Katie Lutz

ORCID: 0000-0002-0762-6220
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About
Contact & Profiles
Research Areas
  • Pulmonary Hypertension Research and Treatments
  • Religion, Spirituality, and Psychology
  • Palliative Care and End-of-Life Issues
  • Medical Imaging and Pathology Studies
  • Bladder and Urothelial Cancer Treatments
  • Pelvic floor disorders treatments
  • Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
  • Grief, Bereavement, and Mental Health
  • Colorectal Cancer Screening and Detection
  • Systemic Sclerosis and Related Diseases
  • Advanced Neuroimaging Techniques and Applications
  • Shoulder Injury and Treatment
  • Shoulder and Clavicle Injuries
  • Vascular Anomalies and Treatments
  • Sports injuries and prevention
  • RNA modifications and cancer
  • Protease and Inhibitor Mechanisms
  • Advanced MRI Techniques and Applications
  • Urinary Tract Infections Management

Children's Medical Center
2024

University of Cincinnati
2024

Cincinnati Children's Hospital Medical Center
2019-2024

Stetson University
2022

Hitit Üniversitesi
2022

University of San Francisco
2017

DKFZ-ZMBH Alliance
2009

German Cancer Research Center
2009

Rationale: Pulmonary arterial hypertension (PAH) is characterized by structural remodeling of pulmonary arteries and arterioles. Underlying biological processes are likely reflected in a perturbation circulating proteins. Objectives: To quantify analyze the plasma proteome patients with PAH using inherited genetic variation to inform on underlying molecular drivers. Methods: An aptamer-based assay was used measure proteins 357 idiopathic or heritable PAH, 103 healthy volunteers, 23 relatives...

10.1164/rccm.202109-2106oc article EN American Journal of Respiratory and Critical Care Medicine 2022-04-08

Abstract Background Approximately 25% of patients with pulmonary arterial hypertension (PAH) have been found to harbor rare mutations in disease-causing genes. To identify missing heritability PAH we integrated deep phenotyping whole-genome sequencing data using Bayesian statistics. Methods We analyzed 13,037 participants enrolled the NIHR BioResource - Rare Diseases (NBR) study, which 1,148 were recruited domain. test for genetic associations between genes and selected phenotypes (PH), used...

10.1101/2019.12.11.871210 preprint EN cc-by-nd bioRxiv (Cold Spring Harbor Laboratory) 2019-12-12

Ziele: Detection of white matter hyperintensities (WMH) by using visual rating scales or manual volumetric measurement is problematic, because both methods rely heavily on the human eye and are hampered floor ceiling effects to detect changes in cerebral matter. Especially describe WMH a qualitative semi-quantitative way. Hence, intra- interrater reliability usually modest low as previous studies have shown. Our first purpose was evaluate clinical acceptability new fully automated method...

10.1055/s-0029-1221753 article EN RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren 2009-04-01
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