Works by Narisu, Narisu

Results: 28

Association Analysis of Genetic Variants with Type 2 Diabetes in a Mongolian Population in China.

Published in:

Journal of Diabetes Research, 2015, v. 2015, p. 1, doi. 10.1155/2015/613236

By:

Haihua Bai;
Haiping Liu;
Suyalatu Suyalatu;
Xiaosen Guo;
Shandan Chu;
Ying Chen;
Tianming Lan;
Burenbatu Borjigin;
Orlov, Yuriy L.;
Posukh, Olga L.;
Xiuqin Yang;
Guilan Guilan;
Osipova, Ludmila P.;
Qizhu Wu;
Narisu Narisu

Publication type:

Article

Use of microarray hybrid capture and next-generation sequencing to identify the anatomy of a transgene.

Published in:

Nucleic Acids Research, 2013, v. 41, n. 6, p. e70, doi. 10.1093/nar/gks1463

By:

DuBose, Amanda J.;
Lichtenstein, Stephen T.;
Narisu, Narisu;
Bonnycastle, Lori L.;
Swift, Amy J.;
Chines, Peter S.;
Collins, Francis S.

Publication type:

Article

Newly identified loci that influence lipid concentrations and risk of coronary artery disease.

Published in:

Nature Genetics, 2008, v. 40, n. 2, p. 161, doi. 10.1038/ng.76

By:

Willer, Cristen J.;
Sanna, Serena;
Jackson, Anne U.;
Scuteri, Angelo;
Bonnycastle, Lori L.;
Clarke, Robert;
Heath, Simon C.;
Timpson, Nicholas J.;
Najjar, Samer S.;
Stringham, Heather M.;
Strait, James;
Duren, William L.;
Maschio, Andrea;
Busonero, Fabio;
Mulas, Antonella;
Albai, Giuseppe;
Swift, Amy J.;
Morken, Mario A.;
Narisu, Narisu;
Bennett, Derrick

Publication type:

Article

The Genome of a Mongolian Individual Reveals the Genetic Imprints of Mongolians on Modern Human Populations.

Published in:

Genome Biology & Evolution, 2014, v. 6, n. 12, p. 3122, doi. 10.1093/gbe/evu242

By:

Haihua Bai;
Xiaosen Guo;
Dong Zhang;
Narisu Narisu;
Junjie Bu;
Jirimutu Jirimutu;
Fan Liang;
Xiang Zhao;
Yanping Xing;
Dingzhu Wang;
Tongda Li;
Yanru Zhang;
Baozhu Guan;
Xukui Yang;
Zili Yang;
Shuangshan Shuangshan;
Zhe Su;
Huiguang Wu;
Wenjing Li;
Ming Chen

Publication type:

Article

Interactions between genetic variation and cellular environment in skeletal muscle gene expression.

Published in:

PLoS ONE, 2018, v. 13, n. 4, p. 1, doi. 10.1371/journal.pone.0195788

By:

Taylor, D. Leland;
Knowles, David A.;
Scott, Laura J.;
Ramirez, Andrea H.;
Casale, Francesco Paolo;
Wolford, Brooke N.;
Guan, Li;
Varshney, Arushi;
Albanus, Ricardo D’Oliveira;
Parker, Stephen C. J.;
Narisu, Narisu;
Chines, Peter S.;
Erdos, Michael R.;
Welch, Ryan P.;
Kinnunen, Leena;
Saramies, Jouko;
Sundvall, Jouko;
Lakka, Timo A.;
Laakso, Markku;
Tuomilehto, Jaakko

Publication type:

Article

A Drosophila functional evaluation of candidates from human genome-wide association studies of type 2 diabetes and related metabolic traits identifies tissue-specific roles for dHHEX.

Published in:

BMC Genomics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2164-14-136

By:

Pendse, Jay;
Ramachandran, Prasanna V.;
Jianbo Na;
Narisu, Narisu;
Fink, Jill L.;
Cagan, Ross L.;
Collins, Francis S.;
Baranski, Thomas J.

