Qasim Ayub
TitleCited byYear
A map of human genome variation from population-scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
66782010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
60702012
A systematic survey of loss-of-function variants in human protein-coding genes
DG MacArthur, S Balasubramanian, A Frankish, N Huang, J Morris, ...
Science 335 (6070), 823-828, 2012
9482012
Insights into hominid evolution from the gorilla genome sequence
A Scally, JY Dutheil, LDW Hillier, GE Jordan, I Goodhead, J Herrero, ...
Nature 483 (7388), 169, 2012
6012012
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
5302003
Demographic history and rare allele sharing among human populations
S Gravel, BM Henn, RN Gutenkunst, AR Indap, GT Marth, AG Clark, F Yu, ...
Proceedings of the National Academy of Sciences 108 (29), 11983-11988, 2011
4552011
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
Integrative annotation of variants from 1092 humans: application to cancer genomics
E Khurana, Y Fu, V Colonna, XJ Mu, HM Kang, T Lappalainen, A Sboner, ...
Science 342 (6154), 1235587, 2013
3142013
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 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
2472009
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
Deleterious-and disease-allele prevalence in healthy individuals: insights from current predictions, mutation databases, and population-scale resequencing
Y Xue, Y Chen, Q Ayub, N Huang, EV Ball, M Mort, AD Phillips, K Shaw, ...
The American Journal of Human Genetics 91 (6), 1022-1032, 2012
2322012
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
2302000
A recent bottleneck of Y chromosome diversity coincides with a global change in culture
M Karmin, L Saag, M Vicente, MAW Sayres, M Järve, UG Talas, S Rootsi, ...
Genome research 25 (4), 459-466, 2015
2062015
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
O Delaneau, J Marchini, GA McVean, P Donnelly, G Lunter, JL Marchini, ...
Nature communications 5, 3934, 2014
2042014
Genomic analyses inform on migration events during the peopling of Eurasia
L Pagani, DJ Lawson, E Jagoda, A Mörseburg, A Eriksson, M Mitt, ...
Nature 538 (7624), 238, 2016
1892016
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
Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences
GD Poznik, Y Xue, FL Mendez, TF Willems, A Massaia, MAW Sayres, ...
Nature genetics 48 (6), 593, 2016
1702016
A global analysis of Y-chromosomal haplotype diversity for 23 STR loci
J Purps, S Siegert, S Willuweit, M Nagy, C Alves, R Salazar, ...
Forensic Science International: Genetics 12, 12-23, 2014
1692014
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
1562012
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