Müller Amelie Johanna - Institute of Medical Genetics and Applied Genomics, University of Tuebingen

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论文共 17 篇作者统计合作学者相似作者

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Rare Predicted Deleterious FEZF2 Variants Are Associated with a Neurodevelopmental Phenotype

Alison Garber, Lisa S. Weingarten,Nicolas J. Abreu,Houda Zghal Elloumi,Tobias Haack, Clara Hildebrant,Nuria Martinez-Gil,Jennifer Mathews,Amelie Johanna Mueller,Irene Valenzuela Palafoll,Connolly Steigerwald,Wendy K. Chung

AMERICAN JOURNAL OF MEDICAL GENETICS PART Ano. 7 (2024)

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Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder

Maria B. Christensen,Amanda M. Levy,Nazanin A. Mohammadi,Marcello Niceta,Rauan Kaiyrzhanov,Maria Lisa Dentici,Chadi Al Alam,Viola Alesi,Valerie Benoit, Kailash P. Bhatia,Tatjana Bierhals,Christian M. Bosselmann,Julien Buratti,Bert Callewaert,Berten Ceulemans,Perrine Charles,Matthias De Wachter,Mohammadreza Dehghani,Erika D'haenens,Martine Doco-Fenzy, Michaela Gessner, Cyrielle Gobert,Ulviyya Guliyeva,Tobias B. Haack,Trine B. Hammer,Tilman Heinrich,Maja Hempel,Theresia Herget,Ute Hoffmann,Judit Horvath,Henry Houlden,Boris Keren,Christina Kresge,Candy Kumps,Damien Lederer,Alban Lermine,Francesca Magrinelli,Reza Maroofian,Mohammad Yahya Vahidi Mehrjardi,Mahdiyeh Moudi,Amelie J. Mueller,Anna J. Oostra,Beth A. Pletcher,David Ros-Pardo, Shanika Samarasekera,Marco Tartaglia,Kristof Van Schil,Julie Vogt,Evangeline Wassmer,Juliane Winkelmann,Maha S. Zaki,Michael Zech,Holger Lerche,Francesca Clementina Radio,Paulino Gomez-Puertas,Rikke S. Moller,Zeynep Tuemer

CLINICAL GENETICS（2022）

引用2浏览0WOS引用

Variant in the PLCG2 Gene May Cause a Phenotypic Overlap of APLAID/PLAID: Case Series and Literature Review

Tatjana Welzel,Lea Oefelein,Ursula Holzer,Amelie Müller,Benita Menden,Tobias B Haack, Miriam Groβ,Jasmin B Kuemmerle-Deschner

JOURNAL OF CLINICAL MEDICINE（2022）

引用3浏览0WOS引用

Agustí Rodríguez-Palmero,Melissa Maria Boerrigter,David Gómez-Andrés,Kimberly A. Aldinger,Íñigo Marcos-Alcalde,Bernt Popp,David B. Everman,Alysia Kern Lovgren,Stephanie Arpin,Vahid Bahrambeigi,Gea Beunders,Anne-Marie Bisgaard,V. A. Bjerregaard,Ange-Line Bruel,Thomas D. Challman,Benjamin Cogné,Christine Coubes,Stella A. de Man,Anne-Sophie Denommé-Pichon,Thomas J. Dye,Frances Elmslie,Lars Feuk,Sixto García-Miñaúr,Tracy Gertler,Elisa Giorgio,Nicolas Gruchy,Tobias B. Haack,Chad R. Haldeman-Englert,Bjørn Ivar Haukanes,Juliane Hoyer,Anna C. E. Hurst,Bertrand Isidor,Maria Johansson Soller,Sulagna Kushary,Malin Kvarnung,Yuval E. Landau,Kathleen A. Leppig,Anna Lindstrand,Lotte Kleinendorst,Alex MacKenzie,Giorgia Mandrile,Bryce A. Mendelsohn,Setareh Moghadasi,Jenny E. Morton,Sebastien Moutton,Amelie J. Müller,Melanie O’Leary,Marta Pacio-Míguez,Maria Palomares-Bralo,Sumit Parikh,Rolph Pfundt,Ben Pode-Shakked,Anita Rauch,Elena Repnikova,Anya Revah-Politi,Meredith J. Ross,Claudia A. L. Ruivenkamp,Elisabeth Sarrazin,Juliann M. Savatt,Agatha Schlüter,Bitten Schönewolf-Greulich,Zohra Shad,Charles Shaw-Smith,Joseph T. Shieh, Motti Shohat,Stephanie Spranger,Heidi Thiese,Frederic Tran Mau-Them,Bregje van Bon, Ineke van de Burgt,Ingrid M. B. H. van de Laar, Esmée van Drie,Mieke M. van Haelst,Conny M. van Ravenswaaij-Arts,Edgard Verdura,Antonio Vitobello,Stephan Waldmüller,Sharon Whiting,Christiane Zweier,Carlos E. Prada,Bert B. A. de Vries,William B. Dobyns,Simone F. Reiter,Paulino Gómez-Puertas,Aurora Pujol,Zeynep Tümer

Genetics in Medicine（2021）

引用11浏览0WOS引用

Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia

American journal of human genetics（2020）

引用26浏览0WOS引用

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