Cette page présente les publications de la plateforme P3S en génomique uniquement
68 documents
Articles dans une revue
- Julie Lerond, Bertrand Mathon, Mélina Scopin, Lucia Nichelli, Justine Guégan, et al.. Hippocampal and neocortical BRAF mutant non‐expansive lesions in focal epilepsies. Neuropathology and Applied Neurobiology, 2023, 49 (5), pp.e12937. ⟨10.1111/nan.12937⟩. ⟨inserm-04432712⟩
- Emma Bergsten, Denis Mestivier, Francoise Donnadieu, Thierry Pedron, Caroline Barau, et al.. Parvimonas micra, an oral pathobiont associated with colorectal cancer, epigenetically reprograms human colonocytes. Gut microbes, 2023, 15 (2), pp.2265138. ⟨10.1080/19490976.2023.2265138⟩. ⟨pasteur-04250370⟩
- Suzanne Tran, Alice Thomas, Ilyes Aliouat, Carine Karachi, Fernando Lozano, et al.. A threshold for mitotic activity and post‐surgical residual volume defines distinct prognostic groups for astrocytoma IDH‐mutant. Neuropathology and Applied Neurobiology, 2023, 49 (4), pp.e12928. ⟨10.1111/nan.12928⟩. ⟨hal-04195333⟩
- Livia Parodi, Mathieu Barbier, Maxime Jacoupy, Claire Pujol, François-Xavier Lejeune, et al.. The mitochondrial seryl-tRNA synthetase SARS2 modifies onset in spastic paraplegia type 4. Genetics in Medicine, 2022, pp.S1098-3600. ⟨10.1016/j.gim.2022.07.023⟩. ⟨pasteur-03813186⟩
- Myriam Rahmouni, Vincent Laville, Jean-Louis Spadoni, Randa Jdid, Leopold Eckhart, et al.. Identification of New Biological Pathways Involved in Skin Aging From the Analysis of French Women Genome-Wide Data. Frontiers in Genetics, 2022, 13, ⟨10.3389/fgene.2022.836581⟩. ⟨hal-03653766⟩
- Julie Lerond, Mony Chenda Morisse, Quentin Letourneur, Coralie Gimonnet, Soledad Navarro, et al.. Immune Microenvironment and Lineage Tracing Help to Decipher Rosette-Forming Glioneuronal Tumors. Journal of Neuropathology and Experimental Neurology, 2022, Publish Ahead of Print, ⟨10.1093/jnen/nlac074⟩. ⟨hal-03771198⟩
- Roberta Armignacco, Parminder Reel, Smarti Reel, Anne Jouinot, Amandine Septier, et al.. Whole blood methylome-derived features to discriminate endocrine hypertension. Clinical Epigenetics, 2022, 14 (1), pp.142. ⟨10.1186/s13148-022-01347-y⟩. ⟨hal-03842638⟩
- Roberta Armignacco, Anne Jouinot, Lucas Bouys, Amandine Septier, Thomas Lartigue, et al.. Identification of glucocorticoid-related molecular signature by whole blood methylome analysis. European Journal of Endocrinology, 2021, pp.EJE-21-0907.R1. ⟨10.1530/EJE-21-0907⟩. ⟨hal-03497285⟩
- Bastien Ducreux, Jean Frappier, Céline Bruno, Abiba Doukani, Magali Guilleman, et al.. Genome-Wide Analysis of DNA Methylation in Buccal Cells of Children Conceived through IVF and ICSI. Genes, 2021, 12 (12), pp.1912. ⟨10.3390/genes12121912⟩. ⟨hal-03467331⟩
- Mathieu Barbier, Agnès Camuzat, Khalid El Hachimi, Justine Guegan, Daisy Rinaldi, et al.. SLITRK2 , an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration. Brain - A Journal of Neurology , 2021, 144 (9), pp.2798-2811. ⟨10.1093/brain/awab171⟩. ⟨hal-03590956⟩
- Camino S M Ruano, Clara Apicella, Sébastien Jacques, Géraldine Gascoin, Cassandra Gaspar, et al.. Alternative splicing in normal and pathological human placentas is correlated to genetic variants. Human Genetics, In press, ⟨10.1007/s00439-020-02248-x⟩. ⟨hal-03113232⟩
