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EKV mutant connexin 31 associated cell death is mediated by ER stress
EKV mutant connexin 31 associated cell death is mediated by ER stress
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EKV mutant connexin 31 associated cell death is mediated by ER stress

Tattersall, Daniel ; Scott, Claire A. ; Gray, Colin ; Zicha, Daniel ; Kelsell, David P.

Human molecular genetics, 2009-12, Vol.18 (24), p.4734-4745 [Periódico revisado por pares]

Oxford: Oxford University Press

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2
Dazl binds in vivo to specific transcripts and can regulate the pre-meiotic translation of Mvh in germ cells
Dazl binds in vivo to specific transcripts and can regulate the pre-meiotic translation of Mvh in germ cells
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Dazl binds in vivo to specific transcripts and can regulate the pre-meiotic translation of Mvh in germ cells

Reynolds, Nicola ; Collier, Brian ; Maratou, Klio ; Bingham, Victoria ; Speed, Robert M. ; Taggart, Mary ; Semple, Colin A. ; Gray, Nicola K. ; Cooke, Howard J.

Human molecular genetics, 2005-12, Vol.14 (24), p.3899-3909 [Periódico revisado por pares]

England: Oxford University Press

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3
CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1
CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1
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CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1

Rees, Elliott ; Walters, James T R ; Chambert, Kimberly D ; O'Dushlaine, Colm ; Szatkiewicz, Jin ; Richards, Alexander L ; Georgieva, Lyudmila ; Mahoney-Davies, Gerwyn ; Legge, Sophie E ; Moran, Jennifer L ; Genovese, Giulio ; Levinson, Douglas ; Morris, Derek W ; Cormican, Paul ; Kendler, Kenneth S ; O'Neill, Francis A ; Riley, Brien ; Gill, Michael ; Corvin, Aiden ; Sklar, Pamela ; Hultman, Christina ; Pato, Carlos ; Pato, Michele ; Sullivan, Patrick F ; Gejman, Pablo V ; McCarroll, Steven A ; O'Donovan, Michael C ; Owen, Michael J ; Kirov, George

Human molecular genetics, 2014-03, Vol.23 (6), p.1669-1676 [Periódico revisado por pares]

England: Oxford University Press

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4
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21
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Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21

Spencer, Chris C A ; Plagnol, Vincent ; Strange, Amy ; Gardner, Michelle ; Paisan-Ruiz, Coro ; Band, Gavin ; Barker, Roger A ; Bellenguez, Celine ; Bhatia, Kailash ; Blackburn, Hannah ; Blackwell, Jennie M ; Bramon, Elvira ; Brown, Martin A ; Brown, Matthew A ; Burn, David ; Casas, Juan-Pablo ; Chinnery, Patrick F ; Clarke, Carl E ; Corvin, Aiden ; Craddock, Nicholas ; Deloukas, Panos ; Edkins, Sarah ; Evans, Jonathan ; Freeman, Colin ; Gray, Emma ; Hardy, John ; Hudson, Gavin ; Hunt, Sarah ; Jankowski, Janusz ; Langford, Cordelia ; Lees, Andrew J ; Markus, Hugh S ; Mathew, Christopher G ; McCarthy, Mark I ; Morrison, Karen E ; Palmer, Colin N A ; Pearson, Justin P ; Peltonen, Leena ; Pirinen, Matti ; Plomin, Robert ; Potter, Simon ; Rautanen, Anna ; Sawcer, Stephen J ; Su, Zhan ; Trembath, Richard C ; Viswanathan, Ananth C ; Williams, Nigel W ; Morris, Huw R ; Donnelly, Peter ; Wood, Nicholas W

Human molecular genetics, 2011-01, Vol.20 (2), p.345-353 [Periódico revisado por pares]

Oxford: Oxford University Press

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5
Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus
Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus
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Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus

Strange, Amy ; Bellenguez, Céline ; Sim, Xueling ; Luben, Robert ; Hysi, Pirro G. ; Ramdas, Wishal D. ; van Koolwijk, Leonieke M.E. ; Freeman, Colin ; Pirinen, Matti ; Su, Zhan ; Band, Gavin ; Pearson, Richard ; Vukcevic, Damjan ; Langford, Cordelia ; Deloukas, Panos ; Hunt, Sarah ; Gray, Emma ; Dronov, Serge ; Potter, Simon C. ; Tashakkori-Ghanbaria, Avazeh ; Edkins, Sarah ; Bumpstead, Suzannah J. ; Blackwell, Jenefer M. ; Bramon, Elvira ; Brown, Matthew A. ; Casas, Juan P. ; Corvin, Aiden ; Duncanson, Audrey ; Jankowski, Janusz A.Z. ; Markus, Hugh S. ; Mathew, Christopher G. ; Palmer, Colin N.A. ; Plomin, Robert ; Rautanen, Anna ; Sawcer, Stephen J. ; Trembath, Richard C. ; Wood, Nicholas W. ; Barroso, Ines ; Peltonen, Leena ; Healey, Paul ; McGuffin, Peter ; Topouzis, Fotis ; Klaver, Caroline C.W. ; van Duijn, Cornelia M. ; Mackey, David A. ; Young, Terri L. ; Hammond, Christopher J. ; Khaw, Kay-Tee ; Wareham, Nick ; Wang, Jie Jin ; Wong, Tien Y. ; Foster, Paul J. ; Mitchell, Paul ; Spencer, Chris C.A. ; Donnelly, Peter ; Viswanathan, Ananth C.

