Identification of six new genetic loci associated with atrial fibrillation in the Japanese population
Kaoru Ito, Yoichiro Kamatani, Toshihiro Tanaka and colleagues report a genome-wide association study for atrial fibrillation in the Japanese population. They identify six new loci, five of which are not associated with atrial fibrillation in individuals of European ancestry, suggesting that they may...
Saved in:
Published in | Nature genetics Vol. 49; no. 6; pp. 953 - 958 |
---|---|
Main Authors | , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Nature Publishing Group US
01.06.2017
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
ISSN | 1061-4036 1546-1718 1546-1718 |
DOI | 10.1038/ng.3842 |
Cover
Abstract | Kaoru Ito, Yoichiro Kamatani, Toshihiro Tanaka and colleagues report a genome-wide association study for atrial fibrillation in the Japanese population. They identify six new loci, five of which are not associated with atrial fibrillation in individuals of European ancestry, suggesting that they may be specific to the Japanese population.
Atrial fibrillation is the most common cardiac arrhythmia and leads to stroke. To investigate genetic loci associated with atrial fibrillation in the Japanese population, we performed a genome-wide association study (GWAS) that included 8,180 atrial fibrillation cases and 28,612 controls with follow-up in an additional 3,120 cases and 125,064 controls. We replicated previously reported loci and identified six new loci, near the
KCND3
,
PPFIA4
,
SLC1A4
–
CEP68
,
HAND2
,
NEBL
and
SH3PXD2A
genes. Five of the six new loci were specifically associated with atrial fibrillation in the Japanese population after comparing our data to those from individuals of European ancestry, suggesting that there might be different genetic factors affecting susceptibility across ancestry groups. Our study discovered variants in the
HAND2
,
KCND3
and
NEBL
genes, which are relevant to atrial fibrillation susceptibility. The involvement of
PPFIA4
and
SH3PXD2A
in axon guidance also suggested a role in disease pathogenesis. Our findings may contribute to a better understanding of atrial fibrillation susceptibility and pathogenesis. |
---|---|
AbstractList | Kaoru Ito, Yoichiro Kamatani, Toshihiro Tanaka and colleagues report a genome-wide association study for atrial fibrillation in the Japanese population. They identify six new loci, five of which are not associated with atrial fibrillation in individuals of European ancestry, suggesting that they may be specific to the Japanese population.
Atrial fibrillation is the most common cardiac arrhythmia and leads to stroke. To investigate genetic loci associated with atrial fibrillation in the Japanese population, we performed a genome-wide association study (GWAS) that included 8,180 atrial fibrillation cases and 28,612 controls with follow-up in an additional 3,120 cases and 125,064 controls. We replicated previously reported loci and identified six new loci, near the
KCND3
,
PPFIA4
,
SLC1A4
–
CEP68
,
HAND2
,
NEBL
and
SH3PXD2A
genes. Five of the six new loci were specifically associated with atrial fibrillation in the Japanese population after comparing our data to those from individuals of European ancestry, suggesting that there might be different genetic factors affecting susceptibility across ancestry groups. Our study discovered variants in the
HAND2
,
KCND3
and
NEBL
genes, which are relevant to atrial fibrillation susceptibility. The involvement of
PPFIA4
and
SH3PXD2A
in axon guidance also suggested a role in disease pathogenesis. Our findings may contribute to a better understanding of atrial fibrillation susceptibility and pathogenesis. Atrial fibrillation is the most common cardiac arrhythmia and leads to stroke. To investigate genetic loci associated with atrial fibrillation in the Japanese population, we performed a genome-wide association study (GWAS) that included 8,180 atrial fibrillation cases and 28,612 controls with follow-up in an additional 3,120 cases and 125,064 controls. We replicated previously reported loci and identified six new loci, near the KCND3, PPFIA4, SLC1A4-CEP68, HAND2, NEBL and SH3PXD2A genes. Five of the six new loci were specifically associated with atrial fibrillation in the Japanese population after comparing our data to those from individuals of European ancestry, suggesting that there might be different genetic factors affecting susceptibility across ancestry groups. Our study discovered variants in the HAND2, KCND3 and NEBL genes, which are relevant to atrial fibrillation susceptibility. The involvement of PPFIA4 and SH3PXD2A in axon guidance also suggested a role in disease pathogenesis. Our findings may contribute to a better understanding of atrial fibrillation susceptibility and pathogenesis. Atrial fibrillation is the most common cardiac arrhythmia and leads to stroke. To investigate genetic loci associated with atrial fibrillation in the Japanese population, we performed a genome-wide association study (GWAS) that included 8,180 atrial fibrillation cases and 28,612 controls with follow-up in an additional 3,120 cases and 125,064 controls. We replicated previously reported loci and identified six new loci, near the KCND3, PPFIA4, SLC1A4-CEP68, HAND2, NEBL and SH3PXD2A genes. Five of the six new loci were specifically associated with atrial fibrillation in the Japanese population after comparing our data to those from individuals of European ancestry, suggesting that there might be different genetic factors affecting susceptibility across ancestry groups. Our study discovered variants in the HAND2, KCND3 and NEBL genes, which are relevant to atrial fibrillation susceptibility. The involvement of PPFIA4 and SH3PXD2A in axon guidance also suggested a role in disease pathogenesis. Our findings may contribute to a better understanding of atrial fibrillation susceptibility and pathogenesis.Atrial fibrillation is the most common cardiac arrhythmia and leads to stroke. To investigate genetic loci associated with atrial fibrillation in the Japanese