Author details

Full Name

Anastasia P Grigorenko

Affiliation

ORCID

Career Start Year

1996

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37153504	An Analysis of Genetic Predisposition to Hereditary Catalepsy in a Mouse Model of Neuropsychiatric Disorders Using Whole-Genome Sequencing Data.		2023
35159210	Neurodevelopmental Syndrome with Intellectual Disability, Speech Impairment, and Quadrupedia Is Associated with Glutamate Receptor Delta 2 Gene Defect.	Cells	2022
35526848	Studying of Molecular Regulation of Developmental Processes of Lower Metazoans Exemplified by Cnidaria Using High-Throughput Sequencing.	Biochemistry (Moscow)	2022
32117220	Dissection of the Human T-Cell Receptor Î³ Gene Repertoire in the Brain and Peripheral Blood Identifies Age- and Alzheimer's Disease-Associated Clonotype Profiles.	Frontiers in Immunology	2020
30970224	Epigenetic-genetic chromatin footprinting identifies novel and subject-specific genes active in prefrontal cortex neurons.	FASEB J	2019
31624234	Chromatin profiling of cortical neurons identifies individual epigenetic signatures in schizophrenia.	Transl Psychiatry	2019
27845203	Complete mitochondrial genome and evolutionary analysis of Turritopsis dohrnii, the "immortal" jellyfish with a reversible life-cycle.	Molecular Phylogenetics and Evolution	2017
28941465	Quantitative Analysis of L1-Retrotransposons in Alzheimer's Disease and Aging.	Biochemistry (Moscow)	2017
29137240	Mutational re-modeling of di-aspartyl intramembrane proteases: uncoupling physiologically-relevant activities from those associated with Alzheimer's disease.	Oncotarget	2017
26242992	Whole-genome sequencing identifies a novel ABCB7 gene mutation for X-linked congenital cerebellar ataxia in a large family of Mongolian ancestry.	European Journal of Human Genetics	2016
27216912	Whole exome sequencing links dental tumor to an autosomal-dominant mutation in ANO5 gene associated with gnathodiaphyseal dysplasia and muscle dystrophies.	Scientific Reports	2016
25480889	Epigenetic dysregulation of hairy and enhancer of split 4 (HES4) is associated with striatal degeneration in postmortem Huntington brains.	Hum Mol Genet	2015
24847885	The ctenophore genome and the evolutionary origins of neural systems.	Nature	2014
23390425	Studying micro RNA Function and Dysfunction in Alzheimer's Disease.	Frontiers in Genetics	2012
20873220	[Analysis of clusterin gene (CLU/APOJ) polymorphism in Alzheimer's disease patients and in normal cohorts from Russian populations].	Molekulyarnaya Biologiya	2010
19815722	Genotype analysis identifies the cause of the "royal disease".	Science	2009
22649615	Achievements and peculiarities in studies of ancient DNA and DNA from complicated forensic specimens.	Acta Naturae	2009
19251637	Genomic identification in the historical case of the Nicholas II royal family.	Proceedings of the National Academy of Sciences of the United States of America	2009
18632683	A set of differentially expressed miRNAs, including miR-30a-5p, act as post-transcriptional inhibitors of BDNF in prefrontal cortex.	Human Molecular Genetics	2008
18988525	[Human microRNA in norm and pathology].	Molekulyarnaya Biologiya	2008
17514900	[Molecular basics of Alzheimer's disease].	Molekulyarnaya Biologiya	2007
17564961	Conversion and compensatory evolution of the gamma-crystallin genes and identification of a cataractogenic mutation that reverses the sequence of the human CRYGD gene to an ancestral state.	American Journal of Human Genetics	2007
17095700	Human hair growth deficiency is linked to a genetic defect in the phospholipase gene LIPH.	Science	2006
16448217	Complete mitochondrial genome and phylogeny of Pleistocene mammoth Mammuthus primigenius.	PLoS Biology	2006
16446740	Polymorphism in the 5'-promoter region of serine racemase gene in schizophrenia.	Molecular Psychiatry	2006
14741365	Impas 1 possesses endoproteolytic activity against multipass membrane protein substrate cleaving the presenilin 1 holoprotein.	FEBS Letters	2004
15469912	The Caenorhabditis elegans IMPAS gene, imp-2, is essential for development and is functionally distinct from related presenilins.	Proceedings of the National Academy of Sciences of the United States of America	2004
12943504	Effects of human presenilin 1 isoforms on proliferation and survival of rat pheochromocytoma cell line PC12.	Biochemistry (Moscow)	2003
12884513	[Loach spermatozoa transfer foreign DNA, which expression is discovered in the early development stages].	Genetika	2003
12139484	Novel class of polytopic proteins with domains associated with putative protease activity.	Biochemistry (Moscow)	2002
12232783	Regulatory region variability in the human presenilin-2 (PSEN2) gene: potential contribution to the gene activity and risk for AD.	Mol Psychiatry	2002
10477119	Alpha-2 macroglobulin gene in early- and late-onset Alzheimer disease.	Neurosci Lett	1999
9102356	[Expression of the CMV-lacZ- and RSV-lacZ-genes in transgenic fish and mouse embryos].	Genetika	1996