Project 1: Genetic Discovery Within Diverse Ancestry Cohorts
项目 1:不同血统群体中的基因发现
基本信息
- 批准号:10333060
- 负责人:
- 金额:$ 63.43万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2022
- 资助国家:美国
- 起止时间:2022-07-01 至 2027-06-30
- 项目状态:未结题
- 来源:
- 关键词:AccountingAddressAfricanAfrican AmericanAfrican American populationAfrican CaribbeanAgingAllelesAlzheimer&aposs DiseaseAlzheimer&aposs disease modelAlzheimer&aposs disease riskAmericanBiologicalBiological MarkersCaribbean HispanicCellsChromosomesCodeCommunitiesComplexCustomDataData CollectionEconomicsEnrollmentEpigenetic ProcessEthnic groupGenesGeneticGenetic VariationGenomicsGenotypeGoalsHealth PolicyHeritabilityHispanicLatinxLatinx populationLocalized DiseaseLogisticsMethodsModelingMolecularNeurodegenerative DisordersNot Hispanic or LatinoParticipantPathway AnalysisPathway interactionsPhenotypePopulationPopulation HeterogeneityPublic HealthRaceRegulatory ElementResourcesRiskRisk FactorsSample SizeSamplingSiteStandardizationStatistical Data InterpretationTestingTissuesTrans-Omics for Precision MedicineVariantadjudicateadjudicationbaseclinical practicecohortdata managementgenetic architecturegenetic risk factorgenetic testinggenetic variantgenome wide association studygenome-widegenomic biomarkerhealth disparityimprovedmulti-ethnicnoveloutreachpredictive modelingrecruitsocialtranscriptome
项目摘要
PROJECT SUMMARY
The genomics of Alzheimer Disease is complex and evidence to date suggests that different ancestry groups
have distinct genetic factors that influence risk. In this project, we will perform multiple statistical analyses of
generated genetic data in African American, African, and Hispanic/Latinx populations to identify genetic factors
that are distinct within those groups. We will develop and apply new methods for identifying regulatory elements
and leveraging admixed chromosomes that are features of these populations. Finally, we will summarize results
through polygenic and pathway analyses to identify specific molecular mechanisms that harbor genetic variants
influence Alzheimer risk in each of these populations.
项目概要
阿尔茨海默病的基因组学很复杂,迄今为止的证据表明不同的血统群体
具有影响风险的独特遗传因素。在这个项目中,我们将进行多项统计分析
生成非裔美国人、非洲人和西班牙裔/拉丁裔人群的遗传数据,以识别遗传因素
在这些群体中是不同的。我们将开发并应用新方法来识别监管要素
并利用这些种群特征的混合染色体。最后我们来总结一下结果
通过多基因和途径分析来识别包含遗传变异的特定分子机制
影响每个人群的阿尔茨海默病风险。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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William S Bush其他文献
DNA from multiple viral species is associated with Alzheimer's disease risk
来自多种病毒物种的 DNA 与阿尔茨海默病风险相关
- DOI:
10.1002/alz.13414 - 发表时间:
2023-08-14 - 期刊:
- 影响因子:0
- 作者:
Marlene Tejeda;J. Farrell;Congcong Zhu;L. Wetzler;Kathryn L. Lunetta;William S Bush;Eden Martin;Li;Gerard D Schellenberg;M. Pericak;J. Haines;Lindsay A Farrer;Richard Sherva - 通讯作者:
Richard Sherva
Methylome-wide analysis reveals epigenetic marks associated with resistance to tuberculosis in HIV-infected individuals from East Africa.
