Akira Narita

ORCID: 0000-0002-9076-0710
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About
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Research Areas
  • Genetic Associations and Epidemiology
  • Metabolomics and Mass Spectrometry Studies
  • Antibiotics Pharmacokinetics and Efficacy
  • Birth, Development, and Health
  • Nutritional Studies and Diet
  • Genetic and phenotypic traits in livestock
  • Genetic Mapping and Diversity in Plants and Animals
  • Pharmaceutical studies and practices
  • Advanced Chemical Physics Studies
  • Neonatal Health and Biochemistry
  • Sodium Intake and Health
  • Nutrition, Genetics, and Disease
  • Posttraumatic Stress Disorder Research
  • Metabolism and Genetic Disorders
  • Genomic variations and chromosomal abnormalities
  • Disaster Response and Management
  • Health, Environment, Cognitive Aging
  • Health disparities and outcomes
  • Liver Disease Diagnosis and Treatment
  • Rare-earth and actinide compounds
  • Pregnancy and preeclampsia studies
  • Bioinformatics and Genomic Networks
  • Advanced Physical and Chemical Molecular Interactions
  • Blood Pressure and Hypertension Studies
  • Gestational Diabetes Research and Management

Tohoku Medical Megabank Organization
2015-2025

Tohoku University
2015-2025

Tokyo High School
1991-2021

Tokyo Institute of Technology
2021

Japanese Red Cross Narita Hospital
2018-2019

Akira (France)
2018-2019

South Texas Accelerated Research Therapeutics
2017

Start Treatment & Recovery Centers
2017

Start
2016

Nagoya University
2014

Background: We established a community-based cohort study to assess the long-term impact of Great East Japan Earthquake on disaster victims and gene-environment interactions incidence major diseases, such as cancer cardiovascular diseases.

10.2188/jea.je20190271 article EN cc-by Journal of Epidemiology 2020-01-10
Fumihiko Takeuchi Masato Akiyama Nana Matoba Tomohiro Katsuya Masahiro Nakatochi and 95 more Yasuharu Tabara Akira Narita Woei‐Yuh Saw Sanghoon Moon Cassandra N. Spracklen Jin Fang Chai Young‐Jin Kim Liang Zhang Chaolong Wang Huaixing Li Honglan Li Jer‐Yuarn Wu Rajkumar Dorajoo Jovia L. Nierenberg Ya Xing Wang Jing He Derrick Bennett Atsushi Takahashi Yukihide Momozawa Makoto Hirata Koichi Matsuda Hiromi Rakugi Eitaro Nakashima Masato Isono Matsuyuki Shirota Atsushi Hozawa Sahoko Ichihara Tatsuaki Matsubara Ken Yamamoto Katsuhiko Kohara Michiya Igase Sohee Han Penny Gordon‐Larsen Wei Huang Sang Lee Linda S. Adair Mi Yeong Hwang Juyoung Lee Miao Li Chee Charumathi Sabanayagam Wanting Zhao Jianjun Liu Dermot F. Reilly Liang Sun Shaofeng Huo Todd L. Edwards Jirong Long Li-Ching Chang Chien-Hsiun Chen Jian‐Min Yuan Woon‐Puay Koh Yechiel Friedlander Tanika N. Kelly Wen Bin Wei Liang Xu Hui Cai Yong‐Bing Xiang Kuang Lin Robert Clarke Robin Walters Iona Y. Millwood Liming Li John C. Chambers Jaspal S. Kooner Paul Elliott Pim van der Harst Marie Loh Niek Verweij Weihua Zhang Benjamin Lehne Irene Mateo Leach Alexander Drong James Abbott Han Sun William R. Scott Gianluca Campanella Marc Chadeau‐Hyam Uzma Afzal Tõnu Esko Sarah E. Harris Jaana Hartiala Marcus E. Kleber Richa Saxena Alexandre F.R. Stewart Tarunveer S. Ahluwalia Imke Aits Alexessander Couto Alves Shikta Das Jemma C. Hopewell Robert W. Koivula Leo‐Pekka Lyytikäinen Iris Postmus Olli Raitakari Robert A. Scott Rossella Sorice

Abstract Blood pressure (BP) is a major risk factor for cardiovascular disease and more than 200 genetic loci associated with BP are known. Here, we perform multi-stage genome-wide association study (max N = 289,038) principally in East Asians meta-analysis Europeans. We report 19 new ancestry-specific variants, conforming to common variant model. At 10 unique loci, distinct non-rare variants colocalize within the same linkage disequilibrium block despite significantly discordant effects...