- S. Saget, R. Cong, L. Decourtye, M. L. Endale, L. Martinerie, et al.. Changes in circulating miRNA19a-3p precede insulin resistance programmed by intra-uterine growth retardation in mice. Molecular metabolism, 2020, 42 (Supplement_C), pp.101083. ⟨10.1016/j.molmet.2020.101083⟩. ⟨hal-03170970⟩
- Signe Hässler, Delphine Bachelet, Julianne Duhazé, Natacha Szely, Aude Gleizes, et al.. Clinicogenomic factors of biotherapy immunogenicity in autoimmune disease: A prospective multicohort study of the ABIRISK consortium. PLoS Medicine, 2020, 17 (10), pp.e1003348. ⟨10.1371/journal.pmed.1003348⟩. ⟨hal-03979090⟩
- Roberta Armignacco, Thomas Lartigue, Anne Jouinot, Amandine Septier, Mario Neou, et al.. Identification d’une signature moléculaire d’hypercortisolisme par analyse du methylome du sang total. Annales d'Endocrinologie, 2020, 81 (4), pp.180. ⟨10.1016/j.ando.2020.07.117⟩. ⟨hal-03035962⟩
- Isabelle Audo, Kinga Bujakowska, Saddek Mohand-Saïd, Sophie Tronche, Marie-Elise Lancelot, et al.. A novel DFNB31 mutation associated with Usher type 2 syndrome showing variable degrees of auditory loss in a consanguineous Portuguese family.. Molecular Vision, 2020, 17, pp.1598-606. ⟨hal-02565839⟩
- Mario Neou, Chiara Villa, Roberta Armignacco, A. Jouinot, Marie-Laure Raffin-Sanson, et al.. Pangenomic classification of pituitary neuroendocrine tumors. Cancer Cell, 2020, 37 (1), pp.123-134. ⟨10.1016/j.ccell.2019.11.002⟩. ⟨hal-02441511⟩
- Aurore Siegfried, Julien Masliah-Planchon, Franck-Emmanuel Roux, Delphine Larrieu-Ciron, Gaëlle Pierron, et al.. Brain tumor with an ATXN1-NUTM1 fusion gene expands the histologic spectrum of NUTM1-rearranged neoplasia. Acta Neuropathologica Communications, 2019, 7 (1), pp.220. ⟨10.1186/s40478-019-0870-8⟩. ⟨inserm-02440672⟩
- Kévin Baranger, Manuel van Gijsel-Bonnello, Delphine Stephan, Wassila Carpentier, Santiago Rivera, et al.. Long-Term Pantethine Treatment Counteracts Pathologic Gene Dysregulation and Decreases Alzheimer’s Disease Pathogenesis in a Transgenic Mouse Model. Neurotherapeutics, 2019, ⟨10.1007/s13311-019-00754-z⟩. ⟨hal-02339537⟩
- Maud Blanluet, Julien Masliah-Planchon, Irina Giurgea, Franck Bielle, Élodie Girard, et al.. SHH medulloblastoma in a young adult with a TCF4 germline pathogenic variation. Acta Neuropathologica, 2019, 137 (4), pp.675-678. ⟨10.1007/s00401-019-01983-4⟩. ⟨hal-02347134⟩
- Fabian Christoph Franke, Johannes Müller, Miguel Abal, Eduardo Domínguez Medina, Ulrich Nitsche, et al.. The Tumor Suppressor SASH1 Interacts With the Signal Adaptor CRKL to Inhibit Epithelial–Mesenchymal Transition and Metastasis in Colorectal Cancer. Cellular and Molecular Gastroenterology and Hepatology, 2019, 7 (1), pp.33-53. ⟨10.1016/j.jcmgh.2018.08.007⟩. ⟨hal-01976847⟩
- Emmanuelle Uro-Coste, Julien Masliah-Planchon, Aurore Siegfried, Maud Blanluet, Sander Lambo, et al.. ETMR-like infantile cerebellar embryonal tumors in the extended morphologic spectrum of DICER1-related tumors. Acta Neuropathologica, 2018, ⟨10.1007/s00401-018-1935-7⟩. ⟨hal-01984537⟩
- Aurélien Bataille, Pierre Galichon, Nadjim Chelghoum, Badreddine Mohand Oumoussa, Marie-Julia Ziliotis, et al.. Increased Fatty Acid Oxidation in Differentiated Proximal Tubular Cells Surviving a Reversible Episode of Acute Kidney Injury. Cellular Physiology and Biochemistry, 2018, 47 (4), pp.1338 - 1351. ⟨10.1159/000490819⟩. ⟨hal-02565135⟩