population, we performed a genome-wide association study (GWAS) that included 8,180 atrial fibrillation cases and 28,612 controls with follow-up in an additional 3,120 cases and 125,064 controls. We replicated previously reported loci and identified six new loci, near the KCND3, PPFIA4, SLC1A4-CEP68, HAND2, NEBL and SH3PXD2A genes. Five of the six new loci were specifically associated with atrial fibrillation in the Japanese population after comparing our data to those from individuals of European ancestry, suggesting that there might be different genetic factors affecting susceptibility across ancestry groups. Our study discovered variants in the HAND2, KCND3 and NEBL genes, which are relevant to atrial fibrillation susceptibility. The involvement of PPFIA4 and SH3PXD2A in axon guidance also suggested a role in disease pathogenesis. Our findings may contribute to a better understanding of atrial fibrillation susceptibility and pathogenesis. |
Audience | Academic |
Author | Tsugane, Shoichiro Christophersen, Ingrid E Yamamoto, Masayuki Tanaka, Hideo Ellinor, Patrick T Tanaka, Keitaro Kamatani, Yoichiro Furukawa, Tetsushi Sasaki, Makoto Ebana, Yusuke Ozaki, Kouichi Takahashi, Atsushi Iwasaki, Motoki Kubo, Michiaki Ito, Kaoru Wakai, Kenji Ogishima, Soichi Satoh, Mamoru Yamaji, Taiki Low, Siew-Kee Tanaka, Toshihiro Naito, Mariko |
Author_xml | – sequence: 1 givenname: Siew-Kee surname: Low fullname: Low, Siew-Kee organization: Laboratory for Statistical Analysis, RIKEN Center for Integrative Medical Sciences, Faculty of Pharmacy, University of Sydney – sequence: 2 givenname: Atsushi surname: Takahashi fullname: Takahashi, Atsushi organization: Laboratory for Statistical Analysis, RIKEN Center for Integrative Medical Sciences, Department of Genomic Medicine, Research Institute, National Cerebral and Cardiovascular Center – sequence: 3 givenname: Yusuke surname: Ebana fullname: Ebana, Yusuke organization: Department of Bio-Informational Pharmacology, Medical Research Institute, Tokyo Medical and Dental University – sequence: 4 givenname: Kouichi surname: Ozaki fullname: Ozaki, Kouichi organization: Laboratory for Cardiovascular Diseases, RIKEN Center for Integrative Medical Sciences, Laboratory for Medical Genome Sciences, Medical Genome Center, National Center for Geriatrics and Gerontology – sequence: 5 givenname: Ingrid E surname: Christophersen fullname: Christophersen, Ingrid E organization: Broad Institute of Harvard and MIT, Cardiovascular Research Center, Massachusetts General Hospital, Department of Medical Research, Bærum Hospital, Vestre Viken Hospital Trust – sequence: 6 givenname: Patrick T orcidid: 0000-0002-2067-0533 surname: Ellinor fullname: Ellinor, Patrick T organization: Broad Institute of Harvard and MIT – sequence: 8 givenname: Soichi surname: Ogishima fullname: Ogishima, Soichi organization: Tohoku Medical Megabank Organization, Tohoku University – sequence: 9 givenname: Masayuki surname: Yamamoto fullname: Yamamoto, Masayuki organization: Tohoku Medical Megabank Organization, Tohoku University – sequence: 10 givenname: Mamoru surname: Satoh fullname: Satoh, Mamoru organization: Iwate Tohoku Medical Megabank Organization, Iwate Medical University – sequence: 11 givenname: Makoto surname: Sasaki fullname: Sasaki, Makoto organization: Iwate Tohoku Medical Megabank Organization, Iwate Medical University – sequence: 12 givenname: Taiki surname: Yamaji fullname: Yamaji, Taiki organization: Division of Epidemiology, Center for Public Health Sciences, National Cancer Center – sequence: 13 givenname: Motoki surname: Iwasaki fullname: Iwasaki, Motoki organization: Division of Epidemiology, Center for Public Health Sciences, National Cancer Center – sequence: 14 givenname: Shoichiro orcidid: 0000-0003-4105-2774 surname: Tsugane fullname: Tsugane, Shoichiro organization: Center for Public Health Sciences, National Cancer Center – sequence: 15 givenname: Keitaro surname: Tanaka fullname: Tanaka, Keitaro organization: Department of Preventive Medicine, Faculty of Medicine, Saga University – sequence: 16 givenname: Mariko surname: Naito fullname: Naito, Mariko organization: Department of Preventive Medicine, Nagoya University Graduate School of Medicine – sequence: 17 givenname: Kenji surname: Wakai fullname: Wakai, Kenji organization: Department of Preventive Medicine, Nagoya University Graduate School of Medicine – sequence: 18 givenname: Hideo surname: Tanaka fullname: Tanaka, Hideo organization: Division of Epidemiology and Prevention, Aichi Cancer Center Research Institute, Department of Epidemiology, Nagoya University Graduate School of Medicine – sequence: 19 givenname: Tetsushi surname: Furukawa fullname: Furukawa, Tetsushi organization: Department of Bio-Informational Pharmacology, Medical Research Institute, Tokyo Medical and Dental University – sequence: 20 givenname: Michiaki surname: Kubo fullname: Kubo, Michiaki organization: RIKEN Center for Integrative Medical Sciences – sequence: 21 givenname: Kaoru surname: Ito fullname: Ito, Kaoru email: kaoru.ito@riken.jp organization: Laboratory for Cardiovascular Diseases, RIKEN Center for Integrative Medical Sciences – sequence: 22 givenname: Yoichiro surname: Kamatani fullname: Kamatani, Yoichiro email: yoichiro.kamatani@riken.jp organization: Laboratory for Statistical Analysis, RIKEN Center for Integrative Medical Sciences – sequence: 23 givenname: Toshihiro orcidid: 0000-0001-6201-9784 surname: Tanaka fullname: Tanaka, Toshihiro email: ttana.brc@tmd.ac.jp organization: Laboratory for Cardiovascular Diseases, RIKEN Center for Integrative Medical Sciences, Department of Human Genetics and Disease Diversity, Tokyo Medical and Dental University Graduate School of Medical and Dental Sciences |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28416822$$D View this record in MEDLINE/PubMed |
