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Onofre Combarros

Showing results (81-90 of 92) with videos related to

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European Journal of Human Genetics : EJHG|June 6, 2013
The sex-specific associations of the aromatase gene with Alzheimer's disease and its interaction with IL10 in the Epistasis ProjectChristopher Medway, Onofre Combarros, Mario Cortina-Borja, et al.
Plos One|April 29, 2015
A genome wide association study links glutamate receptor pathway to sporadic Creutzfeldt-Jakob disease riskPascual Sanchez-Juan, Matthew T Bishop, Gabor G Kovacs, et al.
Neurobiology of Aging|September 7, 2010
Transferrin and HFE genes interact in Alzheimer's disease risk: the Epistasis ProjectDonald J Lehmann, Maaike Schuur, Donald R Warden, et al.
Neurobiology of Aging|September 18, 2013
Assessing the role of the TREM2 p.R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementiaAgustín Ruiz, Oriol Dols-Icardo, María J Bullido, et al.
Plos One|September 27, 2013
Rare variants in calcium homeostasis modulator 1 (CALHM1) found in early onset Alzheimer's disease patients alter calcium homeostasisFanny Rubio-Moscardo, Núria Setó-Salvia, Marta Pera, et al.
Neurobiology of Aging|January 12, 2011
Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populationsJean-Charles Lambert, Diana Zelenika, Mikko Hiltunen, et al.
Journal of Alzheimer'S Disease : JAD|October 8, 2015
MAPT H1 Haplotype is Associated with Late-Onset Alzheimer's Disease Risk in APOEɛ4 Noncarriers: Results from the Dementia Genetics Spanish ConsortiumPau Pastor, Fermín Moreno, Jordi Clarimón, et al.
Nature Genetics|September 8, 2009
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's diseaseJean-Charles Lambert, Simon Heath, Gael Even, et al.
Journal of Alzheimer'S Disease : JAD|September 18, 2010
The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis studyJean-Charles Lambert, Kristel Sleegers, Antonio González-Pérez, et al.
Nature Genetics|April 5, 2011
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's diseasePaul Hollingworth, Denise Harold, Rebecca Sims, et al.
Pageof 10

Showing results (81-90 of 92) with videos related to

Sort By:
Pageof 10
European Journal of Human Genetics : EJHG|June 6, 2013
The sex-specific associations of the aromatase gene with Alzheimer's disease and its interaction with IL10 in the Epistasis ProjectChristopher Medway, Onofre Combarros, Mario Cortina-Borja, et al.
Plos One|April 29, 2015
A genome wide association study links glutamate receptor pathway to sporadic Creutzfeldt-Jakob disease riskPascual Sanchez-Juan, Matthew T Bishop, Gabor G Kovacs, et al.
Neurobiology of Aging|September 7, 2010
Transferrin and HFE genes interact in Alzheimer's disease risk: the Epistasis ProjectDonald J Lehmann, Maaike Schuur, Donald R Warden, et al.
Neurobiology of Aging|September 18, 2013
Assessing the role of the TREM2 p.R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementiaAgustín Ruiz, Oriol Dols-Icardo, María J Bullido, et al.
Plos One|September 27, 2013
Rare variants in calcium homeostasis modulator 1 (CALHM1) found in early onset Alzheimer's disease patients alter calcium homeostasisFanny Rubio-Moscardo, Núria Setó-Salvia, Marta Pera, et al.
Neurobiology of Aging|January 12, 2011
Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populationsJean-Charles Lambert, Diana Zelenika, Mikko Hiltunen, et al.
Journal of Alzheimer'S Disease : JAD|October 8, 2015
MAPT H1 Haplotype is Associated with Late-Onset Alzheimer's Disease Risk in APOEɛ4 Noncarriers: Results from the Dementia Genetics Spanish ConsortiumPau Pastor, Fermín Moreno, Jordi Clarimón, et al.
Nature Genetics|September 8, 2009
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's diseaseJean-Charles Lambert, Simon Heath, Gael Even, et al.
Journal of Alzheimer'S Disease : JAD|September 18, 2010
The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis studyJean-Charles Lambert, Kristel Sleegers, Antonio González-Pérez, et al.
Nature Genetics|April 5, 2011
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's diseasePaul Hollingworth, Denise Harold, Rebecca Sims, et al.
Pageof 10