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Prof. Dr. André Wiesmann da Silva Reis
List of publications:
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Lehrstuhl für Humangenetik
Award(s)
(2)
Project Leads
(5)
Project Memberships
(2)
Publications
(234)
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Journal article
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Book chapter / Article in edited volumes
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ARID1B-related disorder in 87 adults: Natural history and self-sustainability (2024)
van der Sluijs PJ, Gösgens M, Dingemans AJ, Striano P, Riva A, Mignot C, Faudet A, et al.
Journal article
Nachruf John M. Opitz, geboren in Hamburg am 15.08.1935, verstorben 31. Oktober 2023 in Salt Lake City, Utah, U. S. A. (2024)
Rauch A, Reis A
Journal article
Further delineation of the SCAF4-associated neurodevelopmental disorder (2024)
Schmid CM, Gregor A, Ruiz A, Manso Bazús C, Herman I, Ammouri F, Kotzaeridou U, et al.
Journal article
Determinants Affecting the Clinical Implementation of a Molecularly Informed Molecular Tumor Board Recommendation: Experience from a Tertiary Cancer Center. (2023)
Tögel L, Schubart C, Lettmaier S, Neufert C, Hoyer J, Wolff K, Moskalev E, et al.
Journal article
Association of mineral and bone biomarkers with adverse cardiovascular outcomes and mortality in the German Chronic Kidney Disease (GCKD) cohort (2023)
Reimer KC, Nadal J, Meiselbach H, Schmid M, Schultheiss UT, Kotsis F, Stockmann H, et al.
Journal article
Different MAPT haplotypes influence expression of total MAPT in postmortem brain tissue (2023)
Tauber CV, Schwarz SC, Rösler TW, Arzberger T, Gentleman S, Windl O, Krumbiegel M, et al.
Journal article
Analysis of genetically determined gene expression suggests role of inflammatory processes in exfoliation syndrome (2023)
Hirbo JB, Pasutto F, Gamazon ER, Evans P, Pawar P, Berner D, Sealock J, et al.
Journal article
Ex Vivo Chromosomal Radiosensitivity Testing in Patients with Pathological Germline Variants in Breast Cancer High-Susceptibility Genes BReast CAncer 1 and BReast CAncer 2 (2023)
Zuhair Kassem T, Wunderle M, Kuhlmann L, Rübner M, Hübner H, Hoyer J, Reis A, et al.
Journal article
LHX2 haploinsufficiency causes a variable neurodevelopmental disorder (2023)
Schmid CM, Gregor A, Costain G, Morel CF, Massingham L, Schwab J, Quélin C, et al.
Journal article
Pathogenic SCN2A variants cause early-stage dysfunction in patient-derived neurons (2023)
Asadollahi R, Delvendahl , Muff R, Tan G, Rodrieguez DG, Turan S, Russo M, et al.
Journal article
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