Publication type:

Article

Single-cell transcriptomic profiling of human pancreatic islets reveals genes responsive to glucose exposure over 24 h.

Published in:

Diabetologia, 2024, v. 67, n. 10, p. 2246, doi. 10.1007/s00125-024-06214-4

By:

Grenko, Caleb M.;
Taylor, Henry J.;
Bonnycastle, Lori L.;
Xue, Dongxiang;
Lee, Brian N.;
Weiss, Zoe;
Yan, Tingfen;
Swift, Amy J.;
Mansell, Erin C.;
Lee, Angela;
Robertson, Catherine C.;
Narisu, Narisu;
Erdos, Michael R.;
Chen, Shuibing;
Collins, Francis S.;
Taylor, D. Leland

Publication type:

Article

Bone dysplasia in Hutchinson‐Gilford progeria syndrome is associated with dysregulated differentiation and function of bone cell populations.

Published in:

Aging Cell, 2023, v. 22, n. 9, p. 1, doi. 10.1111/acel.13903

By:

Cabral, Wayne A.;
Stephan, Chris;
Terajima, Masahiko;
Thaivalappil, Abhirami A.;
Blanchard, Owen;
Tavarez, Urraca L.;
Narisu, Narisu;
Yan, Tingfen;
Wincovitch, Stephen M.;
Taga, Yuki;
Yamauchi, Mitsuo;
Kozloff, Kenneth M.;
Erdos, Michael R.;
Collins, Francis S.

Publication type:

Article

Analysis of somatic mutations identifies signs of selection during in vitro aging of primary dermal fibroblasts.

Published in:

Aging Cell, 2019, v. 18, n. 6, p. N.PAG, doi. 10.1111/acel.13010

By:

Narisu, Narisu;
Rothwell, Rebecca;
Vrtačnik, Peter;
Rodríguez, Sofía;
Didion, John;
Zöllner, Sebastian;
Erdos, Michael R.;
Collins, Francis S.;
Eriksson, Maria

Publication type:

Article

The genetic regulatory signature of type 2 diabetes in human skeletal muscle.

Published in:

Nature Communications, 2016, v. 7, n. 6, p. 11764, doi. 10.1038/ncomms11764

By:

Scott, Laura J.;
Erdos, Michael R.;
Huyghe, Jeroen R.;
Welch, Ryan P.;
Beck, Andrew T.;
Wolford, Brooke N.;
Chines, Peter S.;
Didion, John P.;
Narisu, Narisu;
Stringham, Heather M.;
Taylor, D. Leland;
Jackson, Anne U.;
Vadlamudi, Swarooparani;
Bonnycastle, Lori L.;
Kinnunen, Leena;
Saramies, Jouko;
Sundvall, Jouko;
Albanus, Ricardo D'Oliveira;
Kiseleva, Anna;
Hensley, John

Publication type:

Article

Mitochondrial polymorphisms and susceptibility to type 2 diabetes-related traits in Finns.

Published in:

Human Genetics, 2005, v. 118, n. 2, p. 245, doi. 10.1007/s00439-005-0046-4

By:

Mohlke, Karen L.;
Jackson, Anne U.;
Scott, Laura J.;
Peck, Erin C.;
Suh, Yong D.;
Chines, Peter S.;
Watanabe, Richard M.;
Buchanan, Thomas A.;
Conneely, Karen N.;
Erdos, Michael R.;
Narisu, Narisu;
Enloe, Sareena;
Valle, Timo T.;
Tuomilehto, Jaakko;
Bergman, Richard N.;
Boehnke, Michael;
Collins, Francis S.

Publication type:

Article

Autosomal Dominant Diabetes Arising From a Wolfram Syndrome 1 Mutation.

