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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 Project
Christopher Medway, Onofre Combarros, Mario Cortina-Borja, et al.
Neurobiology of Aging
|
September 7, 2010
Transferrin and HFE genes interact in Alzheimer's disease risk: the Epistasis Project
Donald 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 dementia
Agustín Ruiz, Oriol Dols-Icardo, María J Bullido, et al.
Gastroenterology
|
September 15, 2019
White-Light Endoscopy Is Adequate for Lynch Syndrome Surveillance in a Randomized and Noninferiority Study
Liseth Rivero-Sánchez, Coral Arnau-Collell, Jesús Herrero, et al.
Plos Medicine
|
October 24, 2023
Screening uptake of colonoscopy versus fecal immunochemical testing in first-degree relatives of patients with non-syndromic colorectal cancer: A multicenter, open-label, parallel-group, randomized trial (ParCoFit study)
Natalia González-López, Enrique Quintero, Antonio Z Gimeno-Garcia, et al.
Neurobiology of Aging
|
January 12, 2011
Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populations
Jean-Charles Lambert, Diana Zelenika, Mikko Hiltunen, et al.
Brain : a Journal of Neurology
|
October 23, 2021
SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration
Mathieu Barbier, Agnès Camuzat, Khalid El Hachimi, et al.
Nature Genetics
|
September 8, 2009
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease
Jean-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 study
Jean-Charles Lambert, Kristel Sleegers, Antonio González-Pérez, et al.
Plos One
|
October 3, 2023
Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project
Eva-Juliane Vollstedt, Harutyun Madoev, Anna Aasly, et al.
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of 19
Search research articles
Search
Showing results (161-170 of 181) with videos related to
Sort By:
Page
of 19
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 Project
Christopher Medway, Onofre Combarros, Mario Cortina-Borja, et al.
Neurobiology of Aging
|
September 7, 2010
Transferrin and HFE genes interact in Alzheimer's disease risk: the Epistasis Project
Donald 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 dementia
Agustín Ruiz, Oriol Dols-Icardo, María J Bullido, et al.
Gastroenterology
|
September 15, 2019
White-Light Endoscopy Is Adequate for Lynch Syndrome Surveillance in a Randomized and Noninferiority Study
Liseth Rivero-Sánchez, Coral Arnau-Collell, Jesús Herrero, et al.
Plos Medicine
|
October 24, 2023
Screening uptake of colonoscopy versus fecal immunochemical testing in first-degree relatives of patients with non-syndromic colorectal cancer: A multicenter, open-label, parallel-group, randomized trial (ParCoFit study)
Natalia González-López, Enrique Quintero, Antonio Z Gimeno-Garcia, et al.
Neurobiology of Aging
|
January 12, 2011
Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populations
Jean-Charles Lambert, Diana Zelenika, Mikko Hiltunen, et al.
Brain : a Journal of Neurology
|
October 23, 2021
SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration
Mathieu Barbier, Agnès Camuzat, Khalid El Hachimi, et al.
Nature Genetics
|
September 8, 2009
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease
Jean-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 study
Jean-Charles Lambert, Kristel Sleegers, Antonio González-Pérez, et al.
Plos One
|
October 3, 2023
Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project
Eva-Juliane Vollstedt, Harutyun Madoev, Anna Aasly, et al.
Page
of 19