全甲基化分析揭示了东非艾滋病毒感染者与结核病抵抗力相关的表观遗传标记。
- DOI:
- 发表时间:
2021 - 期刊:
- 影响因子:6.4
- 作者:
Catherine M. Stein;Penelope Benchek;J. Bartlett;R. Igo;Rafal S. Sobota;K. Chervenak;Harriet Mayanja;C. F. von Reyn;Timothy Lahey;William S Bush;W. H. Boom;William K. Scott;Carmen J. Marsit;Giorgio Sirugo;Scott M. Williams - 通讯作者:
Scott M. Williams
T-cell receptor diversity in minimal change disease in the NEPTUNE study
NEPTUNE 研究中微小病变性疾病中 T 细胞受体的多样性
- DOI:
10.1007/s00467-022-05696-x - 发表时间:
2023-04 - 期刊:
- 影响因子:3
- 作者:
Shiying Liu;William S Bush;K. Miskimen;Agustin Gonzalez;Jessica N. Cooke Bailey;I. Konidari;Jacob L. McCauley;J. Sedor;John F. O'Toole;Dana C Crawford - 通讯作者:
Dana C Crawford
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants
通过多祖先全基因组发现 187 种新风险变异来表征前列腺癌风险
- DOI:
10.1038/s41588-023-01534-4 - 发表时间:
2023-11-09 - 期刊:
- 影响因子:30.8
- 作者:
Anqi Wang;Jiayi Shen;Alex Rodriguez;E. Saunders;Fei Chen;Rohini Janivara;B. Darst;Xin Sheng;Yili Xu;Alisha Chou;S. Benlloch;Tokhir Dadaev;M. Brook;A. Plym;A. Sahimi;Thomas J Hoffman;Atushi Takahashi;K. Matsuda;Y. Momozawa;Masashi Fujita;T. Laisk;Jessica Figueredo;Kenneth R. Muir;Shuji Ito;Xiaoxi Liu;Yuji Uchio;M. Kubo;Y. Kamatani;A. Lophatananon;Peggy Wan;Caroline Andrews;Adriana Lori;P. Choudhury;J. Schleutker;T. Tammela;C. Sipeky;Anssi Auvinen;Graham G. Giles;M. Southey;R. MacInnis;C. Cybulski;D. Wokołorczyk;J. Lubiński;C. Rentsch;Kelly Cho;Benjamin H. McMahon;D. Neal;J. Donovan;F. Hamdy;Richard M. Martin;B. Nordestgaard;S. F. Nielsen;Maren Weischer;S. Bojesen;Andreas Røder;H. V. Stroomberg;J. Batra;Suzanne K. Chambers;L. Horvath;Judith A. Clements;Wayne Tilly;G. Risbridger;H. Gronberg;M. Aly;R. Szulkin;Martin Eklund;T. Nordstrom;Nora Pashayan;A. Dunning;M. Ghoussaini;R. Travis;Tim J Key;E. Riboli;Jong Y. Park;T. A. Sellers;Hui Lin;D. Albanes;S. Weinstein;Michael B. Cook;L. Mucci;E. Giovannucci;S. Lindstrom;P. Kraft;David J Hunter;K. Penney;Constance Turman;C. Tangen;P. Goodman;Ian M. Thompson;Robert J. Hamilton;Neil Fleshner;A. Finelli;M. Parent;Janet L. Stanford;Elaine A. Ostrander;Stella Koutros;L. B. Beane Freeman;M. Stampfer;A. Wolk;N. Håkansson;Gerald L. Andriole;R. N. Hoover;M. Machiela;K. D. Sørensen;Michael Borre;William J Blot;W. Zheng;E. Yeboah;James E Mensah;Yong;Hong;Ninghan Feng;Xueying Mao;Yudong Wu;Shan;Zan Sun;S N Thibodeau;S. McDonnell;D. Schaid;C. West;Gill Barnett;C. Maier;T. Schnoeller;Manuel Luedeke;A. Kibel;Bettina F Drake;O. Cussenot;G. Cancel;F. Menegaux;Thérèse Truong;Y. Koudou;Esther M John;E. Grindedal;L. Maehle;K. Khaw;S. Ingles;M. Stern;Ana Vega;A. Gómez;L. Fachal;B. Rosenstein;Sarah L. Kerns;H. Ostrer;Manuel R Teixeira;P. Paulo;Andreia