BookMark | eNqNkktr3DAQx0VJaB4t_QZF0EPag7eSLdvaYwh9bAgE0sdVzMojR8EruZJM0m9fbXfbZpccig4jpN_853lCDpx3SMgrzmacVfK962eVFOUzcsxr0RS85fIg31nDC8Gq5oicxHjHGBeCyefkqJSCN7IsjwkuOnTJGqshWe-oNzTaB-rwnvboMFlNB68thRizgYQdvbfplkIKFgZq7DLYYdj4WkfTLdJLGMFhRDr6cdp8vSCHBoaIL7f2lHz7-OHrxefi6vrT4uL8qtCibVPRAjYMJetgDrAEwbFpNdMIdbmstQEp69bwmiED6IRpWVXxCiQTogHG27o6JW83umPwPyaMSa1s1JgTdOinqLiU80q2rCwz-mYPvfNTcDk7xeesbhqZdf9RPQyorDM-BdBrUXUu5qWsZC3XYWdPUPl0uLI6T8rY_L7j8G7HITMJH1IPU4xq8eXm_9nr77vs621R03KFnRqDXUH4qf7MOwNnG0AHH2NA8xfhTK03SblerTcpk8UeqW36Pcxcmx2e4Letj1nR9Rge9XMP_QWzXdQd |
CitedBy_id | crossref_primary_10_1038_s41588_022_01284_9 crossref_primary_10_1136_openhrt_2021_001898 crossref_primary_10_1016_j_ejmg_2022_104429 crossref_primary_10_1093_eurheartj_ehx389 crossref_primary_10_1161_CIRCGEN_117_001980 crossref_primary_10_1161_CIRCGENETICS_117_001902 crossref_primary_10_1002_cpt_1706 crossref_primary_10_1073_pnas_1907418116 crossref_primary_10_1002_ajmg_a_61571 crossref_primary_10_7554_eLife_80317 crossref_primary_10_1016_j_bbagrm_2021_194702 crossref_primary_10_1136_heartjnl_2024_324506 crossref_primary_10_1097_HCO_0000000000000505 crossref_primary_10_1111_eci_14084 crossref_primary_10_12677_ACM_2022_122209 crossref_primary_10_21518_ms2024_379 crossref_primary_10_1038_s41439_024_00308_6 crossref_primary_10_3390_ijms22031265 crossref_primary_10_1111_cas_13815 crossref_primary_10_1186_s12864_023_09425_y crossref_primary_10_1080_0886022X_2025_2477318 crossref_primary_10_1097_HCO_0000000000001031 crossref_primary_10_1161_CIR_0000000000000558 crossref_primary_10_1161_CIRCRESAHA_120_316575 crossref_primary_10_1093_cvr_cvaa144 crossref_primary_10_1093_cvr_cvab073 crossref_primary_10_1093_schbul_sbaa179 crossref_primary_10_1136_heartjnl_2016_311027 crossref_primary_10_1371_journal_pone_0277242 crossref_primary_10_1161_CIRCULATIONAHA_117_031431 crossref_primary_10_1038_s41586_022_05165_3 crossref_primary_10_1016_j_cjca_2024_07_029 crossref_primary_10_1186_s13023_022_02542_z crossref_primary_10_1016_j_jjcc_2019_05_018 crossref_primary_10_1007_s42835_024_01998_2 crossref_primary_10_1016_j_hrthm_2020_01_006 crossref_primary_10_1093_europace_euae043 crossref_primary_10_1371_journal_pone_0238304 crossref_primary_10_1016_j_cpcardiol_2023_102024 crossref_primary_10_1186_s10020_024_00999_1 crossref_primary_10_1038_s41431_018_0295_z crossref_primary_10_1016_j_hlc_2021_04_006 crossref_primary_10_1111_jce_15446 crossref_primary_10_1161_CIR_0000000000000659 crossref_primary_10_3389_fonc_2021_653200 crossref_primary_10_1002_cai2_70004 crossref_primary_10_1253_circj_CJ_23_0926 crossref_primary_10_1016_j_cpcardiol_2024_102439 crossref_primary_10_1016_j_hlc_2017_04_008 crossref_primary_10_3389_fcvm_2019_00127 crossref_primary_10_1016_j_numecd_2022_03_008 crossref_primary_10_1097_HCO_0000000000000840 crossref_primary_10_1159_000496150 crossref_primary_10_1038_s41598_018_35789_3 crossref_primary_10_1161_CIR_0000000000001193 crossref_primary_10_1210_clinem_dgac532 crossref_primary_10_1016_j_yjmcc_2021_04_003 crossref_primary_10_1007_s10840_024_01771_5 crossref_primary_10_1161_CIRCRESAHA_119_316006 crossref_primary_10_1016_j_ijcha_2019_100383 crossref_primary_10_1097_MD_0000000000015953 crossref_primary_10_1038_s41467_021_21286_1 crossref_primary_10_1007_s00395_024_01038_0 crossref_primary_10_1038_s41467_019_12721_5 crossref_primary_10_1161_CIRCGEN_118_002107 crossref_primary_10_1161_CIRCGEN_118_002109 crossref_primary_10_1016_j_tcm_2020_12_002 crossref_primary_10_1101_cshperspect_a037408 crossref_primary_10_1186_s40168_020_00923_9 crossref_primary_10_3389_fphys_2021_650449 crossref_primary_10_1007_s00438_023_02035_z crossref_primary_10_1161_CIRCRESAHA_121_319146 crossref_primary_10_1016_j_jacc_2017_09_005 crossref_primary_10_1093_jb_mvy096 crossref_primary_10_1111_eci_13584 crossref_primary_10_1016_j_ahjo_2022_100221 crossref_primary_10_1371_journal_pone_0209096 crossref_primary_10_1186_s12944_021_01482_0 crossref_primary_10_1093_cvr_cvab153 crossref_primary_10_1109_TIT_2021_3100108 crossref_primary_10_1152_physiolgenomics_00012_2019 crossref_primary_10_3389_fphys_2018_01458 crossref_primary_10_1161_CIRCGENETICS_117_001838 crossref_primary_10_20538_1682_0363_2020_1_180_189 crossref_primary_10_1111_cge_14443 crossref_primary_10_1016_j_ebiom_2024_105194 crossref_primary_10_1210_jc_2018_01551 crossref_primary_10_1016_j_jjcc_2022_09_006 crossref_primary_10_1038_s41397_018_0038_0 crossref_primary_10_1016_j_hrthm_2024_03_017 crossref_primary_10_3390_ijms23010006 crossref_primary_10_1002_mgg3_835 crossref_primary_10_1093_ije_dyac212 crossref_primary_10_1016_j_ccep_2020_10_010 crossref_primary_10_1016_j_ajhg_2017_12_003 crossref_primary_10_1038_s41588_018_0047_6 crossref_primary_10_1186_s40246_023_00498_0 crossref_primary_10_1172_JCI127750 crossref_primary_10_3389_fgene_2019_00108 crossref_primary_10_1016_j_jacc_2023_08_017 crossref_primary_10_1007_s00439_020_02203_w crossref_primary_10_1038_s41467_019_12267_6 crossref_primary_10_1016_j_amjcard_2023_08_007 crossref_primary_10_1038_s41588_018_0133_9 crossref_primary_10_1007_s12551_018_0435_2 crossref_primary_10_1038_s44161_023_00294_y crossref_primary_10_1136_annrheumdis_2020_217663 crossref_primary_10_1016_j_mgene_2020_100689 crossref_primary_10_1093_hmg_ddac153 crossref_primary_10_1038_s41598_019_53654_9 crossref_primary_10_1002_joa3_13082 crossref_primary_10_2188_jea_JE20190271 crossref_primary_10_1016_j_ijbiomac_2024_135125 crossref_primary_10_1007_s11033_022_07420_2 crossref_primary_10_1007_s12311_018_0927_4 crossref_primary_10_18632_aging_103615 crossref_primary_10_1016_j_hlc_2018_03_028 crossref_primary_10_20538_1682_0363_2021_3_203_212 crossref_primary_10_1093_carcin_bgy026 crossref_primary_10_3389_fphys_2023_1181510 crossref_primary_10_1093_eurheartjsupp_suae072 crossref_primary_10_1007_s00380_019_01418_w crossref_primary_10_1253_jjcsc_29_0_56 crossref_primary_10_1038_s41467_023_36491_3 |
