Sandy S Sung

发表

High-resolution whole genome tiling path array CGH analysis of CD34+ cells from patients with low-risk myelodysplastic syndromes reveals cryptic copy number alterations and predicts overall and leukemia-free survival.

A. Telenius, D. Horsman, W. Lam, 2008, Blood.

Mutations in TNNT3 cause multiple congenital contractures: a second locus for distal arthrogryposis type 2B.

M. Bamshad, L. Jorde, J. Carey, 2003, American journal of human genetics.

Correlation of clinical response and response duration with miR-145 induction by lenalidomide in CD34+ cells from patients with del(5q) myelodysplastic syndrome

A. Karsan, U. Platzbecker, Sandy S Sung, 2013, Haematologica.

Mutations in genes encoding fast-twitch contractile proteins cause distal arthrogryposis syndromes.

M. Bamshad, L. Jorde, J. Carey, 2003, American journal of human genetics.

Identification of Mir-145 and Mir-146a as Micrornas Involved in the Pathogenesis of 5q- Syndrome

W. Lam, M. Marra, M. Hirst, 2008 .

Copy number alterations at polymorphic loci may be acquired somatically in patients with myelodysplastic syndromes.

W. Lam, A. Brooks-Wilson, A. Karsan, 2009, Leukemia research.

T cells of patients with myelodysplastic syndrome are frequently derived from the malignant clone

W. Lam, A. Karsan, H. Bruyèrè, 2011, British journal of haematology.

Identification of miR-145 and miR-146a as mediators of the 5q– syndrome phenotype

Ryan D. Morin, W. Lam, M. Marra, 2010, Nature Medicine.

Barnacle: detecting and characterizing tandem duplications and fusions in transcriptome assemblies

Inanc Birol, Ka Ming Nip, Jenny Q. Qian, 2013, BMC Genomics.

Array comparative genomic hybridization of peripheral blood granulocytes of patients with myelodysplastic syndrome detects karyotypic abnormalities.

D. Horsman, W. Lam, A. Karsan, 2010, American journal of clinical pathology.

Directional migration in the Hindu castes: inferences from mitochondrial, autosomal and Y-chromosomal data

M. Bamshad, L. Jorde, W. Watkins, 2004, Human Genetics.

Heterogeneity of breast cancer stem cells as evidenced with Notch-dependent and Notch-independent populations

A. Karsan, M. Fuller, Sandy S Sung, 2012, Cancer medicine.

Expressivity of Holt-Oram syndrome is not predicted by TBX5 genotype.

M. Bamshad, L. Jorde, Anna-Marie E Brassington, 2003, American journal of human genetics.

Predisposition to Myelodysplastic Syndrome with Deletion 5q Is Associated with TP53 Codon 72 Genotype

F. Solé, A. Karsan, M. Calasanz, 2010 .