Ian McLaughlin - Concepedia

Author

Ian McLaughlin

Pacific Biosciences (United States)ORCID

Also Known As

I. McLaughlin, I.J. McLaughlin, Ian J McLaughlin, Ian J. McLaughlin, Ian McLaughlin, Ian Mclaughlin, Laird-Metke, Elisa, Primo Bayabyan

Publications

614

Citations

H-Index

Concepts

All Affiliations

Pacific Biosciences (United States)Mayo Clinic in Florida Mayo Clinic in Arizona Stanford University Mayo Clinic

About

Ian McLaughlin is an author at Pacific Biosciences (United States) specializing in medicine, genetics, and genomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	361
2	Biology	2	2	48
3	Engineering	1	1	65
4	Natural Sciences	1	1	65
5	Public Health	1	1	21

Ian McLaughlin

Publications

592

Citations

H-Index

Page 1

	Year	Citations
Does Blood of Healthy Subjects Contain Bacterial Ribosomal DNA? Simo Nikkari, Ian McLaughlin, Wanli Bi, Journal of Clinical Microbiology Ribosomal DnaPolymerase Chain ReactionMedical MicrobiologyMedicineBlood Specimens	2001	259
Long-read sequencing across the C9orf72 ‘GGGGCC’ repeat expansion: implications for clinical use and genetic discovery efforts in human disease Mark Ebbert, Stefan L. Farrugia, Jonathon Sens, Molecular Neurodegeneration	2018	127
Some Comments on a Formal Theory of Photochemical Dissociation Reactions Stuart A. Rice, Ian McLaughlin, Joshua Jortner The Journal of Chemical Physics EngineeringExcitation Energy TransferComputational ChemistryChemistryFormal Theory	1968	65
Long-read targeted sequencing uncovers clinicopathological associations for<i>C9orf72</i>-linked diseases Mariely DeJesus‐Hernandez, Ross A. Aleff, Jazmyne L. Jackson, Brain	2021	29
ATTCT and ATTCC repeat expansions in the ATXN10 gene affect disease penetrance of spinocerebellar ataxia type 10 C. Alejandra Morato Torres, Faria Zafar, Yu‐Chih Tsai, Human Genetics and Genomics Advances Genetic DisorderMedicineGeneticsDegenerative DiseaseNeurology	2022	29
Synchronized long-read genome, methylome, epigenome and transcriptome profiling resolve a Mendelian condition Mitchell R. Vollger, Jonas Korlach, Kiara C. Eldred, Nature Genetics BiologyBioinformaticsChromatinLong-read GenomeMendelian Disorder	2025	27
Amplification-free long-read sequencing of TCF4 expanded trinucleotide repeats in Fuchs Endothelial Corneal Dystrophy Eric D. Wieben, Ross A. Aleff, Shubham Basu, PLoS ONE Ocular DiseaseCag ExpansionsElderly PatientsGeneticsMolecular Biology	2019	25
<scp>MR1</scp> encompasses at least six allele groups with coding region alterations Erik H. Rozemuller, Sidonia B. G. Eckle, Ian McLaughlin, HLA HlaHistocompatibilityGeneticsHla ImmunogeneticsGenetic Epidemiology	2021	21
Validated assays for the quantification of C9orf72 human pathology Sally Salomonsson, A. M. Maltos, Kamaljot Gill, Scientific Reports	2024	10

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