Cites_doi | 10.1253/circj.CJ-15-0854 10.1002/ana.23701 10.1002/gepi.20579 10.1038/nn1416 10.1161/CIRCULATIONAHA.114.009892 10.1016/j.yjmcc.2013.04.021 10.1001/jama.291.23.2851 10.1006/excr.2001.5423 10.1038/ng1333 10.1038/ejhg.2011.39 10.1242/dev.108266 10.1016/j.ijcard.2008.06.029 10.1038/ng.537 10.1038/ng.2261 10.1007/s00018-015-1894-2 10.1007/s10048-013-0370-0 10.1038/nature06007 10.1038/ng.416 10.1002/ana.23700 10.1002/gepi.20303 10.1093/cvr/cvt028 10.1016/j.jacc.2010.05.045 10.1091/mbc.e13-04-0202 10.1161/CIRCULATIONAHA.109.886440 10.1016/0012-1606(83)90100-8 10.1086/512821 10.1161/CIRCULATIONAHA.113.002449 10.1161/CIRCRESAHA.108.180083 10.1186/s12881-015-0200-3 10.2188/jea.JE20150268 10.1371/journal.pgen.1001058 10.1253/circj.CJ-66-0092 10.1242/dev.127.24.5331 |
ContentType | Journal Article |
Copyright | Springer Nature America, Inc. 2017 COPYRIGHT 2017 Nature Publishing Group Copyright Nature Publishing Group Jun 2017 |
Copyright_xml | – notice: Springer Nature America, Inc. 2017 – notice: COPYRIGHT 2017 Nature Publishing Group – notice: Copyright Nature Publishing Group Jun 2017 |
CorporateAuthor | AFGen Consortium |
CorporateAuthor_xml | – name: AFGen Consortium |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM IOV ISR 3V. 7QL 7QP 7QR 7SS 7T7 7TK 7TM 7U9 7X7 7XB 88A 88E 8AO 8C1 8FD 8FE 8FH 8FI 8FJ 8FK 8G5 ABUWG AEUYN AFKRA AZQEC BBNVY BENPR BHPHI C1K CCPQU DWQXO FR3 FYUFA GHDGH GNUQQ GUQSH H94 HCIFZ K9. LK8 M0S M1P M2O M7N M7P MBDVC P64 PHGZM PHGZT PJZUB PKEHL PPXIY PQEST PQGLB PQQKQ PQUKI PRINS Q9U RC3 7X8 |
DOI | 10.1038/ng.3842 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed Gale In Context: Opposing Viewpoints Gale In Context: Science ProQuest Central (Corporate) Bacteriology Abstracts (Microbiology B) Calcium & Calcified Tissue Abstracts Chemoreception Abstracts Entomology Abstracts (Full archive) Industrial and Applied Microbiology Abstracts (Microbiology A) Neurosciences Abstracts Nucleic Acids Abstracts Virology and AIDS Abstracts Health & Medical Collection ProQuest Central (purchase pre-March 2016) Biology Database (Alumni Edition) Medical Database (Alumni Edition) ProQuest Pharma Collection Public Health Database (ProQuest) Technology Research Database ProQuest SciTech Collection ProQuest Natural Science Collection Hospital Premium Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) Research Library (Alumni) ProQuest Central (Alumni) ProQuest One Sustainability ProQuest Central UK/Ireland ProQuest Central Essentials Biological Science Collection ProQuest Central Natural Science Collection Environmental Sciences and Pollution Management ProQuest One ProQuest Central Engineering Research Database Health Research Premium Collection Health Research Premium Collection (Alumni) ProQuest Central Student ProQuest Research Library AIDS and Cancer Research Abstracts SciTech Premium Collection ProQuest Health & Medical Complete (Alumni) Biological Sciences ProQuest Health & Medical Collection Medical Database Research Library Algology Mycology and Protozoology Abstracts (Microbiology C) Biological Science Database Research Library (Corporate) Biotechnology and BioEngineering Abstracts Proquest Central Premium ProQuest One Academic (New) ProQuest Health & Medical Research Collection ProQuest One Academic Middle East (New) ProQuest One Health & Nursing ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Applied & Life Sciences ProQuest One Academic ProQuest One Academic UKI Edition ProQuest Central China ProQuest Central Basic Genetics Abstracts MEDLINE - Academic |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) Research Library Prep ProQuest Central Student ProQuest Central Essentials Nucleic Acids Abstracts SciTech Premium Collection ProQuest Central China Environmental Sciences and Pollution Management ProQuest One Applied & Life Sciences ProQuest One Sustainability Health Research Premium Collection Natural Science Collection Health & Medical Research Collection Biological Science Collection Chemoreception Abstracts Industrial and Applied Microbiology Abstracts (Microbiology A) ProQuest Central (New) ProQuest Medical Library (Alumni) Virology and AIDS Abstracts ProQuest Biological Science Collection ProQuest One Academic Eastern Edition ProQuest Hospital Collection Health Research Premium Collection (Alumni) Biological Science Database Neurosciences Abstracts ProQuest Hospital Collection (Alumni) Biotechnology and BioEngineering Abstracts Entomology Abstracts ProQuest Health & Medical Complete ProQuest One Academic UKI Edition Engineering Research Database ProQuest One Academic Calcium & Calcified Tissue Abstracts ProQuest One Academic (New) Technology Research Database ProQuest One Academic Middle East (New) ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) ProQuest One Community College ProQuest One Health & Nursing Research Library (Alumni Edition) ProQuest Natural Science Collection ProQuest Pharma Collection ProQuest Biology Journals (Alumni Edition) ProQuest Central ProQuest Health & Medical Research Collection Genetics Abstracts Health and Medicine Complete (Alumni Edition) ProQuest Central Korea Bacteriology Abstracts (Microbiology B) Algology Mycology and Protozoology Abstracts (Microbiology C) AIDS and Cancer Research Abstracts ProQuest Research Library ProQuest Public Health ProQuest Central Basic ProQuest SciTech Collection ProQuest Medical Library ProQuest Central (Alumni) MEDLINE - Academic |
DatabaseTitleList | Research Library Prep MEDLINE MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database – sequence: 3 dbid: BENPR name: ProQuest Central url: http://www.proquest.com/pqcentral?accountid=15518 sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Agriculture Biology |
EISSN | 1546-1718 |
EndPage | 958 |
ExternalDocumentID | A492838585 28416822 10_1038_ng_3842 |
Genre | Journal Article Correspondence |
GeographicLocations | Japan |
GeographicLocations_xml | – name: Japan |
