (1976), 2017-06, Vol.141 (6), p.749-750

Weck, Karen E

2017

Volltextzugriff (PDF)

PIK3CA Mutation in HPV-Associated OPSCC Patients Receiving Deintensified Chemoradiation

JNCI : Journal of the National Cancer Institute, 2020-08, Vol.112 (8), p.855-858

2020

Volltextzugriff (PDF)

A phase II trial of UGT1A1 genotype-guided FOLFIRI plus bevacizumab as first-line therapy for advanced, unresectable colorectal cancer

The oncologist (Dayton, Ohio), 2024-06

2024

Volltextzugriff (PDF)

Recommendations for Clinical Warfarin Genotyping Allele Selection: A Report of the Association for Molecular Pathology and the College of American Pathologists

The Journal of molecular diagnostics : JMD, 2020-07, Vol.22 (7), p.847-859

2020

Volltextzugriff (PDF)

A panoramic view of the accuracy of molecular genetic testing

Genetics in medicine, 2016-12, Vol.18 (12), p.1188-1189

2016

Volltextzugriff (PDF)

Clinical Outcomes and Sustainability of Using CYP2C19 Genotype-Guided Antiplatelet Therapy After Percutaneous Coronary Intervention

Circulation. Genomic and precision medicine, 2018-04, Vol.11 (4), p.e002069-e002069

2018

Volltextzugriff (PDF)

1 – 25 von 131

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(126)
Mit Volltextzugriff
(127)

Publikationsform

Artikel
(130)
magazinearticle
(1)

Sprache

Englisch
(131)
Japanisch
(13)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(2)
... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

College of American Pathologists' laboratory standards for next-generation sequencing clinical tests

Frequency and clinical outcomes of CYP2C19 genotype-guided escalation and de-escalation of antiplatelet therapy in a real-world clinical setting

Genotype-Guided Tamoxifen Dosing Increases Active Metabolite Exposure in Women With Reduced CYP2D6 Metabolism: A Multicenter Study

Public Interest in Population Genetic Screening for Cancer Risk

Verifying nomenclature of DNA variants in submitted manuscripts: Guidance for journals

Interpretation of genomic sequencing: variants should be considered uncertain until proven guilty

FNA smears as a potential source of DNA for targeted next‐generation sequencing of lung adenocarcinomas

Recommendations for Clinical CYP2C19 Genotyping Allele Selection: A Report of the Association for Molecular Pathology

Hepatitis C Virus Genotyping: Interrogation of the 5′ Untranslated Region Cannot Accurately Distinguish Genotypes 1a and 1b

Next generation massively parallel sequencing of targeted exomes to identify genetic mutations in primary ciliary dyskinesia: implications for application to clinical testing

The phenotype of multiple congenital anomalies-hypotonia-seizures syndrome 1: Report and review

Murine Gammaherpesvirus 68 Infection Is Associated with Lymphoproliferative Disease and Lymphoma in BALB β2 Microglobulin-Deficient Mice

Recommendations for Clinical CYP2C9 Genotyping Allele Selection: A Joint Recommendation of the Association for Molecular Pathology and College of American Pathologists

Acute Myeloid Leukemia with Co‐mutated ASXL1 and SRSF2 Exhibits Monocytic Differentiation and has a Mutational Profile Overlapping with Chronic Myelomonocytic Leukemia

Cri du Chat Syndrome and Primary Ciliary Dyskinesia: A Common Genetic Cause on Chromosome 5p

An approach to integrating exome sequencing for fetal structural anomalies into clinical practice

Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project

Development and Validation of Clinical Whole-Exome and Whole-Genome Sequencing for Detection of Germline Variants in Inherited Disease

The Next Generation of Molecular Pathology is Here: Validation of Next-Generation Sequencing Technology for Clinical Molecular Testing Across Multiple Different Disciplines

PIK3CA Mutation in HPV-Associated OPSCC Patients Receiving Deintensified Chemoradiation

A phase II trial of UGT1A1 genotype-guided FOLFIRI plus bevacizumab as first-line therapy for advanced, unresectable colorectal cancer

Recommendations for Clinical Warfarin Genotyping Allele Selection: A Report of the Association for Molecular Pathology and the College of American Pathologists

A panoramic view of the accuracy of molecular genetic testing

Clinical Outcomes and Sustainability of Using CYP2C19 Genotype-Guided Antiplatelet Therapy After Percutaneous Coronary Intervention

Suchergebnisse filtern