H Turner

ORCID: 0009-0006-7198-714X
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About
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Research Areas
  • Biomedical Text Mining and Ontologies
  • Topic Modeling
  • CRISPR and Genetic Engineering
  • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
  • Asthma and respiratory diseases
  • Machine Learning in Bioinformatics
  • Cancer, Hypoxia, and Metabolism
  • Telecommunications and Broadcasting Technologies
  • Adrenal and Paraganglionic Tumors
  • RNA and protein synthesis mechanisms
  • Infectious Diseases and Mycology
  • Eosinophilic Disorders and Syndromes
  • Urticaria and Related Conditions
  • Genomics and Chromatin Dynamics
  • Renal cell carcinoma treatment
  • Renal and related cancers
  • Bladder and Urothelial Cancer Treatments
  • Medical Imaging Techniques and Applications
  • Urinary and Genital Oncology Studies
  • Machine Learning in Healthcare
  • Sinusitis and nasal conditions
  • SARS-CoV-2 and COVID-19 Research
  • Nasal Surgery and Airway Studies
  • Insects and Parasite Interactions
  • Advanced MIMO Systems Optimization

Georgia Institute of Technology
2023-2025

Emory University
2025

Newcastle upon Tyne Hospitals NHS Foundation Trust
2018-2022

Uppsala University
2021

John Radcliffe Hospital
2015

Abstract De novo mutations are known to play a prominent role in sporadic disorders with reduced fitness. We hypothesize that de an important severe male infertility and explain portion of the genetic causes this understudied disorder. To test hypothesis, we utilize trio-based exome sequencing cohort 185 infertile males their unaffected parents. Following systematic analysis, 29 145 rare (MAF < 0.1%) protein-altering classified as possibly causative phenotype. observed significant...

10.1038/s41467-021-27132-8 article EN cc-by Nature Communications 2022-01-10

This work introduces TrialSieve, a novel framework for biomedical information extraction that enhances clinical meta-analysis and drug repurposing. By extending traditional PICO (Patient, Intervention, Comparison, Outcome) methodologies, TrialSieve incorporates hierarchical, treatment group-based graphs, enabling more comprehensive quantitative comparisons of outcomes. was used to annotate 1609 PubMed abstracts, 170,557 annotations, 52,638 final spans, incorporating 20 unique annotation...

10.3390/bioengineering12050486 article EN cc-by Bioengineering 2025-05-02

This work presents a new, original document classification dataset, BioSift, to expedite the initial selection and labeling of studies for drug repurposing. The dataset consists 10,000 human-annotated abstracts from scientific articles in PubMed. Each abstract is labeled with up eight attributes necessary perform meta-analysis utilizing popular patient-intervention-comparator-outcome (PICO) method: has human subjects, clinical trial/cohort, population size, target disease, study drug,...

10.1145/3539618.3591897 article EN cc-by Proceedings of the 45th International ACM SIGIR Conference on Research and Development in Information Retrieval 2023-07-18

10.1136/bmj.2.4065.1178-a article EN BMJ 1938-12-03

admits the reality of maleuces Dr. Scripture's " unconscious mind," one cannot afford to say single word against doctrine possession by devils.Indeed, all hard words that have been uttered divines with regard this matter must be retracted ; and we hope they do not retort on us sending back some epithets so freely hurled at them (gullible, credulous, reactionary, unscientific, on, ad nauseam).But does Scripture claim Unconscious Mind is devil ?Milton has assured that- The mind its own place,...

10.1016/s0140-6736(00)62624-7 article EN ˜The œLancet 1922-10-01

10.1136/bmj.2.4172.882-b article EN BMJ 1940-12-21

10.5594/j07364iia article EN Journal of the SMPTE 1956-03-01

Introduction De novo mutations (DNMs) are known to play a prominent role in sporadic disorders with reduced fitness 1 . We hypothesize that DNMs an important male infertility and explain significant fraction of the genetic causes this understudied disorder. To test hypothesis, we performed trio-based exome-sequencing unique cohort 185 infertile males their unaffected parents. Following systematic analysis, 29 145 rare protein altering were classified as possibly causative phenotype. observed...

10.1101/2021.02.27.433155 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2021-02-27
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