Karin M. Dent - Concepedia

Author

Karin M. Dent

University of Utah

Also Known As

K Dent, K M Dent, K. Dent, K. M. Dent, K.M. Dent, Karin Dent, Karin M Dent, Karin M. Dent, Kylie Dent, M. Nauman Akhtar

Publications

3.3K

Citations

H-Index

Concepts

All Affiliations

University of Utah University of Washington Seattle Children's Hospital University of Pittsburgh Intermountain Healthcare

About

Karin M. Dent is an author at University of Utah specializing in medicine, genetics, and genomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	2.4K
2	Public Health	3	3	129
3	Social Sciences	2	2	406
4	Education	1	1	23
5	Health Sciences	1	1	14

Karin M. Dent

Publications

3.1K

Citations

H-Index

Page 1

	Year	Citations
Exome sequencing identifies the cause of a mendelian disorder Sarah Ng, Kati J. Buckingham, Choli Lee, Nature Genetics Mendelian DisorderGenetic DisorderGeneticsMolecular GeneticsGenomics	2009	1.9K
Aggression and anger-related traits associated with a polymorphism of the tryptophan hydroxylase gene Stephen B. Manuck, Janine D. Flory, Robert E. Ferrell, Biological Psychiatry Behavioral SciencesAnger-related TraitsBehavioral NeuroscienceSocial BehaviorAffective Neuroscience	1999	277
Improved molecular diagnosis of dystrophinopathies in an unselected clinical cohort Karin M. Dent, Diane M. Dunn, Andrew C. von Niederhausern, American Journal of Medical Genetics Part A Molecular DiagnosisDmd MutationsGeneticsDiagnosisGynecology	2005	147
Neuroticism is not associated with the serotonin transporter (5-HTTLPR) polymorphism J.D. Flory, Stephen B. Manuck, R E Ferrell, Molecular Psychiatry NeuropsychologyMolecular NeuroscienceSerotonin TransporterPsychiatryNeurophysiology	1999	129
Informed consent for whole genome sequencing: A qualitative analysis of participant expectations and perceptions of risks, benefits, and harms Holly K. Tabor, Jacquie Stock, Tracy Brazg, American Journal of Medical Genetics Part A	2012	118
Practices and Policies of Clinical Exome Sequencing Providers: Analysis and Implications Seema M. Jamal, Joon‐Ho Yu, Jessica X. Chong, American Journal of Medical Genetics Part A Genetic TestingGeneticsGynecologyGenomicsResearch Ethics	2013	75
The spectrum of <i>DNMT3A</i> variants in Tatton–Brown–Rahman syndrome overlaps with that in hematologic malignancies Wei Shen, Jennifer Heeley, Colleen M. Carlston, American Journal of Medical Genetics Part A	2017	48
My46: a Web-based tool for self-guided management of genomic test results in research and clinical settings Holly K. Tabor, Seema M. Jamal, Joon‐Ho Yu, Genetics in Medicine Genetic AnalysisGenetic TestingFunctional GenomicsWeb-based ToolGenetics	2016	37
Methodology of a multistate study of congenital hearing loss: Preliminary data from Utah newborn screening Karin M. Dent, Aileen Kenneson, Janice C. Palumbos, American Journal of Medical Genetics Part C Seminars in Medical Genetics	2004	34
Empagliflozin in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial Obbina Abani, Amr E. Abbas, Fatima Abbas, The Lancet Diabetes & Endocrinology	2023	34

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