Ninette Cohen

Northwell Health — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

19h-index1.9kcitations50works0.02yr avg
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Research Topics

Genomic variations and chromosomal abnormalities(15), Genetic Syndromes and Imprinting(6), Cardiomyopathy and Myosin Studies(5), Prenatal Screening and Diagnostics(5), Chronic Myeloid Leukemia Treatments(5)

Publications49 total

Incorporating automation in a cytogenetics laboratory: three practitioners’ perspectives on benefits and limitations
Molecular Cytogenetics·2025Open Access
Author response: Integrated transcriptomic analysis of human induced pluripotent stem cell-derived osteogenic differentiation reveals a regulatory role of KLF16
2025Open Access
Integrated transcriptomic analysis of human induced pluripotent stem cell-derived osteogenic differentiation reveals a regulatory role of KLF16
2025Open Access
Integrated transcriptomic analysis of human induced pluripotent stem cell-derived osteogenic differentiation reveals a regulatory role of KLF16
2025Open Access
Integrated transcriptomic analysis of human induced pluripotent stem cell-derived osteogenic differentiation reveals a regulatory role of KLF16
2024Open Access
P558: Improving patient care for recurrent pregnancy loss patients via a multidisciplinary relationship between OBGYN and Northwell Labs across Northwell Health
Genetics in Medicine Open·2024Open Access
Chromothripsis in lipoblastoma: second reported case with complex PLAG1 rearrangement
Molecular Cytogenetics·2023· 3 citedOpen Access
Myeloid/lymphoid neoplasm with a novel cryptic <i>RBPMS::FGFR1</i> rearrangement presenting as de novo acute leukemias
Leukemia & lymphoma/Leukemia and lymphoma·2023· 1 cited
Transient abnormal myelopoiesis with extramedullary involvement in a down syndrome preemie leading to an unresponsive course despite chemotherapy
Leukemia Research Reports·2023· 2 citedOpen Access
25. Novel translocation t(5;19)(q35;p13.3) in a patient with T-Cell large granular lymphocytic leukemia: report of a rare case
Cancer Genetics·2022
A new translocation partner for CBFB in acute myeloid leukemia, t(10;16)(p13;q22)
Molecular Genetics and Metabolism·2021
Optimal Tissue Size for Successful Cytogenetic Yield in Lymphoma Work-Up
2020
Familial inheritance of the 3q29 microdeletion syndrome: case report and review
BMC Medical Genomics·2019· 10 citedOpen Access
De Novo Interstitial Deletion of 9q in a Pediatric Patient With Global Developmental Delay
Child Neurology Open·2019Open Access
Functional and transcriptomic insights into pathogenesis of R9C phospholamban mutation using human induced pluripotent stem cell-derived cardiomyocytes
Journal of Molecular and Cellular Cardiology·2018· 31 citedOpen Access
Prospective longitudinal overnight video-EEG evaluation in Phelan–McDermid Syndrome
Epilepsy & Behavior·2018· 22 cited
Cytogenomic identification and long-read single molecule real-time (SMRT) sequencing of a Bardet–Biedl Syndrome 9 (BBS9) deletion
npj Genomic Medicine·2018· 121 citedOpen Access
Abstract 185: Genome Editing of Isogenic Human Induced Pluripotent Stem Cells Allows for Functional and Transcriptomic Insights Into Hereditary Dilated Cardiomyopathy Caused by Phospholamban Mutations
Circulation Research·2017
Maternal uniparental disomy of chromosome 15 and concomitant <i>STRC</i> and <i>CATSPER2</i> deletion‐mediated deafness‐infertility syndrome
American Journal of Medical Genetics Part A·2017· 10 citedOpen Access
Chromosomal Microarray Detection of Constitutional Copy Number Variation Using Saliva DNA
Journal of Molecular Diagnostics·2017· 13 citedOpen Access
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Frequent Co-authors

Gideon Rechavi(15), Luba Trakhtenbrot(15), Ninette Amariglio(14), Lisa Edelmann(10), David R. Betts(8), Sunita L. D’Souza(7), Christoph Schaniel(6), Bruce D. Gelb(5), Ethylin Wang Jabs(5), Stuart A. Scott(5), Izhar Hardan(5), F. Brok‐Simoni(5), Meng Wu(5), Eric E. Schadt(4), Felix Niggli(4), Nayyara Mahmood(4), Ru Ying(4), Meng Ma(4), Xianxiao Zhou(4), Divya Kriti(4)