Brandão;S. Watya;Alex Lubwama;J. Bensen;Eboneé N. Butler;James L Mohler;Jack A. Taylor;M. Kogevinas;T. Dierssen;G. Castaño‐Vinyals;L. Cannon;C. Teerlink;Chad D Huff;P. Pilié;Yao Yu;R. Bohlender;Jian Gu;Sara S. Strom;L. Multigner;P. Blanchet;L. Brureau;R. Kaneva;C. Slavov;V. Mitev;Robin J. Leach;H. Brenner;Xuechen Chen;Bernd Holleczek;B. Schöttker;Eric A Klein;A. Hsing;Rick A. Kittles;Adam B. Murphy;Christopher J. Logothetis;Jeri Kim;S. Neuhausen;L. Steele;Y. Ding;W. Isaacs;B. Nemesure;A. Hennis;J. Carpten;H. Pandha;Agnieszka Michael;K. De Ruyck;G. De Meerleer;P. Ost;Jianfeng Xu;A. Razack;Jasmine Lim;Soo;Lisa F. Newcomb;Daniel W. Lin;J. Fowke;C. Neslund;B. Rybicki;Marija Gamulin;D. Lessel;T. Kuliš;N. Usmani;A. Abraham;Sandeep Singhal;M. Parliament;Frank Claessens;Steven Joniau;T. Van den Broeck;M. Gago;J. Castelao;María Elena Martínez;Samantha E. T. Larkin;Paul A. Townsend;Claire Aukim;William S Bush;M. Aldrich;Dana C Crawford;S. Srivastava;Jennifer Cullen;G. Petrovics;G. Casey;Ying Wang;Y. Tettey;J. Lachance;Wei Tang;R. Biritwum;A. Adjei;Evelyn Tay;A. Truelove;S. Niwa;K. Yamoah;K. Govindasami;A. Chokkalingam;Jacob M. Keaton;J. Hellwege;Peter E. Clark;M. Jalloh;S. Gueye;L. Niang;O. Ogunbiyi;Olayiwola Shittu;O. Amodu;A. Adebiyi;O. Aisuodionoe;Hafees O Ajibola;M. Jamda;O. Oluwole;Maxwell Nwegbu;B. Adusei;S. Mante;Afua Darkwa;H. Diop;Susan M Gundell;M. Roobol;G. Jenster;Ron H N van Schaik;Jennifer J Hu;M. Sanderson;L. Kachuri;Rohit Varma;R. Mckean;M. Torres;Michael H. Preuss;R. Loos;M. Zawistowski;Sebastian Zöllner;Zeyun Lu;S. K. Van Den Eeden;D. Easton;S. Ambs;T. Edwards;R. Mägi;Timothy R Rebbeck;L. Fritsche;S. Chanock;S. I. Berndt;F. Wiklund;H. Nakagawa;John S. Witte;J. Gaziano;Amy C Justice;N. Mancuso;C. Terao;R. Eeles;Z. Kote;R. Madduri;David V Conti;C. Haiman - 通讯作者:
C. Haiman
the genetic etiology
遗传病因学
- DOI:
- 发表时间:
2024-09-14 - 期刊:
- 影响因子:0
- 作者:
C. Bellenguez;L. Kleineidam;Amin Najaf Sonia;A. Naj;Grenier;Andrade Victor Holmans Peter A Benjamin;A. Bol;van der Lee Vincent;Costa Sven J.;Kuulasmaa Marcos R.;Carla Abdelnour;Alcolea Emilio;Alegret Daniel;Alvarez Ignacio Álvarez Victoria Armstrong Montserrat;Arosio Beatrice Athanasiu Lavinia Bailly Henri Banaj Neri Alfonso Arias;Below Ana Belén;Blesa Rafael Boada Mercè Boerwinkle Eric Borroni Barbara Aless;ra;Henry;Keeley J. Brookes;Luis Ignacio;Buiza;Katharina Burholt Vanessa Dolores Bûrger;William S Bush;Cantwell Miguel;Laura Cervera;C. Charbonnier;Hung;J. A. Claassen;A. Corma;Carolina;Daniele;Dardiotis Efthimios Dartigues Jean;D. Deyn;Peter Paul;Paiva Lopes;de Witte Lot D Katia;del Ser;Denning Teodoro;Nicola DeStefano;Dichgans Anita;Diez;Djurovic Srdjan