Syed Qasim Mehdi
Syed Qasim Mehdi
HEC Distinguished National Professor
Verified email at comsats.net.pk
TitleCited byYear
Y chromosome sequence variation and the history of human populations
PA Underhill, P Shen, AA Lin, L Jin, G Passarino, WH Yang, E Kauffman, ...
Nature genetics 26 (3), 358, 2000
12262000
A human genome diversity cell line panel
HM Cann, C De Toma, L Cazes, MF Legrand, V Morel, L Piouffre, ...
Science 296 (5566), 261-262, 2002
9402002
Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography
PA Underhill, L Jin, AA Lin, SQ Mehdi, T Jenkins, D Vollrath, RW Davis, ...
Genome research 7 (10), 996-1005, 1997
8041997
The genetic legacy of the Mongols
T Zerjal, Y Xue, G Bertorelle, RS Wells, W Bao, S Zhu, R Qamar, Q Ayub, ...
The American Journal of Human Genetics 72 (3), 717-721, 2003
5282003
Where west meets east: the complex mtDNA landscape of the southwest and Central Asian corridor
L Quintana-Murci, R Chaix, RS Wells, DM Behar, H Sayar, R Scozzari, ...
The American Journal of Human Genetics 74 (5), 827-845, 2004
4432004
Polarity and temporality of high-resolution y-chromosome distributions in India identify both indigenous and exogenous expansions and reveal minor genetic influence of Central …
S Sengupta, LA Zhivotovsky, R King, SQ Mehdi, CA Edmonds, CET Chow, ...
The American Journal of Human Genetics 78 (2), 202-221, 2006
4322006
Independent introduction of two lactase-persistence alleles into human populations reflects different history of adaptation to milk culture
NS Enattah, TGK Jensen, M Nielsen, R Lewinski, M Kuokkanen, ...
The American Journal of Human Genetics 82 (1), 57-72, 2008
3112008
Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis
MM Sohocki, SJ Bowne, LS Sullivan, S Blackshaw, CL Cepko, AM Payne, ...
Nature genetics 24 (1), 79, 2000
2972000
Y-chromosomal DNA variation in Pakistan
R Qamar, Q Ayub, A Mohyuddin, A Helgason, K Mazhar, A Mansoor, ...
The American Journal of Human Genetics 70 (5), 1107-1124, 2002
2652002
A comprehensive survey of human Y-chromosomal microsatellites
M Kayser, R Kittler, A Erler, M Hedman, AC Lee, A Mohyuddin, SQ Mehdi, ...
The American Journal of Human Genetics 74 (6), 1183-1197, 2004
2562004
A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia
PS Dhandapany, S Sadayappan, Y Xue, GT Powell, DS Rani, P Nallari, ...
Nature genetics 41 (2), 187, 2009
2462009
Separating the post-Glacial coancestry of European and Asian Y chromosomes within haplogroup R1a
PA Underhill, NM Myres, S Rootsi, M Metspalu, LA Zhivotovsky, RJ King, ...
European Journal of Human Genetics 18 (4), 479, 2010
2352010
Identification and characterisation of novel human Y-chromosomal microsatellites from sequence database information
Q Ayub, A Mohyuddin, R Qamar, K Mazhar, T Zerjal, SQ Mehdi, ...
Nucleic acids research 28 (2), e8-e8, 2000
2292000
Insertion of β-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness
HS Scott, J Kudoh, M Wattenhofer, K Shibuya, A Berry, R Chrast, ...
Nature genetics 27 (1), 59, 2001
2162001
Y-chromosome lineages trace diffusion of people and languages in southwestern Asia
L Quintana-Murci, C Krausz, T Zerjal, SH Sayar, MF Hammer, SQ Mehdi, ...
The American Journal of Human Genetics 68 (2), 537-542, 2001
1802001
Refined Geographic Distribution of the Oriental ALDH2*504Lys (nee 487Lys) Variant
H Li, S Borinskaya, K Yoshimura, N Kal’Ina, A Marusin, VA Stepanov, ...
Annals of human genetics 73 (3), 335-345, 2009
1762009
Evidence of still-ongoing convergence evolution of the lactase persistence T-13910 alleles in humans
NS Enattah, A Trudeau, V Pimenoff, L Maiuri, S Auricchio, L Greco, ...
The American Journal of Human Genetics 81 (3), 615-625, 2007
1582007
Ethiopian genetic diversity reveals linguistic stratification and complex influences on the Ethiopian gene pool
L Pagani, T Kivisild, A Tarekegn, R Ekong, C Plaster, IG Romero, Q Ayub, ...
The American journal of Human genetics 91 (1), 83-96, 2012
1572012
Connexin 50 mutation in a family with congenital" zonular nuclear" pulverulent cataract of Pakistani origin
V Berry, D Mackay, S Khaliq, PJ Francis, A Hameed, K Anwar, SQ Mehdi, ...
Human genetics 105 (1-2), 168-170, 1999
1551999
Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan
A Veske, R Oehlmann, F Younus, A Mohyuddin, B Müller-Myhsok, ...
Human molecular genetics 5 (1), 165-168, 1996
1301996
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