A. Sano

发表

The Val66Met polymorphism of the brain‐derived neurotrophic factor gene is associated with psychotic feature and suicidal behavior in Japanese major depressive patients

Hongwei Song, T. Ohmori, K. Hokoishi, 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

The human serotonin transporter gene linked polymorphism (5-HTTLPR) shows ten novel allelic variants

H. Tanabe, A. Sano, M. Nakamura, 2000, Molecular Psychiatry.

Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy

Koji Abe, Sumio Sugano, Akio Ikeda, 2018, Nature Genetics.

A gene‐targeted mouse model for chorea‐acanthocytosis

Daisuke Sato, Kenji Nakamura, M. Katsuki, 2005, Journal of neurochemistry.

Working Memory-Related Prefrontal Hemodynamic Responses in University Students: A Correlation Study of Subjective Well-Being and Lifestyle Habits

A. Sano, Masayuki Nakamura, C. Koriyama, 2019, Front. Behav. Neurosci..

Mitochondrial DNA deletion mutations in patients with neuropsychiatric symptoms

A. Sano, S. Ueno, I. Higuchi, 2011, Neuroscience Research.

Different Clinical Phenotypes in Siblings with a Presenilin-1 P264L Mutation

S. Fujita, K. Takeuchi, A. Sano, 2012, Dementia and Geriatric Cognitive Disorders.

Sleep Disorders in Four Patients With Myotonic Dystrophy Type 1

A. Sano, Masayuki Nakamura, T. Ishizuka, 2020, Frontiers in Neurology.

A Case of Metabolic Syndrome with the Change of Ultrasonogram of the Pancreas

T. Oki, A. Sano, Hiroaki Kobayashi, 2017 .

Predictive validity of the Japanese version of Postpartum Depression Predictors Inventory-Revised (PDPI-R) during pregnancy and the postpartum period

T. Douchi, T. Oki, A. Sano, 2016 .

A patient with McLeod syndrome showing involvement of the central sensorimotor tracts for the legs

M. Abe, H. Matsumoto, Y. Ugawa, 2019, BMC Neurology.

Association of the TaqI A polymorphism of the dopamine D(2) receptor gene with predisposition to neuroleptic malignant syndrome.

N. Yasui-Furukori, K. Otani, A. Suzuki, 2001, The American journal of psychiatry.

Identification of a novel polymorphism of the human dopamine transporter (DAT1) gene and the significant association with alcoholism

T. Arinami, H. Tanabe, A. Sano, 1999, Molecular Psychiatry.

Association of the Taq I A Polymorphism of the Dopamine D 2 Receptor Gene With Predisposition to Neuroleptic Malignant Syndrome

N. Yasui-Furukori, K. Otani, A. Suzuki, 2001 .

Cytochrome P-450 2D6 gene polymorphism is not associated with neuroleptic malignant syndrome

K. Otani, S. Kaneko, A. Sano, 1996, Biological Psychiatry.

Chorein interacts with α‐tubulin and histone deacetylase 6, and overexpression preserves cell viability during nutrient deprivation in human embryonic kidney 293 cells

A. Sano, Natsuki Sasaki, Masayuki Nakamura, 2016, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Chorea-acanthocytosis with upper motor neuron degeneration and 3419_3420 delCA and 3970_3973 delAGTC VPS13A mutations

K. Wakabayashi, F. Mori, A. Sano, 2010, Acta Neuropathologica.

Phenotypic abnormalities in a chorea-acanthocytosis mouse model are modulated by strain background.

A. Sano, Masayuki Nakamura, H. Sakimoto, 2016, Biochemical and biophysical research communications.

Novel pathogenic XK mutations in McLeod syndrome and interaction between XK protein and chorein

Y. Ugawa, T. Murakami, A. Sano, 2019, Neurology: Genetics.

Novel pathogenic VPS13A gene mutations in Japanese patients with chorea-acanthocytosis

T. Fujii, Yuji Takahashi, H. Mochizuki, 2019, Neurology: Genetics.

Seizures as presenting and prominent symptom in chorea‐acanthocytosis with c.2343del VPS13A gene mutation

S. Berkovic, A. Korczyn, Manuela Pendziwiat, 2016, Epilepsia.

Chorein, the protein responsible for chorea-acanthocytosis, interacts with β-adducin and β-actin.

