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Genome-Wide Analysis Identifies Two Susceptibility Loci for Positive Thyroid Peroxidase and Thyroglobulin Antibodies.
Published in:
2019
By:
- Matana, Antonela;
- Boutin, Thibaud;
- Torlak, Vesela;
- Brdar, Dubravka;
- Gunjača, Ivana;
- Kolčić, Ivana;
- Boraska Perica, Vesna;
- Punda, Ante;
- Polašek, Ozren;
- Barbalić, Maja;
- Hayward, Caroline;
- Zemunik, Tatijana
Publication type:
journal article
Genome-Wide Association Analysis and Genomic Prediction of Thyroglobulin Plasma Levels.
Published in:
International Journal of Molecular Sciences, 2022, v. 23, n. 4, p. 2173, doi. 10.3390/ijms23042173
By:
- Pleić, Nikolina;
- Babić Leko, Mirjana;
- Gunjača, Ivana;
- Boutin, Thibaud;
- Torlak, Vesela;
- Matana, Antonela;
- Punda, Ante;
- Polašek, Ozren;
- Hayward, Caroline;
- Zemunik, Tatijana
Publication type:
Article
Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH.
Published in:
Diabetologia, 2023, v. 66, n. 7, p. 1260, doi. 10.1007/s00125-023-05922-7
By:
- Li, Josephine H.;
- Brenner, Laura N.;
- Kaur, Varinderpal;
- Figueroa, Katherine;
- Schroeder, Philip;
- Huerta-Chagoya, Alicia;
- MAGIC Investigators;
- Chen, Ji;
- Spracklen, Cassandra N.;
- Marenne, Gaëlle;
- Varshney, Arushi;
- Corbin, Laura J.;
- Luan, Jian'an;
- Willems, Sara M.;
- Wu, Ying;
- Zhang, Xiaoshuai;
- Horikoshi, Momoko;
- Boutin, Thibaud S.;
- Mägi, Reedik;
- Waage, Johannes
Publication type:
Article
Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits.
Published in:
PLoS Genetics, 2020, v. 16, n. 7, p. 1, doi. 10.1371/journal.pgen.1008785
By:
- Bretherick, Andrew D.;
- Canela-Xandri, Oriol;
- Joshi, Peter K.;
- Clark, David W.;
- Rawlik, Konrad;
- Boutin, Thibaud S.;
- Zeng, Yanni;
- Amador, Carmen;
- Navarro, Pau;
- Rudan, Igor;
- Wright, Alan F.;
- Campbell, Harry;
- Vitart, Veronique;
- Hayward, Caroline;
- Wilson, James F.;
- Tenesa, Albert;
- Ponting, Chris P.;
- Baillie, J. Kenneth;
- Haley, Chris
Publication type:
Article
Genetic Variants in the ST6GAL1 Gene Are Associated with Thyroglobulin Plasma Level in Healthy Individuals.
Published in:
Thyroid, 2019, v. 29, n. 6, p. 886, doi. 10.1089/thy.2018.0661
By:
- Matana, Antonela;
- Popović, Marijana;
- Gunjača, Ivana;
- Boraska Perica, Vesna;
- Barbalić, Maja;
- Zemunik, Tatijana;
- Boutin, Thibaud;
- Hayward, Caroline;
- Torlak, Vesela;
- Brdar, Dubravka;
- Punda, Ante;
- Kolčić, Ivana;
- Polašek, Ozren;
- Rudan, Igor
Publication type:
Article
Publisher Correction: Parent of origin genetic effects on methylation in humans are common and influence complex trait variation.
Published in:
2019
By:
- Zeng, Yanni;
- Amador, Carmen;
- Xia, Charley;
- Marioni, Riccardo;
- Sproul, Duncan;
- Walker, Rosie M.;
- Morris, Stewart W.;
- Bretherick, Andrew;
- Canela-Xandri, Oriol;
- Boutin, Thibaud S.;
- Clark, David W.;
- Campbell, Archie;
- Rawlik, Konrad;
- Hayward, Caroline;
- Nagy, Reka;
- Tenesa, Albert;
- Porteous, David J.;
- Wilson, James F.;
- Deary, Ian J.;
- Evans, Kathryn L.
Publication type:
Correction Notice
Parent of origin genetic effects on methylation in humans are common and influence complex trait variation.
Published in:
Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-09301-y
By:
- Zeng, Yanni;
- Amador, Carmen;
- Xia, Charley;
- Marioni, Riccardo;
- Sproul, Duncan;
- Walker, Rosie M.;
- Morris, Stewart W.;
- Bretherick, Andrew;
- Canela-Xandri, Oriol;
- Boutin, Thibaud S.;
- Clark, David W.;
- Campbell, Archie;
- Rawlik, Konrad;
- Hayward, Caroline;
- Nagy, Reka;
- Tenesa, Albert;
- Porteous, David J.;
- Wilson, James F.;
- Deary, Ian J.;
- Evans, Kathryn L.