- Maguelonne Roux, Claire Perret, Eva Feigerlova, Badreddine Mohand Oumoussa, Pierre-Jean Saulnier, et al.. Plasma levels of hsa-miR-152-3p are associated with diabetic nephropathy in patients with type 2 diabetes. Nephrology Dialysis Transplantation, 2018, 33 (12), pp.2201-2207. ⟨10.1093/ndt/gfx367⟩. ⟨hal-02272317⟩
- Esther Lopez-Rivera, Yangfan Liu, Miguel Verbitsky, Blair Anderson, Valentina Capone, et al.. Genetic Drivers of Kidney Defects in the DiGeorge Syndrome. New England Journal of Medicine, 2017, 376 (8), pp.742-754. ⟨10.1056/NEJMoa1609009⟩. ⟨hal-02565169⟩
- Marjorie Poggi, Matthias Canault, Marie Favier, Ernest Turro, Paul Saultier, et al.. Germline variants in ETV6 underlie reduced platelet formation, platelet dysfunction and increased levels of circulating CD34+ progenitors.. Haematologica, 2017, 102 (2), pp.282-294. ⟨10.3324/haematol.2016.147694⟩. ⟨hal-01478347⟩
- Aude Carillion, Sarah Feldman, Na Na, Matthieu Biais, Wassila Carpentier, et al.. Atorvastatin reduces β-Adrenergic dysfunction in rats with diabetic cardiomyopathy. PLoS ONE, 2017, 12 (7), pp.e0180103. ⟨10.1371/journal.pone.0180103⟩. ⟨hal-01579491⟩
- Reham Khalaf-Nazzal, Melissa A. Stouffer, Robert Olaso, Leila Muresan, Audrey Roumegous, et al.. Early born neurons are abnormally positioned in the doublecortin knockout hippocampus. Human Molecular Genetics, 2017, 26 (1), pp.90-108. ⟨10.1093/hmg/ddw370⟩. ⟨hal-01512718⟩
- Damien Ulveling, Sigrid Le Clerc, Aurélie Cobat, Taoufik Labib, Josselin Noirel, et al.. A new 3p25 locus is associated with liver fibrosis progression in human immunodeficiency virus/hepatitis C virus-coinfected patients. Hepatology, 2016, 64 (5), pp.1462-1472. ⟨10.1002/hep.28695⟩. ⟨hal-01515298⟩
- Vincent Laville, Sigrid Le Clerc, Khaled Ezzedine, Randa Jdid, Lieng Taing, et al.. A genome-wide association study in Caucasian women suggests the involvement of HLA genes in the severity of facial solar lentigines. PIGMENT CELL & MELANOMA RESEARCH, 2016, 29 (5), pp.550-558. ⟨10.1111/pcmr.12502⟩. ⟨hal-01515300⟩
- Mariam Meddeb, Wassila Carpentier, Nicolas Cagnard, Sophie Nadaud, Antoine Grillon, et al.. Homogeneous Inflammatory Gene Profiles Induced in Human Dermal Fibroblasts in Response to the Three Main Species of Borrelia burgdorferi sensu lato. PLoS ONE, 2016, 11 (10), pp.e0164117. ⟨10.1371/journal.pone.0164117.s004⟩. ⟨hal-01380244⟩
- Alexandra Richard, Jean-Christophe Corvol, Rabab Debs, Pauline Reach, Khadija Tahiri, et al.. Transcriptome Analysis of Peripheral Blood in Chronic Inflammatory Demyelinating Polyradiculoneuropathy Patients Identifies TNFR1 and TLR Pathways in the IVIg Response. Medicine, 2016, 95 (19), pp.e3370. ⟨10.1097/MD.0000000000003370⟩. ⟨hal-01319866⟩
- Claire Bouvard, Isabelle Galy-Fauroux, Françoise Grelac, Wassila Carpentier, Anna Lokajczyk, et al.. Low-Molecular-Weight Fucoidan Induces Endothelial Cell Migration via the PI3K/AKT Pathway and Modulates the Transcription of Genes Involved in Angiogenesis. Marine drugs, 2015, 13 (12), pp.7446 - 7462. ⟨10.3390/md13127075⟩. ⟨hal-01514447⟩
- Tangui Le Guen, Fabien Touzot, Isabelle André-Schmutz, Chantal Lagresle-Peyrou, Benoit France, et al.. An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiation. Journal of Allergy and Clinical Immunology, 2015, 136, pp.1619-26. ⟨10.1016/j.jaci.2015.06.008⟩. ⟨hal-01252419⟩
