Ninette Cohen

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Identification and Purification of Human Induced Pluripotent Stem Cell-Derived Atrial-Like Cardiomyocytes Based on Sarcolipin Expression

G. Fishman, B. Gelb, E. Sobie, 2014, PloS one.

Detection of unidentified chromosome abnormalities in human neuroblastoma by spectral karyotyping (SKY)

L. Trakhtenbrot, N. Amariglio, G. Rechavi, 2001, Genes, chromosomes & cancer.

Multiple hemangiomas in a patient with a t(3q;4p) translocation: An infrequent association with Wolf–Hirschhorn syndrome

K. Hirschhorn, L. Edelmann, N. Cohen, 2008, American journal of medical genetics. Part A.

Determination of chromosome 13 status in bone marrow cells of patients with multiple myeloma using combined morphologic and fluorescence in situ hybridization analysis.

A. Nagler, L. Trakhtenbrot, N. Amariglio, 2004, Experimental Hematology.

Patient-specific induced pluripotent stem-cell-derived models of LEOPARD syndrome

Yongchao Ge, Yen-Sin Ang, Roye Rozov, 2010 .

An atypical deletion of the Williams–Beuren syndrome interval implicates genes associated with defective visuospatial processing and autism

Uta Francke, Barbara K Burton, U. Francke, 2006, Journal of Medical Genetics.

Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: Efficient identification of known microduplications and identification of a novel microduplication in ASMT

Evdokia Anagnostou, Eric Hollander, L. Soorya, 2008, BMC Medical Genomics.

Large inverted repeats within Xp11.2 are present at the breakpoints of isodicentric X chromosomes in Turner syndrome.

S. Scott, P. Warburton, L. Edelmann, 2010, Human molecular genetics.

Novel, Compound Heterozygous, Single‐Nucleotide Variants in MARS2 Associated with Developmental Delay, Poor Growth, and Sensorineural Hearing Loss

E. Schadt, T. Naidich, R. Rodenburg, 2015, Human mutation.

Karyotypic evolution pathways in medulloblastoma/primitive neuroectodermal tumor determined with a combination of spectral karyotyping, G-banding, and fluorescence in situ hybridization.

L. Trakhtenbrot, N. Amariglio, G. Rechavi, 2004, Cancer genetics and cytogenetics.

Familial inheritance of the 3q29 microdeletion syndrome: case report and review

Wahab A. Khan, S. Scott, N. Cohen, 2019, BMC Medical Genomics.

Myeloid Dysregulation in a Human Induced Pluripotent Stem Cell Model of PTPN11-Associated Juvenile Myelomonocytic Leukemia.

H. Cavé, B. Gelb, L. Edelmann, 2015, Cell reports.

Prenatal Cytogenetic and Cytogenomic Diagnosis

L. Edelmann, N. Cohen, Ninette Cohen, 2013 .

Transient abnormal myelopoiesis with extramedullary involvement in a down syndrome preemie leading to an unresponsive course despite chemotherapy

S. Geetha, M. Shaham, Ram Singh, 2023, Leukemia research reports.

Subgroup of patients with Philadelphia-positive chronic myelogenous leukemia characterized by a deletion of 9q proximal to ABL gene: expression profiling, resistance to interferon therapy, and poor prognosis.

L. Trakhtenbrot, N. Amariglio, G. Rechavi, 2001, Cancer genetics and cytogenetics.

Correction of human phospholamban R14del mutation associated with cardiomyopathy using targeted nucleases and combination therapy

Ronald A. Li, Despina Sanoudou, Roger J Hajjar, 2015, Nature Communications.

SKY reveals a high frequency of unbalanced translocations involving chromosome 6 in t(12;21)-positive acute lymphoblastic leukemia.

L. Trakhtenbrot, N. Amariglio, G. Rechavi, 2008, Leukemia research.

Maternal uniparental disomy of chromosome 15 and concomitant STRC and CATSPER2 deletion‐mediated deafness‐infertility syndrome

Wahab A. Khan, S. Scott, Amy C Yang, 2017, American journal of medical genetics. Part A.

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

Wahab A. Khan, R. Sebra, E. Jabs, 2018, npj Genomic Medicine.

Interphase fluorescence in situ hybridization detection of chromosome 17 and 17q region gains in neuroblastoma: are they secondary events?

