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  1. Münnich, Fanny [Author] ; Universität Leipzig, Sächsische Akademie der Wissenschaften zu Leipzig, Franz Steiner Verlag

    Der sächsische Adel an den Universitäten Europas : Universitätsbesuch, Studienalltag und Lebenswege in Spätmittelalter und beginnender Frühneuzeit

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    [Leipzig]: Sächsische Akademie der Wissenschaften zu Leipzig, [2020] ; Stuttgart: In Kommission bei Franz Steiner Verlag, [2020]

    Published in: Quellen und Forschungen zur sächsischen und mitteldeutschen Geschichte ; Band 45

    Saxon Bibliography (Sächsische Bibliografie)
  2. Münnich, Fanny [Author] ; Universität Leipzig

    Der sächsische Adel an den Universitäten Europas : Universitätsbesuch, Studienalltag und Lebenswege in Spätmittelalter und beginnender Frühneuzeit / Teilband 1

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    Leipzig: Sächsische Akademie der Wissenschaften zu Leipzig, [2020] ; Stuttgart: In Kommission bei Franz Steiner Verlag, [2020]

    Published in: Der sächsische Adel an den Universitäten Europas ; 1 - Quellen und Forschungen zur sächsischen und mitteldeutschen Geschichte ; 45,1

    Saxon Bibliography (Sächsische Bibliografie)
  3. Münnich, Fanny [Author] ; Universität Leipzig

    Der sächsische Adel an den Universitäten Europas : Universitätsbesuch, Studienalltag und Lebenswege in Spätmittelalter und beginnender Frühneuzeit / Teilband 2, Anhang

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    [Leipzig]: Sächsische Akademie der Wissenschaften zu Leipzig, [2020] ; Stuttgart: In Kommission bei Franz Steiner Verlag, [2020]

    Published in: Der sächsische Adel an den Universitäten Europas ; 2 - Quellen und Forschungen zur sächsischen und mitteldeutschen Geschichte ; 45,2

    Saxon Bibliography (Sächsische Bibliografie)
  7. Mendelssohn Bartholdy, Felix [Author] ; Münnich, Stefan [Editor]; Schiwietz, Lucian [Editor]; Wald, Uta [Editor]

    Sämtliche Briefe / Band 12, Februar 1847 bis November 1847 : Gesamtregister der Bände 1 bis 12 / herausgegeben und kommentiert von Stefan Münnich, Lucian Schiwietz und Uta Wald - [Kassel ; Basel ; London ; New York ; Praha$nBärenreiter]

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    [2017]

    Published in: Sämtliche Briefe / Felix Mendelssohn Bartholdy ; 12

  8. Münnich, Fanny [Author] ; Franz Steiner Verlag

    Der sächsische Adel an den Universitäten Europas : Universitätsbesuch, Studienalltag und Lebenswege in Spätmittelalter und beginnender Frühneuzeit - [1. Auflage]

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    Stuttgart: Franz Steiner Verlag, 2021

    Published in: Quellen und Forschungen zur sächsischen und mitteldeutschen Geschichte ; 47

    Saxon Bibliography (Sächsische Bibliografie)
  10. Münnich, Fanny [Author]

    Konrad Wimpinas Beschreibung der Stadt und Universität Leipzig : Edition und Übersetzung der Almae universitatis studii Lipczensis descriptio

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    2011

    Published in: Neues Archiv für sächsische Geschichte ; 82(2011), Seite 1-60

    Saxon Bibliography (Sächsische Bibliografie)
  13. Le Goff, Carine; Morice-Picard, Fanny; Dagoneau, Nathalie; Wang, Lauren W; Perrot, Claire; Crow, Yanick J; Bauer, Florence; Flori, Elisabeth; Prost-Squarcioni, Catherine; Krakow, Deborah; Ge, Gaoxiang; Greenspan, Daniel S; Bonnet, Damien; Le Merrer, Martine; Munnich, Arnold; Apte, Suneel S; Cormier-Daire, Valérie

    ADAMTSL2 mutations in geleophysic dysplasia demonstrate a role for ADAMTS-like proteins in TGF-β bioavailability regulation

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    Springer Science and Business Media LLC, 2008

    Published in: Nature Genetics

  14. Alby, Caroline; Piquand, Kevin; Huber, Céline; Megarbané, André; Ichkou, Amale; Legendre, Marine; Pelluard, Fanny; Encha-Ravazi, Ferechté; Abi-Tayeh, Georges; Bessières, Bettina; El Chehadeh-Djebbar, Salima; Laurent, Nicole; Faivre, Laurence; Sztriha, László; Zombor, Melinda; Szabó, Hajnalka; Failler, Marion; Garfa-Traore, Meriem; Bole, Christine; Nitschké, Patrick; Nizon, Mathilde; Elkhartoufi, Nadia; Clerget-Darpoux, Françoise; Munnich, Arnold; [...]