A. Sano, Natsuki Sasaki, Masayuki Nakamura, 2013, Biochemical and biophysical research communications.

Subcellular localization and putative role of VPS13A/chorein in dopaminergic neuronal cells.

M. Iijima, A. Sano, Masayuki Nakamura, 2012, Biochemical and biophysical research communications.

Novel pathogenic mutations and copy number variations in the VPS13A Gene in patients with chorea‐acanthocytosis

K. Kotschet, D. Babovic‐Vuksanovic, K. Wakabayashi, 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

In vivo distribution and localization of chorein.

S. Izumo, A. Sano, Masayuki Nakamura, 2007, Biochemical and biophysical research communications.

Chorea-acanthocytosis with a novel mutation in the vacuolar protein sorting 13 homolog a gene: A case report

Yoshihisa Ikeda, K. Iwasa, M. Yamada, 2020, Journal of the Neurological Sciences.

Chorea-Acanthocytosis with the Ehime-Deletion Mutation

Y. Maruki, M. Ikeda, K. Kamae, 2004 .

Differences in two mice strains on kainic acid-induced amygdalar seizures.

A. Sano, Masayuki Nakamura, Motofumi Kasugai, 2007, Biochemical and biophysical research communications.

Quetiapine-induced frequent premature ventricular contraction.

A. Sano, Masayuki Nakamura, Takehiro Hayashi, 2012, General hospital psychiatry.

Discriminating chorea-acanthocytosis from Huntington's disease with single-case voxel-based morphometry analysis

O. Abe, H. Matsuda, M. Ota, 2019, Journal of the Neurological Sciences.

Mouse model of chorea-acanthocytosis exhibits male infertility caused by impaired sperm motility as a result of ultrastructural morphological abnormalities in the mitochondrial sheath in the sperm midpiece.

A. Sano, Natsuki Sasaki, Masayuki Nakamura, 2018, Biochemical and biophysical research communications.

Clinical and molecular genetic assessment of a chorea-acanthocytosis pedigree

A. Sano, Masayuki Nakamura, Y. Tomemori, 2007, Journal of the Neurological Sciences.

A new phenotype of chorea‐acanthocytosis with dilated cardiomyopathy and myopathy

Keiji Matsumoto, A. Sano, S. Ueno, 2007, Movement disorders : official journal of the Movement Disorder Society.

The gene encoding a newly discovered protein, chorein, is mutated in chorea-acanthocytosis

Y. Maruki, K. Kamae, H. Tanabe, 2001, Nature Genetics.

A PRIMPOL mutation and variants in multiple genes may contribute to phenotypes in a familial case with chronic progressive external ophthalmoplegia symptoms

Akira Sano, Masayuki Nakamura, A. Sano, 2020, Neuroscience Research.

Gene expression and association analysis of vascular endothelial growth factor in major depressive disorder

Hongwei Song, T. Ohmori, K. Hokoishi, 2007, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

Microarray comparative genomic hybridization analysis of 59 patients with schizophrenia

N. Niikawa, M. Itokawa, R. Hashimoto, 2008, Journal of Human Genetics.

Positional cloning and comprehensive mutation analysis identified a novel KDM2B mutation in a Japanese family with minor malformations, intellectual disability, and schizophrenia

A. Sano, S. Ueno, Natsuki Sasaki, 2021, Journal of Human Genetics.

Association of AKT1 haplotype with the risk of schizophrenia in Iranian population

M. R. Sargolzaee, K. Arimura, H. Najmabadi, 2006, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p

A. Sano, K. Umino, I. Kanazawa, 1994, Nature Genetics.

No association between the NDE1 gene and schizophrenia in the Japanese population

K. Ohi, R. Hashimoto, M. Takeda, 2008, Schizophrenia Research.

Transgenic mice harboring a full-length human mutant DRPLA gene exhibit age-dependent intergenerational and somatic instabilities of CAG repeats comparable with those in DRPLA patients.

I. Kanazawa, G. Sobue, T. Shimohata, 1999, Human molecular genetics.

Somatic mosaicism of CAG repeat in dentatorubral-pallidoluysian atrophy (DRPLA).

F. Hazama, A. Sano, S. Ueno, 1995, Human molecular genetics.

A unique origin and multistep process for the generation of expanded DRPLA triplet repeats.

