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Sheikh Amer Riazuddin

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Pakistan

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Saima Riazuddin; Sheikh Amer Riazuddin; Ghanshyam P Sinha; Asli Sirmaci; Mustafa Tekin; David Terrell; Abdul Wali; Rizwan Yousaf; Wasim Ahmad; Javed Akram; Rana A Ali; Paula B Andrade-Elizondo; Muhammad Ansar; Saima Anwar; Muhammad Ayub; Sulman Basit; Inna A Belyantseva; Elke K Buschbeck; Tiffany Cook; Thomas B Friedman; Gregory I Frolenkov; Arnaud P J Giese; Rashmi S Hegde; Artur A Indzhykulian; Shaheen N Khan; Suzanne M Leal; Kwanghyuk Lee; Sue Lee; Sri Pratima Nandamuri; Leslie V Parise; Zubair M Ahmed
Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48.
Mahmood S Choudhery; Mohsin Khan; Shaheen N Khan; Ruhma Mahmood; Sadia Mohsin; Shoaib Akhtar; Fatima Ali; Sheikh Amer Riazuddin
Mesenchymal stem cells conditioned with glucose depletion augments their ability to repair-infarcted myocardium.
Mahmood Saba Choudhery; Mohsin Khan; Shaheen N Khan; Ruhma Mahmood; Azra Mehmood; Sheikh Amer Riazuddin
Bone marrow derived mesenchymal stem cells from aged mice have reduced wound healing, angiogenesis, proliferation and anti-apoptosis capabilities.

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All Publications

2012: Saima Riazuddin; Sheikh Amer Riazuddin; Ghanshyam P Sinha; Asli Sirmaci; Mustafa Tekin; David Terrell; Abdul Wali; Rizwan Yousaf; Wasim Ahmad; Javed Akram; Rana A Ali; Paula B Andrade-Elizondo; Muhammad Ansar; Saima Anwar; Muhammad Ayub; Sulman Basit; Inna A Belyantseva; Elke K Buschbeck; Tiffany Cook; Thomas B Friedman; Gregory I Frolenkov; Arnaud P J Giese; Rashmi S Hegde; Artur A Indzhykulian; Shaheen N Khan; Suzanne M Leal; Kwanghyuk Lee; Sue Lee; Sri Pratima Nandamuri; Leslie V Parise; Zubair M Ahmed
Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48.
Nature genetics 2012;44(11):1265-71.
2012: Mahmood S Choudhery; Mohsin Khan; Shaheen N Khan; Ruhma Mahmood; Sadia Mohsin; Shoaib Akhtar; Fatima Ali; Sheikh Amer Riazuddin
Mesenchymal stem cells conditioned with glucose depletion augments their ability to repair-infarcted myocardium.
Journal of cellular and molecular medicine 2012;16(10):2518-29.
2012: Mahmood Saba Choudhery; Mohsin Khan; Shaheen N Khan; Ruhma Mahmood; Azra Mehmood; Sheikh Amer Riazuddin
Bone marrow derived mesenchymal stem cells from aged mice have reduced wound healing, angiogenesis, proliferation and anti-apoptosis capabilities.
Cell biology international 2012;36(8):747-53.
2012: Allen O Eghrari; David Emmert; Benjamin W Iliff; Nicholas Katsanis; Elyse J McGlumphy; Sheikh Amer Riazuddin; Jiangxia Wang; John D Gottsch
Prevalence and severity of fuchs corneal dystrophy in Tangier Island.
American journal of ophthalmology 2012;153(6):1067-72.
2012: Benjamin W Iliff; Sheikh Amer Riazuddin; John D Gottsch
Documenting the corneal phenotype associated with the MIR184 c.57C>T mutation.
American journal of human genetics 2012;90(5):934; author reply 934-5.
2012: Zafar Iqbal; Michael P Kwint; Kornelia Neveling; Muhammad Qasim; Attia Razzaq; Sheikh Amer Riazuddin; Mohsin Shahzad; Arjan P M de Brouwer; Sabine Gijsen; Christian Gilissen; Joris A Veltman; Nienke Wieskamp; Muhammad Yasir Zahoor; Hans van Bokhoven
Targeted next generation sequencing reveals a novel intragenic deletion of the TPO gene in a family with intellectual disability.
Archives of medical research 2012;43(4):312-6.
2012: R A Ali; T B Friedman; Tayyab Husnain; S N Khan; A U Rehman; Z M Ahmed; Sheikh Amer Riazuddin; S Riazuddin
DFNB86, a novel autosomal recessive non-syndromic deafness locus on chromosome 16p13.3.
Clinical genetics 2012;81(5):498-500.
2012: Sheikh Amer Riazuddin; Robert Schleif; Thore Schmedt; Benjamin W Iliff; Ula V Jurkunas; Nicholas Katsanis; Elyse J McGlumphy; Edwin C Oh; David S Parker; John D Gottsch
Mutations in LOXHD1, a recessive-deafness locus, cause dominant late-onset Fuchs corneal dystrophy.
American journal of human genetics 2012;90(3):533-9.
2012: Muhammad Asif Naeem; Saima Riazuddin; Sheikh Riazuddin; Shahbaz Ali; Radha Ayyagari; Venkata R M Chavali; J Fielding Hejtmancik; Tayyab Husnain; Muhammad Iqbal; Shaheen N Khan; Paul Sieving; Sheikh Amer Riazuddin
GNAT1 associated with autosomal recessive congenital stationary night blindness.
Investigative ophthalmology & visual science 2012;53(3):1353-61.
2012: Muhammad Hashim Raza; Sheikh Amer Riazuddin; Rana Amjad; Dennis Drayna
Studies in a consanguineous family reveal a novel locus for stuttering on chromosome 16q.
Human genetics 2012;131(2):311-3.
2012: Lisa Ann Brennan; Daniel Chauss; Ales Cvekl; Shuying He; J Fielding Hejtmancik; Wanda Lee Kantorow; Lyndzie Mattucci; Rebecca McGreal; Sheikh Amer Riazuddin; Jianning Wei; Marc Kantorow
Spatial expression patterns of autophagy genes in the eye lens and induction of autophagy in lens cells.
Molecular vision 2012;18():1773-86.
2012: Gibran Ali; Mohsin Khan; Shaheen N Khan; Sadia Mohsin; Ghazanfar Ali Nasir; Sulaiman Shams; Sheikh Amer Riazuddin
Nitric oxide augments mesenchymal stem cell ability to repair liver fibrosis.
Journal of translational medicine 2012;10():75.
2012: Benjamin W Iliff; Sheikh Amer Riazuddin; John D Gottsch
A single-base substitution in the seed region of miR-184 causes EDICT syndrome.
Investigative ophthalmology & visual science 2012;53(1):348-53.
2011: Atteeq U Rehman; Saima Riazuddin; Sheikh Amer Riazuddin; Mohsin Shahzad; Wasim Ahmad; Zubair M Ahmed; Rana A Ali; Paula B Andrade; Carmen C Brewer; Khitab Gul; Ateeq-Ul Jaleel; Saadullah Khan; Shaheen N Khan; Suzanne M Leal; Kwanghyuk Lee; Robert J Morell; Thomas B Friedman
Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p.
Human genetics 2011;130(6):759-65.
2011: Julie M Schultz; Ekaterini T Tsilou; Amy Turriff; Christopher K Zalewski; Wadih M Zein; Nazir Ahmad; Zubair M Ahmed; Rashid Bhatti; Carmen C Brewer; Manju Ghosh; Andrew J Griffith; Zawar Hussain; Shaheen N Kahn; Kelly A King; Xue Zhong Liu; Anne C Madeo; Meira R Meltzer; Murali Munisamy; Julie A Muskett; Muhammad Qasim; Heidi L Rehm; Sheikh Amer Riazuddin; Saima Riazuddin; Thomas B Friedman
Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes.
Journal of medical genetics 2011;48(11):767-75.
