A. Bernheim

Guidelines for cytogenetic investigations in tumours
201533 citationsauthor #10
Genome-Wide Microarray Expression and Genomic Alterations by Array-CGH Analysis in Neuroblastoma Stem-Like Cells
20147 citationsauthor #8
Abstract 3051: Genome-wide microarray expression and genomic alteration by array-CGH analysis in neuroblastoma stem-like cells
20140 citationsauthor #10
Guidelines and Quality Assurance for Acquired Cytogenetics
20138 citationsauthor #16
Monozygotic twins discordant for submicroscopic chromosomal anomalies in 2p25.3 region detected by array CGH
201333 citationsauthor #6
Abstract 413: Genome-wide microarray expression and array-CGH analysis in neuroblastoma stem-like cells by use of the neurosphere-formation assay
20120 citationsauthor #7
Genome-Wide High-Resolution aCGH Analysis of Gestational Choriocarcinomas
201236 citationsauthor #12
Immunohistochemistry to identify EGFR mutations or ALK rearrangements in patients with lung adenocarcinoma.
201265 citationsauthor #6
Atlas of Genetics and Cytogenetics in Oncology and Haematology in 2013
2012176 citationsauthor #4
[Cytogenomic studies of hydatiform moles and gestational choriocarcinoma].
20126 citationsauthor #11
24 colour multifish karyotype showing the complexity of the genomic rearrangements with rearranged c
20110 citationsauthor #7
t(8;13)(p12;q12)
20110 citationsauthor #3
P3-05-07: Genetic Heterogeneity of Amplification Status in Breast Invasive Carcinoma with 2+ HER2 Immunostaining: What Can We Learn?
20111 citationsauthor #4
Chromosomal Minimal Critical Regions in Therapy-Related Leukemia Appear Different from Those of De Novo Leukemia by High-Resolution aCGH
201129 citationsauthor #12
Cytogenomics of cancers: From chromosome to sequence
201027 citationsauthor #1
Genomic Aberrations in Lung Adenocarcinoma in Never Smokers
201077 citationsauthor #2
t(12;21)(p12;q22)
20100 citationsauthor #2
Non-randomness in complex translocations of chronic myeloid leukaemia.
200911 citationsauthor #2
High Resolution Genome-Wide Analysis of Chromosomal Alterations in Burkitt's Lymphoma
200976 citationsauthor #15
Acute monoblastic leukaemia. Clinical, biological data and survival in 45 cases.
20098 citationsauthor #4
Intragenic breakpoints localized by array CGH in a t(2;6) familial translocation
20085 citationsauthor #1
High-resolution array comparative genomic hybridization analysis of human bronchial and salivary adenoid cystic carcinoma
200846 citationsauthor #1
Contents Vol. 119, 2007
20080 citationsauthor #75
Constitutional C-band polymorphism in lymphocytes from patients with chronic myeloid leukemia.
20084 citationsauthor #2
Differences in human C-band pattern between two European populations.
200814 citationsauthor #2
Specific cytogenetic abnormalities are associated with a significantly inferior outcome in children and adolescents with mature B-cell Non-Hodgkin’s Lymphoma: Results of the FAB/LMB 96 international study
2008129 citationsauthor #16
C-band polymorphism in non-Hodgkin lymphoma.
20085 citationsauthor #3
No abnormal C-band polymorphism in lung cancer patients.
20082 citationsauthor #3
Safe selection of genetically manipulated human primary keratinocytes with very high growth potential using CD24.
200731 citationsauthor #4
Prognostic Impact of Cytogenetic Abnormalities in Elderly Patients with Acute Myeloid Leukemia (AML) Enrolled in the ALFA-9803 Trial.
20072 citationsauthor #9
Cryptic del(13q14.2) and physiological deletions of immunoglobulin genes detected by high-resolution array comparative genomic hybridization in a patient with indolent chronic lymphocytic leukemia.
20074 citationsauthor #1
Telomere shortening and associated chromosomal instability in peripheral blood lymphocytes of patients with Hodgkin's lymphoma prior to any treatment are predictive of second cancers.
200764 citationsauthor #15
Biological characterization of two xenografts derived from human CUPs (carcinomas of unknown primary)
20074 citationsauthor #7
An unusual case of a lymphoblastic lymphoma with initial bilateral breast lesions but with c-myc and bcl-2 rearrangements
20072 citationsauthor #6
Integration of Myeloblastosis Associated Virus proviral sequences occurs in the vicinity of genes encoding signaling proteins and regulators of cell proliferation
200618 citationsauthor #3
JC human polyomavirus (JCV) and Epstein-Barr virus (EBV) replicative activities are detected in Hodgkin/Reed Sternberg cells (HRS) and circulating lymphocytes (PBL) of Hodgkin lymphoma (HL) and associated with relapse, especially in younger patients.
