skip to main content
Idioma:
Mostrar Somente
Refinado por: assunto: Fundamental And Applied Biological Sciences. Psychology remover assunto: Genetics & Heredity remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
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

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

Texto completo disponível

Citações Citado por
2
Sequence variants at CHRNB3 - CHRNA6 and CYP2A6 affect smoking behavior
Sequence variants at CHRNB3 - CHRNA6 and CYP2A6 affect smoking behavior
Material Type:
Artigo 		Adicionar ao Meu Espaço

Sequence variants at CHRNB3 - CHRNA6 and CYP2A6 affect smoking behavior

Perola, Markus ; McCarthy, Mark I ; Keskitalo, Kaisu ; Pergadia, Michele L ; Salomaa, Veikko ; Stefansson, Hreinn ; Kovacs, Peter ; Aben, Katja K ; Peltonen, Leena ; Giegling, Ina ; Lezcano, Victoria ; Mueller, Thomas ; Thorsteinsdottir, Unnur ; Geller, Frank ; Hartikainen, Anna-Liisa ; Rujescu, Dan ; Franklin, Wilbur A ; Ashraf, Haseem ; Stefansson, Kari ; Walter, Stefan ; van Duijn, Cornelia M ; Mayordomo, Jose I ; Willemsen, Gonneke ; Kiemeney, Lambertus A ; Pedersen, Jesper Holst ; Huei-Yi, Shen ; Tyrfingsson, Thorarinn ; Stumvoll, Michael ; Jones, Gregory T ; Uitterlinden, André G ; Allen, Maxine ; Dieplinger, Benjamin ; Krestyaninova, Maria ; Amin, Najaf ; van Rij, Andre M ; Gulcher, Jeffrey R ; Valdes, Ana M ; Mangino, Massimo ; Heath, Andrew C ; Döring, Angela ; Gieger, Christian ; Gudjonsdottir, Iris H ; Hofman, Albert ; Jonsson, Steinn ; Kaprio, Jaakko ; Mägi, Reedik ; Dirksen, Asger ; Nelis, Mari ; Thompson, John R ; Hottenga, Jouke Jan ; Garcia-Prats, Maria D ; Metspalu, Andres ; Hall, Alistair S ; Oostra, Ben A ; Matthiasson, Stefan E ; Prokopenko, Inga ; Dahmen, Norbert ; Madden, Pamela A F ; Wolf, Holly ; Steves, Claire ; Nitz, Barbara ; Kettunen, Johannes ; Martin, Nicholas G ; Spector, Tim D ; Thorgeirsson, Thorgeir E ; Haltmayer, Meinhard ; Ripatti, Samuli ; Gudbjartsson, Daniel F ; Esko, Tõnu ; Rafnar, Thorunn ; Soranzo, Nicole ; Vink, Jacqueline M ; De Diego, Veronica ; Laitinen, Jaana ; Järvelin, Marjo-Riitta ; Wichmann, H-Erich ; Pouta, Anneli ; Penninx, Brenda W ; Boomsma, Dorret I ; Surakka, Ida ; Rawal, Rajesh ; Aulchenko, Yurii S ; Sulem, Patrick ; Gretarsdottir, Solveig ; Oskarsson, Hogni ; Isohanni, Matti ; Tönjes, Anke ; Saez, Berta ; Lindholt, Jes S ; Tiemeier, Henning ; Samani, Nilesh J ; den Heijer, Martin ; Vogelzangs, Nicole ; Montgomery, Grant W

Nature Genetics, 2010-05, Vol.42 (5), p.448-453 [Periódico revisado por pares]

New York, NY: Nature Publishing Group

Texto completo disponível

Citações Citado por
3
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
Material Type:
Artigo 		Adicionar ao Meu Espaço

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

Texto completo disponível

Citações Citado por
4
Fine mapping and association studies of a high-density lipoprotein cholesterol linkage region on chromosome 16 in French-Canadian subjects
Fine mapping and association studies of a high-density lipoprotein cholesterol linkage region on chromosome 16 in French-Canadian subjects
Material Type:
Artigo 		Adicionar ao Meu Espaço

Fine mapping and association studies of a high-density lipoprotein cholesterol linkage region on chromosome 16 in French-Canadian subjects

DASTANI, Zari ; PAJUKANTA, Päivi ; RIOUX, John ; HUDSON, Thomas J ; GAUDET, Daniel ; ENGERT, James C ; GENEST, Jacques ; MARCIL, Michel ; RUDZICZ, Nicholas ; RUEL, Isabelle ; BAILEY, Swneke D ; LEE, Jenny C ; LEMIRE, Mathieu ; FAITH, Janet ; PLATKO, Jill

European journal of human genetics : EJHG, 2010-03, Vol.18 (3), p.342-347 [Periódico revisado por pares]

Basingstoke: Nature Publishing Group

Texto completo disponível

Citações Citado por
5
Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms
Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms
Material Type:
Artigo 		Adicionar ao Meu Espaço

Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms

Hudson, Thomas J. ; Engelstein, Marcy ; Lee, Matthias K. ; Ho, Elizabeth C. ; Rubenfield, Marc J. ; Adams, Christopher P. ; Housman, David E. ; Dracopoli, Nicholas C.

Genomics (San Diego, Calif.), 1992-07, Vol.13 (3), p.622-629 [Periódico revisado por pares]

SAN DIEGO: Elsevier Inc

Texto completo disponível

Citações Citado por
6
A PCR-Based Linkage Map of Human Chromosome 1
A PCR-Based Linkage Map of Human Chromosome 1
Material Type:
Artigo 		Adicionar ao Meu Espaço

A PCR-Based Linkage Map of Human Chromosome 1

Engelstein, Marcy ; Hudson, Thomas J. ; Lane, Joan M. ; Lee, Matthias K. ; Leverone, Ben ; Landes, Gregory M. ; Peltonen, Elena ; Weber, James L. ; Dracopoli, Nicholas C.

Genomics (San Diego, Calif.), 1993-02, Vol.15 (2), p.251-258 [Periódico revisado por pares]

San Diego, CA: Elsevier Inc

Texto completo disponível

Citações Citado por
7
Dinucleotide repeat polymorphism at the D9S126 locus (9p21)
Dinucleotide repeat polymorphism at the D9S126 locus (9p21)
Material Type:
Artigo 		Adicionar ao Meu Espaço

Dinucleotide repeat polymorphism at the D9S126 locus (9p21)

Fountain, Jane W. ; Hudson, Thomas J. ; Engelstein, Marcy ; Housman, David E. ; Dracopoli, Nicholas C.

Human molecular genetics, 1993-06, Vol.2 (6), p.823-823 [Periódico revisado por pares]

Oxford: Oxford University Press

Sem texto completo

Citações Citado por

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Mostrar Somente

  1. Recursos Online (6)

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.