2011: Muhammad Iqbal; Shaheen N Khan; Muhammad Asif Naeem; Zaheeruddin A Qazi; Saima Riazuddin; Shahbaz Ali; Tahir Farooq; J Fielding Hejtmancik; Tayyab Husnain; Sheikh Amer Riazuddin; Paul A Sieving; Sheikh Riazuddin
Association of pathogenic mutations in TULP1 with retinitis pigmentosa in consanguineous Pakistani families.
Archives of ophthalmology 2011;129(10):1351-7.
2011: Jianjun Chen; Monia Ben Hamed Hammer; Shyana Harper; Xiaodong Jiao; Nicholas Katsanis; Sheikh Riazuddin; Sheikh Amer Riazuddin; Nizar Smaoui; Eliot L Berson; Habiba Chaabouni; J Fielding Hejtmancik
Molecular analysis of Bardet-Biedl syndrome families: report of 21 novel mutations in 10 genes.
Investigative ophthalmology & visual science 2011;52(8):5317-24.
2011: Ali M Waryah; Munir A Bhinder; Mohsin Shahzad; Robert A Sisk; Zubair M Ahmed; Munir A Binder; Daniel I Choo; Thomas B Friedman; Shaheen N Khan; Sheikh Amer Riazuddin; Saima Riazuddin
Molecular and clinical studies of X-linked deafness among Pakistani families.
Journal of human genetics 2011;56(7):534-40.
2011: Sadaf Naz; Sheikh Amer Riazuddin; Paul A Sieving; Ahmad U Zafar; Shahbaz Ali; Nadeem H Butt; Tahir Farooq; J Fielding Hejtmancik; Tayyab Husnain; Shaheen N Khan; Ian M MacDonald; Sheikh Riazuddin
Mutations in RLBP1 associated with fundus albipunctatus in consanguineous Pakistani families.
The British journal of ophthalmology 2011;95(7):1019-24.
2011: Mohsin Khan; Shaheen N Khan; Sadia Mohsin; Sheikh Amer Riazuddin
Repair of senescent myocardium by mesenchymal stem cells is dependent on the age of donor mice.
Journal of cellular and molecular medicine 2011;15(7):1515-27.
2011: Jianjun Chen; Robert Fariss; Moshe Frydman; Xiaodong Jiao; Marc Kantorow; Wanda Lee Kantorow; Zhiwei Ma; Elon Pras; Elon Pras; Sheikh Riazuddin; Sheikh Amer Riazuddin; J Fielding Hejtmancik
Mutations in FYCO1 cause autosomal-recessive congenital cataracts.
American journal of human genetics 2011;88(6):827-38.
2011: Abdul Qayyum Rao; Muhammad Irfan; Zafar Saleem; Idrees Ahmad Nasir; Sheikh Amer Riazuddin; Tayyab Husnain
Overexpression of the phytochrome B gene from Arabidopsis thaliana increases plant growth and yield of cotton (Gossypium hirsutum).
Journal of Zhejiang University. Science. B 2011;12(4):326-34.
2011: Sheikh Amer Riazuddin; Elyse J McGlumphy; William S Yeo; Jiangxia Wang; Nicholas Katsanis; John D Gottsch
Replication of the TCF4 intronic variant in late-onset Fuchs corneal dystrophy and evidence of independence from the FCD2 locus.
Investigative ophthalmology & visual science 2011;52(5):2825-9.
2011: Guntram Borck; Atteeq Ur Rehman; Kwanghyuk Lee; Hans-Martin Pogoda; Naseebullah Kakar; Simon von Ameln; Nicolas Grillet; Michael S Hildebrand; Zubair M Ahmed; Gudrun Nürnberg; Muhammad Ansar; Sulman Basit; Qamar Javed; Robert J Morell; Nabilah Nasreen; A Eliot Shearer; Adeel Ahmad; Kimia Kahrizi; Rehan S Shaikh; Rana A Ali; Shaheen N Khan; Ingrid Goebel; Nicole C Meyer; William J Kimberling; Jennifer A Webster; Dietrich A Stephan; Martin R Schiller; Melanie Bahlo; Hossein Najmabadi; Peter G Gillespie; Peter Nürnberg; Bernd Wollnik; Saima Riazuddin; Richard J H Smith; Wasim Ahmad; Ulrich Müller; Matthias Hammerschmidt; Thomas B Friedman; Sheikh Amer Riazuddin; Suzanne M Leal; Jamil Ahmad; Christian Kubisch
Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42.
American journal of human genetics 2011;88(2):127-37.
2011: Zubair M Ahmed; Rizwan Yousaf; Byung Cheon Lee; Shaheen N Khan; Sue Lee; Kwanghyuk Lee; Tayyab Husnain; Atteeq Ur Rehman; Sarah Bonneux; Muhammad Ansar; Wasim Ahmad; Suzanne M Leal; Vadim N Gladyshev; Inna A Belyantseva; Guy Van Camp; Sheikh Amer Riazuddin; Thomas B Friedman; Saima Riazuddin
Functional null mutations of MSRB3 encoding methionine sulfoxide reductase are associated with human deafness DFNB74.
American journal of human genetics 2011;88(1):19-29.
2011: Humera Kausar; Zafar Nawaz; Sheikh Amer Riazuddin; Muhammad Tahir Sarwar; Waqar Ahmad; Sana Gull; Bushra Ijaz; Zafar Iqbal; Sajida Hassan
Huh-7 cell line as an alternative cultural model for the production of human like erythropoietin (EPO).
Journal of translational medicine 2011;9():186.
2011: Usman A Ashfaq; Muhammad S Masoud; Zafar Nawaz; Sheikh Amer Riazuddin
Glycyrrhizin as antiviral agent against Hepatitis C Virus.
Journal of translational medicine 2011;9():112.
2011: Shahbaz Ali; J Fielding Hejtmancik; Tayyab Husnain; Shaheen N Khan; Idrees A Nasir; Sheikh Amer Riazuddin; Amber Shahzadi; Paul A Sieving; Javed Akram; Sheikh Riazuddin
Mutations in the β-subunit of rod phosphodiesterase identified in consanguineous Pakistani families with autosomal recessive retinitis pigmentosa.
Molecular vision 2011;17():1373-80.
2011: Usman A Ashfaq; sabahat Khaliq; Muhammad S Masoud; Zafar Nawaz; Sheikh Amer Riazuddin
Inhibition of hepatitis C virus 3a genotype entry through Glanthus Nivalis Agglutinin.
Virology journal 2011;8():248.
2011: Sidra Rehman; Sana Riaz; Usman A Ashfaq; Tariq Javed; Sheikh Amer Riazuddin
Antiviral activity of Acacia nilotica against Hepatitis C Virus in liver infected cells.
Virology journal 2011;8():220.
2011: Muhammad Ansar; Usman Ali Ashfaq; Imran Shahid; Muhammad Tahir Sarwar; Tariq Javed; Sidra Rehman; Sajida Hassan; Sheikh Amer Riazuddin
Inhibition of full length hepatitis C virus particles of 1a genotype through small interference RNA.
Virology journal 2011;8():203.
2011: Yi-Ju Li; Mollie A Minear; Jacqueline B Rimmler; Bei Zhao; Elmer Balajonda; Michael A Hauser; R Rand Allingham; Allen O Eghrari; Sheikh Amer Riazuddin; Nicholas Katsanis; John D Gottsch; Simon G Gregory; Gordon K Klintworth; Natalie A Afshari
Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy.
PloS one 2011;6(4):e18044.
2011: Usman A Ashfaq; Tariq Javed; Sidra Rehman; Zafar Nawaz; Sheikh Amer Riazuddin
Lysosomotropic agents as HCV entry inhibitors.
Virology journal 2011;8():163.
2011: Usman A Ashfaq; Tariq Javed; Sidra Rehman; Zafar Nawaz; Sheikh Amer Riazuddin
An overview of HCV molecular biology, replication and immune responses.
Virology journal 2011;8():161.
2011: Usman Ali Ashfaq; Shaheen N Khan; Zafar Nawaz; Sheikh Amer Riazuddin
In-vitro model systems to study Hepatitis C Virus.
Genetic vaccines and therapy 2011;9():7.