GroupedDBID | --- -DZ -~X .55 .GJ 0R~ 123 29M 2FS 36B 39C 3O- 3V. 4.4 53G 5BI 5M7 5RE 5S5 70F 7X7 85S 88A 88E 8AO 8C1 8FE 8FH 8FI 8FJ 8G5 8R4 8R5 AAEEF AAHBH AARCD AAYOK AAYZH AAZLF ABAWZ ABCQX ABDBF ABDPE ABEFU ABJNI ABLJU ABOCM ABTAH ABUWG ACBWK ACGFO ACGFS ACIWK ACMJI ACNCT ACPRK ACUHS ADBBV ADFRT AENEX AEUYN AFBBN AFFNX AFKRA AFRAH AFSHS AGAYW AGCDD AGHTU AHBCP AHMBA AHOSX AHSBF AIBTJ ALFFA ALIPV ALMA_UNASSIGNED_HOLDINGS AMTXH ARMCB ASPBG AVWKF AXYYD AZFZN AZQEC B0M BBNVY BENPR BHPHI BKKNO BPHCQ BVXVI CCPQU CS3 DB5 DU5 DWQXO EAD EAP EBC EBD EBS EE. EJD EMB EMK EMOBN EPL ESX EXGXG F5P FEDTE FQGFK FSGXE FYUFA GNUQQ GUQSH GX1 HCIFZ HMCUK HVGLF HZ~ IAO IH2 IHR INH INR IOV ISR ITC L7B LGEZI LK8 LOTEE M0L M1P M2O M7P MVM N9A NADUK NNMJJ NXXTH ODYON P2P PKN PQQKQ PROAC PSQYO Q2X RIG RNS RNT RNTTT RVV SHXYY SIXXV SJN SNYQT SOJ SV3 TAOOD TBHMF TDRGL TN5 TSG TUS UKHRP VQA X7M XJT XOL Y6R YHZ ZGI ZXP ZY4 ~8M ~KM AAYXX ABFSG ACMFV ACSTC AETEA AFANA ALPWD ATHPR CITATION PHGZM PHGZT CGR CUY CVF ECM EIF NPM AEIIB PMFND 7QL 7QP 7QR 7SS 7T7 7TK 7TM 7U9 7XB 8FD 8FK C1K FR3 H94 K9. M7N MBDVC P64 PJZUB PKEHL PPXIY PQEST PQGLB PQUKI PRINS Q9U RC3 7X8 PUEGO |
ID | FETCH-LOGICAL-c477t-7ae60e80da9aaba41e67c0cea52b5cfa8857f150e0aad4f703313a80446a01753 |
IEDL.DBID | 8C1 |
ISSN | 1061-4036 1546-1718 |
IngestDate | Thu Sep 04 21:57:33 EDT 2025 Fri Jul 25 08:45:26 EDT 2025 Tue Jun 17 21:05:30 EDT 2025 Tue Jun 10 20:40:37 EDT 2025 Fri Jun 27 04:10:04 EDT 2025 Fri Jun 27 03:36:50 EDT 2025 Wed Feb 19 02:13:42 EST 2025 Tue Jul 01 01:50:14 EDT 2025 Thu Apr 24 23:06:33 EDT 2025 Fri Feb 21 02:39:06 EST 2025 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 6 |
Language | English |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c477t-7ae60e80da9aaba41e67c0cea52b5cfa8857f150e0aad4f703313a80446a01753 |
Notes | SourceType-Scholarly Journals-1 ObjectType-Correspondence-1 content type line 14 ObjectType-Article-1 ObjectType-Feature-2 content type line 23 |
ORCID | 0000-0001-6201-9784 0000-0003-4105-2774 0000-0002-2067-0533 |
PMID | 28416822 |
PQID | 1905668804 |
PQPubID | 33429 |
PageCount | 6 |
ParticipantIDs | proquest_miscellaneous_1889387022 proquest_journals_1905668804 gale_infotracmisc_A492838585 gale_infotracacademiconefile_A492838585 gale_incontextgauss_ISR_A492838585 gale_incontextgauss_IOV_A492838585 pubmed_primary_28416822 crossref_primary_10_1038_ng_3842 crossref_citationtrail_10_1038_ng_3842 springer_journals_10_1038_ng_3842 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2017-06-01 |
PublicationDateYYYYMMDD | 2017-06-01 |
PublicationDate_xml | – month: 06 year: 2017 text: 2017-06-01 day: 01 |
PublicationDecade | 2010 |
PublicationPlace | New York |
PublicationPlace_xml | – name: New York – name: United States |
PublicationTitle | Nature genetics |
PublicationTitleAbbrev | Nat Genet |
PublicationTitleAlternate | Nat Genet |
PublicationYear | 2017 |
Publisher | Nature Publishing Group US Nature Publishing Group |
Publisher_xml | – name: Nature Publishing Group US – name: Nature Publishing Group |
References | Duarri (CR19) 2015; 72 Purevjav (CR28) 2010; 56 Gudbjartsson (CR3) 2007; 448 Yang (CR32) 2011; 19 Sinner (CR7) 2014; 130 Moncman, Wang (CR26) 2002; 273 Duarri (CR18) 2012; 72 CR11 McFadden (CR13) 2000; 127 Ellinor (CR5) 2010; 42 Kuriyama (CR30) 2016; 26 Santiago-Medina, Gregus, Nichol, O'Toole, Gomez (CR16) 2015; 142 Ellinor (CR6) 2012; 44 Zollner, Pritchard (CR12) 2007; 80 Dunah (CR15) 2005; 8 Lee (CR21) 2012; 72 Olesen (CR23) 2013; 98 Bang, Chen (CR24) 2015; 79 Smets (CR22) 2015; 16 So, Gui, Cherny, Sham (CR10) 2011; 35 Pe'er, Yelensky, Altshuler, Daly (CR9) 2008; 32 Freedman (CR31) 2004; 36 Morikawa, Cserjesi (CR14) 2008; 103 Kirby, Stewart (CR17) 1983; 97 Benjamin (CR4) 2009; 41 Segrè, Groop, Mootha, Daly, Altshuler (CR33) 2010; 6 Fox (CR2) 2004; 291 Maiellaro-Rafferty (CR27) 2013; 60 Duarri (CR20) 2013; 14 Dewland, Olgin, Vittinghoff, Marcus (CR8) 2013; 128 Lubitz (CR29) 2010; 122 Inoue (CR1) 2009; 137 Eulitz (CR25) 2013; 24 M Santiago-Medina (BFng3842_CR16) 2015; 142 MF Sinner (BFng3842_CR7) 2014; 130 S Kuriyama (BFng3842_CR30) 2016; 26 J Yang (BFng3842_CR32) 2011; 19 AV Segrè (BFng3842_CR33) 2010; 6 S Eulitz (BFng3842_CR25) 2013; 24 Y Morikawa (BFng3842_CR14) 2008; 103 BFng3842_CR11 A Duarri (BFng3842_CR20) 2013; 14 ML Kirby (BFng3842_CR17) 1983; 97 I Pe'er (BFng3842_CR9) 2008; 32 ML Freedman (BFng3842_CR31) 2004; 36 S Zollner (BFng3842_CR12) 2007; 80 K Smets (BFng3842_CR22) 2015; 16 CS Fox (BFng3842_CR2) 2004; 291 A Duarri (BFng3842_CR19) 2015; 72 EJ Benjamin (BFng3842_CR4) 2009; 41 TA Dewland (BFng3842_CR8) 2013; 128 HC So (BFng3842_CR10) 2011; 35 ML Bang (BFng3842_CR24) 2015; 79 DG McFadden (BFng3842_CR13) 2000; 127 H Inoue (BFng3842_CR1) 2009; 137 A Duarri (BFng3842_CR18) 2012; 72 YC Lee (BFng3842_CR21) 2012; 72 DF Gudbjartsson (BFng3842_CR3) 2007; 448 PT Ellinor (BFng3842_CR6) 2012; 44 E Purevjav (BFng3842_CR28) 2010; 56 AW Dunah (BFng3842_CR15) 2005; 8 CL Moncman (BFng3842_CR26) 2002; 273 MS Olesen (BFng3842_CR23) 2013; 98 PT Ellinor (BFng3842_CR5) 2010; 42 SA Lubitz (BFng3842_CR29) 2010; 122 K Maiellaro-Rafferty (BFng3842_CR27) 2013; 60 23400760 - Cardiovasc Res. 2013 Jun 1;98(3):488-95 26321576 - Circ J. 2015;79(10):2081-7 21407268 - Eur J Hum Genet. 2011 Jul;19(7):807-12 25854634 - Cell Mol Life Sci. 2015 Sep;72(17):3387-99 20173747 - Nat Genet. 2010 Mar;42(3):240-4 22544366 - Nat Genet. 2012 Apr 29;44(6):670-5 23985323 - Mol Biol Cell. 2013 Oct;24(20):3215-26 25124494 - Circulation. 2014 Oct 7;130(15):1225-35 23963749 - Neurogenetics. 2013 Nov;14(3-4):257-8 21374718 - Genet Epidemiol. 2011 Jul;35(5):310-7 24103419 - Circulation. 2013 Dec 3;128(23):2470-7 24965079 - Circ J. 2014;78(8):1997-2021 23280838 - Ann Neurol. 2012 Dec;72(6):870-80 15750591 - Nat Neurosci. 2005 Apr;8(4):458-67 23632046 - J Mol Cell Cardiol. 2013 Jul;60:151-60 20951326 - J Am Coll Cardiol. 2010 Oct 26;56(18):1493-502 18348202 - Genet Epidemiol. 2008 May;32(4):381-5 15052270 - Nat Genet. 2004 Apr;36(4):388-93 19008477 - Circ Res. 2008 Dec 5;103(12):1422-9 6852374 - Dev Biol. 1983 Jun;97(2):433-43 20733104 - Circulation. 2010 Sep 7;122(10):976-84 25564649 - Development. 2015 Feb 1;142(3):486-96 26189493 - BMC Med Genet. 2015 Jul 21;16:51 18691774 - Int J Cardiol. 2009 Oct 2;137(2):102-7 27374138 - J Epidemiol. 2016 Sep 5;26(9):493-511 23280837 - Ann Neurol. 2012 Dec;72(6):859-69 11076755 - Development. 2000 Dec;127(24):5331-41 20714348 - PLoS Genet. 2010 Aug 12;6(8):null 17603472 - Nature. 2007 Jul 19;448(7151):353-7 17357068 - Am J Hum Genet. 2007 Apr;80(4):605-15 19597492 - Nat Genet. 2009 Aug;41(8):879-81 11822876 - Exp Cell Res. 2002 Feb 15;273(2):204-18 15199036 - JAMA. 2004 Jun 16;291(23):2851-5 |