- Ludovic Arnold, Hélène Perrin, Camille Baudesson de Chanville, Marielle Saclier, Patricia Hermand, et al.. CX3CR1 deficiency promotes muscle repair and regeneration by enhancing macrophage ApoE production. Nature Communications, 2015, 6, pp.8972. ⟨10.1038/ncomms9972⟩. ⟨hal-01514445⟩
- Christine Poitou, Claire Perret, François Mathieu, Vinh Truong, Yuna Blum, et al.. Bariatric Surgery Induces Disruption in Inflammatory Signaling Pathways Mediated by Immune Cells in Adipose Tissue: A RNA-Seq Study. PLoS ONE, 2015, 10 (5), pp.e0125718. ⟨10.1371/journal.pone.0125718⟩. ⟨hal-01227880⟩
- Kinga M. Bujakowska, Qi Zhang, Anna M. Siemiatkowska, Qin Liu, Emily Place, et al.. Mutations in IFT172 cause isolated retinal degeneration and Bardet-Biedl syndrome. Human Molecular Genetics, 2015, 24 (1), pp.230-242. ⟨10.1093/hmg/ddu441⟩. ⟨hal-01514441⟩
- Fanny Charbonnier-Beaupel, Marion Malerbi, Cristina Alcacer, Khadija Tahiri, Wassila Carpentier, et al.. Gene Expression Analyses Identify Narp Contribution in the Development of L-DOPA-Induced Dyskinesia. Journal of Neuroscience, 2015, 35 (1), pp.96-111. ⟨10.1523/JNEUROSCI.5231-13.2015⟩. ⟨hal-01514443⟩
- Cyril Dalmasso, Wassila Carpentier, Catherine Guettier, Sophie Camilleri-Broët, Wyllians Vendramini Borelli, et al.. Patterns of chromosomal copy-number alterations in intrahepatic cholangiocarcinoma. BMC Cancer, 2015, 15, pp.126. ⟨10.1186/s12885-015-1111-6⟩. ⟨hal-01211706⟩
- Michel Kielar, Francoise Phan Dinh Tuy, Sara Bizzotto, Cécile Lebrand, Camino De Juan Romero, et al.. Mutations in Eml1 lead to ectopic progenitors and neuronal heterotopia in mouse and human. Nature Neuroscience, 2014, 17 (7), pp.923-933. ⟨10.1038/nn.3729⟩. ⟨hal-01514452⟩
- C. Chauvin, V. Koka, A. Nouschi, V. Mieulet, C. Hoareau-Aveilla, et al.. Ribosomal protein S6 kinase activity controls the ribosome biogenesis transcriptional program. Oncogene, 2014, 33 (4), pp.474-483. ⟨10.1038/onc.2012.606⟩. ⟨hal-01514455⟩
- Mélanie Eyries, David Montani, Barbara Girerd, Claire Perret, Anne Leroy, et al.. EIF2AK4 mutations cause pulmonary veno-occlusive disease, a recessive form of pulmonary hypertension. Nature Genetics, 2014, 46 (1), pp.65+. ⟨10.1038/ng.2844⟩. ⟨hal-01514453⟩
- Ashley Beecham, Nikolaos Patsopoulos, Dionysia Xifara, Mary Davis, Anu Kemppinen, et al.. Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Nature Genetics, 2013, 45 (11), pp.1353-1360. ⟨10.1038/ng.2770⟩. ⟨hal-02565210⟩
- Audrey Baeyens, Louis Pérol, Gwladys Fourcade, Nicolas Cagnard, Wassila Carpentier, et al.. Limitations of IL-2 and Rapamycin in Immunotherapy of Type 1 Diabetes. Diabetes, 2013, 62 (9), pp.3120-3131. ⟨10.2337/db13-0214⟩. ⟨hal-02565238⟩
- Despina Moshous, Emmanuel Martin, Wassila Carpentier, Annick Lim, Isabelle Callebaut, et al.. Whole-exome sequencing identifies Coronin-1A deficiency in 3 siblings with immunodeficiency and EBV-associated B-cell lymphoproliferation. Journal of Allergy and Clinical Immunology, 2013, 131 (6), pp.1594-1603.e9. ⟨10.1016/j.jaci.2013.01.042⟩. ⟨hal-02565338⟩
- Marine Germain, Mélanie Eyries, David Montani, Odette Poirier, Barbara Girerd, et al.. Genome-wide association analysis identifies a susceptibility locus for pulmonary arterial hypertension. Nature Genetics, 2013, 45 (5), pp.518-521. ⟨10.1038/ng.2581⟩. ⟨hal-02565627⟩