    Mutations in KIAA0586 Cause Lethal Ciliopathies Ranging from a Hydrolethalus Phenotype to Short-Rib Polydactyly Syndrome

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    Elsevier BV, 2015

    Published in: The American Journal of Human Genetics

  15. Alby, Caroline; Piquand, Kevin; Huber, Céline; Megarbané, André; Ichkou, Amale; Legendre, Marine; Pelluard, Fanny; Encha-Ravazi, Ferechté; Abi-Tayeh, Georges; Bessières, Bettina; El Chehadeh-Djebbar, Salima; Laurent, Nicole; Faivre, Laurence; Sztriha, László; Zombor, Melinda; Szabó, Hajnalka; Failler, Marion; Garfa-Traore, Meriem; Bole, Christine; Nitschké, Patrick; Nizon, Mathilde; Elkhartoufi, Nadia; Clerget-Darpoux, Françoise; Munnich, Arnold; [...]

    Mutations in KIAA0586 Cause Lethal Ciliopathies Ranging from a Hydrolethalus Phenotype to Short-Rib Polydactyly Syndrome

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    Elsevier BV, 2015

    Published in: The American Journal of Human Genetics

  16. Juven, Aurélien; Nambot, Sophie; Piton, Amélie; Jean-Marçais, Nolwenn; Masurel, Alice; Callier, Patrick; Marle, Nathalie; Mosca-Boidron, Anne-Laure; Kuentz, Paul; Philippe, Christophe; Chevarin, Martin; Duffourd, Yannis; Gautier, Elodie; Munnich, Arnold; Rio, Marlène; Rondeau, Sophie; El Chehadeh, Salima; Schaefer, Élise; Gérard, Bénédicte; Bouquillon, Sonia; Delorme, Catherine Vincent; Francannet, Christine; Laffargue, Fanny; Gouas, Laetitia; [...]

    Primrose syndrome: a phenotypic comparison of patients with a ZBTB20 missense variant versus a 3q13.31 microdeletion including ZBTB20

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    Springer Science and Business Media LLC, 2020

    Published in: European Journal of Human Genetics

  17. Bal, Elodie; Park, Hyun-Sook; Belaid-Choucair, Zakia; Kayserili, Hülya; Naville, Magali; Madrange, Marine; Chiticariu, Elena; Hadj-Rabia, Smail; Cagnard, Nicolas; Kuonen, Francois; Bachmann, Daniel; Huber, Marcel; Le Gall, Cindy; Côté, Francine; Hanein, Sylvain; Rosti, Rasim Özgür; Aslanger, Ayca Dilruba; Waisfisz, Quinten; Bodemer, Christine; Hermine, Olivier; Morice-Picard, Fanny; Labeille, Bruno; Caux, Frédéric; Mazereeuw-Hautier, Juliette; [...]

    Mutations in ACTRT1 and its enhancer RNA elements lead to aberrant activation of Hedgehog signaling in inherited and sporadic basal cell carcinomas

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    Springer Science and Business Media LLC, 2017

    Published in: Nature Medicine

  18. Démurger, Florence; Ichkou, Amale; Mougou-Zerelli, Soumaya; Le Merrer, Martine; Goudefroye, Géraldine; Delezoide, Anne-Lise; Quélin, Chloé; Manouvrier, Sylvie; Baujat, Geneviève; Fradin, Mélanie; Pasquier, Laurent; Megarbané, André; Faivre, Laurence; Baumann, Clarisse; Nampoothiri, Sheela; Roume, Joëlle; Isidor, Bertrand; Lacombe, Didier; Delrue, Marie-Ange; Mercier, Sandra; Philip, Nicole; Schaefer, Elise; Holder, Muriel; Krause, Amanda; [...]

    New insights into genotype–phenotype correlation for GLI3 mutations

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    Springer Science and Business Media LLC, 2015

    Published in: European Journal of Human Genetics

  19. Laquerriere, Annie; Jaber, Dana; Abiusi, Emanuela; Maluenda, Jérome; Mejlachowicz, Dan; Vivanti, Alexandre; Dieterich, Klaus; Stoeva, Radka; Quevarec, Loic; Nolent, Flora; Biancalana, Valerie; Latour, Philippe; Sternberg, Damien; Capri, Yline; Verloes, Alain; Bessieres, Bettina; Loeuillet, Laurence; Attie-Bitach, Tania; Martinovic, Jelena; Blesson, Sophie; Petit, Florence; Beneteau, Claire; Whalen, Sandra; Marguet, Florent; [...]

    Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita

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    BMJ, 2022

    Published in: Journal of Medical Genetics

  20. Chevarin, Martin; Duffourd, Yannis; A. Barnard, Rebecca; Moutton, Sébastien; Lecoquierre, François; Daoud, Fatma; Kuentz, Paul; Cabret, Caroline; Thevenon, Julien; Gautier, Elodie; Callier, Patrick; St-Onge, Judith; Jouan, Thibaud; Lacombe, Didier; Delrue, Marie Ange; Goizet, Cyril; Morice-Picard, Fanny; Van-Gils, Julien; Munnich, Arnold; Lyonnet, Stanislas; Cormier-Daire, Valérie; Baujat, Geneviève; Holder, Muriel; Petit, Florence; [...]

    Excess of de novo variants in genes involved in chromatin remodelling in patients with marfanoid habitus and intellectual disability

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    BMJ, 2020

    Published in: Journal of Medical Genetics