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Tytuł :
Age-dependent changes in mean and variance of gene expression across tissues in a twin cohort
Autorzy :
Viñuela, Ana
Brown, Andrew A.
Buil, Alfonso
Tsai, Pei-Chien
Davies, Matthew N
Bell, Jordana Tzenova
Dermitzakis, Emmanouil T
Spector, Timothy D
Small, Kerrin S.
Pokaż więcej
Temat :
ddc:576.5
ddc:590
ddc:025.063/570
Association Studies Articles
Źródło :
Human Molecular Genetics, Vol. 27, No 4 (2018) pp. 732-741
Viñuela, A, Brown, A A, Buil, A, Tsai, P-C, Davies, M N, Bell, J T, Dermitzakis, E T, Spector, T D & Small, K S 2018, ' Age-dependent changes in mean and variance of gene expression across tissues in a twin cohort ', Human Molecular Genetics, vol. 27, no. 4, pp. 732–741 . https://doi.org/10.1093/hmg/ddx424
Opis pliku :
application/pdf
Tytuł :
Discovery of novel heart rate-associated loci using the Exome Chip
Autorzy :
Dominiczak, Anna F.
Padmanabhan, Sandosh
Sattar, Naveed
van den Berg, Marten E.
Warren, Helen R.
Cabrera, Claudia P.
Verweij, Niek
Mifsud, Borbala
Harssler, Jeffrey
Bihlmeyer, Nathan A.
Fu, Yi-Ping
Weiss, Stefan
Lin, Henry J.
Grarup, Niels
Li-Gao, Ruifang
Pistis, Giorgio
Shah, Nabi
Brody, Jennifer A.
Müller-Nurasyid, Martina
Lin, Honghuang
Mei, Hao
Smith, Albert V.
Lyytikäinen, Leo-Pekka
Hall, Leanne M.
van Setten, Jessica
Trompet, Stella
Prins, Bram P.
Isaacs, Aaron
Radmanesh, Farid
Marten, Jonathan
Entwistle, Aiman
Kors, Jan A.
Silva, Claudia T.
Alonso, Alvaro
Bis, Joshua C.
de Boer, Rudolf
de Haan, Hugoline G.
de Mutsert, Renée
Dedoussis, George
Doney, Alex S.F.
Ellinor, Patrick T.
Eppinga, Ruben N.
Felix, Stephan B.
Guo, Xiuqing
Hagemeijer, Yanick
Hansen, Torben
Harris, Tamara B.
Heckbert, Susan R.
Huang, Paul L.
Hwang, Shih-Jen
Kähönen, Mika
Kanters, Jørgen K.
Kolcic, Ivana
Launer, Lenore J.
Li, Man
Yao, Jie
Linneberg, Allan
Liu, Simin
Macfarlane, Peter W.
Mangino, Massimo
Morris, Andrew D.
Mulas, Antonella
Murray, Alison D.
Nelson, Christopher P.
Orrú, Marco
Peters, Annette
Porteous, David J.
Poulter, Neil
Pstay, Bruce M.
Qi, Lihong
Raitakari, Olli T.
Rivadeneira, Fernando
Roselli, Carolina
Rudan, Igor
Sever, Peter
Sinner, Moritz F.
Soliman, Elsayed Z.
Spector, Timothy D.
Stanton, Alice V.
Stirrups, Kathleen E.
Taylor, Kent D.
Tobin, Martin D.
Uitterlinden, André
Vaartjes, Ilonca
Hoes, Arno W.
van der Meer, Peter
Völker, Uwe
Waldenberger, Melanie
Xie, Zhijun
Zoledziewska, Magdalena
Tinker, Andrew
Polasek, Ozren
Rosand, Jonathan
Jamshidi, Yalda
van Duijn, Cornelia M.
Zeggini, Eleftheria
Jukema, J. Wouter
Asselbergs, Folkert W.
Samani, Nilesh J.
