Gary J. Latham - Concepedia

Author

Gary J. Latham

Asuragen (United States)ORCID

Also Known As

G. Latham, G.J. Latham, Gary J Latham, Gary J. Latham, Gary Latham, Latham, G, Latham, Gary J.

Publications

3.6K

Citations

H-Index

Concepts

All Affiliations

Asuragen (United States)University of Oregon University of California, Davis The University of Texas Medical Branch at Galveston New York State Office for People With Developmental Disabilities

About

Gary J. Latham is an author at Asuragen (United States) specializing in medicine, molecular biology, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	13	1.6K
2	Natural Sciences	5	5	164
3	Engineering	2	2	988
4	Health Sciences	2	2	185
5	Public Health	1	1	177

Gary J. Latham

Publications

3.4K

Citations

H-Index

Page 1

	Year	Citations
Normalization of microRNA expression levels in quantitative RT-PCR assays: Identification of suitable reference RNA targets in normal and cancerous human solid tissues Heidi J. Peltier, Gary J. Latham RNA EngineeringPathologyRigorous NormalizationQuantitative Rt-pcr AssaysProper Normalization	2008	796
A Novel FMR1 PCR Method for the Routine Detection of Low Abundance Expanded Alleles and Full Mutations in Fragile X Syndrome Stela Filipovic-Sadic, Sachin Sah, Liangjing Chen, Clinical Chemistry	2010	272
Activation of the <i>NOTCH</i> Pathway in Head and Neck Cancer Wenyue Sun, Daria A. Gaykalova, Michael F. Ochs, Cancer Research	2013	199
Targeted, High-Depth, Next-Generation Sequencing of Cancer Genes in Formalin-Fixed, Paraffin-Embedded and Fine-Needle Aspiration Tumor Specimens Andrew G. Hadd, Jeff Houghton, Ashish Choudhary, Journal of Molecular Diagnostics Tumor BiologySystems BiologyOncologyEngineeringTumor Heterogeneity	2013	192
An Information-Rich CGG Repeat Primed PCR That Detects the Full Range of Fragile X Expanded Alleles and Minimizes the Need for Southern Blot Analysis Liangjing Chen, Andrew G. Hadd, Sachin Sah, Journal of Molecular Diagnostics Genetic AnalysisAllelic VariantFull RangeGeneticsFragile X Spectrum	2010	177
Fragile X full mutation expansions are inhibited by one or more AGG interruptions in premutation carriers Sarah L. Nolin, Anne Glicksman, Nicole Ersalesi, Genetics in Medicine	2014	135
Fragile X AGG analysis provides new risk predictions for 45–69 repeat alleles Sarah L. Nolin, Sachin Sah, Anne Glicksman, American Journal of Medical Genetics Part A	2013	124
AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission Carolyn M. Yrigollen, Loreto Martorell, Blythe Durbin‐Johnson, Journal of Neurodevelopmental Disorders	2014	109
Functional DNA quantification guides accurate next-generation sequencing mutation detection in formalin-fixed, paraffin-embedded tumor biopsies Sachin Sah, Liangjing Chen, Jeffrey Houghton, Genome Medicine Mutation DetectionDna AnalysisPathologyHigh Throughput SequencingTumor Biology	2013	98
High-resolution methylation polymerase chain reaction for fragile X analysis: Evidence for novel FMR1 methylation patterns undetected in Southern blot analyses Liangjing Chen, Andrew G. Hadd, Sachin Sah, Genetics in Medicine ChromatinFragile X AnalysisEpigenetic ChangeGeneticsFragile X Spectrum	2011	91

Page 1