User profiles for "author:Tatsuhiko Naito"
Tatsuhiko NaitoIcahn School of Medicine at Mount Sinai Verified email at umin.ac.jp Cited by 420 |
[HTML][HTML] HLA imputation and its application to genetic and molecular fine-mapping of the MHC region in autoimmune diseases
Variations of human leukocyte antigen (HLA) genes in the major histocompatibility complex
region (MHC) significantly affect the risk of various diseases, especially autoimmune …
region (MHC) significantly affect the risk of various diseases, especially autoimmune …
Effects of mindfulness training on posttraumatic growth: A systematic review and meta-analysis
MP Shiyko, S Hallinan, T Naito - Mindfulness, 2017 - Springer
Posttraumatic growth (PTG) is a process of personal transformation following a traumatic life
event in domains of life appreciation, interpersonal relationships, recognition of personal …
event in domains of life appreciation, interpersonal relationships, recognition of personal …
[HTML][HTML] DOCK2 is involved in the host genetics and biology of severe COVID-19
H Namkoong, R Edahiro, T Takano, H Nishihara… - Nature, 2022 - nature.com
Identifying the host genetic factors underlying severe COVID-19 is an emerging challenge,,,–
. Here we conducted a genome-wide association study (GWAS) involving 2,393 cases of …
. Here we conducted a genome-wide association study (GWAS) involving 2,393 cases of …
[HTML][HTML] A deep learning method for HLA imputation and trans-ethnic MHC fine-mapping of type 1 diabetes
Conventional human leukocyte antigen (HLA) imputation methods drop their performance
for infrequent alleles, which is one of the factors that reduce the reliability of trans-ethnic …
for infrequent alleles, which is one of the factors that reduce the reliability of trans-ethnic …
[HTML][HTML] Multifaceted analysis of cross-tissue transcriptomes reveals phenotype–endotype associations in atopic dermatitis
A Sekita, H Kawasaki, A Fukushima-Nomura… - Nature …, 2023 - nature.com
Atopic dermatitis (AD) is a skin disease that is heterogeneous both in terms of clinical
manifestations and molecular profiles. It is increasingly recognized that AD is a systemic …
manifestations and molecular profiles. It is increasingly recognized that AD is a systemic …
Multiancestry analysis of the HLA locus in Alzheimer's and Parkinson's diseases uncovers a shared adaptive immune response mediated by HLA-DRB1*04 subtypes
Across multiancestry groups, we analyzed Human Leukocyte Antigen (HLA) associations in
over 176,000 individuals with Parkinson's disease (PD) and Alzheimer's disease (AD) …
over 176,000 individuals with Parkinson's disease (PD) and Alzheimer's disease (AD) …
Trans‐Ethnic Fine‐Mapping of the Major Histocompatibility Complex Region Linked to Parkinson's Disease
Background Despite evidence for the role of human leukocyte antigen (HLA) in the genetic
predisposition to Parkinson's disease (PD), the complex haplotype structure and highly …
predisposition to Parkinson's disease (PD), the complex haplotype structure and highly …
[HTML][HTML] The whole blood transcriptional regulation landscape in 465 COVID-19 infected samples from Japan COVID-19 Task Force
QS Wang, R Edahiro, H Namkoong… - Nature …, 2022 - nature.com
Abstract Coronavirus disease 2019 (COVID-19) is a recently-emerged infectious disease
that has caused millions of deaths, where comprehensive understanding of disease …
that has caused millions of deaths, where comprehensive understanding of disease …
[HTML][HTML] Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative
Host genetics is a key determinant of COVID-19 outcomes. Previously, the COVID-19 Host
Genetics Initiative genome-wide association study used common variants to identify multiple …
Genetics Initiative genome-wide association study used common variants to identify multiple …
[PDF][PDF] Genome-wide association study identifies risk loci within the major histocompatibility complex region for Hunner-type interstitial cystitis
Hunner-type interstitial cystitis (HIC) is a rare, chronic inflammatory disease of the urinary
bladder with unknown etiology and genetic background. Here, we conduct a genome-wide …
bladder with unknown etiology and genetic background. Here, we conduct a genome-wide …