Lehtimäki, Terho
Gudnason, Vilmundur
Wilson, James
Lubitz, Steven A.
Kääb, Stefan
Sotoodehnia, Nona
Caulfield, Mark J.
Palmer, Colin N.A.
Sanna, Serena
Mook-Kanamori, Dennis O.
Deloukas, Panos
Pedersen, Oluf
Rotter, Jerome I.
Dörr, Marcus
O'Donnell, Chris J.
Hayward, Caroline
Arking, Dan E.
Kooperberg, Charles
van der Harst, Pim
Eijgelsheim, Mark
Stricker, Bruno H.
Munroe, Patricia B.
Pokaż więcej
Temat :
Biochemistry & Molecular Biology
06 Biological Sciences
PROJECT
VARIANTS
Research Support, Non-U.S. Gov't
RISK-FACTOR
IDENTIFICATION
Biokemia, solu- ja molekyylibiologia - Biochemistry, cell and molecular biology
PROTEIN
ddc:610
Genetiikka, kehitysbiologia, fysiologia - Genetics, developmental biology, physiology
DISEASE
Life Sciences & Biomedicine
GENE
COMPLEX TRAITS
Sisätaudit - Internal medicine
Medizin
Science & Technology
Research Support, N.I.H., Extramural
ALL-CAUSE MORTALITY
11 Medical And Health Sciences
Genetics & Heredity
Journal Article
GENOME-WIDE ASSOCIATION
Association Studies Articles
Źródło :
van den Berg, M E, Warren, H R, Cabrera, C P, Verweij, N, Mifsud, B, Haessler, J, Bihlmeyer, N A, Fu, Y-P, Weiss, S, Lin, H J, Grarup, N, Li-Gao, R, Pistis, G, Shah, N, Brody, J A, Müller-Nurasyid, M, Lin, H, Mei, H, Smith, A V, Lyytikäinen, L-P, Hall, L M, van Setten, J, Trompet, S, Prins, B P, Isaacs, A, Radmanesh, F, Marten, J, Entwistle, A, Kors, J A, Silva, C T, Alonso, A, Bis, J C, de Boer, R, de Haan, H G, de Mutsert, R, Dedoussis, G, Dominiczak, A F, Doney, A S F, Ellinor, P T, Eppinga, R N, Felix, S B, Guo, X, Hagemeijer, Y, Hansen, T, Harris, T B, Heckbert, S R, Huang, P L, Hwang, S-J, Kähönen, M, Kanters, J K, Kolcic, I, Launer, L J, Li, M, Yao, J, Linneberg, A, Liu, S, Macfarlane, P W, Mangino, M, Morris, A D, Mulas, A, Murray, A D, Nelson, C P, Orrú, M, Padmanabhan, S, Peters, A, Porteous, D J, Poulter, N, Psaty, B M, Qi, L, Raitakari, O T, Rivadeneira, F, Roselli, C, Rudan, I, Sattar, N, Sever, P, Sinner, M F, Soliman, E Z, Spector, T D, Stanton, A V, Stirrups, K E, Taylor, K D, Tobin, M D, Uitterlinden, A, Vaartjes, I, Hoes, A W, van der Meer, P, Völker, U, Waldenberger, M, Xie, Z, Zoledziewska, M, Tinker, A, Polasek, O, Rosand, J, Jamshidi, Y, van Duijn, C M, Zeggini, E, Wouter Jukema, J, Asselbergs, F W, Samani, N J, Lehtimäki, T, Gudnason, V, Wilson, J, Lubitz, S A, Kääb, S, Sotoodehnia, N, Caulfield, M J, Palmer, C N A, Sanna, S, Mook-Kanamori, D O, Deloukas, P, Pedersen, O, Rotter, J I, Dörr, M, O'Donnell, C J, Hayward, C, Arking, D E, Kooperberg, C, van der Harst, P, Eijgelsheim, M, Stricker, B H & Munroe, P B 2017, ' Discovery of novel heart rate-associated loci using the Exome Chip ', Human Molecular Genetics . https://doi.org/10.1093/hmg/ddx113
