FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

REGISTER

now for free

Ali Khan

Research Profile

Disorders

Procedures

Physiology

Chemicals & Drugs

Genes & Molecular Sequences

Single Nucleotide Polymorphism

Concepts & Ideas

Pedigree

Anatomy

Living Beings

Asian Americans

Register to see full profile

Co-author Network

Register to see all co-authors

Publications

TOP 3
Anthony J Aldave; V Yellore; Baris Sonmez; Nirit Bourla; Andrew K Salem; M Ali Khan; Sylvia A Rayner; Ben J Glasgow
A novel variant of combined granular-lattice corneal dystrophy associated with the Met619Lys mutation in the TGFBI gene.
Anthony J Aldave; Nirit Bourla; V Yellore; Sylvia A Rayner; M Ali Khan; Andrew K Salem; Baris Sonmez
Keratoconus is not associated with mutations in COL8A1 and COL8A2.
Anthony J Aldave; V Yellore; Nirit Bourla; Rominder S Momi; M Ali Khan; Andrew K Salem; Sylvia A Rayner; Ben J Glasgow; Ira Kurtz
Autosomal recessive CHED associated with novel compound heterozygous mutations in SLC4A11.

Register to see all publications

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Register to see more

Geonetwork of Ali Khan (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

Register to see more

All Publications

2008: Anthony J Aldave; V Yellore; Baris Sonmez; Nirit Bourla; Andrew K Salem; M Ali Khan; Sylvia A Rayner; Ben J Glasgow
A novel variant of combined granular-lattice corneal dystrophy associated with the Met619Lys mutation in the TGFBI gene.
Archives of ophthalmology 2008;126(3):371-7.
2007: Anthony J Aldave; Nirit Bourla; V Yellore; Sylvia A Rayner; M Ali Khan; Andrew K Salem; Baris Sonmez
Keratoconus is not associated with mutations in COL8A1 and COL8A2.
Cornea 2007;26(8):963-5.
2007: Anthony J Aldave; V Yellore; Nirit Bourla; Rominder S Momi; M Ali Khan; Andrew K Salem; Sylvia A Rayner; Ben J Glasgow; Ira Kurtz
Autosomal recessive CHED associated with novel compound heterozygous mutations in SLC4A11.
Cornea 2007;26(7):896-900.
2007: V Yellore; Jeanette C Papp; Eric Sobel; M Ali Khan; Sylvia A Rayner; Debora B Farber; Anthony J Aldave
Replication and refinement of linkage of posterior polymorphous corneal dystrophy to the posterior polymorphous corneal dystrophy 1 locus on chromosome 20.
Genetics in medicine : official journal of the American College of Medical Genetics 2007;9(4):228-34.
2007: V Yellore; M Ali Khan; Nirit Bourla; Sylvia A Rayner; Michael C Chen; Baris Sonmez; Rominder S Momi; Kapil M Sampat; Michael B Gorin; Anthony J Aldave
Identification of mutations in UBIAD1 following exclusion of coding mutations in the chromosome 1p36 locus for Schnyder crystalline corneal dystrophy.
Molecular vision 2007;13():1777-82.

Register to see more

Copyright © 2011 Elsevier Inc. All rights reserved.