2011: Usman Ali Ashfaq; Tariq Javed; Sidra Rehman; Zafar Nawaz; Sheikh Amer Riazuddin
Inhibition of HCV 3a core gene through Silymarin and its fractions.
Virology journal 2011;8():153.
2011: Usman Ali Ashfaq; Muhammad Ansar; Muhammad Tahir Sarwar; Tariq Javed; Sidra Rehman; Sheikh Amer Riazuddin
Post-transcriptional inhibition of hepatitis C virus replication through small interference RNA.
Virology journal 2011;8():112.
2011: Saima Riazuddin; Zubair M Ahmed; Rashmi S Hegde; Shaheen N Khan; Idrees Nasir; Uzma Shaukat; Sheikh Amer Riazuddin; John A Butman; Andrew J Griffith; Thomas B Friedman; Byung Yoon Choi
Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome.
BMC medical genetics 2011;12():21.
2011: Tariq Javed; Usman Ali Ashfaq; Sana Riaz; Sidra Rehman; Sheikh Amer Riazuddin
In-vitro antiviral activity of Solanum nigrum against Hepatitis C Virus.
Virology journal 2011;8():26.
2011: Sadia Mohsin; Sulaiman Shams; Ghazanfar Ali Nasir; Mohsin Khan; Sana Javaid Awan; Shaheen N Khan; Sheikh Amer Riazuddin
Enhanced hepatic differentiation of mesenchymal stem cells after pretreatment with injured liver tissue.
Differentiation; research in biological diversity 2011;81(1):42-8.
2011: Mohsin Khan; Shoaib Akhtar; Sadia Mohsin; Shaheen N Khan; Sheikh Amer Riazuddin
Growth factor preconditioning increases the function of diabetes-impaired mesenchymal stem cells.
Stem cells and development 2011;20(1):67-75.
2010: Elyse J McGlumphy; William S Yeo; Sheikh Amer Riazuddin; Amr Al-Saif; Jiangxia Wang; Allen O Eghrari; Danielle N Meadows; David G Emmert; Nicholas Katsanis; John D Gottsch
Age-severity relationships in families linked to FCD2 with retroillumination photography.
Investigative ophthalmology & visual science 2010;51(12):6298-302.
2010: Sheikh Amer Riazuddin; Eranga N Vithana; Li-Fong Seet; Yangjian Liu; Amr Al-Saif; Li Wei Koh; Yee Meng Heng; Tin Aung; Danielle N Meadows; Allen O Eghrari; John D Gottsch; Nicholas Katsanis
Missense mutations in the sodium borate cotransporter SLC4A11 cause late-onset Fuchs corneal dystrophy.
Human mutation 2010;31(11):1261-8.
2010: Sheikh Amer Riazuddin; Amber Shahzadi; Christina Zeitz; Zubair M Ahmed; Radha Ayyagari; Venkata R M Chavali; Virgilio G Ponferrada; Isabelle Audo; Christelle Michiels; Marie-Elise Lancelot; Idrees A Nasir; Ahmad U Zafar; Shaheen N Khan; Tayyab Husnain; Xiaodong Jiao; Ian M MacDonald; Sheikh Riazuddin; Paul Sieving; Nicholas Katsanis; J Fielding Hejtmancik
A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness.
American journal of human genetics 2010;87(4):523-31.
2010: Muhammad Hashim Raza; Sheikh Amer Riazuddin; Dennis Drayna
Identification of an autosomal recessive stuttering locus on chromosome 3q13.2-3q13.33.
Human genetics 2010;128(4):461-3.
2010: Lin Li; Naoki Nakaya; Venkata R M Chavali; Zhiwei Ma; Xiaodong Jiao; Paul Sieving; Sheikh Riazuddin; Stanislav I Tomarev; Radha Ayyagari; Sheikh Amer Riazuddin; J Fielding Hejtmancik
A mutation in ZNF513, a putative regulator of photoreceptor development, causes autosomal-recessive retinitis pigmentosa.
American journal of human genetics 2010;87(3):400-9.
2010: Ronna Hertzano; Chandrakala Puligilla; Siaw-Lin Chan; Caroline Timothy; Didier Depireux; Zubair Ahmed; Jeffrey S Wolf; David J Eisenman; Thomas B Friedman; Sheikh Amer Riazuddin; Matthew W Kelley; Scott E Strome
CD44 is a marker for the outer pillar cells in the early postnatal mouse inner ear.
Journal of the Association for Research in Otolaryngology : JARO 2010;11(3):407-18.
2010: Haiba Kaul; Sheikh Amer Riazuddin; Zaheeruddin A Qazi; Idrees A Nasir; Ahmad U Zafar; Shaheen N Khan; Tayyab Husnain; Javed Akram; J Fielding Hejtmancik; Sheikh Riazuddin
Ectopia lentis in a consanguineous pakistani family and a novel locus on chromosome 8q.
Archives of ophthalmology 2010;128(8):1046-9.
2010: Amber Shahzadi; Sheikh Amer Riazuddin; Shahbaz Ali; David Li; Shaheen N Khan; Tayyab Husnain; Javed Akram; Paul Sieving; J Fielding Hejtmancik; Sheikh Riazuddin
Nonsense mutation in MERTK causes autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family.
The British journal of ophthalmology 2010;94(8):1094-9.
2010: Shin-ichiro Kitajiri; Takeshi Sakamoto; Inna A Belyantseva; Richard J Goodyear; Ruben Stepanyan; Ikuko Fujiwara; Jonathan E Bird; Sheikh Amer Riazuddin; Sheikh Riazuddin; Zubair M Ahmed; Jenny E Hinshaw; James Sellers; James R Bartles; John A Hammer; Guy P Richardson; Andrew J Griffith; Gregory I Frolenkov; Thomas B Friedman
Actin-bundling protein TRIOBP forms resilient rootlets of hair cell stereocilia essential for hearing.
Cell 2010;141(5):786-98.
2010: Sheikh Amer Riazuddin; Muhammad Iqbal; Yue Wang; Tomohiro Masuda; Yuhng Chen; Sara Bowne; Lori S Sullivan; Naushin H Waseem; Shomi Bhattacharya; Stephen P Daiger; Kang Zhang; Shaheen N Khan; Sheikh Riazuddin; J Fielding Hejtmancik; Paul Sieving; Donald J Zack; Nicholas Katsanis
A splice-site mutation in a retina-specific exon of BBS8 causes nonsyndromic retinitis pigmentosa.
American journal of human genetics 2010;86(5):805-12.
2010: Shagufta Naz; Sheikh Amer Riazuddin; Lin Li; Mariam Shahid; Samra Kousar; Paul Sieving; J Fielding Hejtmancik; Sheikh Riazuddin
A novel locus for autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family maps to chromosome 2p.
American journal of ophthalmology 2010;149(5):861-6.
2010: Atteeq Ur Rehman; Robert J Morell; Inna A Belyantseva; Shahid Y Khan; Erich T Boger; Mohsin Shahzad; Zubair M Ahmed; Saima Riazuddin; Shaheen N Khan; Sheikh Amer Riazuddin; Thomas B Friedman
Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79.
American journal of human genetics 2010;86(3):378-88.
2010: Changsoo Kang; Sheikh Amer Riazuddin; Jennifer Mundorff; Donna Krasnewich; Penelope Friedman; James C Mullikin; Dennis Drayna
Mutations in the lysosomal enzyme-targeting pathway and persistent stuttering.
The New England journal of medicine 2010;362(8):677-85.
2010: Namerah Sabir; Sheikh Amer Riazuddin; Haiba Kaul; Farheena Iqbal; Idrees A Nasir; Ahmad U Zafar; Zaheeruddin A Qazi; Nadeem H Butt; Shaheen N Khan; Tayyab Husnain; J Fielding Hejtmancik; Sheikh Riazuddin
Mapping of a novel locus associated with autosomal recessive congenital cataract to chromosome 8p.
Molecular vision 2010;16():2911-5.
