Gary J. Latham

3.6k total citations · 1 hit paper
52 papers, 2.7k citations indexed

About

Gary J. Latham is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Gary J. Latham has authored 52 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 23 papers in Genetics and 16 papers in Cancer Research. Recurrent topics in Gary J. Latham's work include Genetics and Neurodevelopmental Disorders (17 papers), Autism Spectrum Disorder Research (12 papers) and DNA Repair Mechanisms (10 papers). Gary J. Latham is often cited by papers focused on Genetics and Neurodevelopmental Disorders (17 papers), Autism Spectrum Disorder Research (12 papers) and DNA Repair Mechanisms (10 papers). Gary J. Latham collaborates with scholars based in United States, Italy and United Kingdom. Gary J. Latham's co-authors include Heidi J. Peltier, Andrew G. Hadd, Sachin Sah, Liangjing Chen, Flora Tassone, R. Stephen Lloyd, Stela Filipovic-Sadic, Peter H. von Hippel, Paul J. Hagerman and Paola Pietroni and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Gary J. Latham

50 papers receiving 2.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Normalization of microRNA expression levels in quantitative RT-PCR assays: Identification of suitable reference RNA targets in normal and cancerous human solid tissues

2008 682 citations Heidi J. Peltier, Gary J. Latham RNA profile →

Peers

Gary J. Latham

GENET

ONCOL

Scott A. Tenenbaum United States

Giovanni Stefani United States

Kirk B. Jensen United States

Shaun Webb United Kingdom

Ingrid Maurer-Fogy Austria

Guy Froyen Belgium

Peter J. Skene United States

Ru Cao United States

John J. Schwarz United States

H.F. Willard United States

Scott A. Tenenbaum United States

Gary J. Latham

3.3k ×1.7

783 ×0.7

GENET

518 ×0.5

252 ×0.4

157 ×0.9

ONCOL

Citations per year, relative to Gary J. Latham Gary J. Latham (= 1×) peers Scott A. Tenenbaum

Countries citing papers authored by Gary J. Latham

Since Specialization

Citations

This map shows the geographic impact of Gary J. Latham's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Gary J. Latham with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gary J. Latham more than expected).

Fields of papers citing papers by Gary J. Latham

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gary J. Latham. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Gary J. Latham. The network helps show where Gary J. Latham may publish in the future.

Co-authorship network of co-authors of Gary J. Latham

This figure shows the co-authorship network connecting the top 25 collaborators of Gary J. Latham. A scholar is included among the top collaborators of Gary J. Latham based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Gary J. Latham. Gary J. Latham is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Hall, B. D., et al.. (2025). A Dual-Mode Targeted Nanopore Sequencing Assay for Comprehensive SMN1 and SMN2 Variant Analysis. Journal of Molecular Diagnostics. 27(6). 502–510.

Milligan, John N., Jessica L. Larson, Stela Filipovic-Sadic, et al.. (2021). Multisite Evaluation and Validation of a Sensitive Diagnostic and Screening System for Spinal Muscular Atrophy that Reports SMN1 and SMN2 Copy Number, along with Disease Modifier and Gene Duplication Variants. Journal of Molecular Diagnostics. 23(6). 753–764. 6 indexed citations

Nolin, Sarah L., Anne Glicksman, Emily G. Allen, et al.. (2019). Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation alleles. American Journal of Medical Genetics Part A. 179(7). 1148–1156. 47 indexed citations

Lee, Stacey, Jennifer Taylor, Andrew G. Hadd, et al.. (2019). Validation of Fragile X Screening in the Newborn Population Using a Fit-for-Purpose FMR1 PCR Assay System. Journal of Molecular Diagnostics. 22(3). 346–354. 8 indexed citations

Blidner, Richard, Brian C. Haynes, Stephen Hyter, et al.. (2018). Design, Optimization, and Multisite Evaluation of a Targeted Next-Generation Sequencing Assay System for Chimeric RNAs from Gene Fusions and Exon-Skipping Events in Non–Small Cell Lung Cancer. Journal of Molecular Diagnostics. 21(2). 352–365. 10 indexed citations

