Kristy Damjanovich - Concepedia

Author

Kristy Damjanovich

University of Utah

Also Known As

K Damjanovich, K. DAMJANOVICH, Kristy Damjanovich

Publications

1.2K

Citations

H-Index

Concepts

All Affiliations

University of Utah ARUP Laboratories (United States)ARUP Institute for Clinical and Experimental Pathology Austrian Academy of Sciences

About

Kristy Damjanovich is an author at University of Utah specializing in medicine, genetics, and molecular epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	892
2	Engineering	1	1	80
3	Health Sciences	1	1	685
4	Public Health	1	1	101
5	Biomolecular Engineering	1	1	80

Kristy Damjanovich

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
MHC heterozygosity confers a selective advantage against multiple-strain infections Dustin J. Penn, Kristy Damjanovich, Wayne K. Potts Proceedings of the National Academy of Sciences Molecular EpidemiologySusceptible HostGeneticsImmunologyGenetic Epidemiology	2002	685
Major Histocompatibility Complex Heterozygosity Reduces Fitness in Experimentally Infected Mice Petteri Ilmonen, Dustin J. Penn, Kristy Damjanovich, Genetics HistocompatibilityMolecular EpidemiologySusceptible HostGeneticsImmunology	2007	101
Unlabeled Oligonucleotides as Internal Temperature Controls for Genotyping by Amplicon Melting Michael Seipp, Jacob Durtschi, Michael Liew, Journal of Molecular Diagnostics EngineeringMolecular Biological MethodMedicineGeneticsOligonucleotide	2007	80
Molecular diagnosis in hereditary hemorrhagic telangiectasia: findings in a series tested simultaneously by sequencing and deletion/duplication analysis Jamie McDonald, Kristy Damjanovich, Alison Millson, Clinical Genetics	2010	66
Experimental infection magnifies inbreeding depression in house mice Petteri Ilmonen, Dustin J. Penn, Kristy Damjanovich, Journal of Evolutionary Biology	2008	66
Mosaic <i>ACVRL1</i> and <i>ENG</i> mutations in hereditary haemorrhagic telangiectasia patients D. Hunter Best, Cecily P. Vaughn, Jamie McDonald, Journal of Medical Genetics	2011	40
5'UTR mutations of ENG cause hereditary hemorrhagic telangiectasia Kristy Damjanovich, Carmen Langa, Francisco J. Blanco, Orphanet Journal of Rare Diseases	2011	38
A novel X‐linked multiple congenital anomaly syndrome associated with an <i>EBP</i> mutation Larissa V. Furtado, Pınar Bayrak‐Toydemir, Becki Hulinsky, American Journal of Medical Genetics Part A	2010	33
Mosaicism in Stickler syndrome David A. Stevenson, Rena Vanzo, Kristy Damjanovich, European Journal of Medical Genetics Down SyndromeGenetic DisorderPathologyMedicineMosaicism	2012	14
p.R672C Mutation of MYH3 Gene in an Egyptian Infant Presented with Freeman-Sheldon Syndrome Mohammad Al-Haggar, Soheir Yahia, Kristy Damjanovich, The Indian Journal of Pediatrics Developmental AnomalyP.r672c MutationDevelopmental BiologyMendelian DisorderGenetic Disorder	2010	12

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