2010: Namerah Sabir; Sheikh Amer Riazuddin; Tariq Butt; Farheena Iqbal; Idrees A Nasir; Ahmad U Zafar; Zaheeruddin A Qazi; Nadeem H Butt; Shaheen N Khan; Tayyab Husnain; J Fielding Hejtmancik; Sheikh Riazuddin
Mapping of a new locus associated with autosomal recessive congenital cataract to chromosome 3q.
Molecular vision 2010;16():2634-8.
2010: Afshan Yasmeen; Sheikh Amer Riazuddin; Haiba Kaul; Sadia Mohsin; Mohsin Khan; Zaheeruddin A Qazi; Idrees A Nasir; Ahmad U Zafar; Shaheen N Khan; Tayyab Husnain; Javed Akram; J Fielding Hejtmancik; Sheikh Riazuddin
Autosomal recessive congenital cataract in consanguineous Pakistani families is associated with mutations in GALK1.
Molecular vision 2010;16():682-8.
2010: Haiba Kaul; Sheikh Amer Riazuddin; Mariam Shahid; Samra Kousar; Nadeem H Butt; Ahmad U Zafar; Shaheen N Khan; Tayyab Husnain; Javed Akram; J Fielding Hejtmancik; Sheikh Riazuddin
Autosomal recessive congenital cataract linked to EPHA2 in a consanguineous Pakistani family.
Molecular vision 2010;16():511-7.
2010: Haiba Kaul; Sheikh Amer Riazuddin; Afshan Yasmeen; Sadia Mohsin; Mohsin Khan; Idrees A Nasir; Shaheen N Khan; Tayyab Husnain; Javed Akram; J Fielding Hejtmancik; Sheikh Riazuddin
A new locus for autosomal recessive congenital cataract identified in a Pakistani family.
Molecular vision 2010;16():240-5.
2010: Sheikh Amer Riazuddin; Norann Zaghloul; Amr Al-Saif; Lisa Davey; Bill H Diplas; Danielle N Meadows; Allen O Eghrari; Mollie A Minear; Yi-Ju Li; Gordon K Klintworth; Natalie Afshari; Simon G Gregory; John D Gottsch; Nicholas Katsanis
Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p.
American journal of human genetics 2010;86(1):45-53.
2010: Asma Maqbool; Waseem Abbas; Abdul Qayyum Rao; Muhammad Irfan; Muzna Zahur; Allah Bakhsh; Sheikh Amer Riazuddin; Tayyab Husnain
Gossypium arboreum GHSP26 enhances drought tolerance in Gossypium hirsutum.
Biotechnology progress 2010;26(1):21-5.
2010: sabahat Khaliq; Sadaf A Khaliq; Muzna Zahur; Bushra Ijaz; shah Jahan; Muhammad Ansar; Sheikh Amer Riazuddin; Sajida Hassan
RNAi as a new therapeutic strategy against HCV.
Biotechnology advances 2010;28(1):27-34.
2010: Shahid Yar Khan; Sheikh Amer Riazuddin; Mohsin Shahzad; Nazir Ahmed; Ahmad Usman Zafar; Atteeq Ur Rehman; Robert J Morell; Andrew J Griffith; Zubair M Ahmed; Sheikh Riazuddin; Thomas B Friedman
DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3.
European journal of human genetics : EJHG 2010;18(1):125-9.
2009: Danielle N Meadows; Allen O Eghrari; Sheikh Amer Riazuddin; David G Emmert; Nicholas Katsanis; John D Gottsch
Progression of Fuchs corneal dystrophy in a family linked to the FCD1 locus.
Investigative ophthalmology & visual science 2009;50(12):5662-6.
2009: Sheikh Amer Riazuddin; Allen O Eghrari; Amr Al-Saif; Lisa Davey; Danielle N Meadows; Nicholas Katsanis; John D Gottsch
Linkage of a mild late-onset phenotype of Fuchs corneal dystrophy to a novel locus at 5q33.1-q35.2.
Investigative ophthalmology & visual science 2009;50(12):5667-71.
2009: Mohsin Abbas Zaidi; Gongyin Ye; Hongwei Yao; Taek H You; Evelin Loit; Donald H Dean; Sheikh Amer Riazuddin; Illimar Altosaar
Transgenic rice plants expressing a modified cry1Ca1 gene are resistant to Spodoptera litura and Chilo suppressalis.
Molecular biotechnology 2009;43(3):232-42.
2009: Abdul Qayyum Rao; Allah Bakhsh; Sarfraz Kiani; Kamran Shahzad; Ahmad Ali Shahid; Tayyab Husnain; Sheikh Amer Riazuddin
The myth of plant transformation.
Biotechnology advances 2009;27(6):753-63.
2009: Muhammad Idrees; Shazia Rafique; Irshadur Rehman; Haji Akbar; Muhammad-Zubair Yousaf; Sadia Butt; Zunaira Awan; Sobia Manzoor; Madiha Akram; Mahwish Aftab; Bushra Khubaib; Sheikh Amer Riazuddin
Hepatitis C virus genotype 3a infection and hepatocellular carcinoma: Pakistan experience.
World journal of gastroenterology : WJG 2009;15(40):5080-5.
2009: A M Waryah; A Rehman; Zubair M Ahmed; Z-H Bashir; Shahid Y Khan; A U Zafar; Sheikh Amer Riazuddin; Thomas B Friedman; S Riazuddin
DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15.
Clinical genetics 2009;76(3):270-5.
2009: Muzna Zahur; Asma Maqbool; Muhammad Irfan; Muhammad Younas Khan Barozai; Uzma Qaiser; Bushra Rashid; Tayyab Husnain; Sheikh Amer Riazuddin
Functional analysis of cotton small heat shock protein promoter region in response to abiotic stresses in tobacco using Agrobacterium-mediated transient assay.
Molecular biology reports 2009;36(7):1915-21.
2009: Sheikh Amer Riazuddin; Saima Anwar; Martin Fischer; Zubair M Ahmed; Shahid Y Khan; Audrey G H Janssen; Ahmad U Zafar; Ute Scholl; Tayyab Husnain; Inna A Belyantseva; Penelope L Friedman; Sheikh Riazuddin; Thomas B Friedman; Christoph Fahlke
Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome.
American journal of human genetics 2009;85(2):273-80.
2009: Muzna Zahur; Asma Maqbool; Muhamad Ifran; Muhammad Younas Khan Barozai; Bushra Rashid; Sheikh Amer Riazuddin; Tayyab Husnain
[Isolation and functional analysis of cotton universal stress protein promoter in response to phytohormones and abiotic stresses].
Molekuliarnaia biologiia 2009;43(4):628-35.
2009: Julie M Schultz; Shaheen N Khan; Zubair M Ahmed; Saima Riazuddin; Ali M Waryah; Dhananjay Chhatre; Matthew F Starost; Barbara Ploplis; Stephanie Buckley; David Velásquez; Madhulika Kabra; Kwanghyuk Lee; Muhammad J Hassan; Ghazanfar Ali; Muhammad Ansar; Manju Ghosh; Edward R Wilcox; Wasim Ahmad; Glenn Merlino; Suzanne M Leal; Sheikh Amer Riazuddin; Thomas B Friedman; Robert J Morell
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
American journal of human genetics 2009;85(1):25-39.
2009: Manir Ali; Martin McKibbin; Adam Booth; David A Parry; Payal Jain; Sheikh Amer Riazuddin; J Fielding Hejtmancik; Shaheen N Khan; Sabika Firasat; Mike Shires; David F Gilmour; Katherine Towns; Anna-Louise Murphy; Dimitar Azmanov; Ivailo Tournev; Sylvia Cherninkova; Hussain Jafri; Yasmin Raashid; Carmel Toomes; Jamie Craig; David A Mackey; Luba Kalaydjieva; Sheikh Riazuddin; Chris F Inglehearn
Null mutations in LTBP2 cause primary congenital glaucoma.
American journal of human genetics 2009;84(5):664-71.
2009: Saima Anwar; Saima Riazuddin; Zubair M Ahmed; Saba Tasneem; Shahid Y Khan; Andrew J Griffith; Thomas B Friedman; Sheikh Amer Riazuddin
SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis.
