C. Popovici

发表

Neural Tissue in Ascidian Embryos Is Induced by FGF9/16/20, Acting via a Combination of Maternal GATA and Ets Transcription Factors

Vincent Bertrand, P. Lemaire, C. Hudson, 2003, Cell.

Caenorhabditis elegans receptors related to mammalian vascular endothelial growth factor receptors are expressed in neural cells

D. Birnbaum, D. Isnardon, C. Popovici, 2002, Neuroscience Letters.

The power of high-resolution non-targeted array-CGH in identifying intragenic rearrangements responsible for Cohen syndrome

P. Rump, L. Faivre, C. Thauvin-Robinet, 2011, Journal of Medical Genetics.

Intragenic rearrangements in X‐linked intellectual deficiency: Results of a‐CGH in a series of 54 patients and identification of TRPC5 and KLHL15 as potential XLID genes

A. Mégarbané, S. Julia, N. Philip, 2014, American journal of medical genetics. Part A.

Molecular Profiles of Advanced Urological Cancers in the PERMED-01 Precision Medicine Clinical Trial

F. Bertucci, D. Birnbaum, P. Finetti, 2022, Cancers.

A recurrent chromosome translocation breakpoint in breast and pancreatic cancer cell lines targets the neuregulin/NRG1 gene

P. Edwards, D. Birnbaum, C. Theillet, 2003, Genes, chromosomes & cancer.

TAKTIC: A prospective, multicentre, uncontrolled, phase IB/II study of LY2780301, a p70S6K/AKT inhibitor, in combination with weekly paclitaxel in HER2-negative advanced breast cancer patients.

F. Bertucci, D. Birnbaum, F. Dalenc, 2021, European journal of cancer.

Ovarian cancer patients at high risk of BRCA mutation: the constitutional genetic characterization does not change prognosis

P. Viens, H. Sobol, C. Popovici, 2016, Familial Cancer.

Phylogenetic Analysis of Ciona intestinalis Gene Superfamilies Supports the Hypothesis of Successive Gene Expansions

D. Birnbaum, F. Coulier, C. Popovici, 2004, Journal of Molecular Evolution.

LET-756/FGF is Implicated in the Control of C. elegans Body Size

D. Birnbaum, C. Popovici, R. Roubin, 2008 .

Syndromic mental retardation with thrombocytopenia due to 21q22.11q22.12 deletion: Report of three patients

N. Philip, A. Renieri, F. Mari, 2010, American journal of medical genetics. Part A.

Fibroblast growth factor receptor 1 is fused to FIM in stem-cell myeloproliferative disorder with t(8;13).

D. Birnbaum, M. Pébusque, G. Guasch, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Y253H mutation appearing in a μ-BCR-ABL (e19a2) CML

S. Olschwang, M. Mozziconacci, O. Gisserot, 2008 .

Mosaic 15q13.3 deletion including CHRNA7 gene in monozygotic twins.

N. Philip, M. Milh, A. Moncla, 2013, European journal of medical genetics.

Direct and heterologous approaches to identify the LET-756/FGF interactome

D. Birnbaum, C. Popovici, Fabien Conchonaud, 2006, BMC Genomics.

Ovarian cancer patients at high risk of BRCA mutation: the constitutional genetic characterization does not change prognosis

P. Viens, H. Sobol, C. Popovici, 2016, Familial Cancer.

Fluorescent in situ hybridization (FISH) on corneal impression cytology specimens (CICS): study of epithelial cell survival after keratoplasty.

F. Matonti, L. Hoffart, J. Conrath, 2011, Investigative ophthalmology & visual science.

Chromosome region 8p11‐p21: Refined mapping and molecular alterations in breast cancer

A. Børresen-Dale, D. Birnbaum, R. Zeillinger, 1998, Genes, chromosomes & cancer.

ZNF703 gene amplification at 8p12 specifies luminal B breast cancer

C. Sotiriou, F. Bertucci, D. Birnbaum, 2011, EMBO molecular medicine.

Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach.

F. Révillion, R. Lidereau, N. Sevenet, 2021, American journal of human genetics.

Prospective high-throughput genome profiling of advanced cancers: results of the PERMED-01 clinical trial

F. Bertucci, D. Birnbaum, P. Finetti, 2021, Genome Medicine.

Major Response to Carboplatin in a Patient With Metastatic Triple-Negative Breast Cancer With Somatic Mutation of BRCA1 and Loss of RAD51B.