Publication type:
Article
Fine-mapping and cell-specific enrichment at corneal resistance factor loci prioritize candidate causal regulatory variants.
Published in:
Communications Biology, 2020, v. 3, n. 1, p. 1, doi. 10.1038/s42003-020-01497-w
By:
- Jiang, Xinyi;
- Dellepiane, Nefeli;
- Pairo-Castineira, Erola;
- Boutin, Thibaud;
- Kumar, Yatendra;
- Bickmore, Wendy A.;
- Vitart, Veronique
Publication type:
Article
Genome-wide meta-analyses of stratified depression in Generation Scotland and UK Biobank.
Published in:
Translational Psychiatry, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41398-017-0034-1
By:
- Hall, Lynsey S.;
- Adams, Mark J.;
- Arnau-Soler, Aleix;
- Clarke, Toni-Kim;
- Howard, David M.;
- Zeng, Yanni;
- Davies, Gail;
- Hagenaars, Saskia P.;
- Maria Fernandez-Pujals, Ana;
- Gibson, Jude;
- Wigmore, Eleanor M.;
- Boutin, Thibaud S.;
- Hayward, Caroline;
- Scotland, Generation;
- Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium;
- Porteous, David J.;
- Deary, Ian J.;
- Thomson, Pippa A.;
- Haley, Chris S.;
- McIntosh, Andrew M.
Publication type:
Article
An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort.
Published in:
Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-47436-6
By:
- Kerr, Shona M.;
- Klaric, Lucija;
- Halachev, Mihail;
- Hayward, Caroline;
- Boutin, Thibaud S.;
- Meynert, Alison M.;
- Semple, Colin A.;
- Tuiskula, Annukka M.;
- Swan, Heikki;
- Santoyo-Lopez, Javier;
- Vitart, Veronique;
- Haley, Chris;
- Dean, John;
- Miedzybrodzka, Zosia;
- Aitman, Timothy J.;
- Wilson, James F.
Publication type:
Article
Insights into the genetic basis of retinal detachment.
Published in:
Human Molecular Genetics, 2020, v. 29, n. 4, p. 689, doi. 10.1093/hmg/ddz294
By:
- Boutin, Thibaud S;
- Charteris, David G;
- Chandra, Aman;
- Campbell, Susan;
- Hayward, Caroline;
- Campbell, Archie;
- Consortium, UK Biobank Eye & Vision;
- Nandakumar, Priyanka;
- Hinds, David;
- Team, 23andMe Research;
- Mitry, Danny;
- Vitart, Veronique
Publication type:
Article
New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics.
Published in:
Human Molecular Genetics, 2017, v. 26, n. 2, p. 438, doi. 10.1093/hmg/ddw399
By:
- Springelkamp, Henriët;
- Iglesias, Adriana I.;
- Mishra, Aniket;
- Höhn, René;
- Wojciechowski, Robert;
- Khawaja, Anthony P.;
- Nag, Abhishek;
- Ya Xing Wang;
- Jie Jin Wang;
- Cuellar-Partida, Gabriel;
- Gibson, Jane;
- Cooke Bailey, Jessica N.;
- Vithana, Eranga N.;
- Gharahkhani, Puya;
- Boutin, Thibaud;
- Ramdas, Wishal D.;
- Zeller, Tanja;
- Luben, Robert N.;
- Yonova-Doing, Ekaterina;
- Viswanathan, Ananth C.
Publication type:
Article
Characterisation of an inflammation-related epigenetic score and its association with cognitive ability.
Published in:
Clinical Epigenetics, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s13148-020-00903-8
By:
- Stevenson, Anna J.;
- McCartney, Daniel L.;
- Hillary, Robert F.;
- Campbell, Archie;
- Morris, Stewart W.;
- Bermingham, Mairead L.;
- Walker, Rosie M.;
- Evans, Kathryn L.;
- Boutin, Thibaud S.;
- Hayward, Caroline;
- McRae, Allan F.;
- McColl, Barry W.;
- Spires-Jones, Tara L.;
- McIntosh, Andrew M.;
- Deary, Ian J.;
- Marioni, Riccardo E.
Publication type:
Article
Genome-wide meta-analysis identifies novel loci associated with parathyroid hormone level.
Published in:
Molecular Medicine, 2018, v. 24, n. 1, p. N.PAG, doi. 10.1186/s10020-018-0018-5
By:
- Matana, Antonela;
- Brdar, Dubravka;
- Torlak, Vesela;
- Boutin, Thibaud;
- Popović, Marijana;
- Gunjača, Ivana;
- Kolčić, Ivana;
- Boraska Perica, Vesna;
- Punda, Ante;
- Polašek, Ozren;
- Barbalić, Maja;
- Hayward, Caroline;
- Zemunik, Tatijana
Publication type:
Article
SNP and Haplotype Regional Heritability Mapping (SNHap-RHM): Joint Mapping of Common and Rare Variation Affecting Complex Traits.