van den Berg, M E, Warren, H R, Cabrera, C P, Verweij, N, Mifsud, B, Haessler, J, Bihlmeyer, N A, Fu, Y-P, Weiss, S, Lin, H J, Grarup, N, Li-Gao, R, Pistis, G, Shah, N, Brody, J A, Müller-Nurasyid, M, Lin, H, Mei, H, Smith, A V, Lyytikäinen, L-P, Hall, L M, van Setten, J, Trompet, S, Prins, B P, Isaacs, A, Radmanesh, F, Marten, J, Entwistle, A, Kors, J A, Silva, C T, Alonso, A, Bis, J C, de Boer, R A, de Haan, H G, de Mutsert, R, Dedoussis, G, Dominiczak, A F, Doney, A S F, Ellinor, P T, Eppinga, R N, Felix, S B, Guo, X, Hagemeijer, Y, Hansen, T, Harris, T B, Heckbert, S R, Huang, P L, Hwang, S-J, Kähönen, M, Kanters, J K, Kolcic, I, Launer, L J, Li, M, Yao, X J, Linneberg, A, Liu, S, Macfarlane, P W, Mangino, M, Morris, A D, Mulas, A, Murray, A D, Nelson, C P, Orrù, M, Padmanabhan, S, Peters, A, Porteous, D J, Poulter, N, Psaty, B M, Qi, L, Raitakari, O T, Rivadeneira, F, Roselli, C, Rudan, I, Sattar, N, Sever, P, Sinner, M F, Soliman, E Z, Spector, T D, Stanton, A V, Stirrups, K E, Taylor, K D, Tobin, M D, Uitterlinden, A, Vaartjes, I, Hoes, A W, van der Meer, P, Völker, U, Waldenberger, M, Xie, Z, Zoledziewska, M, Tinker, A, Polasek, O, Rosand, J, Jamshidi, Y, van Duijn, C M, Zeggini, E, Jukema, J W, Asselbergs, F W, Samani, N J, Lehtimäki, T, Gudnason, V, Wilson, J, Lubitz, S A, Kääb, S, Sotoodehnia, N, Caulfield, M J, Palmer, C N A, Sanna, S, Mook-Kanamori, D O, Deloukas, P, Pedersen, O, Rotter, J I, Dörr, M, O'Donnell, C J, Hayward, C, Arking, D E, Kooperberg, C, van der Harst, P, Eijgelsheim, M, Stricker, B H C & Munroe, P B 2017, ' Discovery of novel heart rate-associated loci using the Exome Chip ', Human Molecular Genetics, vol. 26, no. 12, pp. 2346-2363 . https://doi.org/10.1093/hmg/ddx113
Opis pliku :
application/pdf; fulltext
Tytuł :
Mapping eQTLs with RNA-seq reveals novel susceptibility genes, non-coding RNAs and alternative-splicing events in systemic lupus erythematosus
Autorzy :
Odhams, Christopher A.
Cortini, Andrea
Chen, Lingyan
Roberts, Amy L.
Viñuela, Ana
Buil, Alfonso
Small, Kerrin S.
Dermitzakis, Emmanouil T
Morris, David L.
Vyse, Timothy J.
Cunninghame Graham, Deborah S.
