UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 210

Sortiert nach

Increasing the diagnostic yield of exome sequencing by copy number variant analysis

PloS one, 2018-12, Vol.13 (12), p.e0209185-e0209185

2018

Volltextzugriff (PDF)

Indexing the ‘dark side of addiction’: substance‐induced affective symptoms and alcohol use disorders

Addiction (Abingdon, England), 2019-01, Vol.114 (1), p.139-149

2019

Volltextzugriff (PDF)

Pleiotropic loci for cannabis use disorder severity in multi-ancestry high-risk populations

Molecular and cellular neuroscience, 2023-06, Vol.125, p.103852-103852, Article 103852

2023

Volltextzugriff (PDF)

SMNN: batch effect correction for single-cell RNA-seq data via supervised mutual nearest neighbor detection

Briefings in bioinformatics, 2021-05, Vol.22 (3)

2021

Volltextzugriff (PDF)

Developing, implementing, and evaluating the visiting Neighbors' program in rural Appalachia: A quality improvement protocol

PloS one, 2024-01, Vol.19 (1), p.e0296438-e0296438

2024

Volltextzugriff (PDF)

Focused ultrasound-mediated blood-brain barrier opening in Alzheimer's disease: long-term safety, imaging, and cognitive outcomes

Journal of neurosurgery, 2023-07, Vol.139 (1), p.275-283

2023

Volltextzugriff (PDF)

Germline Analysis from Tumor-Germline Sequencing Dyads to Identify Clinically Actionable Secondary Findings

Clinical cancer research, 2016-08, Vol.22 (16), p.4087-4094

2016

Volltextzugriff (PDF)

The feasibility of genetic dissection of endophenotypes

Psychophysiology, 2014-12, Vol.51 (12), p.1337-1338

Wilhelmsen, Kirk C.

2014

Volltextzugriff (PDF)

scRNA-seq in medulloblastoma shows cellular heterogeneity and lineage expansion support resistance to SHH inhibitor therapy

Nature communications, 2019-12, Vol.10 (1), p.5829-17, Article 5829

2019

Volltextzugriff (PDF)

A greedy regression algorithm with coarse weights offers novel advantages

Scientific reports, 2022-03, Vol.12 (1), p.5440-14, Article 5440

2022

Volltextzugriff (PDF)

Genetic risk for trait aggression and alcohol use predict unique facets of alcohol-related aggression

Psychology of addictive behaviors, 2024-06

2024

Volltextzugriff (PDF)

An informatics approach to analyzing the incidentalome

Genetics in medicine, 2013-01, Vol.15 (1), p.36-44

2013

Volltextzugriff (PDF)

Common genetic substrates of alcohol and substance use disorder severity revealed by pleiotropy detection against GWAS catalog in two populations

Addiction biology, 2021-01, Vol.26 (1), p.e12877-n/a

2021

Volltextzugriff (PDF)

Can Genetic Analysis of Putative Blood Alzheimer's Disease Biomarkers Lead to Identification of Susceptibility Loci?

PloS one, 2015-12, Vol.10 (12), p.e0142360-e0142360

2015

Volltextzugriff (PDF)

Genetic variation in FAAH is associated with cannabis use disorders in a young adult sample of Mexican Americans

Drug and alcohol dependence, 2016-09, Vol.166, p.249-253

2016

Volltextzugriff (PDF)

Projected t-SNE for batch correction

Bioinformatics, 2020-06, Vol.36 (11), p.3522-3527

2020

Volltextzugriff (PDF)

Pre-capture multiplexing provides additional power to detect copy number variation in exome sequencing

BMC bioinformatics, 2021-07, Vol.22 (1), p.1-374, Article 374

2021

Volltextzugriff (PDF)

A blood-based screening tool for Alzheimer's disease that spans serum and plasma: findings from TARC and ADNI

PloS one, 2011-12, Vol.6 (12), p.e28092

2011

Volltextzugriff (PDF)

