author-photo

Malini Sathanoori

University of Pittsburgh

26

Papers

278

Citations

Citation Trend

Filter By

Papers (17) Sort By

Journal Conference Others

Optical genome mapping for assessment of genomic aberrations in acute myeloid leukemia: a multicenter evaluation

2021 Molecular Genetics and Metabolism
Show All
- Source
- Cite
- Save
Citations (0)
20. A resource for our clinical genomics community: The Compendium of Cancer Genome Aberrations (CCGA)

2020 Cancer Genetics and Cytogenetics
Show All
- Source
- Cite
- Save
Citations (0)
Addition of chromosomal microarray and next generation sequencing to FISH and classical cytogenetics enhances genomic profiling of myeloid malignancies

2017 Cancer Genetics and Cytogenetics
Show All
- Source
- Cite
- Save
Citations (11)
Chromosomal microarray provides enhanced targetable gene aberration detection when paired with next generation sequencing panel in profiling lung and colorectal tumors

2016 Cancer Genetics and Cytogenetics
Show All
- Source
- Cite
- Save
Citations (5)
CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders.

2015 Journal of Neurodevelopmental Disorders
Show All
- Source
- Cite
- Save
Citations (50)
Whole-Genome Single Nucleotide Polymorphism Array Analysis Is Complementary to Classical Cytogenetic Analysis in the Evaluation of Lymphoid Proliferations

2014 American Journal of Clinical Pathology
Show All
- Source
- Cite
- Save
Citations (6)
Co‐existence of 9p deletion and Silver‐Russell syndromes in a patient with maternally inherited cryptic complex chromosome rearrangement involving chromosomes 4, 9, and 11

2013 American Journal of Medical Genetics Part A
Show All
- Source
- Cite
- Save
Citations (9)
Double-hit B-cell lymphomas with BCL6 and MYC translocations are aggressive, frequently extranodal lymphomas distinct from BCL2 double-hit B-cell lymphomas.

2013 The American Journal of Surgical Pathology
Show All
- Source
- Cite
- Save
Citations (121)
Thyroid carcinoma-associated genetic mutations also occur in thyroid lymphomas.

2012 Modern Pathology
Show All
- Source
- Cite
- Save
Citations (15)
Prenatal detection of del(10)(q11.2) mosaicism in chorionic villus specimens likely caused by a common chromosomal fragile site FRA10G is associated with a normal phenotype

2012 Prenatal Diagnosis
Show All
- Source
- Cite
- Save
Citations (3)