Detalhe da pesquisa
1.
Reconstructing the demographic history of the Himalayan and adjoining populations.
Hum Genet
; 137(2): 129-139, 2018 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-29356938
2.
A Complete Absence of Missense Mutation in Myosin Regulatory and Essential Light Chain Genes of South Indian Hypertrophic and Dilated Cardiomyopathies.
Cardiology
; 141(3): 156-166, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30605904
3.
Mechanistic heterogeneity in contractile properties of α-tropomyosin (TPM1) mutants associated with inherited cardiomyopathies.
J Biol Chem
; 290(11): 7003-15, 2015 Mar 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-25548289
4.
Indian Siddis: African descendants with Indian admixture.
Am J Hum Genet
; 89(1): 154-61, 2011 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21741027
5.
Novel MYBPC3 Mutations in Indian Population with Cardiomyopathies.
Pharmgenomics Pers Med
; 16: 883-893, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37750083
6.
High prevalence of Arginine to Glutamine substitution at 98, 141 and 162 positions in Troponin I (TNNI3) associated with hypertrophic cardiomyopathy among Indians.
BMC Med Genet
; 13: 69, 2012 Aug 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-22876777
7.
Novel Mutations in ß-MYH7 Gene in Indian Patients With Dilated Cardiomyopathy.
CJC Open
; 4(1): 1-11, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-35072022
8.
No evidence for association between SLC11A1 and visceral leishmaniasis in India.
BMC Med Genet
; 12: 71, 2011 May 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-21599885
9.
Genetic and functional evaluation of the role of CXCR1 and CXCR2 in susceptibility to visceral leishmaniasis in north-east India.
BMC Med Genet
; 12: 162, 2011 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22171941
10.
CAG repeat variation in the mtDNA polymerase gamma is not associated with oligoasthenozoospermia.
Int J Androl
; 32(6): 647-55, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-18798765
11.
High frequencies of Non Allelic Homologous Recombination (NAHR) events at the AZF loci and male infertility risk in Indian men.
Sci Rep
; 9(1): 6276, 2019 04 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-31000748
12.
Mitochondrial genome variations in idiopathic dilated cardiomyopathy.
Mitochondrion
; 48: 51-59, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30910572
13.
"Like sugar in milk": reconstructing the genetic history of the Parsi population.
Genome Biol
; 18(1): 110, 2017 06 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-28615043
14.
A novel human sex-determining gene linked to Xp11.21-11.23.
J Clin Endocrinol Metab
; 91(10): 4028-36, 2006 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16868052
15.
Y chromosome deletions in azoospermic men in India.
J Androl
; 24(4): 588-97, 2003.
Artigo
em Inglês
| MEDLINE | ID: mdl-12826698
16.
A novel arginine to tryptophan (R144W) mutation in troponin T (cTnT) gene in an indian multigenerational family with dilated cardiomyopathy (FDCM).
PLoS One
; 9(7): e101451, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24992688
17.
Mitochondrial DNA variations associated with hypertrophic cardiomyopathy.
Mitochondrion
; 16: 65-72, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24215792
18.
RAF1 mutations in childhood-onset dilated cardiomyopathy.
Nat Genet
; 46(6): 635-639, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24777450
19.
Genetic evidence of TAP1 gene variant as a susceptibility factor in Indian leprosy patients.
Hum Immunol
; 74(6): 803-7, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23395648
20.
Genetic structure of Tibeto-Burman populations of Bangladesh: evaluating the gene flow along the sides of Bay-of-Bengal.
PLoS One
; 8(10): e75064, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24130682