References_xml | – volume: 79 start-page: 2081 year: 2015 end-page: 2087 ident: CR24 article-title: Roles of nebulin family members in the heart publication-title: Circ. J. doi: 10.1253/circj.CJ-15-0854 – volume: 72 start-page: 859 year: 2012 end-page: 869 ident: CR21 article-title: Mutations in cause spinocerebellar ataxia type 22 publication-title: Ann. Neurol. doi: 10.1002/ana.23701 – volume: 35 start-page: 310 year: 2011 end-page: 317 ident: CR10 article-title: Evaluating the heritability explained by known susceptibility variants: a survey of ten complex diseases publication-title: Genet. Epidemiol. doi: 10.1002/gepi.20579 – volume: 8 start-page: 458 year: 2005 end-page: 467 ident: CR15 article-title: LAR receptor protein tyrosine phosphatases in the development and maintenance of excitatory synapses publication-title: Nat. Neurosci. doi: 10.1038/nn1416 – volume: 130 start-page: 1225 year: 2014 end-page: 1235 ident: CR7 article-title: Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation publication-title: Circulation doi: 10.1161/CIRCULATIONAHA.114.009892 – volume: 60 start-page: 151 year: 2013 end-page: 160 ident: CR27 article-title: Altered regional cardiac wall mechanics are associated with differential cardiomyocyte calcium handling due to nebulette mutations in preclinical inherited dilated cardiomyopathy publication-title: J. Mol. Cell. Cardiol. doi: 10.1016/j.yjmcc.2013.04.021 – volume: 6 start-page: e1001058 year: 2010 ident: CR33 article-title: Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits publication-title: PLoS Genet. – volume: 127 start-page: 5331 year: 2000 end-page: 5341 ident: CR13 article-title: A GATA-dependent right ventricular enhancer controls dHAND transcription in the developing heart publication-title: Development – volume: 291 start-page: 2851 year: 2004 end-page: 2855 ident: CR2 article-title: Parental atrial fibrillation as a risk factor for atrial fibrillation in offspring publication-title: J. Am. Med. Assoc. doi: 10.1001/jama.291.23.2851 – volume: 273 start-page: 204 year: 2002 end-page: 218 ident: CR26 article-title: Targeted disruption of nebulette protein expression alters cardiac myofibril assembly and function publication-title: Exp. Cell Res. doi: 10.1006/excr.2001.5423 – volume: 36 start-page: 388 year: 2004 end-page: 393 ident: CR31 article-title: Assessing the impact of population stratification on genetic association studies publication-title: Nat. Genet. doi: 10.1038/ng1333 – volume: 19 start-page: 807 year: 2011 end-page: 812 ident: CR32 article-title: Genomic inflation factors under polygenic inheritance publication-title: Eur. J. Hum. Genet. doi: 10.1038/ejhg.2011.39 – volume: 142 start-page: 486 year: 2015 end-page: 496 ident: CR16 article-title: Regulation of ECM degradation and axon guidance by growth cone invadosomes publication-title: Development doi: 10.1242/dev.108266 – volume: 137 start-page: 102 year: 2009 end-page: 107 ident: CR1 article-title: Prevalence of atrial fibrillation in the general population of Japan: an analysis based on periodic health examination publication-title: Int. J. Cardiol. doi: 10.1016/j.ijcard.2008.06.029 – volume: 42 start-page: 240 year: 2010 end-page: 244 ident: CR5 article-title: Common variants in are associated with lone atrial fibrillation publication-title: Nat. Genet. doi: 10.1038/ng.537 – volume: 44 start-page: 670 year: 2012 end-page: 675 ident: CR6 article-title: Meta-analysis identifies six new susceptibility loci for atrial fibrillation publication-title: Nat. Genet. doi: 10.1038/ng.2261 – volume: 72 start-page: 3387 year: 2015 end-page: 3399 ident: CR19 article-title: Spinocerebellar ataxia type 19/22 mutations alter heterocomplex K 4.3 channel function and gating in a dominant manner publication-title: Cell. Mol. Life Sci. doi: 10.1007/s00018-015-1894-2 – volume: 14 start-page: 257 year: 2013 end-page: 258 ident: CR20 article-title: The L450F mutation in brings spinocerebellar ataxia and Brugada syndrome closer together publication-title: Neurogenetics doi: 10.1007/s10048-013-0370-0 – volume: 448 start-page: 353 year: 2007 end-page: 357 ident: CR3 article-title: Variants conferring risk of atrial fibrillation on chromosome 4q25 publication-title: Nature doi: 10.1038/nature06007 – volume: 41 start-page: 879 year: 2009 end-page: 881 ident: CR4 article-title: Variants in are associated with atrial fibrillation in individuals of European ancestry publication-title: Nat. Genet. doi: 10.1038/ng.416 – volume: 72 start-page: 870 year: 2012 end-page: 880 ident: CR18 article-title: Mutations in potassium channel cause spinocerebellar ataxia type 19 publication-title: Ann. Neurol. doi: 10.1002/ana.23700 – volume: 32 start-page: 381 year: 2008 end-page: 385 ident: CR9 article-title: Estimation of the multiple testing burden for genomewide association studies of nearly all common variants publication-title: Genet. Epidemiol. doi: 10.1002/gepi.20303 – volume: 98 start-page: 488 year: 2013 end-page: 495 ident: CR23 article-title: A novel gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation publication-title: Cardiovasc. Res. doi: 10.1093/cvr/cvt028 – volume: 56 start-page: 1493 year: 2010 end-page: 1502 ident: CR28 article-title: Nebulette mutations are associated with dilated cardiomyopathy and endocardial fibroelastosis publication-title: J. Am. Coll. Cardiol. doi: 10.1016/j.jacc.2010.05.045 – volume: 24 start-page: 3215 year: 2013 end-page: 3226 ident: CR25 article-title: Identification of Xin-repeat proteins as novel ligands of the SH3 domains of nebulin and nebulette and analysis of their interaction during myofibril formation and remodeling publication-title: Mol. Biol. Cell doi: 10.1091/mbc.e13-04-0202 – volume: 122 start-page: 976 year: 2010 end-page: 984 ident: CR29 article-title: Independent susceptibility markers for atrial fibrillation on chromosome 4q25 publication-title: Circulation doi: 10.1161/CIRCULATIONAHA.109.886440 – volume: 97 start-page: 433 year: 1983 end-page: 443 ident: CR17 article-title: Neural crest origin of cardiac ganglion cells in the chick embryo: identification and extirpation publication-title: Dev. Biol. doi: 10.1016/0012-1606(83)90100-8 – ident: CR11 – volume: 80 start-page: 605 year: 2007 end-page: 615 ident: CR12 article-title: Overcoming the winner's curse: estimating penetrance parameters from case–control data publication-title: Am. J. Hum. Genet. doi: 10.1086/512821 – volume: 128 start-page: 2470 year: 2013 end-page: 2477 ident: CR8 article-title: Incident atrial fibrillation among Asians, Hispanics, blacks, and whites publication-title: Circulation doi: 10.1161/CIRCULATIONAHA.113.002449 – volume: 103 start-page: 1422 year: 2008 end-page: 1429 ident: CR14 article-title: Cardiac neural crest expression of Hand2 regulates outflow and second heart field development publication-title: Circ. Res. doi: 10.1161/CIRCRESAHA.108.180083 – volume: 16 start-page: 51 year: 2015 ident: CR22 article-title: First mutation causes severe K 4.3 channel dysfunction leading to early onset cerebellar ataxia, intellectual disability, oral apraxia and epilepsy publication-title: BMC Med. Genet. doi: 10.1186/s12881-015-0200-3 – volume: 26 start-page: 493 year: 2016 end-page: 511 ident: CR30 article-title: The Tohoku Medical Megabank Project: design and mission publication-title: J. Epidemiol. doi: 10.2188/jea.JE20150268 – volume: 8 start-page: 458 year: 2005 ident: BFng3842_CR15 publication-title: Nat. Neurosci. doi: 10.1038/nn1416 – volume: 103 start-page: 1422 year: 2008 ident: BFng3842_CR14 publication-title: Circ. Res. doi: 10.1161/CIRCRESAHA.108.180083 – volume: 56 start-page: 1493 year: 2010 ident: BFng3842_CR28 publication-title: J. Am. Coll. Cardiol. doi: 10.1016/j.jacc.2010.05.045 – volume: 6 start-page: e1001058 year: 2010 ident: BFng3842_CR33 publication-title: PLoS Genet. doi: 10.1371/journal.pgen.1001058 – volume: 35 start-page: 310 year: 2011 ident: BFng3842_CR10 publication-title: Genet. Epidemiol. doi: 10.1002/gepi.20579 – volume: 24 start-page: 3215 year: 2013 ident: BFng3842_CR25 publication-title: Mol. Biol. Cell doi: 10.1091/mbc.e13-04-0202 – volume: 60 start-page: 151 year: 2013 ident: BFng3842_CR27 publication-title: J. Mol. Cell. Cardiol. doi: 10.1016/j.yjmcc.2013.04.021 – volume: 41 start-page: 879 year: 2009 ident: BFng3842_CR4 publication-title: Nat. Genet. doi: 10.1038/ng.416 – ident: BFng3842_CR11 doi: 10.1253/circj.CJ-66-0092 – volume: 44 start-page: 670 year: 2012 ident: BFng3842_CR6 publication-title: Nat. Genet. doi: 10.1038/ng.2261 – volume: 14 start-page: 257 year: 2013 ident: BFng3842_CR20 publication-title: Neurogenetics doi: 10.1007/s10048-013-0370-0 – volume: 122 start-page: 976 year: 2010 ident: BFng3842_CR29 publication-title: Circulation doi: 10.1161/CIRCULATIONAHA.109.886440 – volume: 80 start-page: 605 year: 2007 ident: BFng3842_CR12 publication-title: Am. J. Hum. Genet. doi: 10.1086/512821 – volume: 448 start-page: 353 year: 2007 ident: BFng3842_CR3 publication-title: Nature doi: 10.1038/nature06007 – volume: 72 start-page: 870 year: 2012 ident: BFng3842_CR18 publication-title: Ann. Neurol. doi: 10.1002/ana.23700 – volume: 72 start-page: 3387 year: 2015 ident: BFng3842_CR19 publication-title: Cell. Mol. Life Sci. doi: 10.1007/s00018-015-1894-2 – volume: 127 start-page: 5331 year: 2000 ident: BFng3842_CR13 publication-title: Development doi: 10.1242/dev.127.24.5331 – volume: 36 start-page: 388 year: 2004 ident: BFng3842_CR31 publication-title: Nat. Genet. doi: 10.1038/ng1333 – volume: 291 start-page: 2851 year: 2004 ident: BFng3842_CR2 publication-title: J. Am. Med. Assoc. doi: 10.1001/jama.291.23.2851 – volume: 32 start-page: 381 year: 2008 ident: BFng3842_CR9 publication-title: Genet. Epidemiol. doi: 10.1002/gepi.20303 – volume: 16 start-page: 51 year: 2015 ident: BFng3842_CR22 publication-title: BMC Med. Genet. doi: 10.1186/s12881-015-0200-3 – volume: 137 start-page: 102 year: 2009 ident: BFng3842_CR1 publication-title: Int. J. Cardiol. doi: 10.1016/j.ijcard.2008.06.029 – volume: 98 start-page: 488 year: 2013 ident: BFng3842_CR23 publication-title: Cardiovasc. Res. doi: 10.1093/cvr/cvt028 – volume: 26 start-page: 493 year: 2016 ident: BFng3842_CR30 publication-title: J. Epidemiol. doi: 10.2188/jea.JE20150268 – volume: 97 start-page: 433 year: 1983 ident: BFng3842_CR17 publication-title: Dev. Biol. doi: 10.1016/0012-1606(83)90100-8 – volume: 128 start-page: 2470 year: 2013 ident: BFng3842_CR8 publication-title: Circulation doi: 10.1161/CIRCULATIONAHA.113.002449 – volume: 79 start-page: 2081 year: 2015 ident: BFng3842_CR24 publication-title: Circ. J. doi: 10.1253/circj.CJ-15-0854 – volume: 42 start-page: 240 year: 2010 ident: BFng3842_CR5 publication-title: Nat. Genet. doi: 10.1038/ng.537 – volume: 130 start-page: 1225 year: 2014 ident: BFng3842_CR7 publication-title: Circulation doi: 10.1161/CIRCULATIONAHA.114.009892 – volume: 72 start-page: 859 year: 2012 ident: BFng3842_CR21 publication-title: Ann. Neurol. doi: 10.1002/ana.23701 – volume: 273 start-page: 204 year: 2002 ident: BFng3842_CR26 publication-title: Exp. Cell Res. doi: 10.1006/excr.2001.5423 – volume: 19 start-page: 807 year: 2011 ident: BFng3842_CR32 publication-title: Eur. J. Hum. Genet. doi: 10.1038/ejhg.2011.39 – volume: 142 start-page: 486 year: 2015 ident: BFng3842_CR16 publication-title: Development doi: 10.1242/dev.108266 – reference: 22544366 - Nat Genet. 2012 Apr 29;44(6):670-5 – reference: 23280838 - Ann Neurol. 2012 Dec;72(6):870-80 – reference: 21374718 - Genet Epidemiol. 2011 Jul;35(5):310-7 – reference: 27374138 - J Epidemiol. 2016 Sep 5;26(9):493-511 – reference: 23400760 - Cardiovasc Res. 2013 Jun 1;98(3):488-95 – reference: 17357068 - Am J Hum Genet. 2007 Apr;80(4):605-15 – reference: 17603472 - Nature. 2007 Jul 19;448(7151):353-7 – reference: 20951326 - J Am Coll Cardiol. 2010 Oct 26;56(18):1493-502 – reference: 20733104 - Circulation. 2010 Sep 7;122(10):976-84 – reference: 23632046 - J Mol Cell Cardiol. 2013 Jul;60:151-60 – reference: 15052270 - Nat Genet. 