Louise W. Gane - Concepedia

Author

Louise W. Gane

Also Known As

Guadalupe Mendoza-Morales, L Gane, L. Gane, L. W. Gane, L.W. Gane, LOUISE GANE, LOUISE W. GANE, Louise Gane, Louise W Gane, Louise W. Gane

Publications

5.1K

Citations

H-Index

Concepts

All Affiliations

University of California, Davis University of California Davis Medical Center Rush University Medical Center University of Colorado Denver University of Colorado Health

About

Louise W. Gane is an author at University of California, Davis specializing in medicine, fragile x spectrum, and fragile x premutation.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	18	2.3K
2	Social Sciences	3	3	169
3	Education	2	2	403
4	Public Health	2	2	45
5	Cell Biology	1	1	27

Louise W. Gane

Publications

3.8K

Citations

H-Index

Page 1

	Year	Citations
Elevated Levels of FMR1 mRNA in Carrier Males: A New Mechanism of Involvement in the Fragile-X Syndrome Flora Tassone, Randi J. Hagerman, Annette K. Taylor, The American Journal of Human Genetics Fragile-x SyndromeDevelopmental BiologyMendelian DisorderFmr1 MrnaGenetic Disorder	2000	764
Autism Spectrum Disorders and Attention-Deficit/Hyperactivity Disorder in Boys with the Fragile X Premutation Faraz Farzin, Hazel Perry, David Hessl, Journal of Developmental & Behavioral Pediatrics Autism Spectrum DisordersGeneticsDisabilityEducationNeurodiversity	2006	326
Fragile-X–Associated Tremor/Ataxia Syndrome (FXTAS) in Females with the FMR1 Premutation Randi J. Hagerman, Blair R. Leavitt, F. Farzin, The American Journal of Human Genetics Fragile X SpectrumRehabilitationNeurologyMotor DisorderNeuropathology	2004	325
FMR1 CGG allele size and prevalence ascertained through newborn screening in the United States Flora Tassone, Ka Pou Iong, Tzuhan Tong, Genome Medicine	2012	315
Abnormal elevation of<i>FMR1</i>mRNA is associated with psychological symptoms in individuals with the fragile X premutation David Hessl, Flora Tassone, Danuta Z. Loesch, American Journal of Medical Genetics Part B Neuropsychiatric Genetics	2005	232
Clinical involvement and protein expression in individuals with theFMR1 premutation Flora Tassone, Randi J. Hagerman, Annette K. Taylor, American Journal of Medical Genetics	2000	216
<i>FMR1</i> CGG repeat length predicts motor dysfunction in premutation carriers Maureen A. Leehey, Elizabeth Berry‐Kravis, Christopher G. Goetz, Neurology	2007	183
AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome Carolyn M. Yrigollen, Blythe Durbin‐Johnson, Louise W. Gane, Genetics in Medicine Fragile X SyndromeDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	2012	174
Psychiatric Phenotype of the Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS) in Males Susan Bacalman, Faraz Farzin, James A. Bourgeois, The Journal of Clinical Psychiatry	2006	171
Aging in Individuals With the FMR1 Mutation Sebastian Jacquemont, F. Farzin, Deborah A. Hall, American Journal on Mental Retardation AgingNeurological SyndromeNeurological DisorderGeneticsPathology	2004	152

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