Works by Narisu, Narisu

Results: 28

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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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