Published in:

Diabetes, 2013, v. 62, n. 11, p. 3943, doi. 10.2337/db13-0571

By:

Bonnycastle, Lori L.;
Chines, Peter S.;
Takashi Hara;
Huyghe, Jeroen R.;
Swift, Amy J.;
Heikinheimo, Pirkko;
Mahadevan, Jana;
Peltonen, Sirkku;
Huopio, Hanna;
Nuutila, Pirjo;
Narisu, Narisu;
Goldfeder, Rachel L.;
Stitzel, Michael L.;
Simin Lu;
Boehnke, Michael;
Urano, Fumihiko;
Collins, Francis S.;
Laakso, Markku

Publication type:

Article

Comprehensive Association Study of Type 2 Diabetes and Related Quantitative Traits With 222 Candidate Genes.

Published in:

Diabetes, 2008, v. 57, n. 11, p. 3136, doi. 10.2337/db07-1731

By:

Gaulton, Kyle J.;
Willer, Cristen J.;
Yun Li;
Scott, Laura J.;
Conneely, Karen N.;
Jackson, Anne U.;
Duren, William L.;
Chines, Peter S.;
Narisu, Narisu;
Bonnycastle, Lori L.;
Luo, Jingchun;
Tong, Maurine;
Sprau, Andrew G.;
Pugh, Elizabeth W.;
Doheny, Kimberly F.;
Valle, Timo T.;
Abecasis, Gonçalo R.;
Tuomilehto, Jaakko;
Bergman, Richard N.;
Collins, Francis S.

Publication type:

Article

Screening of 134 Single Nucleotide Polymorphisms (SNPs) Previously Associated With Type 2 Diabetes Replicates Association With 12 SNPs in Nine Genes.

Published in:

Diabetes, 2007, v. 56, n. 1, p. 256, doi. 10.2337/db06-0461

By:

Willer, Cristen J.;
Bonnycastle, Lori L.;
Conneely, Karen N.;
Duren, William L.;
Jackson, Anne U.;
Scott, Laura J.;
Narisu, Narisu;
Chines, Peter S.;
Skol, Andrew;
Stringham, Heather M.;
Petrie, John;
Erdos, Michael R.;
Swift, Amy J.;
Enloe, Sareena T.;
Sprau, Andrew G.;
Smith, Eboni;
Tong, Maurine;
Doheny, Kimberly F.;
Pugh, Elizabeth W.;
Watanabe, Richard M.

Publication type:

Article

Association of Transcription Factor 7-Like 2 (TCF7L2) Variants With Type 2 Diabetes in a Finnish Sample.

Published in:

Diabetes, 2006, v. 55, n. 9, p. 2649, doi. 10.2337/db06-0341

By:

Scott, Laura J.;
Bonnycastle, Lori L.;
Willer, Cristen J.;
Sprau, Andrew G.;
Jackson, Anne U.;
Narisu, Narisu;
Duren, William L.;
Chines, Peter S.;
Stringham, Heather M.;
Erdos, Michael R.;
Valle, Timo T.;
Tuomilehto, Jaakko;
Bergman, Richard N.;
Mohlke, Karen L.;
Collins, Francis S.;
Boehnke, Michael

Publication type:

Article

Common Variants in Maturity-Onset Diabetes of the Young Genes Contribute to Risk of Type 2 Diabetes in Finns.

Published in:

Diabetes, 2006, v. 55, n. 9, p. 2534, doi. 10.2337/db06-0178

By:

Bonnycastle, Lori L.;
Willer, Cristen J.;
Conneely, Karen N.;
Jackson, Anne U.;
Burrill, Cecily P.;
Watanabe, Richard M.;
Chines, Peter S.;
Narisu, Narisu;
Scott, Laura J.;
Enloe, Sareena T.;
Swift, Amy J.;
Duren, William L.;
Stringham, Heather M.;
Erdos, Michael R.;
Riebow, Nancy L.;
Buchanan, Thomas A.;
Valle, Timo T.;
Tuomilehto, Jaakko;
Bergman, Richard N.;
Mohlke, Karen L.

Publication type:

Article

Genetic variation near the hepatocyte nuclear factor-4 alpha gene predicts susceptibility to type 2 diabetes.