20062 citationsauthor #7
High promoter hypermethylation frequency of p14/ARF in supratentorial PNET but not in medulloblastoma
200629 citationsauthor #7
In Pediatric Mature B-Cell Non Hodgkin Lymphoma (NHL), Complex Karyotype or del(13q) Are Linked Prognostic Factors in Burkitt Lymphoma (BL) While 8q24/c-myc Rearrangement Is Associated with a Strong Adverse Effect in Diffuse Large B-Cell Lymphoma (DLBCL).
20051 citationsauthor #15
Genetic heterogeneity in supratentorial and infratentorial primitive neuroectodermal tumours of the central nervous system
200537 citationsauthor #13
Duplication of the Ph-chromosome as a possible mechanism of resistance to imatinib mesylate in patients with chronic myelogenous leukemia.
200514 citationsauthor #2
Conventional and array-based comparative genomic hybridization analysis of nasopharyngeal carcinomas from the Mediterranean area.
200526 citationsauthor #8
Cytogenetic repartition of chicken CR1 sequences evidenced by PRINS in Galliformes and some other birds
200519 citationsauthor #8
State of the Art and Future Needs in Cytogenetic/Molecular Genetics/Arrays in childhood lymphoma: Summary report of workshop at the First International Symposium on childhood and adolescent non‐Hodgkin lymphoma, April 9, 2003, New York City, NY
200519 citationsauthor #2
Mesenchymal cells generated from patients with myelodysplastic syndromes are devoid of chromosomal clonal markers and support short- and long-term hematopoiesis in vitro
200576 citationsauthor #7
Detecting single DNA copy number variations in complex genomes using one nanogram of starting DNA and BAC-array CGH.
200543 citationsauthor #10
High frequency trans-splicing in a cell line producing spliced and polyadenylated RNA polymerase I transcripts from an rDNA-myc chimeric gene
20057 citationsauthor #8
BCR/ABL promotes dendritic cell-mediated natural killer cell activation.
200539 citationsauthor #8
Characterization of quantitative chromosomal abnormalities in renal cell carcinomas by interphase four-color fluorescence in situ hybridization.
200525 citationsauthor #9
Shortened telomeres in peripheral lymphocytes are associated to complex chromosome anomalies and to second cancers in Hodgkin's lymphoma patients
20051 citationsauthor #5
Characteristic Pattern of Chromosomal Imbalances in Posttransplantation Lymphoproliferative Disorders: Correlation with Histopathological Subcategories and EBV Status
200576 citationsauthor #2
PTEN and DMBT1 homozygous deletion and expression in medulloblastomas and supratentorial primitive neuroectodermal tumors.
200423 citationsauthor #10
Multiple excitation confocal analysis of targets in nuclei of cytogenetic preparations.
20043 citationsauthor #7
Complex translocation (8;12;21): a new variant of t(8;21) in acute myeloid leukemia.
200433 citationsauthor #5
Alternative pathways of MYCN gene copy number increase in primary neuroblastoma tumors.
200413 citationsauthor #12
A Tsp509I variant in exon 13 of the neurofibromatosis type 1 (NF1) gene allows the identification of both alleles at the mRNA level
20042 citationsauthor #4
A report from the LALA-94 and LALA-SA groups on hypodiploidy with 30 to 39 chromosomes and near-triploidy: 2 possible expressions of a sole entity conferring poor prognosis in adult acute lymphoblastic leukemia (ALL).
200482 citationsauthor #10
A simple method for R-banding combined with in situ hybridization
20040 citationsauthor #1
A simple method for improving the reproductibility of the R-banding technique
20043 citationsauthor #1
[Cytogenetics, cytogenomics and cancer: 2004 update].
20041 citationsauthor #1
An Atlas on genes and chromosomes in oncology and haematology.
200430 citationsauthor #3
Simultaneous Fluorescence In-situ Hybridization (FISH) and R-Banding By Primed In-situ Labelling (PRINS)
20047 citationsauthor #4
Hypodiploidy with 30-39 chromosomes and near-triploidy: two possible expressions of a sole entity conferring poor prognosis in Adult Acute Lymphoblastic Leukemia (ALL). A report from the LALA-94 and LALA-SA Groups
20041 citationsauthor #10
Short Communication. Double Hybridization Signals on the Chromatid Revealed by Telomeric Probes
20043 citationsauthor #3
Localization of actin-related sequences by in situ hybridization to R-banded human chromosomes
20042 citationsauthor #1
Characterization of the atypical karyotype of the black-winged kite Elanus caeruleus (Falconiformes: Accipitridae) by means of classical and molecular cytogenetic techniques
200438 citationsauthor #5
Chromosomal abnormalities in human glioblastomas: Gain in chromosome 7p correlating with loss in chromosome 10q
200343 citationsauthor #15
Therapy‐related myelodysplasia and/or acute myeloid leukaemia after autologous haematopoietic progenitor cell transplantation in a prospective single centre cohort of 221 patients
200316 citationsauthor #4
An internet database on genetics in oncology
200310 citationsauthor #3
Risk of secondary leukemia after a solid tumor in childhood according to the dose of epipodophyllotoxins and anthracyclines: a case-control study by the Société Française d'Oncologie Pédiatrique.