F. Bertucci, D. Birnbaum, A. Gonçalves, 2019, JCO precision oncology.

Fibroblast growth factor receptor 1 is fused to FIM in stem-cell myeloproliferative disorder with t(8;13).

D. Birnbaum, M. Pébusque, G. Guasch, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Coparalogy: physical and functional clusterings in the human genome.

D. Birnbaum, F. Coulier, C Popovici, 2001, Biochemical and biophysical research communications.

CDKN2A/B Deletion and Double-hit Mutations of the MAPK Pathway Underlie the Aggressive Behavior of Langerhans Cell Tumors

F. Bertucci, R. Bouabdallah, P. Brousset, 2018, The American journal of surgical pathology.

National recommendations of the French Genetics and Cancer Group - Unicancer on the modalities of multi-genes panel analyses in hereditary predispositions to tumors of the digestive tract.

B. Buecher, C. Lasset, P. Berthet, 2020, European journal of medical genetics.

Variant MYST4‐CBP gene fusion in a t(10;16) acute myeloid leukaemia

D. Birnbaum, F. Birg, A. Murati, 2004, British journal of haematology.

An evolutionary history of the FGF superfamily.

D. Birnbaum, F. Coulier, C. Popovici, 2005, BioEssays : news and reviews in molecular, cellular and developmental biology.

Chromosome arm 8p and cancer: a fragile hypothesis.

D. Birnbaum, E. Charafe-Jauffret, M. Mozziconacci, 2003, The Lancet. Oncology.

Incidental findings on array comparative genomic hybridization: detection of carrier females of dystrophinopathy without any family history

S. Julia, N. Philip, M. Till, 2015, Clinical genetics.

MetaHox gene clusters.

D. Birnbaum, F. Coulier, C. Popovici, 2000, The Journal of experimental zoology.

Reciprocal translocations in breast tumor cell lines: Cloning of a t(3;20) that targets the FHIT gene

F. Bertucci, D. Birnbaum, S. Ethier, 2002, Genes, chromosomes & cancer.

Targeted NGS, array-CGH, and patient-derived tumor xenografts for precision medicine in advanced breast cancer: a single-center prospective study

F. Bertucci, D. Birnbaum, P. Finetti, 2016, Oncotarget.

t(6;8), t(8;9) and t(8;13) translocations associated with stem cell myeloproliferative disorders have close or identical breakpoints in chromosome region 8p11-12

D. Birnbaum, A. Hagemeijer, M. Pébusque, 1998, Oncogene.

Translocation and coamplification of loci from chromosome arms 8p and 11q in the MDA-MB-175 mammary carcinoma cell line.

D. Birnbaum, D. Ron, M. Pébusque, 2000, International journal of oncology.

stem cell myeloproliferative disorder with t(8;19)(p12;q13.3) Endogenous retroviral sequence is fused to FGFR1 kinase in the 8p12

M. Pébusque, G. Guasch, C. Popovici, 2013 .

Endogenous retroviral sequence is fused to FGFR1 kinase in the 8p12 stem-cell myeloproliferative disorder with t(8;19)(p12;q13.3).

D. Birnbaum, M. Pébusque, P. Pontarotti, 2003, Blood.

FGFR1 is fused to the centrosome-associated protein CEP110 in the 8p12 stem cell myeloproliferative disorder with t(8;9)(p12;q33).

D. Birnbaum, J. B. Rattner, M. Pébusque, 2000, Blood.

The t(6;8)(q27;p11) translocation in a stem cell myeloproliferative disorder fuses a novel gene, FOP, to fibroblast growth factor receptor 1.

D. Birnbaum, M. Pébusque, P. Jonveaux, 1999, Blood.

Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers: an international cohort study

R. Eeles, J. Hopper, D. Easton, 2021, American journal of obstetrics and gynecology.

Loss of FHIT protein expression is a marker of adverse evolution in good prognosis localized breast cancer

F. Bertucci, D. Birnbaum, V. Bardou, 2003, International journal of cancer.

A pair as a minimum: The two fibroblast growth factors of the nematode Caenorhabditis elegans

D. Birnbaum, C. Popovici, R. Roubin, 2005, Developmental dynamics : an official publication of the American Association of Anatomists.