L. Trakhtenbrot, N. Amariglio, G. Rechavi, 2002 .

De Novo Interstitial Deletion of 9q in a Pediatric Patient With Global Developmental Delay

Ram Singh, N. Cohen, Dennis Keselman, 2019, Child neurology open.

SKY detection of chromosome rearrangements in two cases of tMDS with a complex karyotype.

L. Trakhtenbrot, N. Amariglio, G. Rechavi, 2002, Cancer genetics and cytogenetics.

Standardization criteria for the detection of BCR/ABL fusion in interphase nuclei of chronic myelogenous leukemia patients by fluorescence in situ hybridization.

L. Trakhtenbrot, N. Amariglio, G. Rechavi, 2000, Cancer genetics and cytogenetics.

Detection of low-level mosaicism and placental mosaicism by oligonucleotide array comparative genomic hybridization

R. Desnick, S. Scott, L. Edelmann, 2010, Genetics in Medicine.

Chromosomal Microarray Detection of Constitutional Copy Number Variation Using Saliva DNA.

S. Scott, L. Edelmann, N. Cohen, 2017, The Journal of molecular diagnostics : JMD.

Autonomous and Non-autonomous Defects Underlie Hypertrophic Cardiomyopathy in BRAF-Mutant hiPSC-Derived Cardiomyocytes

L. Weiss, E. Ullian, B. Gelb, 2016, Stem cell reports.

Patient-specific induced pluripotent stem cell derived models of LEOPARD syndrome

Lei Yang, Roye Rozov, Jie Su, 2010, Nature.

Complex autism spectrum disorder in a patient with a 17q12 microduplication

A. Kolevzon, L. Soorya, A. Tryfon, 2012, American journal of medical genetics. Part A.

Characterization of karyotypic events and evolution in neuroblastoma

K. Leibundgut, D. Betts, F. Niggli, 2005, Pediatric blood & cancer.

Prospective longitudinal overnight video-EEG evaluation in Phelan–McDermid Syndrome

S. Inati, A. Thurm, A. Gropman, 2018, Epilepsy & Behavior.

Clonal expansion and not cell interconversion is the basis for the neuroblast and nonneuronal types of the SK-N-SH neuroblastoma cell line.

L. Trakhtenbrot, N. Amariglio, G. Rechavi, 2003, Cancer genetics and cytogenetics.

Interphase fluorescence in situ hybridization detection of chromosome 17 and 17q region gains in neuroblastoma: are they secondary events?

L. Trakhtenbrot, N. Amariglio, G. Rechavi, 2002, Cancer genetics and cytogenetics.

Short communication Clonal expansion and not cell interconversion is the basis for the neuroblast and nonneuronal types of the SK-N-SH neuroblastoma cell line

L. Trakhtenbrot, N. Amariglio, G. Rechavi, 2003 .

Myeloid Dysregulation in a Human Induced Pluripotent Stem Cell Model of PTPN 11-Associated Juvenile Myelomonocytic Leukemia Graphical

H. Cavé, B. Gelb, L. Edelmann, 2015 .

L. Soorya, J. Buxbaum, C. Betancur, 2008, BMC Medical Genomics.

Functional and transcriptomic insights into pathogenesis of R9C phospholamban mutation using human induced pluripotent stem cell-derived cardiomyocytes.

Ronald A. Li, Daniel R. Stroik, J. Björkegren, 2018, Journal of molecular and cellular cardiology.

Acquisition of a Ph chromosome with minor BCR/ABL fusion in treatment-related myelodysplastic syndrome with chromosome 7 abnormalities in a patient treated for Hodgkin disease.

A. Nagler, L. Trakhtenbrot, N. Amariglio, 2005, Cancer genetics and cytogenetics.

Bmc Medical Genomics Multiplex Ligation-dependent Probe Amplification for Genetic Screening in Autism Spectrum Disorders: Efficient Identification of Known Microduplications and Identification of a Novel Microduplication in Asmt

L. Soorya, Danielle Zurawiecki, J. Buxbaum, 2008 .

Chromosomal Microarray Detection of Constitutional Copy Number Variation Using Saliva DNA.

L. Edelmann, L. Mehta, Lisa Karger, 2017, The Journal of molecular diagnostics : JMD.