2003198 citationsauthor #10
Sensitivity to Radiation and Alkylating Agent of Peripheral Lymphocytes and Fibroblasts in a Hoyeraal-Hreidarsson Syndrome Patient
200317 citationsauthor #12
Baseline and treatment-induced chromosomal abnormalities in peripheral blood lymphocytes of Hodgkin's lymphoma patients.
200337 citationsauthor #9
Atlas of Genetics and Cytogenetics in Oncology and Haematology, year 2003
200352 citationsauthor #3
Chicken fucosyltransferase genes compared to human
20031 citationsauthor #8
Werner Schmid, 1930–2002
20020 citationsauthor #74
[Recommendations for the treatment of neurofibromatosis type 1].
20024 citationsauthor #8
Brief Gene Mapping Reports A / B / C / D / E / F / G
200225 citationsauthor #74
Assignment1 of the chicken NOV gene (alias CCN3) to chromosome 2q34→q36: Conserved and compared synteny between avian, mouse and human
20021 citationsauthor #5
PRINS, the other in situ DNA labeling method useful in cellular biology.
200224 citationsauthor #7
[From the cytogenetics to the cytogenomics of thyroid tumors].
20020 citationsauthor #2
MYCN gene overrepresentation detected in primary neuroblastoma tumour cells without amplification
200222 citationsauthor #10
Modulation of tumor growth by inhibitory Fc(gamma) receptor expressed by human melanoma cells.
200222 citationsauthor #8
Initiation of the breakage-fusion-bridge mechanism through common fragile site activation in human breast cancer cells: the model of PIP gene duplication from a break at FRA7I.
2002142 citationsauthor #9
[Cytogenetics, cytogenomics and cancer].
20023 citationsauthor #1
Improved confocal characterization of targets in nuclei of cytogenetic preparations.
20020 citationsauthor #5
Assignment1 of the homologue of human JAG1 to chicken chromosome 3q11 by in situ hybridization
20020 citationsauthor #6
Assignment of the chicken NOV gene (alias CCN3) to chromosome 2q34-->q36: Conserved and compared synteny between avian, mouse and human.
20022 citationsauthor #5
Modulation of tumor growth by inhibitory Fcγ receptor expressed by human melanoma cells
200235 citationsauthor #8
[Neurofibromatosis 1: recommendations for management].
20020 citationsauthor #8
Lead article Patterns of specific genomic alterations associated with poor prognosis in high-grade renal cell carcinomas
20010 citationsauthor #7
Prognostic impact of cytogenetics in untreated AML patients aged 16-60 years: preliminary results of the randomized AML-10 phase III trial of the EORTC and GIMEMA Leukemia Groups
20010 citationsauthor #6
Stromal cells and human malignant neuroblasts derived from bone marrow metastasis may share common karyotypic abnormalities: the case of the IGR-N-91 cell line.
20017 citationsauthor #6
Chromosome 3q abnormalities in 43 untreated AML patients aged 15-60 years: preliminary results of the randomized AML-10 phase III trial of the EORTC and GIMEMA Leukemia Groups
20011 citationsauthor #5
Atlas of Genetics and Cytogenetics in Oncology and Haematology, updated
200123 citationsauthor #3
Chromosomal abnormalities in liver cell dysplasia detected by comparative genomic hybridisation
200158 citationsauthor #7
An Atlas on Chromosomes in Hematological Malignancies. Example: 11q23 and MLL partners
2001133 citationsauthor #3
[Neurofibromatosis 1: recommendations for management].
200124 citationsauthor #8
P 9 POTENTIAL FUNCTIONAL INTERACTIONS OF THE NOVH C-TERMINAL DOMAIN IN NORMAL AND TUMOR TISSUES FROM ADRENAL CORTEX
20010 citationsauthor #7
Mapping of the 7q31 subregion common to the small chromosome 7 derivatives from two sporadic papillary renal cell carcinomas: increased copy number and overexpression of the MET proto-oncogene
200040 citationsauthor #7
Distinct chromosomal abnormality pattern in primary liver cancer of non-B, non-C patients
2000107 citationsauthor #6
Revised guidelines for authors of gene mapping reports
20000 citationsauthor #100

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