I. Kanazawa, T. Miyashita, Koichiro Nakamura, 1996, Human molecular genetics.

Positional cloning and comprehensive mutation analysis of a Japanese family with lithium-responsive bipolar disorder identifies a novel DOCK5 mutation

A. Sano, S. Ueno, Masayuki Nakamura, 2020, Journal of Human Genetics.

Polymorphisms of the human homologue of the Drosophila white gene are associated with mood and panic disorders

S. Ueno, H. Tanabe, A. Sano, 1999, Molecular Psychiatry.

The silencer activity of the novel human serotonin transporter linked polymorphic regions

Y. Shirai, N. Saito, A. Sano, 2002, Neuroscience Letters.

Familial Semantic Dementia with P301L Mutation in the Tau Gene

A. Sano, Masayuki Nakamura, M. Ichiba, 2011, Dementia and Geriatric Cognitive Disorders.

Positional Candidate Approach for the Gene Responsible for Benign Adult Familial Myoclonic Epilepsy

H. Tanabe, A. Sano, S. Ueno, 2002, Epilepsia.

Localization of a gene for benign adult familial myoclonic epilepsy to chromosome 8q23.3-q24.1.

Toshihiro Tanaka, H. Tanabe, A. Sano, 1999, American journal of human genetics.

Positive association of the PDE4B (phosphodiesterase 4B) gene with schizophrenia in the Japanese population.

Hongwei Song, M. Tomotake, T. Ohmori, 2008, Journal of psychiatric research.

Gene expression and association analyses of the phosphodiesterase 4B (PDE4B) gene in major depressive disorder in the Japanese population

T. Asada, H. Kunugi, M. Tomotake, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Adult‐type metachromatic leukodystrophy with compound heterozygous ARSA mutations: A case report and phenotypic comparison with a previously reported case

K. Arimura, A. Sano, Y. Okamoto, 2011, Psychiatry and clinical neurosciences.

DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA repeat expansion in TNRC6A

Y. Goto, S. Niwa, A. Sano, 2020, Journal of Human Genetics.

Psychiatric Morbidity in Neuroacanthocytosis

A. Sano, 2008 .

DNA analysis in hereditary dentatorubral-pallidoluysian atrophy

I. Kanazawa, M. Yamada, I. Kondo, 1995, Neurology.

Predicting postpartum depression by evaluating temperament during pregnancy.

T. Douchi, A. Sano, Hiroaki Kobayashi, 2021, Journal of affective disorders.

Gene expression and association analysis of LIM (PDLIM5) in major depression

Hongwei Song, K. Morita, K. Rokutan, 2006, Neuroscience Letters.

Comprehensive analysis of the genes responsible for neuroacanthocytosis in mood disorder and schizophrenia

A. Sano, S. Ueno, Masayuki Nakamura, 2011, Neuroscience Research.

Relationship between functional dopamine D2 and D3 receptors gene polymorphisms and neuroleptic malignant syndrome

K. Otani, A. Suzuki, S. Kaneko, 2003, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Remapping and mutation analysis of benign adult familial myoclonic epilepsy in a Japanese pedigree

A. Sano, S. Ueno, T. Yasuda, 2011, Journal of Human Genetics.

A. Sano, Masayuki Nakamura, Yuka Urata, 2023, The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry.

Exome sequencing identifies a novel missense variant in RRM2B associated with autosomal recessive progressive external ophthalmoplegia

S. Kanba, A. Takata, T. Yoshikawa, 2011, Genome Biology.

Brain-specific transcript variants of 5' and 3' ends of mouse VPS13A and VPS13C.

A. Sano, Masayuki Nakamura, M. Ichiba, 2007, Biochemical and biophysical research communications.

Chorein deficiency leads to upregulation of gephyrin and GABA(A) receptor.

S. Izumo, A. Sano, Masayuki Nakamura, 2006, Biochemical and biophysical research communications.

A Mouse Model of Chorea-Acanthocytosis

Y. Katoh, A. Sano, S. Ueno, 2008 .

The effects of olanzapine treatment on brain regional glucose metabolism in neuroleptic‐naive first‐episode schizophrenic patients

S. Fujita, K. Takeuchi, A. Sano, 2016, Human psychopharmacology.

Neurologic phenotypes associated with acanthocytosis

A. Danek, C. Dobson-Stone, F. Tison, 2007, Neurology.