Journal of human genetics 2009;54(5):266-70.
2009: Mounira Hmani-Aifa; Zeineb Benzina; Fareeha Zulfiqar; Houria Dhouib; Amber Shahzadi; Ali Ghorbel; Ahmed Rebaï; Peter Söderkvist; Sheikh Amer Riazuddin; William J Kimberling; Hammadi Ayadi
Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family.
European journal of human genetics : EJHG 2009;17(4):474-82.
2009: B Y Choi; Z M Ahmed; Sheikh Amer Riazuddin; M A Bhinder; M Shahzad; Tayyab Husnain; S Riazuddin; A J Griffith; T B Friedman
Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan.
Clinical genetics 2009;75(3):237-43.
2009: Muhammad Idrees; Sadia Butt; Zunaira Awan; Mahwish Aftab; Bushra Khubaib; Irshad-Ur Rehman; Madiha Akram; Sobia Manzoor; Haji Akbar; Shazia Rafiqe; Sheikh Amer Riazuddin
Nucleotide identity and variability among different Pakistani hepatitis C virus isolates.
Virology journal 2009;6():130.
2009: Sheikh Amer Riazuddin; Laleh Amiri-Kordestani; Haiba Kaul; Tariq Butt; Xiaodong Jiao; Sheikh Riazuddin; J Fielding Hejtmancik
Novel SIL1 mutations in consanguineous Pakistani families mapping to chromosomes 5q31.
Molecular vision 2009;15():1050-6.
2009: Muhammad Idrees; Sheikh Amer Riazuddin
A study of best positive predictors for sustained virologic response to interferon alpha plus ribavirin therapy in naive chronic hepatitis C patients.
BMC gastroenterology 2009;9():5.
2009: Muhammad Akram Tariq; Muhammad Farooq Sabir; Sheikh Amer Riazuddin; Sheikh Riazuddin
Haplotype analysis of two X-chromosome STR clusters in the Pakistani population.
International journal of legal medicine 2009;123(1):85-7.
2009: Zubair M Ahmed; Sheikh Amer Riazuddin; Shaheen N Khan; P L Friedman; S Riazuddin; Thomas B Friedman
USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23.
Clinical genetics 2009;75(1):86-91.
2008: Zubair M Ahmed; Saber Masmoudi; Ersan Kalay; Inna A Belyantseva; Mohamed Ali Mosrati; Rob W J Collin; Saima Riazuddin; Mounira Hmani-Aifa; Hanka Venselaar; Mayya N Kawar; Abdelaziz Tlili; Bert van der Zwaag; Shahid Y Khan; Leila Ayadi; Sheikh Amer Riazuddin; Robert J Morell; Andrew J Griffith; Ilhem Charfedine; Refik Caylan; Jaap Oostrik; Ahmet Karaguzel; Abdelmonem Ghorbel; Sheikh Riazuddin; Thomas B Friedman; Hammadi Ayadi; Hannie Kremer
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.
Nature genetics 2008;40(11):1335-40.
2008: Muhammad Akram Tariq; Obaid Ullah; Sheikh Amer Riazuddin; Sheikh Riazuddin
Allele frequency distribution of 13 X-chromosomal STR loci in Pakistani population.
International journal of legal medicine 2008;122(6):525-8.
2008: Ahmad Ali Shahid; Tayyab Husnain; Sheikh Amer Riazuddin
Ascochyta blight of chickpea: production of phytotoxins and disease management.
Biotechnology advances 2008;26(6):511-5.
2008: Zubair M Ahmed; Saima Riazuddin; Sandar Aye; Rana A Ali; Hanka Venselaar; Saima Anwar; Polina P Belyantseva; Muhammad Qasim; Sheikh Amer Riazuddin; Thomas B Friedman
Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome.
Human genetics 2008;124(3):215-23.
2008: Muhammad Younas Khan Barozai; Muhammad Irfan; Rizwan Yousaf; Imran Ali; Uzma Qaisar; Asma Maqbool; Muzna Zahoor; Bushra Rashid; Tayyab Hussnain; Sheikh Amer Riazuddin
Identification of micro-RNAs in cotton.
Plant physiology and biochemistry : PPB / Société française de physiologie végétale 2008;46(8-9):739-51.
2008: A Maqbool; M Zahur; M Irfan; M Younas; K Barozai; B Rashid; T Husnain; Sheikh Amer Riazuddin
[Identification and expression of six drought responsive transcripts through differential display in desi cottion (Gossypium aroreum)].
Molekuliarnaia biologiia 2008;42(4):559-65.
2008: Idrees Ahmad Nasir; Sheikh Amer Riazuddin
In vitro selection for Fusarium wilt resistance in Gladiolus.
Journal of integrative plant biology 2008;50(5):601-12.
2008: Imran Ali; Tayyab Husnain; Sheikh Amer Riazuddin
RNA interference: the story of gene silencing in plants and humans.
Biotechnology advances 2008;26(3):202-9.
2008: Sheikh Amer Riazuddin; Sabiha Nazli; Zubair M Ahmed; Yi Yang; Fareeha Zulfiqar; Rehan S Shaikh; Ahmed U Zafar; Shaheen N Khan; Farooq Sabar; Fouzia T Javid; Edward R Wilcox; Ekaterini Tsilou; Erich T Boger; James R Sellers; Inna A Belyantseva; Sheikh Riazuddin; Thomas B Friedman
Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.
Human mutation 2008;29(4):502-11.
2008: Sabika Firasat; Sheikh Amer Riazuddin; Shaheen N Khan; Sheikh Riazuddin
Novel CYP1B1 mutations in consanguineous Pakistani families with primary congenital glaucoma.
Molecular vision 2008;14():2002-9.
2008: Sabika Firasat; Sheikh Amer Riazuddin; J Fielding Hejtmancik; Sheikh Riazuddin
Primary congenital glaucoma localizes to chromosome 14q24.2-24.3 in two consanguineous Pakistani families.
Molecular vision 2008;14():1659-65.
2008: Muhammad T Idrees; Sheikh Amer Riazuddin
Frequency distribution of hepatitis C virus genotypes in different geographical regions of Pakistan and their possible routes of transmission.
BMC infectious diseases 2008;8():69.
2008: Rob W J Collin; Ersan Kalay; Muhammad Tariq; Theo Peters; Bert van der Zwaag; Hanka Venselaar; Jaap Oostrik; Kwanghyuk Lee; Zubair M Ahmed; Refik Caylan; Yun Li; Henk A Spierenburg; Erol Eyupoglu; Angelien Heister; Saima Riazuddin; Elif Bahat; Muhammad Ansar; Selcuk Arslan; Bernd Wollnik; Han G Brunner; Cor W R J Cremers; Ahmet Karaguzel; Wasim Ahmad; Frans P M Cremers; Gert Vriend; Thomas B Friedman; Sheikh Amer Riazuddin; Suzanne M Leal; Hannie Kremer
Mutations of ESRRB encoding estrogen-related receptor beta cause autosomal-recessive nonsyndromic hearing impairment DFNB35.
American journal of human genetics 2008;82(1):125-38.
2007: Shin-ichiro Kitajiri; R McNamara; Tomoko Makishima; Tayyab Husnain; A U Zafar; Rick Kittles; Zubair M Ahmed; Thomas B Friedman; Sheikh Amer Riazuddin; Andrew J Griffith
Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in Pakistan.
Clinical genetics 2007;72(6):546-50.
2007: Quratul Ain; Sabiha Nazli; Saima Riazuddin; Ateeq-ul Jaleel; Sheikh Amer Riazuddin; Ahmad U Zafar; Shaheen N Khan; Tayyab Husnain; Andrew J Griffith; Zubair M Ahmed; Thomas B Friedman; Sheikh Riazuddin
The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3.
Human genetics 2007;122(5):445-50.
2007: Qingjiong Zhang; Fareeha Zulfiqar; Xueshan Xiao; Sheikh Amer Riazuddin; Zahoor Ahmad; Raphael Caruso; Ian MacDonald; Paul Sieving; Sheikh Riazuddin; J Fielding Hejtmancik
Severe retinitis pigmentosa mapped to 4p15 and associated with a novel mutation in the PROM1 gene.
