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1.
Methods and Software to Analyze Gene-Environment Interactions under a Case-Mother-Control-Mother Design with Partially Missing Child Genotype.
Hum Hered;
88(1): 38-49, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37100044
2.
Heterogeneity in the longitudinal courses of global functioning in children at familial risk of major psychiatric disorders: Association with trauma and familial characteristics.
Bipolar Disord;
2023 Nov 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-37957788
3.
Time trends in social contacts before and during the COVID-19 pandemic: the CONNECT study.
BMC Public Health;
22(1): 1032, 2022 05 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-35606703
4.
Exploring polypharmacy with artificial intelligence: data analysis protocol.
BMC Med Inform Decis Mak;
21(1): 219, 2021 07 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-34284765
5.
Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants.
Genet Epidemiol;
43(1): 37-49, 2019 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-30246882
6.
Detection of rare disease variants in extended pedigrees using RVS.
Bioinformatics;
35(14): 2509-2511, 2019 07 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-30500888
7.
Exposure to polychlorinated biphenyls and organochlorine pesticides and risk of dementia, Alzheimer's disease and cognitive decline in an older population: a prospective analysis from the Canadian Study of Health and Aging.
Environ Health;
18(1): 57, 2019 06 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-31200706
8.
Whole exome association of rare deletions in multiplex oral cleft families.
Genet Epidemiol;
41(1): 61-69, 2017 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-27910131
9.
Polyunphased: an extension to polytomous outcomes of the Unphased package for family-based genetic association analysis.
Stat Appl Genet Mol Biol;
16(1): 75-81, 2017 03 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-28186960
10.
Polygenic risk scores distinguish patients from non-affected adult relatives and from normal controls in schizophrenia and bipolar disorder multi-affected kindreds.
Am J Med Genet B Neuropsychiatr Genet;
177(3): 329-336, 2018 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-29193655
11.
Reduced Antibody Response to Infant Measles Vaccination: Effects Based on Type and Timing of the First Vaccine Dose Persist After the Second Dose.
Clin Infect Dis;
65(7): 1094-1102, 2017 10 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-28595358
12.
When Is an Endophenotype Useful to Detect Association to a Disease? Exploring the Relationships between Disease Status, Endophenotype and Genetic Polymorphisms.
Hum Hered;
81(1): 11-25, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-27475094
13.
On the validity of within-nuclear-family genetic association analysis in samples of extended families.
Stat Appl Genet Mol Biol;
14(6): 533-49, 2015 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-26544107
14.
Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives.
Bioinformatics;
30(15): 2189-96, 2014 Aug 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-24740360
15.
A genome-wide association study of suicidal behavior.
Am J Med Genet B Neuropsychiatr Genet;
168(7): 557-63, 2015 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-26079190
16.
Detection of phenotype modifier genes using two-locus linkage analysis in complex disorders such as major psychosis.
Hum Hered;
73(4): 195-207, 2012.
Artículo
en Inglés
| MEDLINE | ID: mdl-22907187
17.
Multivariate extension of penalized regression on summary statistics to construct polygenic risk scores for correlated traits.
HGG Adv;
4(3): 100209, 2023 07 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-37333772
18.
A novel rare variants association test for binary traits in family-based designs via copulas.
Stat Methods Med Res;
32(11): 2096-2122, 2023 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-37832140
19.
Molecular test of Paget's disease of bone in families not linked to SQSTM1 gene mutations.
Bone Rep;
18: 101670, 2023 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-36915391
20.
Latent class model with familial dependence to address heterogeneity in complex diseases: adapting the approach to family-based association studies.
Genet Epidemiol;
35(3): 182-9, 2011 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-21308764