10.1038/s41467-018-07345-0 article EN cc-by Nature Communications 2018-11-22
Konstantinos Hatzikotoulas Lorraine Southam Lilja Stefánsdóttir Cindy G. Boer Merry‐Lynn McDonald and 95 more J. Patrick Pett Young‐Chan Park Margo Tuerlings Rick Mulders Andrei Barysenka Ana Luiza Arruda Vinicius Tragante Alison Rocco Norbert Bittner Shibo Chen Susanne Horn Vinodh Srinivasasainagendra Ken To Georgia Katsoula Peter Kreitmaier Amabel Tenghe Arthur Gilly Liubov Arbeeva Lane G. Chen Agathe de Pins Daniel Dochtermann Cecilie Henkel Jonas Höijer Shuji Ito Penelope A. Lind Bitota Lukusa-Sawalena Aye Ko Ko Minn Marina Mola-Caminal Akira Narita Chelsea Nguyen Ene Reimann Micah Silberstein Anne Heidi Skogholt Hemant K. Tiwari Michelle S. Yau Ming Yue Wei Zhao Jin Zhou George Alexiadis Karina Banasik Søren Brunak Archie Campbell Jackson T S Cheung Joseph Dowsett Tariq Faquih Jessica D. Faul Lijiang Fei Anne Marie Fenstad Takamitsu Funayama Maiken E. Gabrielsen Chinatsu Gocho Kirill Gromov Thomas Hansen Georgi Hudjashov Þorvaldur Ingvarsson Jessica Johnson Helgi Jónsson Saori Kakehi Juha Karjalainen Elisa Kasbohm Susanna Lemmelä Kuang Lin Xiaoxi Liu M. Loef Massimo Mangino Daniel L. McCartney Iona Y. Millwood Joshua Richman Mary B. Roberts Kathleen A. Ryan Dino Samartzis Manu Shivakumar Søren Thorgaard Skou Sachiyo Sugimoto Ken Suzuki Hiroshi Takuwa Maris Teder‐Laving Laurent F. Thomas Kohei Tomizuka Constance Turman Stefan Weiß Tian Wu Eleni Zengini Yanfei Zhang Manuel A. R. Ferreira George C. Babis Aris Baras Tyler Barker David J. Carey Kathryn S.E. Cheah Zhengming Chen Jason Pui Yin Cheung Mark Daly Renée de Mutsert Charles B. Eaton

Abstract Osteoarthritis is the third most rapidly growing health condition associated with disability, after dementia and diabetes 1 . By 2050, total number of patients osteoarthritis estimated to reach billion worldwide 2 As no disease-modifying treatments exist for osteoarthritis, a better understanding disease aetiopathology urgently needed. Here we perform genome-wide association study meta-analyses across up 489,975 cases 1,472,094 controls, establishing 962 independent associations,...

10.1038/s41586-025-08771-z article EN cc-by Nature 2025-04-09

The existence of familial aggregation mandibular prognathism (MP) suggests that genetic components play an important role in its etiology. In this study, a genome-wide linkage analysis to identify loci susceptible MP was conducted with 90 affected sibling-pairs 42 families, comprised 40 Korean and 50 Japanese sibling-pairs. Two non-parametric analyses, GENEHUNTER-PLUS SIBPAL, were applied detected nominal statistical significance at chromosomes 1p36, 6q25, 19p13.2. best evidence near D1S234...

10.1177/154405910508400309 article EN Journal of Dental Research 2005-03-01
Shweta Ramdas Jonathan Judd Sarah E. Graham Stavroula Kanoni Yuxuan Wang and 95 more Ida Surakka Brandon M. Wenz Shoa L. Clarke Alessandra Chesi Andrew D. Wells Konain Fatima Bhatti Sailaja Vedantam Thomas W. Winkler Adam E. Locke Eirini Marouli Greg J.M. Zajac Kuan-Han Wu Ιωάννα Ντάλλα Qin Hui Derek Klarin Austin T. Hilliard Zeyuan Wang Chao Xue Guðmar Þorleifsson Anna Helgadóttir Daníel F. Guðbjartsson Hilma Hólm Ísleifur Ólafsson Mi Yeong Hwang Sohee Han Masato Akiyama Saori Sakaue Chikashi Terao Masahiro Kanai Wei Zhou Ben Brumpton Humaira Rasheed Aki S. Havulinna Yogasudha Veturi Jennifer A. Pacheco Elisabeth A. Rosenthal Todd Lingren QiPing Feng Iftikhar J. Kullo Akira Narita Jun Takayama Hilary C. Martin Karen A. Hunt Bhavi Trivedi Jeffrey Haessler Franco Giulianini Yuki Bradford Jason E. Miller Archie Campbell Kuang Lin Iona Y. Millwood Asif Rasheed George Hindy Jessica D. Faul Wei Zhao David R. Weir Constance Turman Hongyan Huang Mariaelisa Graff Ananyo Choudhury Dhriti Sengupta Anubha Mahajan Michael R. Brown Weihua Zhang Ketian Yu Ellen M. Schmidt Anita Pandit Stefan Gustafsson Xianyong Yin Jian’an Luan Jinghua Zhao Fumihiko Matsuda Hye-Mi Jang Kyungheon Yoon Carolina Medina‐Gómez Achilleas Pitsillides Jouke‐Jan Hottenga Andrew R. Wood Yingji Ji Zishan Gao Simon Haworth Ruth E. Mitchell Jin Fang Chai Mette Aadahl Anne A. Bjerregaard Jie Yao Ani Manichaikul Wen‐Jane Lee Chao A. Hsiung Helen R. Warren Julia Ramírez Jette Bork‐Jensen Line Lund Kårhus Anuj Goel Maria Sabater‐Lleal