- Sigrid Le Clerc, Lieng Taing, Khaled Ezzedine, Julie Latreille, Olivier Delaneau, et al.. A Genome-Wide Association Study in Caucasian Women Points Out a Putative Role of the STXBP5L Gene in Facial Photoaging. Journal of Investigative Dermatology, 2013, 133 (4), pp.929 - 935. ⟨10.1038/jid.2012.458⟩. ⟨hal-01614378⟩
- Laure Ségurel, Frédéric Austerlitz, Bruno Toupance, Mathieu M. Gautier, Joanna L Kelley, et al.. Positive selection of protective variants for type 2 diabetes from the Neolithic onward: a case study in Central Asia. European Journal of Human Genetics, 2013, 21 (10), pp.1146-1151. ⟨10.1038/ejhg.2012.295⟩. ⟨hal-02120826⟩
- Tangui Leguen, Laurent Jullien, Fabien Touzot, Michael Schertzer, Laetitia Gaillard, et al.. Human RTEL1 deficiency causes Hoyeraal- Hreidarsson syndrome with short telomeres and genome instability. Human Molecular Genetics, 2013, 22 (16), pp.3239-3249. ⟨10.1093/hmg/ddt178⟩. ⟨hal-00858583⟩
- Benjamin Terrier, Nicolas Derian, Yoland Schoindre, Wahiba Chaara, Guillaume Geri, et al.. Restoration of regulatory and effector T cell balance and B cell homeostasis in systemic lupus erythematosus patients through vitamin D supplementation.. Arthritis Research and Therapy, 2012, 14 (5), pp.R221. ⟨10.1186/ar4060⟩. ⟨inserm-00768700⟩
- Stephan Klebe, Alexander Lossos, Hamid Azzedine, Emeline Mundwiller, Ruth Sheffer, et al.. KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutations. European Journal of Human Genetics, 2012, 20 (6), pp.645-649. ⟨10.1038/ejhg.2011.261⟩. ⟨hal-02565698⟩
- Kinga Bujakowska, Isabelle Audo, Saddek Mohand-Saïd, Marie-Elise Lancelot, Aline Antonio, et al.. CRB1 mutations in inherited retinal dystrophies.. Human Mutation, 2012, 33 (2), pp.306-15. ⟨10.1002/humu.21653⟩. ⟨inserm-00640122⟩
- Christel Depienne, Delphine Bouteiller, Aurélie Méneret, Ségolène Billot, Sergiu Groppa, et al.. RAD51 haploinsufficiency causes congenital mirror movements in humans. American Journal of Human Genetics, 2012, 90 (2), pp.301--307. ⟨10.1016/j.ajhg.2011.12.002⟩. ⟨hal-01543631⟩
- Hayet Ait Ghezala, Béatrice Jolles, Samia Salhi, Katia Castrillo, Wassila Carpentier, et al.. Translation termination efficiency modulates ATF4 response by regulating ATF4 mRNA translation at 5' short ORFs. Nucleic Acids Research, 2012, 40 (19), pp.9557 - 9570. ⟨10.1093/nar/gks762⟩. ⟨hal-01544180⟩
- Benjamin Terrier, Florence Joly, Thomas Vazquez, Philippe Benech, Michelle Rosenzwajg, et al.. Expansion of Functionally Anergic CD21 −/low Marginal Zone-like B Cell Clones in Hepatitis C Virus Infection-Related Autoimmunity. Journal of Immunology, 2011, 187 (12), pp.6550-6563. ⟨10.4049/jimmunol.1102022⟩. ⟨hal-02565763⟩
- Cécile Jeanpierre, Guillaume Macé, Mélanie Parisot, Vincent Morinière, Audrey Pawtowsky, et al.. RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects. Journal of Medical Genetics, 2011, 48 (7), pp.497. ⟨10.1136/jmg.2010.088526⟩. ⟨hal-00622876⟩
- Yenkel Grinberg-Bleyer, David Saadoun, Audrey Baeyens, Fabienne Billiard, Jérémie D. Goldstein, et al.. Pathogenic T cells have a paradoxical protective effect in murine autoimmune diabetes by boosting Tregs. Journal of Clinical Investigation, 2010, 120 (12), pp.4558-4568. ⟨10.1172/JCI42945⟩. ⟨hal-02565872⟩
- Boris Keren, Aurelia Jacquette, Christel Depienne, Patricia Leite, Alexandra Dürr, et al.. Evidence against haploinsuffiency of human ataxin 10 as a cause of spinocerebellar ataxia type 10. neurogenetics, 2010, 11 (2), pp.273-274. ⟨10.1007/s10048-009-0227-8⟩. ⟨hal-02566579⟩