Duron Emmanuelle Düzel Emrah Dufouil Carole Paolo Dionigi;Espinosa Valentina;Ewers Michael Faber Ana;Sune Fallgaard;D. Fardo;Fenoglio;Chiara;Harald Hanon Kara L Hampel;Hardy John Hartmann Annette M Olivier;Holmes Clive Holstege Henne Vilas Raquel Huerto Per;Seshadri Sudha Andreassen Ole A Giacomina;M. Ingelsson;Cornelia M. Van Duijn;R. Sims;W. M. van der Flier;Agustin Ruiz;Jean;A. Palotie;M. Daly;H. Jacob;A. Matakidou;H. Runz;S. John;R. Plenge;M. Mccarthy;J. Hunkapiller;Meg Ehm;D. Waterworth;Caroline Fox;A. Malarstig;K. Klinger;Kathy Call;tim Behrens;P. Loerch;T. Mäkelä;J. Kaprio;P. Virolainen;Kari Pulkki;Kilpi;M. Perola;J. Partanen;A. Pitkäranta;Kaarteenaho;S. Vainio;M. Turpeinen;R. Serpi;Tarja Laitinen;J. Mäkelä;V. Kosma;Kujala;Outi Tuovila;Minna Hendolin;Pakkanen;J. Waring;B. Riley;Jimmy Z Liu;Shameek Biswas;D. Diogo;C. Marshall;Xinli Hu;M. Gossel;Rob Graham;Beryl B. Cummings;S. Ripatti;J. Schleutker;Mikko Arvas;reetta Hinttala Olli carpén 347;J. Kettunen;A. Mannermaa;J. Laukkanen;Valtteri Julkunen;A. Remes;Kälviäinen;J. Peltola;P. Tienari;Juha O. Rinne;A. Ziemann;S. Esmaeeli;N. Smaoui;A. Lehtonen;Susan Eaton;S. Lahdenperä;J. Adelsberg;J. Michon;Geoff Kerchner;Natalie Bowers;John D. Eicher;Vinay Mehta;P. Gormley;K. Lindén;Christopher Whelan;Fanli Xu;D. Pulford;Martti A Färkkilä;S. Pikkarainen;A. Jussila;T. Blomster;M. Kiviniemi;M. Voutilainen;Bob Georgantas;Graham A. R. Heap;F. Rahimov;K. Usiskin;Tim Lu;D. Oh;Kirsi Kalpala;Melissa Miller;L. Mccarthy;Kari K Eklund;A. Palomäki;P. Isomäki;L. Pirilä;O. Kaipiainen;Johanna Huhtakangas;A. Lertratanakul;M. Hochfeld;N. Bing;J. Gordillo;N. Mars;Margit K. Pelkonen;P. Kauppi;H. Kankaanranta;Harju;David W. Close;Steven Greenberg;Hubert Chen;Jo Betts;Soumitra Ghosh;V. Salomaa;Niiranen;M. Juonala;K. Metsärinne;M. Kähönen;J. Junttila;Markku Laakso;J. Pihlajamäki;J. Sinisalo;M. Taskinen;Bennett Challis;Andrew Peterson;Audrey M. Chu;J. Parkkinen;Anthony Muslin;H. Joensuu;Meretoja;L. Aaltonen;Johanna Mattson;A. Auranen;P. Karihtala;S. Kauppila;P. Auvinen;K. Elenius;Popovic;J. Schutzman;Andrey Loboda;A. Chhibber;Heli J. Lehtonen;S. McDonough;Marika Crohns;Diptee A. Kulkarni;K. Kaarniranta;terhi Ollila Joni A. turunen 356;S. Seitsonen;Hannu Uusitalo;V. Aaltonen;H. Uusitalo;M. Luodonpää;N. Hautala;Stephanie Loomis;Erich Strauss;Hao Chen;Anna I. Podgornaia;Joshua Hoffman;K. Tasanen;L. Huilaja;K. Hannula;Salmi;S. Peltonen;L. Koulu;Harvima;Ying Wu;David Choy;P. Pussinen;A. Salminen;Salo;Dave Rice;Pekka Nieminen;U. Palotie;M. Siponen;L. Suominen;P. Mäntylä;Gursoy;V. Anttonen;K. Sipilä;J. Davis;D. Quarless;S. Petrovski;Eleonor Wigmore;Chia;P. Bronson;Ellen A. Tsai;Yunfeng