Detalhe da pesquisa
1.
Ethiopian genetic diversity reveals linguistic stratification and complex influences on the Ethiopian gene pool.
Am J Hum Genet
; 91(1): 83-96, 2012 Jul 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-22726845
2.
ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous.
Hum Mol Genet
; 21(16): 3681-94, 2012 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22645276
3.
Independent introduction of two lactase-persistence alleles into human populations reflects different history of adaptation to milk culture.
Am J Hum Genet
; 82(1): 57-72, 2008 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-18179885
4.
Genetic heterogeneity for autosomal dominant familial hypertrophic cardiomyopathy in a Pakistani family.
J Coll Physicians Surg Pak
; 21(4): 202-6, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21453614
5.
Sub-Saharan African coding sequence variation and haplotype diversity at the NAT2 gene.
Hum Mutat
; 27(7): 720, 2006 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-16786516
6.
DC-SIGN interacts with Mycobacterium leprae but sequence variation in this lectin is not associated with leprosy in the Pakistani population.
Hum Immunol
; 67(1-2): 102-7, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-16698431
7.
Cloning and characterization of WDR17, a novel WD repeat-containing gene on chromosome 4q34.
Biochim Biophys Acta
; 1579(1): 18-25, 2002 Nov 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-12401215
8.
Genetic instability in EBV-transformed lymphoblastoid cell lines.
Biochim Biophys Acta
; 1670(1): 81-3, 2004 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-14729144
9.
Locus heterogeneity and Knobloch syndrome.
Am J Med Genet A
; 152A(11): 2880-1, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-20979194
10.
A novel locus for autosomal dominant nuclear cataract mapped to chromosome 2p12 in a Pakistani family.
Invest Ophthalmol Vis Sci
; 43(7): 2083-7, 2002 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-12091400
11.
Frequency of CCR5 Gene 32-bp deletion in Pakistani ethnic groups.
Genet Test
; 6(2): 123-7, 2002.
Artigo
em Inglês
| MEDLINE | ID: mdl-12215252
12.
Contrasting signals of positive selection in genes involved in human skin-color variation from tests based on SNP scans and resequencing.
Investig Genet
; 2(1): 24, 2011 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22133426
13.
Separating the post-Glacial coancestry of European and Asian Y chromosomes within haplogroup R1a.
Eur J Hum Genet
; 18(4): 479-84, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19888303
14.
Population differentiation as an indicator of recent positive selection in humans: an empirical evaluation.
Genetics
; 183(3): 1065-77, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19737746
15.
A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia.
Nat Genet
; 41(2): 187-91, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19151713
16.
Geographically separate increases in the frequency of the derived ADH1B*47His allele in eastern and western Asia.
Am J Hum Genet
; 81(4): 842-6, 2007 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-17847010
17.
Evidence of still-ongoing convergence evolution of the lactase persistence T-13910 alleles in humans.
Am J Hum Genet
; 81(3): 615-25, 2007 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17701907
18.
Detection of novel Y SNPs provides further insights into Y chromosomal variation in Pakistan.
J Hum Genet
; 51(4): 375-378, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-16470330
19.
Y-chromosomal DNA variation in Pakistan.
Am J Hum Genet
; 70(5): 1107-24, 2002 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-11898125
20.
Mutation screening of Pakistani families with congenital eye disorders.
Exp Eye Res
; 76(3): 343-8, 2003 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-12573663