Heidi Stöhr - Institute for Human Genetics, University of Regensburg

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论文共 54 篇作者统计合作学者相似作者

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18-Years of Single-Centre DNA Testing in over 7000 Index Cases with Inherited Retinal Dystrophies and Optic Neuropathies

Christina Kiel, Fabiola Biasella,Heidi Stöhr, Philipp Rating,Georg Spital, Ulrich Kellner, Karsten Hufendiek,Cord Huchzermeyer, Herbert Jaegle,Klaus Ruether, Bernhard H F Weber

Scientific reportsno. 1 (2024): 25529-25529

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Mitochondrial and Cellular Function in Fibroblasts and Reprogrammed Neural Cells: Insights into Major Depression As a Mitochondria-Associated Disease

Christian Wetzel,Iseline Cardon,Sonja Grobecker, Selin Kücükoktay,Stefanie Bader,Tatjana Jahner,Caroline Nothdurfter, Kevin-Thomas Koschitzki,Mark Berneburg,Heidi Stöhr,Bernhard Weber,Marcus Höring, Gerhard Liebisch,Frank Braun, Tanja Rothammer-Hampl,Markus Riemenschneider,Rainer Rupprecht,Vladimir Milenkovic

crossref（2023）

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Mitochondrial and cellular function in fibroblasts and reprogrammed neural cells: insights into major depression as a mitochondria-associated disease

Christian H. Wetzel,Iseline Cardon,Sonja Grobecker, Selin Kücükoktay,Stefanie Bader,Tatjana Jahner,Caroline Nothdurfter, Kevin-Thomas Koschitzki,Mark Berneburg,Heidi Stöhr,Bernhard H. F. Weber,Marcus Höring,Gerhard Liebisch,Frank Braun, Tanja Rothammer-Hampl,Markus J. Riemenschneider,Rainer Rupprecht,Vladimir M. Milenkovic

Research Square (Research Square) (2023)

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Association of Sex With Frequent and Mild ABCA4 Alleles in Stargardt Disease (vol 138, pg 1035, 2020)

Esmee H. Runhart,Mubeen Khan, Stephaine S. Cornelis,Susanne Roosing,Marta Del Pozo-Valero,Tina M. Lamey,Petra Liskova,Lisa Roberts,Heidi Stohr,Caroline C. W. Klaver,Carel B. Hoyng,Frans P. M. Cremers,Claire-Marie Dhaenens

JAMA OPHTHALMOLOGY（2021）

引用1浏览0引用

Wide-field Optical Coherence Tomography in ABCA4-associated Inherited Retinal Dystrophies

Mohammad Saleh,Heidi Stöhr,Christina Kiel,Simone Kellner,Silke Weinitz,Ghazaleh Farmand,Bernhard H. F. Weber,Albrecht Lommatzsch,Ulrich Kellner

Journal of Translational Genetics and Genomics (2021)

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Neue Techniken Zur Quantifizierung Des Farbsinns Bei Störungen Der Zapfenfunktion

Huchzermeyer Cord,Fars Julien,Stöhr Heidi,Kremers Jan

Der Ophthalmologeno. 2 (2020): 144-153

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Resolving the Dark Matter of ABCA4 for 1054 Stargardt Disease Probands Through Integrated Genomics and Transcriptomics

Mubeen Khan,Stéphanie S. Cornelis,Marta Del Pozo-Valero,Laura Whelan,Esmee H. Runhart,Ketan Mishra, Femke Bults,Yahya AlSwaiti,Alaa AlTalbishi,Elfride De Baere,Sandro Banfi,Eyal Banin,Miriam Bauwens,Tamar Ben-Yosef,Camiel J. F. Boon,L. Ingeborgh van den Born,Sabine Defoort,Aurore Devos,Adrian Dockery,Lubica Dudakova,Ana Fakin,G. Jane Farrar,Juliana Maria Ferraz Sallum,Kaoru Fujinami,Christian Gilissen,Damjan Glavač,Michael B. Gorin,Jacquie Greenberg,Takaaki Hayashi,Ymkje M. Hettinga,Alexander Hoischen,Carel B. Hoyng,Karsten Hufendiek,Herbert Jägle,Smaragda Kamakari,Marianthi Karali,Ulrich Kellner,Caroline C. W. Klaver,Bohdan Kousal,Tina M. Lamey,Ian M. MacDonald,Anna Matynia,Terri L. McLaren,Marcela D. Mena,Isabelle Meunier, Rianne Miller,Hadas Newman, Buhle Ntozini,Monika Oldak,Marc Pieterse,Osvaldo L. Podhajcer,Bernard Puech,Raj Ramesar,Klaus Rüther,Manar Salameh,Mariana Vallim Salles,Dror Sharon,Francesca Simonelli,Georg Spital,Marloes Steehouwer,Jacek P. Szaflik,Jennifer A. Thompson,Caroline Thuillier,Anna M. Tracewska, Martine van Zweeden,Andrea L. Vincent,Xavier Zanlonghi,Petra Liskova,Heidi Stöhr,John N. De Roach,Carmen Ayuso,Lisa Roberts,Bernhard H. F. Weber,Claire‐Marie Dhaenens,Frans P. M. Cremers

Genetics in medicine（2020）

引用87浏览0WOS引用

Stufendiagnostik Einer CSNB1 Mit NYX- Genmutation

P. Rating,H. Stöhr, C. Neuhaus,B. Schaperdoth-Gerlings,M. R. R. Böhm, M.‑A. Freimuth,N. E. Bechrakis

Der Ophthalmologeno. 12 (2019): 1207-1211

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