Associations Between Genomic Variants in Alcohol Dehydrogenase Genes and Alcohol Symptomatology in American Indians and European Americans: Distinctions and Convergence

Alcoholism, clinical and experimental research, 2017-10, Vol.41 (10), p.1695-1704

2017

Volltextzugriff (PDF)

Effects of genetic risk for alcohol dependence and onset of regular drinking on the progression to alcohol dependence: A polygenic risk score approach

Drug and alcohol dependence, 2022-01, Vol.230, p.109117-109117, Article 109117

2022

Volltextzugriff (PDF)

Effects of Common and Rare Chromosome 4 GABAergic Gene Variation on Alcohol Use and Antisocial Behavior

Journal of studies on alcohol and drugs, 2019-11, Vol.80 (6), p.585

2019

Volltextzugriff (PDF)

Genome‐wide meta‐analysis identifies a novel susceptibility signal at CACNA2D3 for nicotine dependence

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2017-07, Vol.174 (5), p.557-567

2017

Volltextzugriff (PDF)

A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing

Genetics in medicine, 2016-05, Vol.18 (5), p.467-475

2016

Volltextzugriff (PDF)

Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly

Cell, 2018-02, Vol.172 (5), p.897-909.e21

2018

Volltextzugriff (PDF)

Variant calling in low-coverage whole genome sequencing of a Native American population sample

BMC genomics, 2014-01, Vol.15 (1), p.85-85, Article 85

2014

Volltextzugriff (PDF)

1 – 25 von 210

Suche als RSS-Feed

Aktive Filter

KollektionSpringer journals

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(195)
Mit Volltextzugriff
(186)

Publikationsform

Sprache

Englisch
(210)
Japanisch
(27)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Increasing the diagnostic yield of exome sequencing by copy number variant analysis

Indexing the ‘dark side of addiction’: substance‐induced affective symptoms and alcohol use disorders

Pleiotropic loci for cannabis use disorder severity in multi-ancestry high-risk populations

SMNN: batch effect correction for single-cell RNA-seq data via supervised mutual nearest neighbor detection

Developing, implementing, and evaluating the visiting Neighbors' program in rural Appalachia: A quality improvement protocol

Focused ultrasound-mediated blood-brain barrier opening in Alzheimer's disease: long-term safety, imaging, and cognitive outcomes

Germline Analysis from Tumor-Germline Sequencing Dyads to Identify Clinically Actionable Secondary Findings

The feasibility of genetic dissection of endophenotypes

scRNA-seq in medulloblastoma shows cellular heterogeneity and lineage expansion support resistance to SHH inhibitor therapy

A greedy regression algorithm with coarse weights offers novel advantages

Genetic risk for trait aggression and alcohol use predict unique facets of alcohol-related aggression

An informatics approach to analyzing the incidentalome

Common genetic substrates of alcohol and substance use disorder severity revealed by pleiotropy detection against GWAS catalog in two populations

Can Genetic Analysis of Putative Blood Alzheimer's Disease Biomarkers Lead to Identification of Susceptibility Loci?

Genetic variation in FAAH is associated with cannabis use disorders in a young adult sample of Mexican Americans

Projected t-SNE for batch correction

Pre-capture multiplexing provides additional power to detect copy number variation in exome sequencing

A blood-based screening tool for Alzheimer's disease that spans serum and plasma: findings from TARC and ADNI

Associations Between Genomic Variants in Alcohol Dehydrogenase Genes and Alcohol Symptomatology in American Indians and European Americans: Distinctions and Convergence

Effects of genetic risk for alcohol dependence and onset of regular drinking on the progression to alcohol dependence: A polygenic risk score approach

Effects of Common and Rare Chromosome 4 GABAergic Gene Variation on Alcohol Use and Antisocial Behavior

Genome‐wide meta‐analysis identifies a novel susceptibility signal at CACNA2D3 for nicotine dependence

A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing

Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly

Variant calling in low-coverage whole genome sequencing of a Native American population sample

Aktive Filter

Suchergebnisse filtern