Human genetics 2007;122(3-4):293-9.
2007: Nevra Nal; Zubair M Ahmed; Engin Erkal; Özgül M Alper; Güven Lüleci; Oktay Dinç; Ali Muhammad Waryah; Quratul Ain; Saba Tasneem; Tayyab Husnain; Parna Chattaraj; Sheikh Amer Riazuddin; Erich T Boger; Manju Ghosh; Madhulika Kabra; Sheikh Riazuddin; Robert J Morell; Thomas B Friedman
Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearing.
Human mutation 2007;28(10):1014-9.
2007: Shahid Y Khan; Zubair M Ahmed; Muhammad I Shabbir; Shin-ichiro Kitajiri; Saeeda Kalsoom; Saba Tasneem; Sara Shayiq; Arabandi Ramesh; Srikumari Srisailpathy; Shaheen N Khan; Richard J H Smith; Sheikh Amer Riazuddin; Thomas B Friedman; Sheikh Riazuddin
Mutations of the RDX gene cause nonsyndromic hearing loss at the DFNB24 locus.
Human mutation 2007;28(5):417-23.
2007: Sadia Sharif; Takayuki Nakagawa; Tsunehisa Ohno; Masahiro Matsumoto; Tomoko Kita; Sheikh Amer Riazuddin; Juichi Ito
The potential use of bone marrow stromal cells for cochlear cell therapy.
Neuroreport 2007;18(4):351-4.
2007: Shahid Y Khan; Saima Riazuddin; Muhammad Tariq; Saima Anwar; Muhammad I Shabbir; Sheikh Amer Riazuddin; Shaheen N Khan; Tayyab Husnain; Zubair M Ahmed; Thomas B Friedman; Sheikh Riazuddin
Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2-q13.3.
Human genetics 2007;120(6):789-93.
2007: Tariq Butt; Wenliang Yao; Haiba Kaul; Jiao Xiaodong; Libe Gradstein; Yan Zhang; Tayyab Husnain; Sheikh Riazuddin; J Fielding Hejtmancik; Sheikh Amer Riazuddin
Localization of autosomal recessive congenital cataracts in consanguineous Pakistani families to a new locus on chromosome 1p.
Molecular vision 2007;13():1635-40.
2006: Sheikh Amer Riazuddin; Zubair M Ahmed; Alan S Fanning; Ayala Lagziel; Shin-ichiro Kitajiri; Khushnooda Ramzan; Shaheen N Khan; Parna Chattaraj; Penelope L Friedman; James M Anderson; Inna A Belyantseva; Andrew Forge; Sheikh Riazuddin; Thomas B Friedman
Tricellulin is a tight-junction protein necessary for hearing.
American journal of human genetics 2006;79(6):1040-51.
2006: Muhammad I Shabbir; Zubair M Ahmed; Shahid Y Khan; Sheikh Amer Riazuddin; A M Waryah; Shaheen N Khan; R D Camps; M Ghosh; M Kabra; Inna A Belyantseva; Thomas B Friedman; Sheikh Riazuddin
Mutations of human TMHS cause recessively inherited non-syndromic hearing loss.
Journal of medical genetics 2006;43(8):634-40.
2006: Zubair M Ahmed; Richard J Goodyear; Sheikh Amer Riazuddin; Ayala Lagziel; P Kevin Legan; Martine Behra; Shawn M Burgess; Kathryn S Lilley; Edward R Wilcox; Sheikh Riazuddin; Andrew J Griffith; Gregory I Frolenkov; Inna A Belyantseva; Guy P Richardson; Thomas B Friedman
The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2006;26(26):7022-34.
2006: Abdul Qayyum Rao; S Sarfraz Hussain; M Saqib Shahzad; S Yassir Abbas Bokhari; M Hashim Raza; Allah Rakha; A Majeed; A Ali Shahid; Zafar Saleem; Tayyab Husnain; Sheikh Amer Riazuddin
Somatic embryogenesis in wild relatives of cotton (Gossypium Spp.).
Journal of Zhejiang University. Science. B 2006;7(4):291-8.
2006: Sheikh Amer Riazuddin; Fareeha Zulfiqar; Qingjiong Zhang; Wenliang Yao; Shouling Li; Xiaodong Jiao; Amber Shahzadi; MUHAMMAD AMER; Muhammad Iqbal; Tayyab Hussnain; Paul Sieving; Sheikh Riazuddin; J Fielding Hejtmancik
Mutations in the gene encoding the alpha-subunit of rod phosphodiesterase in consanguineous Pakistani families.
Molecular vision 2006;12():1283-91.
2006: Sheikh Amer Riazuddin; Shaheen N Khan; Zubair M Ahmed; Manju Ghosh; Kyle Caution; Sabiha Nazli; Madhulika Kabra; Ahmad U Zafar; Kevin Chen; Sadaf Naz; Anthony Antonellis; William J Pavan; Eric Green; Edward R Wilcox; Penelope L Friedman; Robert J Morell; Sheikh Riazuddin; Thomas B Friedman
Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness.
American journal of human genetics 2006;78(1):137-43.
2005: Qingjiong Zhang; Fareeha Zulfiqar; Xueshan Xiao; Sheikh Amer Riazuddin; Radha Ayyagari; Farooq Sabar; Raphael Caruso; Paul Sieving; Sheikh Riazuddin; J Fielding Hejtmancik
Severe autosomal recessive retinitis pigmentosa maps to chromosome 1p13.3-p21.2 between D1S2896 and D1S457 but outside ABCA4.
Human genetics 2005;118(3-4):356-65.
2005: Rehan Sadiq Shaikh; Khushnooda Ramzan; Sabiha Nazli; Sameera Sattar; Shaheen N Khan; Sheikh Amer Riazuddin; Zubair M Ahmed; Thomas B Friedman; Sheikh Riazuddin
A new locus for nonsyndromic deafness DFNB51 maps to chromosome 11p13-p12.
American journal of medical genetics. Part A 2005;138(4):392-5.
2005: Sheikh Amer Riazuddin; Fareeha Zulfiqar; Qingjiong Zhang; Yuri V Sergeev; Zaheeruddin A Qazi; Tayyab Husnain; Raphael Caruso; Sheikh Riazuddin; Paul Sieving; J Fielding Hejtmancik
Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani families.
Investigative ophthalmology & visual science 2005;46(7):2264-70.
2005: Sheikh Amer Riazuddin; Afshan Yasmeen; Wenliang Yao; Yuri V Sergeev; Qingjiong Zhang; Fareeha Zulfiqar; Assad Riaz; Sheikh Riazuddin; J Fielding Hejtmancik
Mutations in betaB3-crystallin associated with autosomal recessive cataract in two Pakistani families.
Investigative ophthalmology & visual science 2005;46(6):2100-6.
2005: Naveeda Riaz; Stacy Steinberg; Jamil Ahmad; Anna Pluzhnikov; Sheikh Amer Riazuddin; Nancy J Cox; Dennis Drayna
Genomewide significant linkage to stuttering on chromosome 12.
American journal of human genetics 2005;76(4):647-51.
2005: Jamil Ahmad; Shaheen N Khan; Shahid Y Khan; Khushnooda Ramzan; Sheikh Amer Riazuddin; Zubair M Ahmed; Edward R Wilcox; Thomas B Friedman; Sheikh Riazuddin
DFNB48, a new nonsyndromic recessive deafness locus, maps to chromosome 15q23-q25.1.
Human genetics 2005;116(5):407-12.
2005: Sheikh Amer Riazuddin; Afshan Yasmeen; Qingjiong Zhang; Wenliang Yao; Muhammad Farooq Sabar; Zahoor Ahmed; Sheikh Riazuddin; J Fielding Hejtmancik
A new locus for autosomal recessive nuclear cataract mapped to chromosome 19q13 in a Pakistani family.
Investigative ophthalmology & visual science 2005;46(2):623-6.
