Pesquisa | BVS Doenças Infecciosas e Parasitárias

1.

GDF15 linked to maternal risk of nausea and vomiting during pregnancy.

Fejzo, M; Rocha, N; Cimino, I; Lockhart, S M; Petry, C J; Kay, R G; Burling, K; Barker, P; George, A L; Yasara, N; Premawardhena, A; Gong, S; Cook, E; Rimmington, D; Rainbow, K; Withers, D J; Cortessis, V; Mullin, P M; MacGibbon, K W; Jin, E; Kam, A; Campbell, A; Polasek, O; Tzoneva, G; Gribble, F M; Yeo, G S H; Lam, B Y H; Saudek, V; Hughes, I A; Ong, K K; Perry, J R B; Sutton Cole, A; Baumgarten, M; Welsh, P; Sattar, N; Smith, G C S; Charnock-Jones, D S; Coll, A P; Meek, C L; Mettananda, S; Hayward, C; Mancuso, N; O'Rahilly, S.

Nature ; 625(7996): 760-767, 2024 Jan.

Artigo em Inglês | MEDLINE | ID: mdl-38092039

2.

Author Correction: A massive core for a cluster of galaxies at a redshift of 4.3.

Miller, T B; Chapman, S C; Aravena, M; Ashby, M L N; Hayward, C C; Vieira, J D; Weiß, A; Babul, A; Béthermin, M; Bradford, C M; Brodwin, M; Carlstrom, J E; Chen, Chian-Chou; Cunningham, D J M; De Breuck, C; Gonzalez, A H; Greve, T R; Harnett, J; Hezaveh, Y; Lacaille, K; Litke, K C; Ma, J; Malkan, M; Marrone, D P; Morningstar, W; Murphy, E J; Narayanan, D; Pass, E; Perry, R; Phadke, K A; Rennehan, D; Rotermund, K M; Simpson, J; Spilker, J S; Sreevani, J; Stark, A A; Strandet, M L; Strom, A L.

Nature ; 561(7721): E2, 2018 09.

Artigo em Inglês | MEDLINE | ID: mdl-29930351

3.

A massive core for a cluster of galaxies at a redshift of 4.3.

Miller, T B; Chapman, S C; Aravena, M; Ashby, M L N; Hayward, C C; Vieira, J D; Weiß, A; Babul, A; Béthermin, M; Bradford, C M; Brodwin, M; Carlstrom, J E; Chen, Chian-Chou; Cunningham, D J M; De Breuck, C; Gonzalez, A H; Greve, T R; Harnett, J; Hezaveh, Y; Lacaille, K; Litke, K C; Ma, J; Malkan, M; Marrone, D P; Morningstar, W; Murphy, E J; Narayanan, D; Pass, E; Perry, R; Phadke, K A; Rennehan, D; Rotermund, K M; Simpson, J; Spilker, J S; Sreevani, J; Stark, A A; Strandet, M L; Strom, A L.

Nature ; 556(7702): 469-472, 2018 04.

Artigo em Inglês | MEDLINE | ID: mdl-29695849

4.

Galaxy growth in a massive halo in the first billion years of cosmic history.

Marrone, D P; Spilker, J S; Hayward, C C; Vieira, J D; Aravena, M; Ashby, M L N; Bayliss, M B; Béthermin, M; Brodwin, M; Bothwell, M S; Carlstrom, J E; Chapman, S C; Chen, Chian-Chou; Crawford, T M; Cunningham, D J M; De Breuck, C; Fassnacht, C D; Gonzalez, A H; Greve, T R; Hezaveh, Y D; Lacaille, K; Litke, K C; Lower, S; Ma, J; Malkan, M; Miller, T B; Morningstar, W R; Murphy, E J; Narayanan, D; Phadke, K A; Rotermund, K M; Sreevani, J; Stalder, B; Stark, A A; Strandet, M L; Tang, M; Weiß, A.

Nature ; 553(7686): 51-54, 2018 01 04.

Artigo em Inglês | MEDLINE | ID: mdl-29211721

5.

Genome-wide meta-analysis identifies novel loci associated with free triiodothyronine and thyroid-stimulating hormone.

Popovic, M; Matana, A; Torlak, V; Boutin, T; Brdar, D; Gunjaca, I; Kalicanin, D; Kolcic, I; Boraska Perica, V; Punda, A; Polasek, O; Barbalic, M; Hayward, C; Zemunik, T.

J Endocrinol Invest ; 42(10): 1171-1180, 2019 Oct.

Artigo em Inglês | MEDLINE | ID: mdl-30843173

6.

Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112 117).

Clarke, T-K; Adams, M J; Davies, G; Howard, D M; Hall, L S; Padmanabhan, S; Murray, A D; Smith, B H; Campbell, A; Hayward, C; Porteous, D J; Deary, I J; McIntosh, A M.