Huang;Joseph C Maranville;Samir Wadhawan;E. Kvikstad;Minal caliskan;tushar Bhangale Diana chang 336;S. Pendergrass;E. Holzinger;Xing Chen;Å. Hedman;Karen S. King;C;E. Xu;F. Augé;C. Chatelain;D. Rajpal;Dongyu Liu;Kathy Call;Tai;Matt Brauer;M. Kurki;J. Karjalainen;A. Havulinna;A. Jalanko;P. Palta;Pietro della;Briotta Parolo;Wei Zhou;S. Lemmelä;M. Rivas;J. Harju;Arto A Lehisto;A. Ganna;V. Llorens;H. Laivuori;S. Rüeger;Mari E. K. Niemi;tukiainen 331;Mary Pat reeve 331;H. Heyne;Kimmo Palin;Javier Garcia;H. Siirtola;Kiiskinen;Jiwoo Lee;K. Tsuo;A. Elliott;K. Kristiansson;K. Hyvärinen;J. Ritari;Miika Koskinen;K. Pylkäs;Marita Kalaoja;Minna M. Karjalainen;Mantere;Kangasniemi;S. Heikkinen;Laakkonen;Sipeky;S. Heron;A. Karlsson;Dhanaprakash Jambulingam;V. Rathinakannan;Risto Kajanne;M. Aavikko;Manuel González Jiménez;Pietro della Briotta Parola;Arto Lehistö;M. Kanai;M. Kaunisto;Elina Kilpeläinen;P. Sipilä;Georg Brein;Ghazal Awaisa;Anastasia Shcherban;K. Donner;A. Loukola;P. Laiho;Sistonen;Kaiharju;Markku Laukkanen;Elina Järvensivu;S. Lähteenmäki;Lotta Männikkö;Wong;Hannele Mattsson;T. Hiekkalinna;Paajanen;K. Pärn;Javier Gracia;Martin Woon;B. Wright;chuang;S. Younkin;chang;Lei Yu;Yuanchao Zhang;Yi Zhao;Xiongwei Zhu - 通讯作者:
Xiongwei Zhu
William S Bush的其他文献
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{{ truncateString('William S Bush', 18)}}的其他基金
Project 1: Genetic Discovery Within Diverse Ancestry Cohorts
项目 1:不同血统群体中的基因发现
- 批准号:
10654539 - 财政年份:2022
- 资助金额:
$ 63.43万 - 项目类别:
Genomic, Epigenomic, and Transcriptomic Mechanisms of Contributing to Alzheimer's Disease Risk in Diverse Ancestral Populations
不同祖先人群中阿尔茨海默病风险的基因组、表观基因组和转录组机制
- 批准号:
10301691 - 财政年份:2021
- 资助金额:
$ 63.43万 - 项目类别:
The Alzheimer's Disease Translational Data Science Training Program
阿尔茨海默病转化数据科学培训计划
- 批准号:
10475653 - 财政年份:2021
- 资助金额:
$ 63.43万 - 项目类别:
The Alzheimer's Disease Translational Data Science Training Program
阿尔茨海默病转化数据科学培训计划
- 批准号:
10686916 - 财政年份:2021
- 资助金额:
$ 63.43万 - 项目类别:
The Alzheimer Disease Sequence Analysis Collaborative
阿尔茨海默病序列分析协作组织
- 批准号:
9788240 - 财政年份:2018
- 资助金额:
$ 63.43万 - 项目类别:
The Alzheimer Disease Sequence Analysis Collaborative
阿尔茨海默病序列分析协作组织
- 批准号:
10474474 - 财政年份:2018
- 资助金额:
$ 63.43万 - 项目类别:
The Alzheimer Disease Sequence Analysis Collaborative
阿尔茨海默病序列分析协作组织
- 批准号:
10000822 - 财政年份:2018
- 资助金额:
$ 63.43万 - 项目类别:
The Alzheimer Disease Sequence Analysis Collaborative
阿尔茨海默病序列分析协作组织
- 批准号:
9661768 - 财政年份:2018
- 资助金额:
$ 63.43万 - 项目类别:
The Alzheimer Disease Sequence Analysis Collaborative
阿尔茨海默病序列分析协作组织
- 批准号:
10242911 - 财政年份:2018
- 资助金额:
$ 63.43万 - 项目类别:
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