- Sigrid Le Clerc, Sophie Limou, Cédric Coulonges, Wassila Carpentier, Christian Dina, et al.. Genomewide Association Study of a Rapid Progression Cohort Identifies New Susceptibility Alleles for AIDS (ANRS Genomewide Association Study 03). Journal of Infectious Diseases, 2009, 200 (8), pp.1194-1201. ⟨10.1086/605892⟩. ⟨hal-02566721⟩
- Marie-Paule Beaujard, Sandra Chantot, Michèle Dubois, Boris Keren, Wassila Carpentier, et al.. Atypical deletion of 22q11.2: Detection using the FISH TBX1 probe and molecular characterization with high-density SNP arrays. European Journal of Medical Genetics, 2009, 52 (5), pp.321-327. ⟨10.1016/j.ejmg.2009.05.010⟩. ⟨hal-02566730⟩
- Sophie Limou, Sigrid Le Clerc, Cédric Coulonges, Wassila Carpentier, Christian Dina, et al.. Genomewide Association Study of an AIDS‐Nonprogression Cohort Emphasizes the Role Played by HLA Genes (ANRS Genomewide Association Study 02). Journal of Infectious Diseases, 2009, 199 (3), pp.419-426. ⟨10.1086/596067⟩. ⟨hal-02566791⟩
- Christel Depienne, Delphine Bouteiller, Boris Keren, Emmanuel Cheuret, Karine Poirier, et al.. Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females. PLoS Genetics, 2009, 5 (2), pp.e1000381. ⟨10.1371/journal.pgen.1000381⟩. ⟨hal-02566769⟩
- C Depienne, O Trouillard, C. Saint-Martin, I Gourfinkel-An, D Bouteiller, et al.. Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients. Journal of Medical Genetics, 2008, 46 (3), pp.183-191. ⟨10.1136/jmg.2008.062323⟩. ⟨hal-02566795⟩
- Cyril Dalmasso, Wassila Carpentier, Laurence Meyer, Christine Rouzioux, Cécile Goujard, et al.. Distinct Genetic Loci Control Plasma HIV-RNA and Cellular HIV-DNA Levels in HIV-1 Infection: The ANRS Genome Wide Association 01 Study. PLoS ONE, 2008, 3 (12), pp.e3907. ⟨10.1371/journal.pone.0003907⟩. ⟨hal-02566809⟩
- Irene Mowszowicz, Abiba Doukani, Martine Giacomini. Binding of the androgen receptor to the nuclear matrix of human foreskin. Journal of Steroid Biochemistry, 1988, 29 (6), pp.715-719. ⟨10.1016/0022-4731(88)90173-2⟩. ⟨hal-02575627⟩
Communications dans un congrès
- L. Benarroch, I. Nelson, T. Stojkovic, B Mohand Oumoussa, H. Madry, et al.. P166 Deciphering the genetic cause of oculopharyngodistal myopathy in a French cohort using Cas9-targeted long-read sequencing. 28th International Annual Congress of the World Muscle Society, Oct 2023, Charleston SC, United States. pp.S141, ⟨10.1016/j.nmd.2023.07.298⟩. ⟨hal-04280249⟩
- Karine Zeitouni, Nadjim Chelghoum. Spatial decision tree-application to traffic risk analysis. ACS/IEEE International Conference on Computer Systems and Applications, Jun 2001, Beirut, Lebanon. pp.203-207, ⟨10.1109/aiccsa.2001.933978⟩. ⟨hal-04371594⟩
Poster de conférence
- Badreddine Mohand Oumoussa, Abiba Doukani, Cassandra Gaspar, Franck Bielle. Analyse de la méthylation d’ADN sur puces : étude comparative d’échantillons de tissus congelés et tissus FFPE. 10eme Assises de Génétique Humaine et Médicale, Jan 2020, Tours, France. ⟨hal-02539624⟩
Pré-publications, Documents de travail
- Emma Bergsten, Denis Mestivier, Francoise Donnadieu, Thierry Pedron, Landry Tsoumtsa, et al.. Parvimonas micra , an oral pathobiont associated with colorectal cancer, epigenetically reprograms human primary intestinal epithelial cells. 2022. ⟨pasteur-03689065⟩
Documents récupérés de l'archive ouverte HAL 