Published in:

2004

By:

Silander, Kaisa;
Mohlke, Karen L.;
Scott, Laura J.;
Peck, Erin C.;
Hollstein, Pablo;
Skol, Andrew D.;
Jackson, Anne U.;
Deloukas, Panagiotis;
Hunt, Sarah;
Stavrides, George;
Chines, Peter S.;
Erdos, Michael R.;
Narisu, Narisu;
Conneely, Karen N.;
Li, Chun;
Fingerlin, Tasha E.;
Dhanjal, Sharanjeet K.;
Valle, Timo T.;
Bergman, Richard N.;
Tuomilehto, Jaakko

Publication type:

journal article

A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14.

Published in:

2004

By:

Silander, Kaisa;
Scott, Laura J.;
Valle, Timo T.;
Mohlke, Karen L.;
Stringham, Heather M.;
Wiles, Kerry R.;
Duren, William L.;
Doheny, Kimberly F.;
Pugh, Elizabeth W.;
Chines, Peter;
Narisu, Narisu;
White, Peggy P.;
Fingerlin, Tasha E.;
Jackson, Anne U.;
Li, Chun;
Ghosh, Soumitra;
Magnuson, Victoria L.;
Colby, Kimberly;
Erdos, Michael R.;
Hill, Jason E.

Publication type:

journal article

Adiponectin GWAS loci harboring extensive allelic heterogeneity exhibit distinct molecular consequences.

Published in:

PLoS Genetics, 2020, v. 16, n. 9, p. 1, doi. 10.1371/journal.pgen.1009019

By:

Spracklen, Cassandra N.;
Iyengar, Apoorva K.;
Vadlamudi, Swarooparani;
Raulerson, Chelsea K.;
Jackson, Anne U.;
Brotman, Sarah M.;
Wu, Ying;
Cannon, Maren E.;
Davis, James P.;
Crain, Aaron T.;
Currin, Kevin W.;
Perrin, Hannah J.;
Narisu, Narisu;
Stringham, Heather M.;
Fuchsberger, Christian;
Locke, Adam E.;
Welch, Ryan P.;
Kuusisto, Johanna K.;
Pajukanta, Päivi;
Scott, Laura J.

Publication type:

Article

Genetic variant effects on gene expression in human pancreatic islets and their implications for T2D.

Published in:

Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-18581-8

By:

Viñuela, Ana;
Varshney, Arushi;
van de Bunt, Martijn;
Prasad, Rashmi B.;
Asplund, Olof;
Bennett, Amanda;
Boehnke, Michael;
Brown, Andrew A.;
Erdos, Michael R.;
Fadista, João;
Hansson, Ola;
Hatem, Gad;
Howald, Cédric;
Iyengar, Apoorva K.;
Johnson, Paul;
Krus, Ulrika;
MacDonald, Patrick E.;
Mahajan, Anubha;
Manning Fox, Jocelyn E.;
Narisu, Narisu

Publication type:

Article

A Transcription Start Site Map in Human Pancreatic Islets Reveals Functional Regulatory Signatures.

Published in:

2021

By:

Varshney, Arushi;
Kyono, Yasuhiro;
Elangovan, Venkateswaran Ramamoorthi;
Wang, Collin;
Erdos, Michael R.;
Narisu, Narisu;
Albanus, Ricardo D'Oliveira;
Orchard, Peter;
Stitzel, Michael L.;
Collins, Francis S.;
Kitzman, Jacob O.;
Parker, Stephen C.J.

Publication type:

journal article

Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.

Published in:

PLoS Genetics, 2017, v. 13, n. 10, p. 1, doi. 10.1371/journal.pgen.1007079

By:

Davis, James P.;
Huyghe, Jeroen R.;
Locke, Adam E.;
Jackson, Anne U.;
Sim, Xueling;
Stringham, Heather M.;
Teslovich, Tanya M.;
Welch, Ryan P.;
Fuchsberger, Christian;
Narisu, Narisu;
Chines, Peter S.;
Kangas, Antti J.;
Soininen, Pasi;
Ala-Korpela, Mika;
Kuusisto, Johanna;
Collins, Francis S.;
Laakso, Markku;
Boehnke, Michael;
Mohlke, Karen L.