Published in:
Frontiers in Genetics, 2022, v. 12, p. 1, doi. 10.3389/fgene.2021.791712
By:
- Oppong, Richard F.;
- Boutin, Thibaud;
- Campbell, Archie;
- McIntosh, Andrew M.;
- Porteous, David;
- Hayward, Caroline;
- Haley, Chris S.;
- Navarro, Pau;
- Knott, Sara
Publication type:
Article
Genome-wide meta-analysis associates HLADQA1/ DRB1 and LPA and lifestyle factors with human longevity.
Published in:
Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00934-5
By:
- Joshi, Peter K.;
- Pirastu, Nicola;
- Kentistou, Katherine A.;
- Fischer, Krista;
- Hofer, Edith;
- Schraut, Katharina E.;
- Clark, David W.;
- Nutile, Teresa;
- Barnes, Catriona L. K.;
- Timmers, Paul R. H. J.;
- Xia Shen;
- Gandin, Ilaria;
- McDaid, Aaron F.;
- Hansen, Thomas Folkmann;
- Gordon, Scott D.;
- Giulianini, Franco;
- Boutin, Thibaud S.;
- Abdellaoui, Abdel;
- Wei Zhao;
- Medina-Gomez, Carolina
Publication type:
Article
The struggle for life of the genome's selfish architects.
Published in:
Biology Direct, 2011, v. 6, n. 1, p. 19, doi. 10.1186/1745-6150-6-19
By:
- Hua-Van, Aurélie;
- Le Rouzic, Arnaud;
- Boutin, Thibaud S.;
- Filée, Jonathan;
- Capy, Pierre
Publication type:
Article
Colocalization of corneal resistance factor GWAS loci with GTEx e/sQTLs highlights plausible candidate causal genes for keratoconus postnatal corneal stroma weakening.
Published in:
Frontiers in Genetics, 2023, p. 01, doi. 10.3389/fgene.2023.1171217
By:
- Xinyi Jiang;
- Boutin, Thibaud;
- Vitart, Veronique
Publication type:
Article
When do myopia genes have their effect? Comparison of genetic risks between children and adults.
Published in:
Genetic Epidemiology, 2016, v. 40, n. 8, p. 756, doi. 10.1002/gepi.21999
By:
- Tideman, J. Willem L.;
- Fan, Qiao;
- Polling, Jan Roelof;
- Guo, Xiaobo;
- Yazar, Seyhan;
- Khawaja, Anthony;
- Höhn, René;
- Lu, Yi;
- Jaddoe, Vincent W.V.;
- Yamashiro, Kenji;
- Yoshikawa, Munemitsu;
- Gerhold‐Ay, Aslihan;
- Nickels, Stefan;
- Zeller, Tanja;
- He, Mingguang;
- Boutin, Thibaud;
- Bencic, Goran;
- Vitart, Veronique;
- Mackey, David A.;
- Foster, Paul J.
Publication type:
Article
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.
Published in:
Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-15706-x
By:
- Ntalla, Ioanna;
- Weng, Lu-Chen;
- Cartwright, James H.;
- Hall, Amelia Weber;
- Sveinbjornsson, Gardar;
- Tucker, Nathan R.;
- Choi, Seung Hoan;
- Chaffin, Mark D.;
- Roselli, Carolina;
- Barnes, Michael R.;
- Mifsud, Borbala;
- Warren, Helen R.;
- Hayward, Caroline;
- Marten, Jonathan;
- Cranley, James J.;
- Concas, Maria Pina;
- Gasparini, Paolo;
- Boutin, Thibaud;
- Kolcic, Ivana;
- Polasek, Ozren
Publication type:
Article
An epigenome-wide association study of sex-specific chronological ageing.
Published in:
Genome Medicine, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s13073-019-0693-z
By:
- McCartney, Daniel L.;
- Zhang, Futao;
- Hillary, Robert F.;
- Zhang, Qian;
- Stevenson, Anna J.;
- Walker, Rosie M.;
- Bermingham, Mairead L.;
- Boutin, Thibaud;
- Morris, Stewart W.;
- Campbell, Archie;
- Murray, Alison D.;
- Whalley, Heather C.;
- Porteous, David J.;
- Hayward, Caroline;
- Evans, Kathryn L.;
- Chandra, Tamir;
- Deary, Ian J.;
- McIntosh, Andrew M.;
- Yang, Jian;
- Visscher, Peter M.
Publication type:
Article
Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.
Published in:
Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0414-4
By:
- Nagy, Reka;
- Boutin, Thibaud S.;
- Marten, Jonathan;
- Huffman, Jennifer E.;
- Kerr, Shona M.;
- Campbell, Archie;
- Evenden, Louise;
- Gibson, Jude;
- Amador, Carmen;
- Howard, David M.;
- Navarro, Pau;
- Morris, Andrew;
- Deary, Ian J.;
- Hocking, Lynne J.;
- Padmanabhan, Sandosh;
- Smith, Blair H.;
- Joshi, Peter;
- Wilson, James F.;
- Hastie, Nicholas D.;
- Wright, Alan F.
Publication type:
Article

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