S
Stefan A. Haas
Researcher at Max Planck Society
Publications - 88
Citations - 13764
Stefan A. Haas is an academic researcher from Max Planck Society. The author has contributed to research in topics: Gene & X-linked intellectual disability. The author has an hindex of 47, co-authored 86 publications receiving 11715 citations. Previous affiliations of Stefan A. Haas include German Cancer Research Center.
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Intellectual Disability and Early-Onset Parkinson Disease with a-Synuclein Pathology
Gabrielle R. Wilson,Catriona McLean,Maila Giannandrea,Charles A. Galea,Jessica R. Riseley,Elizabeth A. Fitzpatrick,Stefan A. Haas,Kate Pope,Kirk J. Hogan,Ronald G. Gregg,Catherine J. Bromhead,David S. Wargowski,Christopher Lawrence,Paul A. James,Andrew Churchyard,Yujing Gao,Dean Phelan,Greta Gillies,Nicholas Salce,Lynn Stanford,Maria Lidia Mignogna,Susan J. Hayflick,Richard J. Leventer,Martin B. Delatycki,George D. Mellick,Vera M. Kalscheuer,Melanie Bahlo,David J. Amor,Paul J. Lockhart +28 more
TL;DR: Overall, it is shown that loss-of-function mutations in RAB39B cause intellectual disability and pathologically confirmed early-onset Parkinson disease and potentially other neurodegenerative disorders.
Massively parallel sequencing in >250 families with X-linked intellectual disability
Vera M. Kalscheuer,Hao Hu,Stefan A. Haas,Jamel Chelly,Hilde Van Esch,M Rayknaud,A.P.M. de Brouwer,T Zemotjel,Stefanie Weinert,Guy Froyen,Sgm Frynts,Frédéric Laumonnier,Michael I. Love,Hugues Richard,Anne-Katrin Emde,M Bienek,C Jensen,Melanie Hambrock,Claudia Langnick,Mirjam Feldkamp,Willemijn M. Wissink-Lindhout,Nicolas Lebrun,L. Castelnau,Marie Shaw,Mark A. Corbett,Alison Gardner,Saffron A.G. Willis-Owen,C Tan,Kathryn Friend,Stefanie Belet,Kep Van Roozendaal,M Jimenez-Pocquet,Marie-Pierre Moizard,Nathalie Ronce,Ruping Sun,S O'Keeffef,Ramu Chenna,A Mysickova,Jonathan Göke,Anna Hackett,Michael Field,Eric Haan,John Nelson,Gillian Turner,Gareth Baynam,Gabriele Gillessen-Kaesbach,Ulrich Müller,Daniela Steinberger,Bartłomiej Budny,Magdalena Badura-Stronka,Anna Latos-Bielenska,Lilian Bomme Ousager,Peter Wieacker,GR Criado,Marie-Louise Bondeson,Andreas Dufke,Monika Cohen,L. Van Maldergem,C Cincent-delorme,Bernard Echenne,B. Simon-Bouy,Tjitske Kleefstra,Marjolein H. Willemsen,Jean-Pierre Fryns,Koenraad Devriendt,Martin Vingron,Klaus Wrogemann,Reinhard Ullmann,Jozef Gecz,Andreas Tzschach,H Van Bokhoven,J Jentsch,Wei Chen,Hans-Hilger Ropers +73 more
Next-generation sequencing in >240 families with X-linked intellectual disability
Vera M. Kalscheuer,Hao Hu,Stefan A. Haas,Jamel Chelly,Hilde Van Esch,Martine Raynaud,Sgm Frints,De Brouwer A,Jozef Gecz,Stefanie Weinert,Z Zemojtel,Michael I. Love,Guy Froyen,Frédéric Laumonnier,Hugues Richard,A Emde,M Bienek,C Jensen,M Hambrock,Nicolas Lebrun,Mark A. Corbett,C Tan,Cep Van Rozendaal,M Pocquet,Nathalie Ronce,E Sun,A Hacket,Michael Field,Eric Haan,John Nelson,Gillian M. Turner,G Baynam,G Gillessen-Kaesbach,U Mueller,Bartłomiej Budny,Magdalena Badura-Stronka,Anna Latos-Bielenska,Monika Cohen,Tjitske Kleefstra,Reinhard Ullmann,P Wieacker,Andreas Dufke,GR Criado,M Bondeson,H Van Bokhoven,A Rzschach,Klaus Wrogemann,Thomas J. Jentsch,Wei Chen,H.H. Ropers +49 more