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.
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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)
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)
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.
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)
Homologous Association of Oppositely Imprinted Chromosomal Domains
Janine M. LaSalle;Marc Lalande.
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)
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)
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)
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)
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)
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