Detalles de la búsqueda
1.
Whole genome-wide sequence analysis of long-lived families (Long-Life Family Study) identifies MTUS2 gene associated with late-onset Alzheimer's disease.
Alzheimers Dement
; 20(4): 2670-2679, 2024 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-38380866
2.
Midlife Vascular Factors and Prevalence of Mild Cognitive Impairment in Late-Life in Mexico.
J Int Neuropsychol Soc
; 28(4): 351-361, 2022 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-34376262
3.
Integration of GWAS and brain transcriptomic analyses in a multiethnic sample of 35,245 older adults identifies DCDC2 gene as predictor of episodic memory maintenance.
Alzheimers Dement
; 18(10): 1797-1811, 2022 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-34873813
4.
Analysis of pedigree data in populations with multiple ancestries: Strategies for dealing with admixture in Caribbean Hispanic families from the ADSP.
Genet Epidemiol
; 42(6): 500-515, 2018 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-29862559
5.
Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project.
Dement Geriatr Cogn Disord
; 45(1-2): 1-17, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-29486463
6.
Rare coding mutations identified by sequencing of Alzheimer disease genome-wide association studies loci.
Ann Neurol
; 78(3): 487-98, 2015 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-26101835
7.
Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease.
Alzheimers Dement
; 12(1): 2-10, 2016 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-26365416
8.
Linkage analyses in Caribbean Hispanic families identify novel loci associated with familial late-onset Alzheimer's disease.
Alzheimers Dement
; 11(12): 1397-1406, 2015 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-26433351
9.
Genetic variants associated with lung function: the long life family study.
Respir Res
; 15: 134, 2014 Nov 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-25409777
10.
Emerging science of hydroxyurea therapy for pediatric sickle cell disease.
Pediatr Res
; 75(1-2): 196-204, 2014 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-24252885
11.
The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia.
Nat Genet
; 37(9): 931-3, 2005 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-16116424
12.
Systemic inflammation in relation to exceptional memory in the Long Life Family Study (LLFS).
Brain Behav Immun Health
; 37: 100746, 2024 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-38476338
13.
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies LRRC4C, LHX5-AS1 and nominates ancestry-specific loci PTPRK , GRB14 , and KIAA0825 as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics Consortium.
medRxiv
; 2023 Jul 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-37461624
14.
Association between late maternal age and age-related endophenotypes in the Long Life Family Study.
Neurosci Lett
; 784: 136737, 2022 07 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-35709880
15.
New insights into the genetic etiology of Alzheimer's disease and related dementias.
Nat Genet
; 54(4): 412-436, 2022 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-35379992
16.
X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1.
Am J Hum Genet
; 82(1): 208-13, 2008 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-18179901
17.
Genetic modifiers of HbF and response to hydroxyurea in sickle cell disease.
Pediatr Blood Cancer
; 56(2): 177-81, 2011 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-20830771
18.
Fetal hemoglobin levels in African American and Hispanic children with sickle cell disease at baseline and in response to hydroxyurea.
J Pediatr Hematol Oncol
; 33(7): 496-9, 2011 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-21941141
19.
MEF2C Common Genetic Variation Is Associated With Different Aspects of Cognition in Non-Hispanic White and Caribbean Hispanic Non-demented Older Adults.
Front Genet
; 12: 642327, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34386032
20.
ABCB1 (MDR1) genetic variants are associated with methadone doses required for effective treatment of heroin dependence.
Hum Mol Genet
; 17(14): 2219-27, 2008 Jul 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-18424454