Human molecular genetics, 2013-11, Vol.22 (22), p.4653-4660 [Periódico revisado por pares]

England: Oxford University Press

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6
Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease
Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease
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Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

KELLER, Margaux F ; SAAD, Mohamad ; SCHULTE, Claudia ; MOSKVINA, Valentina ; DURR, Alexandra ; HOLMANS, Peter ; KILARSKI, Laura L ; GUERREIRO, Rita ; HERNANDEZ, Dena G ; BRICE, Alexis ; YLIKOTILA, Pauli ; STEFANSSON, Hreinn ; BRAS, Jose ; MAJAMAA, Kari ; MORRIS, Huw R ; WILLIAMS, Nigel ; GASSER, Thomas ; HEUTINK, Peter ; WOOD, Nicholas W ; HARDY, John ; MARTINEZ, Maria ; SINGLETON, Andrew B ; NALLS, Michael A ; BETTELLA, Francesco ; NICOLAOU, Nayia ; SIMON-SANCHEZ, Javier ; MITTAG, Florian ; BÜCHEL, Finja ; SHARMA, Manu ; RAPHAEL GIBBS, J

Human molecular genetics, 2012-11, Vol.21 (22), p.4996-5009 [Periódico revisado por pares]

Oxford: Oxford University Press

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7
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21
Material Type:
Artigo 		Adicionar ao Meu Espaço

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21

UK Parkinson's Disease Consortium ; Wellcome Trust Case Control Consortium 2 ; Spencer, Chris CA ; Plagnol, Vincent ; Strange, Amy ; Gardner, Michelle ; Paisan-Ruiz, Coro ; Band, Gavin ; Barker, Roger A ; Bellenguez, Celine ; Bhatia, Kailash ; Blackburn, Hannah ; Blackwell, Jennie M ; Bramon, Elvira ; Brown, Martin A ; Brown, Matthew A ; Burn, David ; Casas, Juan-Pablo ; Chinnery, Patrick F ; Clarke, Carl E ; Corvin, Aiden ; Craddock, Nicholas ; Deloukas, Panos ; Edkins, Sarah ; Evans, Jonathan ; Freeman, Colin ; Gray, Emma ; Hardy, John ; Hudson, Gavin ; Hunt, Sarah ; Jankowski, Janusz ; Langford, Cordelia ; Lees, Andrew J ; Markus, Hugh S ; Mathew, Christopher G ; McCarthy, Mark I ; Morrison, Karen E ; Palmer, Colin NA ; Pearson, Justin P ; Peltonen, Leena ; Pirinen, Matti ; Plomin, Robert ; Potter, Simon ; Rautanen, Anna ; Sawcer, Stephen J ; Su, Zhan ; Trembath, Richard C ; Viswanathan, Ananth C ; Williams, Nigel W ; Morris, Huw R ; Donnelly, Peter ; Wood, Nicholas W

Human molecular genetics, 2011, Vol.20 (2), p.345-353 [Periódico revisado por pares]

Oxford University Press (OUP)

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8
Dazi binds in vivo to specific transcripts and can regulate the pre-meiotic translation of Mvh in germ cells
Dazi binds in vivo to specific transcripts and can regulate the pre-meiotic translation of Mvh in germ cells
Material Type:
Artigo 		Adicionar ao Meu Espaço

Dazi binds in vivo to specific transcripts and can regulate the pre-meiotic translation of Mvh in germ cells

REYNOLDS, Nicola ; COLLIER, Brian ; MARNTO, Kilo ; BINGHAM, Victoria ; SPEED, Robert M ; TAGGART, Mary ; SEMPLE, Colin A ; GRAY, Nicola K ; COOKE, Howard J

Human molecular genetics, 2005, Vol.14 (24), p.3899-3909 [Periódico revisado por pares]

Oxford: Oxford University Press

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