Pokaż więcej
Temat :
Lupus Erythematosus, Systemic
Alternative Splicing
Quantitative Trait Loci
RNA, Untranslated
Gene Expression Regulation
Carbon-Nitrogen Ligases with Glutamine as Amide-N-Donor
Haplotypes
ddc:576.5
Chromosome Mapping
Polymorphism, Single Nucleotide
T Cell Transcription Factor 1
Genome-Wide Association Study
Genetic Predisposition to Disease
Female
Humans
Male
Association Studies Articles
Źródło :
Human Molecular Genetics (2017) P. ddw417
Odhams, C A, Cortini, A, Chen, L, Roberts, A L, Viñuela, A, Buil, A, Small, K S, Dermitzakis, E T, Morris, D L, Vyse, T J & Cunninghame Graham, D S 2017, ' Mapping eQTLs with RNA-Seq Reveals Novel Susceptibility Genes, Non-Coding RNAs, and Alternative-Splicing Events in Systemic Lupus Erythematosus ', Human Molecular Genetics, vol. 26, no. 5, pp. 1003-1017 . https://doi.org/10.1093/hmg/ddw417
Opis pliku :
application/pdf; Print
Tytuł :
Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease
Autorzy :
Orlando, Giulia
Law, Philip J.
Palin, Kimmo
Tuupanen, Sari
Gylfe, Alexandra
Hänninen, Ulrika A.
Cajuso, Tatiana
Tanskanen, Tomas
Kondelin, Johanna
Kaasinen, Eevi
Sarin, Antti-Pekka
Kaprio, Jaakko
Eriksson, Johan G.
Rissanen, Harri
Knekt, Paul
Pukkala, Eero
Jousilahti, Pekka
Salomaa, Veikko
Ripatti, Samuli
Palotie, Aarno
Järvinen, Heikki
Renkonen-Sinisalo, Laura
Lepistö, Anna
Böhm, Jan
Mecklin, Jukka-Pekka
Al-Tassan, Nada A.
Palles, Claire
Martin, Lynn
Barclay, Ella
Tenesa, Albert
Farrington, Susan
Timofeeva, Maria N.
Meyer, Brian F.
Wakil, Salma M.
Campbell, Harry
Smith, Christopher G.
Idziaszczyk, Shelley
Maughan, Timothy S.
Kaplan, Richard
Kerr, Rachel
Kerr, David
Buchanan, Daniel D.
Ko Win, Aung
Hopper, John
Jenkins, Mark
Lindor, Noralane M.
Newcomb, Polly A.
Gallinger, Steve
Conti, David
Schumacher, Fred
Casey, Graham
Taipale, Jussi
Cheadle, Jeremy P.
Dunlop, Malcolm G.
Tomlinson, Ian P.
Aaltonen, Lauri A.
Houlston, Richard S.
Pokaż więcej
Temat :
3122 Cancers
RC0254
METAANALYSIS
SUSCEPTIBILITY LOCI
3126 Surgery, anesthesiology, intensive care, radiology
FUNCTIONAL VARIATION
COHORT PROFILE
INTESTINAL INFLAMMATION
VARIANTS
digestive system diseases
3121 Internal medicine
CROHNS-DISEASE
Terveystiede - Health care science
3111 Biomedicine
IMPUTATION
BIRTH COHORT
GENOME-WIDE ASSOCIATION
Syöpätaudit - Cancers
Association Studies Articles
Źródło :
Orlando, G, Law, P J, Palin, K, Tuupanen, S, Gylfe, A, Hanninen, U, Cajuso, T, Tanskanen, T, Kondelin, J, Kaasinen, E, Sarin, A-P, Kaprio, J, Eriksson, J G, Rissanen, H, Knekt, P, Pukkala, E, Jousilahti, P, Salomaa, V, Ripatti, S, Palotie, A, Jarvinen, H J, Renkonen-Sinisalo, L, Lepisto, A, Bohm, J, Meklin, J-P, Al-Tassan, N A, Palles, C, Martin, L, Barclay, E, Tenesa, A, Farrington, S, Timofeeva, M, Meyer, B F, Wakil, S M, Campbell, H, Smith, C G, Idziaszczyk, S, Maughan, T S, Kaplan, R, Kerr, R, Kerr, D, Buchanan, D, Win, A K, Hopper, J L, Jenkins, M C, Lindor, N M, Newcomb, P A, Gallinger, S, Conti, D, Schumacher, F, Casey, G, Taipale, J, Cheadle, J P, Dunlop, M, Tomlinson, I, Aaltonen, L A & Houlston, R S 2016, ' Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease ', Human Molecular Genetics, vol. 25, no. 11, pp. 2349-2359 . https://doi.org/10.1093/hmg/ddw087
Opis pliku :
application/pdf; fulltext
Tytuł :