2005: Qingjiong Zhang; Fareeha Zulfiqar; Sheikh Amer Riazuddin; Xueshan Xiao; Afshan Yasmeen; Peter K Rogan; Raphael Caruso; Paul Sieving; Sheikh Riazuddin; J Fielding Hejtmancik
A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 gene.
Molecular vision 2005;11():977-85.
2005: Khushnooda Ramzan; Rehan S Shaikh; Jamil Ahmad; Shaheen N Khan; Sheikh Amer Riazuddin; Zubair M Ahmed; Thomas B Friedman; Edward R Wilcox; Sheikh Riazuddin
A new locus for nonsyndromic deafness DFNB49 maps to chromosome 5q12.3-q14.1.
Human genetics 2005;116(1-2):17-22.
2004: Qingjiong Zhang; Fareeha Zulfiqar; Sheikh Amer Riazuddin; Xueshan Xiao; Zahoor Ahmad; Sheikh Riazuddin; J Fielding Hejtmancik
Autosomal recessive retinitis pigmentosa in a Pakistani family mapped to CNGA1 with identification of a novel mutation.
Molecular vision 2004;10():884-9.
2004: M Saqib Shahzad; S Yassir Abbas Bokhari; Abdul Qayyum Rao; M Hashim Raza; Obaid Ullah; A Ali Shahid; Zahoor Ahmad; Sheikh Amer Riazuddin
Population studies for STR loci (D3S1358, D5S818, D7S820, D18S51 and FGA) in NWFP and Sindhi populations of Pakistan for forensic use.
Archiwum medycyny sa̧dowej i kryminologii 2004;54(4):215-22.
2004: Zubair M Ahmed; Xiaoyan Cindy Li; Shontell D Powell; Sheikh Amer Riazuddin; Terry-Lynn Young; Khushnooda Ramzan; Zahoor Ahmad; Sandra Luscombe; Kiran Dhillon; Linda MacLaren; Barbara Ploplis; Lawrence I Shotland; Elizabeth Ives; Sheikh Riazuddin; Thomas B Friedman; Robert J Morell; Edward R Wilcox
Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan.
BMC medical genetics 2004;5():24.
2004: Sadaf Naz; Andrew J Griffith; S Riazuddin; Lori L Hampton; James F Battey; Shaheen N Khan; Sheikh Amer Riazuddin; Edward R Wilcox; Thomas B Friedman
Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction.
Journal of medical genetics 2004;41(8):591-5.
2004: Muhammad Idrees; Sanaullah Khan; Sheikh Amer Riazuddin
Common genotypes of hepatitis B virus.
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP 2004;14(6):344-7.
2003: Zubair M Ahmed; Sheikh Amer Riazuddin; Jamil Ahmad; Steven L Bernstein; Yan Guo; Muhammad F Sabar; Paul Sieving; Sheikh Riazuddin; Andrew J Griffith; Thomas B Friedman; Inna A Belyantseva; Edward R Wilcox
PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23.
Human molecular genetics 2003;12(24):3215-23.
2003: Thomas B Friedman; Julie M Schultz; Tamar Ben-Yosef; Shannon P Pryor; Ayala Lagziel; Rachel A Fisher; Edward R Wilcox; Sheikh Amer Riazuddin; Zubair M Ahmed; Inna A Belyantseva; Andrew J Griffith
Recent advances in the understanding of syndromic forms of hearing loss.
Ear and hearing 2003;24(4):289-302.
2003: Shaheen N Khan; Farrukh Hasan; Carla Sollaino; Luciana Perseu; Sheikh Amer Riazuddin
Molecular characterization of alpha-thalassemia in Pakistan.
Hemoglobin 2003;27(3):161-6.
2003: Zubair M Ahmed; Sheikh Amer Riazuddin; S Riazuddin; Edward R Wilcox
The molecular genetics of Usher syndrome.
Clinical genetics 2003;63(6):431-44.
2003: Sadaf Naz; F Alasti; Alireza Mowjoodi; Sheikh Amer Riazuddin; Mohammad Hossein Sanati; Thomas B Friedman; Andrew J Griffith; Edward R Wilcox; S Riazuddin
Distinctive audiometric profile associated with DFNB21 alleles of TECTA.
Journal of medical genetics 2003;40(5):360-3.
2003: Zubair M Ahmed; Robert J Morell; Sheikh Amer Riazuddin; Andrea Gropman; Shahzad Shaukat; Mussaber M Ahmad; Saidi Mohiddin; Lameh Fananapazir; Rafael C Caruso; Tayyab Husnain; Shaheen N Khan; Sheikh Riazuddin; Andrew J Griffith; Thomas B Friedman; Edward R Wilcox
Mutations of MYO6 are associated with recessive deafness, DFNB37.
American journal of human genetics 2003;72(5):1315-22.
2003: H-J Park; S Shaukat; Xue Zhong Liu; S H Hahn; Sadaf Naz; M Ghosh; H-N Kim; S-K Moon; S Abe; K Tukamoto; S Riazuddin; M Kabra; Raadnabazar Erdenetungalag; J Radnaabazar; S Khan; Arti Pandya; S-I Usami; Walter E Nance; Edward R Wilcox; Sheikh Amer Riazuddin; Andrew J Griffith
Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness.
Journal of medical genetics 2003;40(4):242-8.
2002: Sadaf Naz; Chantal M Giguere; David C Kohrman; Kristina L Mitchem; Sheikh Amer Riazuddin; Robert J Morell; Arabandi Ramesh; Srikumari Srisailpathy; Dilip Deshmukh; Sheikh Riazuddin; Andrew J Griffith; Thomas B Friedman; Richard J H Smith; Edward R Wilcox
Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus.
American journal of human genetics 2002;71(3):632-6.
2002: G Rasul Chaudhry; A Mateen; B Kaskar; M Bloda; Sheikh Amer Riazuddin
Purification and biochemical characterization of the carbamate hydrolase from Pseudomonas sp. 50432.
Biotechnology and applied biochemistry 2002;36(Pt 1):63-70.
2002: Lisa M Astuto; Julie M Bork; Michael D Weston; James W Askew; R R Fields; Dana J Orten; S J Ohliger; Sheikh Amer Riazuddin; Robert J Morell; Shaheen Khan; S Riazuddin; Hannie Kremer; Peter Van Hauwe; CG Moller; Cor W R J Cremers; C Ayuso; John R Heckenlively; Klaus Rohrschneider; Ulrich H M Spandau; J Greenberg; Rajkumar Ramesar; William Reardon; P Bitoun; J Millan; R Legge; Thomas B Friedman; William J Kimberling
CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness.
American journal of human genetics 2002;71(2):262-75.
2002: Zubair M Ahmed; Tenesha N Smith; Sheikh Amer Riazuddin; Tomoko Makishima; Manju Ghosh; Sirosh Bokhari; P S N Menon; Dilip Deshmukh; Andrew J Griffith; Sheikh Riazuddin; Thomas B Friedman; Edward R Wilcox
Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC.
Human genetics 2002;110(6):527-31.
2002: Kiyoto Kurima; Linda M Peters; Yandan Yang; Sheikh Amer Riazuddin; Zubair M Ahmed; Sadaf Naz; Deidre Arnaud; Stacy Drury; Jianhong Mo; Tomoko Makishima; Manju Ghosh; P S N Menon; Dilip Deshmukh; Carole Oddoux; Harry Ostrer; Shaheen Khan; Sheikh Riazuddin; Prescott L Deininger; Lori L Hampton; Susan L Sullivan; James F Battey; Bronya J B Keats; Edward R Wilcox; Thomas B Friedman; Andrew J Griffith
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
Nature genetics 2002;30(3):277-84.
2002: Sheikh Amer Riazuddin; Zubair M Ahmed; Thomas B Friedman; Andrew J Griffith; Sheikh Riazuddin; Edward R Wilcox
Genetic modifiers of hereditary hearing loss.
Advances in oto-rhino-laryngology 2002;61():224-9.
2002: Zubair M Ahmed; Sheikh Amer Riazuddin; Thomas B Friedman; Sheikh Riazuddin; Edward R Wilcox; Andrew J Griffith
Clinical manifestations of DFNB29 deafness.