Zhu, Huiping, S. Gokul, & Gary J. Latham. (2018). P3.09-20 A Simple and Versatile Next-Generation Sequencing Technology for Co-Detection of RNA Structural Variants and DNA Mutations in Lung Cancer. Journal of Thoracic Oncology. 13(10). S955–S956. 1 indexed citations

Chen, Xiaoli, Jingmin Wang, Hua Xie, et al.. (2015). Fragile X syndrome screening in Chinese children with unknown intellectual developmental disorder. BMC Pediatrics. 15(1). 77–77. 10 indexed citations

Pretto, Dalyir, Joyce Lo, Ru Cao, et al.. (2014). CGG allele size somatic mosaicism and methylation in FMR1 premutation alleles. Journal of Medical Genetics. 51(5). 309–318. 66 indexed citations

Latham, Gary J., Justine Coppinger, Andrew G. Hadd, & Sarah L. Nolin. (2014). The role of AGG interruptions in fragile X repeat expansions: a twenty-year perspective. Frontiers in Genetics. 5. 244–244. 42 indexed citations

10.

Yrigollen, Carolyn M., Loreto Martorell, Blythe Durbin‐Johnson, et al.. (2014). AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission. Journal of Neurodevelopmental Disorders. 6(1). 24–24. 82 indexed citations

11.

Nolin, Sarah L., Sachin Sah, Anne Glicksman, et al.. (2013). Fragile X AGG analysis provides new risk predictions for 45–69 repeat alleles. American Journal of Medical Genetics Part A. 161(4). 771–778. 99 indexed citations

12.

Sah, Sachin, et al.. (2013). Functional DNA quantification guides accurate next-generation sequencing mutation detection in formalin-fixed, paraffin-embedded tumor biopsies. Genome Medicine. 5(8). 77–77. 67 indexed citations

13.

Hadd, Andrew G., Ashish Choudhary, Sachin Sah, et al.. (2013). Targeted, High-Depth, Next-Generation Sequencing of Cancer Genes in Formalin-Fixed, Paraffin-Embedded and Fine-Needle Aspiration Tumor Specimens. Journal of Molecular Diagnostics. 15(2). 234–247. 141 indexed citations

14.

Latham, Gary J.. (2010). Normalization of MicroRNA Quantitative RT-PCR Data in Reduced Scale Experimental Designs. Methods in molecular biology. 667. 19–31. 52 indexed citations

15.

Peltier, Heidi J., Bin Lü, Manoj Bhasin, et al.. (2008). Gene expression profile of mouse prostate tumors reveals dysregulations in major biological processes and identifies potential murine targets for preclinical development of human prostate cancer therapy. The Prostate. 68(14). 1517–1530. 29 indexed citations

16.

Peltier, Heidi J. & Gary J. Latham. (2008). Normalization of microRNA expression levels in quantitative RT-PCR assays: Identification of suitable reference RNA targets in normal and cancerous human solid tissues. RNA. 14(5). 844–852. 682 indexed citations breakdown →

17.

Feng, Dong, et al.. (1999). Interactions of Bacteriophage T4-coded Primase (gp61) with the T4 Replication Helicase (gp41) and DNA in Primosome Formation. Journal of Biological Chemistry. 274(38). 27287–27298. 28 indexed citations

18.

Pietroni, Paola, Mark C. Young, Gary J. Latham, & Peter H. von Hippel. (1997). Structural Analyses of gp45 Sliding Clamp Interactions during Assembly of the Bacteriophage T4 DNA Polymerase Holoenzyme. Journal of Biological Chemistry. 272(50). 31666–31676. 45 indexed citations

19.

Latham, Gary J., et al.. (1997). Structural Analyses of gp45 Sliding Clamp Interactions during Assembly of the Bacteriophage T4 DNA Polymerase Holoenzyme. Journal of Biological Chemistry. 272(50). 31685–31692. 29 indexed citations

20.

Latham, Gary J., Constance M. Harris, Thomas M. Harris, & R. Stephen Lloyd. (1995). The Efficiency of Translesion Synthesis Past Single Styrene Oxide DNA Adducts in Vitro Is Polymerase-Specific. Chemical Research in Toxicology. 8(3). 422–430. 17 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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