FGFR 1 is fused to the centrosome-associated protein CEP 110 in the 8 p 12 stem cell myeloproliferative disorder with t ( 8 ; 9 ) ( p 12 ; q 33 )

D. Birnbaum, J. B. Rattner, M. Pébusque, 2022 .

E6a2 BCR-ABL fusion with BCR exon 5-deleted transcript in a Philadelphia positive CML responsive to Imatinib

M. Mozziconacci, Cornel Popovici, Sylvie Cailleres, 2005, Leukemia & lymphoma.

Coffin-Siris syndrome with multiple congenital malformations and intrauterine death: towards a better delineation of the severe end of the spectrum.

N. Girard, A. Tasei, B. Coulibaly, 2010, European journal of medical genetics.

Is there a correlation between peripheral blood expression of angiogenic transcriptional factors/receptors and colorectal cancer?

I. Berindan‐Neagoe, T. Ciuleanu, O. Bălăcescu, 2015, Journal of B.U.ON. : official journal of the Balkan Union of Oncology.

Introduction Is there a correlation between peripheral blood expression of angiogenic transcriptional factors / receptors and colorectal cancer ?

I. Berindan‐Neagoe, T. Ciuleanu, O. Bălăcescu, 2015 .

Dual lympho-myeloproliferative disorder in a patient with t(8;22) with BCR-FGFR1 gene fusion.

D. Birnbaum, L. Xerri, B. Delaval, 2005, International journal of oncology.

TUMOSPEC: A Nation-Wide Study of Hereditary Breast and Ovarian Cancer Families with a Predicted Pathogenic Variant Identified through Multigene Panel Testing

J. Lemonnier, N. Sevenet, D. Stoppa-Lyonnet, 2021, Cancers.

Whole ARX gene duplication is compatible with normal intellectual development

N. Philip, J. Andrieux, A. Moncla, 2014, American journal of medical genetics. Part A.

let-756, a C. elegans fgf essential for worm development

D. Birnbaum, J. Thierry-Mieg, D. Thierry-Mieg, 1999, Oncogene.

Bernard–Soulier syndrome: first human case due to a homozygous deletion of GP9 gene

M. Alessi, H. Chambost, N. Saut, 2020, British journal of haematology.

A further case of acute myelomonocytic leukemia with inv(8) chromosomal rearrangement and MOZ-NCOA2 gene fusion.

D. Birnbaum, C. Arnoulet, A. Murati, 2003, International journal of molecular medicine.

The family of Caenorhabditis elegans tyrosine kinase receptors: similarities and differences with mammalian receptors.

D. Birnbaum, P. Pontarotti, F. Coulier, 1999, Genome research.

Nectin-4 is a new histological and serological tumor associated marker for breast cancer

D. Birnbaum, P. Finetti, P. Viens, 2007, BMC Cancer.

Use of DOP-PCR for amplification and labeling of BAC DNA for FISH

A. Moncla, C. Popovici, C. Missirian, 2012, Biotechnic & histochemistry : official publication of the Biological Stain Commission.

Functional Phylogeny Relates LET-756 to Fibroblast Growth Factor 9*

D. Birnbaum, C. Popovici, Fabien Conchonaud, 2004, Journal of Biological Chemistry.

Intracellular trafficking of LET-756, a fibroblast growth factor of C. elegans, is controlled by a balance of export and nuclear signals.

D. Birnbaum, D. Marguet, C. Popovici, 2006, Experimental cell research.

Homeobox gene clusters and the human paralogy map

D. Birnbaum, F. Coulier, C. Popovici, 2001, FEBS letters.

[FGFR1 and MOZ, two key genes involved in malignant hemopathies linked to rearrangements within the chromosomal region 8p11-12].

D. Birnbaum, M. Pébusque, M. Chaffanet, 2000, Bulletin du cancer.

ZNF703 gene amplification at 8p12 specifies luminal B breast cancer

C. Sotiriou, F. Bertucci, D. Birnbaum, 2011, EMBO Molecular Medicine.

[A solid variant of a serous cystadenocarcinoma of the pancreas].

B. Terris, F. Poizat, J. Thomassin-Piana, 2016, Annales de pathologie.

Intragenic rearrangements in X‐linked intellectual deficiency: Results of a‐CGH in a series of 54 patients and identification of TRPC5 and KLHL15 as potential XLID genes

A. Mégarbané, S. Julia, N. Philip, 2014, American journal of medical genetics. Part A.