10.1016/j.ajhg.2022.06.012 article EN publisher-specific-oa The American Journal of Human Genetics 2022-08-01

Social capital has been considered an important factor affecting mental-health outcomes, such as psychological distress in post-disaster settings. Although disaster-related house condition and displacement could affect both social distress, limited studies have investigated interactions. This study aimed to examine the association between taking into consideration interaction of after Great East Japan Earthquake 2011.Using data from 3793 adults living Shichigahama, Miyagi Prefecture, Japan,...

10.1111/pcn.12467 article EN cc-by-nc-nd Psychiatry and Clinical Neurosciences 2016-10-15

Abstract Autism spectrum disorder (ASD) has phenotypically and genetically heterogeneous characteristics. A simulation study demonstrated that attempts to categorize patients with a complex disease into more homogeneous subgroups could have power elucidate hidden heritability. We conducted cluster analyses using the k-means algorithm number of 15 based on phenotypic variables from Simons Simplex Collection (SSC). As preliminary study, we conventional genome-wide association (GWAS) data set...

10.1038/s41398-020-00951-x article EN cc-by Translational Psychiatry 2020-08-17

Recently, the sodium (Na)/potassium (K) ratio was reported to be associated with blood pressure (BP). A Na/K self-monitoring device using spot urine established recently. Here, we assessed whether urinary change measured BP in a health checkup setting. We targeted 12,890 participants who attended Tome City, Miyagi between 2017 and 2018. City introduced measurements during checkups since 2017. For each year, compared baseline characteristics according level. relationship multiple regression...

10.1038/s41440-020-00536-7 article EN cc-by Hypertension Research 2020-08-17

Abstract No study, to our knowledge, has constructed a polygenic risk score based on clinical blood pressure and investigated the association of genetic lifestyle risks with home hypertension. We examined associations combined hypertension In cross-sectional study 7027 Japanese individuals aged ≥20 years, we developed body mass index, alcohol consumption, physical activity, sodium-to-potassium ratio, categorized into ideal, intermediate, poor lifestyles. A was target data ( n = 1405) using...

10.1038/s41440-024-01705-8 article EN cc-by Hypertension Research 2024-06-24

Abstract Massively parallel sequencing of target regions, exomes, and complete genomes has begun to increase the opportunities for identifying genetic variants underlying rare common diseases dramatically. Here we applied exome resequencing primary failure tooth eruption (PFE) identify causality disease. Two Japanese families having PFE were recruited examined by genome-wide linkage study subsequently analyses. Linkage analyses these two comprising eight affected individuals unaffected...

10.1002/jbmr.385 article EN Journal of Bone and Mineral Research 2011-03-14

Since the Great East Japan Earthquake in 2011, many of affected have been forced to live temporary housing or at a relative's house. Special attention needs be paid negative health impacts resulting from such changes living conditions. This study examined association between future prospects and risk psychological distress 1 year after earthquake.In 2012, questionnaire was completed by cross-sectional people aged 20 years older Shichigahama Town, Miyagi, northeastern Japan, an area that had...

10.1111/pcn.12377 article EN Psychiatry and Clinical Neurosciences 2015-12-11

Ethnic-specific SNP arrays are becoming more important to increase the power of genome-wide association studies in diverse population. In Tohoku Medical Megabank Project, we have been developing a series Japonica Arrays (JPA) for genotyping participants based on reference panels constructed from whole-genome sequence data Japanese Here, designed novel version array population, called Array NEO (JPA NEO), comprising total 666,883 markers. Among them, 654,246 tag SNPs autosomes and X...

10.1093/jb/mvab060 article EN cc-by The Journal of Biochemistry 2021-05-12

Abstract Aims/hypothesis Clustering-based subclassification of type 2 diabetes, which reflects pathophysiology and genetic predisposition, is a promising approach for providing personalised effective therapeutic strategies. Ahlqvist’s classification currently the most vigorously validated method because its superior ability to predict diabetes complications but it does not have strong consistency over time requires HOMA2 indices, are routinely available in clinical practice standard cohort...

10.1007/s00125-024-06248-8 article EN cc-by Diabetologia 2024-08-21

It has been reported that chronic inflammation may play an important role in the pathogenesis of several serious diseases and could be modulated by diet. Recently, Dietary Inflammatory Index (DII®) was developed to assess inflammatory potential overall The DII as relevant various but not validated Japanese. Thus, present study, we analyzed relationship between scores high-sensitivity C-reactive protein (hs-CRP) levels a Japanese population.Data National Integrated Project for Prospective...

10.2188/jea.je20180156 article EN cc-by Journal of Epidemiology 2019-02-08
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