2004 Apr;36(4):388-93 – reference: 20714348 - PLoS Genet. 2010 Aug 12;6(8):null – reference: 25854634 - Cell Mol Life Sci. 2015 Sep;72(17):3387-99 – reference: 24965079 - Circ J. 2014;78(8):1997-2021 – reference: 19597492 - Nat Genet. 2009 Aug;41(8):879-81 – reference: 23985323 - Mol Biol Cell. 2013 Oct;24(20):3215-26 – reference: 25564649 - Development. 2015 Feb 1;142(3):486-96 – reference: 11076755 - Development. 2000 Dec;127(24):5331-41 – reference: 6852374 - Dev Biol. 1983 Jun;97(2):433-43 – reference: 25124494 - Circulation. 2014 Oct 7;130(15):1225-35 – reference: 23280837 - Ann Neurol. 2012 Dec;72(6):859-69 – reference: 20173747 - Nat Genet. 2010 Mar;42(3):240-4 – reference: 26321576 - Circ J. 2015;79(10):2081-7 – reference: 19008477 - Circ Res. 2008 Dec 5;103(12):1422-9 – reference: 15199036 - JAMA. 2004 Jun 16;291(23):2851-5 – reference: 15750591 - Nat Neurosci. 2005 Apr;8(4):458-67 – reference: 18348202 - Genet Epidemiol. 2008 May;32(4):381-5 – reference: 11822876 - Exp Cell Res. 2002 Feb 15;273(2):204-18 – reference: 18691774 - Int J Cardiol. 2009 Oct 2;137(2):102-7 – reference: 21407268 - Eur J Hum Genet. 2011 Jul;19(7):807-12 – reference: 26189493 - BMC Med Genet. 2015 Jul 21;16:51 – reference: 24103419 - Circulation. 2013 Dec 3;128(23):2470-7 – reference: 23963749 - Neurogenetics. 2013 Nov;14(3-4):257-8 |
SSID | ssj0014408 |
Score | 2.5744743 |
Snippet | Kaoru Ito, Yoichiro Kamatani, Toshihiro Tanaka and colleagues report a genome-wide association study for atrial fibrillation in the Japanese population. They... Atrial fibrillation is the most common cardiac arrhythmia and leads to stroke. To investigate genetic loci associated with atrial fibrillation in the Japanese... |
SourceID | proquest gale pubmed crossref springer |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 953 |
SubjectTerms | 45/43 631/208/205/2138 631/208/457 692/699/75/29/1309 Adult Aged Agriculture Animal Genetics and Genomics Arrhythmia Asian Continental Ancestry Group - genetics Atrial fibrillation Atrial Fibrillation - genetics Axon guidance Basic Helix-Loop-Helix Transcription Factors - genetics Biomedicine Cancer Research Cardiac arrhythmia Chromosomes, Human, Pair 4 Electrocardiography Fibrillation Gene Function Gene loci Genes Genetic aspects Genetic factors Genetic Loci Genetic Predisposition to Disease Genetic research Genetic susceptibility Genome-wide association studies Genome-Wide Association Study - methods Genomes Heart diseases Human Genetics Humans Identification and classification letter Loci Middle Aged Pathogenesis Polymorphism, Single Nucleotide Preventive medicine Quantitative trait loci Risk factors Shal Potassium Channels - genetics Stroke |
Title | Identification of six new genetic loci associated with atrial fibrillation in the Japanese population |
URI | https://link.springer.com/article/10.1038/ng.3842 https://www.ncbi.nlm.nih.gov/pubmed/28416822 https://www.proquest.com/docview/1905668804 https://www.proquest.com/docview/1889387022 |
Volume | 49 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3db9MwED-xTUi8THyvY1QeQvAUljlO7D6hMW0akxhoMNQ36-I4VaUpKaSVxn_PXeKGZQiefbFi-873830CvMY8LyTXqZz4HCPSUHFkUjehpwopM-U16oIN-p8usrMrdT5Np8Hg1oSwyvWd2F7URe3YRn5AiouQB3Gber_4EXHXKPauhhYaG7DFOaD8-DLHfYgH-y27VLiM30nsptzu0szNQTV7lxglB9ro7p18Synd8ZK2yuf0IWwH1CiOumN-BPd89Rjud30kfz0B36XblsH-JupSNPMbQYhZEH9wmqIgnTUXGM7CF4LtrwLbnh2i5LD_6y4oTswrQZhQnJMS5eaUYtF3-HoKV6cn347PotA_IXJK62Wk0WexN3GBE8Qc1aHPtIudx1TmqSvRmFSXBAh9jFiokmQ_OUzQsIsXY67g-Qw2q7ryOyByp70sMudN4hTKFGkuqdJClnnCCGgEb9b7aF0oLs49Lq5t6-ROjK1mljd8BKInXHT1NP4mecUHYbk6RcXhLzNcNY39-Pm7PVITgkPsyvwX0dfLAdHbQFTW9DcOQ8oBrYmrXg0o9waUJGNuOLxmChtkvLF_OHIE-_0wf8lxa5WvV0RjCA_SlShpVc87ZuqXLdnja3hkf81dtyYf7snu_3_gBTyQDDda69AebC5_rvxLAkvLfAwbeqrHrVyMYevDycWXy996hxR2 |
linkProvider | ProQuest |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9QwELbKVgguFW-2FHARj1No6jiJ91ChAq12-1hQaVFvZuI4q5WqZEt2Bf1z_DZmEic0RXDr2RMrtseezzOe-Rh7CUmSCqpTObAJeGihfE-FZoBXFTRm0sYQp-TQPxxHwxO5dxqeLrFfTS4MPatszsTqoE4LQz7yDTRciDxQ2-S72blHrFEUXW0oNMBRK6RbVYkxl9ixby9-4BWu3Bp9xPV-JcTuzvGHoedYBjwj43juxWAj3yo_hQFAAnLTRrHxjYVQJKHJQKkwzhA2WR8glRnukGAzAEWBUPCpziX2e4MtS3Kg9Njy-53x56M2jkF8zlW8NaKbGgVKV-pEd7WRT94GSoqOPbxqFS6ZxStx2sr87d5hKw638u1a0e6yJZvfYzdrJsuL-8zWCb-Z8wDyIuPl9CdHzM5RQylRkqPVnHJw2mBTTh5gDhVrCM8o8eCsfpbHpzlHVMr30IwTPSaftRxjD9jJtcztQ9bLi9w-ZjwxsRVpZKwKjAQRAvYlZJiKLAkIg_XZ62YetXHlzYll40xXYfZA6XyiacL7jLeCs7qix98iL2ghNNXHyOkBzgQWZalHn77qbTlAQEbB1H8JfTnqCL1xQlmBf2PAJT3gmKjuVkdyrSOJu9x0mxul0O6UKfWfPdFn620zfUkv53JbLFBGISLFQ1ngqB7VytQOW1DMWVHLeqNdlzrvzsnq_3_gObs1PD480Aej8f4TdlsQ-Kl8VWusN_--sE8Rus2TZ25_cPbturfkb2vDVeo |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9QwELZKEYhLxZuFAi7icQqbOk7sPSBUUVbdFgoCWu3NTBx7tVKVLGRX0L_Gr2MmL5oiuPXsiRXbM57P82TsKaRpJqhO5cilEKCGCgMd2xE-VVCZSadAZWTQf3-Y7B3J_Wk8XWO_2lwYCqts78Tqos4KSzbyISouRB7IbXLom7CIj7vj14tvAXWQIk9r206jZpEDd_oDn2_lq8kunvUzIcZvv7zZC5oOA4GVSi0DBS4JnQ4zGAGkILddomxoHcQija0HrWPlETK5ECCTHqUj2o5AkxMUQqpxifNeYpdVJCW1jVDT7rFHPtM6DS-hNxq5SDfqFHc9zGcvIy1FTxOe1wdnFOI5D22l-MbX2UaDWPlOzWI32JrLb7IrdQ_L01vM1am-vrH98cLzcv6TI1rnyJuUIslRX845NHzgMk62Xw5VvxDuKeXgpA7I4_OcIx7l-6jAqTEmX3TdxW6zowvZ2TtsPS9yd4_x1ConssQ6HVkJIgacS8g4Ez6NCH0N2PN2H41tCptTf40TUznYI23ymaENHzDeES7qWh5_kzyhgzBUGSMnHpvBqizN5MOx2ZEjhGLkRv0X0edPPaIXDZEv8G8sNOkOuCaquNWj3OxRonzb_nDLFKa5X0rzRxoGbKsbpi8pZi53xQppNGJRvI4FrupuzUzdsgV5mzWNbLXcdWby_p7c__8PPGZXURDNu8nhwQN2TRDqqYxUm2x9-X3lHiJmW6aPKuHg7OtFS-NvFitThg |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Identification+of+six+new+genetic+loci+associated+with+atrial+fibrillation+in+the+Japanese+population&rft.jtitle=Nature+genetics&rft.au=Low%2C+Siew-Kee&rft.au=Takahashi%2C+Atsushi&rft.au=Ebana%2C+Yusuke&rft.au=Ozaki%2C+Kouichi&rft.date=2017-06-01&rft.eissn=1546-1718&rft.volume=49&rft.issue=6&rft.spage=953&rft_id=info:doi/10.1038%2Fng.3842&rft_id=info%3Apmid%2F28416822&rft.externalDocID=28416822 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1061-4036&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1061-4036&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1061-4036&client=summon |