Megan Martin - Concepedia

Author

Megan Martin

Lineage Cell Therapeutics (United States)ORCID

Also Known As

M MARTIN, M Martin, M. Martin, M. Martín, MEGAN MARTIN, Megan M Martin, Megan M. Martin, Megan Martin, Monica Pulido Martín, Mr. Justin Martin

Publications

595

Citations

H-Index

Concepts

All Affiliations

Lineage Cell Therapeutics (United States)University of Utah ARUP Laboratories (United States)Columbia University Irving Medical Center Georgia Institute of Technology

About

Megan Martin is an author at Lineage Cell Therapeutics (United States) specializing in genetics, medicine, and public health.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	192
2	Public Health	3	3	73
3	Health Sciences	2	2	118
4	Social Sciences	2	2	190
5	Engineering	1	1	10

Megan Martin

Publications

549

Citations

H-Index

Page 1

	Year	Citations
Neural correlates of the complexity of rhythmic finger tapping Mukeshwar Dhamala, Giuseppe Pagnoni, Kurt Wiesenfeld, NeuroImage Cognitive ScienceNeurodynamicsComputational NeuroscienceRhythmic FingerMotor Control	2003	108
Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders Karen S. Ho, E. Robert Wassman, Adrianne L. Baxter, International Journal of Molecular Sciences Consecutive IndividualsAutism Spectrum DisordersGeneticsPathologyDisease Gene Identification	2016	82
Limbic Hyperreactivity in Bipolar II Disorder Gregory S. Berns, Megan Martin, Shawnette M. Proper American Journal of Psychiatry	2002	50
Chromosomal microarray testing identifies a 4p terminal region associated with seizures in Wolf–Hirschhorn syndrome Karen S. Ho, Sarah T. South, Amanda Lortz, Journal of Medical Genetics	2016	49
Mosaic deletion of 20pter due to rescue by somatic recombination Megan Martin, Rena Vanzo, Mallory R. Sdano, American Journal of Medical Genetics Part A	2015	42
The Context of Uncertainty Modulates the Subcortical Response to Predictability Amanda Bischoff‐Grethe, Megan Martin, Hui Mao, Journal of Cognitive Neuroscience	2001	40
Variants of unknown significance on chromosomal microarray analysis: parental perspectives Stephanie Jez, Megan Martin, Sarah T. South, Journal of Community Genetics Genetic AnalysisUnknown SignificanceGenetic TestingGeneticsGenetic Epidemiology	2015	33
Familial KANK1 deletion that does not follow expected imprinting pattern Rena Vanzo, Megan Martin, Mallory R. Sdano, European Journal of Medical Genetics Gene Deletion DataDevelopmental BiologyGenetic DisorderGeneticsFamilial Kank1 Deletion	2013	24
Clinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders Karen J. Ho, Hope Twede, Rena Vanzo, BioMed Research International NeurogenomicsGeneticsGenetic EpidemiologyDisease Gene IdentificationEpigenetics	2016	23
Clinical significance of copy number variants involving KANK1 in patients with neurodevelopmental disorders Rena Vanzo, Hope Twede, Karen S. Ho, European Journal of Medical Genetics	2018	22

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