Syed Qasim Mehdi

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	Wszystkie	Od 2020
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Dr. Shagufta Khaliq, Dir. Research, U...University College of Medicine & Dentistry-The University of LahoreZweryfikowany adres z ucm.uol.edu.pk
aisha mohyuddinShifa College of Medicine, Islamabad, PakistanZweryfikowany adres z shifacollege.edu
Qasim AyubWellcome Trust Sanger InstituteZweryfikowany adres z sanger.ac.uk
Annette PayneLecturer Brunel UniversityZweryfikowany adres z brunel.ac.uk
Antonio TorroniProfessor of Genetics, Department of Biology and Biotechnology, University of Pavia, ItalyZweryfikowany adres z unipv.it
Luca PaganiFull Professor, Department of Biology, University of Padova, ItalyZweryfikowany adres z unipd.it
Kumarasamy ThangarajCentre for Cellular and Molecular BiologyZweryfikowany adres z ccmb.res.in
Prof. Dr. Muhammed MubarakProfessor of Pathology and Head of Histopathology Department, Sindh Institute of Urology andZweryfikowany adres z siut.org
Mark SeielstadUniversity of California San FranciscoZweryfikowany adres z ucsf.edu
Giuseppe PassarinoUniversità della CalabriaZweryfikowany adres z unical.it
Jaume BertranpetitIBE (UPF-CSIC), Universitat Pompeu FabraZweryfikowany adres z upf.edu
Mark G ThomasProfessor of Evolutionary Genetics, University College LondonZweryfikowany adres z ucl.ac.uk
Stylianos E. AntonarakisProfessor of Genetic Medicine, University of Geneva Medical SchoolZweryfikowany adres z unige.ch
Hamish S ScottCenter of Cancer BiologyZweryfikowany adres z sa.gov.au
DAVID COMASFull professor, Universitat Pompeu Fabra, Institut de Biologia Evolutiva (CSIC-UPF)Zweryfikowany adres z upf.edu
Agnar HelgasondeCODE Genetics and University of IcelandZweryfikowany adres z hi.is
Deepa Selvi RaniCentre for Cellular and Molecular BiologyZweryfikowany adres z ccmb.res.in
Bertorelle GiorgioProfessor in Genetics, University of FerraraZweryfikowany adres z unife.it
Cheryl-Emiliane ChowUSC; UBC; Second Genome; GenentechZweryfikowany adres z gene.com
Giovanni Destro BisolUniversity of Rome "La Sapienza" and Istituto Italiano di AntropologiaZweryfikowany adres z uniroma1.it

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Syed Qasim Mehdi

HEC Distinguished National Professor

Zweryfikowany adres z comsats.net.pk

Human Genome Diversity


Tytuł Sortuj wg cytatów Sortuj wg roku Sortuj wg tytułu	Cytowane przez Cytowane przez	Rok
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), 358-361, 2000	1414	2000
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	1183	2002
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	878	1997
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	756	2003
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	546	2006
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	541	2004
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	398	2008
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	346	2004
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), 79-83, 2000	339	2000
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), 479-484, 2010	338	2010
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), 187-191, 2009	338	2009
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	333	2002
Refined Geographic Distribution of the Oriental ALDH2504Lys* (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	330	2009
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), 59-63, 2001	291	2001
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	273	2000
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	260	2012
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	210	2007
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	210	2001
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, ... Human genetics 105, 168-170, 1999	178	1999
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	158	1996

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