Loretta W Mahon - Concepedia

Author

Loretta W Mahon

Quest Diagnostics (United States)

Also Known As

L MAHON, Loretta Mahon, Loretta W Mahon, Loretta W. Mahon, Mahon, Loretta

Publications

239

Citations

H-Index

Concepts

All Affiliations

Quest Diagnostics (United States)Rady Children's Hospital-San Diego

About

Loretta W Mahon is an author at Quest Diagnostics (United States) specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	122
2	Health Sciences	1	1	17
3	Natural Sciences	1	1	27
4	Public Health	1	1	78
5	Molecular Biology	1	1	27

Loretta W Mahon

Publications

222

Citations

H-Index

Page 1

	Year	Citations
Regions of homozygosity identified by oligonucleotide SNP arrays: evaluating the incidence and clinical utility Jia‐Chi Wang, Leslie Ross, Loretta W Mahon, European Journal of Human Genetics Genetic AnalysisAllelic VariantClinical UtilityGeneticsMedicine	2014	78
Effects of platforms, size filter cutoffs, and targeted regions of cytogenomic microarray on detection of copy number variants and uniparental disomy in prenatal diagnosis: Results from 5026 pregnancies Jia‐Chi Wang, Jeff Radcliff, Sandra Coe, Prenatal Diagnosis	2019	57
Short stature, digit anomalies and dysmorphic facial features are associated with the duplication of miR-17 ~ 92 cluster Morteza Hemmat, Melissa Rumple, Loretta W Mahon, Molecular Cytogenetics	2014	29
Concurrent triplication and uniparental isodisomy: evidence for microhomology-mediated break-induced replication model for genomic rearrangements Trilochan Sahoo, Jia‐Chi Wang, Pedro A. Sanchez‐Lara, European Journal of Human Genetics Genome InstabilityNatural SciencesGeneticsConcurrent TriplicationGenomic Mechanism	2014	27
Spectral Karyotyping for identification of constitutional chromosomal abnormalities at a national reference laboratory Arturo Anguiano, Boris T Wang, Shirong R Wang, Molecular Cytogenetics Genetic TestingCytogeneticsGeneticsPathologySpectral Imaging System	2012	17
Enrichment of small pathogenic deletions at chromosome 9p24.3 and 9q34.3 involving DOCK8, KANK1, EHMT1 genes identified by using high-resolution oligonucleotide-single nucleotide polymorphism array analysis Jia‐Chi Wang, Loretta W Mahon, Leslie Ross, Molecular Cytogenetics	2016	14

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