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Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion.
Published in:
Nature Genetics, 2013, v. 45, n. 2, p. 197, doi. 10.1038/ng.2507
By:
- Huyghe, Jeroen R;
- Jackson, Anne U;
- Fogarty, Marie P;
- Buchkovich, Martin L;
- Stan?áková, Alena;
- Stringham, Heather M;
- Sim, Xueling;
- Yang, Lingyao;
- Fuchsberger, Christian;
- Cederberg, Henna;
- Chines, Peter S;
- Teslovich, Tanya M;
- Romm, Jane M;
- Ling, Hua;
- McMullen, Ivy;
- Ingersoll, Roxann;
- Pugh, Elizabeth W;
- Doheny, Kimberly F;
- Neale, Benjamin M;
- Daly, Mark J
Publication type:
Article
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes.
Published in:
Nature Genetics, 2012, v. 44, n. 9, p. 981, doi. 10.1038/ng.2383
By:
- Morris, Andrew P;
- Voight, Benjamin F;
- Teslovich, Tanya M;
- Ferreira, Teresa;
- Segrè, Ayellet V;
- Steinthorsdottir, Valgerdur;
- Strawbridge, Rona J;
- Khan, Hassan;
- Grallert, Harald;
- Mahajan, Anubha;
- Prokopenko, Inga;
- Kang, Hyun Min;
- Dina, Christian;
- Esko, Tonu;
- Fraser, Ross M;
- Kanoni, Stavroula;
- Kumar, Ashish;
- Lagou, Vasiliki;
- Langenberg, Claudia;
- Luan, Jian'an
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
The centrosome in human genetic disease.
Published in:
Nature Reviews Genetics, 2005, v. 6, n. 3, p. 194, doi. 10.1038/nrg1557
By:
- Badano, Jose L.;
- Teslovich, Tanya M.;
- Katsanis, Nicholas
Publication type:
Article
A major locus for hereditary prostate cancer in Finland: localization by linkage disequilibrium of a haplotype in the HPCX region.
Published in:
2005
By:
- Baffoe-Bonnie, Agnes B.;
- Smith, Jeffrey R.;
- Stephan, Dietrich A.;
- Schleutker, Johanna;
- Carpten, John D.;
- Kainu, Tommi;
- Gillanders, Elizabeth M.;
- Matikainen, Mika;
- Teslovich, Tanya M.;
- Tammela, Teuvo;
- Sood, Raman;
- Balshem, Andrew M.;
- Scarborough, Sheehan D.;
- Jianfeng Xu;
- Isaacs, William B.;
- Trent, Jeffrey M.;
- Kallioniemi, Olli-P.;
- Bailey-Wilson, Joan E.
Publication type:
Correction Notice
A major locus for hereditary prostate cancer in Finland: localization by linkage disequilibrium of a haplotype in the HPCX region.
Published in:
Human Genetics, 2005, v. 117, n. 4, p. 307, doi. 10.1007/s00439-005-1306-z
By:
- Baffoe-Bonnie, Agnes B.;
- Smith, Jeffrey R.;
- Stephan, Dietrich A.;
- Schleutker, Johanna;
- Carpten, John D.;
- Kainu, Tommi;
- Gillanders, Elizabeth M.;
- Matikainen, Mika;
- Teslovich, Tanya M.;
- Tammela, Teuvo;
- Sood, Raman;
- Balshem, Andrew M.;
- Scarborough, Sheehan D.;
- Jianfeng Xu;
- Isaacs, William B.;
- Trent, Jeffrey;
- Kallioniemi, Olli-P.;
- Bailey-Wilson, Joan
Publication type:
Article
Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13.
Published in:
Human Genetics, 2003, v. 113, n. 3, p. 293, doi. 10.1007/s00439-003-0967-8
By:
- Tranebjaerg, Lisbeth;
- Teslovich, Tanya M.;
- Jones, MaryPat;
- Barmada, M. Michael;
- Fagerheim, Toril;
- Dahl, Arve;
- Escolar, Diana M.;
- Trent, Jeffrey M.;
- Gillanders, Elizabeth M.;
- Stephan, Dietrich A.
Publication type:
Article
A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment.
Published in:
European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1097, doi. 10.1038/sj.ejhg.5201670
By:
- Rendtorff, Nanna D.;
- Mei Zhu;
- Fagerheim, Toril;
- Antal, Torben L.;
- Jones, MaryPat;
- Teslovich, Tanya M.;
- Gillanders, Elizabeth M.;
- Barmada, Michael;
- Teig, Erik;
- Trent, Jeffrey M.;
- Friderici, Karen H.;
- Stephan, Dietrich A.;
- Tranebjærg, Lisbeth
Publication type:
Article
Development and production of an oligonucleotide MuscleChip: use for validation of ambiguous ESTs.