Advances in oto-rhino-laryngology 2002;61():156-60.
2002: Julie M Bork; Robert J Morell; Shaheen Khan; Sheikh Amer Riazuddin; Edward R Wilcox; Thomas B Friedman; Andrew J Griffith
Clinical presentation of DFNB12 and Usher syndrome type 1D.
Advances in oto-rhino-laryngology 2002;61():145-52.
2002: Thomas B Friedman; John T Hinnant; Manju Ghosh; Erich T Boger; Sheikh Amer Riazuddin; James R Lupski; Lorraine Potocki; Edward R Wilcox
DFNB3, spectrum of MYO15A recessive mutant alleles and an emerging genotype-phenotype correlation.
Advances in oto-rhino-laryngology 2002;61():124-30.
2001: John M Old; S N Khan; I Verma; Suthat Fucharoen; Marina Kleanthous; P Ioannou; N Kotea; Chris Fisher; Sheikh Amer Riazuddin; Renu Saxena; Pranee Winichagoon; Kyriacos Kyriacou; F Al-Quobaili; Baldip Khan
A multi-center study in order to further define the molecular basis of beta-thalassemia in Thailand, Pakistan, Sri Lanka, Mauritius, Syria, and India, and to develop a simple molecular diagnostic strategy by amplification refractory mutation system-polymerase chain reaction.
Hemoglobin 2001;25(4):397-407.
2001: NA Liburd; Manju Ghosh; S Riazuddin; Sadaf Naz; S Khan; Zubair M Ahmed; Sheikh Amer Riazuddin; Y Liang; P S N Menon; T Smith; A C Smith; Ken-Shiung Chen; James R Lupski; Edward R Wilcox; L Potocki; Thomas B Friedman
Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome.
Human genetics 2001;109(5):535-41.
2001: Z M Ahmed; Sheikh Amer Riazuddin; Steven L Bernstein; Zubair M Ahmed; Shaheen Khan; Andrew J Griffith; Robert J Morell; Thomas B Friedman; S Riazuddin; Edward R Wilcox
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.
American journal of human genetics 2001;69(1):25-34.
2001: Tamar Ben-Yosef; Marie Wattenhofer; S Riazuddin; Z M Ahmed; Hamish Scott; Jun Kudoh; Kazunori Shibuya; Stylianos E Antonarakis; Batsheva Bonne-Tamir; Uppala Radhakrishna; Sadaf Naz; Zubair M Ahmed; Sheikh Amer Riazuddin; Arti Pandya; Walter E Nance; Edward R Wilcox; Thomas B Friedman; Robert J Morell
Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness.
Journal of medical genetics 2001;38(6):396-400.
2001: E Wilcox; Sheikh Amer Riazuddin; S Riazuddin
Some deafness-causing mutations can be silenced with the appropriate gene partner.
TheScientificWorldJournal 2001;1():202-3.
2001: Edward R Wilcox; Quianna Burton; Sadaf Naz; Sheikh Amer Riazuddin; Tenesha N Smith; B Ploplis; Inna A Belyantseva; Tamar Ben-Yosef; NA Liburd; Robert J Morell; Anne E White-Olson; Doris K Wu; Andrew J Griffith; S Riazuddin; Thomas B Friedman
Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29.
Cell 2001;104(1):165-72.
2001: Julie M Bork; Linda M Peters; S Riazuddin; Steven L Bernstein; Z M Ahmed; Seth L Ness; R Polomeno; Arabandi Ramesh; M Schloss; C R Srisailpathy; S Wayne; S Bellman; D Desmukh; Zubair M Ahmed; Shaheen N Khan; V M Kaloustian; XC Li; Anil K Lalwani; Sheikh Amer Riazuddin; Maria Bitner-Glindzicz; Walter E Nance; Xue Zhong Liu; G Wistow; Richard J H Smith; Andrew J Griffith; Edward R Wilcox; Thomas B Friedman; Robert J Morell
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.
American journal of human genetics 2001;68(1):26-37.
2000: Sheikh Amer Riazuddin; Caley M Castelein; Zubair M Ahmed; Anil K Lalwani; Mary Ann Mastroianni; Sadaf Naz; Tenesha N Smith; NA Liburd; Thomas B Friedman; Andrew J Griffith; S Riazuddin; Edward R Wilcox
Dominant modifier DFNM1 suppresses recessive deafness DFNB26.
Nature genetics 2000;26(4):431-4.
2000: T Friedman; James F Battey; Anne E White-Olson; Sheikh Amer Riazuddin; Konrad Noben-Trauth; Andrew J Griffith; Edward R Wilcox
Modifier genes of hereditary hearing loss.
Current opinion in neurobiology 2000;10(4):487-93.
2000: Shaheen N Khan; F I Butt; Sheikh Amer Riazuddin; R Galanello
Hb Sallanches [alpha104(G11)Cys-->Tyr]: a rare alpha2-globin chain variant found in the homozygous state in three members of a Pakistani family.
Hemoglobin 2000;24(1):31-5.
2000: Shaheen N Khan; Sheikh Amer Riazuddin; R Galanello
Identification of three rare beta-thalassemia mutations in the Pakistani population.
Hemoglobin 2000;24(1):15-22.
1998: Shaheen N Khan; Sheikh Amer Riazuddin
Molecular characterization of beta-thalassemia in Pakistan.
Hemoglobin 1998;22(4):333-45.
1995: S N Khan; A U Zafar; Sheikh Amer Riazuddin
Molecular genetic diagnosis of beta thalassemia in Pakistan.
JPMA. The Journal of the Pakistan Medical Association 1995;45(3):66-70.
1993: R Mushtaq; S Naeem; anjum sohail; Sheikh Amer Riazuddin
BseRI a novel restriction endonuclease from a Bacillus species which recognizes the sequence 5'...GAGGAG...3'.
Nucleic acids research 1993;21(15):3585.
1989: Sheikh Amer Riazuddin; A Nasim
Future growth in biotechnology in the developing countries.
Genome / National Research Council Canada = Génome / Conseil national de recherches Canada 1989;31(2):1042-5.
1988: Sheikh Amer Riazuddin
Development of training programmes in biotechnology safety and risk assessment.
BioEssays : news and reviews in molecular, cellular and developmental biology 1988;9(4):131-2.
1987: Sheikh Amer Riazuddin; A Athar; anjum sohail
Methyl transferases induced during chemical adaptation of M. luteus.
Nucleic acids research 1987;15(22):9471-86.
1987: Sheikh Amer Riazuddin; A Athar; Z Ahmed; S M Lali; anjum sohail
DNA glycosylase enzymes induced during chemical adaptation of M. luteus.
Nucleic acids research 1987;15(16):6607-24.
1985: Sheikh Amer Riazuddin; A Athar; R Saffhill
Chemical adaptation of M. luteus induces repair functions for O-alkylated DNA pyrimidines.
Nucleic acids research 1985;13(19):7153-66.
1984: A Ather; Z Ahmed; Sheikh Amer Riazuddin
Adaptive response of Micrococcus luteus to alkylating chemicals.
Nucleic acids research 1984;12(4):2111-26.
1980: Sheikh Amer Riazuddin
Purification and properties of pyrimidine dimer specific endonucleases from Micrococcus luteus.
Methods in enzymology 1980;65(1):185-91.
1977: Sheikh Amer Riazuddin; L Grossman
Micrococcus luteus correndonucleases. III. Evidence for involvement in repair in vivo of two endonucleases specific for DNA containing pyrimidine dimers.
The Journal of biological chemistry 1977;252(18):6294-8.
1977: Sheikh Amer Riazuddin; L Grossman
Micrococcus luteus correndonucleases. I. resolution and purification of two endonucleases specific for DNA containing pyrimidine dimers.
The Journal of biological chemistry 1977;252(18):6280-6.
1977: Sheikh Amer Riazuddin; L Grossman
Micrococcus luteus correndonucleases. II. Mechanism of action of two endonucleases specific for DNA containing pyrimidine dimers.
The Journal of biological chemistry 1977;252(18):6287-93.