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Co-authors
(103)
Wasim Ahmad
30
Muhammad Ansar
13
Suzanne M. Leal
10
Muhammad Salman Chishti
10
Muhammad Jawad Hassan
10
Journals
(16)
CLIN GENET
6
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6
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3
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3
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Authors
Ghazanfar Ali
Ghazanfar Ali,Aga Khan University,Genetics & Genealogy,Dermatology,Neuroscience
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Ghazanfar Ali
Aga Khan University
Publications:
33
|
Citations:
168
Fields:
Genetics & Genealogy
,
Dermatology
,
Neuroscience
View FAQ about top research areas and Fields of study
Collaborated with
103 co-authors
from 2004 to 2011
|
Cited by
669 authors
Cumulative
Annual
Sort by:
Publications
(33)
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A novel deletion mutation in the TUSC3 gene in a consanguineous Pakistani family with autosomal recessive nonsyndromic intellectual disability
(
Citations: 1
)
Muzammil Ahmad Khan
,
Muhammad Arshad Rafiq
,
Abdul Noor
,
Nadir Ali
,
Ghazanfar Ali
,
John B Vincent
,
Muhammad Ansar
Journal:
BMC Medical Genetics - BMC MED GENET
, vol. 12, no. 1, pp. 1-7, 2011
Mutations in the Alpha 1,2Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability
(
Citations: 1
)
Lucia Puettmann
,
Abdul Noor
,
Annapoorani Ramiah
,
Ghazanfar Ali
,
Hao Hu
,
Yong Xiang
,
Masoud Garshasbi
,
Rosanna Weksberg
,
Reinhard Ullmann
,
Andreas Tzschach
,
Kimia Kahrizi
,
Khalid Mahmood
http://academic.research.microsoft.com/io.ashx?type=5&id=49005488&selfId1=24431658&selfId2=0&maxNumber=12&query=
Journal:
American Journal of Human Genetics - AMER J HUM GENET
, vol. 89, no. 1, pp. 176-182, 2011
Novel Autosomal Recessive Nonsyndromic Hearing Impairment Locus DFNB90 Maps to 7p22.1-p15.3
Ghazanfar Ali
,
Kwanghyuk Lee
,
Paula B. Andrade
,
Sulman Basit
,
Regie Lyn P. Santos-Cortez
,
Leon Chen
,
Musharraf Jelani
,
Muhammad Ansar
,
Wasim Ahmad
,
Suzanne M. Leal
Journal:
Human Heredity - HUM HERED
, vol. 71, pp. 106-112, 2011
Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment
(
Citations: 7
)
Margit Schraders
,
Kwanghyuk Lee
,
Jaap Oostrik
,
Patrick L. M. Huygen
,
Ghazanfar Ali
,
Lies H. Hoefsloot
,
Joris A. Veltman
,
Frans P. M. Cremers
,
Sulman Basit
,
Muhammad Ansar
,
Cor W. R. J. Cremers
,
Henricus P. M. Kunst
http://academic.research.microsoft.com/io.ashx?type=5&id=36196472&selfId1=24431658&selfId2=0&maxNumber=12&query=
Journal:
American Journal of Human Genetics - AMER J HUM GENET
, vol. 86, no. 2, pp. 138-147, 2010
Mapping of three novel loci for non-syndromic autosomal recessive mental retardation (NS-ARMR) in consanguineous families from Pakistan
(
Citations: 4
)
MA Rafiq
,
M Ansar
,
CR Marshall
,
A Noor
,
N Shaheen
,
A Mowjoodi
,
MA Khan
,
G Ali
,
M Amin-ud-Din
,
L Feuk
,
JB Vincent
,
SW Scherer
Journal:
Clinical Genetics - CLIN GENET
, 2010
Sort by:
Citations
(168 times by 107 publications)
Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
Regina C Betz
,
Rita M Cabral
,
Angela M Christiano
,
Eli Sprecher
Published in 2012.
Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots
(
Citations: 4
)
Andreas Walter Kuss
,
Masoud Garshasbi
,
Kimia Kahrizi
,
Andreas Tzschach
,
Farkhondeh Behjati
,
Hossein Darvish
,
Lia Abbasi-Moheb
,
Lucia Puettmann
,
Agnes Zecha
,
Robert Weißmann
,
Hao Hu
,
Marzieh Mohseni
http://academic.research.microsoft.com/io.ashx?type=5&id=48065794&selfId1=24431658&selfId2=0&maxNumber=12&query=
Journal:
Human Genetics - HUM GENET
, vol. 129, no. 2, pp. 141-148, 2011
Deep sequencing reveals 50 novel genes for recessive cognitive disorders
(
Citations: 2
)
Hossein Najmabadi
,
Hao Hu
,
Masoud Garshasbi
,
Tomasz Zemojtel
,
Seyedeh Sedigheh Abedini
,
Wei Chen
,
Masoumeh Hosseini
,
Farkhondeh Behjati
,
Stefan Haas
,
Payman Jamali
,
Agnes Zecha
,
Marzieh Mohseni
http://academic.research.microsoft.com/io.ashx?type=5&id=52420420&selfId1=24431658&selfId2=0&maxNumber=12&query=
Journal:
Nature
, vol. 478, no. 7367, pp. 57-63, 2011
Homozygosity mapping in 64 Syrian consanguineous families with non-specific intellectual disability reveals 11 novel loci and high heterogeneity
R Abou Jamra
,
Sigrun Wohlfart
,
Markus Zweier
,
Steffen Uebe
,
Lutz Priebe
,
Arif Ekici
,
Susanne Giesebrecht
,
Ahmad Abboud
,
Mohammed Ayman Al Khateeb
,
Mahmoud Fakher
,
Saber Hamdan
,
Amina Ismael
http://academic.research.microsoft.com/io.ashx?type=5&id=56548600&selfId1=24431658&selfId2=0&maxNumber=12&query=
Journal:
European Journal of Human Genetics - EUR J HUMAN GENET
, vol. 19, no. 11, pp. 1161-1166, 2011
Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human
(
Citations: 1
)
Nikoletta Charizopoulou
,
Andrea Lelli
,
Margit Schraders
,
Kausik Ray
,
Michael S. Hildebrand
,
Arabandi Ramesh
,
C. R. Srikumari Srisailapathy
,
Jaap Oostrik
,
Ronald J. C. Admiraal
,
Harold R. Neely
,
Joseph R. Latoche
,
Richard J. H. Smith
http://academic.research.microsoft.com/io.ashx?type=5&id=53381775&selfId1=24431658&selfId2=0&maxNumber=12&query=
Journal:
Nature Communications
, vol. 2, pp. 201-201, 2011
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