Detalhe da pesquisa
1.
Transmission of human mtDNA heteroplasmy in the Genome of the Netherlands families: support for a variable-size bottleneck.
Genome Res
; 26(4): 417-26, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26916109
2.
Population data of 17 Y-STRs (Yfiler) from Punjabis and Kashmiris of Pakistan.
Int J Legal Med
; 132(1): 137-138, 2018 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-28516222
3.
Mitochondrial DNA diversity of present-day Aboriginal Australians and implications for human evolution in Oceania.
J Hum Genet
; 62(3): 343-353, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27904152
4.
MSeqDR: A Centralized Knowledge Repository and Bioinformatics Web Resource to Facilitate Genomic Investigations in Mitochondrial Disease.
Hum Mutat
; 37(6): 540-548, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26919060
5.
Phy-Mer: a novel alignment-free and reference-independent mitochondrial haplogroup classifier.
Bioinformatics
; 31(8): 1310-2, 2015 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25505086
6.
Antiquity and diversity of aboriginal Australian Y-chromosomes.
Am J Phys Anthropol
; 159(3): 367-81, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26515539
7.
Simultaneous analysis of hundreds of Y-chromosomal SNPs for high-resolution paternal lineage classification using targeted semiconductor sequencing.
Hum Mutat
; 36(1): 151-9, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25338970
8.
Simultaneous Whole Mitochondrial Genome Sequencing with Short Overlapping Amplicons Suitable for Degraded DNA Using the Ion Torrent Personal Genome Machine.
Hum Mutat
; 36(12): 1236-47, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26387877
9.
The Basque paradigm: genetic evidence of a maternal continuity in the Franco-Cantabrian region since pre-Neolithic times.
Am J Hum Genet
; 90(3): 486-93, 2012 Mar 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-22365151
10.
A "Copernican" reassessment of the human mitochondrial DNA tree from its root.
Am J Hum Genet
; 90(4): 675-84, 2012 Apr 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-22482806
11.
Mitochondrial Disease Sequence Data Resource (MSeqDR): a global grass-roots consortium to facilitate deposition, curation, annotation, and integrated analysis of genomic data for the mitochondrial disease clinical and research communities.
Mol Genet Metab
; 114(3): 388-96, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25542617
12.
Seeing the wood for the trees: a minimal reference phylogeny for the human Y chromosome.
Hum Mutat
; 35(2): 187-91, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24166809
13.
Recent radiation within Y-chromosomal haplogroup R-M269 resulted in high Y-STR haplotype resemblance.
Ann Hum Genet
; 78(2): 92-103, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24571229
14.
Bridging near and remote Oceania: mtDNA and NRY variation in the Solomon Islands.
Mol Biol Evol
; 29(2): 545-64, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21771715
15.
Multiplex genotyping assays for fine-resolution subtyping of the major human Y-chromosome haplogroups E, G, I, J, and R in anthropological, genealogical, and forensic investigations.
Electrophoresis
; 34(20-21): 3029-38, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23893838
16.
Mitochondrial DNA analysis of Swedish population samples.
Int J Legal Med
; 127(6): 1097-9, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24077990
17.
Indian Ocean crossroads: human genetic origin and population structure in the Maldives.
Am J Phys Anthropol
; 151(1): 58-67, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23526367
18.
Unexpected island effects at an extreme: reduced Y chromosome and mitochondrial DNA diversity in Nias.
Mol Biol Evol
; 28(4): 1349-61, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21059792
19.
Population genetic structure in Indian Austroasiatic speakers: the role of landscape barriers and sex-specific admixture.
Mol Biol Evol
; 28(2): 1013-24, 2011 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20978040
20.
A multiplex SNP assay for the dissection of human Y-chromosome haplogroup O representing the major paternal lineage in East and Southeast Asia.
J Hum Genet
; 57(1): 65-9, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22048658