Published in:
BMC Bioinformatics, 2002, v. 3, p. 33, doi. 10.1186/1471-2105-3-33
By:
- Borup, Rehannah H. A.;
- Toppo, Stefano;
- Yi-Wen Chen;
- Teslovich, Tanya M.;
- Lanfranchi, Gerolamo;
- Valle, Giorgio;
- Hoffman, Eric P.
Publication type:
Article
Biological, clinical and population relevance of 95 loci for blood lipids.
Published in:
Nature, 2010, v. 466, n. 7307, p. 707, doi. 10.1038/nature09270
By:
- Teslovich, Tanya M.;
- Musunuru, Kiran;
- Smith, Albert V.;
- Edmondson, Andrew C.;
- Stylianou, Ioannis M.;
- Koseki, Masahiro;
- Pirruccello, James P.;
- Ripatti, Samuli;
- Chasman, Daniel I.;
- Willer, Cristen J.;
- Johansen, Christopher T.;
- Fouchier, Sigrid W.;
- Isaacs, Aaron;
- Peloso, Gina M.;
- Barbalic, Maja;
- Ricketts, Sally L.;
- Bis, Joshua C.;
- Aulchenko, Yurii S.;
- Thorleifsson, Gudmar;
- Feitosa, Mary F.
Publication type:
Article
Omics-squared: human genomic, transcriptomic and phenotypic data for genetic analysis workshop 19.
Published in:
BMC Proceedings, 2016, v. 10, p. 71, doi. 10.1186/s12919-016-0008-y
By:
- Blangero, John;
- Teslovich, Tanya M.;
- Xueling Sim;
- Almeida, Marcio A.;
- Goo Jun;
- Dyer, Thomas D.;
- Johnson, Matthew;
- Peralta, Juan M.;
- Manning, Alisa;
- Wood, Andrew R.;
- Fuchsberger, Christian;
- Kent Jr, Jack W.;
- Aguilar, David A.;
- Below, Jennifer E.;
- Farook, Vidya S.;
- Arya, Rector;
- Fowler, Sharon;
- Blackwell, Tom W.;
- Puppala, Sobha;
- Kumar, Satish
Publication type:
Article
Whole genome sequencing of 4,787 individuals identifies gene-based rare variants in age-related macular degeneration.
Published in:
Human Molecular Genetics, 2024, v. 33, n. 4, p. 374, doi. 10.1093/hmg/ddad189
By:
- Kwong, Alan;
- Zawistowski, Matthew;
- Fritsche, Lars G;
- Zhan, Xiaowei;
- Bragg-Gresham, Jennifer;
- Branham, Kari E;
- Advani, Jayshree;
- Othman, Mohammad;
- Ratnapriya, Rinki;
- Teslovich, Tanya M;
- Stambolian, Dwight;
- Chew, Emily Y;
- Abecasis, Gonçalo R;
- Swaroop, Anand
Publication type:
Article
Prosaposin is a regulator of progranulin levels and oligomerization.
Published in:
Nature Communications, 2016, v. 7, n. 6, p. 11992, doi. 10.1038/ncomms11992
By:
- Nicholson, Alexandra M.;
- Finch, NiCole A.;
- Almeida, Marcio;
- Perkerson, Ralph B.;
- van Blitterswijk, Marka;
- Wojtas, Aleksandra;
- Cenik, Basar;
- Rotondo, Sergio;
- Inskeep, Venette;
- Almasy, Laura;
- Dyer, Thomas;
- Peralta, Juan;
- Jun, Goo;
- Wood, Andrew R.;
- Frayling, Timothy M.;
- Fuchsberger, Christian;
- Fowler, Sharon;
- Teslovich, Tanya M.;
- Manning, Alisa K.;
- Kumar, Satish
Publication type:
Article
Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome.
Published in:
Nature, 2003, v. 425, n. 6958, p. 628, doi. 10.1038/nature02030
By:
- Ansley, Stephen J.;
- Badano, Jose L.;
- Blacque, Oliver E.;
- Hill, Josephine;
- Hoskins, Bethan E.;
- Leitch, Carmen C.;
- Jun Chul Kim, Carmen C.;
- Ross, Alison J.;
- Eichers, Erica R.;
- Teslovich, Tanya M.;
- Mah, Allan K.;
- Johnsen, Robert C.;
- Cavender, John C.;
- Lewis, Richard Alan;
- Leroux, Michel R.;
- Beales, Philip L.;
- Katsanis, Nicholas
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 inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes.
