• 
  Binnaz Yalcin, Jonathan Flint. Association studies in outbred mice in a new era of full-genome sequencing. Mammalian Genome, 2012, 23, pp.719 - 726. ⟨10.1007/s00335-012-9409-z⟩. ⟨inserm-03949489⟩
• 
  Binnaz Yalcin, David J Adams, Jonathan Flint, Thomas M Keane. Next-generation sequencing of experimental mouse strains. Mammalian Genome, 2012, 23, pp.490 - 498. ⟨10.1007/s00335-012-9402-6⟩. ⟨inserm-03949475⟩
• 
  Thomas Keane, Kim Wong, David Adams, Jonathan Flint, Alexandre Reymond, et al.. Identification of structural variation in mouse genomes. Frontiers in Genetics, 2014, 5, pp.192. ⟨10.3389/fgene.2014.00192⟩. ⟨inserm-03949464⟩
• 
  Maria Nicla Loviglio, Thomas Arbogast, Aia Elise Jønch, Stephan C Collins, Konstantin Popadin, et al.. The Immune Signaling Adaptor LAT Contributes to the Neuroanatomical Phenotype of 16p11.2 BP2-BP3 CNVs. American Journal of Human Genetics, 2017, 101, pp.564 - 577. ⟨10.1016/j.ajhg.2017.08.016⟩. ⟨inserm-03948660⟩
• 
  Zhengzheng S Liang, Irene Cimino, Binnaz Yalcin, Narayanan Raghupathy, Valerie E Vancollie, et al.. Trappc9 deficiency causes parent-of-origin dependent microcephaly and obesity. PLoS Genetics, 2020, 16 (9), pp.e1008916. ⟨10.1371/journal.pgen.1008916⟩. ⟨inserm-03948614⟩
• 
  Norine Voisin, Rhonda E Schnur, Sofia Douzgou, Susan M Hiatt, Cecilie F Rustad, et al.. Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy. American Journal of Human Genetics, 2021, 108, pp.857 - 873. ⟨10.1016/j.ajhg.2021.04.001⟩. ⟨inserm-03948529⟩
• 
  Delphine Lapaillerie, Benoît Lelandais, Eric Mauro, Floriane Lagadec, Camille Tumiotto, et al.. Modulation of the intrinsic chromatin binding property of HIV-1 integrase by LEDGF/p75. Nucleic Acids Research, 2021, 49 (19), pp.11241-11256. ⟨10.1093/nar/gkab886⟩. ⟨hal-03795503⟩
• 
  Lettie E Rawlins, Hashem Almousa, Shazia Khan, Stephan C Collins, Miroslav P Milev, et al.. Biallelic variants in TRAPPC10 cause a microcephalic TRAPPopathy disorder in humans and mice. PLoS Genetics, 2022, 18 (3), pp.e1010114. ⟨10.1371/journal.pgen.1010114⟩. ⟨inserm-03944752⟩
• 
  Sylvie Nguyen, Meghna Kannan, Marion Gaborit, Stephan C Collins, Binnaz Yalcin. Quantitative Neuroanatomical Phenotyping of the Embryonic Mouse Brain. Current Protocols, 2022, 2, pp.e509. ⟨10.1002/cpz1.509⟩. ⟨inserm-03944654⟩
• 
  Stephan C Collins, Valerie E Vancollie, Anna Mikhaleva, Christel Wagner, Rebecca Balz, et al.. Characterization of Two Mouse Chd7 Heterozygous Loss-of-Function Models Shows Dysgenesis of the Corpus Callosum and Previously Unreported Features of CHARGE Syndrome. International Journal of Molecular Sciences, 2022, 23 (19), pp.11509. ⟨10.3390/ijms231911509⟩. ⟨inserm-03944621⟩
• 
  Evgeny B. Pichkur, Alena Paleskava, Andrey G. Tereshchenkov, Pavel Kasatsky, Ekaterina S. Komarova, et al.. Insights into the improved macrolide inhibitory activity from the high-resolution cryo-EM structure of dirithromycin bound to the E. coli 70S ribosome. RNA, 2020, 26 (6), pp.715-723. ⟨10.1261/rna.073817.119⟩. ⟨hal-03700147⟩
• 
  Juliette Piard, Matthieu Béreau, Wenshu Xiang Wei, Thomas Wirth, Daniel Amsallem, et al.. The GRIA3 c.2477G > A Variant Causes an Exaggerated Startle Reflex, Chorea, and Multifocal Myoclonus. Movement Disorders, 2020, 35 (7), pp.1224-1232. ⟨10.1002/mds.28058⟩. ⟨hal-03669746⟩
• 
  Susanna Säisä-Borreill, Guillaume Davidson, Thomas Kleiber, Andréa Thevenot, Elisabeth Martin, et al.. General transcription factor TAF4 antagonizes epigenetic silencing by Polycomb to maintain intestine stem cell functions.. Cell death and differentiation, 2023, ⟨10.1038/s41418-022-01109-6⟩. ⟨hal-03942206⟩
• 
  Raquel Mela López. Thioredoxin reductase in Anopheles gambiae mosquitoes : role in redox homeostasis maintenance and manipulation for vector control. Human health and pathology. Université de Strasbourg; Justus-Liebig-Universität (Giessen, Allemagne), 2019. English. ⟨NNT : 2019STRAJ116⟩. ⟨tel-03941394⟩
• 
  Birgit Ritschka, Tania Knauer-Meyer, Daniel Sampaio Gonçalves, Alba Mas Malavila, Jean-Luc Plassat, et al.. The senotherapeutic drug ABT-737 disrupts aberrant p21 expression to restore liver regeneration in adult mice. Genes and Development, 2020, 34 (7-8), pp.489-494. ⟨10.1101/gad.332643.119⟩. ⟨hal-03715508⟩
• 
  Anna Niewiadomska-Cimicka, Antoine Hache, Stéphanie Le Gras, Céline Keime, Tao Ye, et al.. Polyglutamine-expanded ATXN7 alters a specific epigenetic signature underlying photoreceptor identity gene expression in SCA7 mouse retinopathy. Journal of Biomedical Science, 2022, 107, ⟨10.1186/s12929-022-00892-1⟩. ⟨hal-03935562⟩
• 
  Monica Peña Luna. Functional study of the Elongator complex from activity to diseases : characterization of Kti12, a cofactor with a kinase domain. Human health and pathology. Université de Strasbourg, 2021. English. ⟨NNT : 2021STRAJ033⟩. ⟨tel-03934767⟩
• 
  Guilherme Monteiro Oliveira. Modeling chromatin dynamics using Gaussian processes and polymer physics. Human health and pathology. Université de Strasbourg, 2021. English. ⟨NNT : 2021STRAJ006⟩. ⟨tel-03934754⟩
• 
  Karima Habbas. La diacyglycérol kinase kappa (Dgkκ) comme nouvelle cible thérapeutique dans le modèle murin Fmrl-KO du syndrome de l'X fragile. Médecine humaine et pathologie. Université de Strasbourg, 2020. Français. ⟨NNT : 2020STRAJ087⟩. ⟨tel-03934698⟩
• 
  Ioanna Mitrentsi. Double strand break repair in human heterochromatin. Human health and pathology. Université de Strasbourg, 2020. English. ⟨NNT : 2020STRAJ082⟩. ⟨tel-03934681⟩

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