Mol Psychiatry ; 22(10): 1376-1384, 2017 10.

Artigo em Inglês | MEDLINE | ID: mdl-28937693

7.

Assessing the genetic overlap between BMI and cognitive function.

Marioni, R E; Yang, J; Dykiert, D; Mõttus, R; Campbell, A; Davies, G; Hayward, C; Porteous, D J; Visscher, P M; Deary, I J.

Mol Psychiatry ; 21(10): 1477-82, 2016 10.

Artigo em Inglês | MEDLINE | ID: mdl-26857597

8.

Genome-wide association study of cognitive functions and educational attainment in UK Biobank (N=112 151).

Davies, G; Marioni, R E; Liewald, D C; Hill, W D; Hagenaars, S P; Harris, S E; Ritchie, S J; Luciano, M; Fawns-Ritchie, C; Lyall, D; Cullen, B; Cox, S R; Hayward, C; Porteous, D J; Evans, J; McIntosh, A M; Gallacher, J; Craddock, N; Pell, J P; Smith, D J; Gale, C R; Deary, I J.

Mol Psychiatry ; 21(6): 758-67, 2016 06.

Artigo em Inglês | MEDLINE | ID: mdl-27046643

9.

Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population.

Clarke, T-K; Lupton, M K; Fernandez-Pujals, A M; Starr, J; Davies, G; Cox, S; Pattie, A; Liewald, D C; Hall, L S; MacIntyre, D J; Smith, B H; Hocking, L J; Padmanabhan, S; Thomson, P A; Hayward, C; Hansell, N K; Montgomery, G W; Medland, S E; Martin, N G; Wright, M J; Porteous, D J; Deary, I J; McIntosh, A M.

Mol Psychiatry ; 21(3): 419-25, 2016 Mar.

Artigo em Inglês | MEDLINE | ID: mdl-25754080

10.

Genome-wide analysis of over 106 000 individuals identifies 9 neuroticism-associated loci.

Smith, D J; Escott-Price, V; Davies, G; Bailey, M E S; Colodro-Conde, L; Ward, J; Vedernikov, A; Marioni, R; Cullen, B; Lyall, D; Hagenaars, S P; Liewald, D C M; Luciano, M; Gale, C R; Ritchie, S J; Hayward, C; Nicholl, B; Bulik-Sullivan, B; Adams, M; Couvy-Duchesne, B; Graham, N; Mackay, D; Evans, J; Smith, B H; Porteous, D J; Medland, S E; Martin, N G; Holmans, P; McIntosh, A M; Pell, J P; Deary, I J; O'Donovan, M C.

Mol Psychiatry ; 21(6): 749-57, 2016 06.

Artigo em Inglês | MEDLINE | ID: mdl-27067015

11.

Molecular phenotype and bleeding risks of an inherited platelet disorder in a family with a RUNX1 frameshift mutation.

Badin, M S; Iyer, J K; Chong, M; Graf, L; Rivard, G E; Waye, J S; Paterson, A D; Pare, G; Hayward, C P M.

Haemophilia ; 23(3): e204-e213, 2017 May.

Artigo em Inglês | MEDLINE | ID: mdl-28181366

12.

Genomic approaches to bleeding disorders.

Peyvandi, F; Hayward, C P M.

Haemophilia ; 22 Suppl 5: 42-5, 2016 Jul.

Artigo em Inglês | MEDLINE | ID: mdl-27405675

13.

Regional heritability mapping method helps explain missing heritability of blood lipid traits in isolated populations.

Shirali, M; Pong-Wong, R; Navarro, P; Knott, S; Hayward, C; Vitart, V; Rudan, I; Campbell, H; Hastie, N D; Wright, A F; Haley, C S.

Heredity (Edinb) ; 116(3): 333-8, 2016 Mar.

Artigo em Inglês | MEDLINE | ID: mdl-26696135

14.

Potential role of coenzyme Q10 in facilitating recovery from statin-induced rhabdomyolysis.

Wang, L W; Jabbour, A; Hayward, C S; Furlong, T J; Girgis, L; Macdonald, P S; Keogh, A M.

Intern Med J ; 45(4): 451-3, 2015 Apr.

Artigo em Inglês | MEDLINE | ID: mdl-25827512

15.

A K(ATP) channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila.

Allebrandt, K V; Amin, N; Müller-Myhsok, B; Esko, T; Teder-Laving, M; Azevedo, R V D M; Hayward, C; van Mill, J; Vogelzangs, N; Green, E W; Melville, S A; Lichtner, P; Wichmann, H-E; Oostra, B A; Janssens, A C J W; Campbell, H; Wilson, J F; Hicks, A A; Pramstaller, P P; Dogas, Z; Rudan, I; Merrow, M; Penninx, B; Kyriacou, C P; Metspalu, A; van Duijn, C M; Meitinger, T; Roenneberg, T.