Publication type:

Article

Putative Prostate Cancer Risk SNP in an Androgen Receptor-Binding Site of the Melanophilin Gene Illustrates Enrichment of Risk SNPs in Androgen Receptor Target Sites.

Published in:

Human Mutation, 2016, v. 37, n. 1, p. 52, doi. 10.1002/humu.22909

By:

Bu, Huajie;
Narisu, Narisu;
Schlick, Bettina;
Rainer, Johannes;
Manke, Thomas;
Schäfer, Georg;
Pasqualini, Lorenza;
Chines, Peter;
Schweiger, Michal R.;
Fuchsberger, Christian;
Klocker, Helmut

Publication type:

Article

Comprehensive Analysis of Pathogenic Deletion Variants in Fanconi Anemia Genes.

Published in:

Human Mutation, 2014, v. 35, n. 11, p. 1342, doi. 10.1002/humu.22680

By:

Flynn, Elizabeth K.;
Kamat, Aparna;
Lach, Francis P.;
Donovan, Frank X.;
Kimble, Danielle C.;
Narisu, Narisu;
Sanborn, Erica;
Boulad, Farid;
Davies, Stella M.;
Gillio, Alfred P.;
Harris, Richard E.;
MacMillan, Margaret L.;
Wagner, John E.;
Smogorzewska, Agata;
Auerbach, Arleen D.;
Ostrander, Elaine A.;
Chandrasekharappa, Settara C.

Publication type:

Article

Colocalization of GWAS and eQTL signals at loci with multiple signals identifies additional candidate genes for body fat distribution.

Published in:

Human Molecular Genetics, 2019, v. 28, n. 24, p. 4161, doi. 10.1093/hmg/ddz263

By:

Wu, Ying;
Broadaway, K Alaine;
Raulerson, Chelsea K;
Scott, Laura J;
Pan, Calvin;
Ko, Arthur;
He, Aiqing;
Tilford, Charles;
Fuchsberger, Christian;
Locke, Adam E;
Stringham, Heather M;
Jackson, Anne U;
Narisu, Narisu;
Kuusisto, Johanna;
Pajukanta, Päivi;
Collins, Francis S;
Boehnke, Michael;
Laakso, Markku;
Lusis, Aldons J;
Civelek, Mete

Publication type:

Article

Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study.

Published in:

Human Molecular Genetics, 2018, v. 27, n. 9, p. 1664, doi. 10.1093/hmg/ddy067

By:

Teslovich, Tanya M.;
Kim, Daniel Seung;
Xianyong Yin;
Stančcáková, Alena;
Jackson, Anne U.;
Wielscher, Matthias;
Naj, Adam;
Perry, John R. B.;
Huyghe, Jeroen R.;
Stringham, Heather M.;
Davis, James P.;
Raulerson, Chelsea K.;
Welch, Ryan P.;
Fuchsberger, Christian;
Locke, Adam E.;
Xueling Sim;
Chines, Peter S.;
Narisu, Narisu;
Kangas, Antti J.;
Soininen, Pasi

Publication type:

Article

Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 3, p. 535, doi. 10.1093/hmg/ddp522

By:

Perry, John R.B.;
Weedon, Michael N.;
Langenberg, Claudia;
Jackson, Anne U.;
Lyssenko, Valeriya;
Sparsø, Thomas;
Thorleifsson, Gudmar;
Grallert, Harald;
Ferrucci, Luigi;
Maggio, Marcello;
Paolisso, Giuseppe;
Walker, Mark;
Palmer, Colin N.A.;
Payne, Felicity;
Young, Elizabeth;
Herder, Christian;
Narisu, Narisu;
Morken, Mario A.;
Bonnycastle, Lori L.;
Owen, Katharine R.

Publication type:

Article

A rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian family.

Published in:

BMC Medical Genetics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2350-15-34

By:

Haihua Bai;
Xukui Yang;
Temuribagen;
Guilan;
Suyalatu;
Narisu Narisu;
Huiguang Wu;
Yujie Chen;
Yangjian Liu;
Qizhu Wu

Publication type:

Article