Detalhe da pesquisa
1.
Inferring Transmission Histories of Rare Alleles in Population-Scale Genealogies.
Am J Hum Genet
; 103(6): 893-906, 2018 12 06.
Artigo
Inglês
| MEDLINE | ID: mdl-30526866
2.
Historical human remains identification through maternal and paternal genetic signatures in a founder population with extensive genealogical record.
Am J Phys Anthropol
; 171(4): 645-658, 2020 04.
Artigo
Inglês
| MEDLINE | ID: mdl-32064591
3.
Molecular characterization of a large group of Mucopolysaccharidosis type IIIC patients reveals the evolutionary history of the disease.
Hum Mutat
; 40(8): 1084-1100, 2019 08.
Artigo
Inglês
| MEDLINE | ID: mdl-31228227
4.
Joubert Syndrome in French Canadians and Identification of Mutations in CEP104.
Am J Hum Genet
; 97(5): 744-53, 2015 Nov 05.
Artigo
Inglês
| MEDLINE | ID: mdl-26477546
5.
Genome diversity in the Neolithic Globular Amphorae culture and the spread of Indo-European languages.
Proc Biol Sci
; 284(1867)2017 Nov 29.
Artigo
Inglês
| MEDLINE | ID: mdl-29167359
6.
Genetic Structure of First Nation Communities in the Pacific Northwest.
Hum Biol
; 88(4): 251-263, 2016 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-28826319
7.
Disruption of CLPB is associated with congenital microcephaly, severe encephalopathy and 3-methylglutaconic aciduria.
J Med Genet
; 52(5): 303-11, 2015 May.
Artigo
Inglês
| MEDLINE | ID: mdl-25650066
8.
Reconciling migration models to the Americas with the variation of North American native mitogenomes.
Proc Natl Acad Sci U S A
; 110(35): 14308-13, 2013 Aug 27.
Artigo
Inglês
| MEDLINE | ID: mdl-23940335
9.
GENLIB: an R package for the analysis of genealogical data.
BMC Bioinformatics
; 16: 160, 2015 May 15.
Artigo
Inglês
| MEDLINE | ID: mdl-25971991
10.
Mutations in C5ORF42 cause Joubert syndrome in the French Canadian population.
Am J Hum Genet
; 90(4): 693-700, 2012 Apr 06.
Artigo
Inglês
| MEDLINE | ID: mdl-22425360
11.
Female-to-male breeding ratio in modern humans-an analysis based on historical recombinations.
Am J Hum Genet
; 86(3): 353-63, 2010 Mar 12.
Artigo
Inglês
| MEDLINE | ID: mdl-20188344
12.
Mutability of Y-chromosomal microsatellites: rates, characteristics, molecular bases, and forensic implications.
Am J Hum Genet
; 87(3): 341-53, 2010 Sep 10.
Artigo
Inglês
| MEDLINE | ID: mdl-20817138
13.
Mutations in TMEM231 cause Joubert syndrome in French Canadians.
J Med Genet
; 49(10): 636-41, 2012 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-23012439
14.
An X-linked haplotype of Neandertal origin is present among all non-African populations.
Mol Biol Evol
; 28(7): 1957-62, 2011 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-21266489
15.
The effective family size of immigrant founders predicts their long-term demographic outcome: From Québec settlers to their 20th-century descendants.
PLoS One
; 17(5): e0266079, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-35507549
16.
When genetics and genealogies tell different stories-maternal lineages in Gaspesia.
Ann Hum Genet
; 75(2): 247-54, 2011 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-21058944
17.
Genomic and genealogical investigation of the French Canadian founder population structure.
Hum Genet
; 129(5): 521-31, 2011 May.
Artigo
Inglês
| MEDLINE | ID: mdl-21234765
18.
Admixed ancestry and stratification of Quebec regional populations.
Am J Phys Anthropol
; 144(3): 432-41, 2011 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-21302269
19.
Haplotype allelic classes for detecting ongoing positive selection.
BMC Bioinformatics
; 11: 65, 2010 Jan 28.
Artigo
Inglês
| MEDLINE | ID: mdl-20109229
20.
Contrasting patterns of nuclear and mtDNA diversity in Native American populations.
Ann Hum Genet
; 74(6): 525-38, 2010 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-20887376