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Wahab A. Khan

Researcher at Icahn School of Medicine at Mount Sinai

Publications -  15
Citations -  208

Wahab A. Khan is an academic researcher from Icahn School of Medicine at Mount Sinai. The author has contributed to research in topics: Cytogenetics & Fluorescence in situ hybridization. The author has an hindex of 7, co-authored 12 publications receiving 163 citations. Previous affiliations of Wahab A. Khan include University of Western Ontario & Mount Sinai Hospital.

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Journal ArticleDOI

Cytogenomic identification and long-read single molecule real-time (SMRT) sequencing of a Bardet-Biedl Syndrome 9 (BBS9) deletion.

TL;DR: A 1-year-old male child from Guyana with obesity, postaxial polydactyly on his right foot, hypotonia, ophthalmologic abnormalities, and developmental delay together indicated a clinical diagnosis of Bardet–Biedl syndrome, and the identification of this shared haplotype in the parents suggests that this pathogenic aberration may be a BBS founder mutation in the Guyanese population.
Proceedings ArticleDOI

An image processing algorithm for accurate extraction of the centerline from human metaphase chromosomes

TL;DR: A hybrid algorithm that uses Gradient Vector Flow active contours, Discrete Curve Evolution based skeleton pruning and morphological thinning to provide a reliable centerline that is robust to shape variations of the chromosomes is proposed.
Journal ArticleDOI

Automating dicentric chromosome detection from cytogenetic biodosimetry data

TL;DR: A prototype software system with sufficient capacity and speed to estimate radiation exposures in a mass casualty event by counting dicentric chromosomes (DCs) in metaphase cells from many individuals is presented.
Proceedings ArticleDOI

An Accurate Image Processing Algorithm for Detecting FISH Probe Locations Relative to Chromosome Landmarks on DAPI Stained Metaphase Chromosome Images

TL;DR: A hybrid algorithm is proposed that utilizes Gradient Vector Flow active contours, Discrete Curve Evolution based skeleton pruning and morphological thinning to provide a robust and accurate centerline of the chromosome, which is then used for the measurement of the FISH probe signals.
Journal ArticleDOI

Localized, non-random differences in chromatin accessibility between homologous metaphase chromosomes

TL;DR: There are localized differences in compaction of homologs during mitotic metaphase and that these differences may arise during or preceding metaphase chromosome compaction, providing evidence that DA is non-random and reproducible.