Janine M. LaSalle

University of California, Davis
United States

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name Citations Publications World Ranking National Ranking

Genetics D-index 61 Citations 10,162 156 World Ranking 2291 National Ranking 1017

Overview

What are the main themes of her work throughout her whole career to date

Her primary areas of investigation include Genetics. She integrates many fields, such as Gene and Gene isoform, in her works. Gene isoform and Gene are two areas of study in which Janine M. LaSalle engages in interdisciplinary work. Rett syndrome and MECP2 are two areas of study in which she engages in interdisciplinary research. In her works, she undertakes multidisciplinary study on MECP2 and Rett syndrome. Janine M. LaSalle performs multidisciplinary study in Phenotype and Genetics in her work. Janine M. LaSalle performs integrative study on Mutation and Phenotype. Exon and Mutation are two areas of study in which she engages in interdisciplinary work. Bisulfite sequencing and Differentially methylated regions are two areas of study in which Janine M. LaSalle engages in interdisciplinary research.

Janine M. LaSalle most often published in these fields:

Gene (100.00%)
Genetics (100.00%)
Rett syndrome (50.00%)

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Best Publications

Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3

Rodney C. Samaco;Amber Hogart;Janine M. LaSalle.
Human Molecular Genetics (2005)

492 Citations

Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes

Dag H. Yasui;Sailaja Peddada;Mark C. Bieda;Roxanne O. Vallero.
Proceedings of the National Academy of Sciences of the United States of America (2007)

426 Citations

Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation.

Raman P Nagarajan;Amber R Hogart;Ynnez Gwye;Michelle R Martin.
Epigenetics (2006)

365 Citations

Rett Syndrome Astrocytes Are Abnormal and Spread MeCP2 Deficiency through Gap Junctions

Izumi Maezawa;Susan Swanberg;Danielle J Harvey;Janine M LaSalle.
The Journal of Neuroscience (2009)

310 Citations

Homologous Association of Oppositely Imprinted Chromosomal Domains

Janine M. LaSalle;Marc Lalande.
Science (1996)

304 Citations

The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13

Amber Hogart;David Wu;Janine M. LaSalle;N. Carolyn Schanen;N. Carolyn Schanen;N. Carolyn Schanen.
Neurobiology of Disease (2010)

303 Citations

RAB22 and RAB163/mouse BRCA2: Proteins that specifically interact with the RAD51 protein

Ryushin Mizuta;Janine M. LaSalle;Hwei Ling Cheng;Akira Shinohara.
Proceedings of the National Academy of Sciences of the United States of America (1997)

295 Citations

The human placenta methylome

Diane I. Schroeder;John D. Blair;Paul Lott;Hung On Ken Yu.
Proceedings of the National Academy of Sciences of the United States of America (2013)

274 Citations

15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders

Amber Hogart;Raman P. Nagarajan;Katherine A. Patzel;Dag H. Yasui.
Human Molecular Genetics (2007)

259 Citations

Small-Magnitude Effect Sizes in Epigenetic End Points are Important in Children's Environmental Health Studies: The Children's Environmental Health and Disease Prevention Research Center's Epigenetics Working Group.

Carrie V. Breton;Carmen J. Marsit;Elaine Faustman;Kari Nadeau;Kari Nadeau.
Environmental Health Perspectives (2017)

252 Citations

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