Prenatal and early life influences on epigenetic age in children:a study of mother-offspring pairs from two cohort studies
Autorzy :
Simpkin, Andrew J
Hemani, Gibran
Suderman, Matthew
Gaunt, Tom R
Lyttleton, Oliver
Mcardle, Wendy L
Ring, Susan M
Sharp, Gemma C
Tilling, Kate
Horvath, Steve
Kunze, Sonja
Peters, Annette
Waldenberger, Melanie
Ward-Caviness, Cavin
Nohr, Ellen A
Sørensen, Thorkild I A
Relton, Caroline L
Smith, George Davey
Pokaż więcej
Temat :
Research Support, N.I.H., Extramural
Journal Article
Association Studies Articles
Research Support, Non-U.S. Gov't
Źródło :
Simpkin, A J, Hemani, G, Suderman, M, Gaunt, T R, Lyttleton, O, Mcardle, W L, Ring, S M, Sharp, G C, Tilling, K, Horvath, S, Kunze, S, Peters, A, Waldenberger, M, Ward-Caviness, C, Nohr, E A, Sørensen, T I A, Relton, C L & Smith, G D 2016, ' Prenatal and early life influences on epigenetic age in children : a study of mother-offspring pairs from two cohort studies ', Human Molecular Genetics, vol. 25, no. 1, pp. 191-201 . https://doi.org/10.1093/hmg/ddv456
Simpkin, A J, Hemani, G, Suderman, M, Gaunt, T R, Lyttleton, O, McArdle, W L, Ring, S M, Sharp, G C, Tilling, K, Horvath, S, Kunze, S, Peters, A, Waldenberger, M, Ward-Caviness, C, Nohr, E A, Sorensen, T, Relton, C L & Smith, G D 2016, ' Prenatal and early life influences on epigenetic age in children : a study of mother-offspring pairs from two cohort studies ', Human Molecular Genetics, vol. 25, no. 1, pp. 191-201 . https://doi.org/10.1093/hmg/ddv456
Opis pliku :
application/pdf
Tytuł :
Genomic prediction of complex human traits: relatedness, trait architecture and predictive meta-models
Autorzy :
Spiliopoulou, Athina
Nagy, Reka
Bermingham, Mairead L.
Huffman, Jennifer E.
Hayward, Caroline
Vitart, Veronique
Rudan, Igor
Campbell, Harry
Wright, Alan F.
Wilson, James F.
Pong-Wong, Ricardo
Agakov, Felix
Navarro, Pau
Haley, Chris S.
Pokaż więcej
Temat :
Association Studies Articles
Źródło :
Spiliopoulou, A, Nagy, R, Bermingham, M L, Huffman, J E, Hayward, C, Vitart, V, Rudan, I, Campbell, H, Wright, A F, Wilson, J F, Pong-Wong, R, Agakov, F, Navarro, P & Haley, C S 2015, ' Genomic prediction of complex human traits: relatedness, trait architecture and predictive meta-models ', Human Molecular Genetics, vol. 24, no. 14, pp. 4167-4182 . https://doi.org/10.1093/hmg/ddv145
Opis pliku :
application/pdf
Tytuł :
Salt-inducible kinase 3, SIK3, is a new gene associated with hearing
Autorzy :
Wolber, Lisa E
Girotto, Giorgia
Buniello, Annalisa
Vuckovic, Dragana
Pirastu, Nicola
Lorente-Cánovas, Beatriz
Rudan, Igor
Hayward, Caroline
Polasek, Ozren
Ciullo, Marina
Mangino, Massimo
Steves, Claire
Concas, Maria Pina
Cocca, Massilimiliano
Spector, Tim D
Gasparini, Paolo
Steel, Karen P
Williams, Frances M K
Pokaż więcej
Temat :
otorhinolaryngologic diseases
Association Studies Articles
Źródło :
Wolber, L E, Girotto, G, Buniello, A, Vuckovic, D, Pirastu, N, Lorente-Cánovas, B, Rudan, I, Hayward, C, Polasek, O, Ciullo, M, Mangino, M, Steves, C, Concas, M P, Cocca, M, Spector, T D, Gasparini, P, Steel, K P & Williams, F M K 2014, ' Salt-inducible kinase 3, SIK3, is a new gene associated with hearing ', Human Molecular Genetics . https://doi.org/10.1093/hmg/ddu346
Opis pliku :
application/pdf
Tytuł :
Germline Sequence Variants in TGM3 and RGS22 Confer Risk of Basal Cell Carcinoma
Autorzy :
Stacey, Simon N.