Mol Psychiatry ; 18(1): 122-32, 2013 Jan.

Artigo em Inglês | MEDLINE | ID: mdl-22105623

16.

Fetally-encoded GDF15 and maternal GDF15 sensitivity are major determinants of nausea and vomiting in human pregnancy.

Fejzo, M; Rocha, N; Cimino, I; Lockhart, S M; Petry, C; Kay, R G; Burling, K; Barker, P; George, A L; Yasara, N; Premawardhena, A; Gong, S; Cook, E; Rainbow, K; Withers, D J; Cortessis, V; Mullin, P M; MacGibbon, K W; Jin, E; Kam, A; Campbell, A; Polasek, O; Tzoneva, G; Gribble, F M; Yeo, Gsh; Lam, Byh; Saudek, V; Hughes, I A; Ong, K K; Perry, Jrb; Sutton Cole, A; Baumgarten, M; Welsh, P; Sattar, N; Smith, Gcs; Charnock Jones, D S; Coll, A P; Meek, C L; Mettananda, S; Hayward, C; Mancuso, N; O'Rahilly, S.

bioRxiv ; 2023 Jun 04.

Artigo em Inglês | MEDLINE | ID: mdl-37398065

17.

SNP mistyping in genotyping arrays--an important cause of spurious association in case-control studies.

Mitry, D; Campbell, H; Charteris, D G; Fleck, B W; Tenesa, A; Dunlop, M G; Hayward, C; Wright, A F; Vitart, V.

Genet Epidemiol ; 35(5): 423-6, 2011 Jul.

Artigo em Inglês | MEDLINE | ID: mdl-21254221

18.

Genome-wide analysis of over 106 000 individuals identifies 9 neuroticism-associated loci.

Smith, D J; Escott-Price, V; Davies, G; Bailey, M E S; Colodro-Conde, L; Ward, J; Vedernikov, A; Marioni, R; Cullen, B; Lyall, D; Hagenaars, S P; Liewald, D C M; Luciano, M; Gale, C R; Ritchie, S J; Hayward, C; Nicholl, B; Bulik-Sullivan, B; Adams, M; Couvy-Duchesne, B; Graham, N; Mackay, D; Evans, J; Smith, B H; Porteous, D J; Medland, S E; Martin, N G; Holmans, P; McIntosh, A M; Pell, J P; Deary, I J; O'Donovan, M C.

Mol Psychiatry ; 21(11): 1644, 2016 11.

Artigo em Inglês | MEDLINE | ID: mdl-27620839

19.

Global haemostasis and point of care testing.

Dargaud, Y; Sorensen, B; Shima, M; Hayward, C; Srivastava, A; Negrier, C.

Haemophilia ; 18 Suppl 4: 81-8, 2012 Jul.

Artigo em Inglês | MEDLINE | ID: mdl-22726088

20.

Take heart: bariatric surgery in obese patients with severe heart failure. Two case reports.

Samaras, K; Connolly, S M; Lord, R V; Macdonald, P; Hayward, C S.

Heart Lung Circ ; 21(12): 847-9, 2012 Dec.

Artigo em Inglês | MEDLINE | ID: mdl-22743291

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GDF15 linked to maternal risk of nausea and vomiting during pregnancy.

Author Correction: A massive core for a cluster of galaxies at a redshift of 4.3.

A massive core for a cluster of galaxies at a redshift of 4.3.

Galaxy growth in a massive halo in the first billion years of cosmic history.

Genome-wide meta-analysis identifies novel loci associated with free triiodothyronine and thyroid-stimulating hormone.

Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112 117).

Assessing the genetic overlap between BMI and cognitive function.

Genome-wide association study of cognitive functions and educational attainment in UK Biobank (N=112 151).

Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population.

Genome-wide analysis of over 106 000 individuals identifies 9 neuroticism-associated loci.

Molecular phenotype and bleeding risks of an inherited platelet disorder in a family with a RUNX1 frameshift mutation.

Genomic approaches to bleeding disorders.

Regional heritability mapping method helps explain missing heritability of blood lipid traits in isolated populations.

Potential role of coenzyme Q10 in facilitating recovery from statin-induced rhabdomyolysis.

A K(ATP) channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila.

Fetally-encoded GDF15 and maternal GDF15 sensitivity are major determinants of nausea and vomiting in human pregnancy.

SNP mistyping in genotyping arrays--an important cause of spurious association in case-control studies.

Genome-wide analysis of over 106 000 individuals identifies 9 neuroticism-associated loci.

Global haemostasis and point of care testing.

Take heart: bariatric surgery in obese patients with severe heart failure. Two case reports.