Published in:
Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-04611-z
By:
- Gusarova, Viktoria;
- O’Dushlaine, Colm;
- Teslovich, Tanya M.;
- Benotti, Peter N.;
- Mirshahi, Tooraj;
- Gottesman, Omri;
- Van Hout, Cristopher V.;
- Murray, Michael F.;
- Mahajan, Anubha;
- Nielsen, Jonas B.;
- Fritsche, Lars;
- Wulff, Anders Berg;
- Gudbjartsson, Daniel F.;
- Sjögren, Marketa;
- Emdin, Connor A.;
- Scott, Robert A.;
- Wen-Jane Lee;
- Small, Aeron;
- Kwee, Lydia C.;
- Dwivedi, Om Prakash
Publication type:
Article
Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 Locus.
Published in:
PLoS Genetics, 2015, v. 11, n. 1, p. 1, doi. 10.1371/journal.pgen.1004876
By:
- Mahajan, Anubha;
- Sim, Xueling;
- Ng, Hui Jin;
- Manning, Alisa;
- Rivas, Manuel A.;
- Highland, Heather M.;
- Locke, Adam E.;
- Grarup, Niels;
- Im, Hae Kyung;
- Cingolani, Pablo;
- Flannick, Jason;
- Fontanillas, Pierre;
- Fuchsberger, Christian;
- Gaulton, Kyle J.;
- Teslovich, Tanya M.;
- Rayner, N. William;
- Robertson, Neil R.;
- Beer, Nicola L.;
- Rundle, Jana K.;
- Bork-Jensen, Jette
Publication type:
Article
Re-sequencing Expands Our Understanding of the Phenotypic Impact of Variants at GWAS Loci.
Published in:
PLoS Genetics, 2014, v. 10, n. 1, p. 1, doi. 10.1371/journal.pgen.1004147
By:
- Service, Susan K.;
- Teslovich, Tanya M.;
- Fuchsberger, Christian;
- Ramensky, Vasily;
- Yajnik, Pranav;
- Koboldt, Daniel C.;
- Larson, David E.;
- Zhang, Qunyuan;
- Lin, Ling;
- Welch, Ryan;
- Ding, Li;
- McLellan, Michael D.;
- O'Laughlin, Michele;
- Fronick, Catrina;
- Fulton, Lucinda L.;
- Magrini, Vincent;
- Swift, Amy;
- Elliott, Paul;
- Jarvelin, Marjo-Riitta;
- Kaakinen, Marika
Publication type:
Article
Population Bottlenecks as a Potential Major Shaping Force of Human Genome Architecture.
Published in:
PLoS Genetics, 2007, v. 3, n. 7, p. e119, doi. 10.1371/journal.pgen.0030119
By:
- Gherman, Adrian;
- Chen, Peter E.;
- Teslovich, Tanya M.;
- Stankiewicz, Pawel;
- Withers, Marjorie;
- Kashuk, Carl S.;
- Chakravarti, Aravinda;
- Lupski, James R.;
- Cutler, David J.;
- Katsanis, Nicholas
Publication type:
Article
LocusZoom: regional visualization of genome-wide association scan results.
Published in:
Bioinformatics, 2010, v. 26, n. 18, p. 2336, doi. 10.1093/bioinformatics/btq419
By:
- Pruim, Randall J.;
- Welch, Ryan P.;
- Sanna, Serena;
- Teslovich, Tanya M.;
- Chines, Peter S.;
- Gliedt, Terry P.;
- Boehnke, Michael;
- Abecasis, Gonçalo R.;
- Willer, Cristen J.
Publication type:
Article
Therapeutic targets for HIV-1 infection in the host proteome.
Published in:
Retrovirology, 2005, v. 2, p. 20, doi. 10.1186/1742-4690-2-20
By:
- Liang, Winnie S.;
- Maddukuri, Anil;
- Teslovich, Tanya M.;
- de la Fuente, Cynthia;
- Agbottah, Emmanuel;
- Dadgar, Shabnam;
- Kehn, Kylene;
- Hautaniemi, Sampsa;
- Pumfery, Anne;
- Stephan, Dietrich A.;
- Kashanchi, Fatah
Publication type:
Article

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