Sulem, Patrick
Gudbjartsson, Daniel F.
Jonasdottir, Aslaug
Thorleifsson, Gudmar
Gudjonsson, Sigurjon A.
Masson, Gisli
Gudmundsson, Julius
Sigurgeirsson, Bardur
Benediktsdottir, Kristrun R.
Thorisdottir, Kristin
Ragnarsson, Rafn
Fuentelsaz, Victoria
Corredera, Cristina
Grasa, Matilde
Planelles, Dolores
Sanmartin, Onofre
Rudnai, Peter
Gurzau, Eugene
Koppova, Kvetoslava
Hemminki, Kari
Nexø, Bjørn A
Tjønneland, Anne
Overvad, Kim
Johannsdottir, Hrefna
Helgadottir, Hafdis T.
Thorsteinsdottir, Unnur
Kong, Augustine
Vogel, Ulla
Kumar, Rajiv
Nagore, Eduardo
Mayordomo, José I.
Rafnar, Thorunn
Olafsson, Jon H.
Stefansson, Kari
Pokaż więcej
Temat :
Association Studies Articles
Źródło :
Stacey, S N, Sulem, P, Gudbjartsson, D F, Jonasdottir, A, Thorleifsson, G, Gudjonsson, S A, Masson, G, Gudmundsson, J, Sigurgeirsson, B, Benediktsdottir, K R, Thorisdottir, K, Ragnarsson, R, Fuentelsaz, V, Corredera, C, Grasa, M, Planelles, D, Sanmartin, O, Rudnai, P, Gurzau, E, Koppova, K, Hemminki, K, Nexø, B A, Tjønneland, A, Overvad, K, Johannsdottir, H, Helgadottir, H T, Thorsteinsdottir, U, Kong, A, Vogel, U, Kumar, R, Nagore, E, Mayordomo, J I, Rafnar, T, Olafsson, J H & Stefansson, K 2014, ' Germline Sequence Variants in TGM3 and RGS22 Confer Risk of Basal Cell Carcinoma ', Human Molecular Genetics, vol. 23, no. 11, pp. 3045-53 . https://doi.org/10.1093/hmg/ddt671
Tytuł :
GWAS of human bitter taste perception identifies new loci and reveals additional complexity of bitter taste genetics
Autorzy :
Ledda, Mirko
Kutalik, Zoltán
Souza Destito, Maria C.
Souza, Milena M.
Cirillo, Cintia A.
Zamboni, Amabilene
Martin, Nathalie
Morya, Edgard
Sameshima, Koichi
Beckmann, Jacques S.
le Coutre, Johannes
Bergmann, Sven
Genick, Ulrich K.
Pokaż więcej
Temat :
genetic structures
psychological phenomena and processes
Association Studies Articles
stomatognathic system
Źródło :
Human Molecular Genetics, vol. 23, no. 1, pp. 259-267
Opis pliku :
application/pdf

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